Item | Value |
---|---|
geneid | 23067 |
ensemblid | ENSG00000139718.12 |
hgncid | 29187 |
symbol | SETD1B |
name | SET domain containing 1B, histone lysine methyltransferase |
refseq_nuc | NM_001353345.2 |
refseq_prot | NP_001340274.1 |
ensembl_nuc | ENST00000604567.6 |
ensembl_prot | ENSP00000474253.1 |
mane_status | MANE Select |
chr | chr12 |
start | 121804009 |
end | 121832656 |
strand | + |
ver | v1.2 |
region | chr12:121804009-121832656 |
region5000 | chr12:121799009-121837656 |
regionname0 | SETD1B_chr12_121804009_121832656 |
regionname5000 | SETD1B_chr12_121799009_121837656 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1966 | 199 | 58 | 44 | 55 | 14 | 26 | 39 | SETD1B_chr12_121799009_121837656 | SETD1B | MENSH others(1961): Show |
chr12 | 121799009 | 121837656 |
a0002 | 0/0 | 840 | 22 | 6 | 2 | 10 | 0 | 4 | 6 | SETD1B_chr12_121799009_121837656 | SETD1B | MENSH others(835): Show |
chr12 | 121799009 | 121837656 |
a0003 | 0/0 | 1966 | 8 | 5 | 1 | 1 | 0 | 1 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | MENSH others(1961): Show |
chr12 | 121799009 | 121837656 |
a0004 | 0/0 | 840 | 7 | 3 | 2 | 2 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | MENSH others(835): Show |
chr12 | 121799009 | 121837656 |
a0005 | 0/0 | 723 | 4 | 2 | 1 | 1 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | MENSH others(718): Show |
chr12 | 121799009 | 121837656 |
a0006 | 0/0 | 1966 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | MENSH others(1961): Show |
chr12 | 121799009 | 121837656 |
a0007 | 0/0 | 1966 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | MENSH others(1961): Show |
chr12 | 121799009 | 121837656 |
a0008 | 0/0 | 1966 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | MENSH others(1961): Show |
chr12 | 121799009 | 121837656 |
a0009 | 0/0 | 1966 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | MENSH others(1961): Show |
chr12 | 121799009 | 121837656 |
a0010 | 0/0 | 1966 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | MENSH others(1961): Show |
chr12 | 121799009 | 121837656 |
a0011 | 0/0 | 1966 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | MENSH others(1961): Show |
chr12 | 121799009 | 121837656 |
a0012 | 0/0 | 1966 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | MENSH others(1961): Show |
chr12 | 121799009 | 121837656 |
a0013 | 0/0 | 1966 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | MENSH others(1961): Show |
chr12 | 121799009 | 121837656 |
a0014 | 0/0 | 1966 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | MENSH others(1961): Show |
chr12 | 121799009 | 121837656 |
a0015 | 0/0 | 1966 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | MENSH others(1961): Show |
chr12 | 121799009 | 121837656 |
a0016 | 0/0 | 1966 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | MENSH others(1961): Show |
chr12 | 121799009 | 121837656 |
a0017 | 0/0 | 1966 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | MENSH others(1961): Show |
chr12 | 121799009 | 121837656 |
a0018 | 0/0 | 840 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | MENSH others(835): Show |
chr12 | 121799009 | 121837656 |
a0019 | 0/0 | 1966 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | MENSH others(1961): Show |
chr12 | 121799009 | 121837656 |
a0020 | 0/0 | 1966 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | MENSH others(1961): Show |
chr12 | 121799009 | 121837656 |
a0021 | 0/0 | 1966 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | MENSH others(1961): Show |
chr12 | 121799009 | 121837656 |
a0022 | 0/0 | 1966 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | MENSH others(1961): Show |
chr12 | 121799009 | 121837656 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 5898 | 73 | 23 | 12 | 25 | 3 | 10 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0001c0002 | 0/1 | 5898 | 60 | 0 | 18 | 21 | 8 | 12 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0001c0003 | 1/0 | 5898 | 42 | 28 | 6 | 0 | 3 | 4 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0001c0005 | 0/0 | 5898 | 5 | 3 | 2 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0001c0009 | 0/0 | 5898 | 3 | 1 | 0 | 2 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0001c0012 | 0/0 | 5898 | 2 | 2 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0001c0015 | 0/0 | 5898 | 2 | 0 | 2 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0001c0019 | 0/0 | 5898 | 2 | 1 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0001c0025 | 0/0 | 5898 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0001c0029 | 0/0 | 5898 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0001c0031 | 0/0 | 5898 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0001c0034 | 0/0 | 5898 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0001c0037 | 0/0 | 5898 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0001c0041 | 0/0 | 5898 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0001c0045 | 0/0 | 5898 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0001c0048 | 0/0 | 5898 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0001c0051 | 0/0 | 5898 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0001c0053 | 0/0 | 5898 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0002c0004 | 0/0 | 5899 | 9 | 4 | 1 | 3 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5894): Show |
