Item | Value |
---|---|
geneid | 64423 |
ensemblid | ENSG00000203485.14 |
hgncid | 23791 |
symbol | INF2 |
name | inverted formin 2 |
refseq_nuc | NM_022489.4 |
refseq_prot | NP_071934.3 |
ensembl_nuc | ENST00000392634.9 |
ensembl_prot | ENSP00000376410.4 |
mane_status | MANE Select |
chr | chr14 |
start | 104689618 |
end | 104722535 |
strand | + |
ver | v1.2 |
region | chr14:104689618-104722535 |
region5000 | chr14:104684618-104727535 |
regionname0 | INF2_chr14_104689618_104722535 |
regionname5000 | INF2_chr14_104684618_104727535 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1249 | 282 | 63 | 63 | 116 | 10 | 28 | 83 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1244): Show |
chr14 | 104684618 | 104727535 |
a0002 | 0/0 | 1245 | 33 | 5 | 6 | 10 | 3 | 9 | 6 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1240): Show |
chr14 | 104684618 | 104727535 |
a0003 | 0/0 | 1247 | 12 | 8 | 2 | 1 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1242): Show |
chr14 | 104684618 | 104727535 |
a0004 | 0/0 | 1247 | 7 | 2 | 2 | 1 | 0 | 2 | 1 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1242): Show |
chr14 | 104684618 | 104727535 |
a0005 | 0/0 | 1249 | 6 | 0 | 1 | 5 | 0 | 0 | 4 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1244): Show |
chr14 | 104684618 | 104727535 |
a0006 | 0/0 | 1249 | 6 | 0 | 1 | 5 | 0 | 0 | 4 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1244): Show |
chr14 | 104684618 | 104727535 |
a0007 | 0/0 | 1249 | 4 | 1 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1244): Show |
chr14 | 104684618 | 104727535 |
a0008 | 0/0 | 1249 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1244): Show |
chr14 | 104684618 | 104727535 |
a0009 | 0/0 | 1247 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1242): Show |
chr14 | 104684618 | 104727535 |
a0010 | 0/0 | 1249 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1244): Show |
chr14 | 104684618 | 104727535 |
a0011 | 0/0 | 1249 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1244): Show |
chr14 | 104684618 | 104727535 |
a0012 | 0/0 | 1249 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1244): Show |
chr14 | 104684618 | 104727535 |
a0013 | 0/0 | 1249 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1244): Show |
chr14 | 104684618 | 104727535 |
a0014 | 0/0 | 1245 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1240): Show |
chr14 | 104684618 | 104727535 |
a0015 | 0/0 | 1209 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1204): Show |
chr14 | 104684618 | 104727535 |
a0016 | 0/0 | 1249 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1244): Show |
chr14 | 104684618 | 104727535 |
a0017 | 0/0 | 1249 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1244): Show |
chr14 | 104684618 | 104727535 |
a0018 | 0/0 | 1249 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1244): Show |
chr14 | 104684618 | 104727535 |
a0019 | 0/0 | 1249 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1244): Show |
chr14 | 104684618 | 104727535 |
a0020 | 0/0 | 1249 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1244): Show |
chr14 | 104684618 | 104727535 |
a0021 | 0/0 | 552 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(547): Show |
chr14 | 104684618 | 104727535 |
a0022 | 0/0 | 1249 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1244): Show |
chr14 | 104684618 | 104727535 |
a0023 | 0/0 | 1249 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1244): Show |
chr14 | 104684618 | 104727535 |
a0024 | 0/0 | 1249 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | MSVKE others(1244): Show |
chr14 | 104684618 | 104727535 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3747 | 187 | 39 | 37 | 86 | 7 | 17 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0001c0002 | 0/0 | 3747 | 35 | 11 | 17 | 1 | 3 | 3 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0001c0004 | 0/0 | 3747 | 26 | 0 | 4 | 17 | 0 | 5 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0001c0005 | 0/0 | 3747 | 8 | 7 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0001c0009 | 0/0 | 3747 | 5 | 0 | 0 | 3 | 0 | 2 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0001c0014 | 0/0 | 3747 | 3 | 0 | 0 | 3 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0001c0017 | 0/0 | 3747 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0001c0020 | 0/0 | 3747 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0001c0021 | 0/0 | 3747 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0001c0022 | 0/0 | 3747 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0001c0025 | 0/0 | 3747 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0001c0026 | 1/0 | 3747 | 1 | 0 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0001c0031 | 0/0 | 3747 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0001c0035 | 0/0 | 3747 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0001c0036 | 0/0 | 3747 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0001c0038 | 0/0 | 3747 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0001c0041 | 0/0 | 3747 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0001c0051 | 0/0 | 3747 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0002c0003 | 0/0 | 3735 | 26 | 0 | 6 | 10 | 2 | 8 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3730): Show |
chr14 | 104684618 | 104727535 | ||
a0002c0013 | 0/0 | 3735 | 4 | 4 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3730): Show |
chr14 | 104684618 | 104727535 | ||
a0002c0046 | 0/0 | 3735 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3730): Show |
chr14 | 104684618 | 104727535 | ||
a0002c0047 | 0/0 | 3735 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3730): Show |
chr14 | 104684618 | 104727535 | ||
a0002c0048 | 0/0 | 3735 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3730): Show |
chr14 | 104684618 | 104727535 | ||
a0003c0010 | 0/0 | 3741 | 5 | 5 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3736): Show |
chr14 | 104684618 | 104727535 | ||
a0003c0019 | 0/0 | 3741 | 3 | 0 | 1 | 1 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3736): Show |
chr14 | 104684618 | 104727535 | ||
a0003c0042 | 0/0 | 3741 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3736): Show |
chr14 | 104684618 | 104727535 | ||
a0003c0043 | 0/0 | 3741 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3736): Show |
chr14 | 104684618 | 104727535 | ||
a0003c0044 | 0/0 | 3741 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3736): Show |
chr14 | 104684618 | 104727535 | ||
a0003c0045 | 0/0 | 3741 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3736): Show |
chr14 | 104684618 | 104727535 | ||
a0004c0006 | 0/0 | 3741 | 7 | 2 | 2 | 1 | 0 | 2 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3736): Show |
chr14 | 104684618 | 104727535 | ||
a0005c0007 | 0/0 | 3747 | 6 | 0 | 1 | 5 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0006c0008 | 0/0 | 3747 | 6 | 0 | 1 | 5 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0007c0016 | 0/0 | 3747 | 3 | 0 | 3 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0007c0029 | 0/0 | 3747 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0008c0015 | 0/0 | 3747 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0008c0032 | 0/0 | 3747 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0009c0012 | 0/0 | 3741 | 4 | 4 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3736): Show |
chr14 | 104684618 | 104727535 | ||
a0010c0011 | 0/0 | 3747 | 4 | 0 | 0 | 4 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0011c0018 | 0/0 | 3747 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0012c0024 | 0/0 | 3747 | 2 | 0 | 1 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0013c0023 | 0/0 | 3747 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0014c0049 | 0/0 | 3735 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3730): Show |
chr14 | 104684618 | 104727535 | ||
a0015c0030 | 0/0 | 3782 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3777): Show |
chr14 | 104684618 | 104727535 | ||
a0016c0033 | 0/0 | 3747 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0017c0034 | 0/0 | 3747 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0018c0050 | 0/0 | 3747 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0019c0037 | 0/0 | 3747 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0020c0052 | 0/0 | 3747 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0021c0028 | 0/0 | 3734 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3729): Show |
chr14 | 104684618 | 104727535 | ||
a0022c0027 | 0/0 | 3747 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0023c0040 | 0/0 | 3747 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 | ||
a0024c0039 | 0/0 | 3747 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | ATGTC others(3742): Show |
chr14 | 104684618 | 104727535 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7615 | 77 | 17 | 16 | 32 | 6 | 6 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0002 | 0/0 | 7615 | 38 | 1 | 7 | 28 | 0 | 2 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0003 | 0/0 | 7589 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7584): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0004 | 0/0 | 7579 | 13 | 13 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7574): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0006 | 0/0 | 7616 | 10 | 0 | 0 | 9 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7611): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0007 | 0/0 | 7763 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7758): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0009 | 0/0 | 7615 | 5 | 0 | 3 | 1 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0010 | 0/0 | 7616 | 4 | 1 | 1 | 1 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7611): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0012 | 0/0 | 7616 | 5 | 4 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7611): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0017 | 0/0 | 7615 | 3 | 0 | 0 | 3 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0019 | 0/0 | 7615 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0020 | 0/0 | 7615 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0021 | 0/0 | 7616 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7611): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0024 | 0/0 | 7615 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0027 | 0/0 | 7615 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0031 | 0/0 | 7615 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0032 | 0/0 | 7615 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0033 | 0/0 | 7719 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7714): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0047 | 0/0 | 7615 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0048 | 0/0 | 7615 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0049 | 0/0 | 7615 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0050 | 0/0 | 7623 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7618): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0053 | 0/0 | 7615 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0057 | 0/0 | 7692 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7687): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0058 | 0/0 | 7616 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7611): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0062 | 0/0 | 7479 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7474): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0063 | 0/0 | 7615 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0064 | 0/0 | 7615 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0065 | 0/0 | 7615 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0066 | 0/0 | 7615 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0067 | 0/0 | 7615 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0073 | 0/0 | 7579 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7574): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0075 | 0/0 | 7579 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7574): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0076 | 0/0 | 7579 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7574): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0078 | 0/0 | 7614 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7609): Show |
chr14 | 104684618 | 104727535 |
a0001c0001t0079 | 0/1 | 7654 | 1 | 0 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7649): Show |
chr14 | 104684618 | 104727535 |
a0001c0002t0003 | 0/0 | 7589 | 23 | 6 | 10 | 1 | 3 | 3 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7584): Show |
chr14 | 104684618 | 104727535 |
a0001c0002t0018 | 0/0 | 7589 | 3 | 0 | 3 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7584): Show |
chr14 | 104684618 | 104727535 |
a0001c0002t0026 | 0/0 | 7615 | 3 | 2 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0002t0036 | 0/0 | 7582 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7577): Show |
chr14 | 104684618 | 104727535 |
a0001c0002t0038 | 0/0 | 7589 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7584): Show |
chr14 | 104684618 | 104727535 |
a0001c0002t0061 | 0/0 | 7615 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0002t0070 | 0/0 | 7623 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7618): Show |
chr14 | 104684618 | 104727535 |
a0001c0004t0001 | 0/0 | 7615 | 24 | 0 | 4 | 15 | 0 | 5 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0004t0021 | 0/0 | 7616 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7611): Show |
chr14 | 104684618 | 104727535 |
a0001c0004t0051 | 0/0 | 7984 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7979): Show |
chr14 | 104684618 | 104727535 |
a0001c0005t0023 | 0/0 | 7581 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7576): Show |
chr14 | 104684618 | 104727535 |
a0001c0005t0024 | 0/0 | 7615 | 2 | 1 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0005t0035 | 0/0 | 7615 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0005t0039 | 0/0 | 7615 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0009t0007 | 0/0 | 7763 | 3 | 0 | 0 | 1 | 0 | 2 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7758): Show |
chr14 | 104684618 | 104727535 |
a0001c0009t0008 | 0/0 | 7727 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7722): Show |
chr14 | 104684618 | 104727535 |
a0001c0009t0056 | 0/0 | 7763 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7758): Show |
chr14 | 104684618 | 104727535 |
a0001c0014t0014 | 0/0 | 7616 | 3 | 0 | 0 | 3 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7611): Show |
chr14 | 104684618 | 104727535 |
a0001c0017t0004 | 0/0 | 7579 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7574): Show |
chr14 | 104684618 | 104727535 |
a0001c0020t0014 | 0/0 | 7616 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7611): Show |
chr14 | 104684618 | 104727535 |
a0001c0020t0044 | 0/0 | 7616 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7611): Show |
chr14 | 104684618 | 104727535 |
a0001c0021t0001 | 0/0 | 7615 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0021t0077 | 0/0 | 7615 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0022t0071 | 0/0 | 7590 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7585): Show |
chr14 | 104684618 | 104727535 |
a0001c0022t0072 | 0/0 | 7555 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7550): Show |
chr14 | 104684618 | 104727535 |
a0001c0025t0002 | 0/0 | 7615 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0026t0059 | 1/0 | 7623 | 1 | 0 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7618): Show |
chr14 | 104684618 | 104727535 |
a0001c0031t0002 | 0/0 | 7615 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0035t0052 | 0/0 | 7615 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0036t0001 | 0/0 | 7615 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0038t0025 | 0/0 | 7613 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7608): Show |
chr14 | 104684618 | 104727535 |
a0001c0041t0027 | 0/0 | 7615 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0001c0051t0002 | 0/0 | 7615 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0002c0003t0005 | 0/0 | 7751 | 11 | 0 | 3 | 4 | 0 | 4 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7746): Show |
chr14 | 104684618 | 104727535 |
a0002c0003t0007 | 0/0 | 7751 | 3 | 0 | 1 | 0 | 0 | 2 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7746): Show |
chr14 | 104684618 | 104727535 |
a0002c0003t0008 | 0/0 | 7715 | 5 | 0 | 0 | 5 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7710): Show |
chr14 | 104684618 | 104727535 |
a0002c0003t0028 | 0/0 | 7717 | 2 | 0 | 1 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7712): Show |
chr14 | 104684618 | 104727535 |
a0002c0003t0034 | 0/0 | 7716 | 2 | 0 | 0 | 0 | 1 | 1 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7711): Show |
chr14 | 104684618 | 104727535 |
a0002c0003t0041 | 0/0 | 7856 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7851): Show |
chr14 | 104684618 | 104727535 |
a0002c0003t0042 | 0/0 | 7856 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7851): Show |
chr14 | 104684618 | 104727535 |
a0002c0003t0074 | 0/0 | 7715 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7710): Show |
chr14 | 104684618 | 104727535 |
a0002c0013t0013 | 0/0 | 7751 | 4 | 4 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7746): Show |
chr14 | 104684618 | 104727535 |
a0002c0046t0001 | 0/0 | 7603 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7598): Show |
chr14 | 104684618 | 104727535 |
a0002c0047t0003 | 0/0 | 7577 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7572): Show |
chr14 | 104684618 | 104727535 |
a0002c0048t0043 | 0/0 | 7579 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7574): Show |
chr14 | 104684618 | 104727535 |
a0003c0010t0016 | 0/0 | 7583 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7578): Show |
chr14 | 104684618 | 104727535 |
a0003c0010t0068 | 0/0 | 7583 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7578): Show |
chr14 | 104684618 | 104727535 |
a0003c0010t0069 | 0/0 | 7583 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7578): Show |
chr14 | 104684618 | 104727535 |
a0003c0019t0019 | 0/0 | 7609 | 2 | 0 | 0 | 1 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7604): Show |
chr14 | 104684618 | 104727535 |
a0003c0019t0020 | 0/0 | 7609 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7604): Show |
chr14 | 104684618 | 104727535 |
a0003c0042t0020 | 0/0 | 7609 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7604): Show |
chr14 | 104684618 | 104727535 |
a0003c0043t0011 | 0/0 | 7651 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7646): Show |
chr14 | 104684618 | 104727535 |
a0003c0044t0046 | 0/0 | 7609 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7604): Show |
chr14 | 104684618 | 104727535 |
a0003c0045t0016 | 0/0 | 7583 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7578): Show |
chr14 | 104684618 | 104727535 |
a0004c0006t0011 | 0/0 | 7651 | 2 | 1 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7646): Show |
chr14 | 104684618 | 104727535 |
a0004c0006t0029 | 0/0 | 7651 | 2 | 0 | 1 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7646): Show |
chr14 | 104684618 | 104727535 |
a0004c0006t0030 | 0/0 | 7651 | 2 | 1 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7646): Show |
chr14 | 104684618 | 104727535 |
a0004c0006t0045 | 0/0 | 7721 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7716): Show |
chr14 | 104684618 | 104727535 |
a0005c0007t0001 | 0/0 | 7615 | 6 | 0 | 1 | 5 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0006c0008t0002 | 0/0 | 7615 | 4 | 0 | 1 | 3 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0006c0008t0037 | 0/0 | 7624 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7619): Show |
chr14 | 104684618 | 104727535 |
a0007c0016t0002 | 0/0 | 7615 | 3 | 0 | 3 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0007c0029t0003 | 0/0 | 7589 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7584): Show |
chr14 | 104684618 | 104727535 |
a0008c0015t0015 | 0/0 | 7615 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0008c0032t0015 | 0/0 | 7615 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0009c0012t0001 | 0/0 | 7609 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7604): Show |
chr14 | 104684618 | 104727535 |
a0009c0012t0022 | 0/0 | 7610 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7605): Show |
chr14 | 104684618 | 104727535 |
a0010c0011t0001 | 0/0 | 7615 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0010c0011t0040 | 0/0 | 7616 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7611): Show |
chr14 | 104684618 | 104727535 |
a0011c0018t0025 | 0/0 | 7613 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7608): Show |
chr14 | 104684618 | 104727535 |
a0011c0018t0060 | 0/0 | 7613 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7608): Show |
chr14 | 104684618 | 104727535 |
a0012c0024t0054 | 0/0 | 7443 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7438): Show |
chr14 | 104684618 | 104727535 |
a0012c0024t0055 | 0/0 | 7616 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7611): Show |
chr14 | 104684618 | 104727535 |
a0013c0023t0011 | 0/0 | 7657 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7652): Show |
chr14 | 104684618 | 104727535 |
a0014c0049t0007 | 0/0 | 7751 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7746): Show |
chr14 | 104684618 | 104727535 |
a0015c0030t0001 | 0/0 | 7650 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7645): Show |
chr14 | 104684618 | 104727535 |
a0016c0033t0003 | 0/0 | 7589 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7584): Show |
chr14 | 104684618 | 104727535 |
a0017c0034t0001 | 0/0 | 7615 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0018c0050t0001 | 0/0 | 7615 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0019c0037t0002 | 0/0 | 7615 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0020c0052t0027 | 0/0 | 7615 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0021c0028t0005 | 0/0 | 7750 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7745): Show |
chr14 | 104684618 | 104727535 |
a0022c0027t0001 | 0/0 | 7615 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
a0023c0040t0010 | 0/0 | 7616 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7611): Show |
chr14 | 104684618 | 104727535 |
a0024c0039t0035 | 0/0 | 7615 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | GCCAG others(7610): Show |
