Item | Value |
---|---|
geneid | 54790 |
ensemblid | ENSG00000168769.14 |
hgncid | 25941 |
symbol | TET2 |
name | tet methylcytosine dioxygenase 2 |
refseq_nuc | NM_001127208.3 |
refseq_prot | NP_001120680.1 |
ensembl_nuc | ENST00000380013.9 |
ensembl_prot | ENSP00000369351.4 |
mane_status | MANE Select |
chr | chr4 |
start | 105146876 |
end | 105279803 |
strand | + |
ver | v1.2 |
region | chr4:105146876-105279803 |
region5000 | chr4:105141876-105284803 |
regionname0 | TET2_chr4_105146876_105279803 |
regionname5000 | TET2_chr4_105141876_105284803 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 2002 | 133 | 23 | 33 | 51 | 9 | 16 | 39 | TET2_chr4_105141876_105284803 | TET2 | MEQDR others(1997): Show |
chr4 | 105141876 | 105284803 |
a0002 | 0/0 | 2002 | 60 | 2 | 10 | 32 | 4 | 12 | 26 | TET2_chr4_105141876_105284803 | TET2 | MEQDR others(1997): Show |
chr4 | 105141876 | 105284803 |
a0003 | 0/0 | 2002 | 45 | 0 | 5 | 38 | 1 | 1 | 31 | TET2_chr4_105141876_105284803 | TET2 | MEQDR others(1997): Show |
chr4 | 105141876 | 105284803 |
a0004 | 0/0 | 2002 | 45 | 26 | 4 | 14 | 0 | 1 | 13 | TET2_chr4_105141876_105284803 | TET2 | MEQDR others(1997): Show |
chr4 | 105141876 | 105284803 |
a0005 | 0/1 | 2002 | 20 | 7 | 7 | 3 | 0 | 2 | 1 | TET2_chr4_105141876_105284803 | TET2 | MEQDR others(1997): Show |
chr4 | 105141876 | 105284803 |
a0006 | 0/0 | 2002 | 17 | 16 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | MEQDR others(1997): Show |
chr4 | 105141876 | 105284803 |
a0007 | 0/0 | 2002 | 4 | 1 | 1 | 0 | 0 | 2 | 0 | TET2_chr4_105141876_105284803 | TET2 | MEQDR others(1997): Show |
chr4 | 105141876 | 105284803 |
a0008 | 0/0 | 2002 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | MEQDR others(1997): Show |
chr4 | 105141876 | 105284803 |
a0009 | 0/0 | 2002 | 3 | 0 | 0 | 2 | 0 | 1 | 1 | TET2_chr4_105141876_105284803 | TET2 | MEQDR others(1997): Show |
chr4 | 105141876 | 105284803 |
a0010 | 0/0 | 2002 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TET2_chr4_105141876_105284803 | TET2 | MEQDR others(1997): Show |
chr4 | 105141876 | 105284803 |
a0011 | 0/0 | 2002 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | MEQDR others(1997): Show |
chr4 | 105141876 | 105284803 |
a0012 | 0/0 | 2002 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | MEQDR others(1997): Show |
chr4 | 105141876 | 105284803 |
a0013 | 0/0 | 2002 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | MEQDR others(1997): Show |
chr4 | 105141876 | 105284803 |
a0014 | 0/0 | 2002 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | MEQDR others(1997): Show |
chr4 | 105141876 | 105284803 |
a0015 | 0/0 | 2002 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | MEQDR others(1997): Show |
chr4 | 105141876 | 105284803 |
a0016 | 0/0 | 2002 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | MEQDR others(1997): Show |
chr4 | 105141876 | 105284803 |
a0017 | 0/0 | 2002 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | MEQDR others(1997): Show |
chr4 | 105141876 | 105284803 |
a0018 | 0/0 | 2002 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | MEQDR others(1997): Show |
chr4 | 105141876 | 105284803 |
a0019 | 0/0 | 1459 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | MEQDR others(1454): Show |
chr4 | 105141876 | 105284803 |
a0020 | 0/0 | 2002 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | MEQDR others(1997): Show |
chr4 | 105141876 | 105284803 |
a0021 | 0/0 | 2002 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | MEQDR others(1997): Show |
chr4 | 105141876 | 105284803 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 6006 | 123 | 16 | 31 | 50 | 9 | 16 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0001c0007 | 0/0 | 6006 | 7 | 6 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0001c0022 | 0/0 | 6006 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0001c0028 | 0/0 | 6006 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0001c0029 | 0/0 | 6006 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0002c0002 | 0/0 | 6006 | 59 | 2 | 10 | 31 | 4 | 12 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0002c0023 | 0/0 | 6006 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0003c0003 | 0/0 | 6006 | 44 | 0 | 5 | 37 | 1 | 1 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0003c0032 | 0/0 | 6006 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0004c0004 | 0/0 | 6006 | 33 | 16 | 3 | 14 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0004c0008 | 0/0 | 6006 | 6 | 5 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0004c0011 | 0/0 | 6006 | 3 | 3 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0004c0018 | 0/0 | 6006 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0004c0019 | 0/0 | 6006 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0004c0031 | 0/0 | 6006 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0005c0005 | 0/1 | 6006 | 20 | 7 | 7 | 3 | 0 | 2 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0006c0006 | 0/0 | 6006 | 17 | 16 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0007c0009 | 0/0 | 6006 | 4 | 1 | 1 | 0 | 0 | 2 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0008c0010 | 0/0 | 6006 | 4 | 4 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0009c0013 | 0/0 | 6006 | 3 | 0 | 0 | 2 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0010c0012 | 0/0 | 6006 | 3 | 0 | 0 | 3 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0011c0015 | 0/0 | 6006 | 2 | 0 | 1 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0012c0016 | 0/0 | 6006 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0013c0014 | 0/0 | 6006 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0014c0024 | 0/0 | 6006 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0015c0027 | 0/0 | 6006 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0016c0025 | 0/0 | 6006 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0017c0017 | 0/0 | 6006 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0018c0021 | 0/0 | 6006 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0019c0020 | 0/0 | 5956 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(5951): Show |
chr4 | 105141876 | 105284803 | ||
a0020c0026 | 0/0 | 6006 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 | ||
a0021c0030 | 0/0 | 6006 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | ATGGA others(6001): Show |
chr4 | 105141876 | 105284803 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 9589 | 40 | 0 | 3 | 27 | 2 | 7 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9584): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0002 | 0/0 | 9586 | 2 | 0 | 0 | 2 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9581): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0003 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9584): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0004 | 0/0 | 9591 | 13 | 0 | 4 | 8 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9586): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0005 | 0/0 | 9587 | 6 | 1 | 4 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9582): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0006 | 0/0 | 9593 | 10 | 0 | 6 | 0 | 3 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9588): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0007 | 0/0 | 9593 | 7 | 0 | 2 | 4 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9588): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0008 | 0/0 | 9592 | 7 | 0 | 2 | 4 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9587): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0009 | 0/0 | 9591 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9586): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0010 | 0/0 | 9595 | 2 | 0 | 0 | 1 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9590): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0012 | 0/0 | 9590 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9585): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0013 | 0/0 | 9597 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9592): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0015 | 0/0 | 9588 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9583): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0016 | 0/0 | 9595 | 4 | 0 | 3 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9590): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0017 | 0/0 | 9591 | 3 | 0 | 2 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9586): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0028 | 0/0 | 9590 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9585): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0032 | 0/0 | 9607 | 2 | 1 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9602): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0036 | 0/0 | 9584 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9579): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0038 | 0/0 | 9589 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9584): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0041 | 0/0 | 9587 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9582): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0053 | 0/0 | 9598 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9593): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0055 | 0/0 | 9601 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9596): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0061 | 0/0 | 9597 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9592): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0070 | 0/0 | 9610 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9605): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0073 | 0/0 | 9606 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9601): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0075 | 0/0 | 9610 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9605): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0076 | 0/0 | 9612 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9607): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0077 | 0/0 | 9614 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9609): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0078 | 0/0 | 9620 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9615): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0080 | 0/0 | 9603 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9598): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0086 | 0/0 | 9590 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9585): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0088 | 0/0 | 9588 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9583): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0089 | 0/0 | 9585 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9580): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0093 | 0/0 | 9600 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9595): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0095 | 0/0 | 9590 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9585): Show |
chr4 | 105141876 | 105284803 |
a0001c0001t0104 | 0/0 | 9602 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9597): Show |
chr4 | 105141876 | 105284803 |
a0001c0007t0030 | 0/0 | 9604 | 2 | 1 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9599): Show |
chr4 | 105141876 | 105284803 |
a0001c0007t0031 | 0/0 | 9602 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9597): Show |
chr4 | 105141876 | 105284803 |
a0001c0007t0057 | 0/0 | 9604 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9599): Show |
chr4 | 105141876 | 105284803 |
a0001c0007t0071 | 0/0 | 9608 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9603): Show |
chr4 | 105141876 | 105284803 |
a0001c0007t0091 | 0/0 | 9608 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9603): Show |
chr4 | 105141876 | 105284803 |
a0001c0022t0062 | 0/0 | 9592 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9587): Show |
chr4 | 105141876 | 105284803 |
a0001c0028t0001 | 0/0 | 9589 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9584): Show |
chr4 | 105141876 | 105284803 |
a0001c0029t0004 | 0/0 | 9591 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9586): Show |
chr4 | 105141876 | 105284803 |
a0002c0002t0001 | 0/0 | 9589 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9584): Show |
chr4 | 105141876 | 105284803 |
a0002c0002t0003 | 0/0 | 9589 | 27 | 0 | 5 | 16 | 2 | 4 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9584): Show |
chr4 | 105141876 | 105284803 |
a0002c0002t0007 | 0/0 | 9593 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9588): Show |
chr4 | 105141876 | 105284803 |
a0002c0002t0009 | 0/0 | 9591 | 3 | 0 | 0 | 1 | 0 | 2 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9586): Show |
chr4 | 105141876 | 105284803 |
a0002c0002t0011 | 0/0 | 9588 | 5 | 0 | 0 | 5 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9583): Show |
chr4 | 105141876 | 105284803 |
a0002c0002t0020 | 0/0 | 9594 | 3 | 0 | 1 | 1 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9589): Show |
chr4 | 105141876 | 105284803 |
a0002c0002t0021 | 0/0 | 9595 | 3 | 0 | 0 | 1 | 0 | 2 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9590): Show |
chr4 | 105141876 | 105284803 |
a0002c0002t0023 | 0/0 | 9589 | 3 | 1 | 1 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9584): Show |
chr4 | 105141876 | 105284803 |
a0002c0002t0024 | 0/0 | 9587 | 3 | 1 | 0 | 2 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9582): Show |
chr4 | 105141876 | 105284803 |
a0002c0002t0025 | 0/0 | 9589 | 3 | 0 | 0 | 3 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9584): Show |
chr4 | 105141876 | 105284803 |
a0002c0002t0029 | 0/0 | 9590 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9585): Show |
chr4 | 105141876 | 105284803 |
a0002c0002t0035 | 0/0 | 9588 | 2 | 0 | 1 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9583): Show |
chr4 | 105141876 | 105284803 |
a0002c0002t0063 | 0/0 | 9589 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9584): Show |
chr4 | 105141876 | 105284803 |
a0002c0002t0085 | 0/0 | 9591 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9586): Show |
chr4 | 105141876 | 105284803 |
a0002c0002t0087 | 0/0 | 9589 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9584): Show |
chr4 | 105141876 | 105284803 |
a0002c0002t0090 | 0/0 | 9593 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9588): Show |
chr4 | 105141876 | 105284803 |
a0002c0023t0003 | 0/0 | 9589 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9584): Show |
chr4 | 105141876 | 105284803 |
a0003c0003t0002 | 0/0 | 9586 | 33 | 0 | 3 | 30 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9581): Show |
chr4 | 105141876 | 105284803 |
a0003c0003t0004 | 0/0 | 9591 | 2 | 0 | 0 | 2 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9586): Show |
chr4 | 105141876 | 105284803 |
a0003c0003t0012 | 0/0 | 9590 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9585): Show |
chr4 | 105141876 | 105284803 |
a0003c0003t0015 | 0/0 | 9588 | 4 | 0 | 0 | 3 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9583): Show |
chr4 | 105141876 | 105284803 |
a0003c0003t0018 | 0/0 | 9601 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9596): Show |
chr4 | 105141876 | 105284803 |
a0003c0003t0036 | 0/0 | 9584 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9579): Show |
chr4 | 105141876 | 105284803 |
a0003c0003t0096 | 0/0 | 9587 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9582): Show |
chr4 | 105141876 | 105284803 |
a0003c0003t0098 | 0/0 | 9586 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9581): Show |
chr4 | 105141876 | 105284803 |
a0003c0032t0002 | 0/0 | 9586 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9581): Show |
chr4 | 105141876 | 105284803 |
a0004c0004t0004 | 0/0 | 9591 | 5 | 1 | 0 | 4 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9586): Show |
chr4 | 105141876 | 105284803 |
a0004c0004t0007 | 0/0 | 9593 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9588): Show |
chr4 | 105141876 | 105284803 |
a0004c0004t0010 | 0/0 | 9595 | 4 | 0 | 0 | 4 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9590): Show |
chr4 | 105141876 | 105284803 |
a0004c0004t0013 | 0/0 | 9597 | 4 | 1 | 1 | 2 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9592): Show |
chr4 | 105141876 | 105284803 |
a0004c0004t0018 | 0/0 | 9601 | 3 | 3 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9596): Show |
chr4 | 105141876 | 105284803 |
a0004c0004t0028 | 0/0 | 9590 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9585): Show |
chr4 | 105141876 | 105284803 |
a0004c0004t0033 | 0/0 | 9599 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9594): Show |
chr4 | 105141876 | 105284803 |
a0004c0004t0037 | 0/0 | 9593 | 2 | 0 | 0 | 2 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9588): Show |
chr4 | 105141876 | 105284803 |
a0004c0004t0039 | 0/0 | 9599 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9594): Show |
chr4 | 105141876 | 105284803 |
a0004c0004t0042 | 0/0 | 9595 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9590): Show |
chr4 | 105141876 | 105284803 |
a0004c0004t0048 | 0/0 | 9591 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9586): Show |
chr4 | 105141876 | 105284803 |
a0004c0004t0058 | 0/0 | 9611 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9606): Show |
chr4 | 105141876 | 105284803 |
a0004c0004t0072 | 0/0 | 9604 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9599): Show |
chr4 | 105141876 | 105284803 |
a0004c0004t0074 | 0/0 | 9608 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9603): Show |
chr4 | 105141876 | 105284803 |
a0004c0004t0084 | 0/0 | 9591 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9586): Show |
chr4 | 105141876 | 105284803 |
a0004c0004t0094 | 0/0 | 9598 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9593): Show |
chr4 | 105141876 | 105284803 |
a0004c0004t0099 | 0/0 | 9606 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9601): Show |
chr4 | 105141876 | 105284803 |
a0004c0004t0100 | 0/0 | 9597 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9592): Show |
chr4 | 105141876 | 105284803 |
a0004c0004t0101 | 0/0 | 9593 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9588): Show |
chr4 | 105141876 | 105284803 |
a0004c0008t0008 | 0/0 | 9592 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9587): Show |
chr4 | 105141876 | 105284803 |
a0004c0008t0019 | 0/0 | 9598 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9593): Show |
chr4 | 105141876 | 105284803 |
a0004c0008t0059 | 0/0 | 9601 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9596): Show |
chr4 | 105141876 | 105284803 |
a0004c0008t0066 | 0/0 | 9596 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9591): Show |
chr4 | 105141876 | 105284803 |
a0004c0008t0067 | 0/0 | 9594 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9589): Show |
chr4 | 105141876 | 105284803 |
a0004c0011t0008 | 0/0 | 9592 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9587): Show |
chr4 | 105141876 | 105284803 |
a0004c0011t0040 | 0/0 | 9602 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9597): Show |
chr4 | 105141876 | 105284803 |
a0004c0011t0047 | 0/0 | 9597 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9592): Show |
chr4 | 105141876 | 105284803 |
a0004c0018t0019 | 0/0 | 9598 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9593): Show |
chr4 | 105141876 | 105284803 |
a0004c0019t0081 | 0/0 | 9601 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9596): Show |
chr4 | 105141876 | 105284803 |
a0004c0031t0092 | 0/0 | 9606 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9601): Show |
chr4 | 105141876 | 105284803 |
a0005c0005t0005 | 0/0 | 9587 | 11 | 1 | 7 | 3 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9582): Show |
chr4 | 105141876 | 105284803 |
a0005c0005t0014 | 0/0 | 9585 | 5 | 5 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9580): Show |
chr4 | 105141876 | 105284803 |
a0005c0005t0027 | 0/0 | 9597 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9592): Show |
chr4 | 105141876 | 105284803 |
a0005c0005t0049 | 0/0 | 9610 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9605): Show |
chr4 | 105141876 | 105284803 |
a0005c0005t0050 | 0/0 | 9605 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9600): Show |
chr4 | 105141876 | 105284803 |
a0005c0005t0056 | 0/1 | 9592 | 1 | 0 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9587): Show |
chr4 | 105141876 | 105284803 |
a0006c0006t0022 | 0/0 | 9589 | 3 | 3 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9584): Show |
chr4 | 105141876 | 105284803 |
a0006c0006t0026 | 0/0 | 9589 | 3 | 3 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9584): Show |
chr4 | 105141876 | 105284803 |
a0006c0006t0034 | 0/0 | 9591 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9586): Show |
chr4 | 105141876 | 105284803 |
a0006c0006t0045 | 0/0 | 9587 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9582): Show |
chr4 | 105141876 | 105284803 |
a0006c0006t0046 | 0/0 | 9585 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9580): Show |
chr4 | 105141876 | 105284803 |
a0006c0006t0065 | 0/0 | 9596 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9591): Show |
chr4 | 105141876 | 105284803 |
a0006c0006t0068 | 0/0 | 9592 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9587): Show |
chr4 | 105141876 | 105284803 |
a0006c0006t0082 | 0/0 | 9595 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9590): Show |
chr4 | 105141876 | 105284803 |
a0006c0006t0083 | 0/0 | 9593 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9588): Show |
chr4 | 105141876 | 105284803 |
a0006c0006t0097 | 0/0 | 9586 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9581): Show |
chr4 | 105141876 | 105284803 |
a0006c0006t0102 | 0/0 | 9591 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9586): Show |
chr4 | 105141876 | 105284803 |
a0006c0006t0103 | 0/0 | 9591 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9586): Show |
chr4 | 105141876 | 105284803 |
a0007c0009t0027 | 0/0 | 9597 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9592): Show |
chr4 | 105141876 | 105284803 |
a0007c0009t0051 | 0/0 | 9602 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9597): Show |
chr4 | 105141876 | 105284803 |
a0007c0009t0052 | 0/0 | 9598 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9593): Show |
chr4 | 105141876 | 105284803 |
a0007c0009t0054 | 0/0 | 9596 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9591): Show |
chr4 | 105141876 | 105284803 |
a0008c0010t0012 | 0/0 | 9590 | 4 | 4 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9585): Show |
chr4 | 105141876 | 105284803 |
a0009c0013t0001 | 0/0 | 9589 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9584): Show |
chr4 | 105141876 | 105284803 |
a0009c0013t0007 | 0/0 | 9593 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9588): Show |
chr4 | 105141876 | 105284803 |
a0009c0013t0079 | 0/0 | 9609 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9604): Show |
chr4 | 105141876 | 105284803 |
a0010c0012t0003 | 0/0 | 9589 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9584): Show |
chr4 | 105141876 | 105284803 |
a0010c0012t0009 | 0/0 | 9591 | 2 | 0 | 0 | 2 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9586): Show |
chr4 | 105141876 | 105284803 |
a0011c0015t0043 | 0/0 | 9589 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9584): Show |
chr4 | 105141876 | 105284803 |
a0011c0015t0044 | 0/0 | 9585 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9580): Show |
chr4 | 105141876 | 105284803 |
a0012c0016t0001 | 0/0 | 9589 | 2 | 2 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9584): Show |
chr4 | 105141876 | 105284803 |
a0013c0014t0060 | 0/0 | 9599 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9594): Show |
chr4 | 105141876 | 105284803 |
a0013c0014t0064 | 0/0 | 9598 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9593): Show |
chr4 | 105141876 | 105284803 |
a0014c0024t0029 | 0/0 | 9590 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9585): Show |
chr4 | 105141876 | 105284803 |
a0015c0027t0010 | 0/0 | 9595 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9590): Show |
chr4 | 105141876 | 105284803 |
a0016c0025t0017 | 0/0 | 9591 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9586): Show |
chr4 | 105141876 | 105284803 |
a0017c0017t0003 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9584): Show |
chr4 | 105141876 | 105284803 |
a0018c0021t0004 | 0/0 | 9591 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9586): Show |
chr4 | 105141876 | 105284803 |
a0019c0020t0069 | 0/0 | 9589 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9584): Show |
chr4 | 105141876 | 105284803 |
a0020c0026t0009 | 0/0 | 9591 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9586): Show |
chr4 | 105141876 | 105284803 |
a0021c0030t0011 | 0/0 | 9588 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | GTAGA others(9583): Show |
chr4 | 105141876 | 105284803 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0005g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0005g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0005g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0005g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0005g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0006g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0006g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0006g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0006g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0006g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0006g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0006g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0006g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0006g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0007g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0007g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0007g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0007g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0007g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0007g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0007g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0008g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0008g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0008g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0008g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0008g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0008g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0008g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0009g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0009g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0010g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0010g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0012g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0013g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0015g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0016g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0016g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0016g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0016g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0017g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0017g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0017g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0028g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0032g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0032g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0036g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0038g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0038g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0041g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0053g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0055g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0061g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0070g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0073g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0075g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0076g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0077g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0078g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0080g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0086g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0088g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0089g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0093g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0095g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0001t0104g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0007t0030g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0007t0030g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0007t0031g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0007t0031g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0007t0057g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0007t0071g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0007t0091g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0022t0062g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0028t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0001c0029t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0003g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0007g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0009g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0009g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0009g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0011g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0011g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0011g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0011g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0011g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0020g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0020g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0020g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0021g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0021g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0021g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0023g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0023g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0023g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0024g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0024g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0024g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0025g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0025g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0025g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0029g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0035g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0035g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0063g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0085g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0087g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0002t0090g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0002c0023t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0012g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0015g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0015g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0015g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0015g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0018g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0036g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0096g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0003t0098g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0003c0032t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0007g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0010g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0010g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0010g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0010g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0013g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0013g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0013g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0013g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0018g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0018g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0018g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0028g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0033g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0033g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0037g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0037g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0039g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0042g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0048g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0058g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0072g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0074g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0084g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0094g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0099g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0100g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0004t0101g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0008t0008g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0008t0019g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0008t0019g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0008t0059g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0008t0066g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0008t0067g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0011t0008g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0011t0040g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0011t0047g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0018t0019g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0019t0081g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0004c0031t0092g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0005c0005t0005g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0005c0005t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0005c0005t0005g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0005c0005t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0005c0005t0005g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0005c0005t0005g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0005c0005t0005g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0005c0005t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0005c0005t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0005c0005t0005g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0005c0005t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0005c0005t0014g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0005c0005t0014g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0005c0005t0014g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0005c0005t0014g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0005c0005t0014g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0005c0005t0027g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0005c0005t0049g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0005c0005t0050g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0005c0005t0056g0018 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0006c0006t0022g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0006c0006t0022g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0006c0006t0022g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0006c0006t0026g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0006c0006t0026g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0006c0006t0026g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0006c0006t0034g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0006c0006t0034g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0006c0006t0045g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0006c0006t0046g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0006c0006t0065g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0006c0006t0068g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0006c0006t0082g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0006c0006t0083g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0006c0006t0097g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0006c0006t0102g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0006c0006t0103g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0007c0009t0027g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0007c0009t0051g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0007c0009t0052g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0007c0009t0054g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0008c0010t0012g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0008c0010t0012g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0008c0010t0012g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0008c0010t0012g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0009c0013t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0009c0013t0007g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0009c0013t0079g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0010c0012t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0010c0012t0009g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0010c0012t0009g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0011c0015t0043g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0011c0015t0044g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0012c0016t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0012c0016t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0013c0014t0060g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0013c0014t0064g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0014c0024t0029g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0015c0027t0010g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0016c0025t0017g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0017c0017t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0018c0021t0004g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0019c0020t0069g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0020c0026t0009g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
a0021c0030t0011g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | GBR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00140 | hp2 | a0002 | c0002 | t0003 | g0128 | EUR | GBR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00280 | hp1 | a0001 | c0001 | t0013 | g0296 | EUR | FIN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00280 | hp2 | a0002 | c0002 | t0020 | g0176 | EUR | FIN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00323 | hp1 | a0002 | c0002 | t0003 | g0147 | EUR | FIN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00323 | hp2 | a0001 | c0001 | t0006 | g0206 | EUR | FIN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00423 | hp1 | a0009 | c0013 | t0079 | g0264 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00423 | hp2 | a0003 | c0003 | t0002 | g0028 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00438 | hp1 | a0003 | c0003 | t0002 | g0109 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00544 | hp1 | a0003 | c0003 | t0002 | g0085 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00544 | hp2 | a0002 | c0002 | t0003 | g0159 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00558 | hp1 | a0001 | c0001 | t0089 | g0276 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00558 | hp2 | a0002 | c0002 | t0011 | g0157 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00609 | hp1 | a0002 | c0002 | t0021 | g0165 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00609 | hp2 | a0003 | c0003 | t0002 | g0314 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00642 | hp1 | a0001 | c0001 | t0008 | g0205 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00642 | hp2 | a0001 | c0001 | t0055 | g0194 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00673 | hp2 | a0014 | c0024 | t0029 | g0127 | EAS | CHS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00735 | hp1 | a0002 | c0002 | t0020 | g0177 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00735 | hp2 | a0001 | c0007 | t0030 | g0117 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00738 | hp1 | a0002 | c0002 | t0023 | g0134 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00738 | hp2 | a0007 | c0009 | t0027 | g0049 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0196 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG00741 | hp2 | a0001 | c0001 | t0004 | g0186 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01070 | hp1 | a0003 | c0003 | t0018 | g0118 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01070 | hp2 | a0005 | c0005 | t0005 | g0051 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01071 | hp1 | a0005 | c0005 | t0005 | g0050 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01071 | hp2 | a0003 | c0003 | t0002 | g0245 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01074 | hp1 | a0001 | c0001 | t0004 | g0209 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01074 | hp2 | a0003 | c0003 | t0002 | g0089 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01081 | hp1 | a0003 | c0003 | t0036 | g0108 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01081 | hp2 | a0001 | c0001 | t0073 | g0024 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0203 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01099 | hp2 | a0011 | c0015 | t0044 | g0346 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01106 | hp1 | a0001 | c0001 | t0016 | g0215 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01106 | hp2 | a0005 | c0005 | t0005 | g0043 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01109 | hp1 | a0004 | c0004 | t0039 | g0068 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01109 | hp2 | a0001 | c0001 | t0006 | g0318 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01169 | hp1 | a0001 | c0001 | t0006 | g0254 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01169 | hp2 | a0002 | c0002 | t0087 | g0171 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01175 | hp1 | a0004 | c0008 | t0008 | g0071 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01175 | hp2 | a0001 | c0001 | t0006 | g0212 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01192 | hp1 | a0006 | c0006 | t0046 | g0002 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01192 | hp2 | a0004 | c0004 | t0099 | g0060 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01243 | hp2 | a0004 | c0004 | t0013 | g0057 | AMR | PUR | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01255 | hp1 | a0002 | c0002 | t0003 | g0200 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01255 | hp2 | a0001 | c0001 | t0007 | g0244 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01256 | hp1 | a0001 | c0001 | t0016 | g0210 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01256 | hp2 | a0002 | c0002 | t0003 | g0135 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01257 | hp1 | a0001 | c0001 | t0006 | g0204 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01257 | hp2 | a0005 | c0005 | t0005 | g0041 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01258 | hp1 | a0001 | c0001 | t0016 | g0208 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01258 | hp2 | a0005 | c0005 | t0005 | g0042 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01261 | hp1 | a0001 | c0001 | t0005 | g0192 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01261 | hp2 | a0002 | c0002 | t0035 | g0136 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01346 | hp2 | a0002 | c0002 | t0003 | g0150 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01358 | hp1 | a0005 | c0005 | t0005 | g0044 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01358 | hp2 | a0002 | c0002 | t0003 | g0155 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01361 | hp1 | a0001 | c0001 | t0088 | g0030 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01361 | hp2 | a0002 | c0002 | t0085 | g0076 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01496 | hp1 | a0001 | c0028 | t0001 | g0236 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01496 | hp2 | a0015 | c0027 | t0010 | g0255 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01516 | hp1 | a0001 | c0001 | t0006 | g0253 | EUR | IBS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01516 | hp2 | a0002 | c0002 | t0035 | g0153 | EUR | IBS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01517 | hp1 | a0001 | c0001 | t0006 | g0252 | EUR | IBS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01517 | hp2 | a0001 | c0001 | t0008 | g0211 | EUR | IBS | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01884 | hp1 | a0001 | c0001 | t0104 | g0007 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01884 | hp2 | a0001 | c0001 | t0080 | g0053 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01891 | hp1 | a0004 | c0004 | t0018 | g0036 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01891 | hp2 | a0007 | c0009 | t0052 | g0048 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01928 | hp1 | a0001 | c0001 | t0004 | g0243 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01928 | hp2 | a0016 | c0025 | t0017 | g0246 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01943 | hp1 | a0003 | c0003 | t0002 | g0088 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01943 | hp2 | a0001 | c0001 | t0008 | g0298 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01975 | hp1 | a0001 | c0001 | t0005 | g0188 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01975 | hp2 | a0005 | c0005 | t0005 | g0032 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0193 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01981 | hp1 | a0001 | c0001 | t0007 | g0197 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01981 | hp2 | a0002 | c0002 | t0003 | g0173 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02004 | hp1 | a0001 | c0001 | t0017 | g0290 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02004 | hp2 | a0001 | c0001 | t0075 | g0027 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02015 | hp1 | a0003 | c0003 | t0002 | g0081 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02027 | hp1 | a0001 | c0001 | t0004 | g0286 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02027 | hp2 | a0002 | c0002 | t0003 | g0161 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02055 | hp1 | a0006 | c0006 | t0022 | g0336 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02055 | hp2 | a0001 | c0007 | t0071 | g0180 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02056 | hp1 | a0002 | c0002 | t0024 | g0141 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02071 | hp1 | a0002 | c0002 | t0029 | g0170 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02071 | hp2 | a0004 | c0004 | t0010 | g0319 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02080 | hp1 | a0001 | c0001 | t0008 | g0306 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02080 | hp2 | a0003 | c0003 | t0002 | g0090 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02135 | hp1 | a0001 | c0001 | t0007 | g0292 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02135 | hp2 | a0003 | c0003 | t0002 | g0104 | EAS | KHV | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02145 | hp1 | a0008 | c0010 | t0012 | g0012 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02145 | hp2 | a0004 | c0004 | t0072 | g0062 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02155 | hp1 | a0001 | c0001 | t0008 | g0304 | EAS | CDX | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02155 | hp2 | a0005 | c0005 | t0005 | g0294 | EAS | CDX | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | CDX | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CDX | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02257 | hp1 | a0017 | c0017 | t0003 | g0151 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02257 | hp2 | a0004 | c0004 | t0100 | g0055 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02258 | hp1 | a0001 | c0001 | t0038 | g0184 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02258 | hp2 | a0002 | c0002 | t0023 | g0143 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02280 | hp1 | a0005 | c0005 | t0014 | g0343 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02280 | hp2 | a0001 | c0001 | t0078 | g0025 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02300 | hp1 | a0001 | c0001 | t0017 | g0268 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02300 | hp2 | a0001 | c0001 | t0006 | g0214 | AMR | PEL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02451 | hp1 | a0006 | c0006 | t0068 | g0014 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02451 | hp2 | a0012 | c0016 | t0001 | g0020 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02572 | hp1 | a0006 | c0006 | t0082 | g0334 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02572 | hp2 | a0004 | c0008 | t0067 | g0070 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02602 | hp1 | a0001 | c0001 | t0005 | g0267 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02602 | hp2 | a0011 | c0015 | t0043 | g0347 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02615 | hp1 | a0004 | c0004 | t0033 | g0119 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02615 | hp2 | a0005 | c0005 | t0014 | g0342 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02622 | hp1 | a0001 | c0007 | t0031 | g0038 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02622 | hp2 | a0005 | c0005 | t0005 | g0145 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02647 | hp1 | a0008 | c0010 | t0012 | g0011 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02647 | hp2 | a0004 | c0004 | t0074 | g0061 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0133 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02698 | hp2 | a0018 | c0021 | t0004 | g0345 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02723 | hp1 | a0006 | c0006 | t0034 | g0333 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0158 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02735 | hp1 | a0005 | c0005 | t0049 | g0047 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02735 | hp2 | a0002 | c0002 | t0003 | g0344 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02809 | hp1 | a0001 | c0007 | t0057 | g0040 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02809 | hp2 | a0004 | c0018 | t0019 | g0324 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02818 | hp1 | a0006 | c0006 | t0083 | g0335 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02818 | hp2 | a0006 | c0006 | t0026 | g0006 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02886 | hp1 | a0004 | c0004 | t0018 | g0120 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02886 | hp2 | a0006 | c0006 | t0065 | g0340 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02922 | hp1 | a0008 | c0010 | t0012 | g0008 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02922 | hp2 | a0001 | c0001 | t0009 | g0146 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02965 | hp1 | a0006 | c0006 | t0045 | g0121 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02965 | hp2 | a0001 | c0001 | t0095 | g0130 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02970 | hp1 | a0006 | c0006 | t0103 | g0003 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02970 | hp2 | a0005 | c0005 | t0014 | g0065 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02976 | hp1 | a0001 | c0001 | t0009 | g0131 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02976 | hp2 | a0004 | c0004 | t0013 | g0056 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03017 | hp1 | a0003 | c0003 | t0015 | g0093 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03017 | hp2 | a0002 | c0002 | t0009 | g0148 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03041 | hp1 | a0004 | c0004 | t0028 | g0202 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03041 | hp2 | a0001 | c0001 | t0093 | g0179 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03098 | hp1 | a0005 | c0005 | t0014 | g0066 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03098 | hp2 | a0006 | c0006 | t0102 | g0004 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03130 | hp1 | a0013 | c0014 | t0064 | g0073 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03130 | hp2 | a0001 | c0001 | t0070 | g0034 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03139 | hp1 | a0006 | c0006 | t0034 | g0337 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03139 | hp2 | a0004 | c0004 | t0042 | g0059 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03195 | hp1 | a0004 | c0004 | t0033 | g0058 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03195 | hp2 | a0001 | c0001 | t0038 | g0183 | AFR | ESN | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03209 | hp1 | a0004 | c0011 | t0008 | g0325 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03209 | hp2 | a0004 | c0004 | t0101 | g0075 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03225 | hp1 | a0004 | c0011 | t0040 | g0329 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03225 | hp2 | a0001 | c0001 | t0012 | g0185 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03239 | hp2 | a0001 | c0001 | t0010 | g0229 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03453 | hp1 | a0005 | c0005 | t0027 | g0064 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03453 | hp2 | a0013 | c0014 | t0060 | g0074 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03486 | hp1 | a0002 | c0002 | t0024 | g0178 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03486 | hp2 | a0006 | c0006 | t0097 | g0069 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03490 | hp2 | a0005 | c0005 | t0050 | g0046 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03492 | hp1 | a0001 | c0001 | t0053 | g0187 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03540 | hp1 | a0004 | c0019 | t0081 | g0054 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03540 | hp2 | a0001 | c0022 | t0062 | g0039 | AFR | GWD | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03579 | hp1 | a0001 | c0007 | t0091 | g0116 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03579 | hp2 | a0004 | c0004 | t0004 | g0035 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0299 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03654 | hp2 | a0001 | c0001 | t0032 | g0195 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03669 | hp1 | a0002 | c0002 | t0090 | g0144 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03669 | hp2 | a0007 | c0009 | t0054 | g0045 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03688 | hp1 | a0002 | c0002 | t0003 | g0140 | SAS | STU | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03704 | hp1 | a0002 | c0002 | t0003 | g0230 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03704 | hp2 | a0002 | c0002 | t0003 | g0137 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03710 | hp1 | a0019 | c0020 | t0069 | g0162 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03831 | hp1 | a0001 | c0001 | t0007 | g0199 | SAS | BEB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03831 | hp2 | a0004 | c0031 | t0092 | g0021 | SAS | BEB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03927 | hp1 | a0002 | c0002 | t0007 | g0317 | SAS | BEB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03942 | hp1 | a0002 | c0002 | t0023 | g0152 | SAS | BEB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03942 | hp2 | a0001 | c0001 | t0006 | g0239 | SAS | BEB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG04115 | hp1 | a0007 | c0009 | t0051 | g0033 | SAS | STU | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG04115 | hp2 | a0001 | c0001 | t0016 | g0216 | SAS | STU | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG04184 | hp1 | a0009 | c0013 | t0001 | g0321 | SAS | BEB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG04184 | hp2 | a0002 | c0002 | t0009 | g0129 | SAS | BEB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG04199 | hp1 | a0002 | c0002 | t0021 | g0124 | SAS | STU | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG04199 | hp2 | a0001 | c0001 | t0086 | g0031 | SAS | STU | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG04228 | hp1 | a0002 | c0002 | t0021 | g0125 | SAS | STU | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | STU | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18522 | hp1 | a0006 | c0006 | t0022 | g0341 | AFR | YRI | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18522 | hp2 | a0004 | c0004 | t0084 | g0072 | AFR | YRI | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18747 | hp1 | a0005 | c0005 | t0005 | g0293 | EAS | CHB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18747 | hp2 | a0001 | c0001 | t0008 | g0274 | EAS | CHB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18906 | hp1 | a0004 | c0008 | t0066 | g0328 | AFR | YRI | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18906 | hp2 | a0006 | c0006 | t0026 | g0010 | AFR | YRI | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18941 | hp2 | a0003 | c0003 | t0002 | g0084 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18942 | hp1 | a0003 | c0003 | t0002 | g0111 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18942 | hp2 | a0002 | c0002 | t0011 | g0037 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18944 | hp1 | a0003 | c0003 | t0002 | g0082 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18944 | hp2 | a0004 | c0004 | t0037 | g0224 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18946 | hp2 | a0003 | c0003 | t0002 | g0114 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18947 | hp1 | a0001 | c0001 | t0004 | g0310 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18947 | hp2 | a0003 | c0003 | t0002 | g0113 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18948 | hp2 | a0003 | c0003 | t0002 | g0099 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18950 | hp2 | a0003 | c0003 | t0015 | g0097 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18951 | hp1 | a0004 | c0004 | t0013 | g0221 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18951 | hp2 | a0003 | c0003 | t0002 | g0101 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18956 | hp1 | a0003 | c0003 | t0012 | g0105 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18959 | hp1 | a0003 | c0003 | t0002 | g0092 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18959 | hp2 | a0002 | c0023 | t0003 | g0149 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18960 | hp1 | a0001 | c0001 | t0007 | g0300 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18960 | hp2 | a0004 | c0004 | t0004 | g0220 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18963 | hp1 | a0001 | c0001 | t0028 | g0278 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18963 | hp2 | a0003 | c0003 | t0002 | g0078 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18965 | hp1 | a0003 | c0003 | t0002 | g0107 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18969 | hp2 | a0002 | c0002 | t0011 | g0167 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18973 | hp1 | a0002 | c0002 | t0003 | g0142 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18973 | hp2 | a0004 | c0004 | t0010 | g0228 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18978 | hp1 | a0003 | c0003 | t0002 | g0094 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18978 | hp2 | a0010 | c0012 | t0009 | g0233 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18979 | hp1 | a0002 | c0002 | t0003 | g0154 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18980 | hp1 | a0003 | c0003 | t0002 | g0096 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18980 | hp2 | a0005 | c0005 | t0005 | g0303 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18982 | hp1 | a0002 | c0002 | t0003 | g0139 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18982 | hp2 | a0001 | c0001 | t0004 | g0311 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18983 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18983 | hp2 | a0003 | c0003 | t0002 | g0103 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18985 | hp2 | a0002 | c0002 | t0063 | g0013 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18986 | hp1 | a0002 | c0002 | t0024 | g0166 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18986 | hp2 | a0003 | c0003 | t0002 | g0087 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18987 | hp1 | a0003 | c0003 | t0002 | g0098 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18987 | hp2 | a0004 | c0004 | t0010 | g0226 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18988 | hp1 | a0003 | c0003 | t0096 | g0100 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18989 | hp1 | a0002 | c0002 | t0003 | g0156 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18989 | hp2 | a0001 | c0001 | t0007 | g0301 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18990 | hp1 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18990 | hp2 | a0002 | c0002 | t0003 | g0122 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18993 | hp1 | a0004 | c0004 | t0004 | g0015 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18993 | hp2 | a0001 | c0001 | t0008 | g0291 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18997 | hp1 | a0003 | c0003 | t0004 | g0313 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18998 | hp1 | a0004 | c0004 | t0010 | g0227 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19001 | hp1 | a0002 | c0002 | t0003 | g0315 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19001 | hp2 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19003 | hp1 | a0002 | c0002 | t0003 | g0123 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19004 | hp1 | a0001 | c0001 | t0017 | g0266 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19004 | hp2 | a0002 | c0002 | t0003 | g0132 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19007 | hp1 | a0010 | c0012 | t0009 | g0217 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19007 | hp2 | a0003 | c0003 | t0002 | g0083 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19009 | hp1 | a0002 | c0002 | t0011 | g0175 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19009 | hp2 | a0001 | c0001 | t0007 | g0302 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19010 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19012 | hp1 | a0004 | c0004 | t0048 | g0017 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19030 | hp1 | a0004 | c0004 | t0058 | g0312 | AFR | LWK | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19030 | hp2 | a0008 | c0010 | t0012 | g0009 | AFR | LWK | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19043 | hp1 | a0004 | c0008 | t0019 | g0327 | AFR | LWK | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19043 | hp2 | a0001 | c0001 | t0036 | g0029 | AFR | LWK | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19054 | hp1 | a0002 | c0002 | t0025 | g0163 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19054 | hp2 | a0009 | c0013 | t0007 | g0219 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19056 | hp1 | a0001 | c0001 | t0010 | g0235 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19056 | hp2 | a0004 | c0004 | t0037 | g0016 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19057 | hp1 | a0003 | c0003 | t0002 | g0231 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19057 | hp2 | a0002 | c0002 | t0020 | g0201 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19058 | hp1 | a0004 | c0004 | t0004 | g0223 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19058 | hp2 | a0002 | c0002 | t0003 | g0242 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19062 | hp1 | a0003 | c0003 | t0002 | g0079 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19062 | hp2 | a0002 | c0002 | t0003 | g0241 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19064 | hp1 | a0002 | c0002 | t0003 | g0240 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19064 | hp2 | a0004 | c0004 | t0007 | g0283 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19070 | hp2 | a0002 | c0002 | t0011 | g0172 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19072 | hp1 | a0003 | c0003 | t0015 | g0091 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19072 | hp2 | a0002 | c0002 | t0003 | g0316 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19075 | hp2 | a0003 | c0003 | t0004 | g0181 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19079 | hp1 | a0003 | c0003 | t0002 | g0106 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19079 | hp2 | a0002 | c0002 | t0003 | g0138 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19080 | hp1 | a0010 | c0012 | t0003 | g0182 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19080 | hp2 | a0003 | c0003 | t0002 | g0102 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19082 | hp1 | a0020 | c0026 | t0009 | g0168 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19083 | hp1 | a0004 | c0004 | t0013 | g0222 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19083 | hp2 | a0003 | c0003 | t0015 | g0086 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19084 | hp1 | a0002 | c0002 | t0003 | g0126 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19086 | hp1 | a0002 | c0002 | t0025 | g0164 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19086 | hp2 | a0001 | c0001 | t0004 | g0322 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19087 | hp1 | a0003 | c0003 | t0002 | g0095 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19087 | hp2 | a0001 | c0029 | t0004 | g0275 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19088 | hp2 | a0003 | c0032 | t0002 | g0080 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19089 | hp1 | a0001 | c0001 | t0015 | g0330 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19089 | hp2 | a0004 | c0004 | t0004 | g0225 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19090 | hp2 | a0002 | c0002 | t0009 | g0169 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19091 | hp2 | a0021 | c0030 | t0011 | g0160 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19240 | hp1 | a0004 | c0011 | t0047 | g0326 | AFR | YRI | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA19240 | hp2 | a0006 | c0006 | t0026 | g0005 | AFR | YRI | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA20129 | hp1 | a0001 | c0001 | t0077 | g0026 | AFR | ASW | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA20129 | hp2 | a0004 | c0004 | t0094 | g0022 | AFR | ASW | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA20752 | hp1 | a0003 | c0003 | t0098 | g0110 | EUR | TSI | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA20752 | hp2 | a0001 | c0001 | t0076 | g0023 | EUR | TSI | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0247 | EUR | TSI | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA20805 | hp2 | a0001 | c0001 | t0061 | g0213 | EUR | TSI | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01123 | hp1 | a0001 | c0001 | t0041 | g0198 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG01123 | hp2 | a0001 | c0001 | t0006 | g0207 | AMR | CLM | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02559 | hp1 | a0006 | c0006 | t0022 | g0338 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG02559 | hp2 | a0001 | c0001 | t0032 | g0052 | AFR | ACB | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03471 | hp1 | a0001 | c0007 | t0031 | g0115 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG03471 | hp2 | a0005 | c0005 | t0014 | g0067 | AFR | MSL | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG06807 | hp1 | a0004 | c0008 | t0019 | g0332 | AFR | USA | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
HG06807 | hp2 | a0001 | c0007 | t0030 | g0339 | AFR | USA | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA18955 | hp2 | a0002 | c0002 | t0025 | g0174 | EAS | JPT | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA20300 | hp1 | a0004 | c0004 | t0018 | g0063 | AFR | USA | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0190 | AFR | USA | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA21309 | hp1 | a0012 | c0016 | t0001 | g0019 | AFR | LWK | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
NA21309 | hp2 | a0004 | c0008 | t0059 | g0323 | AFR | LWK | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
homoSapiens | chm13v2 | a0005 | c0005 | t0056 | g0018 | REF | REF | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0077 | REF | REF | TET2_chr4_105141876_105284803 | TET2 | chr4 | 105141876 | 105284803 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:105234028 | C | G | 2 | a0003 a0008 |
49 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(46): Show |
missense_variant | MODERATE | c.86C>G | p.Pro29Arg | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 382/9589 | 86/6009 | 29/2002 | chr4 | 105234028 | |||
chr4:105234042 | C | T | 1 | a0011 | 2 | HG01099.hp2 HG02602.hp2 |
missense_variant | MODERATE | c.100C>T | p.Leu34Phe | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 396/9589 | 100/6009 | 34/2002 | chr4 | 105234042 | |||
chr4:105234463 | C | A | 1 | a0017 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.521C>A | p.Pro174His | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 817/9589 | 521/6009 | 174/2002 | chr4 | 105234463 | |||
chr4:105234594 | G | A | 3 | a0004 a0011 a0013 |
49 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(46): Show |
missense_variant | MODERATE | c.652G>A | p.Val218Met | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 948/9589 | 652/6009 | 218/2002 | chr4 | 105234594 | |||
chr4:105235006 | G | A | 1 | a0019 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.1064G>A | p.Gly355Asp | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 1360/9589 | 1064/6009 | 355/2002 | chr4 | 105235006 | |||
chr4:105235030 | C | T | 1 | a0007 | 4 | HG00738.hp2 HG01891.hp2 HG03669.hp2 others(1): Show |
missense_variant | MODERATE | c.1088C>T | p.Pro363Leu | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 1384/9589 | 1088/6009 | 363/2002 | chr4 | 105235030 | |||
chr4:105235666 | C | T | 1 | a0021 | 1 | NA19091.hp2 | missense_variant | MODERATE | c.1724C>T | p.Ala575Val | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 2020/9589 | 1724/6009 | 575/2002 | chr4 | 105235666 | |||
chr4:105236371 | A | G | 1 | a0013 | 2 | HG03130.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.2429A>G | p.Gln810Arg | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 2725/9589 | 2429/6009 | 810/2002 | chr4 | 105236371 | |||
chr4:105236541 | T | C | 1 | a0018 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.2599T>C | p.Tyr867His | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 2895/9589 | 2599/6009 | 867/2002 | chr4 | 105236541 | |||
chr4:105236546 | T | G | 1 | a0010 | 3 | NA18978.hp2 NA19007.hp1 NA19080.hp1 |
missense_variant | MODERATE | c.2604T>G | p.Phe868Leu | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 2900/9589 | 2604/6009 | 868/2002 | chr4 | 105236546 | |||
chr4:105236713 | A | G | 1 | a0008 | 4 | HG02145.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
missense_variant | MODERATE | c.2771A>G | p.His924Arg | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 3067/9589 | 2771/6009 | 924/2002 | chr4 | 105236713 | |||
chr4:105237058 | C | T | 1 | a0009 | 3 | HG00423.hp1 HG04184.hp1 NA19054.hp2 |
missense_variant | MODERATE | c.3116C>T | p.Ser1039Leu | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 3412/9589 | 3116/6009 | 1039/2002 | chr4 | 105237058 | |||
chr4:105237193 | A | C | 1 | a0015 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.3251A>C | p.Gln1084Pro | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 3547/9589 | 3251/6009 | 1084/2002 | chr4 | 105237193 | |||
chr4:105243754 | A | G | 1 | a0020 | 1 | NA19082.hp1 | missense_variant | MODERATE | c.3779A>G | p.Asn1260Ser | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/11 | 4075/9589 | 3779/6009 | 1260/2002 | chr4 | 105243754 | |||
chr4:105272679 | AAGCTCAG others(43): Show |
A | 1 | a0019 | 1 | HG03710.hp1 | frameshift_variant | HIGH | c.4299_4348delAGCTCA others(44): Show |
p.Glu1433fs | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/11 | 4595/9589 | 4299/6009 | 1433/2002 | chr4 | 105272679 | |||
chr4:105275251 | A | G | 1 | a0016 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.4741A>G | p.Asn1581Asp | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 5037/9589 | 4741/6009 | 1581/2002 | chr4 | 105275251 | |||
chr4:105275672 | T | G | 2 | a0005 a0007 |
23 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(20): Show |
missense_variant | MODERATE | c.5162T>G | p.Leu1721Trp | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 5458/9589 | 5162/6009 | 1721/2002 | chr4 | 105275672 | |||
chr4:105275677 | C | T | 1 | a0018 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.5167C>T | p.Pro1723Ser | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 5463/9589 | 5167/6009 | 1723/2002 | chr4 | 105275677 | |||
chr4:105275794 | A | G | 7 | a0002 a0010 a0014 others(4): Show |
68 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(65): Show |
missense_variant | MODERATE | c.5284A>G | p.Ile1762Val | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 5580/9589 | 5284/6009 | 1762/2002 | chr4 | 105275794 | |||
chr4:105275843 | A | G | 4 | a0006 a0011 a0012 others(1): Show |
22 | HG01099.hp2 HG01192.hp1 HG02055.hp1 others(19): Show |
missense_variant | MODERATE | c.5333A>G | p.His1778Arg | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 5629/9589 | 5333/6009 | 1778/2002 | chr4 | 105275843 | |||
chr4:105275927 | A | G | 1 | a0014 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.5417A>G | p.His1806Arg | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 5713/9589 | 5417/6009 | 1806/2002 | chr4 | 105275927 | |||
chr4:105275959 | C | A | 1 | a0012 | 2 | HG02451.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.5449C>A | p.His1817Asn | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 5745/9589 | 5449/6009 | 1817/2002 | chr4 | 105275959 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:105233979 | A | C | 1 | a0012c0016 | 2 | HG02451.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.37A>C | p.Arg13Arg | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 333/9589 | 37/6009 | 13/2002 | chr4 | 105233979 | |||
chr4:105234548 | C | T | 1 | a0004c0031 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.606C>T | p.Asn202Asn | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 902/9589 | 606/6009 | 202/2002 | chr4 | 105234548 | |||
chr4:105235826 | G | A | 2 | a0004c0011 a0004c0018 |
4 | HG02809.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
synonymous_variant | LOW | c.1884G>A | p.Glu628Glu | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 2180/9589 | 1884/6009 | 628/2002 | chr4 | 105235826 | |||
chr4:105236726 | T | C | 1 | a0003c0032 | 1 | NA19088.hp2 | synonymous_variant | LOW | c.2784T>C | p.Phe928Phe | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 3080/9589 | 2784/6009 | 928/2002 | chr4 | 105236726 | |||
chr4:105236978 | A | G | 1 | a0001c0029 | 1 | NA19087.hp2 | synonymous_variant | LOW | c.3036A>G | p.Pro1012Pro | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 3332/9589 | 3036/6009 | 1012/2002 | chr4 | 105236978 | |||
chr4:105237032 | G | A | 1 | a0004c0008 | 6 | HG01175.hp1 HG02572.hp2 HG06807.hp1 others(3): Show |
synonymous_variant | LOW | c.3090G>A | p.Gln1030Gln | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 3386/9589 | 3090/6009 | 1030/2002 | chr4 | 105237032 | |||
chr4:105237059 | G | A | 5 | a0004c0004 a0004c0008 a0004c0011 others(2): Show |
45 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(42): Show |
synonymous_variant | LOW | c.3117G>A | p.Ser1039Ser | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 3413/9589 | 3117/6009 | 1039/2002 | chr4 | 105237059 | |||
chr4:105237176 | C | T | 1 | a0001c0028 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.3234C>T | p.Thr1078Thr | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/11 | 3530/9589 | 3234/6009 | 1078/2002 | chr4 | 105237176 | |||
chr4:105269705 | T | C | 7 | a0001c0007 a0001c0022 a0004c0004 others(4): Show |
52 | HG00735.hp2 HG01109.hp1 HG01175.hp1 others(49): Show |
synonymous_variant | LOW | c.4140T>C | p.His1380His | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/11 | 4436/9589 | 4140/6009 | 1380/2002 | chr4 | 105269705 | |||
chr4:105275820 | G | A | 1 | a0001c0022 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.5310G>A | p.Pro1770Pro | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 5606/9589 | 5310/6009 | 1770/2002 | chr4 | 105275820 | |||
chr4:105276039 | C | T | 1 | a0004c0018 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.5529C>T | p.Asn1843Asn | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 5825/9589 | 5529/6009 | 1843/2002 | chr4 | 105276039 | |||
chr4:105276495 | A | G | 1 | a0002c0023 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.5985A>G | p.Thr1995Thr | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 6281/9589 | 5985/6009 | 1995/2002 | chr4 | 105276495 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:105146960 | G | A | 1 | a0004c0004t0039 | 1 | HG01109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-212G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/11 | 86983 | chr4 | 105146960 | ||||||
chr4:105146972 | A | C | 4 | a0001c0001t0104 a0006c0006t0026 a0006c0006t0102 others(1): Show |
6 | HG01884.hp1 HG02818.hp2 HG02970.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-200A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/11 | 86971 | chr4 | 105146972 | ||||||
chr4:105190388 | T | C | 1 | a0004c0011t0040 | 1 | HG03225.hp1 | 5_prime_UTR_variant | MODIFIER | c.-164T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/11 | 43555 | chr4 | 105190388 | ||||||
chr4:105190394 | T | C | 1 | a0001c0001t0041 | 1 | HG01123.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-158T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/11 | chr4 | 105190394 | |||||||
chr4:105190420 | A | G | 1 | a0004c0004t0101 | 1 | HG03209.hp2 | 5_prime_UTR_variant | MODIFIER | c.-132A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/11 | 43523 | chr4 | 105190420 | ||||||
chr4:105190424 | A | G | 1 | a0001c0001t0038 | 2 | HG02258.hp1 HG03195.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-128A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/11 | chr4 | 105190424 | |||||||
chr4:105190466 | G | C | 1 | a0004c0004t0042 | 1 | HG03139.hp2 | 5_prime_UTR_variant | MODIFIER | c.-86G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/11 | 43477 | chr4 | 105190466 | ||||||
chr4:105276593 | G | A | 7 | a0006c0006t0026 a0006c0006t0045 a0006c0006t0046 others(4): Show |
9 | HG01099.hp2 HG01192.hp1 HG02602.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*74G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 74 | chr4 | 105276593 | ||||||
chr4:105276681 | T | A | 1 | a0004c0011t0047 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*162T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 162 | chr4 | 105276681 | ||||||
chr4:105276779 | C | T | 5 | a0006c0006t0026 a0006c0006t0045 a0006c0006t0046 others(2): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*260C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 260 | chr4 | 105276779 | ||||||
chr4:105276804 | T | A | 1 | a0004c0011t0047 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*285T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 285 | chr4 | 105276804 | ||||||
chr4:105276807 | T | C | 1 | a0004c0011t0047 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*288T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 288 | chr4 | 105276807 | ||||||
chr4:105276837 | A | ATC | 3 | a0004c0004t0037 a0004c0004t0099 a0004c0004t0100 |
4 | HG01192.hp2 HG02257.hp2 NA18944.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*319_*320dupTC | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 321 | INFO_REALIGN_3_PRIME | chr4 | 105276837 | |||||
chr4:105276838 | T | TC | 19 | a0001c0001t0008 a0001c0001t0028 a0001c0001t0104 others(16): Show |
32 | HG00280.hp2 HG00558.hp2 HG00642.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*330dupC | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 331 | INFO_REALIGN_3_PRIME | chr4 | 105276838 | |||||
chr4:105276838 | T | TCC | 11 | a0001c0001t0006 a0001c0001t0016 a0001c0001t0017 others(8): Show |
25 | HG00323.hp2 HG01106.hp1 HG01109.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*329_*330dupCC | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 331 | INFO_REALIGN_3_PRIME | chr4 | 105276838 | |||||
chr4:105276838 | T | TCCCCCCC others(3): Show |
1 | a0001c0001t0055 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*321_*330dupCCCCCC others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 331 | INFO_REALIGN_3_PRIME | chr4 | 105276838 | |||||
chr4:105276838 | T | TCCCCCCC others(4): Show |
2 | a0001c0001t0053 a0007c0009t0054 |
2 | HG03492.hp1 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*320_*330dupCCCCCC others(5): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 331 | INFO_REALIGN_3_PRIME | chr4 | 105276838 | |||||
chr4:105276838 | T | TCCCCCCC others(5): Show |
2 | a0005c0005t0027 a0007c0009t0027 |
2 | HG00738.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*330_*331insCCCCCC others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 331 | INFO_REALIGN_3_PRIME | chr4 | 105276838 | |||||
chr4:105276838 | T | TCCCCCCC others(6): Show |
2 | a0007c0009t0051 a0007c0009t0052 |
2 | HG01891.hp2 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*330_*331insCCCCCC others(7): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 331 | INFO_REALIGN_3_PRIME | chr4 | 105276838 | |||||
chr4:105276838 | T | TCCCCCCC others(13): Show |
1 | a0005c0005t0050 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*330_*331insCCCCCC others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 331 | INFO_REALIGN_3_PRIME | chr4 | 105276838 | |||||
chr4:105276838 | T | TCCCCCCC others(18): Show |
1 | a0005c0005t0049 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*330_*331insCCCCCC others(19): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 331 | INFO_REALIGN_3_PRIME | chr4 | 105276838 | |||||
chr4:105276838 | TC | T | 18 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0015 others(15): Show |
58 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*330delC | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 330 | INFO_REALIGN_3_PRIME | chr4 | 105276838 | |||||
chr4:105276839 | C | CT | 8 | a0004c0004t0004 a0004c0004t0007 a0004c0004t0010 others(5): Show |
17 | HG01243.hp2 HG02071.hp2 HG02145.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*320_*321insT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 321 | chr4 | 105276839 | ||||||
chr4:105276846 | C | A | 1 | a0004c0004t0048 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*327C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 327 | chr4 | 105276846 | ||||||
chr4:105277168 | A | T | 1 | a0001c0007t0091 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*649A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 649 | chr4 | 105277168 | ||||||
chr4:105277179 | A | G | 2 | a0002c0002t0025 a0002c0002t0090 |
4 | HG03669.hp1 NA18955.hp2 NA19054.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*660A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 660 | chr4 | 105277179 | ||||||
chr4:105277601 | C | T | 2 | a0011c0015t0043 a0011c0015t0044 |
2 | HG01099.hp2 HG02602.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1082C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1082 | chr4 | 105277601 | ||||||
chr4:105278071 | A | ATAAAGAA others(43): Show |
1 | a0019c0020t0069 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1554_*1603dupAAAG others(46): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1604 | INFO_REALIGN_3_PRIME | chr4 | 105278071 | |||||
chr4:105278171 | C | CAT | 26 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0008 others(23): Show |
67 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1683_*1684dupAT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | |||||
chr4:105278171 | C | CATACATA others(5): Show |
3 | a0001c0001t0104 a0001c0007t0031 a0001c0007t0057 |
4 | HG01884.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1655_*1656insCATA others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1656 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | |||||
chr4:105278171 | C | CATACATA others(7): Show |
1 | a0001c0007t0030 | 2 | HG00735.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1655_*1656insCATA others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1656 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | |||||
chr4:105278171 | C | CATACATA others(11): Show |
2 | a0001c0007t0071 a0001c0007t0091 |
2 | HG02055.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1655_*1656insCATA others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1656 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | |||||
chr4:105278171 | C | CATACATA others(13): Show |
1 | a0001c0001t0070 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1655_*1656insCATA others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1656 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | |||||
chr4:105278171 | C | CATAT | 10 | a0001c0001t0007 a0001c0001t0016 a0002c0002t0007 others(7): Show |
21 | HG00280.hp2 HG00735.hp1 HG01106.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1681_*1684dupATAT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | |||||
chr4:105278171 | C | CATATAT | 10 | a0001c0001t0010 a0001c0001t0061 a0002c0002t0021 others(7): Show |
16 | HG00609.hp1 HG01496.hp2 HG02071.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1679_*1684dupATAT others(2): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | |||||
chr4:105278171 | C | CATATATA others(1): Show |
7 | a0001c0001t0013 a0004c0004t0013 a0004c0008t0019 others(4): Show |
11 | HG00280.hp1 HG01243.hp2 HG02809.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1677_*1684dupATAT others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | |||||
chr4:105278171 | C | CATATATA others(3): Show |
4 | a0004c0004t0033 a0004c0004t0039 a0004c0004t0094 others(1): Show |
5 | HG01109.hp1 HG02615.hp1 HG03195.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1675_*1684dupATAT others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | |||||
chr4:105278171 | C | CATATATA others(5): Show |
5 | a0001c0001t0093 a0003c0003t0018 a0004c0004t0018 others(2): Show |
7 | HG01070.hp1 HG01891.hp1 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1673_*1684dupATAT others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | |||||
chr4:105278171 | C | CATATATA others(7): Show |
1 | a0001c0001t0080 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1671_*1684dupATAT others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | |||||
chr4:105278171 | C | CATATATA others(11): Show |
2 | a0001c0001t0032 a0004c0031t0092 |
3 | HG02559.hp2 HG03654.hp2 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1667_*1684dupATAT others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | |||||
chr4:105278171 | C | CATATATA others(13): Show |
2 | a0004c0004t0058 a0009c0013t0079 |
2 | HG00423.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1665_*1684dupATAT others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | |||||
chr4:105278171 | CAT | C | 16 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0041 others(13): Show |
70 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1683_*1684delAT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1683 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | |||||
chr4:105278171 | CATAT | C | 12 | a0001c0001t0036 a0001c0001t0089 a0003c0003t0036 others(9): Show |
16 | HG00558.hp1 HG00738.hp2 HG01081.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1681_*1684delATAT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1681 | INFO_REALIGN_3_PRIME | chr4 | 105278171 | |||||
chr4:105278203 | T | TATATATA others(8): Show |
2 | a0004c0004t0072 a0004c0004t0099 |
2 | HG01192.hp2 HG02145.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1684_*1685insATAT others(11): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | chr4 | 105278203 | ||||||
chr4:105278203 | T | TATATATA others(10): Show |
1 | a0001c0001t0073 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1684_*1685insATAT others(13): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | chr4 | 105278203 | ||||||
chr4:105278203 | T | TATATATA others(12): Show |
1 | a0004c0004t0074 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1684_*1685insATAT others(15): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | chr4 | 105278203 | ||||||
chr4:105278203 | T | TATATATA others(14): Show |
1 | a0001c0001t0075 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1684_*1685insATAT others(17): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | chr4 | 105278203 | ||||||
chr4:105278203 | T | TATATATA others(16): Show |
1 | a0001c0001t0076 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1684_*1685insATAT others(19): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | chr4 | 105278203 | ||||||
chr4:105278203 | T | TATATATA others(18): Show |
1 | a0001c0001t0077 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1684_*1685insATAT others(21): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | chr4 | 105278203 | ||||||
chr4:105278203 | T | TATATATA others(24): Show |
1 | a0001c0001t0078 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1684_*1685insATAT others(27): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1685 | chr4 | 105278203 | ||||||
chr4:105278276 | A | G | 1 | a0002c0002t0087 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1757A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1757 | chr4 | 105278276 | ||||||
chr4:105278348 | A | T | 25 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0095 others(22): Show |
70 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1829A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1829 | chr4 | 105278348 | ||||||
chr4:105278358 | A | G | 1 | a0001c0001t0093 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1839A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1839 | chr4 | 105278358 | ||||||
chr4:105278405 | T | TA | 10 | a0001c0001t0070 a0001c0001t0086 a0001c0001t0088 others(7): Show |
12 | HG00735.hp2 HG01361.hp1 HG02055.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1896dupA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 1897 | INFO_REALIGN_3_PRIME | chr4 | 105278405 | |||||
chr4:105278631 | A | G | 1 | a0003c0003t0098 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2112A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 2112 | chr4 | 105278631 | ||||||
chr4:105279048 | C | G | 1 | a0004c0031t0092 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2529C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 2529 | chr4 | 105279048 | ||||||
chr4:105279077 | T | C | 8 | a0006c0006t0022 a0006c0006t0034 a0006c0006t0065 others(5): Show |
11 | HG02055.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2558T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 2558 | chr4 | 105279077 | ||||||
chr4:105279478 | A | G | 2 | a0002c0002t0023 a0002c0002t0085 |
4 | HG00738.hp1 HG01361.hp2 HG02258.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2959A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 2959 | chr4 | 105279478 | ||||||
chr4:105279511 | C | T | 6 | a0004c0004t0058 a0004c0004t0084 a0004c0004t0101 others(3): Show |
6 | HG03130.hp1 HG03209.hp2 HG03453.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2992C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 2992 | chr4 | 105279511 | ||||||
chr4:105279571 | C | T | 1 | a0001c0001t0089 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3052C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 3052 | chr4 | 105279571 | ||||||
chr4:105279624 | C | T | 2 | a0006c0006t0026 a0006c0006t0103 |
4 | HG02818.hp2 HG02970.hp1 NA18906.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3105C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 11/11 | 3105 | chr4 | 105279624 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:105146998 | T | C | 11 | a0001c0001t0104g0007 a0006c0006t0026g0005 a0006c0006t0026g0006 others(8): Show |
11 | HG01192.hp1 HG01884.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-193+19T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105146998 | |||||||
chr4:105147297 | T | G | 1 | a0002c0002t0063g0013 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-193+318T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105147297 | |||||||
chr4:105147341 | C | T | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-193+362C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105147341 | |||||||
chr4:105147342 | A | G | 1 | a0018c0021t0004g0345 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-193+363A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105147342 | |||||||
chr4:105147343 | C | T | 1 | a0002c0002t0003g0344 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-193+364C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105147343 | |||||||
chr4:105147489 | C | T | 11 | a0001c0007t0030g0339 a0005c0005t0014g0342 a0005c0005t0014g0343 others(8): Show |
11 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-193+510C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105147489 | |||||||
chr4:105147545 | A | G | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-193+566A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105147545 | |||||||
chr4:105147574 | G | GT | 11 | a0001c0001t0001g0331 a0001c0001t0015g0330 a0004c0008t0019g0327 others(8): Show |
11 | HG02145.hp1 HG02809.hp2 HG03209.hp1 others(8): Show |
intron_variant | MODIFIER | c.-193+605dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105147574 | ||||||
chr4:105147584 | T | C | 1 | a0006c0006t0068g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-193+605T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105147584 | |||||||
chr4:105147797 | T | C | 3 | a0004c0004t0004g0015 a0004c0004t0037g0016 a0004c0004t0048g0017 |
3 | NA18993.hp1 NA19012.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-193+818T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105147797 | |||||||
chr4:105147841 | A | AG | 12 | a0001c0001t0001g0320 a0001c0001t0004g0322 a0001c0001t0006g0318 others(9): Show |
12 | HG00609.hp2 HG01109.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.-193+867dupG | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105147841 | ||||||
chr4:105147856 | G | T | 103 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0234 others(100): Show |
103 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.-193+877G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105147856 | |||||||
chr4:105147898 | G | A | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-193+919G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105147898 | |||||||
chr4:105148059 | T | TAC | 10 | a0001c0001t0001g0218 a0001c0001t0073g0024 a0001c0001t0075g0027 others(7): Show |
10 | HG00423.hp2 HG01081.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.-193+1103_-193+110 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105148059 | ||||||
chr4:105148082 | A | C | 16 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(13): Show |
16 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+1103A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105148082 | |||||||
chr4:105148155 | T | G | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-193+1176T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105148155 | |||||||
chr4:105148648 | T | G | 2 | a0004c0004t0094g0022 a0004c0031t0092g0021 |
2 | HG03831.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-193+1669T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105148648 | |||||||
chr4:105148715 | T | A | 1 | a0001c0001t0036g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-193+1736T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105148715 | |||||||
chr4:105148754 | G | A | 2 | a0001c0001t0086g0031 a0001c0001t0088g0030 |
2 | HG01361.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-193+1775G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105148754 | |||||||
chr4:105148762 | C | T | 1 | a0002c0002t0020g0201 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-193+1783C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105148762 | |||||||
chr4:105148814 | G | A | 1 | a0005c0005t0005g0032 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-193+1835G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105148814 | |||||||
chr4:105148848 | T | C | 1 | a0007c0009t0051g0033 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-193+1869T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105148848 | |||||||
chr4:105148970 | C | A | 1 | a0001c0001t0070g0034 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-193+1991C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105148970 | |||||||
chr4:105149048 | C | G | 1 | a0004c0004t0048g0017 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-193+2069C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105149048 | |||||||
chr4:105149069 | G | A | 8 | a0004c0008t0019g0327 a0004c0008t0019g0332 a0004c0008t0059g0323 others(5): Show |
8 | HG02809.hp2 HG03209.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.-193+2090G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105149069 | |||||||
chr4:105149092 | A | C | 1 | a0002c0002t0003g0200 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-193+2113A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105149092 | |||||||
chr4:105149105 | G | A | 2 | a0004c0004t0004g0035 a0004c0004t0018g0036 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-193+2126G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105149105 | |||||||
chr4:105149116 | G | T | 1 | a0004c0004t0048g0017 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-193+2137G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105149116 | |||||||
chr4:105149143 | A | T | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+2164A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105149143 | |||||||