chr14 | 104684618 | 104727535 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 4 | 1 | 1 | 1 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0005 | 0/0 | 6 | 1 | 5 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0002g0001 | 0/0 | 12 | 0 | 3 | 8 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0004g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0004g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0006g0001 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0006g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0006g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0006g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0007g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0009g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0009g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0009g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0009g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0010g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0010g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0010g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0012g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0012g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0012g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0012g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0012g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0017g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0017g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0017g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0019g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0020g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0021g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0021g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0024g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0027g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0031g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0032g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0033g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0047g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0048g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0049g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0050g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0053g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0057g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0058g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0062g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0063g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0064g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0065g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0066g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0067g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0073g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0075g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0076g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0078g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0001t0079g0156 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0002t0003g0004 | 0/0 | 10 | 0 | 6 | 0 | 2 | 2 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0002t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0002t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0002t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0002t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0002t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0002t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0002t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0002t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0002t0018g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0002t0026g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0002t0026g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0002t0026g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0002t0036g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0002t0036g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0002t0038g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0002t0061g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0002t0070g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0004t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0004t0001g0003 | 0/0 | 9 | 0 | 4 | 4 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0004t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0004t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0004t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0004t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0004t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0004t0021g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0004t0051g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0005t0023g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0005t0023g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0005t0023g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0005t0024g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0005t0024g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0005t0035g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0005t0039g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0005t0039g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0009t0007g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0009t0007g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0009t0007g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0009t0008g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0009t0056g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0014t0014g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0014t0014g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0017t0004g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0017t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0020t0014g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0020t0044g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0021t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0021t0077g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0022t0071g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0022t0072g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0025t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0026t0059g0139 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0031t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0035t0052g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0036t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0038t0025g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0041t0027g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0001c0051t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0003t0005g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0003t0005g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0003t0005g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0003t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0003t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0003t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0003t0005g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0003t0005g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0003t0005g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0003t0007g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0003t0007g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0003t0008g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0003t0008g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0003t0028g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0003t0028g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0003t0034g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0003t0041g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0003t0042g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0003t0074g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0013t0013g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0013t0013g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0046t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0047t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0002c0048t0043g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0003c0010t0016g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0003c0010t0016g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0003c0010t0016g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0003c0010t0068g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0003c0010t0069g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0003c0019t0019g0029 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0003c0019t0020g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0003c0042t0020g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0003c0043t0011g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0003c0044t0046g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0003c0045t0016g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0004c0006t0011g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0004c0006t0011g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0004c0006t0029g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0004c0006t0030g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0004c0006t0030g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0004c0006t0045g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0005c0007t0001g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0005c0007t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0005c0007t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0006c0008t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0006c0008t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0006c0008t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0006c0008t0037g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0007c0016t0002g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0007c0016t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0007c0029t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0008c0015t0015g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0008c0032t0015g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0009c0012t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0009c0012t0022g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0009c0012t0022g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0010c0011t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0010c0011t0040g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0010c0011t0040g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0011c0018t0025g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0011c0018t0060g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0012c0024t0054g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0012c0024t0055g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0013c0023t0011g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0013c0023t0011g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0014c0049t0007g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0015c0030t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0016c0033t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0017c0034t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0018c0050t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0019c0037t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0020c0052t0027g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0021c0028t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0022c0027t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0023c0040t0010g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
a0024c0039t0035g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0003 | t0028 | g0007 | EUR | GBR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | GBR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | GBR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00140 | hp2 | a0001 | c0002 | t0003 | g0004 | EUR | GBR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00280 | hp1 | a0001 | c0001 | t0078 | g0141 | EUR | FIN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00280 | hp2 | a0002 | c0003 | t0034 | g0034 | EUR | FIN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00323 | hp1 | a0014 | c0049 | t0007 | g0119 | EUR | FIN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00423 | hp1 | a0001 | c0001 | t0065 | g0191 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00423 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00438 | hp2 | a0001 | c0001 | t0006 | g0017 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00544 | hp1 | a0001 | c0004 | t0051 | g0003 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00544 | hp2 | a0005 | c0007 | t0001 | g0002 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00558 | hp1 | a0001 | c0004 | t0001 | g0009 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00558 | hp2 | a0015 | c0030 | t0001 | g0005 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00597 | hp1 | a0001 | c0001 | t0021 | g0002 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00609 | hp2 | a0006 | c0008 | t0002 | g0199 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00639 | hp1 | a0001 | c0002 | t0070 | g0111 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0194 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00642 | hp1 | a0001 | c0004 | t0001 | g0003 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00642 | hp2 | a0007 | c0016 | t0002 | g0187 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00673 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00673 | hp2 | a0002 | c0003 | t0008 | g0007 | EAS | CHS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00733 | hp2 | a0008 | c0032 | t0015 | g0103 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00735 | hp2 | a0004 | c0006 | t0011 | g0104 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00738 | hp2 | a0001 | c0004 | t0001 | g0003 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00741 | hp1 | a0001 | c0002 | t0003 | g0117 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG00741 | hp2 | a0001 | c0001 | t0058 | g0033 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01069 | hp2 | a0001 | c0002 | t0018 | g0023 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01071 | hp1 | a0001 | c0002 | t0018 | g0023 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01071 | hp2 | a0001 | c0001 | t0009 | g0002 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01074 | hp1 | a0001 | c0002 | t0026 | g0157 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01074 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01081 | hp1 | a0001 | c0002 | t0003 | g0075 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01081 | hp2 | a0001 | c0001 | t0024 | g0033 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01099 | hp1 | a0001 | c0001 | t0012 | g0090 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01099 | hp2 | a0003 | c0042 | t0020 | g0093 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01106 | hp1 | a0001 | c0021 | t0077 | g0002 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01106 | hp2 | a0002 | c0003 | t0042 | g0216 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01109 | hp2 | a0002 | c0003 | t0028 | g0221 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01167 | hp1 | a0001 | c0001 | t0033 | g0031 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01167 | hp2 | a0001 | c0004 | t0001 | g0003 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01168 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01168 | hp2 | a0001 | c0025 | t0002 | g0001 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01169 | hp1 | a0001 | c0025 | t0002 | g0001 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01169 | hp2 | a0001 | c0001 | t0033 | g0031 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01175 | hp1 | a0001 | c0001 | t0009 | g0002 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01175 | hp2 | a0001 | c0002 | t0018 | g0023 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01192 | hp1 | a0001 | c0002 | t0003 | g0072 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01192 | hp2 | a0016 | c0033 | t0003 | g0004 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01243 | hp2 | a0004 | c0006 | t0029 | g0030 | AMR | PUR | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01255 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01256 | hp1 | a0001 | c0002 | t0038 | g0004 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01256 | hp2 | a0017 | c0034 | t0001 | g0058 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01257 | hp1 | a0001 | c0001 | t0031 | g0040 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01257 | hp2 | a0002 | c0003 | t0005 | g0052 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01258 | hp1 | a0001 | c0001 | t0031 | g0040 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01258 | hp2 | a0001 | c0002 | t0038 | g0004 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01261 | hp2 | a0001 | c0001 | t0009 | g0114 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01346 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01358 | hp1 | a0007 | c0016 | t0002 | g0047 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01361 | hp2 | a0002 | c0003 | t0007 | g0027 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01433 | hp2 | a0002 | c0003 | t0005 | g0052 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01496 | hp1 | a0001 | c0021 | t0001 | g0002 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01515 | hp1 | a0001 | c0002 | t0003 | g0004 | EUR | IBS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01516 | hp2 | a0012 | c0024 | t0055 | g0032 | EUR | IBS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01517 | hp1 | a0001 | c0002 | t0003 | g0078 | EUR | IBS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01884 | hp1 | a0003 | c0044 | t0046 | g0095 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01884 | hp2 | a0001 | c0001 | t0076 | g0213 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0212 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01891 | hp2 | a0001 | c0005 | t0039 | g0165 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01928 | hp1 | a0001 | c0001 | t0064 | g0001 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01934 | hp1 | a0003 | c0019 | t0020 | g0091 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01943 | hp1 | a0005 | c0007 | t0001 | g0002 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01943 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01952 | hp1 | a0001 | c0002 | t0003 | g0080 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01975 | hp1 | a0007 | c0016 | t0002 | g0047 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01975 | hp2 | a0001 | c0004 | t0001 | g0003 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01978 | hp2 | a0006 | c0008 | t0002 | g0184 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01981 | hp1 | a0012 | c0024 | t0054 | g0032 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01981 | hp2 | a0001 | c0001 | t0048 | g0001 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02015 | hp2 | a0001 | c0004 | t0001 | g0061 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02055 | hp1 | a0009 | c0012 | t0001 | g0121 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02071 | hp1 | a0001 | c0001 | t0021 | g0150 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02074 | hp1 | a0003 | c0019 | t0019 | g0029 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02083 | hp1 | a0001 | c0001 | t0047 | g0099 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02083 | hp2 | a0002 | c0003 | t0005 | g0219 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02132 | hp2 | a0001 | c0020 | t0044 | g0226 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02148 | hp1 | a0001 | c0051 | t0002 | g0190 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02148 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02257 | hp2 | a0001 | c0005 | t0023 | g0154 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0125 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02280 | hp1 | a0001 | c0038 | t0025 | g0168 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02280 | hp2 | a0008 | c0015 | t0015 | g0015 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02300 | hp2 | a0002 | c0003 | t0005 | g0228 | AMR | PEL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02451 | hp1 | a0003 | c0043 | t0011 | g0096 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02523 | hp1 | a0002 | c0003 | t0005 | g0220 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02523 | hp2 | a0001 | c0001 | t0067 | g0020 | EAS | KHV | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02572 | hp1 | a0002 | c0013 | t0013 | g0019 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02572 | hp2 | a0003 | c0010 | t0016 | g0054 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02602 | hp1 | a0001 | c0002 | t0003 | g0004 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02602 | hp2 | a0001 | c0001 | t0010 | g0002 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02615 | hp1 | a0001 | c0017 | t0004 | g0171 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02615 | hp2 | a0001 | c0001 | t0012 | g0089 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02622 | hp1 | a0002 | c0013 | t0013 | g0019 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02622 | hp2 | a0001 | c0002 | t0003 | g0071 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02630 | hp2 | a0003 | c0045 | t0016 | g0054 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02647 | hp1 | a0001 | c0017 | t0004 | g0049 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02647 | hp2 | a0011 | c0018 | t0025 | g0044 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02698 | hp2 | a0001 | c0009 | t0007 | g0108 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02717 | hp1 | a0001 | c0001 | t0075 | g0214 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02723 | hp1 | a0001 | c0002 | t0003 | g0028 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02723 | hp2 | a0001 | c0002 | t0003 | g0026 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02735 | hp1 | a0001 | c0001 | t0009 | g0126 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02809 | hp1 | a0011 | c0018 | t0060 | g0155 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02809 | hp2 | a0001 | c0002 | t0036 | g0158 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02818 | hp1 | a0001 | c0001 | t0012 | g0088 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02818 | hp2 | a0001 | c0005 | t0023 | g0107 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02886 | hp1 | a0001 | c0022 | t0071 | g0112 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02886 | hp2 | a0001 | c0017 | t0004 | g0049 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02922 | hp2 | a0003 | c0010 | t0068 | g0230 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02965 | hp1 | a0001 | c0022 | t0072 | g0113 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02965 | hp2 | a0008 | c0015 | t0015 | g0015 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02970 | hp1 | a0001 | c0002 | t0026 | g0050 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02970 | hp2 | a0001 | c0002 | t0003 | g0028 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02976 | hp1 | a0001 | c0005 | t0039 | g0162 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03017 | hp1 | a0001 | c0001 | t0066 | g0189 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03017 | hp2 | a0001 | c0004 | t0001 | g0003 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03041 | hp2 | a0003 | c0010 | t0069 | g0053 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03130 | hp1 | a0001 | c0002 | t0003 | g0026 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03130 | hp2 | a0003 | c0010 | t0016 | g0053 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03139 | hp1 | a0001 | c0002 | t0061 | g0160 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03139 | hp2 | a0009 | c0012 | t0022 | g0035 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0210 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03209 | hp2 | a0004 | c0006 | t0030 | g0097 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03225 | hp2 | a0001 | c0002 | t0036 | g0050 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03239 | hp1 | a0004 | c0006 | t0029 | g0030 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03239 | hp2 | a0002 | c0003 | t0007 | g0027 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03453 | hp1 | a0002 | c0013 | t0013 | g0172 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0209 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03491 | hp1 | a0002 | c0003 | t0005 | g0051 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03491 | hp2 | a0001 | c0004 | t0001 | g0138 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03492 | hp1 | a0001 | c0004 | t0001 | g0002 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03492 | hp2 | a0002 | c0003 | t0005 | g0051 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03516 | hp1 | a0001 | c0002 | t0026 | g0159 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03516 | hp2 | a0008 | c0015 | t0015 | g0015 | AFR | ESN | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03540 | hp1 | a0001 | c0005 | t0024 | g0181 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03540 | hp2 | a0004 | c0006 | t0011 | g0070 | AFR | GWD | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03579 | hp1 | a0002 | c0013 | t0013 | g0019 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03669 | hp1 | a0002 | c0003 | t0005 | g0224 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03669 | hp2 | a0002 | c0003 | t0034 | g0034 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03688 | hp1 | a0001 | c0001 | t0006 | g0001 | SAS | STU | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03688 | hp2 | a0001 | c0001 | t0019 | g0085 | SAS | STU | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03704 | hp2 | a0001 | c0001 | t0073 | g0134 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03710 | hp1 | a0001 | c0001 | t0050 | g0145 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03831 | hp1 | a0001 | c0005 | t0024 | g0105 | SAS | BEB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03831 | hp2 | a0001 | c0004 | t0001 | g0137 | SAS | BEB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03834 | hp1 | a0002 | c0003 | t0005 | g0225 | SAS | BEB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03834 | hp2 | a0001 | c0001 | t0062 | g0001 | SAS | BEB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03927 | hp1 | a0018 | c0050 | t0001 | g0003 | SAS | BEB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03927 | hp2 | a0001 | c0004 | t0001 | g0065 | SAS | BEB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG04115 | hp1 | a0002 | c0048 | t0043 | g0231 | SAS | STU | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | STU | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG04199 | hp2 | a0001 | c0002 | t0003 | g0004 | SAS | STU | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG04204 | hp1 | a0001 | c0001 | t0020 | g0098 | SAS | STU | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG04204 | hp2 | a0002 | c0003 | t0007 | g0057 | SAS | STU | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG04228 | hp1 | a0002 | c0003 | t0041 | g0007 | SAS | STU | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG04228 | hp2 | a0001 | c0009 | t0007 | g0081 | SAS | STU | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18522 | hp1 | a0003 | c0010 | t0016 | g0229 | AFR | YRI | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | YRI | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18612 | hp2 | a0002 | c0003 | t0005 | g0223 | EAS | CHB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18747 | hp1 | a0019 | c0037 | t0002 | g0017 | EAS | CHB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18747 | hp2 | a0001 | c0001 | t0063 | g0203 | EAS | CHB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18906 | hp1 | a0009 | c0012 | t0022 | g0035 | AFR | YRI | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18906 | hp2 | a0001 | c0002 | t0003 | g0074 | AFR | YRI | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18942 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18942 | hp2 | a0001 | c0001 | t0009 | g0109 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18945 | hp1 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18945 | hp2 | a0010 | c0011 | t0001 | g0002 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18946 | hp1 | a0020 | c0052 | t0027 | g0198 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18946 | hp2 | a0001 | c0009 | t0008 | g0118 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18949 | hp1 | a0004 | c0006 | t0030 | g0094 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18949 | hp2 | a0021 | c0028 | t0005 | g0218 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18950 | hp1 | a0006 | c0008 | t0002 | g0001 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18951 | hp1 | a0001 | c0001 | t0007 | g0166 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18951 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18952 | hp1 | a0001 | c0014 | t0014 | g0045 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18962 | hp1 | a0001 | c0014 | t0014 | g0174 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18962 | hp2 | a0006 | c0008 | t0002 | g0001 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18964 | hp1 | a0001 | c0031 | t0002 | g0001 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18964 | hp2 | a0023 | c0040 | t0010 | g0008 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18967 | hp1 | a0001 | c0036 | t0001 | g0129 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18967 | hp2 | a0002 | c0003 | t0074 | g0012 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18970 | hp1 | a0002 | c0003 | t0008 | g0012 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18970 | hp2 | a0013 | c0023 | t0011 | g0064 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18971 | hp2 | a0010 | c0011 | t0040 | g0002 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18975 | hp2 | a0001 | c0014 | t0014 | g0045 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18977 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18981 | hp1 | a0002 | c0003 | t0005 | g0007 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18981 | hp2 | a0001 | c0041 | t0027 | g0197 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18982 | hp2 | a0001 | c0009 | t0056 | g0060 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18983 | hp1 | a0005 | c0007 | t0001 | g0002 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18983 | hp2 | a0001 | c0001 | t0057 | g0178 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18984 | hp2 | a0010 | c0011 | t0040 | g0115 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18985 | hp1 | a0002 | c0003 | t0008 | g0012 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18985 | hp2 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18986 | hp1 | a0006 | c0008 | t0037 | g0048 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18994 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18994 | hp2 | a0001 | c0002 | t0003 | g0079 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18999 | hp2 | a0001 | c0001 | t0006 | g0059 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19000 | hp1 | a0001 | c0001 | t0006 | g0192 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19000 | hp2 | a0002 | c0003 | t0008 | g0012 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19002 | hp1 | a0001 | c0001 | t0032 | g0002 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19002 | hp2 | a0001 | c0001 | t0049 | g0152 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19004 | hp1 | a0001 | c0004 | t0001 | g0062 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19004 | hp2 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19010 | hp1 | a0001 | c0004 | t0001 | g0024 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19010 | hp2 | a0001 | c0020 | t0014 | g0175 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19011 | hp1 | a0010 | c0011 | t0001 | g0002 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19012 | hp2 | a0001 | c0004 | t0001 | g0046 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19030 | hp1 | a0007 | c0029 | t0003 | g0073 | AFR | LWK | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19030 | hp2 | a0002 | c0046 | t0001 | g0173 | AFR | LWK | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19043 | hp1 | a0001 | c0001 | t0010 | g0110 | AFR | LWK | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19043 | hp2 | a0001 | c0005 | t0035 | g0164 | AFR | LWK | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19056 | hp1 | a0001 | c0004 | t0021 | g0185 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19057 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19057 | hp2 | a0001 | c0001 | t0027 | g0200 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19060 | hp1 | a0001 | c0001 | t0017 | g0222 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19060 | hp2 | a0013 | c0023 | t0011 | g0148 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19062 | hp2 | a0001 | c0001 | t0032 | g0002 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19063 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19063 | hp2 | a0005 | c0007 | t0001 | g0180 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19064 | hp2 | a0005 | c0007 | t0001 | g0013 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19065 | hp1 | a0002 | c0003 | t0008 | g0007 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19065 | hp2 | a0001 | c0001 | t0006 | g0020 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19066 | hp2 | a0001 | c0004 | t0001 | g0069 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19070 | hp1 | a0001 | c0001 | t0010 | g0042 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19070 | hp2 | a0001 | c0001 | t0017 | g0215 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19079 | hp1 | a0001 | c0035 | t0052 | g0063 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19079 | hp2 | a0001 | c0001 | t0006 | g0188 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19085 | hp1 | a0001 | c0009 | t0007 | g0201 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19085 | hp2 | a0005 | c0007 | t0001 | g0013 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19087 | hp1 | a0001 | c0004 | t0001 | g0024 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19088 | hp1 | a0001 | c0004 | t0001 | g0046 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19088 | hp2 | a0006 | c0008 | t0037 | g0048 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19240 | hp1 | a0001 | c0001 | t0012 | g0086 | AFR | YRI | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA19240 | hp2 | a0024 | c0039 | t0035 | g0116 | AFR | YRI | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA20129 | hp1 | a0001 | c0001 | t0012 | g0087 | AFR | ASW | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA20129 | hp2 | a0001 | c0005 | t0023 | g0106 | AFR | ASW | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA20752 | hp1 | a0002 | c0047 | t0003 | g0077 | EUR | TSI | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA20752 | hp2 | a0003 | c0019 | t0019 | g0029 | EUR | TSI | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA20905 | hp1 | a0004 | c0006 | t0045 | g0092 | SAS | GIH | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA20905 | hp2 | a0001 | c0002 | t0003 | g0083 | SAS | GIH | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG01123 | hp2 | a0001 | c0001 | t0010 | g0002 | AMR | CLM | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02109 | hp1 | a0009 | c0012 | t0022 | g0123 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02109 | hp2 | a0001 | c0001 | t0053 | g0124 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0211 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | ACB | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | USA | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0163 | AFR | USA | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18955 | hp1 | a0022 | c0027 | t0001 | g0144 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA18955 | hp2 | a0001 | c0001 | t0017 | g0217 | EAS | JPT | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | USA | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
NA21309 | hp2 | a0011 | c0018 | t0025 | g0044 | AFR | LWK | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
homoSapiens | chm13v2 | a0001 | c0001 | t0079 | g0156 | REF | REF | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
homoSapiens | grch38p0 | a0001 | c0026 | t0059 | g0139 | REF | REF | INF2_chr14_104684618_104727535 | INF2 | chr14 | 104684618 | 104727535 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:104689739 | G | A | 3 | a0001 a0003 a0004 |
13 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(10): Show |
splice_region_variant | LOW | c.-10G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/23 | chr14 | 104689739 | |||||||
chr14:104703409 | C | T | 1 | a0020 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.622C>T | p.Pro208Ser | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 4/23 | 753/7623 | 622/3750 | 208/1249 | chr14 | 104703409 | |||
chr14:104703437 | T | A | 1 | a0022 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.650T>A | p.Leu217Gln | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 4/23 | 781/7623 | 650/3750 | 217/1249 | chr14 | 104703437 | |||
chr14:104707316 | C | T | 1 | a0006 | 6 | HG00609.hp2 HG01978.hp2 NA18950.hp1 others(3): Show |
missense_variant | MODERATE | c.1049C>T | p.Pro350Leu | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1180/7623 | 1049/3750 | 350/1249 | chr14 | 104707316 | |||
chr14:104707525 | ACCCCAC | A | 2 | a0003 a0004 |
19 | HG00735.hp2 HG01099.hp2 HG01243.hp2 others(16): Show |
disruptive_inframe_deletion | MODERATE | c.1280_1285delCACCCC | p.Pro427_Pro428del | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1411/7623 | 1280/3750 | 427/1249 | INFO_REALIGN_3_PRIME | chr14 | 104707525 | ||
chr14:104707525 | ACCCCACC others(5): Show |
A | 2 | a0002 a0014 |
34 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(31): Show |
disruptive_inframe_deletion | MODERATE | c.1274_1285delCACCCC others(6): Show |
p.Pro425_Pro428del | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1405/7623 | 1274/3750 | 425/1249 | INFO_REALIGN_3_PRIME | chr14 | 104707525 | ||
chr14:104707525 | ACCCCACC others(6): Show |
A | 1 | a0021 | 1 | NA18949.hp2 | frameshift_variant | HIGH | c.1262_1274delCACCCC others(7): Show |
p.Pro421fs | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1393/7623 | 1262/3750 | 421/1249 | INFO_REALIGN_3_PRIME | chr14 | 104707525 | ||
chr14:104707543 | C | T | 1 | a0014 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.1276C>T | p.Pro426Ser | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1407/7623 | 1276/3750 | 426/1249 | chr14 | 104707543 | |||
chr14:104707547 | CACCCCT | C | 1 | a0009 | 4 | HG02055.hp1 HG02109.hp1 HG03139.hp2 others(1): Show |
disruptive_inframe_deletion | MODERATE | c.1281_1286delACCCCT | p.Pro428_Leu429del | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1412/7623 | 1281/3750 | 427/1249 | chr14 | 104707547 | |||
chr14:104707615 | G | A | 1 | a0018 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.1348G>A | p.Gly450Arg | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1479/7623 | 1348/3750 | 450/1249 | chr14 | 104707615 | |||
chr14:104707814 | C | T | 1 | a0011 | 3 | HG02647.hp2 HG02809.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.1547C>T | p.Pro516Leu | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1678/7623 | 1547/3750 | 516/1249 | chr14 | 104707814 | |||
chr14:104707849 | C | T | 1 | a0012 | 2 | HG01516.hp2 HG01981.hp1 |
missense_variant | MODERATE | c.1582C>T | p.Pro528Ser | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1713/7623 | 1582/3750 | 528/1249 | chr14 | 104707849 | |||
chr14:104707859 | C | T | 1 | a0023 | 1 | NA18964.hp2 | missense_variant | MODERATE | c.1592C>T | p.Ala531Val | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1723/7623 | 1592/3750 | 531/1249 | chr14 | 104707859 | |||
chr14:104709309 | C | T | 1 | a0010 | 4 | NA18945.hp2 NA18971.hp2 NA18984.hp2 others(1): Show |
missense_variant | MODERATE | c.1978C>T | p.Arg660Trp | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 11/23 | 2109/7623 | 1978/3750 | 660/1249 | chr14 | 104709309 | |||
chr14:104710152 | C | T | 1 | a0003 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.2203C>T | p.Arg735Trp | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/23 | 2334/7623 | 2203/3750 | 735/1249 | chr14 | 104710152 | |||
chr14:104711668 | C | T | 1 | a0024 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.2458C>T | p.Arg820Trp | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/23 | 2589/7623 | 2458/3750 | 820/1249 | chr14 | 104711668 | |||
chr14:104712847 | G | A | 2 | a0003 a0007 |
5 | HG00642.hp2 HG01099.hp2 HG01358.hp1 others(2): Show |
missense_variant | MODERATE | c.2630G>A | p.Arg877Gln | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 18/23 | 2761/7623 | 2630/3750 | 877/1249 | chr14 | 104712847 | |||
chr14:104712941 | C | G | 1 | a0002 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.2724C>G | p.Asp908Glu | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 18/23 | 2855/7623 | 2724/3750 | 908/1249 | chr14 | 104712941 | |||
chr14:104712961 | C | T | 1 | a0019 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.2744C>T | p.Ala915Val | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 18/23 | 2875/7623 | 2744/3750 | 915/1249 | chr14 | 104712961 | |||
chr14:104714356 | A | C | 1 | a0017 | 1 | HG01256.hp2 | missense_variant | MODERATE | c.3194A>C | p.Glu1065Ala | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3325/7623 | 3194/3750 | 1065/1249 | chr14 | 104714356 | |||
chr14:104714448 | C | T | 2 | a0004 a0013 |
9 | HG00735.hp2 HG01243.hp2 HG03209.hp2 others(6): Show |
missense_variant | MODERATE | c.3286C>T | p.Pro1096Ser | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3417/7623 | 3286/3750 | 1096/1249 | chr14 | 104714448 | |||
chr14:104714566 | C | T | 1 | a0005 | 6 | HG00544.hp2 HG01943.hp1 NA18983.hp1 others(3): Show |
missense_variant | MODERATE | c.3404C>T | p.Thr1135Met | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3535/7623 | 3404/3750 | 1135/1249 | chr14 | 104714566 | |||
chr14:104714640 | G | A | 1 | a0008 | 4 | HG00733.hp2 HG02280.hp2 HG02965.hp2 others(1): Show |
missense_variant | MODERATE | c.3478G>A | p.Gly1160Ser | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3609/7623 | 3478/3750 | 1160/1249 | chr14 | 104714640 | |||
chr14:104714664 | C | CCAGGTGG others(28): Show |
1 | a0015 | 1 | HG00558.hp2 | frameshift_variant | HIGH | c.3503_3537dupCAGGTG others(29): Show |
p.Ala1180fs | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3669/7623 | 3538/3750 | 1180/1249 | INFO_REALIGN_3_PRIME | chr14 | 104714664 | ||
chr14:104714800 | G | A | 1 | a0016 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.3638G>A | p.Arg1213Gln | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3769/7623 | 3638/3750 | 1213/1249 | chr14 | 104714800 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:104701407 | G | A | 2 | a0001c0014 a0001c0020 |
5 | HG02132.hp2 NA18952.hp1 NA18962.hp1 others(2): Show |
synonymous_variant | LOW | c.42G>A | p.Leu14Leu | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/23 | 173/7623 | 42/3750 | 14/1249 | chr14 | 104701407 | |||
chr14:104701470 | C | T | 50 | a0001c0001 a0001c0002 a0001c0004 others(47): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
synonymous_variant | LOW | c.105C>T | p.Pro35Pro | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/23 | 236/7623 | 105/3750 | 35/1249 | chr14 | 104701470 | |||
chr14:104701644 | C | T | 1 | a0001c0025 | 2 | HG01168.hp2 HG01169.hp1 |
synonymous_variant | LOW | c.279C>T | p.Ser93Ser | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/23 | 410/7623 | 279/3750 | 93/1249 | chr14 | 104701644 | |||
chr14:104707455 | C | G | 1 | a0001c0051 | 1 | HG02148.hp1 | synonymous_variant | LOW | c.1188C>G | p.Pro396Pro | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1319/7623 | 1188/3750 | 396/1249 | chr14 | 104707455 | |||
chr14:104707494 | G | T | 2 | a0001c0004 a0018c0050 |
27 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(24): Show |
synonymous_variant | LOW | c.1227G>T | p.Ser409Ser | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1358/7623 | 1227/3750 | 409/1249 | chr14 | 104707494 | |||
chr14:104707719 | T | C | 1 | a0008c0015 | 3 | HG02280.hp2 HG02965.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.1452T>C | p.Cys484Cys | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1583/7623 | 1452/3750 | 484/1249 | chr14 | 104707719 | |||
chr14:104707773 | A | C | 1 | a0001c0041 | 1 | NA18981.hp2 | synonymous_variant | LOW | c.1506A>C | p.Pro502Pro | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/23 | 1637/7623 | 1506/3750 | 502/1249 | chr14 | 104707773 | |||
chr14:104711090 | C | T | 3 | a0001c0005 a0003c0044 a0024c0039 |
10 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
synonymous_variant | LOW | c.2322C>T | p.Thr774Thr | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 15/23 | 2453/7623 | 2322/3750 | 774/1249 | chr14 | 104711090 | |||
chr14:104711649 | C | T | 1 | a0003c0044 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.2439C>T | p.Pro813Pro | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/23 | 2570/7623 | 2439/3750 | 813/1249 | chr14 | 104711649 | |||
chr14:104712514 | C | T | 2 | a0001c0038 a0011c0018 |
4 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(1): Show |
synonymous_variant | LOW | c.2571C>T | p.Ser857Ser | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 17/23 | 2702/7623 | 2571/3750 | 857/1249 | chr14 | 104712514 | |||
chr14:104712857 | T | C | 46 | a0001c0001 a0001c0002 a0001c0004 others(43): Show |
344 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(341): Show |
synonymous_variant | LOW | c.2640T>C | p.Asp880Asp | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 18/23 | 2771/7623 | 2640/3750 | 880/1249 | chr14 | 104712857 | |||
chr14:104712983 | C | T | 1 | a0001c0036 | 1 | NA18967.hp1 | synonymous_variant | LOW | c.2766C>T | p.Arg922Arg | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 18/23 | 2897/7623 | 2766/3750 | 922/1249 | chr14 | 104712983 | |||
chr14:104714228 | T | C | 41 | a0001c0001 a0001c0002 a0001c0004 others(38): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
synonymous_variant | LOW | c.3066T>C | p.Asp1022Asp | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3197/7623 | 3066/3750 | 1022/1249 | chr14 | 104714228 | |||
chr14:104714231 | C | T | 1 | a0001c0035 | 1 | NA19079.hp1 | synonymous_variant | LOW | c.3069C>T | p.Pro1023Pro | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3200/7623 | 3069/3750 | 1023/1249 | chr14 | 104714231 | |||
chr14:104714240 | C | T | 1 | a0001c0017 | 3 | HG02615.hp1 HG02647.hp1 HG02886.hp2 |
synonymous_variant | LOW | c.3078C>T | p.Ser1026Ser | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3209/7623 | 3078/3750 | 1026/1249 | chr14 | 104714240 | |||
chr14:104714270 | T | C | 1 | a0012c0024 | 2 | HG01516.hp2 HG01981.hp1 |
synonymous_variant | LOW | c.3108T>C | p.Leu1036Leu | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3239/7623 | 3108/3750 | 1036/1249 | chr14 | 104714270 | |||
chr14:104714315 | C | T | 1 | a0001c0020 | 2 | HG02132.hp2 NA19010.hp2 |
synonymous_variant | LOW | c.3153C>T | p.Asp1051Asp | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3284/7623 | 3153/3750 | 1051/1249 | chr14 | 104714315 | |||
chr14:104714369 | A | C | 33 | a0001c0001 a0001c0004 a0001c0005 others(30): Show |
280 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(277): Show |
synonymous_variant | LOW | c.3207A>C | p.Pro1069Pro | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3338/7623 | 3207/3750 | 1069/1249 | chr14 | 104714369 | |||
chr14:104714369 | A | G | 12 | a0001c0002 a0001c0022 a0002c0047 others(9): Show |
60 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(57): Show |
synonymous_variant | LOW | c.3207A>G | p.Pro1069Pro | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3338/7623 | 3207/3750 | 1069/1249 | chr14 | 104714369 | |||
chr14:104714846 | G | A | 1 | a0001c0031 | 1 | NA18964.hp1 | synonymous_variant | LOW | c.3684G>A | p.Arg1228Arg | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/23 | 3815/7623 | 3684/3750 | 1228/1249 | chr14 | 104714846 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:104689664 | G | A | 9 | a0001c0001t0017 a0001c0002t0018 a0001c0020t0044 others(6): Show |
24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-85G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/23 | 11702 | chr14 | 104689664 | ||||||
chr14:104718929 | C | T | 1 | a0010c0011t0040 | 2 | NA18971.hp2 NA18984.hp2 |
3_prime_UTR_variant | MODIFIER | c.*136C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 3590 | chr14 | 104718929 | ||||||
chr14:104719017 | G | A | 1 | a0001c0001t0031 | 2 | HG01257.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*224G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 3678 | chr14 | 104719017 | ||||||
chr14:104719230 | G | A | 8 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0018 others(5): Show |
33 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*437G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 3891 | chr14 | 104719230 | ||||||
chr14:104719329 | G | T | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(52): Show |
231 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*536G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 3990 | chr14 | 104719329 | ||||||
chr14:104719330 | G | T | 1 | a0001c0001t0078 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*537G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 3991 | chr14 | 104719330 | ||||||
chr14:104719473 | G | T | 1 | a0001c0021t0077 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*680G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4134 | chr14 | 104719473 | ||||||
chr14:104719572 | G | A | 1 | a0001c0001t0048 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*779G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4233 | chr14 | 104719572 | ||||||
chr14:104719685 | ACAGGCCC others(29): Show |
A | 8 | a0001c0001t0004 a0001c0001t0073 a0001c0001t0075 others(5): Show |
26 | HG00673.hp2 HG01884.hp2 HG01891.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*925_*960delCCCCCA others(30): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4379 | INFO_REALIGN_3_PRIME | chr14 | 104719685 | |||||
chr14:104719773 | C | T | 1 | a0001c0005t0039 | 2 | HG01891.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*980C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4434 | chr14 | 104719773 | ||||||