chr4:105149179 | T | C | 1 | a0002c0002t0011g0037 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-193+2200T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105149179 | |||||||
chr4:105149283 | T | G | 4 | a0001c0001t0036g0029 a0004c0031t0092g0021 a0011c0015t0043g0347 others(1): Show |
4 | HG01099.hp2 HG02602.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-193+2304T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105149283 | |||||||
chr4:105149474 | A | G | 4 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0004g0310 others(1): Show |
4 | NA18946.hp1 NA18947.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.-193+2495A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105149474 | |||||||
chr4:105149573 | T | C | 3 | a0001c0007t0031g0038 a0001c0007t0057g0040 a0001c0022t0062g0039 |
3 | HG02622.hp1 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-193+2594T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105149573 | |||||||
chr4:105149907 | A | G | 137 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0234 others(134): Show |
137 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-193+2928A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105149907 | |||||||
chr4:105150231 | G | A | 1 | a0009c0013t0007g0219 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-193+3252G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105150231 | |||||||
chr4:105150440 | T | A | 45 | a0001c0001t0032g0052 a0001c0001t0073g0024 a0001c0001t0075g0027 others(42): Show |
45 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.-193+3461T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105150440 | |||||||
chr4:105150570 | G | A | 13 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(10): Show |
13 | HG02071.hp2 NA18944.hp2 NA18951.hp1 others(10): Show |
intron_variant | MODIFIER | c.-193+3591G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105150570 | |||||||
chr4:105150702 | C | G | 1 | a0003c0003t0004g0181 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-193+3723C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105150702 | |||||||
chr4:105150704 | A | C | 1 | a0003c0003t0004g0181 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-193+3725A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105150704 | |||||||
chr4:105150863 | C | G | 344 | a0001c0001t0001g0112 a0001c0001t0001g0189 a0001c0001t0001g0191 others(341): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.-193+3884C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105150863 | |||||||
chr4:105150952 | G | A | 1 | a0004c0004t0004g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-193+3973G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105150952 | |||||||
chr4:105150999 | G | T | 15 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(12): Show |
15 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.-193+4020G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105150999 | |||||||
chr4:105151045 | C | T | 1 | a0008c0010t0012g0011 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-193+4066C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151045 | |||||||
chr4:105151046 | G | A | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-193+4067G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151046 | |||||||
chr4:105151107 | C | T | 1 | a0018c0021t0004g0345 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-193+4128C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151107 | |||||||
chr4:105151142 | G | T | 1 | a0001c0007t0071g0180 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-193+4163G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151142 | |||||||
chr4:105151179 | G | T | 1 | a0004c0004t0010g0319 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-193+4200G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151179 | |||||||
chr4:105151299 | C | T | 17 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(14): Show |
17 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.-193+4320C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151299 | |||||||
chr4:105151328 | G | A | 48 | a0001c0001t0001g0112 a0001c0001t0015g0330 a0001c0007t0030g0117 others(45): Show |
49 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.-193+4349G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151328 | |||||||
chr4:105151426 | C | T | 16 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(13): Show |
16 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+4447C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151426 | |||||||
chr4:105151791 | G | A | 1 | a0001c0001t0004g0186 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-193+4812G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151791 | |||||||
chr4:105151837 | C | T | 1 | a0004c0004t0004g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-193+4858C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151837 | |||||||
chr4:105151838 | G | A | 16 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(13): Show |
16 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+4859G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151838 | |||||||
chr4:105151849 | T | C | 1 | a0007c0009t0051g0033 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-193+4870T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151849 | |||||||
chr4:105151900 | C | T | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+4921C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151900 | |||||||
chr4:105151932 | G | A | 9 | a0003c0003t0002g0001 a0003c0003t0002g0078 a0003c0003t0002g0079 others(6): Show |
10 | HG00544.hp1 HG02015.hp1 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.-193+4953G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151932 | |||||||
chr4:105151958 | C | G | 16 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(13): Show |
16 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+4979C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151958 | |||||||
chr4:105151959 | C | A | 1 | a0001c0001t0010g0229 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-193+4980C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151959 | |||||||
chr4:105151982 | C | T | 1 | a0001c0001t0007g0199 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-193+5003C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105151982 | |||||||
chr4:105152094 | A | G | 6 | a0001c0007t0030g0339 a0005c0005t0014g0342 a0005c0005t0014g0343 others(3): Show |
6 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-193+5115A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105152094 | |||||||
chr4:105152205 | C | T | 2 | a0004c0004t0004g0035 a0004c0004t0018g0036 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-193+5226C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105152205 | |||||||
chr4:105152352 | A | G | 105 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0234 others(102): Show |
105 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.-193+5373A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105152352 | |||||||
chr4:105152513 | A | G | 1 | a0001c0001t0093g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-193+5534A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105152513 | |||||||
chr4:105152546 | G | GA | 50 | a0001c0001t0001g0112 a0001c0001t0015g0330 a0001c0007t0030g0117 others(47): Show |
51 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.-193+5576dupA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105152546 | ||||||
chr4:105152578 | TTTTC | T | 71 | a0001c0001t0001g0112 a0001c0001t0001g0307 a0001c0001t0004g0311 others(68): Show |
72 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.-193+5619_-193+562 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105152578 | ||||||
chr4:105152595 | TTTC | T | 170 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0218 others(167): Show |
170 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.-193+5619_-193+562 others(7): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105152595 | ||||||
chr4:105152817 | G | A | 2 | a0001c0001t0001g0232 a0003c0003t0002g0231 |
2 | NA19057.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-193+5838G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105152817 | |||||||
chr4:105152910 | A | G | 3 | a0001c0007t0031g0038 a0001c0007t0057g0040 a0001c0022t0062g0039 |
3 | HG02622.hp1 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-193+5931A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105152910 | |||||||
chr4:105153084 | T | C | 51 | a0001c0001t0001g0112 a0001c0001t0015g0330 a0001c0007t0030g0117 others(48): Show |
52 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.-193+6105T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105153084 | |||||||
chr4:105153114 | A | G | 8 | a0004c0008t0019g0327 a0004c0008t0019g0332 a0004c0008t0059g0323 others(5): Show |
8 | HG02809.hp2 HG03209.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.-193+6135A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105153114 | |||||||
chr4:105153375 | T | C | 1 | a0001c0001t0093g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-193+6396T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105153375 | |||||||
chr4:105153420 | TCTTGTGA others(6): Show |
T | 1 | a0018c0021t0004g0345 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-193+6442_-193+645 others(17): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105153420 | |||||||
chr4:105153444 | T | C | 3 | a0001c0007t0031g0038 a0001c0007t0057g0040 a0001c0022t0062g0039 |
3 | HG02622.hp1 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-193+6465T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105153444 | |||||||
chr4:105153588 | A | G | 1 | a0002c0002t0003g0200 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-193+6609A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105153588 | |||||||
chr4:105153669 | T | G | 276 | a0001c0001t0001g0112 a0001c0001t0001g0189 a0001c0001t0001g0191 others(273): Show |
277 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(274): Show |
intron_variant | MODIFIER | c.-193+6690T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105153669 | |||||||
chr4:105153886 | G | A | 1 | a0018c0021t0004g0345 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-193+6907G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105153886 | |||||||
chr4:105153934 | A | G | 2 | a0001c0001t0016g0215 a0001c0001t0016g0216 |
2 | HG01106.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-193+6955A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105153934 | |||||||
chr4:105154027 | G | T | 1 | a0004c0004t0039g0068 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-193+7048G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105154027 | |||||||
chr4:105154031 | C | A | 2 | a0004c0004t0004g0035 a0004c0004t0018g0036 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-193+7052C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105154031 | |||||||
chr4:105154104 | G | T | 1 | a0004c0004t0101g0075 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-193+7125G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105154104 | |||||||
chr4:105154183 | A | G | 13 | a0004c0004t0013g0056 a0004c0004t0013g0057 a0004c0004t0018g0063 others(10): Show |
13 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.-193+7204A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105154183 | |||||||
chr4:105154341 | T | G | 200 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0218 others(197): Show |
200 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.-193+7362T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105154341 | |||||||
chr4:105154477 | G | T | 1 | a0001c0001t0075g0027 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-193+7498G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105154477 | |||||||
chr4:105154601 | A | G | 54 | a0001c0001t0001g0112 a0001c0001t0015g0330 a0001c0007t0030g0117 others(51): Show |
55 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-193+7622A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105154601 | |||||||
chr4:105154659 | A | G | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-193+7680A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105154659 | |||||||
chr4:105154752 | C | T | 12 | a0001c0001t0093g0179 a0001c0007t0030g0339 a0005c0005t0014g0342 others(9): Show |
12 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-193+7773C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105154752 | |||||||
chr4:105154844 | G | A | 1 | a0001c0001t0093g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-193+7865G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105154844 | |||||||
chr4:105155000 | G | A | 43 | a0001c0001t0001g0112 a0001c0001t0015g0330 a0003c0003t0002g0001 others(40): Show |
44 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.-193+8021G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105155000 | |||||||
chr4:105155017 | C | G | 14 | a0004c0004t0013g0056 a0004c0004t0013g0057 a0004c0004t0018g0063 others(11): Show |
14 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-193+8038C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105155017 | |||||||
chr4:105155349 | A | G | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+8370A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105155349 | |||||||
chr4:105155372 | G | A | 1 | a0001c0001t0093g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-193+8393G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105155372 | |||||||
chr4:105155569 | T | A | 50 | a0001c0001t0001g0112 a0001c0001t0015g0330 a0001c0007t0030g0117 others(47): Show |
51 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.-193+8590T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105155569 | |||||||
chr4:105155592 | A | G | 121 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0234 others(118): Show |
121 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-193+8613A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105155592 | |||||||
chr4:105155596 | C | A | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-193+8617C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105155596 | |||||||
chr4:105155791 | A | G | 16 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(13): Show |
16 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+8812A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105155791 | |||||||
chr4:105155885 | T | G | 1 | a0003c0003t0004g0181 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-193+8906T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105155885 | |||||||
chr4:105156161 | C | T | 1 | a0018c0021t0004g0345 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-193+9182C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105156161 | |||||||
chr4:105156258 | G | A | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+9279G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105156258 | |||||||
chr4:105156543 | G | C | 1 | a0001c0001t0075g0027 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-193+9564G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105156543 | |||||||
chr4:105156752 | A | T | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-193+9773A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105156752 | |||||||
chr4:105156827 | A | G | 2 | a0003c0003t0002g0113 a0003c0003t0002g0114 |
2 | NA18946.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.-193+9848A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105156827 | |||||||
chr4:105156888 | T | G | 3 | a0010c0012t0003g0182 a0010c0012t0009g0217 a0010c0012t0009g0233 |
3 | NA18978.hp2 NA19007.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-193+9909T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105156888 | |||||||
chr4:105156924 | C | G | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+9945C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105156924 | |||||||
chr4:105156940 | A | G | 42 | a0001c0001t0032g0052 a0001c0001t0073g0024 a0001c0001t0075g0027 others(39): Show |
42 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.-193+9961A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105156940 | |||||||
chr4:105156958 | C | T | 4 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0004g0310 others(1): Show |
4 | NA18946.hp1 NA18947.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.-193+9979C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105156958 | |||||||
chr4:105157078 | T | G | 1 | a0005c0005t0005g0032 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-193+10099T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105157078 | |||||||
chr4:105157083 | A | C | 1 | a0018c0021t0004g0345 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-193+10104A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105157083 | |||||||
chr4:105157158 | A | G | 2 | a0004c0004t0094g0022 a0004c0031t0092g0021 |
2 | HG03831.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-193+10179A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105157158 | |||||||
chr4:105157187 | ATAT | A | 43 | a0001c0001t0032g0052 a0001c0001t0073g0024 a0001c0001t0075g0027 others(40): Show |
43 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.-193+10211_-193+10 others(9): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105157187 | ||||||
chr4:105157330 | T | G | 3 | a0001c0001t0001g0234 a0001c0001t0010g0235 a0001c0028t0001g0236 |
3 | HG01496.hp1 NA19056.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-193+10351T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105157330 | |||||||
chr4:105157521 | C | T | 1 | a0003c0003t0018g0118 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-193+10542C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105157521 | |||||||
chr4:105157650 | A | G | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+10671A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105157650 | |||||||
chr4:105157802 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-193+10823G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105157802 | |||||||
chr4:105157846 | T | G | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-193+10867T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105157846 | |||||||
chr4:105157955 | G | C | 1 | a0003c0003t0002g0090 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-193+10976G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105157955 | |||||||
chr4:105157999 | C | T | 2 | a0004c0004t0004g0035 a0004c0004t0018g0036 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-193+11020C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105157999 | |||||||
chr4:105158092 | G | T | 3 | a0004c0004t0084g0072 a0013c0014t0060g0074 a0013c0014t0064g0073 |
3 | HG03130.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-193+11113G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105158092 | |||||||
chr4:105158112 | C | T | 1 | a0001c0001t0041g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-193+11133C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105158112 | |||||||
chr4:105158143 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-193+11164G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105158143 | |||||||
chr4:105158177 | C | T | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+11198C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105158177 | |||||||
chr4:105158228 | T | A | 11 | a0001c0007t0030g0339 a0005c0005t0014g0342 a0005c0005t0014g0343 others(8): Show |
11 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-193+11249T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105158228 | |||||||
chr4:105158291 | G | A | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+11312G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105158291 | |||||||
chr4:105158301 | G | A | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-193+11322G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105158301 | |||||||
chr4:105158576 | C | G | 3 | a0004c0004t0058g0312 a0004c0004t0100g0055 a0004c0019t0081g0054 |
3 | HG02257.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-193+11597C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105158576 | |||||||
chr4:105158596 | G | T | 1 | a0004c0004t0018g0120 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-193+11617G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105158596 | |||||||
chr4:105158597 | G | T | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+11618G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105158597 | |||||||
chr4:105158811 | GA | G | 7 | a0001c0001t0004g0322 a0001c0001t0032g0052 a0001c0001t0080g0053 others(4): Show |
7 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-193+11843delA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105158811 | ||||||
chr4:105158929 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-193+11950C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105158929 | |||||||
chr4:105159122 | T | C | 4 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0004g0310 others(1): Show |
4 | NA18946.hp1 NA18947.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.-193+12143T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105159122 | |||||||
chr4:105159251 | C | CT | 30 | a0001c0001t0001g0250 a0001c0001t0001g0308 a0001c0001t0001g0331 others(27): Show |
30 | HG00544.hp2 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.-193+12290dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105159251 | ||||||
chr4:105159255 | T | C | 2 | a0004c0008t0059g0323 a0004c0008t0067g0070 |
2 | HG02572.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-193+12276T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105159255 | |||||||
chr4:105159325 | G | A | 3 | a0001c0007t0031g0038 a0001c0007t0057g0040 a0001c0022t0062g0039 |
3 | HG02622.hp1 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-193+12346G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105159325 | |||||||
chr4:105159339 | T | C | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+12360T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105159339 | |||||||
chr4:105159368 | G | T | 1 | a0001c0001t0008g0306 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-193+12389G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105159368 | |||||||
chr4:105159507 | G | C | 1 | a0001c0001t0006g0239 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-193+12528G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105159507 | |||||||
chr4:105159599 | A | G | 1 | a0003c0003t0018g0118 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-193+12620A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105159599 | |||||||
chr4:105159823 | G | A | 1 | a0002c0002t0003g0315 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-193+12844G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105159823 | |||||||
chr4:105159970 | C | T | 1 | a0001c0001t0006g0214 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-193+12991C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105159970 | |||||||
chr4:105160017 | T | A | 3 | a0002c0002t0003g0240 a0002c0002t0003g0241 a0002c0002t0003g0242 |
3 | NA19058.hp2 NA19062.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-193+13038T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160017 | |||||||
chr4:105160161 | C | T | 1 | a0004c0004t0100g0055 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-193+13182C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160161 | |||||||
chr4:105160401 | G | A | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+13422G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160401 | |||||||
chr4:105160411 | T | A | 4 | a0001c0001t0001g0320 a0001c0001t0004g0243 a0001c0001t0007g0244 others(1): Show |
4 | HG01071.hp2 HG01255.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.-193+13432T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160411 | |||||||
chr4:105160479 | T | C | 124 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0234 others(121): Show |
124 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.-193+13500T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160479 | |||||||
chr4:105160579 | G | A | 3 | a0006c0006t0034g0333 a0006c0006t0082g0334 a0006c0006t0083g0335 |
3 | HG02572.hp1 HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-193+13600G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160579 | |||||||
chr4:105160633 | C | T | 1 | a0001c0001t0016g0216 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-193+13654C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160633 | |||||||
chr4:105160715 | C | A | 5 | a0001c0007t0030g0117 a0001c0007t0031g0115 a0001c0007t0071g0180 others(2): Show |
5 | HG00735.hp2 HG01070.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-193+13736C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160715 | |||||||
chr4:105160774 | G | T | 5 | a0001c0001t0093g0179 a0004c0004t0010g0226 a0004c0004t0010g0227 others(2): Show |
5 | HG02071.hp2 HG03041.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.-193+13795G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160774 | |||||||
chr4:105160774 | GGTTT | G | 11 | a0001c0007t0030g0339 a0005c0005t0014g0342 a0005c0005t0014g0343 others(8): Show |
11 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-193+13812_-193+13 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105160774 | ||||||
chr4:105160907 | C | T | 1 | a0005c0005t0014g0343 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-193+13928C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160907 | |||||||
chr4:105160963 | G | A | 199 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0218 others(196): Show |
199 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.-193+13984G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160963 | |||||||
chr4:105160965 | G | A | 1 | a0001c0001t0004g0203 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-193+13986G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105160965 | |||||||
chr4:105161003 | T | C | 1 | a0006c0006t0022g0338 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-193+14024T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105161003 | |||||||
chr4:105161145 | A | G | 1 | a0004c0004t0028g0202 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-193+14166A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105161145 | |||||||
chr4:105161290 | A | G | 2 | a0004c0008t0008g0071 a0004c0008t0067g0070 |
2 | HG01175.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-193+14311A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105161290 | |||||||
chr4:105161316 | A | G | 12 | a0001c0001t0104g0007 a0006c0006t0026g0005 a0006c0006t0026g0006 others(9): Show |
12 | HG01192.hp1 HG01884.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-193+14337A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105161316 | |||||||
chr4:105161324 | T | C | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-193+14345T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105161324 | |||||||
chr4:105161802 | A | G | 2 | a0013c0014t0060g0074 a0013c0014t0064g0073 |
2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-193+14823A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105161802 | |||||||
chr4:105161898 | G | C | 1 | a0016c0025t0017g0246 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-193+14919G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105161898 | |||||||
chr4:105161921 | T | TGTGTGTA others(4): Show |
1 | a0006c0006t0097g0069 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-193+14954_-193+14 others(17): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105161921 | ||||||
chr4:105162256 | A | G | 1 | a0003c0003t0002g0111 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-193+15277A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105162256 | |||||||
chr4:105162377 | A | T | 2 | a0004c0008t0008g0071 a0004c0008t0067g0070 |
2 | HG01175.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-193+15398A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105162377 | |||||||
chr4:105162433 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-193+15454G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105162433 | |||||||
chr4:105162619 | C | T | 118 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0237 others(115): Show |
118 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-193+15640C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105162619 | |||||||
chr4:105162696 | A | T | 1 | a0001c0001t0061g0213 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-193+15717A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105162696 | |||||||
chr4:105162727 | T | A | 9 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(6): Show |
9 | HG00140.hp1 HG00741.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.-193+15748T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105162727 | |||||||
chr4:105162834 | G | C | 5 | a0001c0001t0073g0024 a0001c0001t0075g0027 a0001c0001t0076g0023 others(2): Show |
5 | HG01081.hp2 HG02004.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-193+15855G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105162834 | |||||||
chr4:105163392 | T | C | 1 | a0018c0021t0004g0345 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-193+16413T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163392 | |||||||
chr4:105163421 | A | G | 1 | a0001c0001t0008g0304 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-193+16442A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163421 | |||||||
chr4:105163435 | C | T | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-193+16456C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163435 | |||||||
chr4:105163485 | C | A | 1 | a0001c0001t0070g0034 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-193+16506C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163485 | |||||||
chr4:105163486 | G | A | 44 | a0001c0001t0032g0052 a0001c0001t0073g0024 a0001c0001t0075g0027 others(41): Show |
44 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.-193+16507G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163486 | |||||||
chr4:105163506 | C | T | 1 | a0004c0011t0040g0329 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-193+16527C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163506 | |||||||
chr4:105163518 | A | C | 1 | a0004c0004t0004g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-193+16539A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163518 | |||||||
chr4:105163621 | C | T | 102 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0237 others(99): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-193+16642C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163621 | |||||||
chr4:105163732 | T | C | 1 | a0002c0002t0003g0316 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-193+16753T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163732 | |||||||
chr4:105163734 | G | A | 1 | a0001c0001t0093g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-193+16755G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163734 | |||||||
chr4:105163761 | A | T | 1 | a0005c0005t0005g0303 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-193+16782A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163761 | |||||||
chr4:105163782 | C | G | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+16803C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163782 | |||||||
chr4:105163806 | C | CGA | 4 | a0002c0002t0003g0123 a0002c0002t0003g0126 a0002c0002t0021g0124 others(1): Show |
4 | HG04199.hp1 HG04228.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.-193+16875_-193+16 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | ||||||
chr4:105163806 | C | CGAGAGA | 3 | a0001c0001t0001g0248 a0002c0002t0003g0122 a0002c0002t0003g0315 |
3 | NA18990.hp2 NA19001.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-193+16871_-193+16 others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | ||||||
chr4:105163806 | C | CGAGAGAG others(3): Show |
2 | a0001c0007t0031g0038 a0001c0022t0062g0039 |
2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-193+16867_-193+16 others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | ||||||
chr4:105163806 | C | CGAGAGAG others(5): Show |
1 | a0001c0001t0053g0187 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-193+16865_-193+16 others(18): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | ||||||
chr4:105163806 | CGA | C | 24 | a0001c0001t0001g0250 a0001c0001t0001g0305 a0001c0001t0002g0249 others(21): Show |
24 | HG00323.hp1 HG00558.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.-193+16875_-193+16 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | ||||||
chr4:105163806 | CGAGA | C | 37 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(34): Show |
37 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.-193+16873_-193+16 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | ||||||
chr4:105163806 | CGAGAGA | C | 70 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0269 others(67): Show |
70 | HG00558.hp1 HG00609.hp1 HG01169.hp2 others(67): Show |
intron_variant | MODIFIER | c.-193+16871_-193+16 others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | ||||||
chr4:105163806 | CGAGAGAG others(1): Show |
C | 22 | a0001c0001t0001g0238 a0001c0001t0001g0297 a0001c0001t0004g0203 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.-193+16869_-193+16 others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | ||||||
chr4:105163806 | CGAGAGAG others(3): Show |
C | 46 | a0001c0001t0001g0247 a0001c0001t0004g0209 a0001c0001t0006g0206 others(43): Show |
47 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.-193+16867_-193+16 others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | ||||||
chr4:105163806 | CGAGAGAG others(5): Show |
C | 8 | a0001c0001t0001g0237 a0001c0001t0008g0211 a0001c0001t0070g0034 others(5): Show |
8 | HG01517.hp2 HG02055.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.-193+16865_-193+16 others(18): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | ||||||
chr4:105163806 | CGAGAGAG others(7): Show |
C | 12 | a0001c0001t0001g0112 a0001c0001t0006g0212 a0004c0004t0033g0058 others(9): Show |
12 | HG01109.hp1 HG01175.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.-193+16863_-193+16 others(20): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | ||||||
chr4:105163806 | CGAGAGAG others(9): Show |
C | 9 | a0001c0001t0006g0214 a0001c0001t0006g0318 a0001c0001t0061g0213 others(6): Show |
9 | HG00438.hp1 HG01074.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.-193+16861_-193+16 others(22): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | ||||||
chr4:105163806 | CGAGAGAG others(11): Show |
C | 18 | a0001c0001t0075g0027 a0004c0004t0018g0063 a0004c0004t0072g0062 others(15): Show |
18 | HG00738.hp2 HG01192.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-193+16859_-193+16 others(24): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | ||||||
chr4:105163806 | CGAGAGAG others(13): Show |
C | 9 | a0001c0001t0073g0024 a0001c0001t0076g0023 a0003c0003t0098g0110 others(6): Show |
9 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.-193+16857_-193+16 others(26): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | ||||||
chr4:105163806 | CGAGAGAG others(15): Show |
C | 5 | a0001c0001t0032g0052 a0001c0001t0077g0026 a0001c0001t0078g0025 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-193+16855_-193+16 others(28): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163806 | ||||||
chr4:105163830 | AGAGAGAG others(19): Show |
A | 1 | a0005c0005t0014g0067 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-193+16853_-193+16 others(32): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163830 | ||||||
chr4:105163832 | AGAGAGAG others(17): Show |
A | 5 | a0004c0004t0013g0057 a0005c0005t0005g0041 a0005c0005t0005g0042 others(2): Show |
5 | HG01106.hp2 HG01243.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-193+16855_-193+16 others(30): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163832 | ||||||
chr4:105163834 | AGAGAGAG others(15): Show |
A | 1 | a0004c0004t0013g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-193+16857_-193+16 others(28): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163834 | ||||||
chr4:105163836 | AGAGAGAG others(13): Show |
A | 2 | a0004c0008t0008g0071 a0004c0008t0067g0070 |
2 | HG01175.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-193+16859_-193+16 others(26): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163836 | ||||||
chr4:105163838 | AGAGAGAG others(11): Show |
A | 1 | a0001c0001t0036g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-193+16861_-193+16 others(24): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163838 | ||||||
chr4:105163840 | AGAGAGAG others(9): Show |
A | 1 | a0002c0002t0009g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-193+16863_-193+16 others(22): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163840 | ||||||
chr4:105163842 | A | T | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+16863A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163842 | |||||||
chr4:105163842 | AGAGAGAG others(7): Show |
A | 1 | a0003c0003t0015g0091 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-193+16865_-193+16 others(20): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163842 | ||||||
chr4:105163844 | A | T | 2 | a0004c0004t0094g0022 a0011c0015t0044g0346 |
2 | HG01099.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-193+16865A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163844 | |||||||
chr4:105163846 | A | T | 3 | a0004c0004t0094g0022 a0011c0015t0043g0347 a0011c0015t0044g0346 |
3 | HG01099.hp2 HG02602.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-193+16867A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163846 | |||||||
chr4:105163847 | G | A | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+16868G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163847 | |||||||
chr4:105163848 | A | T | 4 | a0004c0004t0094g0022 a0011c0015t0043g0347 a0011c0015t0044g0346 others(1): Show |
4 | HG01099.hp2 HG02602.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.-193+16869A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163848 | |||||||
chr4:105163848 | AGAGAGAG others(1): Show |
A | 4 | a0001c0001t0001g0320 a0001c0001t0004g0243 a0001c0001t0007g0244 others(1): Show |
4 | HG01071.hp2 HG01255.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.-193+16871_-193+16 others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163848 | ||||||
chr4:105163850 | A | T | 8 | a0004c0004t0094g0022 a0006c0006t0026g0005 a0006c0006t0026g0006 others(5): Show |
8 | HG01099.hp2 HG01192.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.-193+16871A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163850 | |||||||
chr4:105163851 | G | C | 1 | a0006c0006t0045g0121 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-193+16872G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163851 | |||||||
chr4:105163852 | A | T | 37 | a0001c0001t0001g0247 a0001c0001t0001g0262 a0001c0001t0001g0263 others(34): Show |
37 | HG00673.hp1 HG01099.hp2 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.-193+16873A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163852 | |||||||
chr4:105163854 | A | AGAGAGAG others(19): Show |
1 | a0001c0001t0055g0194 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-193+16876_-193+16 others(32): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163854 | ||||||
chr4:105163854 | A | AGAGAGAG others(9): Show |
1 | a0001c0001t0005g0192 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-193+16876_-193+16 others(22): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163854 | ||||||
chr4:105163854 | A | AGAGAGAG others(11): Show |
1 | a0001c0001t0007g0197 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-193+16876_-193+16 others(24): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163854 | ||||||
chr4:105163854 | A | AGAGAGAG others(7): Show |
2 | a0001c0001t0001g0191 a0001c0001t0088g0030 |
2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.-193+16876_-193+16 others(20): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163854 | ||||||
chr4:105163854 | A | AGAGAGAG others(5): Show |
1 | a0001c0001t0005g0196 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-193+16876_-193+16 others(18): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163854 | ||||||
chr4:105163854 | A | AGAGAGAG others(3): Show |
4 | a0001c0001t0001g0189 a0001c0001t0005g0188 a0001c0001t0041g0198 others(1): Show |
4 | HG00140.hp1 HG01123.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-193+16876_-193+16 others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163854 | ||||||
chr4:105163854 | A | AGAGAGAG others(5): Show |
2 | a0001c0001t0005g0193 a0001c0001t0032g0195 |
2 | HG01978.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-193+16876_-193+16 others(18): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163854 | ||||||
chr4:105163854 | A | T | 152 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0247 others(149): Show |
152 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.-193+16875A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163854 | |||||||
chr4:105163854 | AGTGTGTG others(7): Show |
A | 1 | a0014c0024t0029g0127 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-193+16896_-193+16 others(20): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105163854 | ||||||
chr4:105163856 | T | A | 4 | a0002c0002t0003g0132 a0002c0002t0003g0139 a0002c0002t0021g0124 others(1): Show |
4 | HG04199.hp1 HG04228.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-193+16877T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163856 | |||||||
chr4:105163967 | T | A | 1 | a0001c0001t0001g0248 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-193+16988T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105163967 | |||||||
chr4:105164016 | A | T | 1 | a0003c0003t0002g0107 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-193+17037A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164016 | |||||||
chr4:105164044 | C | T | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+17065C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164044 | |||||||
chr4:105164172 | A | T | 2 | a0004c0004t0013g0056 a0004c0004t0013g0057 |
2 | HG01243.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-193+17193A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164172 | |||||||
chr4:105164235 | G | A | 2 | a0004c0004t0033g0058 a0004c0004t0042g0059 |
2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-193+17256G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164235 | |||||||
chr4:105164247 | G | A | 1 | a0004c0004t0099g0060 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-193+17268G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164247 | |||||||
chr4:105164334 | T | A | 1 | a0006c0006t0046g0002 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-193+17355T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164334 | |||||||
chr4:105164349 | G | A | 1 | a0001c0001t0002g0251 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-193+17370G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164349 | |||||||
chr4:105164367 | C | A | 1 | a0014c0024t0029g0127 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-193+17388C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164367 | |||||||
chr4:105164617 | T | C | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-193+17638T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164617 | |||||||
chr4:105164624 | T | C | 2 | a0002c0002t0020g0176 a0002c0002t0020g0177 |
2 | HG00280.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.-193+17645T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164624 | |||||||
chr4:105164630 | G | A | 1 | a0001c0001t0036g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-193+17651G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164630 | |||||||
chr4:105164931 | C | A | 1 | a0002c0002t0003g0240 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-193+17952C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105164931 | |||||||
chr4:105165028 | T | C | 1 | a0003c0003t0098g0110 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-193+18049T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105165028 | |||||||
chr4:105165145 | C | T | 102 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0237 others(99): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-193+18166C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105165145 | |||||||
chr4:105165203 | C | T | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-193+18224C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105165203 | |||||||
chr4:105165237 | G | T | 1 | a0004c0019t0081g0054 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-193+18258G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105165237 | |||||||
chr4:105165256 | A | T | 11 | a0001c0007t0030g0339 a0005c0005t0014g0342 a0005c0005t0014g0343 others(8): Show |
11 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-193+18277A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105165256 | |||||||
chr4:105165320 | G | A | 1 | a0004c0008t0008g0071 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-193+18341G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105165320 | |||||||
chr4:105165331 | G | A | 4 | a0003c0003t0002g0088 a0003c0003t0002g0089 a0003c0003t0002g0111 others(1): Show |
4 | HG01074.hp2 HG01081.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.-193+18352G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105165331 | |||||||
chr4:105165370 | C | T | 1 | a0004c0004t0084g0072 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-193+18391C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105165370 | |||||||
chr4:105165371 | G | A | 1 | a0001c0001t0008g0211 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-193+18392G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105165371 | |||||||
chr4:105165617 | C | A | 1 | a0018c0021t0004g0345 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-193+18638C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105165617 | |||||||
chr4:105166060 | T | C | 121 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0234 others(118): Show |
121 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-193+19081T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105166060 | |||||||
chr4:105166498 | C | A | 16 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(13): Show |
16 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+19519C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105166498 | |||||||
chr4:105166498 | C | T | 3 | a0004c0004t0058g0312 a0004c0004t0100g0055 a0004c0019t0081g0054 |
3 | HG02257.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-193+19519C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105166498 | |||||||
chr4:105166531 | C | T | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-193+19552C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105166531 | |||||||
chr4:105166545 | G | A | 1 | a0018c0021t0004g0345 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-193+19566G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105166545 | |||||||
chr4:105166610 | G | GA | 44 | a0001c0001t0002g0249 a0001c0001t0015g0330 a0003c0003t0002g0001 others(41): Show |
45 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.-193+19640dupA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105166610 | ||||||
chr4:105166620 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-193+19641G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105166620 | |||||||
chr4:105166620 | GAAAA | G | 5 | a0001c0001t0073g0024 a0001c0001t0075g0027 a0001c0001t0076g0023 others(2): Show |
5 | HG01081.hp2 HG02004.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-193+19647_-193+19 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105166620 | ||||||
chr4:105166621 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-193+19642A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105166621 | |||||||
chr4:105166665 | A | G | 106 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0234 others(103): Show |
106 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.-193+19686A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105166665 | |||||||
chr4:105166786 | T | C | 1 | a0001c0001t0088g0030 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-193+19807T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105166786 | |||||||
chr4:105166875 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-193+19896A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105166875 | |||||||
chr4:105166894 | T | A | 118 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0237 others(115): Show |
118 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-193+19915T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105166894 | |||||||
chr4:105167001 | C | T | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+20022C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105167001 | |||||||
chr4:105167135 | T | A | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+20156T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105167135 | |||||||