chr14:104719798 | C | G | 5 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0075 others(2): Show |
23 | HG01099.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1005C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4459 | chr14 | 104719798 | ||||||
chr14:104719826 | C | T | 14 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0018 others(11): Show |
41 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1033C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4487 | chr14 | 104719826 | ||||||
chr14:104719841 | A | T | 14 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0018 others(11): Show |
41 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1048A>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4502 | chr14 | 104719841 | ||||||
chr14:104719986 | A | G | 23 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0020 others(20): Show |
76 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1193A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4647 | chr14 | 104719986 | ||||||
chr14:104719996 | G | A | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(52): Show |
229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*1203G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4657 | chr14 | 104719996 | ||||||
chr14:104720076 | G | C | 4 | a0003c0010t0016 a0003c0010t0068 a0003c0010t0069 others(1): Show |
6 | HG02572.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1283G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4737 | chr14 | 104720076 | ||||||
chr14:104720179 | C | T | 1 | a0001c0001t0067 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1386C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4840 | chr14 | 104720179 | ||||||
chr14:104720329 | T | G | 1 | a0001c0001t0075 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1536T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4990 | chr14 | 104720329 | ||||||
chr14:104720330 | T | C | 1 | a0001c0001t0049 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1537T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4991 | chr14 | 104720330 | ||||||
chr14:104720336 | A | C | 5 | a0001c0002t0026 a0001c0002t0036 a0001c0002t0061 others(2): Show |
10 | HG00733.hp2 HG01074.hp1 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1543A>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4997 | chr14 | 104720336 | ||||||
chr14:104720336 | A | G | 1 | a0001c0001t0075 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1543A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4997 | chr14 | 104720336 | ||||||
chr14:104720338 | T | G | 1 | a0001c0001t0075 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1545T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 4999 | chr14 | 104720338 | ||||||
chr14:104720339 | C | G | 1 | a0001c0001t0075 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1546C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5000 | chr14 | 104720339 | ||||||
chr14:104720342 | C | T | 15 | a0001c0001t0003 a0001c0001t0075 a0001c0002t0003 others(12): Show |
42 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1549C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5003 | chr14 | 104720342 | ||||||
chr14:104720343 | G | C | 1 | a0001c0001t0075 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1550G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5004 | chr14 | 104720343 | ||||||
chr14:104720348 | G | A | 1 | a0001c0001t0075 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1555G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5009 | chr14 | 104720348 | ||||||
chr14:104720363 | G | A | 1 | a0001c0001t0075 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1570G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5024 | chr14 | 104720363 | ||||||
chr14:104720365 | C | T | 1 | a0001c0001t0075 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1572C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5026 | chr14 | 104720365 | ||||||
chr14:104720371 | C | A | 1 | a0001c0001t0075 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1578C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5032 | chr14 | 104720371 | ||||||
chr14:104720397 | C | T | 1 | a0003c0010t0069 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1604C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5058 | chr14 | 104720397 | ||||||
chr14:104720398 | G | A | 8 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0018 others(5): Show |
33 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1605G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5059 | chr14 | 104720398 | ||||||
chr14:104720403 | C | CGTCGTCC others(97): Show |
1 | a0001c0001t0033 | 2 | HG01167.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1636_*1637insCACG others(100): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5091 | INFO_REALIGN_3_PRIME | chr14 | 104720403 | |||||
chr14:104720409 | CCTCGTGT others(27): Show |
C | 2 | a0001c0022t0071 a0001c0022t0072 |
2 | HG02886.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1648_*1681delAGTC others(30): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5102 | INFO_REALIGN_3_PRIME | chr14 | 104720409 | |||||
chr14:104720409 | CCTCGTGT others(130): Show |
C | 2 | a0001c0001t0062 a0012c0024t0054 |
2 | HG01981.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1671_*1807del | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5125 | INFO_REALIGN_3_PRIME | chr14 | 104720409 | |||||
chr14:104720430 | G | C | 79 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(76): Show |
284 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(281): Show |
3_prime_UTR_variant | MODIFIER | c.*1637G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5091 | chr14 | 104720430 | ||||||
chr14:104720435 | C | T | 19 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0018 others(16): Show |
50 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1642C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5096 | chr14 | 104720435 | ||||||
chr14:104720439 | G | A | 78 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(75): Show |
283 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*1646G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5100 | chr14 | 104720439 | ||||||
chr14:104720441 | A | C | 1 | a0001c0001t0075 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1648A>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5102 | chr14 | 104720441 | ||||||
chr14:104720443 | T | TCTCGTGT others(28): Show |
1 | a0001c0036t0001 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1670_*1671insCACG others(31): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5125 | INFO_REALIGN_3_PRIME | chr14 | 104720443 | |||||
chr14:104720443 | T | TCTCGTGT others(63): Show |
3 | a0001c0001t0001 a0001c0001t0010 a0001c0004t0001 |
6 | HG02056.hp2 HG02135.hp2 HG03017.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1670_*1671insCACG others(66): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5125 | INFO_REALIGN_3_PRIME | chr14 | 104720443 | |||||
chr14:104720443 | T | TCTCGTGT others(98): Show |
1 | a0001c0001t0006 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1670_*1671insCACG others(101): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5125 | INFO_REALIGN_3_PRIME | chr14 | 104720443 | |||||
chr14:104720443 | T | TCTCGTGT others(28): Show |
3 | a0001c0001t0007 a0001c0009t0007 a0001c0009t0056 |
3 | NA18951.hp1 NA18982.hp2 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1674_*1708dupGTCT others(31): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5163 | INFO_REALIGN_3_PRIME | chr14 | 104720443 | |||||
chr14:104720443 | TCTCGTGT others(200): Show |
T | 1 | a0012c0024t0055 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1709_*1915del | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5163 | INFO_REALIGN_3_PRIME | chr14 | 104720443 | |||||
chr14:104720443 | TCTCGTGT others(476): Show |
T | 1 | a0001c0001t0063 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1709_*2191del | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5163 | INFO_REALIGN_3_PRIME | chr14 | 104720443 | |||||
chr14:104720464 | G | C | 77 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(74): Show |
275 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*1671G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5125 | chr14 | 104720464 | ||||||
chr14:104720469 | C | T | 14 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0018 others(11): Show |
41 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1676C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5130 | chr14 | 104720469 | ||||||
chr14:104720473 | G | A | 1 | a0001c0001t0075 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1680G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5134 | chr14 | 104720473 | ||||||
chr14:104720474 | T | G | 3 | a0001c0001t0004 a0001c0001t0076 a0001c0017t0004 |
17 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1681T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5135 | chr14 | 104720474 | ||||||
chr14:104720475 | C | A | 1 | a0001c0001t0075 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1682C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5136 | chr14 | 104720475 | ||||||
chr14:104720478 | CCTCGTGT others(371): Show |
C | 1 | a0001c0001t0064 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1709_*2086del | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5163 | INFO_REALIGN_3_PRIME | chr14 | 104720478 | |||||
chr14:104720499 | G | C | 2 | a0001c0001t0002 a0001c0001t0075 |
2 | HG02074.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1706G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5160 | chr14 | 104720499 | ||||||
chr14:104720499 | GACATCTG others(95): Show |
G | 7 | a0001c0001t0021 a0001c0001t0050 a0001c0001t0058 others(4): Show |
11 | HG00597.hp1 HG00741.hp2 HG02071.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1709_*1810del | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5163 | INFO_REALIGN_3_PRIME | chr14 | 104720499 | |||||
chr14:104720502 | A | G | 75 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(72): Show |
277 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*1709A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5163 | chr14 | 104720502 | ||||||
chr14:104720509 | T | G | 1 | a0001c0001t0075 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1716T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5170 | chr14 | 104720509 | ||||||
chr14:104720510 | A | C | 70 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(67): Show |
271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*1717A>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5171 | chr14 | 104720510 | ||||||
chr14:104720512 | T | TC | 24 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(21): Show |
60 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1720dupC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5175 | INFO_REALIGN_3_PRIME | chr14 | 104720512 | |||||
chr14:104720512 | T | TCCTCGTG others(29): Show |
5 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(2): Show |
11 | HG00621.hp1 HG00735.hp1 HG01123.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1720_*1721insCTCG others(32): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5175 | INFO_REALIGN_3_PRIME | chr14 | 104720512 | |||||
chr14:104720512 | T | TCCTCGTG others(168): Show |
1 | a0006c0008t0037 | 2 | NA18986.hp1 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1720_*1721insCTCG others(171): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5175 | INFO_REALIGN_3_PRIME | chr14 | 104720512 | |||||
chr14:104720513 | CTCGTGTG others(26): Show |
C | 47 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(44): Show |
192 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*1721_*1753delTCGT others(29): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5175 | chr14 | 104720513 | ||||||
chr14:104720513 | CTCGTGTG others(60): Show |
C | 4 | a0001c0005t0023 a0001c0005t0024 a0015c0030t0001 others(1): Show |
6 | HG00558.hp2 HG02257.hp2 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1721_*1787delTCGT others(63): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5175 | chr14 | 104720513 | ||||||
chr14:104720533 | A | G | 26 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(23): Show |
73 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1740A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5194 | chr14 | 104720533 | ||||||
chr14:104720544 | A | C | 26 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(23): Show |
73 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1751A>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5205 | chr14 | 104720544 | ||||||
chr14:104720546 | T | TC | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(22): Show |
71 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1754dupC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5209 | INFO_REALIGN_3_PRIME | chr14 | 104720546 | |||||
chr14:104720547 | CTCGTGTG others(26): Show |
C | 1 | a0001c0002t0036 | 2 | HG02809.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1755_*1787delTCGT others(29): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5209 | chr14 | 104720547 | ||||||
chr14:104720567 | G | C | 2 | a0001c0001t0062 a0012c0024t0054 |
2 | HG01981.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1774G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5228 | chr14 | 104720567 | ||||||
chr14:104720576 | G | A | 2 | a0001c0001t0062 a0012c0024t0054 |
2 | HG01981.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1783G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5237 | chr14 | 104720576 | ||||||
chr14:104720578 | A | C | 66 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(63): Show |
263 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*1785A>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5239 | chr14 | 104720578 | ||||||
chr14:104720580 | T | TC | 66 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(63): Show |
263 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*1788dupC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5243 | INFO_REALIGN_3_PRIME | chr14 | 104720580 | |||||
chr14:104720601 | C | CACGTCTG others(98): Show |
1 | a0002c0003t0034 | 2 | HG00280.hp2 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1823_*1927dupCTCG others(101): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5382 | INFO_REALIGN_3_PRIME | chr14 | 104720601 | |||||
chr14:104720601 | C | CACGTCTG others(133): Show |
11 | a0001c0001t0007 a0001c0009t0007 a0001c0009t0008 others(8): Show |
32 | HG00323.hp1 HG00673.hp2 HG01257.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1927_*1928insCTCG others(136): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5382 | INFO_REALIGN_3_PRIME | chr14 | 104720601 | |||||
chr14:104720601 | C | CACGTCTG others(238): Show |
2 | a0002c0003t0041 a0002c0003t0042 |
2 | HG01106.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1927_*1928insCTCG others(241): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5382 | INFO_REALIGN_3_PRIME | chr14 | 104720601 | |||||
chr14:104720601 | C | G | 71 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(68): Show |
272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*1808C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5262 | chr14 | 104720601 | ||||||
chr14:104720639 | G | A | 1 | a0001c0001t0065 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1846G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5300 | chr14 | 104720639 | ||||||
chr14:104720649 | TC | T | 3 | a0001c0038t0025 a0011c0018t0025 a0011c0018t0060 |
4 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1858delC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5312 | INFO_REALIGN_3_PRIME | chr14 | 104720649 | |||||
chr14:104720671 | G | C | 1 | a0012c0024t0055 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1878G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5332 | chr14 | 104720671 | ||||||
chr14:104720683 | G | A | 2 | a0001c0001t0078 a0001c0004t0051 |
2 | HG00280.hp1 HG00544.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1890G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5344 | chr14 | 104720683 | ||||||
chr14:104720684 | TC | T | 8 | a0001c0001t0078 a0001c0004t0051 a0001c0014t0014 others(5): Show |
11 | HG00280.hp1 HG00544.hp1 HG02132.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1893delC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5347 | INFO_REALIGN_3_PRIME | chr14 | 104720684 | |||||
chr14:104720718 | G | A | 40 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(37): Show |
197 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*1925G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5379 | chr14 | 104720718 | ||||||
chr14:104720719 | T | TC | 19 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0012 others(16): Show |
41 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1927dupC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5382 | INFO_REALIGN_3_PRIME | chr14 | 104720719 | |||||
chr14:104720719 | T | TCCTCGTG others(29): Show |
6 | a0001c0001t0057 a0003c0043t0011 a0004c0006t0011 others(3): Show |
10 | HG00735.hp2 HG01243.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1927_*1928insCTCG others(32): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5382 | INFO_REALIGN_3_PRIME | chr14 | 104720719 | |||||
chr14:104720719 | T | TCCTCGTG others(99): Show |
1 | a0004c0006t0045 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1927_*1928insCTCG others(102): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5382 | INFO_REALIGN_3_PRIME | chr14 | 104720719 | |||||
chr14:104720719 | T | TCCTCGTG others(99): Show |
1 | a0002c0003t0028 | 2 | HG00099.hp1 HG01109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1927_*1928insCTCG others(102): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5382 | INFO_REALIGN_3_PRIME | chr14 | 104720719 | |||||
chr14:104720720 | CTCGTGTG others(26): Show |
C | 13 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0018 others(10): Show |
40 | HG00140.hp2 HG00639.hp2 HG00741.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1928_*1960delTCGT others(29): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5382 | chr14 | 104720720 | ||||||
chr14:104720753 | T | TC | 64 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(61): Show |
243 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*1961dupC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5416 | INFO_REALIGN_3_PRIME | chr14 | 104720753 | |||||
chr14:104720753 | TCTCGTGT others(62): Show |
T | 1 | a0001c0002t0070 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2065_*2133delTCGT others(65): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5519 | INFO_REALIGN_3_PRIME | chr14 | 104720753 | |||||
chr14:104720785 | C | CGTCCTCG others(362): Show |
1 | a0001c0004t0051 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1995_*1996insCTCG others(365): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5450 | INFO_REALIGN_3_PRIME | chr14 | 104720785 | |||||
chr14:104720786 | G | A | 4 | a0001c0001t0021 a0001c0001t0067 a0001c0004t0021 others(1): Show |
6 | HG00597.hp1 HG02071.hp1 HG02523.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1993G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5447 | chr14 | 104720786 | ||||||
chr14:104720787 | T | TC | 8 | a0001c0001t0004 a0001c0001t0075 a0001c0001t0076 others(5): Show |
24 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1995dupC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5450 | INFO_REALIGN_3_PRIME | chr14 | 104720787 | |||||
chr14:104720787 | TCTCGTGT others(28): Show |
T | 2 | a0001c0005t0023 a0001c0022t0072 |
3 | HG02257.hp2 HG02818.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2030_*2064delCTCG others(31): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5484 | INFO_REALIGN_3_PRIME | chr14 | 104720787 | |||||
chr14:104720801 | T | A | 1 | a0001c0001t0078 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2008T>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5462 | chr14 | 104720801 | ||||||
chr14:104720806 | T | C | 1 | a0001c0001t0078 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2013T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5467 | chr14 | 104720806 | ||||||
chr14:104720813 | C | A | 1 | a0001c0001t0032 | 2 | NA19002.hp1 NA19062.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2020C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5474 | chr14 | 104720813 | ||||||
chr14:104720820 | G | A | 1 | a0001c0002t0038 | 2 | HG01256.hp1 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2027G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5481 | chr14 | 104720820 | ||||||
chr14:104720821 | TC | T | 24 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0057 others(21): Show |
69 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*2030delC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5484 | INFO_REALIGN_3_PRIME | chr14 | 104720821 | |||||
chr14:104720822 | CCTCGTGT others(27): Show |
C | 2 | a0001c0022t0071 a0012c0024t0054 |
2 | HG01981.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2065_*2098delTCGT others(30): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5519 | INFO_REALIGN_3_PRIME | chr14 | 104720822 | |||||
chr14:104720846 | G | A | 1 | a0011c0018t0060 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2053G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5507 | chr14 | 104720846 | ||||||
chr14:104720854 | C | T | 5 | a0001c0001t0024 a0001c0001t0058 a0001c0005t0024 others(2): Show |
7 | HG00741.hp2 HG01081.hp2 HG01884.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2061C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5515 | chr14 | 104720854 | ||||||
chr14:104720856 | T | TC | 7 | a0001c0001t0004 a0001c0001t0075 a0001c0001t0076 others(4): Show |
23 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2064dupC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5519 | INFO_REALIGN_3_PRIME | chr14 | 104720856 | |||||
chr14:104720886 | G | A | 1 | a0002c0003t0041 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2093G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5547 | chr14 | 104720886 | ||||||
chr14:104720891 | C | CCTCGTGT others(27): Show |
1 | a0001c0001t0057 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2100_*2133dupTCGT others(30): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5588 | INFO_REALIGN_3_PRIME | chr14 | 104720891 | |||||
chr14:104720925 | TC | T | 8 | a0001c0001t0050 a0001c0001t0067 a0003c0043t0011 others(5): Show |
12 | HG00735.hp2 HG01243.hp2 HG02451.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2134delC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5588 | INFO_REALIGN_3_PRIME | chr14 | 104720925 | |||||
chr14:104720934 | G | T | 1 | a0001c0001t0078 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2141G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5595 | chr14 | 104720934 | ||||||
chr14:104720947 | G | C | 1 | a0001c0001t0063 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2154G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5608 | chr14 | 104720947 | ||||||
chr14:104720965 | G | C | 4 | a0001c0001t0004 a0001c0001t0075 a0001c0001t0076 others(1): Show |
18 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2172G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5626 | chr14 | 104720965 | ||||||
chr14:104721000 | C | G | 19 | a0001c0001t0004 a0001c0001t0050 a0001c0001t0053 others(16): Show |
40 | HG00735.hp2 HG01074.hp1 HG01243.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2207C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5661 | chr14 | 104721000 | ||||||
chr14:104721003 | T | C | 1 | a0012c0024t0054 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2210T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5664 | chr14 | 104721003 | ||||||
chr14:104721024 | GCGTCGTC others(2): Show |
G | 4 | a0001c0001t0004 a0001c0001t0075 a0001c0001t0076 others(1): Show |
18 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2235_*2243delCGTC others(5): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5689 | INFO_REALIGN_3_PRIME | chr14 | 104721024 | |||||
chr14:104721024 | GCGTCGTC others(36): Show |
G | 1 | a0012c0024t0054 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2235_*2277delCGTC others(39): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5689 | INFO_REALIGN_3_PRIME | chr14 | 104721024 | |||||
chr14:104721035 | G | C | 1 | a0001c0001t0057 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2242G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5696 | chr14 | 104721035 | ||||||
chr14:104721038 | T | C | 1 | a0012c0024t0055 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2245T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5699 | chr14 | 104721038 | ||||||
chr14:104721059 | GCGTAGTC others(1): Show |
G | 75 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(72): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
3_prime_UTR_variant | MODIFIER | c.*2270_*2277delAGTC others(4): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5724 | INFO_REALIGN_3_PRIME | chr14 | 104721059 | |||||
chr14:104721061 | G | A | 1 | a0001c0001t0004 | 3 | HG02976.hp2 HG03486.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2268G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5722 | chr14 | 104721061 | ||||||
chr14:104721063 | A | C | 9 | a0001c0001t0050 a0001c0001t0057 a0003c0043t0011 others(6): Show |
14 | HG00735.hp2 HG01243.hp2 HG02451.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2270A>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5724 | chr14 | 104721063 | ||||||
chr14:104721065 | T | TCCTCCTG others(29): Show |
6 | a0003c0043t0011 a0004c0006t0011 a0004c0006t0029 others(3): Show |
10 | HG00735.hp2 HG01243.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2273_*2274insCTCC others(32): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5728 | INFO_REALIGN_3_PRIME | chr14 | 104721065 | |||||
chr14:104721066 | C | CCTCGTGT others(90): Show |
1 | a0006c0008t0037 | 2 | NA18986.hp1 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2273_*2274insCTCG others(93): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5728 | chr14 | 104721066 | ||||||
chr14:104721067 | T | G | 5 | a0001c0001t0004 a0001c0001t0075 a0001c0001t0076 others(2): Show |
20 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2274T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5728 | chr14 | 104721067 | ||||||
chr14:104721069 | G | C | 1 | a0001c0001t0050 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2276G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5730 | chr14 | 104721069 | ||||||
chr14:104721089 | G | T | 4 | a0001c0001t0004 a0001c0001t0075 a0001c0001t0076 others(1): Show |
18 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2296G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5750 | chr14 | 104721089 | ||||||
chr14:104721097 | A | C | 1 | a0001c0001t0050 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2304A>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5758 | chr14 | 104721097 | ||||||
chr14:104721118 | T | C | 4 | a0001c0001t0004 a0001c0001t0075 a0001c0001t0076 others(1): Show |
18 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2325T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5779 | chr14 | 104721118 | ||||||
chr14:104721131 | C | T | 1 | a0001c0001t0033 | 2 | HG01167.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2338C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5792 | chr14 | 104721131 | ||||||
chr14:104721132 | G | A | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(52): Show |
229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*2339G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5793 | chr14 | 104721132 | ||||||
chr14:104721182 | A | G | 15 | a0001c0001t0003 a0001c0001t0057 a0001c0002t0003 others(12): Show |
44 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2389A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5843 | chr14 | 104721182 | ||||||
chr14:104721188 | G | A | 8 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0018 others(5): Show |
33 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2395G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5849 | chr14 | 104721188 | ||||||
chr14:104721230 | C | T | 14 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0018 others(11): Show |
41 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2437C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5891 | chr14 | 104721230 | ||||||
chr14:104721290 | C | T | 1 | a0001c0001t0047 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2497C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5951 | chr14 | 104721290 | ||||||
chr14:104721325 | G | A | 103 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(100): Show |
338 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(335): Show |
3_prime_UTR_variant | MODIFIER | c.*2532G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 5986 | chr14 | 104721325 | ||||||
chr14:104721511 | T | G | 1 | a0001c0035t0052 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2718T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6172 | chr14 | 104721511 | ||||||
chr14:104721645 | T | A | 2 | a0001c0005t0035 a0024c0039t0035 |
2 | NA19043.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2852T>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6306 | chr14 | 104721645 | ||||||
chr14:104721690 | A | G | 1 | a0003c0010t0068 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2897A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6351 | chr14 | 104721690 | ||||||
chr14:104721712 | C | T | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(52): Show |
229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*2919C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6373 | chr14 | 104721712 | ||||||
chr14:104721894 | G | A | 3 | a0001c0001t0027 a0001c0041t0027 a0020c0052t0027 |
3 | NA18946.hp1 NA18981.hp2 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3101G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6555 | chr14 | 104721894 | ||||||
chr14:104721903 | C | T | 5 | a0001c0002t0026 a0001c0002t0036 a0001c0002t0061 others(2): Show |
10 | HG00733.hp2 HG01074.hp1 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3110C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6564 | chr14 | 104721903 | ||||||
chr14:104721997 | A | G | 1 | a0001c0009t0056 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3204A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6658 | chr14 | 104721997 | ||||||
chr14:104722122 | T | G | 1 | a0004c0006t0029 | 2 | HG01243.hp2 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3329T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6783 | chr14 | 104722122 | ||||||
chr14:104722126 | G | A | 1 | a0001c0001t0076 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3333G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6787 | chr14 | 104722126 | ||||||
chr14:104722177 | G | A | 1 | a0001c0002t0061 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3384G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6838 | chr14 | 104722177 | ||||||
chr14:104722207 | T | C | 1 | a0004c0006t0029 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3414T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6868 | chr14 | 104722207 | ||||||
chr14:104722244 | C | T | 1 | a0001c0001t0066 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3451C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6905 | chr14 | 104722244 | ||||||
chr14:104722273 | G | A | 2 | a0001c0005t0035 a0024c0039t0035 |
2 | NA19043.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3480G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 6934 | chr14 | 104722273 | ||||||
chr14:104722364 | T | A | 1 | a0002c0003t0074 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3571T>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 7025 | chr14 | 104722364 | ||||||
chr14:104722499 | G | A | 14 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0018 others(11): Show |
41 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*3706G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 23/23 | 7160 | chr14 | 104722499 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:104689843 | G | A | 24 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(21): Show |
40 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.-10+104G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104689843 | |||||||
chr14:104690040 | C | A | 1 | a0004c0006t0011g0070 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-10+301C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690040 | |||||||
chr14:104690073 | G | A | 38 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0002g0025 others(35): Show |
54 | HG00140.hp2 HG00408.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.-10+334G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690073 | |||||||
chr14:104690156 | T | C | 1 | a0001c0001t0033g0031 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-10+417T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690156 | |||||||
chr14:104690336 | C | A | 1 | a0001c0001t0001g0055 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-10+597C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690336 | |||||||
chr14:104690419 | A | G | 137 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0177 others(134): Show |
198 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.-10+680A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690419 | |||||||
chr14:104690443 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0100 a0001c0001t0001g0101 others(1): Show |
6 | NA18973.hp1 NA18979.hp2 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+704G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690443 | |||||||
chr14:104690606 | G | A | 42 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0002g0025 others(39): Show |
60 | HG00140.hp2 HG00408.hp2 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.-10+867G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690606 | |||||||
chr14:104690705 | C | T | 42 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0002g0025 others(39): Show |
61 | HG00140.hp2 HG00408.hp2 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.-10+966C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690705 | |||||||
chr14:104690706 | G | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0169 a0001c0001t0001g0170 others(1): Show |
6 | HG02280.hp1 HG02922.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+967G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690706 | |||||||
chr14:104690784 | G | A | 5 | a0001c0001t0001g0177 a0001c0001t0002g0176 a0001c0014t0014g0045 others(2): Show |
6 | HG00609.hp1 HG03704.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+1045G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690784 | |||||||
chr14:104690862 | G | A | 1 | a0001c0001t0057g0178 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-10+1123G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690862 | |||||||
chr14:104690891 | A | G | 30 | a0001c0001t0001g0227 a0001c0001t0017g0215 a0001c0001t0017g0217 others(27): Show |
37 | HG00099.hp1 HG00673.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.-10+1152A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690891 | |||||||
chr14:104690981 | G | A | 46 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0002g0001 others(43): Show |
74 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.-10+1242G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104690981 | |||||||
chr14:104690992 | GGGCCCTG others(4): Show |
G | 3 | a0001c0017t0004g0171 a0003c0010t0016g0054 a0003c0045t0016g0054 |
3 | HG02572.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-10+1264_-10+1274d others(13): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr14 | 104690992 | ||||||
chr14:104691114 | G | C | 2 | a0012c0024t0054g0032 a0012c0024t0055g0032 |
2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-10+1375G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691114 | |||||||
chr14:104691142 | G | A | 6 | a0004c0006t0011g0070 a0004c0006t0011g0104 a0008c0015t0015g0015 others(3): Show |
8 | HG00733.hp2 HG00735.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+1403G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691142 | |||||||
chr14:104691204 | G | A | 5 | a0001c0001t0024g0033 a0001c0001t0058g0033 a0001c0005t0023g0106 others(2): Show |
5 | HG00741.hp2 HG01081.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+1465G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691204 | |||||||
chr14:104691328 | G | A | 1 | a0001c0001t0002g0025 | 2 | HG00408.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.-10+1589G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691328 | |||||||
chr14:104691439 | T | C | 1 | a0001c0009t0007g0108 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-10+1700T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691439 | |||||||
chr14:104691470 | G | A | 1 | a0001c0001t0017g0215 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-10+1731G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691470 | |||||||
chr14:104691480 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0007g0166 |
2 | NA18951.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-10+1741C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691480 | |||||||
chr14:104691534 | C | G | 1 | a0002c0048t0043g0231 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-10+1795C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691534 | |||||||
chr14:104691646 | C | T | 2 | a0001c0001t0002g0010 a0001c0001t0002g0206 |
5 | NA18986.hp2 NA19009.hp1 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+1907C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691646 | |||||||
chr14:104691707 | C | T | 40 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0002g0025 others(37): Show |
58 | HG00140.hp2 HG00408.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.-10+1968C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691707 | |||||||
chr14:104691726 | CA | C | 5 | a0001c0001t0001g0177 a0001c0001t0002g0176 a0001c0014t0014g0045 others(2): Show |
6 | HG00609.hp1 HG03704.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+1988delA | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691726 | |||||||
chr14:104691818 | C | T | 3 | a0002c0013t0013g0019 a0002c0013t0013g0172 a0002c0046t0001g0173 |
5 | HG02572.hp1 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+2079C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691818 | |||||||
chr14:104691974 | G | T | 1 | a0004c0006t0011g0070 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-10+2235G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104691974 | |||||||
chr14:104692034 | A | G | 56 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0002g0025 others(53): Show |
75 | HG00140.hp2 HG00408.hp2 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.-10+2295A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692034 | |||||||
chr14:104692056 | G | A | 1 | a0001c0001t0009g0109 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-10+2317G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692056 | |||||||
chr14:104692088 | G | A | 1 | a0001c0001t0010g0110 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10+2349G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692088 | |||||||
chr14:104692101 | C | T | 6 | a0003c0010t0016g0053 a0003c0010t0016g0054 a0003c0010t0016g0229 others(3): Show |
6 | HG02572.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+2362C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692101 | |||||||
chr14:104692199 | C | T | 3 | a0001c0001t0001g0177 a0001c0001t0002g0176 a0001c0020t0014g0175 |
3 | HG00609.hp1 HG03704.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-10+2460C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692199 | |||||||
chr14:104692212 | C | G | 2 | a0002c0003t0005g0052 a0002c0003t0005g0228 |
3 | HG01257.hp2 HG01433.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.-10+2473C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692212 | |||||||
chr14:104692473 | G | A | 1 | a0008c0032t0015g0103 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-10+2734G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692473 | |||||||
chr14:104692666 | C | T | 2 | a0001c0001t0002g0204 a0001c0001t0002g0205 |
2 | HG00733.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-10+2927C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692666 | |||||||
chr14:104692671 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-10+2932C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692671 | |||||||
chr14:104692690 | C | T | 40 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0002g0025 others(37): Show |
58 | HG00140.hp2 HG00408.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.-10+2951C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692690 | |||||||
chr14:104692691 | G | A | 1 | a0002c0003t0042g0216 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-10+2952G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692691 | |||||||
chr14:104692770 | G | A | 1 | a0001c0002t0070g0111 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-10+3031G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692770 | |||||||
chr14:104692901 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-10+3162A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692901 | |||||||
chr14:104692961 | A | C | 2 | a0001c0001t0033g0031 a0001c0017t0004g0171 |
3 | HG01167.hp1 HG01169.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-10+3222A>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104692961 | |||||||
chr14:104693183 | T | C | 5 | a0001c0001t0033g0031 a0001c0002t0070g0111 a0001c0022t0071g0112 others(2): Show |
6 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+3444T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693183 | |||||||
chr14:104693201 | C | T | 3 | a0002c0013t0013g0019 a0002c0013t0013g0172 a0002c0046t0001g0173 |
5 | HG02572.hp1 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+3462C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693201 | |||||||
chr14:104693256 | G | C | 1 | a0001c0002t0003g0072 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-10+3517G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693256 | |||||||
chr14:104693295 | T | C | 1 | a0001c0001t0002g0179 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-10+3556T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693295 | |||||||
chr14:104693372 | T | G | 1 | a0001c0017t0004g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-10+3633T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693372 | |||||||
chr14:104693410 | G | A | 1 | a0007c0029t0003g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-10+3671G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693410 | |||||||
chr14:104693422 | G | A | 10 | a0001c0001t0004g0163 a0001c0001t0024g0033 a0001c0001t0058g0033 others(7): Show |
10 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10+3683G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693422 | |||||||
chr14:104693453 | T | A | 10 | a0001c0001t0004g0163 a0001c0001t0024g0033 a0001c0001t0058g0033 others(7): Show |
10 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10+3714T>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693453 | |||||||
chr14:104693719 | T | C | 1 | a0001c0001t0002g0025 | 2 | HG00408.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.-10+3980T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693719 | |||||||
chr14:104693824 | G | A | 1 | a0001c0001t0009g0114 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-10+4085G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693824 | |||||||
chr14:104693875 | C | T | 3 | a0001c0001t0001g0177 a0001c0001t0002g0176 a0001c0020t0014g0175 |
3 | HG00609.hp1 HG03704.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-10+4136C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693875 | |||||||
chr14:104693895 | G | A | 1 | a0001c0001t0017g0217 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-10+4156G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104693895 | |||||||
chr14:104694178 | C | T | 4 | a0001c0002t0026g0157 a0001c0002t0026g0159 a0001c0002t0036g0158 others(1): Show |
4 | HG01074.hp1 HG02809.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+4439C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694178 | |||||||
chr14:104694377 | G | A | 1 | a0002c0003t0005g0051 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-10+4638G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694377 | |||||||
chr14:104694449 | G | A | 1 | a0010c0011t0040g0115 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-10+4710G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694449 | |||||||
chr14:104694499 | C | T | 3 | a0001c0005t0023g0154 a0011c0018t0025g0044 a0011c0018t0060g0155 |
4 | HG02257.hp2 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+4760C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694499 | |||||||
chr14:104694543 | C | G | 1 | a0001c0004t0001g0069 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-10+4804C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694543 | |||||||
chr14:104694565 | G | A | 9 | a0001c0001t0004g0163 a0001c0001t0024g0033 a0001c0001t0058g0033 others(6): Show |
9 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10+4826G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694565 | |||||||
chr14:104694571 | G | T | 1 | a0001c0001t0063g0203 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-10+4832G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694571 | |||||||
chr14:104694642 | G | A | 21 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0002g0025 others(18): Show |
35 | HG00140.hp2 HG00408.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.-10+4903G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694642 | |||||||
chr14:104694673 | C | T | 3 | a0002c0013t0013g0019 a0002c0013t0013g0172 a0002c0046t0001g0173 |
5 | HG02572.hp1 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+4934C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694673 | |||||||
chr14:104694716 | G | C | 1 | a0001c0001t0063g0203 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-10+4977G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694716 | |||||||
chr14:104694844 | G | A | 1 | a0001c0009t0008g0118 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-10+5105G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694844 | |||||||
chr14:104694938 | G | A | 31 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(28): Show |
45 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.-10+5199G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694938 | |||||||
chr14:104694952 | A | G | 53 | a0001c0001t0001g0068 a0001c0001t0001g0151 a0001c0001t0001g0153 others(50): Show |
83 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.-10+5213A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694952 | |||||||
chr14:104694988 | G | A | 2 | a0001c0002t0003g0026 a0001c0002t0003g0074 |
3 | HG02723.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-10+5249G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104694988 | |||||||
chr14:104695045 | T | C | 3 | a0002c0013t0013g0019 a0002c0013t0013g0172 a0002c0046t0001g0173 |
5 | HG02572.hp1 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+5306T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695045 | |||||||
chr14:104695052 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-10+5313T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695052 | |||||||
chr14:104695117 | C | A | 1 | a0001c0001t0002g0182 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-10+5378C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695117 | |||||||
chr14:104695125 | A | C | 1 | a0021c0028t0005g0218 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-10+5386A>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695125 | |||||||
chr14:104695125 | A | T | 70 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(67): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.-10+5386A>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695125 | |||||||
chr14:104695142 | T | C | 5 | a0001c0001t0012g0086 a0001c0001t0012g0087 a0001c0001t0012g0088 others(2): Show |
5 | HG01099.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+5403T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695142 | |||||||
chr14:104695145 | G | A | 6 | a0003c0010t0016g0053 a0003c0010t0016g0054 a0003c0010t0016g0229 others(3): Show |
6 | HG02572.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+5406G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695145 | |||||||
chr14:104695153 | C | T | 1 | a0001c0001t0075g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-10+5414C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695153 | |||||||
chr14:104695198 | G | A | 9 | a0001c0001t0004g0163 a0001c0001t0024g0033 a0001c0001t0058g0033 others(6): Show |