chr4:105167326 | A | G | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-193+20347A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105167326 | |||||||
chr4:105167342 | A | G | 1 | a0001c0001t0004g0299 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-193+20363A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105167342 | |||||||
chr4:105167441 | TGTA | T | 7 | a0001c0007t0030g0339 a0004c0004t0094g0022 a0005c0005t0014g0342 others(4): Show |
7 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-193+20466_-193+20 others(9): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105167441 | ||||||
chr4:105167511 | A | G | 1 | a0001c0001t0093g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-193+20532A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105167511 | |||||||
chr4:105167890 | G | A | 19 | a0004c0004t0013g0056 a0004c0004t0013g0057 a0004c0004t0018g0063 others(16): Show |
19 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.-193+20911G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105167890 | |||||||
chr4:105167896 | T | C | 1 | a0001c0001t0005g0267 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-193+20917T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105167896 | |||||||
chr4:105167923 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-193+20944C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105167923 | |||||||
chr4:105167995 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-193+21016A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105167995 | |||||||
chr4:105168026 | C | T | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-193+21047C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105168026 | |||||||
chr4:105168172 | A | G | 1 | a0006c0006t0097g0069 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-193+21193A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105168172 | |||||||
chr4:105168222 | C | T | 1 | a0018c0021t0004g0345 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-193+21243C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105168222 | |||||||
chr4:105168405 | T | C | 1 | a0004c0004t0004g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-193+21426T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105168405 | |||||||
chr4:105168498 | C | A | 1 | a0004c0004t0058g0312 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-193+21519C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105168498 | |||||||
chr4:105168580 | T | A | 1 | a0001c0001t0008g0205 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-193+21601T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105168580 | |||||||
chr4:105168581 | A | T | 102 | a0001c0001t0001g0112 a0001c0001t0001g0189 a0001c0001t0001g0191 others(99): Show |
103 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-193+21602A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105168581 | |||||||
chr4:105168833 | T | C | 1 | a0004c0019t0081g0054 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-192-21527T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105168833 | |||||||
chr4:105169398 | G | T | 1 | a0004c0004t0058g0312 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-192-20962G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105169398 | |||||||
chr4:105169488 | C | T | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-192-20872C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105169488 | |||||||
chr4:105169892 | T | C | 1 | a0004c0004t0058g0312 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-192-20468T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105169892 | |||||||
chr4:105169925 | C | A | 1 | a0006c0006t0097g0069 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-192-20435C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105169925 | |||||||
chr4:105169925 | C | CTG | 34 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(31): Show |
34 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-192-20435_-192-20 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105169925 | |||||||
chr4:105169926 | C | T | 34 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(31): Show |
34 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-192-20434C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105169926 | |||||||
chr4:105169927 | C | T | 34 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(31): Show |
34 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-192-20433C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105169927 | |||||||
chr4:105170017 | C | A | 2 | a0013c0014t0060g0074 a0013c0014t0064g0073 |
2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-192-20343C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170017 | |||||||
chr4:105170067 | T | A | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-192-20293T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170067 | |||||||
chr4:105170095 | T | C | 33 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(30): Show |
33 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.-192-20265T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170095 | |||||||
chr4:105170109 | G | A | 41 | a0001c0001t0001g0112 a0001c0001t0015g0330 a0003c0003t0002g0001 others(38): Show |
42 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.-192-20251G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170109 | |||||||
chr4:105170178 | T | C | 1 | a0010c0012t0009g0233 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-192-20182T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170178 | |||||||
chr4:105170299 | C | A | 31 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(28): Show |
31 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.-192-20061C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170299 | |||||||
chr4:105170435 | A | G | 1 | a0001c0001t0104g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-192-19925A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170435 | |||||||
chr4:105170788 | T | C | 1 | a0001c0001t0007g0300 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-192-19572T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170788 | |||||||
chr4:105170789 | T | C | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-192-19571T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170789 | |||||||
chr4:105170821 | G | A | 22 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(19): Show |
22 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-192-19539G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170821 | |||||||
chr4:105170919 | C | T | 2 | a0001c0001t0002g0251 a0001c0001t0004g0295 |
2 | NA19070.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.-192-19441C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170919 | |||||||
chr4:105170963 | A | C | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-192-19397A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170963 | |||||||
chr4:105170966 | A | G | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-192-19394A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105170966 | |||||||
chr4:105171071 | G | A | 6 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(3): Show |
6 | HG01192.hp1 HG02818.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-192-19289G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105171071 | |||||||
chr4:105171342 | A | G | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-192-19018A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105171342 | |||||||
chr4:105171383 | C | T | 18 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(15): Show |
18 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-192-18977C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105171383 | |||||||
chr4:105171710 | A | G | 2 | a0002c0002t0011g0157 a0002c0002t0011g0175 |
2 | HG00558.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-192-18650A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105171710 | |||||||
chr4:105171778 | G | T | 2 | a0001c0001t0077g0026 a0001c0001t0078g0025 |
2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-192-18582G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105171778 | |||||||
chr4:105171865 | T | C | 1 | a0002c0002t0003g0128 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-192-18495T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105171865 | |||||||
chr4:105172270 | T | G | 1 | a0001c0001t0008g0211 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-192-18090T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105172270 | |||||||
chr4:105172321 | A | G | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-192-18039A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105172321 | |||||||
chr4:105172391 | C | T | 17 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(14): Show |
17 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.-192-17969C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105172391 | |||||||
chr4:105172468 | T | C | 1 | a0001c0001t0010g0229 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-192-17892T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105172468 | |||||||
chr4:105173233 | A | C | 2 | a0001c0001t0077g0026 a0001c0001t0078g0025 |
2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-192-17127A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105173233 | |||||||
chr4:105173257 | C | T | 2 | a0007c0009t0027g0049 a0007c0009t0052g0048 |
2 | HG00738.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.-192-17103C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105173257 | |||||||
chr4:105173270 | G | A | 163 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0218 others(160): Show |
163 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.-192-17090G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105173270 | |||||||
chr4:105173363 | C | CA | 121 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0234 others(118): Show |
121 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-192-16982dupA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105173363 | ||||||
chr4:105173370 | A | G | 1 | a0004c0004t0058g0312 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-192-16990A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105173370 | |||||||
chr4:105173374 | A | C | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-192-16986A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105173374 | |||||||
chr4:105173379 | C | A | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-192-16981C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105173379 | |||||||
chr4:105173662 | G | GACATGAG others(5): Show |
1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-192-16687_-192-16 others(18): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105173662 | ||||||
chr4:105173689 | T | G | 18 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(15): Show |
18 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-192-16671T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105173689 | |||||||
chr4:105174062 | T | A | 9 | a0006c0006t0022g0336 a0006c0006t0022g0338 a0006c0006t0022g0341 others(6): Show |
9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-192-16298T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105174062 | |||||||
chr4:105174086 | C | T | 79 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0237 others(76): Show |
79 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-192-16274C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105174086 | |||||||
chr4:105174287 | C | T | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-192-16073C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105174287 | |||||||
chr4:105174348 | A | C | 22 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(19): Show |
22 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-192-16012A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105174348 | |||||||
chr4:105174590 | G | A | 1 | a0018c0021t0004g0345 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-192-15770G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105174590 | |||||||
chr4:105174702 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-192-15658G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105174702 | |||||||
chr4:105174771 | A | G | 1 | a0001c0001t0007g0197 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-192-15589A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105174771 | |||||||
chr4:105174886 | C | G | 1 | a0004c0004t0037g0224 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-192-15474C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105174886 | |||||||
chr4:105174903 | A | G | 4 | a0002c0002t0025g0163 a0002c0002t0025g0164 a0002c0002t0025g0174 others(1): Show |
4 | HG03669.hp1 NA18955.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.-192-15457A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105174903 | |||||||
chr4:105175155 | A | G | 4 | a0001c0007t0031g0038 a0001c0007t0057g0040 a0001c0022t0062g0039 others(1): Show |
4 | HG02622.hp1 HG02809.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-192-15205A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105175155 | |||||||
chr4:105175183 | T | G | 1 | a0001c0001t0017g0268 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-192-15177T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105175183 | |||||||
chr4:105175313 | G | A | 1 | a0001c0001t0007g0197 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-192-15047G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105175313 | |||||||
chr4:105175373 | A | G | 1 | a0014c0024t0029g0127 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-192-14987A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105175373 | |||||||
chr4:105175403 | A | G | 1 | a0006c0006t0097g0069 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-192-14957A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105175403 | |||||||
chr4:105175557 | A | G | 9 | a0004c0004t0028g0202 a0004c0008t0019g0327 a0004c0008t0019g0332 others(6): Show |
9 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.-192-14803A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105175557 | |||||||
chr4:105175560 | A | G | 9 | a0004c0004t0028g0202 a0004c0008t0019g0327 a0004c0008t0019g0332 others(6): Show |
9 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.-192-14800A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105175560 | |||||||
chr4:105175599 | T | C | 11 | a0004c0004t0028g0202 a0004c0008t0019g0327 a0004c0008t0019g0332 others(8): Show |
11 | HG02451.hp2 HG02809.hp2 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.-192-14761T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105175599 | |||||||
chr4:105175607 | G | A | 6 | a0001c0001t0003g0158 a0001c0001t0009g0131 a0001c0001t0009g0146 others(3): Show |
6 | HG00280.hp1 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-192-14753G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105175607 | |||||||
chr4:105175810 | C | T | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-192-14550C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105175810 | |||||||
chr4:105175811 | G | A | 4 | a0001c0001t0001g0320 a0001c0001t0004g0243 a0001c0001t0007g0244 others(1): Show |
4 | HG01071.hp2 HG01255.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.-192-14549G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105175811 | |||||||
chr4:105176182 | T | C | 276 | a0001c0001t0001g0112 a0001c0001t0001g0189 a0001c0001t0001g0191 others(273): Show |
277 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(274): Show |
intron_variant | MODIFIER | c.-192-14178T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105176182 | |||||||
chr4:105176230 | C | G | 1 | a0003c0003t0015g0091 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-192-14130C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105176230 | |||||||
chr4:105176294 | A | C | 1 | a0001c0001t0001g0265 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-192-14066A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105176294 | |||||||
chr4:105176295 | A | G | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-192-14065A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105176295 | |||||||
chr4:105176445 | A | G | 1 | a0002c0002t0003g0173 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-192-13915A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105176445 | |||||||
chr4:105176623 | A | G | 4 | a0001c0001t0036g0029 a0004c0031t0092g0021 a0011c0015t0043g0347 others(1): Show |
4 | HG01099.hp2 HG02602.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-192-13737A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105176623 | |||||||
chr4:105177333 | T | A | 1 | a0001c0001t0007g0199 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-192-13027T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105177333 | |||||||
chr4:105177875 | G | T | 5 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(2): Show |
5 | HG02818.hp2 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-192-12485G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105177875 | |||||||
chr4:105178004 | C | T | 2 | a0001c0001t0007g0292 a0001c0001t0008g0291 |
2 | HG02135.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-192-12356C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178004 | |||||||
chr4:105178119 | C | A | 1 | a0006c0006t0046g0002 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-192-12241C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178119 | |||||||
chr4:105178154 | G | A | 53 | a0001c0001t0001g0112 a0001c0001t0015g0330 a0001c0007t0030g0117 others(50): Show |
54 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.-192-12206G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178154 | |||||||
chr4:105178243 | T | C | 1 | a0001c0001t0036g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-192-12117T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178243 | |||||||
chr4:105178313 | T | A | 4 | a0001c0001t0006g0252 a0001c0001t0006g0253 a0001c0001t0006g0254 others(1): Show |
4 | HG01169.hp1 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-192-12047T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178313 | |||||||
chr4:105178338 | C | T | 2 | a0010c0012t0009g0217 a0010c0012t0009g0233 |
2 | NA18978.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-192-12022C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178338 | |||||||
chr4:105178488 | G | T | 1 | a0003c0003t0002g0085 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-192-11872G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178488 | |||||||
chr4:105178513 | G | A | 1 | a0002c0002t0021g0165 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-192-11847G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178513 | |||||||
chr4:105178522 | C | T | 1 | a0014c0024t0029g0127 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-192-11838C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178522 | |||||||
chr4:105178579 | A | G | 3 | a0003c0003t0002g0001 a0003c0003t0002g0078 a0003c0003t0002g0084 |
4 | NA18941.hp2 NA18963.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.-192-11781A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178579 | |||||||
chr4:105178591 | G | A | 42 | a0001c0001t0001g0112 a0001c0001t0015g0330 a0003c0003t0002g0001 others(39): Show |
43 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.-192-11769G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178591 | |||||||
chr4:105178603 | G | C | 1 | a0001c0007t0057g0040 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-192-11757G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178603 | |||||||
chr4:105178652 | T | C | 111 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0237 others(108): Show |
111 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-192-11708T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178652 | |||||||
chr4:105178685 | C | G | 1 | a0002c0002t0003g0156 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-192-11675C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178685 | |||||||
chr4:105178757 | C | T | 9 | a0006c0006t0022g0336 a0006c0006t0022g0338 a0006c0006t0022g0341 others(6): Show |
9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-192-11603C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105178757 | |||||||
chr4:105179006 | C | T | 1 | a0001c0001t0013g0296 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-192-11354C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105179006 | |||||||
chr4:105179112 | C | T | 1 | a0001c0001t0073g0024 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-192-11248C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105179112 | |||||||
chr4:105179170 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-192-11190A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105179170 | |||||||
chr4:105179502 | A | G | 1 | a0002c0002t0011g0172 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-192-10858A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105179502 | |||||||
chr4:105179528 | A | G | 1 | a0001c0001t0008g0298 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-192-10832A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105179528 | |||||||
chr4:105179901 | T | G | 1 | a0018c0021t0004g0345 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-192-10459T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105179901 | |||||||
chr4:105180100 | C | T | 1 | a0001c0001t0075g0027 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-192-10260C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105180100 | |||||||
chr4:105180279 | C | T | 2 | a0004c0004t0033g0058 a0004c0004t0042g0059 |
2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-192-10081C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105180279 | |||||||
chr4:105180463 | CTTTTAAG | C | 27 | a0001c0001t0017g0266 a0005c0005t0005g0032 a0005c0005t0005g0041 others(24): Show |
27 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.-192-9891_-192-988 others(11): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105180463 | ||||||
chr4:105180487 | T | G | 11 | a0001c0001t0017g0266 a0005c0005t0005g0032 a0005c0005t0005g0041 others(8): Show |
11 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.-192-9873T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105180487 | |||||||
chr4:105180642 | A | AT | 8 | a0006c0006t0022g0336 a0006c0006t0022g0338 a0006c0006t0022g0341 others(5): Show |
8 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-192-9705dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105180642 | ||||||
chr4:105180642 | AT | A | 48 | a0001c0001t0002g0251 a0001c0001t0004g0203 a0001c0001t0004g0209 others(45): Show |
48 | HG00323.hp2 HG00642.hp1 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.-192-9705delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105180642 | ||||||
chr4:105180765 | G | A | 2 | a0002c0002t0011g0157 a0002c0002t0011g0175 |
2 | HG00558.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-192-9595G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105180765 | |||||||
chr4:105181249 | G | C | 107 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0234 others(104): Show |
107 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.-192-9111G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105181249 | |||||||
chr4:105181567 | A | C | 2 | a0005c0005t0049g0047 a0005c0005t0050g0046 |
2 | HG02735.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.-192-8793A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105181567 | |||||||
chr4:105181618 | T | G | 2 | a0007c0009t0051g0033 a0007c0009t0054g0045 |
2 | HG03669.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-192-8742T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105181618 | |||||||
chr4:105181783 | T | C | 3 | a0004c0031t0092g0021 a0011c0015t0043g0347 a0011c0015t0044g0346 |
3 | HG01099.hp2 HG02602.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-192-8577T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105181783 | |||||||
chr4:105181785 | C | G | 9 | a0004c0004t0028g0202 a0004c0008t0019g0327 a0004c0008t0019g0332 others(6): Show |
9 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.-192-8575C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105181785 | |||||||
chr4:105181834 | T | C | 1 | a0002c0002t0090g0144 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-192-8526T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105181834 | |||||||
chr4:105181927 | C | G | 31 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(28): Show |
31 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.-192-8433C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105181927 | |||||||
chr4:105182121 | T | C | 1 | a0005c0005t0005g0145 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-192-8239T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105182121 | |||||||
chr4:105182195 | T | G | 1 | a0002c0002t0001g0133 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-192-8165T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105182195 | |||||||
chr4:105182430 | T | C | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-192-7930T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105182430 | |||||||
chr4:105182572 | A | G | 11 | a0001c0007t0030g0117 a0001c0007t0030g0339 a0001c0007t0031g0038 others(8): Show |
11 | HG00735.hp2 HG01070.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-192-7788A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105182572 | |||||||
chr4:105182727 | T | A | 1 | a0003c0003t0018g0118 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-192-7633T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105182727 | |||||||
chr4:105182844 | T | A | 1 | a0004c0004t0100g0055 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-192-7516T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105182844 | |||||||
chr4:105182940 | A | G | 44 | a0001c0001t0001g0112 a0001c0001t0015g0330 a0003c0003t0002g0001 others(41): Show |
45 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.-192-7420A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105182940 | |||||||
chr4:105183071 | A | G | 1 | a0006c0006t0022g0341 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-192-7289A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105183071 | |||||||
chr4:105183352 | A | G | 1 | a0002c0002t0024g0178 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-192-7008A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105183352 | |||||||
chr4:105183900 | A | T | 31 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(28): Show |
31 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.-192-6460A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105183900 | |||||||
chr4:105183961 | T | C | 1 | a0001c0001t0093g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-192-6399T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105183961 | |||||||
chr4:105184102 | C | T | 1 | a0002c0002t0087g0171 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-192-6258C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184102 | |||||||
chr4:105184103 | G | A | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-192-6257G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184103 | |||||||
chr4:105184142 | A | G | 276 | a0001c0001t0001g0112 a0001c0001t0001g0189 a0001c0001t0001g0191 others(273): Show |
277 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(274): Show |
intron_variant | MODIFIER | c.-192-6218A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184142 | |||||||
chr4:105184252 | C | A | 1 | a0002c0002t0024g0178 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-192-6108C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184252 | |||||||
chr4:105184260 | A | G | 1 | a0001c0001t0017g0290 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-192-6100A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184260 | |||||||
chr4:105184462 | G | T | 1 | a0001c0001t0001g0112 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-192-5898G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184462 | |||||||
chr4:105184529 | A | G | 1 | a0003c0003t0018g0118 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-192-5831A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184529 | |||||||
chr4:105184552 | A | T | 1 | a0002c0002t0003g0230 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-192-5808A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184552 | |||||||
chr4:105184594 | C | T | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-192-5766C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184594 | |||||||
chr4:105184718 | G | T | 28 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(25): Show |
28 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-192-5642G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184718 | |||||||
chr4:105184720 | G | GGT | 34 | a0001c0001t0036g0029 a0001c0001t0104g0007 a0004c0004t0004g0015 others(31): Show |
34 | HG01109.hp1 HG01192.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-192-5621_-192-562 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105184720 | ||||||
chr4:105184720 | G | GGTGT | 3 | a0004c0004t0101g0075 a0004c0008t0008g0071 a0004c0008t0067g0070 |
3 | HG01175.hp1 HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-192-5623_-192-562 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105184720 | ||||||
chr4:105184720 | GGTGT | G | 79 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0237 others(76): Show |
79 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-192-5623_-192-562 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105184720 | ||||||
chr4:105184832 | A | T | 1 | a0002c0002t0003g0240 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-192-5528A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184832 | |||||||
chr4:105184900 | C | A | 1 | a0004c0008t0008g0071 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-192-5460C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184900 | |||||||
chr4:105184974 | G | C | 79 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0237 others(76): Show |
79 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-192-5386G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105184974 | |||||||
chr4:105185055 | A | G | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-192-5305A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105185055 | |||||||
chr4:105185119 | G | A | 1 | a0002c0002t0023g0134 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-192-5241G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105185119 | |||||||
chr4:105185172 | T | G | 2 | a0009c0013t0001g0321 a0009c0013t0007g0219 |
2 | HG04184.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.-192-5188T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105185172 | |||||||
chr4:105185196 | C | A | 161 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0218 others(158): Show |
161 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.-192-5164C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105185196 | |||||||
chr4:105185197 | G | A | 4 | a0002c0002t0025g0163 a0002c0002t0025g0164 a0002c0002t0025g0174 others(1): Show |
4 | HG03669.hp1 NA18955.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.-192-5163G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105185197 | |||||||
chr4:105185238 | T | G | 10 | a0001c0007t0030g0117 a0001c0007t0030g0339 a0001c0007t0031g0038 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-192-5122T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105185238 | |||||||
chr4:105185544 | G | A | 1 | a0002c0002t0085g0076 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-192-4816G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105185544 | |||||||
chr4:105185552 | A | G | 103 | a0001c0001t0001g0218 a0001c0001t0001g0232 a0001c0001t0001g0237 others(100): Show |
103 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.-192-4808A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105185552 | |||||||
chr4:105185568 | C | G | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-192-4792C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105185568 | |||||||
chr4:105185643 | G | A | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-192-4717G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105185643 | |||||||
chr4:105185952 | C | T | 28 | a0001c0001t0017g0266 a0003c0003t0015g0086 a0005c0005t0005g0032 others(25): Show |
28 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.-192-4408C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105185952 | |||||||
chr4:105186334 | C | T | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-192-4026C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105186334 | |||||||
chr4:105186338 | T | C | 1 | a0001c0001t0004g0243 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-192-4022T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105186338 | |||||||
chr4:105186347 | C | T | 50 | a0001c0001t0015g0330 a0001c0007t0030g0117 a0001c0007t0030g0339 others(47): Show |
51 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.-192-4013C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105186347 | |||||||
chr4:105186380 | T | G | 1 | a0004c0004t0028g0202 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-192-3980T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105186380 | |||||||
chr4:105186383 | G | A | 12 | a0003c0003t0002g0001 a0003c0003t0002g0078 a0003c0003t0002g0079 others(9): Show |
13 | HG00544.hp1 HG02015.hp1 NA18941.hp2 others(10): Show |
intron_variant | MODIFIER | c.-192-3977G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105186383 | |||||||
chr4:105186400 | A | AT | 16 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(13): Show |
16 | HG01192.hp2 HG02071.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-192-3953dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105186400 | ||||||
chr4:105186400 | A | ATT | 17 | a0004c0004t0013g0056 a0004c0004t0013g0057 a0004c0004t0018g0063 others(14): Show |
17 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.-192-3954_-192-395 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105186400 | ||||||
chr4:105186473 | C | CT | 29 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(26): Show |
29 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.-192-3867dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105186473 | ||||||
chr4:105186473 | C | CTT | 6 | a0001c0001t0006g0318 a0001c0001t0016g0210 a0001c0001t0016g0216 others(3): Show |
6 | HG01109.hp2 HG01256.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.-192-3868_-192-386 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105186473 | ||||||
chr4:105186473 | CT | C | 8 | a0002c0002t0023g0134 a0003c0003t0002g0084 a0004c0004t0058g0312 others(5): Show |
8 | HG00738.hp1 HG02257.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.-192-3867delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105186473 | ||||||
chr4:105186562 | G | A | 1 | a0018c0021t0004g0345 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-192-3798G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105186562 | |||||||
chr4:105186738 | C | T | 8 | a0001c0001t0070g0034 a0006c0006t0026g0005 a0006c0006t0026g0006 others(5): Show |
8 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-192-3622C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105186738 | |||||||
chr4:105186875 | G | C | 274 | a0001c0001t0001g0112 a0001c0001t0001g0189 a0001c0001t0001g0191 others(271): Show |
275 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.-192-3485G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105186875 | |||||||
chr4:105186900 | T | C | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-192-3460T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105186900 | |||||||
chr4:105186922 | C | T | 1 | a0004c0004t0010g0228 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-192-3438C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105186922 | |||||||
chr4:105186938 | C | T | 13 | a0003c0003t0002g0101 a0003c0003t0002g0102 a0003c0003t0002g0103 others(10): Show |
13 | HG00609.hp2 HG02135.hp2 NA18946.hp2 others(10): Show |
intron_variant | MODIFIER | c.-192-3422C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105186938 | |||||||
chr4:105187280 | A | G | 1 | a0007c0009t0054g0045 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-192-3080A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105187280 | |||||||
chr4:105187482 | T | C | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-192-2878T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105187482 | |||||||
chr4:105187745 | T | C | 28 | a0001c0001t0017g0266 a0003c0003t0015g0086 a0005c0005t0005g0032 others(25): Show |
28 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.-192-2615T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105187745 | |||||||
chr4:105187783 | T | C | 1 | a0001c0001t0016g0215 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-192-2577T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105187783 | |||||||
chr4:105188183 | A | G | 2 | a0004c0004t0004g0035 a0004c0004t0018g0036 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-192-2177A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188183 | |||||||
chr4:105188223 | A | G | 67 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(64): Show |
67 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.-192-2137A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188223 | |||||||
chr4:105188224 | A | G | 271 | a0001c0001t0001g0112 a0001c0001t0001g0189 a0001c0001t0001g0191 others(268): Show |
272 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.-192-2136A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188224 | |||||||
chr4:105188283 | A | G | 4 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0004g0310 others(1): Show |
4 | NA18946.hp1 NA18947.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.-192-2077A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188283 | |||||||
chr4:105188474 | C | T | 22 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(19): Show |
22 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-192-1886C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188474 | |||||||
chr4:105188642 | G | A | 22 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(19): Show |
22 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.-192-1718G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188642 | |||||||
chr4:105188679 | A | G | 2 | a0004c0004t0004g0035 a0004c0004t0018g0036 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-192-1681A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188679 | |||||||
chr4:105188706 | A | G | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-192-1654A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188706 | |||||||
chr4:105188751 | A | G | 1 | a0009c0013t0079g0264 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-192-1609A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188751 | |||||||
chr4:105188762 | T | G | 1 | a0009c0013t0079g0264 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-192-1598T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188762 | |||||||
chr4:105188806 | C | A | 1 | a0013c0014t0064g0073 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-192-1554C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188806 | |||||||
chr4:105188875 | A | G | 8 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(5): Show |
8 | HG02647.hp1 HG02818.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-192-1485A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188875 | |||||||
chr4:105188895 | G | A | 1 | a0001c0001t0005g0267 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-192-1465G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105188895 | |||||||
chr4:105189139 | T | G | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-192-1221T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105189139 | |||||||
chr4:105189204 | GATA | G | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-192-1147_-192-114 others(7): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr4 | 105189204 | ||||||
chr4:105189370 | A | T | 1 | a0003c0003t0002g0078 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-192-990A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105189370 | |||||||
chr4:105189500 | A | T | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-192-860A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105189500 | |||||||
chr4:105189504 | TCC | T | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-192-855_-192-854d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105189504 | |||||||
chr4:105189621 | T | A | 31 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(28): Show |
31 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.-192-739T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105189621 | |||||||
chr4:105189622 | T | G | 1 | a0004c0011t0008g0325 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-192-738T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105189622 | |||||||
chr4:105189636 | A | G | 1 | a0001c0001t0104g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-192-724A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105189636 | |||||||
chr4:105189639 | T | C | 8 | a0006c0006t0022g0336 a0006c0006t0022g0338 a0006c0006t0022g0341 others(5): Show |
8 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-192-721T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105189639 | |||||||
chr4:105189715 | T | G | 1 | a0004c0008t0019g0327 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-192-645T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105189715 | |||||||
chr4:105190114 | G | A | 31 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(28): Show |
31 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.-192-246G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105190114 | |||||||
chr4:105190123 | G | T | 6 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0006g0252 others(3): Show |
6 | HG01169.hp1 HG01516.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.-192-237G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105190123 | |||||||
chr4:105190244 | C | G | 32 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(29): Show |
32 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.-192-116C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105190244 | |||||||
chr4:105190330 | T | C | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-192-30T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 1/10 | chr4 | 105190330 | |||||||
chr4:105190592 | T | C | 34 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(31): Show |
34 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-47+87T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105190592 | |||||||
chr4:105190595 | A | G | 1 | a0010c0012t0009g0217 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-47+90A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105190595 | |||||||
chr4:105190600 | C | T | 1 | a0002c0002t0023g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-47+95C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105190600 | |||||||
chr4:105190704 | T | C | 10 | a0001c0001t0104g0007 a0006c0006t0022g0336 a0006c0006t0022g0338 others(7): Show |
10 | HG01884.hp1 HG02055.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47+199T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105190704 | |||||||
chr4:105190821 | A | G | 1 | a0001c0001t0093g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-47+316A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105190821 | |||||||
chr4:105191075 | C | T | 2 | a0001c0001t0001g0250 a0001c0001t0010g0229 |
2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-47+570C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105191075 | |||||||
chr4:105191103 | T | G | 11 | a0001c0007t0030g0117 a0001c0007t0030g0339 a0001c0007t0031g0038 others(8): Show |
11 | HG00735.hp2 HG01070.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-47+598T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105191103 | |||||||
chr4:105191104 | C | T | 11 | a0001c0007t0030g0117 a0001c0007t0030g0339 a0001c0007t0031g0038 others(8): Show |
11 | HG00735.hp2 HG01070.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-47+599C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105191104 | |||||||
chr4:105191179 | G | A | 1 | a0018c0021t0004g0345 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-47+674G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105191179 | |||||||
chr4:105191226 | C | T | 2 | a0004c0004t0004g0035 a0004c0004t0018g0036 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-47+721C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105191226 | |||||||
chr4:105191381 | A | C | 1 | a0006c0006t0097g0069 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-47+876A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105191381 | |||||||
chr4:105191411 | C | T | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+906C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105191411 | |||||||
chr4:105191422 | A | G | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+917A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105191422 | |||||||
chr4:105191486 | A | G | 1 | a0006c0006t0097g0069 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-47+981A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105191486 | |||||||
chr4:105191519 | T | G | 23 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(20): Show |
23 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.-47+1014T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105191519 | |||||||
chr4:105191987 | C | A | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-47+1482C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105191987 | |||||||
chr4:105192006 | T | G | 2 | a0004c0004t0004g0035 a0004c0004t0018g0036 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-47+1501T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105192006 | |||||||
chr4:105192411 | T | C | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-47+1906T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105192411 | |||||||
chr4:105192489 | A | G | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-47+1984A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105192489 | |||||||
chr4:105192526 | T | C | 47 | a0001c0001t0001g0112 a0001c0001t0015g0330 a0003c0003t0002g0001 others(44): Show |
48 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.-47+2021T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105192526 | |||||||
chr4:105192744 | A | C | 1 | a0002c0002t0011g0157 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-47+2239A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105192744 | |||||||
chr4:105192770 | G | C | 35 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(32): Show |
35 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.-47+2265G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105192770 | |||||||
chr4:105192854 | T | C | 2 | a0001c0001t0006g0206 a0001c0001t0006g0207 |
2 | HG00323.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.-47+2349T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105192854 | |||||||
chr4:105192914 | A | G | 54 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(51): Show |
54 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.-47+2409A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105192914 | |||||||
chr4:105192919 | A | G | 35 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(32): Show |
35 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.-47+2414A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105192919 | |||||||
chr4:105193048 | T | A | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-47+2543T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105193048 | |||||||
chr4:105193056 | C | T | 1 | a0005c0005t0014g0342 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-47+2551C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105193056 | |||||||
chr4:105193218 | G | A | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+2713G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105193218 | |||||||
chr4:105193543 | G | A | 1 | a0001c0001t0093g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-47+3038G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105193543 | |||||||
chr4:105193737 | G | T | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-47+3232G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105193737 | |||||||
chr4:105193876 | G | A | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47+3371G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105193876 | |||||||
chr4:105193994 | C | T | 1 | a0002c0002t0003g0155 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-47+3489C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105193994 | |||||||
chr4:105194020 | A | G | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-47+3515A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105194020 | |||||||
chr4:105194101 | C | T | 1 | a0001c0001t0036g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-47+3596C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105194101 | |||||||
chr4:105194135 | A | G | 33 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(30): Show |