9 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10+5459G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695198 | |||||||
chr14:104695238 | C | T | 1 | a0001c0001t0002g0202 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-10+5499C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695238 | |||||||
chr14:104695239 | G | A | 1 | a0001c0001t0006g0059 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-10+5500G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695239 | |||||||
chr14:104695299 | C | CA | 4 | a0001c0001t0001g0177 a0001c0001t0002g0176 a0001c0020t0014g0175 others(1): Show |
4 | HG00609.hp1 HG02132.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+5561dupA | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr14 | 104695299 | ||||||
chr14:104695311 | C | T | 3 | a0001c0002t0070g0111 a0001c0022t0071g0112 a0001c0022t0072g0113 |
3 | HG00639.hp1 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-10+5572C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695311 | |||||||
chr14:104695337 | C | G | 49 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(46): Show |
68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-10+5598C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695337 | |||||||
chr14:104695377 | C | T | 1 | a0004c0006t0030g0097 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-10+5638C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695377 | |||||||
chr14:104695427 | C | T | 1 | a0001c0001t0017g0215 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-10+5688C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695427 | |||||||
chr14:104695446 | C | T | 1 | a0017c0034t0001g0058 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-10+5707C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695446 | |||||||
chr14:104695463 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-10+5724G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695463 | |||||||
chr14:104695580 | A | ACACCCCT others(12): Show |
4 | a0002c0003t0005g0052 a0002c0003t0005g0225 a0002c0003t0042g0216 others(1): Show |
5 | HG00323.hp1 HG01106.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-5776_-9-5775ins others(19): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr14 | 104695580 | ||||||
chr14:104695580 | A | ACACCCCT others(28): Show |
24 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(21): Show |
34 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.-9-5776_-9-5775ins others(35): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr14 | 104695580 | ||||||
chr14:104695582 | T | C | 28 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(25): Show |
39 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.-9-5775T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695582 | |||||||
chr14:104695582 | T | TCTCCTCC others(25): Show |
13 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0120 others(10): Show |
18 | HG01074.hp1 HG01255.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-5746_-9-5745ins others(32): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr14 | 104695582 | ||||||
chr14:104695587 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-9-5770T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695587 | |||||||
chr14:104695717 | T | C | 91 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(88): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.-9-5640T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695717 | |||||||
chr14:104695822 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-9-5535G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695822 | |||||||
chr14:104695920 | C | T | 163 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(160): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.-9-5437C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695920 | |||||||
chr14:104695956 | G | A | 2 | a0001c0002t0003g0075 a0001c0002t0003g0117 |
2 | HG00741.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.-9-5401G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104695956 | |||||||
chr14:104696006 | T | C | 16 | a0001c0001t0001g0208 a0001c0001t0004g0011 a0001c0001t0004g0022 others(13): Show |
22 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.-9-5351T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696006 | |||||||
chr14:104696011 | C | T | 6 | a0003c0010t0016g0053 a0003c0010t0016g0054 a0003c0010t0016g0229 others(3): Show |
6 | HG02572.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-5346C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696011 | |||||||
chr14:104696049 | G | A | 5 | a0001c0001t0001g0122 a0003c0010t0016g0229 a0009c0012t0001g0121 others(2): Show |
6 | HG02055.hp1 HG02109.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-5308G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696049 | |||||||
chr14:104696082 | G | A | 2 | a0001c0001t0001g0208 a0001c0001t0004g0022 |
4 | HG02976.hp2 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-5275G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696082 | |||||||
chr14:104696125 | T | C | 169 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0055 others(166): Show |
235 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.-9-5232T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696125 | |||||||
chr14:104696156 | T | A | 20 | a0001c0001t0004g0163 a0001c0001t0024g0033 a0001c0001t0058g0033 others(17): Show |
22 | HG00735.hp2 HG00741.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.-9-5201T>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696156 | |||||||
chr14:104696224 | C | T | 3 | a0001c0001t0002g0176 a0001c0020t0014g0175 a0001c0020t0044g0226 |
3 | HG00609.hp1 HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-9-5133C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696224 | |||||||
chr14:104696470 | C | A | 12 | a0002c0003t0005g0051 a0002c0003t0005g0219 a0002c0003t0005g0220 others(9): Show |
15 | HG00735.hp2 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.-9-4887C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696470 | |||||||
chr14:104696544 | C | G | 1 | a0001c0001t0001g0149 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-9-4813C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696544 | |||||||
chr14:104696640 | G | A | 3 | a0001c0001t0002g0176 a0001c0020t0014g0175 a0001c0020t0044g0226 |
3 | HG00609.hp1 HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-9-4717G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696640 | |||||||
chr14:104696735 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-9-4622G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696735 | |||||||
chr14:104696742 | C | G | 1 | a0002c0013t0013g0019 | 3 | HG02572.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-9-4615C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696742 | |||||||
chr14:104696805 | A | G | 166 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(163): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.-9-4552A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696805 | |||||||
chr14:104696991 | C | T | 1 | a0001c0009t0007g0201 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-9-4366C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104696991 | |||||||
chr14:104697027 | G | A | 5 | a0001c0001t0012g0086 a0001c0001t0012g0087 a0001c0001t0012g0088 others(2): Show |
5 | HG01099.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-4330G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697027 | |||||||
chr14:104697090 | C | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(30): Show |
47 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.-9-4267C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697090 | |||||||
chr14:104697195 | C | T | 109 | a0001c0001t0001g0193 a0001c0001t0001g0208 a0001c0001t0002g0001 others(106): Show |
145 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(142): Show |
intron_variant | MODIFIER | c.-9-4162C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697195 | |||||||
chr14:104697209 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-9-4148G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697209 | |||||||
chr14:104697223 | T | C | 144 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(141): Show |
194 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.-9-4134T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697223 | |||||||
chr14:104697279 | G | A | 2 | a0007c0016t0002g0047 a0007c0016t0002g0187 |
3 | HG00642.hp2 HG01358.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.-9-4078G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697279 | |||||||
chr14:104697501 | T | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0131 a0001c0001t0001g0133 others(8): Show |
13 | HG00438.hp2 HG00621.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-3856T>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697501 | |||||||
chr14:104697515 | G | T | 1 | a0001c0002t0061g0160 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-9-3842G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697515 | |||||||
chr14:104697533 | C | A | 1 | a0001c0020t0014g0175 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-9-3824C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697533 | |||||||
chr14:104697729 | C | T | 2 | a0001c0001t0001g0128 a0001c0036t0001g0129 |
2 | HG02027.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.-9-3628C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697729 | |||||||
chr14:104697780 | C | T | 1 | a0009c0012t0022g0123 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-9-3577C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697780 | |||||||
chr14:104697861 | C | A | 3 | a0001c0001t0033g0031 a0012c0024t0054g0032 a0012c0024t0055g0032 |
4 | HG01167.hp1 HG01169.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-3496C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697861 | |||||||
chr14:104697888 | G | T | 57 | a0001c0001t0001g0193 a0001c0001t0002g0001 a0001c0001t0002g0010 others(54): Show |
84 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.-9-3469G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697888 | |||||||
chr14:104697894 | G | C | 5 | a0001c0001t0012g0086 a0001c0001t0012g0087 a0001c0001t0012g0088 others(2): Show |
5 | HG01099.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-3463G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697894 | |||||||
chr14:104697896 | T | G | 1 | a0001c0005t0039g0162 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-9-3461T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697896 | |||||||
chr14:104697906 | G | A | 1 | a0002c0003t0028g0221 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-9-3451G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697906 | |||||||
chr14:104697948 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0073g0134 |
3 | HG00323.hp2 HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-9-3409G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104697948 | |||||||
chr14:104698032 | G | C | 1 | a0001c0001t0004g0209 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-9-3325G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104698032 | |||||||
chr14:104698043 | G | A | 1 | a0001c0002t0070g0111 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-9-3314G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104698043 | |||||||
chr14:104698131 | G | A | 1 | a0001c0005t0023g0154 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-9-3226G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104698131 | |||||||
chr14:104698194 | C | G | 1 | a0001c0001t0002g0204 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-9-3163C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104698194 | |||||||
chr14:104698334 | C | G | 1 | a0001c0002t0070g0111 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-9-3023C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104698334 | |||||||
chr14:104698338 | C | G | 28 | a0001c0001t0001g0208 a0001c0001t0004g0011 a0001c0001t0004g0022 others(25): Show |
35 | HG00741.hp2 HG01081.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.-9-3019C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104698338 | |||||||
chr14:104698380 | G | C | 1 | a0003c0043t0011g0096 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-9-2977G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104698380 | |||||||
chr14:104698418 | C | T | 1 | a0007c0016t0002g0187 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-9-2939C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104698418 | |||||||
chr14:104698597 | C | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(30): Show |
47 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.-9-2760C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104698597 | |||||||
chr14:104698806 | G | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0135 |
3 | HG00099.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-9-2551G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104698806 | |||||||
chr14:104698893 | A | G | 54 | a0001c0001t0001g0128 a0001c0001t0001g0208 a0001c0001t0004g0011 others(51): Show |
63 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.-9-2464A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104698893 | |||||||
chr14:104699201 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-9-2156C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104699201 | |||||||
chr14:104699242 | C | T | 4 | a0001c0001t0012g0087 a0001c0001t0012g0088 a0001c0001t0012g0089 others(1): Show |
4 | HG01099.hp1 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-2115C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104699242 | |||||||
chr14:104699448 | G | A | 6 | a0003c0010t0016g0053 a0003c0010t0016g0054 a0003c0010t0016g0229 others(3): Show |
6 | HG02572.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-1909G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104699448 | |||||||
chr14:104699480 | G | A | 3 | a0003c0010t0016g0053 a0003c0010t0016g0229 a0003c0010t0069g0053 |
3 | HG03041.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-9-1877G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104699480 | |||||||
chr14:104699535 | G | C | 52 | a0001c0001t0001g0128 a0001c0001t0001g0208 a0001c0001t0004g0011 others(49): Show |
61 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.-9-1822G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104699535 | |||||||
chr14:104699665 | A | G | 52 | a0001c0001t0001g0128 a0001c0001t0001g0208 a0001c0001t0004g0011 others(49): Show |
61 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.-9-1692A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104699665 | |||||||
chr14:104699679 | G | A | 1 | a0001c0004t0001g0024 | 2 | NA19010.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-9-1678G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104699679 | |||||||
chr14:104699769 | G | A | 52 | a0001c0001t0001g0128 a0001c0001t0001g0208 a0001c0001t0004g0011 others(49): Show |
61 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.-9-1588G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104699769 | |||||||
chr14:104699785 | A | G | 52 | a0001c0001t0001g0128 a0001c0001t0001g0208 a0001c0001t0004g0011 others(49): Show |
61 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.-9-1572A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104699785 | |||||||
chr14:104699915 | C | T | 58 | a0001c0001t0001g0193 a0001c0001t0002g0001 a0001c0001t0002g0010 others(55): Show |
85 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.-9-1442C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104699915 | |||||||
chr14:104699937 | T | C | 138 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0128 others(135): Show |
190 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.-9-1420T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104699937 | |||||||
chr14:104700113 | G | A | 1 | a0001c0001t0009g0126 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-9-1244G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104700113 | |||||||
chr14:104700171 | C | T | 2 | a0011c0018t0025g0044 a0011c0018t0060g0155 |
3 | HG02647.hp2 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-9-1186C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104700171 | |||||||
chr14:104700500 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-9-857C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104700500 | |||||||
chr14:104700522 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-9-835C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104700522 | |||||||
chr14:104700683 | A | T | 49 | a0001c0001t0001g0208 a0001c0001t0004g0011 a0001c0001t0004g0022 others(46): Show |
58 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.-9-674A>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104700683 | |||||||
chr14:104700775 | C | T | 43 | a0001c0001t0001g0208 a0001c0001t0004g0011 a0001c0001t0004g0022 others(40): Show |
52 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.-9-582C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104700775 | |||||||
chr14:104700785 | G | C | 3 | a0001c0001t0004g0210 a0001c0001t0004g0211 a0001c0001t0004g0212 |
3 | HG01891.hp1 HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-9-572G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104700785 | |||||||
chr14:104700980 | C | T | 50 | a0001c0001t0001g0208 a0001c0001t0004g0011 a0001c0001t0004g0022 others(47): Show |
59 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.-9-377C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104700980 | |||||||
chr14:104701117 | G | T | 1 | a0001c0022t0072g0113 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-9-240G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104701117 | |||||||
chr14:104701118 | C | G | 1 | a0001c0001t0027g0200 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-9-239C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104701118 | |||||||
chr14:104701320 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0153 |
2 | HG01109.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-9-37C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 1/22 | chr14 | 104701320 | |||||||
chr14:104701762 | C | T | 13 | a0001c0001t0001g0208 a0001c0001t0004g0011 a0001c0001t0004g0022 others(10): Show |
19 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
splice_region_variant&intron_variant | LOW | c.391+6C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104701762 | |||||||
chr14:104701773 | G | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0068 a0001c0004t0001g0003 others(10): Show |
27 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.391+17G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104701773 | |||||||
chr14:104701774 | A | T | 5 | a0001c0001t0012g0086 a0001c0002t0026g0157 a0001c0002t0026g0159 others(2): Show |
5 | HG01074.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.391+18A>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104701774 | |||||||
chr14:104701818 | G | A | 1 | a0001c0001t0006g0188 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.391+62G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104701818 | |||||||
chr14:104701879 | G | C | 1 | a0001c0001t0001g0128 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.391+123G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104701879 | |||||||
chr14:104702077 | C | T | 124 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0146 others(121): Show |
172 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.391+321C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702077 | |||||||
chr14:104702084 | A | G | 5 | a0001c0014t0014g0045 a0001c0014t0014g0174 a0001c0020t0014g0175 others(2): Show |
6 | HG00609.hp2 HG02132.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.391+328A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702084 | |||||||
chr14:104702091 | C | T | 39 | a0001c0001t0001g0208 a0001c0001t0004g0011 a0001c0001t0004g0022 others(36): Show |
48 | HG00639.hp1 HG00735.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.391+335C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702091 | |||||||
chr14:104702093 | G | A | 11 | a0001c0001t0012g0086 a0001c0002t0026g0159 a0001c0002t0036g0158 others(8): Show |
14 | HG00733.hp2 HG01884.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.391+337G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702093 | |||||||
chr14:104702178 | C | G | 1 | a0001c0001t0001g0068 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.391+422C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702178 | |||||||
chr14:104702201 | G | C | 1 | a0001c0014t0014g0174 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.391+445G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702201 | |||||||
chr14:104702234 | C | T | 2 | a0012c0024t0054g0032 a0012c0024t0055g0032 |
2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.391+478C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702234 | |||||||
chr14:104702258 | C | T | 1 | a0001c0002t0026g0159 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.391+502C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702258 | |||||||
chr14:104702438 | A | G | 23 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0146 others(20): Show |
39 | HG00140.hp2 HG00408.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.392-667A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702438 | |||||||
chr14:104702502 | T | C | 146 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(143): Show |
196 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.392-603T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702502 | |||||||
chr14:104702556 | T | G | 1 | a0001c0001t0001g0136 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.392-549T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702556 | |||||||
chr14:104702622 | ACAGAGGC others(22): Show |
A | 1 | a0001c0001t0012g0090 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.392-479_392-451del others(29): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr14 | 104702622 | ||||||
chr14:104702748 | T | C | 1 | a0001c0001t0006g0059 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.392-357T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702748 | |||||||
chr14:104702858 | C | G | 6 | a0003c0010t0016g0053 a0003c0010t0016g0054 a0003c0010t0016g0229 others(3): Show |
6 | HG02572.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.392-247C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702858 | |||||||
chr14:104702875 | C | T | 6 | a0003c0010t0016g0053 a0003c0010t0016g0054 a0003c0010t0016g0229 others(3): Show |
6 | HG02572.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.392-230C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702875 | |||||||
chr14:104702914 | G | A | 1 | a0002c0047t0003g0077 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.392-191G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702914 | |||||||
chr14:104702915 | G | T | 1 | a0001c0001t0050g0145 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.392-190G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702915 | |||||||
chr14:104702968 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0100 a0001c0001t0001g0101 |
5 | NA18973.hp1 NA18979.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.392-137G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 2/22 | chr14 | 104702968 | |||||||
chr14:104703666 | T | G | 36 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0146 others(33): Show |
51 | HG00140.hp2 HG00408.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.667+212T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 4/22 | chr14 | 104703666 | |||||||
chr14:104703769 | C | T | 1 | a0020c0052t0027g0198 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.668-147C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 4/22 | chr14 | 104703769 | |||||||
chr14:104703771 | GCATGATG others(2): Show |
G | 9 | a0003c0019t0019g0029 a0003c0019t0020g0091 a0003c0042t0020g0093 others(6): Show |
11 | HG00735.hp2 HG01099.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.668-144_668-136del others(9): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 4/22 | chr14 | 104703771 | |||||||
chr14:104703781 | T | G | 9 | a0003c0019t0019g0029 a0003c0019t0020g0091 a0003c0042t0020g0093 others(6): Show |
11 | HG00735.hp2 HG01099.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.668-135T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 4/22 | chr14 | 104703781 | |||||||
chr14:104703826 | G | A | 23 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0146 others(20): Show |
38 | HG00140.hp2 HG00408.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.668-90G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 4/22 | chr14 | 104703826 | |||||||
chr14:104703838 | T | G | 25 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0146 others(22): Show |
41 | HG00140.hp2 HG00408.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.668-78T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 4/22 | chr14 | 104703838 | |||||||
chr14:104703870 | C | T | 1 | a0001c0001t0033g0031 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.668-46C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 4/22 | chr14 | 104703870 | |||||||
chr14:104703884 | C | T | 16 | a0003c0010t0016g0053 a0003c0010t0016g0054 a0003c0010t0016g0229 others(13): Show |
18 | HG00735.hp2 HG01099.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.668-32C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 4/22 | chr14 | 104703884 | |||||||
chr14:104703885 | G | A | 23 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0146 others(20): Show |
38 | HG00140.hp2 HG00408.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.668-31G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 4/22 | chr14 | 104703885 | |||||||
chr14:104703976 | C | T | 6 | a0003c0010t0016g0053 a0003c0010t0016g0054 a0003c0010t0016g0229 others(3): Show |
6 | HG02572.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.701+27C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104703976 | |||||||
chr14:104704175 | T | C | 2 | a0002c0003t0008g0012 a0002c0003t0074g0012 |
4 | NA18967.hp2 NA18970.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.701+226T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704175 | |||||||
chr14:104704230 | C | G | 2 | a0001c0020t0014g0175 a0001c0020t0044g0226 |
2 | HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.701+281C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704230 | |||||||
chr14:104704293 | G | T | 1 | a0020c0052t0027g0198 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.701+344G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704293 | |||||||
chr14:104704294 | T | G | 1 | a0020c0052t0027g0198 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.701+345T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704294 | |||||||
chr14:104704323 | G | C | 1 | a0001c0004t0001g0137 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.701+374G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704323 | |||||||
chr14:104704415 | C | T | 1 | a0001c0001t0012g0089 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.701+466C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704415 | |||||||
chr14:104704426 | C | T | 1 | a0001c0004t0001g0069 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.701+477C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704426 | |||||||
chr14:104704429 | C | T | 1 | a0006c0008t0037g0048 | 2 | NA18986.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.701+480C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704429 | |||||||
chr14:104704555 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.701+606G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704555 | |||||||
chr14:104704617 | A | G | 1 | a0020c0052t0027g0198 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.701+668A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704617 | |||||||
chr14:104704657 | G | A | 1 | a0001c0001t0076g0213 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.701+708G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704657 | |||||||
chr14:104704685 | C | A | 10 | a0003c0019t0019g0029 a0003c0019t0020g0091 a0003c0042t0020g0093 others(7): Show |
12 | HG00735.hp2 HG01099.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.701+736C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704685 | |||||||
chr14:104704711 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0133 a0001c0001t0017g0215 others(1): Show |
6 | HG02056.hp2 NA18612.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.701+762C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704711 | |||||||
chr14:104704725 | A | G | 1 | a0001c0002t0070g0111 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.701+776A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704725 | |||||||
chr14:104704730 | G | A | 1 | a0001c0051t0002g0190 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.701+781G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704730 | |||||||
chr14:104704763 | C | T | 1 | a0001c0001t0002g0021 | 3 | HG00408.hp1 NA19064.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.701+814C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704763 | |||||||
chr14:104704793 | A | T | 1 | a0002c0003t0005g0224 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.701+844A>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704793 | |||||||
chr14:104704871 | C | T | 27 | a0001c0001t0017g0222 a0001c0009t0056g0060 a0002c0003t0005g0007 others(24): Show |
36 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.701+922C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704871 | |||||||
chr14:104704921 | C | T | 21 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0146 others(18): Show |
36 | HG00140.hp2 HG00408.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.701+972C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104704921 | |||||||
chr14:104705030 | T | TC | 90 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0146 others(87): Show |
118 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.702-1003dupC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr14 | 104705030 | ||||||
chr14:104705145 | G | A | 55 | a0001c0001t0017g0222 a0001c0002t0026g0157 a0001c0002t0026g0159 others(52): Show |
69 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.702-890G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104705145 | |||||||
chr14:104705282 | T | C | 16 | a0003c0010t0016g0053 a0003c0010t0016g0054 a0003c0010t0016g0229 others(13): Show |
18 | HG00735.hp2 HG01099.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.702-753T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104705282 | |||||||
chr14:104705297 | A | T | 1 | a0022c0027t0001g0144 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.702-738A>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104705297 | |||||||
chr14:104705357 | T | C | 89 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0146 others(86): Show |
117 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.702-678T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104705357 | |||||||
chr14:104705369 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.702-666A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104705369 | |||||||
chr14:104705372 | G | A | 1 | a0001c0004t0021g0185 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.702-663G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104705372 | |||||||
chr14:104705416 | CA | C | 85 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0208 others(82): Show |
112 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.702-607delA | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr14 | 104705416 | ||||||
chr14:104705475 | A | G | 62 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0146 others(59): Show |
85 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.702-560A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104705475 | |||||||
chr14:104705510 | G | A | 73 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0146 others(70): Show |
99 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.702-525G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104705510 | |||||||
chr14:104705622 | C | A | 1 | a0001c0022t0071g0112 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.702-413C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104705622 | |||||||
chr14:104705648 | T | C | 9 | a0003c0019t0019g0029 a0003c0019t0020g0091 a0003c0042t0020g0093 others(6): Show |
11 | HG00735.hp2 HG01099.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.702-387T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104705648 | |||||||
chr14:104705978 | G | A | 27 | a0001c0001t0017g0222 a0001c0009t0056g0060 a0002c0003t0005g0007 others(24): Show |
36 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.702-57G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104705978 | |||||||
chr14:104706018 | T | G | 1 | a0021c0028t0005g0218 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.702-17T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104706018 | |||||||
chr14:104706020 | G | C | 1 | a0021c0028t0005g0218 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.702-15G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 5/22 | chr14 | 104706020 | |||||||
chr14:104706192 | C | T | 10 | a0001c0001t0001g0149 a0003c0019t0019g0029 a0003c0019t0020g0091 others(7): Show |
12 | HG00735.hp2 HG01099.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.843+16C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 6/22 | chr14 | 104706192 | |||||||
chr14:104706209 | C | T | 4 | a0001c0014t0014g0045 a0001c0014t0014g0174 a0001c0020t0014g0175 others(1): Show |
5 | HG02132.hp2 NA18952.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.843+33C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 6/22 | chr14 | 104706209 | |||||||
chr14:104706258 | T | G | 1 | a0010c0011t0040g0115 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.843+82T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 6/22 | chr14 | 104706258 | |||||||
chr14:104706263 | C | T | 2 | a0001c0001t0024g0033 a0001c0001t0058g0033 |
2 | HG00741.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.843+87C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 6/22 | chr14 | 104706263 | |||||||
chr14:104706388 | C | T | 2 | a0003c0044t0046g0095 a0008c0032t0015g0103 |
2 | HG00733.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.843+212C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 6/22 | chr14 | 104706388 | |||||||
chr14:104706415 | G | A | 12 | a0001c0001t0033g0031 a0001c0002t0026g0157 a0001c0002t0026g0159 others(9): Show |
16 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.843+239G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 6/22 | chr14 | 104706415 | |||||||
chr14:104706470 | C | T | 2 | a0001c0001t0002g0204 a0001c0001t0002g0205 |
2 | HG00733.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.843+294C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 6/22 | chr14 | 104706470 | |||||||
chr14:104706566 | C | T | 1 | a0003c0043t0011g0096 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.844-344C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 6/22 | chr14 | 104706566 | |||||||
chr14:104706658 | T | C | 2 | a0011c0018t0025g0044 a0011c0018t0060g0155 |
3 | HG02647.hp2 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.844-252T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 6/22 | chr14 | 104706658 | |||||||
chr14:104706788 | C | T | 1 | a0001c0001t0075g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.844-122C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 6/22 | chr14 | 104706788 | |||||||
chr14:104706874 | C | T | 9 | a0001c0002t0026g0157 a0001c0002t0026g0159 a0001c0002t0036g0158 others(6): Show |
12 | HG00733.hp2 HG01074.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.844-36C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 6/22 | chr14 | 104706874 | |||||||
chr14:104707115 | G | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
10 | HG00438.hp1 HG00558.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.985+64G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 7/22 | chr14 | 104707115 | |||||||
chr14:104707116 | G | C | 5 | a0001c0014t0014g0045 a0001c0014t0014g0174 a0001c0017t0004g0049 others(2): Show |
7 | HG02132.hp2 HG02647.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.985+65G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 7/22 | chr14 | 104707116 | |||||||
chr14:104707116 | G | T | 2 | a0001c0041t0027g0197 a0020c0052t0027g0198 |
2 | NA18946.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.985+65G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 7/22 | chr14 | 104707116 | |||||||
chr14:104707117 | G | A | 17 | a0001c0001t0001g0101 a0003c0010t0016g0053 a0003c0010t0016g0054 others(14): Show |
19 | HG00735.hp2 HG01099.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.985+66G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 7/22 | chr14 | 104707117 | |||||||
chr14:104707148 | C | T | 1 | a0004c0006t0030g0094 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.985+97C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 7/22 | chr14 | 104707148 | |||||||
chr14:104708075 | G | A | 1 | a0002c0003t0005g0228 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1735+73G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/22 | chr14 | 104708075 | |||||||
chr14:104708108 | G | A | 18 | a0001c0001t0001g0208 a0001c0001t0004g0011 a0001c0001t0004g0022 others(15): Show |
25 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1735+106G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/22 | chr14 | 104708108 | |||||||
chr14:104708146 | G | A | 1 | a0001c0001t0020g0098 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1735+144G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/22 | chr14 | 104708146 | |||||||
chr14:104708261 | C | T | 27 | a0001c0009t0008g0118 a0001c0009t0056g0060 a0002c0003t0005g0007 others(24): Show |
36 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.1736-175C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/22 | chr14 | 104708261 | |||||||
chr14:104708385 | G | A | 8 | a0003c0019t0019g0029 a0003c0019t0020g0091 a0003c0042t0020g0093 others(5): Show |
10 | HG01099.hp2 HG01243.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.1736-51G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/22 | chr14 | 104708385 | |||||||
chr14:104708388 | A | G | 1 | a0001c0001t0012g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1736-48A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/22 | chr14 | 104708388 | |||||||
chr14:104708394 | C | CG | 14 | a0003c0010t0016g0053 a0003c0010t0016g0054 a0003c0010t0016g0229 others(11): Show |
16 | HG01099.hp2 HG01243.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1736-38dupG | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | 104708394 | ||||||
chr14:104708638 | C | T | 5 | a0001c0001t0012g0086 a0001c0001t0012g0087 a0001c0001t0012g0088 others(2): Show |
5 | HG01099.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1888-33C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 9/22 | chr14 | 104708638 | |||||||
chr14:104708748 | A | G | 47 | a0001c0001t0001g0169 a0001c0001t0004g0011 a0001c0001t0004g0022 others(44): Show |
59 | HG00733.hp2 HG00735.hp2 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.1949+16A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 10/22 | chr14 | 104708748 | |||||||
chr14:104708774 | C | T | 1 | a0001c0022t0072g0113 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1949+42C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 10/22 | chr14 | 104708774 | |||||||
chr14:104708824 | C | T | 1 | a0001c0001t0002g0132 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1949+92C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 10/22 | chr14 | 104708824 | |||||||
chr14:104708873 | A | G | 4 | a0001c0014t0014g0045 a0001c0014t0014g0174 a0001c0020t0014g0175 others(1): Show |
5 | HG02132.hp2 NA18952.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1949+141A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 10/22 | chr14 | 104708873 | |||||||
chr14:104708901 | CT | C | 24 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0146 others(21): Show |
39 | HG00140.hp2 HG00408.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1949+170delT | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 10/22 | chr14 | 104708901 | |||||||
chr14:104708903 | G | A | 24 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0146 others(21): Show |
39 | HG00140.hp2 HG00408.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1949+171G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 10/22 | chr14 | 104708903 | |||||||
chr14:104709028 | G | T | 1 | a0001c0001t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1950-253G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 10/22 | chr14 | 104709028 | |||||||
chr14:104709050 | C | T | 73 | a0001c0001t0001g0014 a0001c0001t0001g0082 a0001c0001t0001g0084 others(70): Show |
89 | HG00408.hp2 HG00639.hp1 HG00733.hp2 others(86): Show |
intron_variant | MODIFIER | c.1950-231C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 10/22 | chr14 | 104709050 | |||||||
chr14:104709117 | C | T | 1 | a0001c0004t0001g0062 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1950-164C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 10/22 | chr14 | 104709117 | |||||||
chr14:104709210 | G | A | 1 | a0007c0029t0003g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1950-71G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 10/22 | chr14 | 104709210 | |||||||
chr14:104709271 | C | A | 1 | a0007c0029t0003g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1950-10C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 10/22 | chr14 | 104709271 | |||||||
chr14:104709717 | C | T | 1 | a0007c0029t0003g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2138+12C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 12/22 | chr14 | 104709717 | |||||||
chr14:104709730 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2138+25C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 12/22 | chr14 | 104709730 | |||||||
chr14:104709807 | A | G | 2 | a0001c0001t0002g0176 a0001c0001t0002g0196 |
2 | HG00609.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.2138+102A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 12/22 | chr14 | 104709807 | |||||||
chr14:104709898 | G | C | 1 | a0001c0001t0001g0082 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2139-190G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 12/22 | chr14 | 104709898 | |||||||
chr14:104710029 | C | G | 1 | a0001c0001t0002g0183 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2139-59C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 12/22 | chr14 | 104710029 | |||||||
chr14:104710244 | C | T | 2 | a0012c0024t0054g0032 a0012c0024t0055g0032 |
2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.2239+56C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | chr14 | 104710244 | |||||||
chr14:104710255 | C | T | 1 | a0002c0003t0005g0052 | 2 | HG01257.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.2239+67C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | chr14 | 104710255 | |||||||
chr14:104710345 | T | C | 27 | a0001c0001t0002g0076 a0001c0002t0003g0004 a0001c0002t0003g0026 others(24): Show |
41 | HG00140.hp2 HG00639.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.2239+157T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | chr14 | 104710345 | |||||||
chr14:104710346 | G | T | 1 | a0001c0001t0001g0056 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2239+158G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | chr14 | 104710346 | |||||||
chr14:104710356 | CG | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(156): Show |
235 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.2239+170delG | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr14 | 104710356 | ||||||
chr14:104710384 | C | A | 1 | a0002c0003t0005g0219 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2239+196C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | chr14 | 104710384 | |||||||
chr14:104710417 | ACACACAC others(27): Show |
A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0130 |
3 | HG00140.hp1 HG02293.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2239+245_2239+278d others(36): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr14 | 104710417 | ||||||
chr14:104710435 | C | T | 1 | a0001c0001t0001g0013 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2239+247C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | chr14 | 104710435 | |||||||
chr14:104710444 | G | A | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(163): Show |
236 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.2239+256G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | chr14 | 104710444 | |||||||
chr14:104710509 | G | A | 1 | a0001c0001t0065g0191 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2239+321G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | chr14 | 104710509 | |||||||
chr14:104710515 | G | A | 1 | a0001c0001t0031g0040 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2239+327G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | chr14 | 104710515 | |||||||
chr14:104710578 | A | C | 3 | a0001c0002t0003g0026 a0001c0002t0003g0071 a0001c0002t0003g0074 |
4 | HG02622.hp2 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2240-359A>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | chr14 | 104710578 | |||||||
chr14:104710637 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2240-300G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 13/22 | chr14 | 104710637 | |||||||
chr14:104711014 | CA | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(193): Show |
280 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(277): Show |
splice_region_variant&intron_variant | LOW | c.2310+8delA | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 14/22 | chr14 | 104711014 | |||||||
chr14:104711229 | C | A | 15 | a0001c0001t0004g0011 a0001c0001t0004g0022 a0001c0001t0004g0125 others(12): Show |
20 | HG01099.hp1 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2418+43C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 15/22 | chr14 | 104711229 | |||||||
chr14:104711273 | C | T | 3 | a0001c0001t0027g0200 a0001c0041t0027g0197 a0020c0052t0027g0198 |
3 | NA18946.hp1 NA18981.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.2418+87C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 15/22 | chr14 | 104711273 | |||||||
chr14:104711316 | T | C | 2 | a0001c0041t0027g0197 a0020c0052t0027g0198 |
2 | NA18946.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.2418+130T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 15/22 | chr14 | 104711316 | |||||||
chr14:104711355 | T | A | 1 | a0001c0001t0031g0040 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2418+169T>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 15/22 | chr14 | 104711355 | |||||||
chr14:104711720 | C | T | 1 | a0001c0020t0014g0175 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2489+21C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104711720 | |||||||
chr14:104711752 | T | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(193): Show |
280 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.2489+53T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104711752 | |||||||
chr14:104711761 | G | C | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(192): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.2489+62G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104711761 | |||||||
chr14:104711813 | C | T | 2 | a0001c0009t0007g0201 a0001c0009t0056g0060 |
2 | NA18982.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.2489+114C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104711813 | |||||||
chr14:104711814 | G | A | 2 | a0001c0020t0014g0175 a0001c0020t0044g0226 |
2 | HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.2489+115G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104711814 | |||||||
chr14:104711816 | C | T | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(192): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.2489+117C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104711816 | |||||||
chr14:104711847 | C | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0020 a0001c0001t0002g0206 others(3): Show |
9 | HG00597.hp2 HG02523.hp2 NA18979.hp1 others(6): Show |
intron_variant | MODIFIER | c.2489+148C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104711847 | |||||||
chr14:104711991 | C | T | 2 | a0012c0024t0054g0032 a0012c0024t0055g0032 |
2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.2489+292C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104711991 | |||||||
chr14:104712080 | A | G | 7 | a0003c0010t0016g0053 a0003c0010t0016g0054 a0003c0010t0016g0229 others(4): Show |
7 | HG02572.hp2 HG02630.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.2490-353A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104712080 | |||||||