33 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.-47+3630A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105194135 | |||||||
chr4:105194293 | G | T | 107 | a0001c0001t0001g0112 a0001c0001t0001g0218 a0001c0001t0001g0232 others(104): Show |
107 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.-47+3788G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105194293 | |||||||
chr4:105194326 | C | A | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+3821C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105194326 | |||||||
chr4:105194417 | A | C | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+3912A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105194417 | |||||||
chr4:105194551 | A | G | 26 | a0005c0005t0005g0032 a0005c0005t0005g0041 a0005c0005t0005g0042 others(23): Show |
26 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.-47+4046A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105194551 | |||||||
chr4:105194663 | A | C | 1 | a0007c0009t0051g0033 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-47+4158A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105194663 | |||||||
chr4:105194825 | C | T | 1 | a0004c0004t0018g0063 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-47+4320C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105194825 | |||||||
chr4:105194938 | C | G | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-47+4433C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105194938 | |||||||
chr4:105195019 | A | G | 1 | a0004c0019t0081g0054 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-47+4514A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105195019 | |||||||
chr4:105195049 | T | C | 1 | a0001c0001t0002g0251 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-47+4544T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105195049 | |||||||
chr4:105195057 | A | AT | 113 | a0001c0001t0001g0112 a0001c0001t0001g0218 a0001c0001t0001g0232 others(110): Show |
113 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.-47+4558dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105195057 | ||||||
chr4:105195165 | G | A | 1 | a0003c0003t0002g0085 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-47+4660G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105195165 | |||||||
chr4:105195293 | C | T | 1 | a0001c0001t0104g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-47+4788C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105195293 | |||||||
chr4:105195598 | G | T | 1 | a0002c0002t0020g0177 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-47+5093G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105195598 | |||||||
chr4:105195651 | T | G | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-47+5146T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105195651 | |||||||
chr4:105195688 | AT | A | 31 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(28): Show |
31 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.-47+5184delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105195688 | |||||||
chr4:105195759 | T | C | 1 | a0002c0002t0011g0037 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-47+5254T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105195759 | |||||||
chr4:105195780 | A | G | 1 | a0019c0020t0069g0162 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-47+5275A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105195780 | |||||||
chr4:105195804 | C | G | 175 | a0001c0001t0001g0234 a0001c0001t0001g0305 a0001c0001t0003g0158 others(172): Show |
176 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.-47+5299C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105195804 | |||||||
chr4:105195967 | C | T | 1 | a0006c0006t0097g0069 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-47+5462C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105195967 | |||||||
chr4:105196011 | C | G | 1 | a0001c0001t0009g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-47+5506C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105196011 | |||||||
chr4:105196165 | C | CTT | 34 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(31): Show |
34 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-47+5671_-47+5672d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105196165 | ||||||
chr4:105196274 | A | G | 1 | a0003c0003t0018g0118 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-47+5769A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105196274 | |||||||
chr4:105196281 | A | G | 1 | a0004c0004t0058g0312 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-47+5776A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105196281 | |||||||
chr4:105196377 | GTGATGTA others(15): Show |
G | 1 | a0001c0001t0053g0187 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-47+5873_-47+5894d others(24): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105196377 | |||||||
chr4:105196401 | C | A | 1 | a0001c0001t0053g0187 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-47+5896C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105196401 | |||||||
chr4:105196625 | C | T | 1 | a0001c0007t0071g0180 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-47+6120C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105196625 | |||||||
chr4:105196632 | C | G | 1 | a0001c0001t0104g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-47+6127C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105196632 | |||||||
chr4:105196762 | C | G | 1 | a0001c0001t0053g0187 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-47+6257C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105196762 | |||||||
chr4:105196850 | A | G | 1 | a0001c0001t0093g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-47+6345A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105196850 | |||||||
chr4:105196900 | T | C | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+6395T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105196900 | |||||||
chr4:105196915 | C | T | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-47+6410C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105196915 | |||||||
chr4:105197046 | C | A | 1 | a0004c0004t0058g0312 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-47+6541C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105197046 | |||||||
chr4:105197114 | T | G | 1 | a0011c0015t0043g0347 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-47+6609T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105197114 | |||||||
chr4:105197164 | G | A | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-47+6659G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105197164 | |||||||
chr4:105197412 | A | T | 1 | a0001c0001t0012g0185 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-47+6907A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105197412 | |||||||
chr4:105197551 | C | T | 1 | a0001c0001t0017g0290 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-47+7046C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105197551 | |||||||
chr4:105197599 | T | C | 52 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(49): Show |
52 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.-47+7094T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105197599 | |||||||
chr4:105197714 | T | A | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-47+7209T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105197714 | |||||||
chr4:105197850 | G | A | 9 | a0006c0006t0022g0336 a0006c0006t0022g0338 a0006c0006t0022g0341 others(6): Show |
9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+7345G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105197850 | |||||||
chr4:105198103 | G | A | 3 | a0006c0006t0022g0338 a0006c0006t0022g0341 a0006c0006t0065g0340 |
3 | HG02559.hp1 HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-47+7598G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105198103 | |||||||
chr4:105198680 | G | A | 1 | a0002c0002t0020g0176 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-47+8175G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105198680 | |||||||
chr4:105198867 | A | G | 1 | a0004c0004t0058g0312 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-47+8362A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105198867 | |||||||
chr4:105198873 | A | G | 1 | a0002c0002t0003g0315 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-47+8368A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105198873 | |||||||
chr4:105198911 | A | G | 1 | a0001c0001t0036g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-47+8406A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105198911 | |||||||
chr4:105199157 | G | T | 1 | a0002c0002t0021g0165 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-47+8652G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105199157 | |||||||
chr4:105199432 | G | A | 6 | a0001c0007t0030g0117 a0001c0007t0031g0038 a0001c0007t0031g0115 others(3): Show |
6 | HG00735.hp2 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47+8927G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105199432 | |||||||
chr4:105199599 | T | G | 74 | a0001c0001t0001g0234 a0001c0001t0001g0305 a0001c0001t0010g0235 others(71): Show |
74 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.-47+9094T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105199599 | |||||||
chr4:105199624 | G | C | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47+9119G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105199624 | |||||||
chr4:105199822 | A | G | 37 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(34): Show |
37 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.-47+9317A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105199822 | |||||||
chr4:105199823 | T | C | 8 | a0006c0006t0022g0336 a0006c0006t0022g0338 a0006c0006t0022g0341 others(5): Show |
8 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47+9318T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105199823 | |||||||
chr4:105199920 | G | GTT | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47+9423_-47+9424d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105199920 | ||||||
chr4:105200031 | T | C | 1 | a0004c0004t0058g0312 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-47+9526T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105200031 | |||||||
chr4:105200259 | T | C | 1 | a0001c0001t0038g0183 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-47+9754T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105200259 | |||||||
chr4:105200311 | CAT | C | 10 | a0004c0004t0094g0022 a0006c0006t0022g0336 a0006c0006t0022g0338 others(7): Show |
10 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47+9809_-47+9810d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105200311 | ||||||
chr4:105200388 | ATGTT | A | 26 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(23): Show |
26 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.-47+9901_-47+9904d others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105200388 | ||||||
chr4:105200448 | A | AAACTT | 39 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(36): Show |
39 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.-47+9943_-47+9944i others(7): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105200448 | |||||||
chr4:105200468 | C | G | 1 | a0006c0006t0097g0069 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-47+9963C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105200468 | |||||||
chr4:105200628 | GT | G | 37 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(34): Show |
37 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.-47+10132delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105200628 | ||||||
chr4:105200642 | G | GTTTTGT | 79 | a0001c0001t0001g0234 a0001c0001t0001g0305 a0001c0001t0003g0158 others(76): Show |
79 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-47+10166_-47+1017 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105200642 | ||||||
chr4:105200642 | G | T | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+10137G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105200642 | |||||||
chr4:105200695 | G | A | 1 | a0004c0004t0100g0055 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-47+10190G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105200695 | |||||||
chr4:105200747 | A | G | 39 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(36): Show |
39 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.-47+10242A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105200747 | |||||||
chr4:105200882 | A | G | 1 | a0006c0006t0026g0006 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-47+10377A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105200882 | |||||||
chr4:105200892 | T | C | 67 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(64): Show |
67 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.-47+10387T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105200892 | |||||||
chr4:105200920 | A | G | 1 | a0002c0002t0023g0134 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-47+10415A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105200920 | |||||||
chr4:105201046 | T | C | 8 | a0001c0007t0030g0117 a0001c0007t0030g0339 a0001c0007t0031g0038 others(5): Show |
8 | HG00735.hp2 HG02055.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47+10541T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201046 | |||||||
chr4:105201331 | G | A | 2 | a0001c0001t0001g0269 a0001c0001t0001g0270 |
2 | NA18941.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-47+10826G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201331 | |||||||
chr4:105201381 | G | C | 3 | a0001c0001t0017g0268 a0001c0001t0017g0290 a0016c0025t0017g0246 |
3 | HG01928.hp2 HG02004.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-47+10876G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201381 | |||||||
chr4:105201448 | T | A | 5 | a0001c0001t0007g0292 a0001c0001t0007g0300 a0001c0001t0007g0301 others(2): Show |
5 | HG02135.hp1 NA18960.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+10943T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201448 | |||||||
chr4:105201449 | T | C | 5 | a0001c0001t0007g0292 a0001c0001t0007g0300 a0001c0001t0007g0301 others(2): Show |
5 | HG02135.hp1 NA18960.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+10944T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201449 | |||||||
chr4:105201450 | G | A | 5 | a0001c0001t0007g0292 a0001c0001t0007g0300 a0001c0001t0007g0301 others(2): Show |
5 | HG02135.hp1 NA18960.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+10945G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201450 | |||||||
chr4:105201451 | T | A | 5 | a0001c0001t0007g0292 a0001c0001t0007g0300 a0001c0001t0007g0301 others(2): Show |
5 | HG02135.hp1 NA18960.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+10946T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201451 | |||||||
chr4:105201452 | T | A | 5 | a0001c0001t0007g0292 a0001c0001t0007g0300 a0001c0001t0007g0301 others(2): Show |
5 | HG02135.hp1 NA18960.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+10947T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201452 | |||||||
chr4:105201500 | A | G | 9 | a0006c0006t0022g0336 a0006c0006t0022g0338 a0006c0006t0022g0341 others(6): Show |
9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+10995A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201500 | |||||||
chr4:105201542 | G | A | 10 | a0001c0001t0104g0007 a0006c0006t0022g0336 a0006c0006t0022g0338 others(7): Show |
10 | HG01884.hp1 HG02055.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47+11037G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201542 | |||||||
chr4:105201613 | A | C | 5 | a0004c0008t0019g0327 a0004c0008t0019g0332 a0004c0008t0059g0323 others(2): Show |
5 | HG02572.hp2 HG06807.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+11108A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201613 | |||||||
chr4:105201638 | T | C | 25 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(22): Show |
25 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.-47+11133T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201638 | |||||||
chr4:105201732 | C | CT | 173 | a0001c0001t0001g0234 a0001c0001t0001g0238 a0001c0001t0001g0250 others(170): Show |
174 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.-47+11253dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105201732 | ||||||
chr4:105201732 | C | CTT | 35 | a0001c0001t0008g0205 a0001c0001t0016g0215 a0001c0001t0016g0216 others(32): Show |
35 | HG00642.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-47+11252_-47+1125 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105201732 | ||||||
chr4:105201732 | C | CTTT | 18 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(15): Show |
18 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-47+11251_-47+1125 others(7): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105201732 | ||||||
chr4:105201732 | C | CTTTT | 7 | a0001c0001t0005g0192 a0001c0001t0005g0193 a0001c0001t0041g0198 others(4): Show |
7 | HG01123.hp1 HG01261.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47+11250_-47+1125 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105201732 | ||||||
chr4:105201732 | C | T | 1 | a0001c0001t0008g0211 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-47+11227C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201732 | |||||||
chr4:105201791 | C | T | 1 | a0001c0001t0016g0216 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-47+11286C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201791 | |||||||
chr4:105201851 | C | G | 1 | a0006c0006t0097g0069 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-47+11346C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201851 | |||||||
chr4:105201869 | G | A | 4 | a0001c0001t0006g0252 a0001c0001t0006g0253 a0001c0001t0006g0254 others(1): Show |
4 | HG01169.hp1 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+11364G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201869 | |||||||
chr4:105201891 | G | A | 5 | a0001c0001t0007g0292 a0001c0001t0007g0300 a0001c0001t0007g0301 others(2): Show |
5 | HG02135.hp1 NA18960.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+11386G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201891 | |||||||
chr4:105201915 | G | A | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-47+11410G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105201915 | |||||||
chr4:105202041 | C | G | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-47+11536C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105202041 | |||||||
chr4:105202263 | AC | A | 3 | a0002c0002t0003g0135 a0002c0002t0023g0143 a0019c0020t0069g0162 |
3 | HG01256.hp2 HG02258.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-47+11759delC | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105202263 | |||||||
chr4:105202302 | A | T | 2 | a0001c0001t0001g0284 a0001c0001t0001g0331 |
2 | NA18985.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-47+11797A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105202302 | |||||||
chr4:105202368 | G | A | 1 | a0003c0003t0018g0118 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-47+11863G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105202368 | |||||||
chr4:105202425 | G | C | 238 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0234 others(235): Show |
239 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.-47+11920G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105202425 | |||||||
chr4:105202481 | A | T | 27 | a0005c0005t0005g0032 a0005c0005t0005g0041 a0005c0005t0005g0042 others(24): Show |
27 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.-47+11976A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105202481 | |||||||
chr4:105202542 | A | T | 1 | a0001c0001t0104g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-47+12037A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105202542 | |||||||
chr4:105202928 | C | T | 2 | a0001c0007t0030g0339 a0001c0007t0071g0180 |
2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-47+12423C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105202928 | |||||||
chr4:105202975 | A | G | 47 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(44): Show |
47 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.-47+12470A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105202975 | |||||||
chr4:105203048 | T | G | 44 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(41): Show |
44 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.-47+12543T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105203048 | |||||||
chr4:105203157 | C | T | 1 | a0005c0005t0005g0145 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-47+12652C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105203157 | |||||||
chr4:105203299 | A | G | 22 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(19): Show |
22 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-47+12794A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105203299 | |||||||
chr4:105203428 | C | G | 243 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0234 others(240): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.-47+12923C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105203428 | |||||||
chr4:105203463 | TCTTTGTA others(58): Show |
T | 45 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(42): Show |
45 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.-47+13044_-47+1310 others(69): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105203463 | ||||||
chr4:105203549 | A | G | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+13044A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105203549 | |||||||
chr4:105203602 | A | ACAATACA others(15): Show |
1 | a0006c0006t0097g0069 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-47+13109_-47+1313 others(26): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105203602 | ||||||
chr4:105203865 | A | G | 23 | a0005c0005t0005g0032 a0005c0005t0005g0041 a0005c0005t0005g0042 others(20): Show |
23 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.-47+13360A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105203865 | |||||||
chr4:105203989 | T | G | 4 | a0002c0002t0009g0169 a0002c0002t0021g0165 a0002c0002t0087g0171 others(1): Show |
4 | HG00609.hp1 HG01169.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+13484T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105203989 | |||||||
chr4:105204022 | G | A | 3 | a0005c0005t0005g0293 a0005c0005t0005g0294 a0005c0005t0005g0303 |
3 | HG02155.hp2 NA18747.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-47+13517G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204022 | |||||||
chr4:105204060 | G | A | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-47+13555G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204060 | |||||||
chr4:105204130 | C | T | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+13625C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204130 | |||||||
chr4:105204152 | C | T | 75 | a0001c0001t0001g0305 a0001c0001t0003g0158 a0001c0001t0009g0131 others(72): Show |
75 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.-47+13647C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204152 | |||||||
chr4:105204193 | G | A | 1 | a0010c0012t0009g0233 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-47+13688G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204193 | |||||||
chr4:105204226 | A | T | 2 | a0004c0004t0004g0035 a0004c0004t0018g0036 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-47+13721A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204226 | |||||||
chr4:105204228 | A | ATAT | 3 | a0002c0002t0003g0241 a0002c0002t0035g0136 a0002c0002t0090g0144 |
3 | HG01261.hp2 HG03669.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-47+13723_-47+1372 others(7): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204228 | |||||||
chr4:105204228 | A | T | 42 | a0004c0004t0004g0035 a0004c0004t0004g0220 a0004c0004t0004g0223 others(39): Show |
42 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.-47+13723A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204228 | |||||||
chr4:105204230 | T | C | 4 | a0002c0002t0003g0241 a0002c0002t0035g0136 a0002c0002t0090g0144 others(1): Show |
4 | HG01261.hp2 HG03669.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+13725T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204230 | |||||||
chr4:105204232 | T | C | 5 | a0002c0002t0003g0241 a0002c0002t0024g0178 a0002c0002t0035g0136 others(2): Show |
5 | HG01261.hp2 HG03486.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+13727T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204232 | |||||||
chr4:105204232 | T | TAC | 9 | a0002c0002t0003g0140 a0002c0002t0003g0155 a0002c0002t0003g0161 others(6): Show |
9 | HG00609.hp1 HG01169.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+13728_-47+1372 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204232 | ||||||
chr4:105204232 | T | TACAC | 45 | a0001c0001t0001g0305 a0001c0001t0003g0158 a0001c0001t0009g0131 others(42): Show |
45 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.-47+13728_-47+1372 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204232 | ||||||
chr4:105204232 | T | TACACAC | 17 | a0001c0001t0001g0234 a0001c0001t0010g0235 a0001c0028t0001g0236 others(14): Show |
17 | HG01496.hp1 HG02071.hp1 HG03704.hp2 others(14): Show |
intron_variant | MODIFIER | c.-47+13728_-47+1372 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204232 | ||||||
chr4:105204232 | T | TACACACA others(1): Show |
3 | a0002c0002t0003g0147 a0006c0006t0026g0010 a0006c0006t0102g0004 |
3 | HG00323.hp1 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-47+13728_-47+1372 others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204232 | ||||||
chr4:105204232 | T | TACACACA others(3): Show |
2 | a0001c0001t0070g0034 a0006c0006t0103g0003 |
2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-47+13728_-47+1372 others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204232 | ||||||
chr4:105204232 | T | TACACACA others(5): Show |
1 | a0006c0006t0046g0002 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-47+13728_-47+1372 others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204232 | ||||||
chr4:105204232 | TATAC | T | 3 | a0001c0001t0041g0198 a0012c0016t0001g0019 a0012c0016t0001g0020 |
3 | HG01123.hp1 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+13729_-47+1373 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204232 | ||||||
chr4:105204232 | TATACAC | T | 13 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0005g0188 others(10): Show |
13 | HG00140.hp1 HG00642.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.-47+13729_-47+1373 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204232 | ||||||
chr4:105204234 | T | C | 97 | a0001c0001t0001g0234 a0001c0001t0001g0305 a0001c0001t0003g0158 others(94): Show |
97 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.-47+13729T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204234 | |||||||
chr4:105204234 | T | TAC | 77 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0250 others(74): Show |
78 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.-47+13763_-47+1376 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204234 | ||||||
chr4:105204234 | T | TACAC | 11 | a0001c0001t0004g0271 a0001c0001t0006g0206 a0001c0001t0032g0052 others(8): Show |
11 | HG00323.hp2 HG00423.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.-47+13761_-47+1376 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204234 | ||||||
chr4:105204234 | T | TACACAC | 13 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(10): Show |
13 | HG00642.hp1 HG01074.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.-47+13759_-47+1376 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204234 | ||||||
chr4:105204234 | TACAC | T | 12 | a0001c0001t0001g0282 a0001c0001t0036g0029 a0002c0002t0035g0153 others(9): Show |
12 | HG01516.hp2 HG02055.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-47+13761_-47+1376 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204234 | ||||||
chr4:105204256 | CACACACA others(7): Show |
C | 1 | a0003c0003t0018g0118 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-47+13755_-47+1376 others(18): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204256 | ||||||
chr4:105204256 | CACACACA others(11): Show |
C | 1 | a0004c0008t0008g0071 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-47+13755_-47+1377 others(22): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204256 | ||||||
chr4:105204258 | CACACACA others(9): Show |
C | 5 | a0004c0008t0019g0327 a0004c0008t0019g0332 a0004c0008t0059g0323 others(2): Show |
5 | HG02572.hp2 HG06807.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+13757_-47+1377 others(20): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204258 | ||||||
chr4:105204262 | CACACACA others(5): Show |
C | 2 | a0004c0004t0004g0035 a0004c0004t0018g0036 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-47+13761_-47+1377 others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204262 | ||||||
chr4:105204266 | C | CACACACA others(11): Show |
2 | a0006c0006t0026g0005 a0006c0006t0026g0006 |
2 | HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-47+13764_-47+1376 others(22): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204266 | ||||||
chr4:105204266 | CACAT | C | 14 | a0001c0001t0004g0186 a0004c0004t0013g0056 a0004c0004t0013g0057 others(11): Show |
14 | HG00741.hp2 HG01243.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-47+13774_-47+1377 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204266 | ||||||
chr4:105204268 | CAT | C | 9 | a0001c0001t0001g0263 a0001c0001t0005g0196 a0001c0001t0006g0252 others(6): Show |
9 | HG00741.hp1 HG01169.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+13765_-47+1376 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204268 | ||||||
chr4:105204268 | CATACAT | C | 22 | a0004c0004t0004g0223 a0004c0004t0004g0225 a0004c0004t0007g0283 others(19): Show |
22 | HG01109.hp1 HG01192.hp2 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.-47+13765_-47+1377 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105204268 | ||||||
chr4:105204270 | T | C | 45 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0005g0188 others(42): Show |
45 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.-47+13765T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204270 | |||||||
chr4:105204274 | T | C | 15 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0013g0056 others(12): Show |
15 | HG01243.hp2 HG02257.hp2 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.-47+13769T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204274 | |||||||
chr4:105204278 | T | C | 2 | a0004c0004t0033g0119 a0004c0004t0101g0075 |
2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-47+13773T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204278 | |||||||
chr4:105204407 | A | G | 1 | a0004c0004t0018g0063 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-47+13902A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204407 | |||||||
chr4:105204513 | T | G | 6 | a0004c0008t0008g0071 a0004c0008t0019g0327 a0004c0008t0019g0332 others(3): Show |
6 | HG01175.hp1 HG02572.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47+14008T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204513 | |||||||
chr4:105204558 | G | A | 44 | a0001c0001t0015g0330 a0003c0003t0002g0001 a0003c0003t0002g0028 others(41): Show |
45 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.-47+14053G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204558 | |||||||
chr4:105204594 | A | G | 1 | a0002c0002t0024g0178 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-47+14089A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204594 | |||||||
chr4:105204667 | G | T | 1 | a0001c0001t0004g0209 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-47+14162G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105204667 | |||||||
chr4:105205003 | G | A | 1 | a0006c0006t0097g0069 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-47+14498G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205003 | |||||||
chr4:105205240 | A | G | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+14735A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205240 | |||||||
chr4:105205256 | G | C | 266 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0234 others(263): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.-47+14751G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205256 | |||||||
chr4:105205279 | G | A | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+14774G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205279 | |||||||
chr4:105205507 | T | TC | 58 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(55): Show |
58 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.-47+15009dupC | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105205507 | ||||||
chr4:105205638 | A | C | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47+15133A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205638 | |||||||
chr4:105205693 | A | T | 1 | a0001c0001t0036g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-47+15188A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205693 | |||||||
chr4:105205785 | C | G | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-47+15280C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205785 | |||||||
chr4:105205806 | C | G | 49 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(46): Show |
49 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.-47+15301C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205806 | |||||||
chr4:105205847 | C | T | 240 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0234 others(237): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.-47+15342C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205847 | |||||||
chr4:105205854 | A | G | 50 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(47): Show |
50 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(47): Show |
intron_variant | MODIFIER | c.-47+15349A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205854 | |||||||
chr4:105205964 | C | A | 1 | a0020c0026t0009g0168 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-47+15459C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205964 | |||||||
chr4:105205964 | C | T | 82 | a0001c0001t0001g0234 a0001c0001t0003g0158 a0001c0001t0009g0131 others(79): Show |
82 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.-47+15459C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105205964 | |||||||
chr4:105206387 | G | A | 3 | a0004c0004t0004g0035 a0004c0004t0018g0036 a0004c0031t0092g0021 |
3 | HG01891.hp1 HG03579.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-47+15882G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105206387 | |||||||
chr4:105206488 | T | C | 1 | a0001c0001t0104g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-47+15983T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105206488 | |||||||
chr4:105206489 | T | C | 50 | a0001c0001t0104g0007 a0004c0004t0004g0015 a0004c0004t0004g0035 others(47): Show |
50 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(47): Show |
intron_variant | MODIFIER | c.-47+15984T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105206489 | |||||||
chr4:105206491 | G | C | 4 | a0001c0001t0104g0007 a0004c0031t0092g0021 a0012c0016t0001g0019 others(1): Show |
4 | HG01884.hp1 HG02451.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+15986G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105206491 | |||||||
chr4:105206617 | G | A | 1 | a0001c0001t0005g0267 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-47+16112G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105206617 | |||||||
chr4:105206777 | A | G | 1 | a0004c0004t0058g0312 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-47+16272A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105206777 | |||||||
chr4:105206946 | C | T | 1 | a0001c0001t0093g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-47+16441C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105206946 | |||||||
chr4:105206951 | G | A | 69 | a0002c0002t0001g0133 a0002c0002t0003g0122 a0002c0002t0003g0123 others(66): Show |
69 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-47+16446G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105206951 | |||||||
chr4:105206952 | A | G | 1 | a0001c0001t0032g0195 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-47+16447A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105206952 | |||||||
chr4:105207034 | G | T | 41 | a0001c0001t0015g0330 a0003c0003t0002g0001 a0003c0003t0002g0028 others(38): Show |
42 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.-47+16529G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207034 | |||||||
chr4:105207035 | A | C | 41 | a0001c0001t0015g0330 a0003c0003t0002g0001 a0003c0003t0002g0028 others(38): Show |
42 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.-47+16530A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207035 | |||||||
chr4:105207037 | G | A | 41 | a0001c0001t0015g0330 a0003c0003t0002g0001 a0003c0003t0002g0028 others(38): Show |
42 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.-47+16532G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207037 | |||||||
chr4:105207207 | A | G | 1 | a0003c0003t0098g0110 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-47+16702A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207207 | |||||||
chr4:105207249 | T | C | 3 | a0004c0031t0092g0021 a0012c0016t0001g0019 a0012c0016t0001g0020 |
3 | HG02451.hp2 HG03831.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+16744T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207249 | |||||||
chr4:105207305 | A | G | 17 | a0004c0004t0028g0202 a0004c0004t0058g0312 a0004c0004t0084g0072 others(14): Show |
17 | HG01175.hp1 HG02572.hp2 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.-47+16800A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207305 | |||||||
chr4:105207499 | A | G | 46 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(43): Show |
46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-47+16994A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207499 | |||||||
chr4:105207531 | G | T | 1 | a0001c0001t0001g0250 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-47+17026G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207531 | |||||||
chr4:105207603 | G | A | 239 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0003g0158 others(236): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.-47+17098G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207603 | |||||||
chr4:105207720 | C | T | 1 | a0006c0006t0097g0069 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-47+17215C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207720 | |||||||
chr4:105207797 | C | T | 148 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0003g0158 others(145): Show |
148 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.-47+17292C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207797 | |||||||
chr4:105207918 | A | G | 1 | a0004c0004t0004g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-47+17413A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105207918 | |||||||
chr4:105208177 | T | TTCATTCT others(323): Show |
1 | a0005c0005t0005g0032 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-47+17683_-47+1768 others(334): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105208177 | ||||||
chr4:105208405 | C | A | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-47+17900C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105208405 | |||||||
chr4:105208416 | A | G | 3 | a0002c0002t0009g0129 a0002c0002t0021g0124 a0002c0002t0021g0125 |
3 | HG04184.hp2 HG04199.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-47+17911A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105208416 | |||||||
chr4:105208441 | A | G | 1 | a0001c0001t0007g0292 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-47+17936A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105208441 | |||||||
chr4:105208721 | A | G | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-47+18216A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105208721 | |||||||
chr4:105209049 | G | GTA | 49 | a0001c0001t0001g0232 a0001c0001t0001g0237 a0001c0001t0001g0259 others(46): Show |
49 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.-47+18592_-47+1859 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | ||||||
chr4:105209049 | G | GTATA | 34 | a0001c0001t0001g0258 a0001c0001t0001g0307 a0001c0001t0001g0331 others(31): Show |
34 | HG00280.hp1 HG00673.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.-47+18590_-47+1859 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | ||||||
chr4:105209049 | G | GTATATA | 38 | a0001c0001t0001g0112 a0001c0001t0001g0218 a0001c0001t0001g0257 others(35): Show |
39 | HG00280.hp2 HG00544.hp2 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.-47+18588_-47+1859 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | ||||||
chr4:105209049 | G | GTATATAT others(1): Show |
34 | a0001c0001t0001g0248 a0001c0001t0001g0250 a0001c0001t0001g0272 others(31): Show |
34 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.-47+18586_-47+1859 others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | ||||||
chr4:105209049 | G | GTATATAT others(3): Show |
19 | a0001c0001t0001g0247 a0001c0001t0001g0261 a0001c0001t0001g0285 others(16): Show |
19 | HG00558.hp2 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-47+18584_-47+1859 others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | ||||||
chr4:105209049 | G | GTATATAT others(5): Show |
9 | a0001c0001t0001g0265 a0001c0001t0005g0188 a0001c0001t0016g0216 others(6): Show |
9 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+18582_-47+1859 others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | ||||||
chr4:105209049 | G | GTATATAT others(7): Show |
2 | a0003c0003t0002g0088 a0003c0003t0002g0101 |
2 | HG01943.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.-47+18580_-47+1859 others(18): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | ||||||
chr4:105209049 | GTA | G | 9 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(6): Show |
9 | HG01517.hp2 HG02155.hp1 NA18998.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+18592_-47+1859 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | ||||||
chr4:105209049 | GTATA | G | 11 | a0001c0001t0001g0297 a0001c0001t0002g0249 a0001c0001t0004g0186 others(8): Show |
11 | HG00741.hp1 HG00741.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47+18590_-47+1859 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | ||||||
chr4:105209049 | GTATATA | G | 13 | a0001c0001t0001g0238 a0001c0001t0001g0320 a0001c0001t0004g0243 others(10): Show |
13 | HG01070.hp1 HG01255.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.-47+18588_-47+1859 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | ||||||
chr4:105209049 | GTATATAT others(1): Show |
G | 4 | a0001c0001t0007g0199 a0001c0001t0104g0007 a0006c0006t0022g0341 others(1): Show |
4 | HG01884.hp1 HG02602.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+18586_-47+1859 others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | ||||||
chr4:105209049 | GTATATAT others(3): Show |
G | 8 | a0001c0001t0001g0191 a0001c0001t0001g0234 a0001c0001t0001g0288 others(5): Show |
8 | HG01256.hp2 HG01346.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47+18584_-47+1859 others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | ||||||
chr4:105209049 | GTATATAT others(5): Show |
G | 9 | a0001c0001t0010g0235 a0001c0001t0017g0266 a0001c0001t0036g0029 others(6): Show |
9 | HG01496.hp1 HG02055.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+18582_-47+1859 others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | ||||||
chr4:105209049 | GTATATAT others(7): Show |
G | 1 | a0011c0015t0044g0346 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-47+18580_-47+1859 others(18): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | ||||||
chr4:105209049 | GTATATAT others(9): Show |
G | 4 | a0003c0003t0015g0086 a0005c0005t0005g0293 a0005c0005t0005g0294 others(1): Show |
4 | HG02155.hp2 NA18747.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+18578_-47+1859 others(20): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | ||||||
chr4:105209049 | GTATATAT others(11): Show |
G | 4 | a0001c0007t0030g0117 a0002c0002t0003g0137 a0002c0002t0003g0230 others(1): Show |
4 | HG00735.hp2 HG01169.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+18576_-47+1859 others(22): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | ||||||
chr4:105209049 | GTATATAT others(13): Show |
G | 15 | a0001c0001t0070g0034 a0001c0007t0030g0339 a0001c0007t0031g0038 others(12): Show |
15 | HG00735.hp1 HG01109.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-47+18574_-47+1859 others(24): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | ||||||
chr4:105209049 | GTATATAT others(15): Show |
G | 23 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(20): Show |
23 | HG01192.hp2 HG01243.hp2 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.-47+18572_-47+1859 others(26): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | ||||||
chr4:105209049 | GTATATAT others(17): Show |
G | 16 | a0004c0004t0058g0312 a0004c0004t0084g0072 a0004c0004t0101g0075 others(13): Show |
16 | HG01175.hp1 HG02572.hp2 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.-47+18570_-47+1859 others(28): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | ||||||
chr4:105209049 | GTATATAT others(19): Show |
G | 2 | a0004c0004t0004g0035 a0004c0004t0018g0036 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-47+18568_-47+1859 others(30): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | ||||||
chr4:105209049 | GTATATAT others(23): Show |
G | 5 | a0001c0001t0007g0300 a0001c0001t0007g0301 a0001c0001t0007g0302 others(2): Show |
5 | NA18960.hp1 NA18979.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+18564_-47+1859 others(34): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | ||||||
chr4:105209049 | GTATATAT others(25): Show |
G | 1 | a0001c0001t0076g0023 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-47+18562_-47+1859 others(36): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105209049 | ||||||
chr4:105209051 | A | G | 1 | a0002c0002t0025g0174 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-47+18546A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209051 | |||||||
chr4:105209071 | A | G | 6 | a0004c0004t0007g0283 a0004c0004t0018g0120 a0004c0004t0033g0058 others(3): Show |
6 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47+18566A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209071 | |||||||
chr4:105209073 | A | G | 22 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(19): Show |
22 | HG01192.hp2 HG01243.hp2 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.-47+18568A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209073 | |||||||
chr4:105209075 | A | G | 16 | a0004c0004t0058g0312 a0004c0004t0084g0072 a0004c0004t0101g0075 others(13): Show |
16 | HG01175.hp1 HG02572.hp2 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.-47+18570A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209075 | |||||||
chr4:105209077 | A | G | 4 | a0004c0004t0004g0035 a0004c0004t0018g0036 a0013c0014t0060g0074 others(1): Show |
4 | HG01891.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+18572A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209077 | |||||||
chr4:105209099 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-47+18594G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209099 | |||||||
chr4:105209120 | A | G | 3 | a0004c0031t0092g0021 a0012c0016t0001g0019 a0012c0016t0001g0020 |
3 | HG02451.hp2 HG03831.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+18615A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209120 | |||||||
chr4:105209153 | G | A | 22 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(19): Show |
22 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-47+18648G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209153 | |||||||
chr4:105209511 | A | C | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47+19006A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209511 | |||||||
chr4:105209641 | G | GA | 49 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(46): Show |
49 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.-47+19136_-47+1913 others(5): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209641 | |||||||
chr4:105209664 | T | C | 46 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(43): Show |
46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-47+19159T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209664 | |||||||
chr4:105209868 | G | A | 48 | a0001c0001t0015g0330 a0003c0003t0002g0001 a0003c0003t0002g0028 others(45): Show |
49 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.-47+19363G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209868 | |||||||
chr4:105209992 | T | G | 4 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(1): Show |
4 | NA18998.hp2 NA19003.hp2 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+19487T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105209992 | |||||||
chr4:105210053 | C | T | 124 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0305 others(121): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.-47+19548C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105210053 | |||||||
chr4:105210071 | T | C | 46 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(43): Show |
46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-47+19566T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105210071 | |||||||
chr4:105210269 | A | C | 46 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(43): Show |
46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-47+19764A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105210269 | |||||||
chr4:105210432 | A | C | 2 | a0001c0001t0001g0284 a0001c0001t0001g0331 |
2 | NA18985.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-47+19927A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105210432 | |||||||
chr4:105211088 | T | G | 1 | a0003c0003t0002g0104 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-47+20583T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105211088 | |||||||
chr4:105211155 | A | G | 8 | a0006c0006t0022g0336 a0006c0006t0022g0338 a0006c0006t0022g0341 others(5): Show |
8 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47+20650A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105211155 | |||||||
chr4:105211163 | A | G | 60 | a0001c0001t0015g0330 a0001c0001t0036g0029 a0001c0001t0104g0007 others(57): Show |
61 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.-47+20658A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105211163 | |||||||
chr4:105211260 | A | C | 2 | a0002c0002t0011g0157 a0002c0002t0011g0175 |
2 | HG00558.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-47+20755A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105211260 | |||||||
chr4:105211608 | A | G | 13 | a0003c0003t0002g0001 a0003c0003t0002g0078 a0003c0003t0002g0079 others(10): Show |
14 | HG00544.hp1 HG02015.hp1 NA18941.hp2 others(11): Show |
intron_variant | MODIFIER | c.-47+21103A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105211608 | |||||||
chr4:105211974 | T | C | 1 | a0002c0002t0003g0242 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-47+21469T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105211974 | |||||||
chr4:105212027 | C | T | 180 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0234 others(177): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.-47+21522C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105212027 | |||||||
chr4:105212314 | G | A | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-21583G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105212314 | |||||||
chr4:105212593 | G | T | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-21304G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105212593 | |||||||
chr4:105212676 | A | G | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-21221A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105212676 | |||||||
chr4:105212761 | G | A | 5 | a0002c0002t0003g0316 a0002c0002t0009g0169 a0002c0002t0021g0165 others(2): Show |
5 | HG00609.hp1 HG01169.hp2 NA19072.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-21136G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105212761 | |||||||
chr4:105212817 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-46-21080C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105212817 | |||||||
chr4:105212860 | C | T | 46 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(43): Show |
46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-21037C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105212860 | |||||||
chr4:105213040 | A | T | 1 | a0003c0003t0002g0090 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-46-20857A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105213040 | |||||||
chr4:105213142 | A | G | 1 | a0001c0001t0036g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-46-20755A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105213142 | |||||||
chr4:105213159 | G | A | 72 | a0001c0001t0003g0158 a0001c0001t0009g0131 a0001c0001t0009g0146 others(69): Show |
72 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.-46-20738G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105213159 | |||||||
chr4:105213219 | A | G | 1 | a0001c0001t0093g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-46-20678A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105213219 | |||||||
chr4:105213328 | A | G | 1 | a0001c0001t0007g0302 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-46-20569A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105213328 | |||||||
chr4:105213500 | G | T | 1 | a0002c0002t0003g0173 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-46-20397G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105213500 | |||||||
chr4:105213732 | A | G | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-20165A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105213732 | |||||||
chr4:105213785 | A | G | 49 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(46): Show |
49 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.-46-20112A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105213785 | |||||||
chr4:105213870 | G | GT | 7 | a0002c0002t0003g0122 a0002c0002t0003g0132 a0002c0002t0003g0142 others(4): Show |
7 | HG00544.hp2 NA18959.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-20020dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105213870 | ||||||
chr4:105214058 | C | T | 1 | a0004c0019t0081g0054 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-46-19839C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105214058 | |||||||
chr4:105214112 | A | C | 3 | a0004c0031t0092g0021 a0012c0016t0001g0019 a0012c0016t0001g0020 |
3 | HG02451.hp2 HG03831.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-19785A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105214112 | |||||||
chr4:105214159 | G | T | 73 | a0001c0001t0003g0158 a0001c0001t0009g0131 a0001c0001t0009g0146 others(70): Show |
73 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.-46-19738G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105214159 | |||||||
chr4:105214172 | G | A | 26 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(23): Show |
26 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.-46-19725G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105214172 | |||||||
chr4:105214291 | C | T | 1 | a0001c0001t0005g0267 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-46-19606C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105214291 | |||||||
chr4:105214301 | A | AT | 25 | a0001c0001t0001g0261 a0001c0001t0001g0272 a0001c0001t0001g0282 others(22): Show |
25 | HG00323.hp1 HG00738.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.-46-19573dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105214301 | ||||||
chr4:105214301 | A | ATT | 81 | a0001c0001t0003g0158 a0001c0001t0004g0203 a0001c0001t0004g0209 others(78): Show |
81 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.-46-19574_-46-1957 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105214301 | ||||||
chr4:105214301 | A | ATTT | 67 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(64): Show |
68 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.-46-19575_-46-1957 others(7): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105214301 | ||||||
chr4:105214301 | A | ATTTT | 7 | a0001c0001t0093g0179 a0001c0007t0091g0116 a0003c0003t0002g0092 others(4): Show |
7 | HG02145.hp1 HG02922.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-19576_-46-1957 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105214301 | ||||||
chr4:105214301 | A | ATTTTT | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02647.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-19577_-46-1957 others(9): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105214301 | ||||||
chr4:105214301 | AT | A | 37 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(34): Show |
37 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.-46-19573delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105214301 | ||||||
chr4:105214301 | ATTTTTTT | A | 28 | a0002c0002t0003g0122 a0002c0002t0003g0123 a0002c0002t0003g0126 others(25): Show |
28 | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.-46-19579_-46-1957 others(11): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105214301 | ||||||
chr4:105214471 | A | AT | 77 | a0001c0001t0001g0112 a0001c0001t0001g0238 a0001c0001t0001g0250 others(74): Show |
77 | HG00423.hp1 HG00673.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.-46-19403dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105214471 | ||||||
chr4:105214471 | A | ATT | 7 | a0001c0001t0001g0237 a0002c0002t0023g0152 a0004c0031t0092g0021 others(4): Show |
7 | HG01192.hp1 HG02572.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-19404_-46-1940 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105214471 | ||||||
chr4:105214499 | A | AGAG | 49 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(46): Show |
49 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.-46-19396_-46-1939 others(7): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105214499 | ||||||
chr4:105214926 | T | C | 1 | a0004c0019t0081g0054 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-46-18971T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105214926 | |||||||
chr4:105215376 | T | A | 1 | a0001c0001t0070g0034 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-46-18521T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105215376 | |||||||
chr4:105215803 | A | G | 5 | a0006c0006t0022g0336 a0006c0006t0034g0333 a0006c0006t0034g0337 others(2): Show |
5 | HG02055.hp1 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-18094A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105215803 | |||||||
chr4:105215876 | G | A | 120 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0003g0158 others(117): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.-46-18021G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105215876 | |||||||
chr4:105215939 | G | C | 2 | a0004c0004t0004g0035 a0004c0004t0018g0036 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-46-17958G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105215939 | |||||||
chr4:105215959 | A | G | 6 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0297 others(3): Show |
6 | HG01255.hp2 HG01928.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46-17938A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105215959 | |||||||
chr4:105216286 | G | C | 2 | a0002c0002t0023g0134 a0002c0002t0023g0152 |
2 | HG00738.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-46-17611G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105216286 | |||||||
chr4:105216288 | G | C | 1 | a0001c0001t0070g0034 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-46-17609G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105216288 | |||||||
chr4:105216602 | T | C | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-17295T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105216602 | |||||||
chr4:105216647 | G | A | 1 | a0001c0001t0004g0209 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-46-17250G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105216647 | |||||||
chr4:105216672 | A | G | 1 | a0003c0003t0018g0118 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-46-17225A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105216672 | |||||||
chr4:105216700 | G | A | 1 | a0006c0006t0046g0002 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-46-17197G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105216700 | |||||||
chr4:105216801 | G | C | 2 | a0004c0004t0004g0035 a0004c0004t0018g0036 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-46-17096G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105216801 | |||||||
chr4:105216980 | G | A | 1 | a0001c0001t0007g0199 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-46-16917G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105216980 | |||||||
chr4:105216989 | T | C | 126 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0234 others(123): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.-46-16908T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105216989 | |||||||
chr4:105217205 | A | C | 26 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(23): Show |
26 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.-46-16692A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217205 | |||||||
chr4:105217250 | G | A | 1 | a0003c0003t0012g0105 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-46-16647G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217250 | |||||||
chr4:105217310 | T | G | 2 | a0004c0004t0004g0035 a0004c0004t0018g0036 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-46-16587T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217310 | |||||||
chr4:105217634 | A | G | 2 | a0001c0007t0030g0117 a0001c0007t0091g0116 |
2 | HG00735.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-46-16263A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217634 | |||||||
chr4:105217700 | T | C | 49 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(46): Show |
49 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.-46-16197T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217700 | |||||||
chr4:105217736 | G | A | 46 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(43): Show |
46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-16161G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217736 | |||||||
chr4:105217765 | A | G | 1 | a0004c0004t0018g0036 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-46-16132A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217765 | |||||||
chr4:105217841 | C | T | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-46-16056C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217841 | |||||||
chr4:105217919 | A | G | 3 | a0004c0031t0092g0021 a0012c0016t0001g0019 a0012c0016t0001g0020 |
3 | HG02451.hp2 HG03831.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-15978A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217919 | |||||||
chr4:105217960 | A | G | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-15937A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217960 | |||||||
chr4:105217962 | C | T | 1 | a0001c0001t0004g0271 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-46-15935C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217962 | |||||||
chr4:105217992 | C | G | 3 | a0004c0031t0092g0021 a0012c0016t0001g0019 a0012c0016t0001g0020 |
3 | HG02451.hp2 HG03831.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-15905C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105217992 | |||||||
chr4:105218230 | T | C | 20 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(17): Show |
20 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.-46-15667T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105218230 | |||||||
chr4:105218388 | T | C | 1 | a0001c0001t0007g0300 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-46-15509T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105218388 | |||||||
chr4:105218428 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-46-15469G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105218428 | |||||||
chr4:105218466 | A | C | 1 | a0001c0001t0008g0304 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-46-15431A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105218466 | |||||||
chr4:105218526 | C | A | 1 | a0004c0004t0100g0055 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-46-15371C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105218526 | |||||||
chr4:105218567 | G | A | 2 | a0002c0002t0003g0241 a0002c0002t0003g0242 |
2 | NA19058.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-46-15330G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105218567 | |||||||
chr4:105218616 | C | T | 9 | a0001c0001t0070g0034 a0001c0007t0030g0117 a0001c0007t0030g0339 others(6): Show |
9 | HG00735.hp2 HG02055.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-46-15281C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105218616 | |||||||
chr4:105218673 | C | T | 2 | a0005c0005t0049g0047 a0005c0005t0050g0046 |
2 | HG02735.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.-46-15224C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105218673 | |||||||
chr4:105218711 | G | A | 3 | a0004c0031t0092g0021 a0012c0016t0001g0019 a0012c0016t0001g0020 |
3 | HG02451.hp2 HG03831.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-15186G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105218711 | |||||||
chr4:105218717 | A | G | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-15180A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105218717 | |||||||
chr4:105218862 | T | C | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-15035T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105218862 | |||||||
chr4:105219161 | T | C | 17 | a0004c0004t0028g0202 a0004c0004t0058g0312 a0004c0004t0084g0072 others(14): Show |
17 | HG01175.hp1 HG02572.hp2 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.-46-14736T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105219161 | |||||||
chr4:105219232 | C | T | 1 | a0003c0003t0002g0314 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-46-14665C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105219232 | |||||||
chr4:105219344 | G | T | 238 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0003g0158 others(235): Show |
239 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.-46-14553G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105219344 | |||||||
chr4:105219363 | G | A | 10 | a0001c0001t0070g0034 a0001c0001t0104g0007 a0001c0007t0030g0117 others(7): Show |
10 | HG00735.hp2 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-46-14534G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105219363 | |||||||
chr4:105219412 | T | C | 1 | a0001c0001t0093g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-46-14485T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105219412 | |||||||
chr4:105219700 | A | G | 2 | a0002c0002t0003g0147 a0002c0002t0003g0150 |
2 | HG00323.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.-46-14197A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105219700 | |||||||
chr4:105219985 | G | A | 1 | a0004c0004t0013g0221 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-46-13912G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105219985 | |||||||
chr4:105219988 | C | G | 2 | a0002c0002t0024g0178 a0006c0006t0068g0014 |
2 | HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-46-13909C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105219988 | |||||||
chr4:105220051 | C | T | 2 | a0001c0001t0032g0052 a0001c0001t0080g0053 |
2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-46-13846C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220051 | |||||||
chr4:105220087 | A | G | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-13810A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220087 | |||||||
chr4:105220102 | C | A | 1 | a0018c0021t0004g0345 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-46-13795C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220102 | |||||||
chr4:105220108 | C | G | 46 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(43): Show |
46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-13789C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220108 | |||||||
chr4:105220170 | C | T | 1 | a0001c0001t0036g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-46-13727C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220170 | |||||||
chr4:105220182 | A | C | 1 | a0018c0021t0004g0345 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-46-13715A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220182 | |||||||
chr4:105220288 | A | G | 9 | a0006c0006t0022g0336 a0006c0006t0022g0338 a0006c0006t0022g0341 others(6): Show |
9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-46-13609A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220288 | |||||||
chr4:105220372 | G | A | 2 | a0002c0002t0025g0163 a0002c0002t0025g0174 |
2 | NA18955.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-46-13525G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220372 | |||||||
chr4:105220520 | C | A | 48 | a0001c0001t0015g0330 a0003c0003t0002g0001 a0003c0003t0002g0028 others(45): Show |
49 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.-46-13377C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220520 | |||||||
chr4:105220579 | G | A | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-46-13318G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220579 | |||||||
chr4:105220649 | A | T | 1 | a0018c0021t0004g0345 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-46-13248A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220649 | |||||||
chr4:105220758 | T | C | 12 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(9): Show |
12 | HG02071.hp2 NA18944.hp2 NA18960.hp2 others(9): Show |
intron_variant | MODIFIER | c.-46-13139T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220758 | |||||||
chr4:105220759 | A | G | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-46-13138A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220759 | |||||||
chr4:105220830 | T | G | 1 | a0017c0017t0003g0151 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-46-13067T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220830 | |||||||
chr4:105220922 | ACTT | A | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-12972_-46-1297 others(7): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105220922 | ||||||
chr4:105220954 | T | G | 1 | a0001c0029t0004g0275 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-46-12943T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105220954 | |||||||
chr4:105221262 | T | C | 1 | a0001c0001t0093g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-46-12635T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221262 | |||||||
chr4:105221384 | T | C | 3 | a0004c0031t0092g0021 a0012c0016t0001g0019 a0012c0016t0001g0020 |
3 | HG02451.hp2 HG03831.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-12513T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221384 | |||||||
chr4:105221709 | A | C | 46 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(43): Show |
46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-12188A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221709 | |||||||
chr4:105221739 | G | A | 1 | a0003c0003t0018g0118 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-46-12158G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221739 | |||||||
chr4:105221803 | C | T | 120 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0003g0158 others(117): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.-46-12094C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221803 | |||||||
chr4:105221821 | G | A | 1 | a0018c0021t0004g0345 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-46-12076G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221821 | |||||||
chr4:105221863 | C | T | 1 | a0006c0006t0065g0340 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-46-12034C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221863 | |||||||
chr4:105221865 | T | TC | 10 | a0001c0001t0001g0237 a0001c0001t0002g0251 a0001c0001t0007g0301 others(7): Show |
10 | HG01192.hp2 HG01256.hp2 HG03942.hp1 others(7): Show |
intron_variant | MODIFIER | c.-46-12026dupC | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105221865 | ||||||
chr4:105221866 | C | CT | 6 | a0001c0001t0004g0310 a0001c0001t0005g0193 a0002c0002t0003g0122 others(3): Show |
6 | HG00140.hp2 HG01978.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46-12031_-46-1203 others(5): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221866 | |||||||
chr4:105221888 | C | T | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-46-12009C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221888 | |||||||
chr4:105221935 | A | G | 1 | a0018c0021t0004g0345 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-46-11962A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221935 | |||||||
chr4:105221943 | C | G | 48 | a0001c0001t0015g0330 a0003c0003t0002g0001 a0003c0003t0002g0028 others(45): Show |
49 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.-46-11954C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221943 | |||||||
chr4:105221983 | T | C | 241 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0305 others(238): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.-46-11914T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105221983 | |||||||
chr4:105222163 | C | T | 1 | a0001c0001t0008g0306 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-46-11734C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222163 | |||||||
chr4:105222164 | G | A | 1 | a0004c0004t0028g0202 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-46-11733G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222164 | |||||||
chr4:105222177 | G | A | 3 | a0001c0007t0030g0117 a0012c0016t0001g0019 a0012c0016t0001g0020 |
3 | HG00735.hp2 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-11720G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222177 | |||||||
chr4:105222225 | A | T | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-11672A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222225 | |||||||
chr4:105222285 | G | A | 5 | a0004c0004t0028g0202 a0004c0011t0008g0325 a0004c0011t0040g0329 others(2): Show |
5 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-11612G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222285 | |||||||
chr4:105222285 | G | T | 3 | a0001c0001t0006g0239 a0001c0001t0013g0296 a0015c0027t0010g0255 |
3 | HG00280.hp1 HG01496.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-46-11612G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222285 | |||||||
chr4:105222318 | T | G | 60 | a0001c0001t0015g0330 a0001c0001t0036g0029 a0001c0001t0104g0007 others(57): Show |
61 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.-46-11579T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222318 | |||||||
chr4:105222335 | C | T | 82 | a0001c0001t0001g0259 a0001c0001t0003g0158 a0001c0001t0009g0131 others(79): Show |
82 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.-46-11562C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222335 | |||||||
chr4:105222406 | T | A | 1 | a0001c0001t0006g0254 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-46-11491T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222406 | |||||||
chr4:105222541 | C | T | 3 | a0006c0006t0034g0333 a0006c0006t0082g0334 a0006c0006t0083g0335 |
3 | HG02572.hp1 HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-46-11356C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222541 | |||||||
chr4:105222553 | G | T | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-46-11344G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222553 | |||||||
chr4:105222559 | A | G | 8 | a0006c0006t0022g0336 a0006c0006t0022g0338 a0006c0006t0022g0341 others(5): Show |
8 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-46-11338A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222559 | |||||||
chr4:105222562 | G | A | 1 | a0001c0001t0104g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-46-11335G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222562 | |||||||
chr4:105222640 | G | A | 123 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0003g0158 others(120): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.-46-11257G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222640 | |||||||
chr4:105222651 | G | C | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-11246G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222651 | |||||||
chr4:105222665 | T | A | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-11232T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222665 | |||||||
chr4:105222689 | C | T | 8 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(5): Show |
8 | HG01192.hp1 HG02698.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-46-11208C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222689 | |||||||
chr4:105222743 | G | T | 2 | a0004c0004t0004g0035 a0004c0004t0018g0036 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-46-11154G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222743 | |||||||
chr4:105222791 | G | A | 177 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0003g0158 others(174): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.-46-11106G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222791 | |||||||
chr4:105222808 | G | A | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | NA18998.hp2 NA19003.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-46-11089G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222808 | |||||||
chr4:105222809 | G | A | 9 | a0006c0006t0022g0336 a0006c0006t0022g0338 a0006c0006t0022g0341 others(6): Show |
9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-46-11088G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222809 | |||||||
chr4:105222811 | G | A | 262 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0003g0158 others(259): Show |
263 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.-46-11086G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222811 | |||||||
chr4:105222860 | A | C | 3 | a0005c0005t0014g0065 a0005c0005t0014g0066 a0005c0005t0027g0064 |
3 | HG02970.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-46-11037A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222860 | |||||||
chr4:105222987 | T | G | 8 | a0001c0001t0001g0262 a0006c0006t0026g0005 a0006c0006t0026g0006 others(5): Show |
8 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-46-10910T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105222987 | |||||||
chr4:105223130 | T | A | 1 | a0001c0001t0001g0262 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-46-10767T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105223130 | |||||||
chr4:105223165 | G | C | 1 | a0001c0001t0001g0262 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-46-10732G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105223165 | |||||||
chr4:105223285 | G | A | 48 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(45): Show |
48 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(45): Show |
intron_variant | MODIFIER | c.-46-10612G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105223285 | |||||||
chr4:105223482 | A | G | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-10415A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105223482 | |||||||
chr4:105223578 | A | C | 183 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0234 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.-46-10319A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105223578 | |||||||
chr4:105223635 | T | C | 1 | a0004c0004t0033g0058 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-46-10262T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105223635 | |||||||
chr4:105224006 | C | T | 46 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(43): Show |
46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-9891C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105224006 | |||||||
chr4:105224115 | A | G | 1 | a0001c0001t0036g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-46-9782A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105224115 | |||||||
chr4:105224273 | G | A | 52 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(49): Show |
52 | HG01109.hp1 HG01175.hp1 HG01192.hp1 others(49): Show |
intron_variant | MODIFIER | c.-46-9624G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105224273 | |||||||
chr4:105224311 | A | G | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-9586A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105224311 | |||||||
chr4:105224471 | C | A | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-9426C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105224471 | |||||||
chr4:105224535 | T | G | 1 | a0002c0023t0003g0149 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-46-9362T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105224535 | |||||||
chr4:105224684 | G | GTC | 62 | a0001c0001t0001g0112 a0001c0001t0001g0232 a0001c0001t0001g0234 others(59): Show |
62 | HG00423.hp1 HG00673.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.-46-9171_-46-9170d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | ||||||
chr4:105224684 | G | GTCTC | 53 | a0001c0001t0001g0238 a0001c0001t0001g0259 a0001c0001t0001g0260 others(50): Show |
53 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.-46-9173_-46-9170d others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | ||||||
chr4:105224684 | G | GTCTCTC | 30 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0269 others(27): Show |
30 | HG00323.hp1 HG01192.hp2 HG02071.hp1 others(27): Show |
intron_variant | MODIFIER | c.-46-9175_-46-9170d others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | ||||||
chr4:105224684 | G | GTCTCTCT others(1): Show |
28 | a0001c0001t0001g0218 a0001c0001t0001g0305 a0001c0001t0001g0308 others(25): Show |
28 | HG00673.hp2 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.-46-9177_-46-9170d others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | ||||||
chr4:105224684 | G | GTCTCTCT others(3): Show |
24 | a0001c0001t0001g0250 a0001c0001t0002g0249 a0001c0001t0003g0158 others(21): Show |
24 | HG00741.hp1 HG01106.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.-46-9179_-46-9170d others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | ||||||
chr4:105224684 | G | GTCTCTCT others(5): Show |
18 | a0001c0001t0001g0189 a0001c0001t0006g0204 a0001c0001t0006g0207 others(15): Show |
18 | HG00140.hp1 HG00738.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.-46-9181_-46-9170d others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | ||||||
chr4:105224684 | G | GTCTCTCT others(7): Show |
19 | a0001c0001t0004g0209 a0001c0001t0005g0188 a0001c0001t0006g0212 others(16): Show |
19 | HG00642.hp1 HG00735.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.-46-9183_-46-9170d others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | ||||||
chr4:105224684 | G | GTCTCTCT others(9): Show |
9 | a0001c0001t0001g0191 a0001c0001t0004g0203 a0001c0001t0005g0192 others(6): Show |
9 | HG00323.hp2 HG01099.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46-9185_-46-9170d others(18): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | ||||||
chr4:105224684 | G | GTCTCTCT others(11): Show |
3 | a0001c0001t0006g0214 a0001c0001t0053g0187 a0005c0005t0005g0044 |
3 | HG01358.hp1 HG02300.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-46-9187_-46-9170d others(20): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | ||||||
chr4:105224684 | G | GTCTCTCT others(13): Show |
1 | a0001c0001t0055g0194 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-46-9189_-46-9170d others(22): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | ||||||
chr4:105224684 | G | GTCTCTCT others(17): Show |
1 | a0001c0007t0071g0180 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-46-9193_-46-9170d others(26): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | ||||||
chr4:105224684 | G | GTCTCTCT others(19): Show |
1 | a0001c0007t0030g0339 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-46-9195_-46-9170d others(28): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | ||||||
chr4:105224684 | G | GTCTCTCT others(21): Show |
1 | a0004c0004t0101g0075 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-46-9197_-46-9170d others(30): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | ||||||
chr4:105224684 | G | GTCTCTCT others(25): Show |
1 | a0004c0004t0084g0072 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-46-9201_-46-9170d others(34): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | ||||||
chr4:105224684 | GTC | G | 24 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 others(21): Show |
24 | HG00280.hp1 HG01243.hp1 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.-46-9171_-46-9170d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | ||||||
chr4:105224684 | GTCTC | G | 3 | a0003c0003t0002g0094 a0006c0006t0045g0121 a0006c0006t0065g0340 |
3 | HG02886.hp2 HG02965.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.-46-9173_-46-9170d others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | ||||||
chr4:105224684 | GTCTCTC | G | 4 | a0003c0003t0002g0028 a0003c0003t0002g0096 a0003c0003t0002g0231 others(1): Show |
4 | HG00423.hp2 NA18980.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46-9175_-46-9170d others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | ||||||
chr4:105224684 | GTCTCTCT others(1): Show |
G | 30 | a0003c0003t0002g0001 a0003c0003t0002g0078 a0003c0003t0002g0079 others(27): Show |
31 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.-46-9177_-46-9170d others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | ||||||
chr4:105224684 | GTCTCTCT others(3): Show |
G | 7 | a0001c0001t0008g0211 a0001c0001t0104g0007 a0003c0003t0018g0118 others(4): Show |
7 | HG01070.hp1 HG01517.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-9179_-46-9170d others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | ||||||
chr4:105224684 | GTCTCTCT others(7): Show |
G | 1 | a0004c0004t0028g0202 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-46-9183_-46-9170d others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | ||||||
chr4:105224684 | GTCTCTCT others(9): Show |
G | 7 | a0001c0001t0015g0330 a0003c0003t0002g0088 a0003c0003t0002g0089 others(4): Show |
7 | HG01071.hp2 HG01074.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-9185_-46-9170d others(18): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | ||||||
chr4:105224684 | GTCTCTCT others(11): Show |
G | 1 | a0003c0003t0015g0093 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-46-9187_-46-9170d others(20): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105224684 | ||||||
chr4:105224727 | T | TCTCTCTC others(4): Show |
1 | a0001c0001t0004g0186 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-46-9170_-46-9169i others(13): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105224727 | |||||||
chr4:105224803 | C | T | 1 | a0002c0002t0087g0171 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-46-9094C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105224803 | |||||||
chr4:105225092 | T | G | 1 | a0001c0001t0053g0187 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-46-8805T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105225092 | |||||||
chr4:105225106 | T | C | 2 | a0001c0001t0001g0238 a0001c0001t0001g0297 |
2 | HG02015.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.-46-8791T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105225106 | |||||||
chr4:105225128 | G | A | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-8769G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105225128 | |||||||
chr4:105225140 | G | A | 1 | a0002c0002t0003g0200 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-46-8757G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105225140 | |||||||
chr4:105225185 | C | CGT | 7 | a0001c0001t0001g0258 a0001c0001t0001g0282 a0001c0001t0008g0291 others(4): Show |
7 | HG02735.hp1 HG03239.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-8688_-46-8687d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105225185 | ||||||
chr4:105225185 | C | CGTGTGTG others(1): Show |
9 | a0001c0001t0032g0052 a0001c0001t0036g0029 a0001c0001t0080g0053 others(6): Show |
9 | HG00609.hp1 HG01169.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46-8694_-46-8687d others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105225185 | ||||||
chr4:105225185 | C | CGTGTGTG others(3): Show |
8 | a0001c0001t0001g0191 a0001c0001t0104g0007 a0002c0002t0003g0242 others(5): Show |
8 | HG01261.hp2 HG01346.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.-46-8696_-46-8687d others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105225185 | ||||||
chr4:105225185 | C | CGTGTGTG others(5): Show |
54 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(51): Show |
54 | HG00323.hp2 HG00558.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.-46-8698_-46-8687d others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105225185 | ||||||
chr4:105225185 | C | CGTGTGTG others(7): Show |
76 | a0001c0001t0001g0189 a0001c0001t0001g0305 a0001c0001t0003g0158 others(73): Show |
76 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.-46-8700_-46-8687d others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105225185 | ||||||
chr4:105225185 | C | CGTGTGTG others(9): Show |
21 | a0001c0001t0032g0195 a0001c0001t0055g0194 a0002c0002t0023g0134 others(18): Show |
21 | HG00642.hp2 HG00738.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.-46-8702_-46-8687d others(18): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105225185 | ||||||
chr4:105225185 | C | CGTGTGTG others(11): Show |
15 | a0001c0001t0053g0187 a0001c0001t0086g0031 a0001c0001t0088g0030 others(12): Show |
15 | HG01109.hp1 HG01361.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-46-8704_-46-8687d others(20): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105225185 | ||||||
chr4:105225185 | C | CGTGTGTG others(13): Show |
7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01099.hp2 HG01192.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-8706_-46-8687d others(22): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105225185 | ||||||
chr4:105225185 | C | CGTGTGTG others(15): Show |
4 | a0004c0004t0074g0061 a0004c0004t0099g0060 a0006c0006t0045g0121 others(1): Show |
4 | HG01192.hp2 HG02602.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-8708_-46-8687d others(24): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105225185 | ||||||
chr4:105225185 | C | CGTGTGTG others(17): Show |
2 | a0004c0004t0013g0222 a0004c0004t0072g0062 |
2 | HG02145.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-46-8710_-46-8687d others(26): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105225185 | ||||||
chr4:105225185 | CGTGTGT | C | 42 | a0001c0001t0015g0330 a0003c0003t0002g0001 a0003c0003t0002g0028 others(39): Show |
43 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.-46-8692_-46-8687d others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105225185 | ||||||
chr4:105225320 | A | C | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-46-8577A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105225320 | |||||||
chr4:105225345 | C | T | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-8552C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105225345 | |||||||
chr4:105225365 | C | T | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-46-8532C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105225365 | |||||||
chr4:105225662 | A | G | 2 | a0002c0002t0024g0178 a0006c0006t0068g0014 |
2 | HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-46-8235A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105225662 | |||||||
chr4:105225878 | T | C | 1 | a0001c0001t0104g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-46-8019T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105225878 | |||||||
chr4:105225909 | G | A | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-7988G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105225909 | |||||||
chr4:105225978 | A | G | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-7919A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105225978 | |||||||
chr4:105226064 | C | T | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-46-7833C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105226064 | |||||||
chr4:105226077 | C | CT | 266 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0234 others(263): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.-46-7818dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105226077 | ||||||
chr4:105226099 | TA | T | 23 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(20): Show |
23 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.-46-7789delA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105226099 | ||||||
chr4:105226416 | G | T | 1 | a0002c0002t0003g0315 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-46-7481G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105226416 | |||||||
chr4:105226633 | CCCTCCCT others(3): Show |
C | 1 | a0001c0001t0016g0215 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-46-7249_-46-7240d others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105226633 | ||||||
chr4:105226721 | A | G | 1 | a0005c0005t0049g0047 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-46-7176A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105226721 | |||||||
chr4:105226756 | A | G | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-7141A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105226756 | |||||||
chr4:105226762 | T | A | 49 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(46): Show |
49 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.-46-7135T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105226762 | |||||||
chr4:105226787 | C | G | 3 | a0004c0031t0092g0021 a0012c0016t0001g0019 a0012c0016t0001g0020 |
3 | HG02451.hp2 HG03831.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-7110C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105226787 | |||||||
chr4:105226841 | T | C | 1 | a0003c0003t0018g0118 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-46-7056T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105226841 | |||||||
chr4:105226922 | C | T | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-46-6975C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105226922 | |||||||
chr4:105226979 | T | G | 49 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(46): Show |
49 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.-46-6918T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105226979 | |||||||
chr4:105226993 | A | G | 1 | a0003c0003t0018g0118 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-46-6904A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105226993 | |||||||
chr4:105227056 | C | T | 3 | a0002c0002t0009g0129 a0002c0002t0021g0124 a0002c0002t0021g0125 |
3 | HG04184.hp2 HG04199.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-46-6841C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227056 | |||||||
chr4:105227058 | G | A | 1 | a0001c0001t0013g0296 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-46-6839G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227058 | |||||||
chr4:105227065 | A | G | 3 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 |
3 | HG01243.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-46-6832A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227065 | |||||||
chr4:105227066 | G | C | 1 | a0004c0004t0013g0222 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-46-6831G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227066 | |||||||
chr4:105227121 | C | A | 4 | a0008c0010t0012g0008 a0008c0010t0012g0009 a0008c0010t0012g0011 others(1): Show |
4 | HG02145.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46-6776C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227121 | |||||||
chr4:105227489 | G | A | 2 | a0004c0004t0004g0035 a0004c0004t0018g0036 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-46-6408G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227489 | |||||||
chr4:105227492 | TAGACCTT others(93): Show |
T | 46 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(43): Show |
46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-6403_-46-6304d others(102): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105227492 | ||||||
chr4:105227596 | A | T | 46 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(43): Show |
46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-6301A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227596 | |||||||
chr4:105227598 | A | T | 46 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(43): Show |
46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-6299A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227598 | |||||||
chr4:105227599 | AGG | A | 46 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(43): Show |
46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-6297_-46-6296d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227599 | |||||||
chr4:105227601 | G | C | 126 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0234 others(123): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.-46-6296G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227601 | |||||||
chr4:105227765 | A | G | 1 | a0004c0004t0013g0221 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-46-6132A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227765 | |||||||
chr4:105227849 | G | C | 27 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(24): Show |