chr14:104712132 | G | A | 5 | a0001c0001t0012g0086 a0001c0001t0012g0087 a0001c0001t0012g0088 others(2): Show |
5 | HG01099.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2490-301G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104712132 | |||||||
chr14:104712141 | T | C | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(217): Show |
318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.2490-292T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104712141 | |||||||
chr14:104712146 | C | T | 1 | a0002c0003t0005g0224 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2490-287C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104712146 | |||||||
chr14:104712270 | C | T | 1 | a0001c0004t0001g0062 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2490-163C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104712270 | |||||||
chr14:104712273 | C | T | 1 | a0001c0004t0001g0061 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2490-160C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104712273 | |||||||
chr14:104712397 | C | T | 1 | a0003c0043t0011g0096 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2490-36C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 16/22 | chr14 | 104712397 | |||||||
chr14:104712706 | G | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(234): Show |
338 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.2611-122G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 17/22 | chr14 | 104712706 | |||||||
chr14:104712744 | G | A | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(174): Show |
260 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.2611-84G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 17/22 | chr14 | 104712744 | |||||||
chr14:104712775 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0007g0166 |
2 | NA18951.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2611-53G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 17/22 | chr14 | 104712775 | |||||||
chr14:104712786 | G | A | 1 | a0001c0002t0003g0079 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2611-42G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 17/22 | chr14 | 104712786 | |||||||
chr14:104712787 | C | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0169 a0001c0001t0001g0170 |
5 | HG02922.hp1 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2611-41C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 17/22 | chr14 | 104712787 | |||||||
chr14:104713007 | C | T | 18 | a0001c0001t0004g0011 a0001c0001t0004g0022 a0001c0001t0004g0125 others(15): Show |
25 | HG01099.hp1 HG01167.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.2775+15C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 18/22 | chr14 | 104713007 | |||||||
chr14:104713010 | G | A | 1 | a0001c0001t0006g0192 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2775+18G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 18/22 | chr14 | 104713010 | |||||||
chr14:104713124 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2776-83G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 18/22 | chr14 | 104713124 | |||||||
chr14:104713126 | C | G | 2 | a0001c0020t0014g0175 a0001c0020t0044g0226 |
2 | HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.2776-81C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 18/22 | chr14 | 104713126 | |||||||
chr14:104713184 | C | T | 1 | a0001c0001t0002g0206 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2776-23C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 18/22 | chr14 | 104713184 | |||||||
chr14:104713330 | C | G | 1 | a0001c0005t0039g0165 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2878+21C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 19/22 | chr14 | 104713330 | |||||||
chr14:104713331 | G | T | 2 | a0001c0020t0014g0175 a0001c0020t0044g0226 |
2 | HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.2878+22G>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 19/22 | chr14 | 104713331 | |||||||
chr14:104713332 | G | A | 1 | a0008c0032t0015g0103 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2878+23G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 19/22 | chr14 | 104713332 | |||||||
chr14:104713370 | C | T | 12 | a0001c0001t0024g0033 a0001c0001t0058g0033 a0001c0005t0023g0106 others(9): Show |
12 | HG00741.hp2 HG01081.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.2878+61C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 19/22 | chr14 | 104713370 | |||||||
chr14:104713417 | C | T | 1 | a0001c0001t0006g0192 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2879-28C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 19/22 | chr14 | 104713417 | |||||||
chr14:104713748 | G | A | 2 | a0001c0001t0001g0208 a0001c0001t0053g0124 |
2 | HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3040+142G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 20/22 | chr14 | 104713748 | |||||||
chr14:104713892 | C | A | 2 | a0008c0015t0015g0015 a0008c0032t0015g0103 |
4 | HG00733.hp2 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3040+286C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 20/22 | chr14 | 104713892 | |||||||
chr14:104713967 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0131 a0001c0001t0001g0161 others(2): Show |
7 | HG02056.hp2 NA18612.hp1 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.3041-236T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 20/22 | chr14 | 104713967 | |||||||
chr14:104714057 | C | G | 5 | a0001c0001t0001g0043 a0001c0001t0001g0149 a0001c0001t0001g0151 others(2): Show |
6 | HG00735.hp1 HG01109.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.3041-146C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 20/22 | chr14 | 104714057 | |||||||
chr14:104714128 | G | A | 13 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0041 others(10): Show |
19 | HG01255.hp2 HG01358.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.3041-75G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 20/22 | chr14 | 104714128 | |||||||
chr14:104714131 | A | G | 3 | a0001c0002t0003g0026 a0001c0002t0003g0071 a0001c0002t0003g0074 |
4 | HG02622.hp2 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.3041-72A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 20/22 | chr14 | 104714131 | |||||||
chr14:104714147 | C | T | 228 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(225): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.3041-56C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 20/22 | chr14 | 104714147 | |||||||
chr14:104714962 | A | G | 1 | a0001c0001t0001g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3694+106A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/22 | chr14 | 104714962 | |||||||
chr14:104714979 | G | A | 1 | a0001c0002t0003g0026 | 2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3694+123G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/22 | chr14 | 104714979 | |||||||
chr14:104715200 | C | T | 2 | a0001c0001t0002g0195 a0001c0001t0076g0213 |
2 | HG01884.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.3695-84C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/22 | chr14 | 104715200 | |||||||
chr14:104715233 | G | A | 1 | a0001c0002t0070g0111 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3695-51G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 21/22 | chr14 | 104715233 | |||||||
chr14:104715455 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.*1+115G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715455 | |||||||
chr14:104715511 | A | G | 229 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(226): Show |
329 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.*1+171A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715511 | |||||||
chr14:104715514 | C | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(155): Show |
234 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.*1+174C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715514 | |||||||
chr14:104715525 | C | T | 12 | a0001c0001t0024g0033 a0001c0001t0058g0033 a0001c0005t0023g0106 others(9): Show |
12 | HG00741.hp2 HG01081.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.*1+185C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715525 | |||||||
chr14:104715565 | C | T | 2 | a0001c0001t0001g0122 a0009c0012t0001g0121 |
2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.*1+225C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715565 | |||||||
chr14:104715601 | G | A | 1 | a0001c0001t0010g0110 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.*1+261G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715601 | |||||||
chr14:104715642 | C | G | 1 | a0001c0005t0024g0181 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.*1+302C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715642 | |||||||
chr14:104715649 | C | T | 3 | a0001c0001t0004g0125 a0001c0001t0004g0163 a0001c0001t0004g0209 |
3 | HG02258.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.*1+309C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715649 | |||||||
chr14:104715653 | CCCTGGGG others(28): Show |
C | 1 | a0001c0001t0078g0141 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.*1+315_*1+349delCT others(33): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104715653 | ||||||
chr14:104715668 | G | A | 1 | a0001c0001t0001g0002 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.*1+328G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715668 | |||||||
chr14:104715714 | G | A | 2 | a0001c0002t0003g0079 a0001c0002t0003g0083 |
2 | NA18994.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.*1+374G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715714 | |||||||
chr14:104715754 | C | T | 1 | a0002c0048t0043g0231 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.*1+414C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715754 | |||||||
chr14:104715969 | C | A | 2 | a0012c0024t0054g0032 a0012c0024t0055g0032 |
2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.*1+629C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104715969 | |||||||
chr14:104716118 | C | T | 1 | a0007c0029t0003g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.*1+778C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716118 | |||||||
chr14:104716123 | G | A | 8 | a0001c0002t0026g0050 a0001c0002t0026g0157 a0001c0002t0026g0159 others(5): Show |
10 | HG00733.hp2 HG01074.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.*1+783G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716123 | |||||||
chr14:104716125 | T | C | 1 | a0001c0004t0001g0024 | 2 | NA19010.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.*1+785T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716125 | |||||||
chr14:104716227 | C | G | 8 | a0001c0002t0026g0050 a0001c0002t0026g0157 a0001c0002t0026g0159 others(5): Show |
10 | HG00733.hp2 HG01074.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.*1+887C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716227 | |||||||
chr14:104716253 | C | T | 1 | a0001c0022t0072g0113 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.*1+913C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716253 | |||||||
chr14:104716375 | G | C | 1 | a0002c0003t0005g0052 | 2 | HG01257.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.*1+1035G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716375 | |||||||
chr14:104716412 | C | A | 5 | a0001c0001t0012g0086 a0001c0001t0012g0087 a0001c0001t0012g0088 others(2): Show |
5 | HG01099.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.*1+1072C>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716412 | |||||||
chr14:104716428 | G | A | 2 | a0001c0005t0039g0162 a0001c0005t0039g0165 |
2 | HG01891.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.*1+1088G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716428 | |||||||
chr14:104716554 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0135 |
3 | HG00099.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.*1+1214G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716554 | |||||||
chr14:104716796 | T | G | 1 | a0001c0001t0033g0031 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.*1+1456T>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716796 | |||||||
chr14:104716899 | T | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(199): Show |
288 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.*1+1559T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716899 | |||||||
chr14:104716966 | A | G | 3 | a0001c0038t0025g0168 a0011c0018t0025g0044 a0011c0018t0060g0155 |
4 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.*1+1626A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716966 | |||||||
chr14:104716992 | C | T | 2 | a0001c0020t0014g0175 a0001c0020t0044g0226 |
2 | HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.*1+1652C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104716992 | |||||||
chr14:104717065 | C | T | 9 | a0001c0022t0071g0112 a0001c0022t0072g0113 a0003c0010t0016g0053 others(6): Show |
9 | HG02572.hp2 HG02630.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.*1+1725C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717065 | |||||||
chr14:104717066 | G | A | 2 | a0001c0020t0014g0175 a0001c0020t0044g0226 |
2 | HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.*1+1726G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717066 | |||||||
chr14:104717159 | A | G | 1 | a0002c0003t0005g0223 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.*2-1636A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717159 | |||||||
chr14:104717226 | CCCGGGCA others(32): Show |
C | 10 | a0001c0002t0003g0080 a0001c0005t0023g0106 a0001c0005t0023g0107 others(7): Show |
10 | HG01884.hp1 HG01891.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.*2-1536_*2-1498del others(39): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104717226 | ||||||
chr14:104717257 | CCGCCCCC others(31): Show |
C | 2 | a0001c0001t0058g0033 a0001c0001t0062g0001 |
2 | HG00741.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.*2-1536_*2-1499del others(38): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104717257 | ||||||
chr14:104717265 | A | C | 2 | a0001c0001t0004g0210 a0024c0039t0035g0116 |
2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.*2-1530A>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717265 | |||||||
chr14:104717265 | ACCGGGCA others(68): Show |
A | 2 | a0001c0001t0004g0022 a0001c0002t0070g0111 |
4 | HG00639.hp1 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.*2-1492_*2-1418del others(75): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104717265 | ||||||
chr14:104717276 | T | C | 3 | a0001c0001t0004g0210 a0001c0009t0007g0108 a0024c0039t0035g0116 |
3 | HG02698.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.*2-1519T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717276 | |||||||
chr14:104717292 | C | T | 1 | a0024c0039t0035g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.*2-1503C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717292 | |||||||
chr14:104717292 | CAGTCCCC others(30): Show |
C | 4 | a0001c0022t0071g0112 a0001c0022t0072g0113 a0012c0024t0054g0032 others(1): Show |
4 | HG01516.hp2 HG01981.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.*2-1497_*2-1461del others(37): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104717292 | ||||||
chr14:104717295 | T | TC | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(150): Show |
226 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.*2-1491dupC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104717295 | ||||||
chr14:104717295 | T | TCCCCCCC others(69): Show |
2 | a0001c0001t0010g0110 a0001c0009t0007g0201 |
2 | NA19043.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.*2-1493_*2-1418dup others(76): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104717295 | ||||||
chr14:104717295 | T | TCCCCCCC others(70): Show |
1 | a0001c0009t0056g0060 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.*2-1494_*2-1418dup others(77): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104717295 | ||||||
chr14:104717304 | C | T | 16 | a0001c0002t0003g0004 a0001c0002t0003g0026 a0001c0002t0003g0028 others(13): Show |
29 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.*2-1491C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717304 | |||||||
chr14:104717313 | C | T | 2 | a0001c0001t0001g0167 a0024c0039t0035g0116 |
2 | NA19080.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.*2-1482C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717313 | |||||||
chr14:104717314 | G | A | 2 | a0001c0001t0002g0017 a0001c0001t0002g0132 |
2 | HG00621.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.*2-1481G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717314 | |||||||
chr14:104717329 | T | C | 1 | a0024c0039t0035g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.*2-1466T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717329 | |||||||
chr14:104717335 | G | GCCCCCCC others(28): Show |
1 | a0002c0013t0013g0019 | 3 | HG02572.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.*2-1443_*2-1409dup others(35): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104717335 | ||||||
chr14:104717349 | G | A | 1 | a0006c0008t0002g0184 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.*2-1446G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717349 | |||||||
chr14:104717351 | T | C | 4 | a0001c0022t0071g0112 a0001c0022t0072g0113 a0012c0024t0054g0032 others(1): Show |
4 | HG01516.hp2 HG01981.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.*2-1444T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717351 | |||||||
chr14:104717359 | C | T | 2 | a0001c0020t0014g0175 a0001c0020t0044g0226 |
2 | HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.*2-1436C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717359 | |||||||
chr14:104717370 | T | TCCCCCCC others(70): Show |
1 | a0001c0001t0007g0166 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.*2-1418_*2-1417ins others(77): Show |
INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104717370 | ||||||
chr14:104717371 | C | T | 2 | a0004c0006t0029g0030 a0004c0006t0045g0092 |
3 | HG01243.hp2 HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.*2-1424C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717371 | |||||||
chr14:104717376 | C | T | 1 | a0001c0001t0031g0040 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.*2-1419C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717376 | |||||||
chr14:104717377 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.*2-1418C>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717377 | |||||||
chr14:104717377 | C | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0133 a0001c0001t0049g0152 others(1): Show |
8 | HG00621.hp2 HG02056.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.*2-1418C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717377 | |||||||
chr14:104717401 | T | C | 3 | a0001c0038t0025g0168 a0011c0018t0025g0044 a0011c0018t0060g0155 |
4 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.*2-1394T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717401 | |||||||
chr14:104717412 | A | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(235): Show |
339 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.*2-1383A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717412 | |||||||
chr14:104717573 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.*2-1222C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717573 | |||||||
chr14:104717576 | CT | C | 3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0186 |
3 | HG01109.hp1 HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.*2-1214delT | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104717576 | ||||||
chr14:104717712 | G | C | 2 | a0008c0015t0015g0015 a0008c0032t0015g0103 |
4 | HG00733.hp2 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.*2-1083G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717712 | |||||||
chr14:104717751 | G | C | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(153): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.*2-1044G>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717751 | |||||||
chr14:104717779 | G | A | 2 | a0001c0020t0014g0175 a0001c0020t0044g0226 |
2 | HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.*2-1016G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717779 | |||||||
chr14:104717863 | C | T | 1 | a0001c0001t0004g0212 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.*2-932C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717863 | |||||||
chr14:104717874 | TC | T | 12 | a0001c0001t0004g0011 a0001c0001t0004g0022 a0001c0001t0004g0125 others(9): Show |
18 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.*2-915delC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr14 | 104717874 | ||||||
chr14:104717880 | C | T | 1 | a0001c0001t0078g0141 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.*2-915C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717880 | |||||||
chr14:104717914 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0073g0134 |
2 | HG02698.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.*2-881C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717914 | |||||||
chr14:104717932 | T | A | 2 | a0001c0020t0014g0175 a0001c0020t0044g0226 |
2 | HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.*2-863T>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717932 | |||||||
chr14:104717976 | G | A | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(198): Show |
287 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.*2-819G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104717976 | |||||||
chr14:104718126 | T | C | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(198): Show |
287 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.*2-669T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718126 | |||||||
chr14:104718287 | G | A | 4 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0140 others(1): Show |
5 | HG02135.hp2 HG03654.hp1 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.*2-508G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718287 | |||||||
chr14:104718294 | G | A | 2 | a0001c0020t0014g0175 a0001c0020t0044g0226 |
2 | HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.*2-501G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718294 | |||||||
chr14:104718325 | C | T | 11 | a0001c0001t0024g0033 a0001c0001t0058g0033 a0001c0005t0023g0107 others(8): Show |
11 | HG00741.hp2 HG01081.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.*2-470C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718325 | |||||||
chr14:104718352 | A | G | 229 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(226): Show |
329 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.*2-443A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718352 | |||||||
chr14:104718402 | C | T | 2 | a0001c0001t0001g0193 a0001c0004t0001g0137 |
2 | HG02015.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.*2-393C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718402 | |||||||
chr14:104718471 | T | C | 1 | a0001c0001t0050g0145 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.*2-324T>C | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718471 | |||||||
chr14:104718500 | C | T | 1 | a0001c0001t0033g0031 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.*2-295C>T | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718500 | |||||||
chr14:104718501 | A | G | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(198): Show |
287 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.*2-294A>G | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718501 | |||||||
chr14:104718517 | G | A | 8 | a0001c0002t0026g0050 a0001c0002t0026g0157 a0001c0002t0026g0159 others(5): Show |
10 | HG00733.hp2 HG01074.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.*2-278G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718517 | |||||||
chr14:104718627 | G | A | 1 | a0001c0001t0076g0213 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.*2-168G>A | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718627 | |||||||
chr14:104718746 | TAC | T | 27 | a0001c0001t0003g0194 a0001c0002t0003g0004 a0001c0002t0003g0026 others(24): Show |
41 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.*2-48_*2-47delAC | INF2 | ENSG00000203485.14 | transcript | ENST00000392634.9 | protein_coding | 22/22 | chr14 | 104718746 |