27 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.-46-6048G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105227849 | |||||||
chr4:105228157 | A | G | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-5740A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105228157 | |||||||
chr4:105228191 | T | C | 1 | a0004c0008t0067g0070 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-46-5706T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105228191 | |||||||
chr4:105228558 | C | T | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-5339C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105228558 | |||||||
chr4:105228573 | A | G | 1 | a0004c0004t0101g0075 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-46-5324A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105228573 | |||||||
chr4:105228679 | T | C | 1 | a0001c0001t0008g0306 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-46-5218T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105228679 | |||||||
chr4:105229011 | T | C | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-4886T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105229011 | |||||||
chr4:105229076 | A | C | 47 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(44): Show |
47 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.-46-4821A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105229076 | |||||||
chr4:105229295 | T | C | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-4602T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105229295 | |||||||
chr4:105229304 | A | G | 1 | a0009c0013t0001g0321 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-46-4593A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105229304 | |||||||
chr4:105229398 | C | T | 24 | a0003c0003t0015g0086 a0005c0005t0005g0032 a0005c0005t0005g0041 others(21): Show |
24 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-46-4499C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105229398 | |||||||
chr4:105229502 | T | G | 49 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(46): Show |
49 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.-46-4395T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105229502 | |||||||
chr4:105229503 | G | T | 46 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(43): Show |
46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-4394G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105229503 | |||||||
chr4:105229516 | GGC | G | 4 | a0001c0001t0006g0252 a0001c0001t0006g0253 a0001c0001t0006g0254 others(1): Show |
4 | HG01169.hp1 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46-4380_-46-4379d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105229516 | |||||||
chr4:105229652 | TA | T | 14 | a0001c0001t0016g0210 a0001c0007t0030g0117 a0001c0007t0030g0339 others(11): Show |
14 | HG00735.hp2 HG01099.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.-46-4231delA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105229652 | ||||||
chr4:105230053 | A | T | 8 | a0001c0001t0017g0266 a0006c0006t0026g0005 a0006c0006t0026g0006 others(5): Show |
8 | HG01192.hp1 HG02818.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-46-3844A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105230053 | |||||||
chr4:105230055 | T | A | 46 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(43): Show |
46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-3842T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105230055 | |||||||
chr4:105230408 | T | C | 44 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(41): Show |
44 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.-46-3489T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105230408 | |||||||
chr4:105230485 | G | A | 125 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0234 others(122): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.-46-3412G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105230485 | |||||||
chr4:105230624 | A | G | 8 | a0006c0006t0022g0336 a0006c0006t0022g0338 a0006c0006t0022g0341 others(5): Show |
8 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-46-3273A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105230624 | |||||||
chr4:105230686 | T | C | 243 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0234 others(240): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.-46-3211T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105230686 | |||||||
chr4:105230760 | C | T | 2 | a0004c0004t0004g0035 a0004c0004t0018g0036 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-46-3137C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105230760 | |||||||
chr4:105230800 | T | C | 1 | a0001c0001t0010g0229 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-46-3097T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105230800 | |||||||
chr4:105230805 | T | G | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-3092T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105230805 | |||||||
chr4:105230880 | G | A | 23 | a0005c0005t0005g0032 a0005c0005t0005g0041 a0005c0005t0005g0042 others(20): Show |
23 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.-46-3017G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105230880 | |||||||
chr4:105230954 | T | G | 77 | a0001c0001t0001g0234 a0001c0001t0001g0305 a0001c0001t0003g0158 others(74): Show |
77 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.-46-2943T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105230954 | |||||||
chr4:105231619 | C | T | 1 | a0002c0002t0020g0201 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-46-2278C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105231619 | |||||||
chr4:105231667 | A | G | 46 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(43): Show |
46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-2230A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105231667 | |||||||
chr4:105231720 | C | A | 108 | a0001c0001t0001g0234 a0001c0001t0003g0158 a0001c0001t0004g0203 others(105): Show |
108 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.-46-2177C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105231720 | |||||||
chr4:105231809 | T | C | 3 | a0005c0005t0014g0065 a0005c0005t0014g0066 a0005c0005t0027g0064 |
3 | HG02970.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-46-2088T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105231809 | |||||||
chr4:105231827 | T | C | 119 | a0001c0001t0001g0234 a0001c0001t0001g0305 a0001c0001t0003g0158 others(116): Show |
119 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.-46-2070T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105231827 | |||||||
chr4:105231828 | G | A | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-2069G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105231828 | |||||||
chr4:105231897 | A | G | 4 | a0001c0001t0032g0052 a0001c0001t0080g0053 a0004c0004t0004g0035 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-2000A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105231897 | |||||||
chr4:105231901 | G | T | 1 | a0002c0002t0021g0165 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-46-1996G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105231901 | |||||||
chr4:105232001 | T | C | 4 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(1): Show |
4 | NA18998.hp2 NA19003.hp2 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-1896T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105232001 | |||||||
chr4:105232022 | C | G | 1 | a0002c0002t0003g0230 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-46-1875C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105232022 | |||||||
chr4:105232063 | C | A | 1 | a0001c0001t0005g0267 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-46-1834C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105232063 | |||||||
chr4:105232395 | G | A | 2 | a0006c0006t0026g0010 a0006c0006t0102g0004 |
2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-46-1502G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105232395 | |||||||
chr4:105232399 | G | A | 1 | a0003c0003t0002g0082 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-46-1498G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105232399 | |||||||
chr4:105232440 | C | G | 1 | a0003c0003t0002g0103 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-46-1457C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105232440 | |||||||
chr4:105232546 | A | C | 2 | a0004c0004t0004g0035 a0004c0004t0018g0036 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-46-1351A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105232546 | |||||||
chr4:105232714 | A | G | 1 | a0004c0004t0084g0072 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-46-1183A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105232714 | |||||||
chr4:105232969 | G | A | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46-928G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105232969 | |||||||
chr4:105233034 | C | A | 1 | a0001c0001t0007g0301 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-46-863C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105233034 | |||||||
chr4:105233102 | G | T | 1 | a0002c0002t0020g0201 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-46-795G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105233102 | |||||||
chr4:105233255 | G | A | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-46-642G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105233255 | |||||||
chr4:105233343 | C | T | 58 | a0001c0001t0036g0029 a0003c0003t0002g0001 a0003c0003t0002g0028 others(55): Show |
59 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.-46-554C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105233343 | |||||||
chr4:105233344 | G | A | 22 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(19): Show |
22 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-46-553G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105233344 | |||||||
chr4:105233356 | C | G | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-46-541C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105233356 | |||||||
chr4:105233378 | C | T | 46 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(43): Show |
46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.-46-519C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105233378 | |||||||
chr4:105233383 | C | CAAAAAAA others(2): Show |
9 | a0001c0001t0093g0179 a0002c0002t0003g0132 a0002c0002t0087g0171 others(6): Show |
9 | HG01169.hp2 HG02080.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46-504_-46-496dup others(9): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233383 | ||||||
chr4:105233383 | C | CAAAAAAA others(3): Show |
119 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(116): Show |
120 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.-46-505_-46-496dup others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233383 | ||||||
chr4:105233383 | C | CAAAAAAA others(4): Show |
34 | a0001c0001t0006g0207 a0001c0001t0006g0212 a0001c0001t0016g0215 others(31): Show |
34 | HG00423.hp2 HG00544.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.-46-506_-46-496dup others(11): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233383 | ||||||
chr4:105233383 | C | CAAAAAAA others(5): Show |
9 | a0001c0001t0009g0131 a0001c0001t0009g0146 a0001c0001t0095g0130 others(6): Show |
9 | HG01891.hp1 HG02572.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46-507_-46-496dup others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233383 | ||||||
chr4:105233383 | C | CAAAAAAA others(6): Show |
12 | a0001c0001t0003g0158 a0004c0004t0018g0063 a0004c0004t0058g0312 others(9): Show |
12 | HG02723.hp2 HG02809.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.-46-508_-46-496dup others(13): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233383 | ||||||
chr4:105233383 | C | CAAAAAAA others(7): Show |
20 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0007g0283 others(17): Show |
20 | HG01109.hp1 HG01175.hp1 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.-46-509_-46-496dup others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233383 | ||||||
chr4:105233383 | C | CAAAAAAA others(8): Show |
11 | a0004c0004t0004g0225 a0004c0004t0010g0226 a0004c0004t0010g0228 others(8): Show |
11 | HG01099.hp2 HG01192.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.-46-510_-46-496dup others(15): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233383 | ||||||
chr4:105233383 | C | CAAAAAAA others(9): Show |
3 | a0004c0004t0004g0223 a0004c0004t0074g0061 a0004c0004t0100g0055 |
3 | HG02257.hp2 HG02647.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.-46-511_-46-496dup others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233383 | ||||||
chr4:105233383 | CA | C | 39 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0289 others(36): Show |
39 | HG00140.hp1 HG00642.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.-46-496delA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233383 | ||||||
chr4:105233542 | G | A | 1 | a0003c0003t0002g0081 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-46-355G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105233542 | |||||||
chr4:105233790 | C | T | 1 | a0004c0004t0101g0075 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-46-107C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | chr4 | 105233790 | |||||||
chr4:105233833 | T | TATAG | 100 | a0003c0003t0002g0001 a0003c0003t0002g0028 a0003c0003t0002g0078 others(97): Show |
101 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.-46-42_-46-39dupTA others(2): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233833 | ||||||
chr4:105233833 | T | TATAGATA others(1): Show |
5 | a0004c0004t0101g0075 a0004c0019t0081g0054 a0004c0031t0092g0021 others(2): Show |
5 | HG01099.hp2 HG02602.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-46_-46-39dupTA others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233833 | ||||||
chr4:105233833 | TATAGATA others(1): Show |
T | 109 | a0001c0001t0001g0234 a0001c0001t0001g0305 a0001c0001t0003g0158 others(106): Show |
109 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.-46-46_-46-39delTA others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr4 | 105233833 | ||||||
chr4:105237369 | A | G | 3 | a0004c0004t0072g0062 a0004c0004t0074g0061 a0004c0004t0099g0060 |
3 | HG01192.hp2 HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.3409+18A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105237369 | |||||||
chr4:105237581 | G | A | 6 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(3): Show |
6 | HG01192.hp1 HG02818.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3409+230G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105237581 | |||||||
chr4:105237663 | T | A | 1 | a0004c0004t0074g0061 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3409+312T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105237663 | |||||||
chr4:105237764 | A | T | 1 | a0004c0004t0018g0063 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3409+413A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105237764 | |||||||
chr4:105237842 | G | T | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3409+491G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105237842 | |||||||
chr4:105237969 | A | C | 1 | a0002c0002t0020g0176 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3409+618A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105237969 | |||||||
chr4:105238107 | C | T | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3409+756C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105238107 | |||||||
chr4:105238114 | AGT | A | 22 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(19): Show |
22 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.3409+767_3409+768d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr4 | 105238114 | ||||||
chr4:105238229 | G | A | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3409+878G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105238229 | |||||||
chr4:105238425 | T | G | 4 | a0007c0009t0027g0049 a0007c0009t0051g0033 a0007c0009t0052g0048 others(1): Show |
4 | HG00738.hp2 HG01891.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.3409+1074T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105238425 | |||||||
chr4:105238850 | C | T | 1 | a0014c0024t0029g0127 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3409+1499C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105238850 | |||||||
chr4:105238874 | G | A | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3409+1523G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105238874 | |||||||
chr4:105238875 | C | A | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3409+1524C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105238875 | |||||||
chr4:105238876 | A | G | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3409+1525A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105238876 | |||||||
chr4:105238976 | G | A | 39 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(36): Show |
39 | HG00140.hp1 HG00642.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.3409+1625G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105238976 | |||||||
chr4:105239004 | A | G | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3409+1653A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239004 | |||||||
chr4:105239062 | G | T | 1 | a0001c0001t0028g0278 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3409+1711G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239062 | |||||||
chr4:105239067 | G | T | 1 | a0001c0001t0008g0298 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.3409+1716G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239067 | |||||||
chr4:105239070 | T | C | 1 | a0001c0001t0008g0205 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3409+1719T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239070 | |||||||
chr4:105239072 | T | TTGTTTTT others(3): Show |
56 | a0001c0001t0001g0259 a0001c0001t0104g0007 a0003c0003t0002g0001 others(53): Show |
57 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.3409+1730_3409+173 others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr4 | 105239072 | ||||||
chr4:105239074 | G | GTTTTTTT others(2): Show |
35 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(32): Show |
35 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.3409+1730_3409+173 others(13): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr4 | 105239074 | ||||||
chr4:105239074 | G | GTTTTTTT others(3): Show |
63 | a0001c0001t0070g0034 a0001c0001t0093g0179 a0001c0007t0030g0117 others(60): Show |
63 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(60): Show |
intron_variant | MODIFIER | c.3409+1730_3409+173 others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr4 | 105239074 | ||||||
chr4:105239074 | G | GTTTTTTT others(4): Show |
103 | a0001c0001t0001g0234 a0001c0001t0001g0305 a0001c0001t0003g0158 others(100): Show |
103 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.3409+1730_3409+173 others(15): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr4 | 105239074 | ||||||
chr4:105239074 | G | GTTTTTTT others(5): Show |
4 | a0002c0002t0024g0141 a0002c0002t0063g0013 a0002c0002t0087g0171 others(1): Show |
4 | HG01169.hp2 HG02056.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.3409+1730_3409+173 others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr4 | 105239074 | ||||||
chr4:105239082 | T | G | 1 | a0006c0006t0045g0121 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3409+1731T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239082 | |||||||
chr4:105239083 | T | G | 4 | a0002c0002t0003g0140 a0002c0002t0025g0163 a0002c0002t0025g0174 others(1): Show |
4 | HG03669.hp1 HG03688.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.3409+1732T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239083 | |||||||
chr4:105239208 | A | C | 111 | a0001c0001t0001g0234 a0001c0001t0001g0305 a0001c0001t0003g0158 others(108): Show |
111 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.3409+1857A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239208 | |||||||
chr4:105239325 | T | C | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3409+1974T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239325 | |||||||
chr4:105239338 | A | G | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3409+1987A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239338 | |||||||
chr4:105239579 | G | C | 3 | a0001c0001t0075g0027 a0001c0001t0077g0026 a0001c0001t0078g0025 |
3 | HG02004.hp2 HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3410-1760G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239579 | |||||||
chr4:105239658 | G | A | 1 | a0009c0013t0001g0321 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3410-1681G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239658 | |||||||
chr4:105239825 | G | A | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3410-1514G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239825 | |||||||
chr4:105239898 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3410-1441T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105239898 | |||||||
chr4:105240118 | A | G | 10 | a0002c0002t0003g0122 a0002c0002t0003g0123 a0002c0002t0003g0126 others(7): Show |
10 | HG00544.hp2 NA18959.hp2 NA18973.hp1 others(7): Show |
intron_variant | MODIFIER | c.3410-1221A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105240118 | |||||||
chr4:105240309 | C | T | 1 | a0013c0014t0060g0074 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3410-1030C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105240309 | |||||||
chr4:105240470 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.3410-869C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105240470 | |||||||
chr4:105240915 | G | A | 3 | a0001c0001t0001g0320 a0001c0001t0004g0243 a0001c0001t0007g0244 |
3 | HG01255.hp2 HG01928.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.3410-424G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105240915 | |||||||
chr4:105241024 | G | A | 1 | a0003c0003t0002g0103 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3410-315G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105241024 | |||||||
chr4:105241058 | GT | G | 8 | a0006c0006t0022g0336 a0006c0006t0022g0338 a0006c0006t0022g0341 others(5): Show |
8 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3410-280delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105241058 | |||||||
chr4:105241161 | A | C | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3410-178A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 3/10 | chr4 | 105241161 | |||||||
chr4:105241546 | G | A | 1 | a0004c0004t0028g0202 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3500+117G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 4/10 | chr4 | 105241546 | |||||||
chr4:105241736 | G | A | 1 | a0018c0021t0004g0345 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3500+307G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 4/10 | chr4 | 105241736 | |||||||
chr4:105241938 | CT | C | 185 | a0001c0001t0001g0112 a0001c0001t0001g0189 a0001c0001t0001g0191 others(182): Show |
186 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.3500+524delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr4 | 105241938 | ||||||
chr4:105241938 | CTT | C | 55 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(52): Show |
55 | HG01109.hp1 HG01175.hp1 HG01192.hp1 others(52): Show |
intron_variant | MODIFIER | c.3500+523_3500+524d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr4 | 105241938 | ||||||
chr4:105241952 | TTC | T | 95 | a0001c0001t0003g0158 a0001c0001t0004g0203 a0001c0001t0004g0209 others(92): Show |
95 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.3500+524_3500+525d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 4/10 | chr4 | 105241952 | |||||||
chr4:105241953 | TC | T | 9 | a0001c0001t0073g0024 a0001c0001t0075g0027 a0001c0001t0076g0023 others(6): Show |
9 | HG00323.hp1 HG01081.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.3500+525delC | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 4/10 | chr4 | 105241953 | |||||||
chr4:105242182 | T | G | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3501-652T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 4/10 | chr4 | 105242182 | |||||||
chr4:105242432 | A | T | 1 | a0001c0001t0004g0271 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3501-402A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 4/10 | chr4 | 105242432 | |||||||
chr4:105242479 | T | G | 1 | a0011c0015t0044g0346 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3501-355T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 4/10 | chr4 | 105242479 | |||||||
chr4:105243040 | C | T | 1 | a0001c0001t0104g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3594+113C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 5/10 | chr4 | 105243040 | |||||||
chr4:105243073 | TAAG | T | 46 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(43): Show |
46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.3594+151_3594+153d others(5): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr4 | 105243073 | ||||||
chr4:105243127 | T | G | 75 | a0001c0001t0001g0305 a0001c0001t0003g0158 a0001c0001t0009g0131 others(72): Show |
75 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.3594+200T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 5/10 | chr4 | 105243127 | |||||||
chr4:105243484 | A | G | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3595-86A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 5/10 | chr4 | 105243484 | |||||||
chr4:105243566 | G | A | 7 | a0002c0002t0003g0316 a0006c0006t0026g0005 a0006c0006t0026g0006 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02970.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.3595-4G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 5/10 | chr4 | 105243566 | |||||||
chr4:105243823 | G | A | 16 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.3803+45G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105243823 | |||||||
chr4:105243834 | T | C | 1 | a0006c0006t0097g0069 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3803+56T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105243834 | |||||||
chr4:105244056 | T | C | 1 | a0001c0001t0005g0267 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3803+278T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244056 | |||||||
chr4:105244267 | A | T | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3803+489A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244267 | |||||||
chr4:105244351 | A | G | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3803+573A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244351 | |||||||
chr4:105244408 | G | T | 1 | a0001c0001t0008g0306 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3803+630G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244408 | |||||||
chr4:105244584 | A | ATC | 6 | a0004c0004t0004g0035 a0004c0004t0018g0036 a0004c0004t0058g0312 others(3): Show |
6 | HG01175.hp1 HG01891.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.3803+807_3803+808i others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244584 | ||||||
chr4:105244584 | A | ATCT | 7 | a0001c0007t0030g0339 a0001c0007t0031g0115 a0001c0007t0057g0040 others(4): Show |
7 | HG02451.hp2 HG02809.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.3803+807_3803+808i others(5): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244584 | ||||||
chr4:105244584 | A | ATCTT | 4 | a0001c0007t0030g0117 a0001c0007t0031g0038 a0001c0007t0071g0180 others(1): Show |
4 | HG00735.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3803+807_3803+808i others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244584 | ||||||
chr4:105244584 | A | ATCTTT | 3 | a0001c0001t0070g0034 a0001c0001t0093g0179 a0001c0001t0104g0007 |
3 | HG01884.hp1 HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3803+807_3803+808i others(7): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244584 | ||||||
chr4:105244584 | A | ATCTTTTT | 5 | a0001c0001t0073g0024 a0001c0001t0075g0027 a0001c0001t0076g0023 others(2): Show |
5 | HG01081.hp2 HG02004.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.3803+807_3803+808i others(9): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244584 | ||||||
chr4:105244584 | A | ATCTTTTT others(2): Show |
9 | a0001c0001t0006g0204 a0001c0001t0006g0206 a0001c0001t0006g0207 others(6): Show |
9 | HG00323.hp2 HG01106.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.3803+807_3803+808i others(11): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244584 | ||||||
chr4:105244584 | A | ATCTTTTT others(3): Show |
7 | a0001c0001t0004g0203 a0001c0001t0006g0214 a0001c0001t0006g0318 others(4): Show |
7 | HG00642.hp1 HG01099.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.3803+807_3803+808i others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244584 | ||||||
chr4:105244584 | ATGTTTTT others(1): Show |
A | 63 | a0001c0001t0001g0305 a0002c0002t0001g0133 a0002c0002t0003g0122 others(60): Show |
63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.3803+808_3803+815d others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244584 | ||||||
chr4:105244584 | ATGTTTTT others(5): Show |
A | 4 | a0002c0002t0003g0155 a0002c0002t0003g0173 a0002c0002t0020g0201 others(1): Show |
4 | HG01358.hp2 HG01981.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.3803+808_3803+819d others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244584 | ||||||
chr4:105244585 | T | TC | 10 | a0004c0004t0010g0319 a0004c0004t0039g0068 a0004c0004t0072g0062 others(7): Show |
10 | HG01109.hp1 HG01192.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.3803+807_3803+808i others(3): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244585 | |||||||
chr4:105244586 | G | C | 38 | a0002c0002t0003g0240 a0004c0004t0004g0015 a0004c0004t0004g0220 others(35): Show |
38 | HG01192.hp2 HG01243.hp2 HG02257.hp2 others(35): Show |
intron_variant | MODIFIER | c.3803+808G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244586 | |||||||
chr4:105244586 | G | GT | 59 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0237 others(56): Show |
59 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.3803+834dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244586 | ||||||
chr4:105244586 | G | GTT | 11 | a0001c0001t0001g0261 a0001c0001t0004g0186 a0001c0001t0005g0193 others(8): Show |
11 | HG00738.hp2 HG00741.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.3803+833_3803+834d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244586 | ||||||
chr4:105244586 | G | T | 52 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(49): Show |
52 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.3803+808G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244586 | |||||||
chr4:105244586 | GT | G | 6 | a0003c0003t0002g0089 a0003c0003t0018g0118 a0006c0006t0022g0341 others(3): Show |
6 | HG01070.hp1 HG01074.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.3803+834delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105244586 | ||||||
chr4:105244587 | T | C | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3803+809T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244587 | |||||||
chr4:105244593 | T | C | 5 | a0001c0001t0003g0158 a0001c0001t0009g0131 a0001c0001t0009g0146 others(2): Show |
5 | HG02723.hp2 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3803+815T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244593 | |||||||
chr4:105244594 | T | C | 63 | a0001c0001t0001g0305 a0002c0002t0001g0133 a0002c0002t0003g0122 others(60): Show |
63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.3803+816T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244594 | |||||||
chr4:105244595 | T | C | 1 | a0002c0002t0003g0242 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.3803+817T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244595 | |||||||
chr4:105244598 | T | C | 4 | a0002c0002t0003g0155 a0002c0002t0003g0173 a0002c0002t0020g0201 others(1): Show |
4 | HG01358.hp2 HG01981.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.3803+820T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244598 | |||||||
chr4:105244625 | C | T | 1 | a0004c0008t0008g0071 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3803+847C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244625 | |||||||
chr4:105244656 | C | T | 1 | a0001c0001t0073g0024 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3803+878C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244656 | |||||||
chr4:105244672 | C | T | 1 | a0006c0006t0097g0069 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3803+894C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244672 | |||||||
chr4:105244715 | C | T | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3803+937C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244715 | |||||||
chr4:105244879 | C | T | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3803+1101C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244879 | |||||||
chr4:105244881 | C | T | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3803+1103C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244881 | |||||||
chr4:105244916 | C | T | 3 | a0004c0011t0040g0329 a0004c0011t0047g0326 a0004c0018t0019g0324 |
3 | HG02809.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3803+1138C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244916 | |||||||
chr4:105244982 | A | G | 8 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(5): Show |
8 | HG01192.hp1 HG02698.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.3803+1204A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105244982 | |||||||
chr4:105245265 | G | A | 1 | a0002c0002t0003g0155 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3803+1487G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105245265 | |||||||
chr4:105245302 | T | C | 1 | a0001c0001t0007g0300 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3803+1524T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105245302 | |||||||
chr4:105245400 | G | A | 1 | a0001c0001t0075g0027 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3803+1622G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105245400 | |||||||
chr4:105245566 | G | T | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3803+1788G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105245566 | |||||||
chr4:105245813 | C | G | 1 | a0006c0006t0022g0336 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3803+2035C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105245813 | |||||||
chr4:105245858 | G | A | 1 | a0003c0003t0002g0113 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3803+2080G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105245858 | |||||||
chr4:105245984 | C | T | 1 | a0001c0001t0036g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3803+2206C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105245984 | |||||||
chr4:105246023 | C | T | 2 | a0002c0002t0003g0154 a0002c0002t0003g0156 |
2 | NA18979.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.3803+2245C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105246023 | |||||||
chr4:105246275 | T | TA | 228 | a0001c0001t0001g0218 a0001c0001t0001g0234 a0001c0001t0001g0272 others(225): Show |
229 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.3803+2503dupA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105246275 | ||||||
chr4:105246501 | TAATGCTT others(4): Show |
T | 6 | a0004c0008t0008g0071 a0004c0008t0019g0327 a0004c0008t0019g0332 others(3): Show |
6 | HG01175.hp1 HG02572.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.3803+2724_3803+273 others(15): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105246501 | |||||||
chr4:105246587 | C | T | 107 | a0001c0001t0001g0234 a0001c0001t0003g0158 a0001c0001t0004g0203 others(104): Show |
107 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.3803+2809C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105246587 | |||||||
chr4:105246602 | T | C | 2 | a0004c0004t0004g0035 a0004c0004t0018g0036 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3803+2824T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105246602 | |||||||
chr4:105246710 | A | T | 1 | a0001c0001t0001g0272 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3803+2932A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105246710 | |||||||
chr4:105246711 | T | A | 1 | a0001c0001t0001g0272 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3803+2933T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105246711 | |||||||
chr4:105246712 | A | T | 1 | a0001c0001t0001g0272 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3803+2934A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105246712 | |||||||
chr4:105246845 | G | A | 2 | a0004c0004t0013g0056 a0004c0004t0013g0057 |
2 | HG01243.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3803+3067G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105246845 | |||||||
chr4:105247137 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3803+3359C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105247137 | |||||||
chr4:105247376 | AAAAG | A | 57 | a0001c0001t0001g0272 a0001c0001t0002g0251 a0001c0001t0005g0267 others(54): Show |
58 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.3803+3603_3803+360 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105247376 | ||||||
chr4:105247466 | C | G | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3803+3688C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105247466 | |||||||
chr4:105247526 | T | G | 1 | a0001c0001t0070g0034 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3803+3748T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105247526 | |||||||
chr4:105247579 | C | G | 46 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(43): Show |
46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.3803+3801C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105247579 | |||||||
chr4:105247642 | GTTTAC | G | 222 | a0001c0001t0001g0272 a0001c0001t0002g0251 a0001c0001t0003g0158 others(219): Show |
223 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.3803+3869_3803+387 others(9): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105247642 | ||||||
chr4:105247664 | A | G | 2 | a0004c0004t0013g0056 a0004c0004t0013g0057 |
2 | HG01243.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3803+3886A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105247664 | |||||||
chr4:105247714 | C | CT | 16 | a0001c0001t0001g0218 a0001c0001t0001g0257 a0001c0001t0001g0258 others(13): Show |
16 | HG00558.hp2 HG00738.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.3803+3961dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105247714 | ||||||
chr4:105247714 | C | CTT | 10 | a0001c0007t0030g0117 a0001c0007t0030g0339 a0001c0007t0031g0038 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.3803+3960_3803+396 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105247714 | ||||||
chr4:105247714 | CT | C | 167 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(164): Show |
168 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.3803+3961delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105247714 | ||||||
chr4:105247714 | CTT | C | 9 | a0002c0002t0003g0137 a0002c0002t0003g0230 a0002c0002t0035g0153 others(6): Show |
9 | HG01169.hp2 HG01516.hp2 HG03704.hp1 others(6): Show |
intron_variant | MODIFIER | c.3803+3960_3803+396 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105247714 | ||||||
chr4:105247723 | T | C | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3803+3945T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105247723 | |||||||
chr4:105247898 | T | G | 45 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(42): Show |
45 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.3803+4120T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105247898 | |||||||
chr4:105248136 | T | C | 3 | a0005c0005t0014g0065 a0005c0005t0014g0066 a0005c0005t0027g0064 |
3 | HG02970.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3803+4358T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105248136 | |||||||
chr4:105248392 | A | G | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3803+4614A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105248392 | |||||||
chr4:105248668 | C | T | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3803+4890C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105248668 | |||||||
chr4:105248766 | C | T | 44 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(41): Show |
44 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.3803+4988C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105248766 | |||||||
chr4:105248909 | A | T | 3 | a0004c0004t0084g0072 a0013c0014t0060g0074 a0013c0014t0064g0073 |
3 | HG03130.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3803+5131A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105248909 | |||||||
chr4:105248914 | G | A | 26 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(23): Show |
26 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.3803+5136G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105248914 | |||||||
chr4:105248936 | A | G | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3803+5158A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105248936 | |||||||
chr4:105249001 | C | CT | 78 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0262 others(75): Show |
79 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.3803+5237dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105249001 | ||||||
chr4:105249001 | CT | C | 27 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(24): Show |
27 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.3803+5237delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105249001 | ||||||
chr4:105249022 | G | A | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3803+5244G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249022 | |||||||
chr4:105249077 | G | A | 46 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(43): Show |
46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.3803+5299G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249077 | |||||||
chr4:105249154 | G | A | 1 | a0001c0007t0031g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3803+5376G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249154 | |||||||
chr4:105249218 | G | C | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3803+5440G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249218 | |||||||
chr4:105249248 | A | T | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3803+5470A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249248 | |||||||
chr4:105249325 | A | T | 1 | a0001c0001t0010g0229 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3803+5547A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249325 | |||||||
chr4:105249357 | C | T | 13 | a0002c0002t0003g0139 a0002c0002t0003g0154 a0002c0002t0003g0156 others(10): Show |
13 | HG00558.hp2 HG02056.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.3803+5579C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249357 | |||||||
chr4:105249402 | A | G | 1 | a0003c0003t0002g0102 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3803+5624A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249402 | |||||||
chr4:105249510 | G | A | 1 | a0004c0004t0094g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3803+5732G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249510 | |||||||
chr4:105249713 | G | A | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3803+5935G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249713 | |||||||
chr4:105249919 | A | G | 44 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(41): Show |
44 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.3803+6141A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249919 | |||||||
chr4:105249966 | A | G | 1 | a0001c0001t0008g0205 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3803+6188A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105249966 | |||||||
chr4:105250361 | T | C | 3 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 |
3 | HG01243.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3803+6583T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105250361 | |||||||
chr4:105250380 | A | AT | 36 | a0001c0001t0001g0112 a0001c0001t0001g0218 a0001c0001t0001g0250 others(33): Show |
36 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.3803+6633dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105250380 | ||||||
chr4:105250380 | A | ATT | 13 | a0001c0001t0001g0237 a0001c0001t0001g0277 a0001c0001t0001g0282 others(10): Show |
13 | HG01099.hp2 HG01258.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.3803+6632_3803+663 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105250380 | ||||||
chr4:105250380 | A | ATTTTT | 9 | a0001c0001t0001g0191 a0001c0001t0005g0188 a0001c0001t0005g0193 others(6): Show |
9 | HG00642.hp2 HG00741.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.3803+6629_3803+663 others(9): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105250380 | ||||||
chr4:105250380 | AT | A | 37 | a0001c0001t0001g0284 a0003c0003t0002g0001 a0003c0003t0002g0078 others(34): Show |
38 | HG00438.hp1 HG00544.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.3803+6633delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105250380 | ||||||
chr4:105250380 | ATT | A | 18 | a0001c0001t0002g0249 a0001c0001t0036g0029 a0003c0003t0002g0092 others(15): Show |
18 | HG01070.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3803+6632_3803+663 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105250380 | ||||||
chr4:105250380 | ATTTT | A | 31 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(28): Show |
31 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.3803+6630_3803+663 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105250380 | ||||||
chr4:105250380 | ATTTTTT | A | 13 | a0001c0001t0006g0204 a0001c0001t0006g0206 a0001c0001t0006g0212 others(10): Show |
13 | HG00323.hp2 HG00735.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.3803+6628_3803+663 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105250380 | ||||||
chr4:105250380 | ATTTTTTT | A | 29 | a0001c0001t0004g0209 a0001c0001t0006g0207 a0001c0001t0006g0214 others(26): Show |
29 | HG00609.hp1 HG00642.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.3803+6627_3803+663 others(11): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105250380 | ||||||
chr4:105250380 | ATTTTTTT others(1): Show |
A | 61 | a0001c0001t0003g0158 a0001c0001t0004g0203 a0001c0001t0009g0131 others(58): Show |
61 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.3803+6626_3803+663 others(12): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105250380 | ||||||
chr4:105250380 | ATTTTTTT others(3): Show |
A | 11 | a0004c0004t0028g0202 a0004c0011t0008g0325 a0004c0011t0040g0329 others(8): Show |
11 | HG02809.hp2 HG02818.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.3803+6624_3803+663 others(14): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105250380 | ||||||
chr4:105250380 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0104g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3803+6622_3803+663 others(16): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105250380 | ||||||
chr4:105250478 | T | G | 161 | a0001c0001t0003g0158 a0001c0001t0004g0203 a0001c0001t0004g0209 others(158): Show |
161 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.3803+6700T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105250478 | |||||||
chr4:105250495 | A | T | 159 | a0001c0001t0003g0158 a0001c0001t0004g0203 a0001c0001t0004g0209 others(156): Show |
159 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.3803+6717A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105250495 | |||||||
chr4:105250702 | A | T | 27 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(24): Show |
27 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.3803+6924A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105250702 | |||||||
chr4:105250714 | A | G | 1 | a0001c0001t0007g0301 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3803+6936A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105250714 | |||||||
chr4:105250826 | C | T | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3803+7048C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105250826 | |||||||
chr4:105250827 | G | A | 1 | a0001c0001t0036g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3803+7049G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105250827 | |||||||
chr4:105251126 | A | G | 46 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(43): Show |
46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.3803+7348A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105251126 | |||||||
chr4:105251294 | A | G | 44 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(41): Show |
44 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.3803+7516A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105251294 | |||||||
chr4:105251480 | A | C | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3803+7702A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105251480 | |||||||
chr4:105251495 | C | T | 1 | a0001c0001t0005g0188 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3803+7717C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105251495 | |||||||
chr4:105251590 | C | T | 1 | a0001c0001t0007g0197 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3803+7812C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105251590 | |||||||
chr4:105251626 | CTGTT | C | 72 | a0001c0001t0003g0158 a0001c0001t0009g0131 a0001c0001t0009g0146 others(69): Show |
72 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.3803+7851_3803+785 others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105251626 | ||||||
chr4:105251827 | C | A | 3 | a0001c0001t0005g0190 a0001c0001t0005g0196 a0001c0001t0041g0198 |
3 | HG00741.hp1 HG01123.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3804-7792C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105251827 | |||||||
chr4:105251940 | G | T | 1 | a0002c0002t0003g0344 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3804-7679G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105251940 | |||||||
chr4:105252020 | G | T | 9 | a0006c0006t0022g0336 a0006c0006t0022g0338 a0006c0006t0022g0341 others(6): Show |
9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.3804-7599G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105252020 | |||||||
chr4:105252042 | A | C | 227 | a0001c0001t0001g0234 a0001c0001t0001g0305 a0001c0001t0002g0249 others(224): Show |
228 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.3804-7577A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105252042 | |||||||
chr4:105252152 | T | G | 1 | a0001c0001t0104g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3804-7467T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105252152 | |||||||
chr4:105252174 | C | T | 1 | a0018c0021t0004g0345 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3804-7445C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105252174 | |||||||
chr4:105252216 | A | G | 4 | a0001c0001t0004g0322 a0001c0001t0017g0268 a0001c0001t0017g0290 others(1): Show |
4 | HG01928.hp2 HG02004.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.3804-7403A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105252216 | |||||||
chr4:105252223 | T | G | 1 | a0001c0001t0070g0034 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3804-7396T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105252223 | |||||||
chr4:105252300 | G | A | 1 | a0004c0004t0004g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3804-7319G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105252300 | |||||||
chr4:105252383 | T | C | 9 | a0006c0006t0022g0336 a0006c0006t0022g0338 a0006c0006t0022g0341 others(6): Show |
9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.3804-7236T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105252383 | |||||||
chr4:105252628 | A | C | 1 | a0003c0003t0002g0109 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3804-6991A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105252628 | |||||||
chr4:105252872 | G | A | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3804-6747G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105252872 | |||||||
chr4:105253225 | A | G | 2 | a0002c0002t0003g0147 a0002c0002t0003g0150 |
2 | HG00323.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.3804-6394A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105253225 | |||||||
chr4:105253309 | A | G | 1 | a0003c0003t0002g0092 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3804-6310A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105253309 | |||||||
chr4:105253317 | A | G | 1 | a0001c0001t0038g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3804-6302A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105253317 | |||||||
chr4:105253442 | T | G | 1 | a0002c0002t0085g0076 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3804-6177T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105253442 | |||||||
chr4:105253546 | G | GT | 58 | a0001c0001t0003g0158 a0001c0001t0009g0131 a0001c0001t0009g0146 others(55): Show |
58 | HG01106.hp2 HG01109.hp1 HG01175.hp1 others(55): Show |
intron_variant | MODIFIER | c.3804-6060dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105253546 | ||||||
chr4:105253674 | A | T | 22 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(19): Show |
22 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.3804-5945A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105253674 | |||||||
chr4:105253779 | T | C | 166 | a0001c0001t0001g0234 a0001c0001t0001g0305 a0001c0001t0003g0158 others(163): Show |
166 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.3804-5840T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105253779 | |||||||
chr4:105254084 | A | G | 1 | a0001c0001t0008g0304 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3804-5535A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105254084 | |||||||
chr4:105254191 | T | C | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3804-5428T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105254191 | |||||||
chr4:105254356 | G | C | 6 | a0004c0004t0058g0312 a0004c0004t0084g0072 a0004c0004t0101g0075 others(3): Show |
6 | HG03130.hp1 HG03209.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.3804-5263G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105254356 | |||||||
chr4:105254428 | T | A | 1 | a0001c0001t0053g0187 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3804-5191T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105254428 | |||||||
chr4:105254445 | C | G | 1 | a0004c0004t0039g0068 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3804-5174C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105254445 | |||||||
chr4:105254477 | T | A | 1 | a0001c0001t0104g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3804-5142T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105254477 | |||||||
chr4:105254747 | A | G | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3804-4872A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105254747 | |||||||
chr4:105254753 | C | T | 1 | a0001c0001t0008g0304 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3804-4866C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105254753 | |||||||
chr4:105254761 | A | G | 2 | a0007c0009t0051g0033 a0007c0009t0054g0045 |
2 | HG03669.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.3804-4858A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105254761 | |||||||
chr4:105254963 | T | G | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3804-4656T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105254963 | |||||||
chr4:105255215 | C | T | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3804-4404C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105255215 | |||||||
chr4:105255236 | G | C | 1 | a0001c0001t0007g0301 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3804-4383G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105255236 | |||||||
chr4:105255450 | A | G | 9 | a0001c0001t0070g0034 a0001c0007t0030g0117 a0001c0007t0030g0339 others(6): Show |
9 | HG00735.hp2 HG02055.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.3804-4169A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105255450 | |||||||
chr4:105255648 | A | T | 2 | a0003c0003t0002g0101 a0003c0003t0002g0107 |
2 | NA18951.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.3804-3971A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105255648 | |||||||
chr4:105255919 | T | TTTATG | 5 | a0004c0004t0028g0202 a0004c0011t0008g0325 a0004c0011t0040g0329 others(2): Show |
5 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.3804-3699_3804-369 others(9): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105255919 | ||||||
chr4:105255921 | G | GATGTT | 222 | a0001c0001t0001g0234 a0001c0001t0001g0305 a0001c0001t0002g0249 others(219): Show |
223 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.3804-3697_3804-369 others(9): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105255921 | ||||||
chr4:105255921 | G | T | 5 | a0004c0004t0028g0202 a0004c0011t0008g0325 a0004c0011t0040g0329 others(2): Show |
5 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.3804-3698G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105255921 | |||||||
chr4:105256295 | A | G | 1 | a0004c0011t0047g0326 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3804-3324A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105256295 | |||||||
chr4:105256315 | C | A | 1 | a0002c0002t0035g0136 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3804-3304C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105256315 | |||||||
chr4:105256330 | G | C | 2 | a0002c0002t0020g0176 a0002c0002t0020g0177 |
2 | HG00280.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.3804-3289G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105256330 | |||||||
chr4:105256607 | G | A | 6 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0297 others(3): Show |
6 | HG01255.hp2 HG01928.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.3804-3012G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105256607 | |||||||
chr4:105256657 | G | A | 14 | a0004c0004t0004g0035 a0004c0004t0018g0036 a0004c0004t0058g0312 others(11): Show |
14 | HG01175.hp1 HG01891.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.3804-2962G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105256657 | |||||||
chr4:105256684 | A | G | 6 | a0004c0004t0058g0312 a0004c0004t0084g0072 a0004c0004t0101g0075 others(3): Show |
6 | HG03130.hp1 HG03209.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.3804-2935A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105256684 | |||||||
chr4:105256725 | G | A | 39 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(36): Show |
39 | HG00140.hp1 HG00642.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.3804-2894G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105256725 | |||||||
chr4:105256916 | A | G | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3804-2703A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105256916 | |||||||
chr4:105256997 | A | G | 5 | a0004c0008t0019g0327 a0004c0008t0019g0332 a0004c0008t0059g0323 others(2): Show |
5 | HG02572.hp2 HG06807.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.3804-2622A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105256997 | |||||||
chr4:105257132 | A | C | 159 | a0001c0001t0001g0234 a0001c0001t0001g0305 a0001c0001t0003g0158 others(156): Show |
159 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.3804-2487A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105257132 | |||||||
chr4:105257139 | A | T | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3804-2480A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105257139 | |||||||
chr4:105257216 | T | G | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3804-2403T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105257216 | |||||||
chr4:105257316 | T | C | 49 | a0001c0001t0002g0249 a0001c0001t0002g0251 a0001c0001t0015g0330 others(46): Show |
50 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.3804-2303T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105257316 | |||||||
chr4:105257471 | T | C | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3804-2148T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105257471 | |||||||
chr4:105257745 | A | G | 157 | a0001c0001t0001g0234 a0001c0001t0003g0158 a0001c0001t0004g0203 others(154): Show |
157 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.3804-1874A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105257745 | |||||||
chr4:105258069 | T | G | 2 | a0001c0001t0086g0031 a0001c0001t0088g0030 |
2 | HG01361.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.3804-1550T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105258069 | |||||||
chr4:105258297 | CAT | C | 73 | a0001c0001t0003g0158 a0001c0001t0009g0131 a0001c0001t0009g0146 others(70): Show |
73 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.3804-1321_3804-132 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105258297 | |||||||
chr4:105258381 | C | T | 9 | a0001c0001t0070g0034 a0001c0007t0030g0117 a0001c0007t0030g0339 others(6): Show |
9 | HG00735.hp2 HG02055.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.3804-1238C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105258381 | |||||||
chr4:105258474 | ATTATAT | A | 4 | a0008c0010t0012g0008 a0008c0010t0012g0009 a0008c0010t0012g0011 others(1): Show |
4 | HG02145.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3804-1141_3804-113 others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr4 | 105258474 | ||||||
chr4:105258484 | G | C | 1 | a0003c0003t0015g0093 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3804-1135G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105258484 | |||||||
chr4:105258550 | A | G | 1 | a0001c0001t0093g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3804-1069A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105258550 | |||||||
chr4:105258857 | T | C | 1 | a0002c0002t0003g0137 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3804-762T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105258857 | |||||||
chr4:105259107 | T | C | 268 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0234 others(265): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.3804-512T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105259107 | |||||||
chr4:105259165 | C | T | 1 | a0001c0001t0017g0268 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3804-454C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105259165 | |||||||
chr4:105259169 | T | C | 1 | a0004c0004t0101g0075 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3804-450T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105259169 | |||||||
chr4:105259550 | C | A | 1 | a0001c0001t0001g0248 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3804-69C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105259550 | |||||||
chr4:105259585 | C | A | 3 | a0003c0003t0018g0118 a0005c0005t0005g0050 a0005c0005t0005g0051 |
3 | HG01070.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.3804-34C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105259585 | |||||||
chr4:105259588 | T | C | 2 | a0001c0001t0001g0269 a0001c0001t0001g0270 |
2 | NA18941.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.3804-31T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 6/10 | chr4 | 105259588 | |||||||
chr4:105259795 | C | A | 1 | a0008c0010t0012g0012 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3954+26C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105259795 | |||||||
chr4:105259997 | A | T | 1 | a0003c0003t0002g0102 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3954+228A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105259997 | |||||||
chr4:105260083 | T | C | 1 | a0004c0018t0019g0324 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3954+314T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105260083 | |||||||
chr4:105260150 | T | TTAAAGTC others(20): Show |
2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3954+409_3954+435d others(29): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr4 | 105260150 | ||||||
chr4:105260233 | ACT | A | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3954+467_3954+468d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr4 | 105260233 | ||||||
chr4:105260266 | T | A | 1 | a0001c0001t0005g0267 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3954+497T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105260266 | |||||||
chr4:105260413 | G | A | 6 | a0002c0002t0003g0135 a0002c0002t0023g0134 a0002c0002t0023g0143 others(3): Show |
6 | HG00738.hp1 HG01256.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.3954+644G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105260413 | |||||||
chr4:105260416 | G | A | 106 | a0001c0001t0003g0158 a0001c0001t0004g0203 a0001c0001t0004g0209 others(103): Show |
106 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.3954+647G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105260416 | |||||||
chr4:105260462 | T | TA | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3954+703dupA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr4 | 105260462 | ||||||
chr4:105260470 | A | G | 4 | a0002c0002t0003g0132 a0002c0002t0003g0159 a0002c0023t0003g0149 others(1): Show |
4 | HG00544.hp2 NA18959.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.3954+701A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105260470 | |||||||
chr4:105260472 | AC | A | 5 | a0003c0003t0018g0118 a0008c0010t0012g0008 a0008c0010t0012g0009 others(2): Show |
5 | HG01070.hp1 HG02145.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3954+704delC | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105260472 | |||||||
chr4:105260600 | C | T | 2 | a0002c0002t0025g0163 a0002c0002t0025g0174 |
2 | NA18955.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.3954+831C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105260600 | |||||||
chr4:105260669 | T | C | 1 | a0001c0001t0007g0292 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3954+900T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105260669 | |||||||
chr4:105260723 | T | G | 2 | a0002c0002t0024g0178 a0006c0006t0068g0014 |
2 | HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3954+954T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105260723 | |||||||
chr4:105260975 | A | T | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3955-784A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105260975 | |||||||
chr4:105261111 | C | A | 1 | a0001c0007t0030g0339 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3955-648C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105261111 | |||||||
chr4:105261163 | T | C | 2 | a0004c0004t0033g0058 a0004c0004t0042g0059 |
2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3955-596T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105261163 | |||||||
chr4:105261167 | A | G | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3955-592A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105261167 | |||||||
chr4:105261289 | A | G | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3955-470A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105261289 | |||||||
chr4:105261321 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3955-438C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105261321 | |||||||
chr4:105261372 | A | C | 1 | a0006c0006t0097g0069 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3955-387A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105261372 | |||||||
chr4:105261437 | A | T | 1 | a0002c0002t0003g0344 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3955-322A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105261437 | |||||||
chr4:105261448 | G | A | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3955-311G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105261448 | |||||||
chr4:105261556 | G | GA | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3955-196dupA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr4 | 105261556 | ||||||
chr4:105261707 | A | G | 1 | a0001c0001t0012g0185 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3955-52A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 7/10 | chr4 | 105261707 | |||||||
chr4:105261958 | C | T | 1 | a0002c0002t0003g0135 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.4044+110C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105261958 | |||||||
chr4:105262084 | A | G | 1 | a0003c0003t0002g0231 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.4044+236A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262084 | |||||||
chr4:105262134 | A | G | 1 | a0002c0002t0003g0147 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4044+286A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262134 | |||||||
chr4:105262266 | A | G | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4044+418A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262266 | |||||||
chr4:105262317 | T | C | 228 | a0001c0001t0001g0234 a0001c0001t0001g0305 a0001c0001t0002g0249 others(225): Show |
229 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.4044+469T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262317 | |||||||
chr4:105262365 | A | AT | 22 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(19): Show |
22 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.4044+527dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105262365 | ||||||
chr4:105262365 | AT | A | 48 | a0001c0001t0006g0239 a0001c0001t0036g0029 a0004c0004t0004g0015 others(45): Show |
48 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(45): Show |
intron_variant | MODIFIER | c.4044+527delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105262365 | ||||||
chr4:105262487 | T | C | 1 | a0002c0002t0011g0157 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.4044+639T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262487 | |||||||
chr4:105262623 | T | G | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4044+775T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262623 | |||||||
chr4:105262664 | C | T | 1 | a0004c0004t0037g0224 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.4044+816C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262664 | |||||||
chr4:105262773 | C | T | 1 | a0001c0001t0008g0205 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.4044+925C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262773 | |||||||
chr4:105262774 | G | A | 1 | a0004c0004t0010g0319 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4044+926G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262774 | |||||||
chr4:105262829 | C | T | 1 | a0001c0001t0005g0188 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4044+981C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262829 | |||||||
chr4:105262857 | G | T | 14 | a0004c0004t0004g0035 a0004c0004t0018g0036 a0004c0004t0058g0312 others(11): Show |
14 | HG01175.hp1 HG01891.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.4044+1009G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262857 | |||||||
chr4:105262881 | C | CA | 92 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0002g0249 others(89): Show |
93 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.4044+1048dupA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105262881 | ||||||
chr4:105262885 | A | G | 1 | a0001c0001t0013g0296 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4044+1037A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262885 | |||||||
chr4:105262916 | G | A | 5 | a0001c0001t0004g0186 a0001c0001t0007g0197 a0001c0001t0007g0199 others(2): Show |
5 | HG00642.hp2 HG00741.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.4044+1068G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105262916 | |||||||
chr4:105263014 | G | C | 2 | a0004c0008t0019g0332 a0004c0008t0066g0328 |
2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4044+1166G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105263014 | |||||||
chr4:105263028 | T | TA | 51 | a0001c0001t0002g0249 a0001c0001t0002g0251 a0001c0001t0005g0267 others(48): Show |
52 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.4044+1189dupA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105263028 | ||||||
chr4:105263028 | TAAA | T | 104 | a0001c0001t0003g0158 a0001c0001t0004g0203 a0001c0001t0004g0209 others(101): Show |
104 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.4044+1187_4044+118 others(7): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105263028 | ||||||
chr4:105263072 | C | T | 104 | a0001c0001t0003g0158 a0001c0001t0004g0203 a0001c0001t0004g0209 others(101): Show |
104 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.4044+1224C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105263072 | |||||||
chr4:105263078 | CATATAAA | C | 8 | a0006c0006t0022g0336 a0006c0006t0022g0338 a0006c0006t0022g0341 others(5): Show |
8 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.4044+1234_4044+124 others(11): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105263078 | ||||||
chr4:105263220 | G | A | 1 | a0001c0001t0004g0209 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4044+1372G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105263220 | |||||||
chr4:105263440 | A | C | 106 | a0001c0001t0003g0158 a0001c0001t0004g0203 a0001c0001t0004g0209 others(103): Show |
106 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.4044+1592A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105263440 | |||||||
chr4:105263564 | T | A | 2 | a0013c0014t0060g0074 a0013c0014t0064g0073 |
2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4044+1716T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105263564 | |||||||
chr4:105263607 | T | C | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4044+1759T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105263607 | |||||||
chr4:105263946 | G | A | 1 | a0003c0003t0002g0103 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.4044+2098G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105263946 | |||||||
chr4:105264083 | G | A | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4044+2235G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264083 | |||||||
chr4:105264092 | C | CA | 267 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0234 others(264): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.4044+2244_4044+224 others(5): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264092 | |||||||
chr4:105264102 | A | AT | 27 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(24): Show |
27 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.4044+2269dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105264102 | ||||||
chr4:105264102 | AT | A | 9 | a0001c0001t0001g0259 a0001c0001t0001g0269 a0001c0001t0001g0270 others(6): Show |
9 | HG00438.hp2 HG03704.hp1 HG03704.hp2 others(6): Show |
intron_variant | MODIFIER | c.4044+2269delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105264102 | ||||||
chr4:105264114 | T | C | 1 | a0002c0002t0003g0147 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4044+2266T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264114 | |||||||
chr4:105264118 | G | C | 110 | a0001c0001t0001g0234 a0001c0001t0001g0305 a0001c0001t0003g0158 others(107): Show |
110 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.4044+2270G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264118 | |||||||
chr4:105264157 | G | A | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4044+2309G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264157 | |||||||
chr4:105264233 | A | T | 1 | a0001c0001t0104g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4044+2385A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264233 | |||||||
chr4:105264256 | G | A | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4044+2408G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264256 | |||||||
chr4:105264273 | A | G | 8 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0005g0188 others(5): Show |
8 | HG00140.hp1 HG00741.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.4044+2425A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264273 | |||||||
chr4:105264299 | C | T | 264 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0305 others(261): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.4044+2451C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264299 | |||||||
chr4:105264371 | A | G | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4044+2523A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264371 | |||||||
chr4:105264500 | A | T | 9 | a0001c0001t0070g0034 a0001c0007t0030g0117 a0001c0007t0030g0339 others(6): Show |
9 | HG00735.hp2 HG02055.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.4044+2652A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264500 | |||||||
chr4:105264506 | C | T | 263 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0305 others(260): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.4044+2658C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264506 | |||||||
chr4:105264865 | G | T | 1 | a0006c0006t0046g0002 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.4044+3017G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264865 | |||||||
chr4:105264902 | T | C | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4044+3054T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105264902 | |||||||
chr4:105265144 | G | A | 50 | a0001c0001t0002g0249 a0001c0001t0002g0251 a0001c0001t0015g0330 others(47): Show |
51 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.4044+3296G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105265144 | |||||||
chr4:105265220 | T | C | 1 | a0001c0007t0030g0339 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4044+3372T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105265220 | |||||||
chr4:105265348 | C | G | 1 | a0006c0006t0065g0340 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4044+3500C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105265348 | |||||||
chr4:105265590 | T | A | 1 | a0001c0001t0036g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4044+3742T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105265590 | |||||||
chr4:105265897 | T | C | 1 | a0008c0010t0012g0008 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4045-3713T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105265897 | |||||||
chr4:105266216 | A | T | 1 | a0002c0002t0003g0344 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4045-3394A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105266216 | |||||||
chr4:105266252 | T | C | 1 | a0002c0002t0085g0076 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4045-3358T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105266252 | |||||||
chr4:105266524 | T | G | 1 | a0003c0003t0002g0109 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4045-3086T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105266524 | |||||||
chr4:105267099 | A | G | 3 | a0001c0001t0075g0027 a0001c0001t0077g0026 a0001c0001t0078g0025 |
3 | HG02004.hp2 HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4045-2511A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105267099 | |||||||
chr4:105267391 | A | T | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.4045-2219A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105267391 | |||||||
chr4:105267535 | C | A | 1 | a0001c0001t0036g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4045-2075C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105267535 | |||||||
chr4:105267539 | T | TA | 12 | a0001c0001t0004g0322 a0003c0003t0002g0113 a0005c0005t0005g0145 others(9): Show |
12 | HG02280.hp1 HG02615.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.4045-2055dupA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105267539 | ||||||
chr4:105267539 | TA | T | 162 | a0001c0001t0003g0158 a0001c0001t0004g0203 a0001c0001t0004g0209 others(159): Show |
162 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.4045-2055delA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105267539 | ||||||
chr4:105267739 | G | T | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.4045-1871G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105267739 | |||||||
chr4:105267962 | A | C | 1 | a0004c0004t0101g0075 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4045-1648A>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105267962 | |||||||
chr4:105267999 | C | A | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.4045-1611C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105267999 | |||||||
chr4:105268101 | A | AAT | 4 | a0005c0005t0014g0065 a0005c0005t0014g0066 a0005c0005t0014g0067 others(1): Show |
4 | HG02970.hp2 HG03098.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4045-1507_4045-150 others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105268101 | ||||||
chr4:105268137 | C | G | 5 | a0004c0004t0028g0202 a0004c0011t0008g0325 a0004c0011t0040g0329 others(2): Show |
5 | HG02809.hp2 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.4045-1473C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105268137 | |||||||
chr4:105268333 | C | CA | 8 | a0001c0007t0030g0117 a0001c0007t0030g0339 a0001c0007t0031g0038 others(5): Show |
8 | HG00735.hp2 HG02055.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.4045-1272dupA | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | 105268333 | ||||||
chr4:105268355 | C | T | 2 | a0013c0014t0060g0074 a0013c0014t0064g0073 |
2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4045-1255C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105268355 | |||||||
chr4:105268457 | G | T | 107 | a0001c0001t0003g0158 a0001c0001t0004g0203 a0001c0001t0004g0209 others(104): Show |
107 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.4045-1153G>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105268457 | |||||||
chr4:105268736 | C | T | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.4045-874C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105268736 | |||||||
chr4:105268898 | A | G | 106 | a0001c0001t0002g0249 a0001c0001t0002g0251 a0001c0001t0005g0267 others(103): Show |
107 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.4045-712A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105268898 | |||||||
chr4:105269069 | C | T | 114 | a0001c0001t0003g0158 a0001c0001t0004g0203 a0001c0001t0004g0209 others(111): Show |
114 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.4045-541C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105269069 | |||||||
chr4:105269282 | G | A | 3 | a0002c0002t0003g0123 a0002c0002t0003g0126 a0002c0002t0003g0138 |
3 | NA19003.hp1 NA19079.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.4045-328G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105269282 | |||||||
chr4:105269300 | A | G | 1 | a0004c0008t0067g0070 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4045-310A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105269300 | |||||||
chr4:105269556 | G | A | 4 | a0001c0001t0001g0218 a0001c0001t0001g0257 a0001c0001t0001g0282 others(1): Show |
4 | HG02027.hp1 HG02165.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.4045-54G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105269556 | |||||||
chr4:105269573 | A | G | 4 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0004g0310 others(1): Show |
4 | NA18946.hp1 NA18947.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.4045-37A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105269573 | |||||||
chr4:105269575 | C | A | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.4045-35C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105269575 | |||||||
chr4:105269583 | G | A | 8 | a0005c0005t0014g0065 a0005c0005t0014g0066 a0005c0005t0014g0067 others(5): Show |
8 | HG02280.hp1 HG02615.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.4045-27G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 8/10 | chr4 | 105269583 | |||||||
chr4:105269756 | G | A | 1 | a0002c0002t0003g0128 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4182+9G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105269756 | |||||||
chr4:105269994 | C | T | 9 | a0006c0006t0022g0336 a0006c0006t0022g0338 a0006c0006t0022g0341 others(6): Show |
9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.4182+247C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105269994 | |||||||
chr4:105270267 | G | A | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4182+520G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105270267 | |||||||
chr4:105270434 | G | C | 1 | a0004c0019t0081g0054 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4182+687G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105270434 | |||||||
chr4:105270510 | C | G | 2 | a0002c0002t0025g0163 a0002c0002t0025g0174 |
2 | NA18955.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.4182+763C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105270510 | |||||||
chr4:105270523 | A | G | 10 | a0005c0005t0005g0032 a0005c0005t0005g0041 a0005c0005t0005g0042 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.4182+776A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105270523 | |||||||
chr4:105270579 | A | T | 46 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(43): Show |
46 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.4182+832A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105270579 | |||||||
chr4:105270586 | G | A | 1 | a0004c0031t0092g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4182+839G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105270586 | |||||||
chr4:105270642 | G | A | 2 | a0011c0015t0043g0347 a0011c0015t0044g0346 |
2 | HG01099.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.4182+895G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105270642 | |||||||
chr4:105270663 | A | G | 1 | a0001c0001t0080g0053 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4182+916A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105270663 | |||||||
chr4:105270674 | T | TTA | 13 | a0001c0001t0001g0250 a0001c0001t0001g0279 a0001c0001t0001g0280 others(10): Show |
13 | HG01169.hp1 HG01516.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.4182+951_4182+952d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | 105270674 | ||||||
chr4:105270674 | T | TTATA | 7 | a0001c0001t0001g0260 a0001c0001t0001g0262 a0001c0001t0001g0263 others(4): Show |
7 | HG03239.hp1 HG03654.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.4182+949_4182+952d others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | 105270674 | ||||||
chr4:105270674 | TTA | T | 34 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(31): Show |
34 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.4182+951_4182+952d others(4): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | 105270674 | ||||||
chr4:105270674 | TTATA | T | 8 | a0004c0004t0033g0119 a0006c0006t0026g0005 a0006c0006t0026g0006 others(5): Show |
8 | HG01192.hp1 HG02615.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.4182+949_4182+952d others(6): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | 105270674 | ||||||
chr4:105270674 | TTATATA | T | 111 | a0001c0001t0002g0249 a0001c0001t0002g0251 a0001c0001t0015g0330 others(108): Show |
112 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.4182+947_4182+952d others(8): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | 105270674 | ||||||
chr4:105270674 | TTATATAT others(1): Show |
T | 104 | a0001c0001t0003g0158 a0001c0001t0004g0203 a0001c0001t0004g0209 others(101): Show |
104 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.4182+945_4182+952d others(10): Show |
TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | 105270674 | ||||||
chr4:105270681 | T | C | 1 | a0004c0004t0033g0119 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4182+934T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105270681 | |||||||
chr4:105270683 | T | C | 45 | a0004c0004t0004g0015 a0004c0004t0004g0035 a0004c0004t0004g0220 others(42): Show |
45 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.4182+936T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105270683 | |||||||
chr4:105270922 | G | C | 2 | a0004c0004t0013g0056 a0004c0004t0013g0057 |
2 | HG01243.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4182+1175G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105270922 | |||||||
chr4:105271057 | T | C | 1 | a0001c0001t0036g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4182+1310T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105271057 | |||||||
chr4:105271067 | C | T | 2 | a0002c0002t0001g0133 a0002c0002t0007g0317 |
2 | HG02698.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.4182+1320C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105271067 | |||||||
chr4:105271147 | A | G | 1 | a0001c0001t0093g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4182+1400A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105271147 | |||||||
chr4:105271229 | T | A | 1 | a0003c0003t0002g0082 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.4183-1335T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105271229 | |||||||
chr4:105271235 | A | G | 26 | a0004c0004t0004g0015 a0004c0004t0004g0220 a0004c0004t0004g0223 others(23): Show |
26 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.4183-1329A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105271235 | |||||||
chr4:105271300 | C | A | 39 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(36): Show |
39 | HG00140.hp1 HG00642.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.4183-1264C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105271300 | |||||||
chr4:105271308 | T | A | 1 | a0001c0001t0004g0322 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.4183-1256T>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105271308 | |||||||
chr4:105271406 | T | C | 39 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0004g0186 others(36): Show |
39 | HG00140.hp1 HG00642.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.4183-1158T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105271406 | |||||||
chr4:105271445 | AG | A | 22 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(19): Show |
22 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.4183-1118delG | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105271445 | |||||||
chr4:105271618 | G | A | 223 | a0001c0001t0002g0249 a0001c0001t0002g0251 a0001c0001t0003g0158 others(220): Show |
224 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.4183-946G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105271618 | |||||||
chr4:105272003 | C | G | 111 | a0001c0001t0001g0234 a0001c0001t0003g0158 a0001c0001t0004g0203 others(108): Show |
111 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.4183-561C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105272003 | |||||||
chr4:105272015 | AT | A | 22 | a0001c0001t0004g0203 a0001c0001t0004g0209 a0001c0001t0006g0204 others(19): Show |
22 | HG00323.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.4183-543delT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr4 | 105272015 | ||||||
chr4:105272177 | T | C | 113 | a0001c0001t0001g0234 a0001c0001t0003g0158 a0001c0001t0004g0203 others(110): Show |
113 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.4183-387T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105272177 | |||||||
chr4:105272378 | T | C | 1 | a0001c0001t0009g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4183-186T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105272378 | |||||||
chr4:105272431 | A | G | 54 | a0001c0001t0002g0249 a0001c0001t0002g0251 a0001c0001t0005g0267 others(51): Show |
55 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.4183-133A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105272431 | |||||||
chr4:105272493 | A | G | 1 | a0002c0002t0003g0147 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4183-71A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 9/10 | chr4 | 105272493 | |||||||
chr4:105272994 | C | T | 1 | a0001c0001t0104g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4537+76C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105272994 | |||||||
chr4:105273189 | C | T | 2 | a0012c0016t0001g0019 a0012c0016t0001g0020 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4537+271C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105273189 | |||||||
chr4:105273262 | C | A | 7 | a0006c0006t0026g0005 a0006c0006t0026g0006 a0006c0006t0026g0010 others(4): Show |
7 | HG01192.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.4537+344C>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105273262 | |||||||
chr4:105273315 | C | T | 1 | a0017c0017t0003g0151 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4537+397C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105273315 | |||||||
chr4:105273485 | C | T | 2 | a0001c0001t0001g0260 a0001c0001t0004g0299 |
2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.4537+567C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105273485 | |||||||
chr4:105273703 | T | C | 1 | a0004c0004t0101g0075 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4537+785T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105273703 | |||||||
chr4:105273764 | T | G | 8 | a0006c0006t0022g0336 a0006c0006t0022g0338 a0006c0006t0022g0341 others(5): Show |
8 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.4537+846T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105273764 | |||||||
chr4:105273869 | T | C | 54 | a0001c0001t0002g0249 a0001c0001t0002g0251 a0001c0001t0005g0267 others(51): Show |
55 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.4537+951T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105273869 | |||||||
chr4:105273879 | A | G | 1 | a0004c0004t0013g0221 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.4537+961A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105273879 | |||||||
chr4:105273886 | C | G | 1 | a0018c0021t0004g0345 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4537+968C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105273886 | |||||||
chr4:105274023 | T | G | 1 | a0001c0001t0104g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4538-1025T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274023 | |||||||
chr4:105274185 | T | C | 1 | a0004c0011t0008g0325 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4538-863T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274185 | |||||||
chr4:105274210 | C | G | 1 | a0001c0001t0076g0023 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4538-838C>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274210 | |||||||
chr4:105274263 | A | G | 1 | a0004c0004t0101g0075 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4538-785A>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274263 | |||||||
chr4:105274279 | A | T | 10 | a0001c0001t0070g0034 a0001c0001t0104g0007 a0001c0007t0030g0117 others(7): Show |
10 | HG00735.hp2 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.4538-769A>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274279 | |||||||
chr4:105274384 | T | C | 264 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0002g0249 others(261): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.4538-664T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274384 | |||||||
chr4:105274415 | G | A | 105 | a0001c0001t0003g0158 a0001c0001t0004g0203 a0001c0001t0004g0209 others(102): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.4538-633G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274415 | |||||||
chr4:105274434 | G | C | 1 | a0001c0001t0104g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4538-614G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274434 | |||||||
chr4:105274491 | T | G | 2 | a0013c0014t0060g0074 a0013c0014t0064g0073 |
2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4538-557T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274491 | |||||||
chr4:105274609 | T | G | 1 | a0019c0020t0069g0162 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4538-439T>G | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274609 | |||||||
chr4:105274680 | G | C | 1 | a0001c0001t0006g0239 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4538-368G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274680 | |||||||
chr4:105274690 | C | T | 5 | a0001c0001t0073g0024 a0001c0001t0075g0027 a0001c0001t0076g0023 others(2): Show |
5 | HG01081.hp2 HG02004.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.4538-358C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274690 | |||||||
chr4:105274691 | G | C | 1 | a0001c0001t0104g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4538-357G>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274691 | |||||||
chr4:105274693 | T | C | 51 | a0001c0001t0002g0249 a0001c0001t0002g0251 a0001c0001t0005g0267 others(48): Show |
52 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.4538-355T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274693 | |||||||
chr4:105274728 | T | C | 4 | a0002c0002t0001g0133 a0002c0002t0003g0137 a0002c0002t0007g0317 others(1): Show |
4 | HG02698.hp1 HG03017.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.4538-320T>C | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274728 | |||||||
chr4:105274736 | G | A | 2 | a0001c0001t0086g0031 a0001c0001t0088g0030 |
2 | HG01361.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.4538-312G>A | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274736 | |||||||
chr4:105274830 | A | AT | 6 | a0001c0001t0073g0024 a0001c0001t0075g0027 a0001c0001t0076g0023 others(3): Show |
6 | HG01081.hp2 HG02004.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.4538-208dupT | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr4 | 105274830 | ||||||
chr4:105274935 | C | T | 282 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0238 others(279): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.4538-113C>T | TET2 | ENSG00000168769.14 | transcript | ENST00000380013.9 | protein_coding | 10/10 | chr4 | 105274935 |