chr12 | 121799009 | 121837656 | ||
a0002c0006 | 0/0 | 5899 | 5 | 0 | 1 | 3 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5894): Show |
chr12 | 121799009 | 121837656 | ||
a0002c0007 | 0/0 | 5899 | 4 | 0 | 0 | 2 | 0 | 2 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5894): Show |
chr12 | 121799009 | 121837656 | ||
a0002c0013 | 0/0 | 5899 | 2 | 2 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5894): Show |
chr12 | 121799009 | 121837656 | ||
a0002c0032 | 0/0 | 5899 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5894): Show |
chr12 | 121799009 | 121837656 | ||
a0002c0050 | 0/0 | 5899 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5894): Show |
chr12 | 121799009 | 121837656 | ||
a0003c0010 | 0/0 | 5898 | 3 | 3 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0003c0011 | 0/0 | 5898 | 2 | 0 | 0 | 1 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0003c0023 | 0/0 | 5898 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0003c0028 | 0/0 | 5898 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0003c0040 | 0/0 | 5898 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0004c0008 | 0/0 | 5899 | 3 | 1 | 2 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5894): Show |
chr12 | 121799009 | 121837656 | ||
a0004c0020 | 0/0 | 5899 | 2 | 0 | 0 | 2 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5894): Show |
chr12 | 121799009 | 121837656 | ||
a0004c0021 | 0/0 | 5899 | 2 | 2 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5894): Show |
chr12 | 121799009 | 121837656 | ||
a0005c0014 | 0/0 | 5900 | 2 | 1 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5895): Show |
chr12 | 121799009 | 121837656 | ||
a0005c0027 | 0/0 | 5900 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5895): Show |
chr12 | 121799009 | 121837656 | ||
a0005c0036 | 0/0 | 5900 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5895): Show |
chr12 | 121799009 | 121837656 | ||
a0006c0016 | 0/0 | 5898 | 2 | 2 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0006c0030 | 0/0 | 5898 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0007c0017 | 0/0 | 5898 | 2 | 2 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0008c0022 | 0/0 | 5898 | 2 | 0 | 0 | 2 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0009c0018 | 0/0 | 5898 | 2 | 2 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0010c0042 | 0/0 | 5898 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0011c0043 | 0/0 | 5898 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0012c0038 | 0/0 | 5898 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0013c0039 | 0/0 | 5898 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0014c0052 | 0/0 | 5898 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0015c0033 | 0/0 | 5898 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0016c0026 | 0/0 | 5898 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0017c0046 | 0/0 | 5898 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0018c0035 | 0/0 | 5899 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5894): Show |
chr12 | 121799009 | 121837656 | ||
a0019c0049 | 0/0 | 5898 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0020c0047 | 0/0 | 5898 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0021c0024 | 0/0 | 5898 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 | ||
a0022c0044 | 0/0 | 5898 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | ATGGA others(5893): Show |
chr12 | 121799009 | 121837656 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8558 | 3 | 0 | 2 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0001c0001t0002 | 0/0 | 8557 | 47 | 20 | 10 | 11 | 3 | 3 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0001c0001t0003 | 0/0 | 8558 | 2 | 0 | 0 | 2 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0001c0001t0004 | 0/0 | 8556 | 12 | 0 | 0 | 9 | 0 | 3 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8551): Show |
chr12 | 121799009 | 121837656 |
a0001c0001t0008 | 0/0 | 8558 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0001c0001t0010 | 0/0 | 8557 | 2 | 2 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0001c0001t0011 | 0/0 | 8558 | 2 | 0 | 0 | 1 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0001c0001t0020 | 0/0 | 8557 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0001c0001t0021 | 0/0 | 8556 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8551): Show |
chr12 | 121799009 | 121837656 |
a0001c0001t0025 | 0/0 | 8556 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8551): Show |
chr12 | 121799009 | 121837656 |
a0001c0001t0026 | 0/0 | 8557 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0001c0002t0001 | 0/0 | 8558 | 53 | 0 | 16 | 18 | 7 | 12 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0001c0002t0003 | 0/0 | 8558 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0001c0002t0007 | 0/0 | 8559 | 3 | 0 | 1 | 1 | 1 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8554): Show |
chr12 | 121799009 | 121837656 |
a0001c0002t0012 | 0/0 | 8559 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8554): Show |
chr12 | 121799009 | 121837656 |
a0001c0002t0018 | 0/0 | 8558 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0001c0002t0024 | 0/1 | 8558 | 1 | 0 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0001c0003t0002 | 1/0 | 8557 | 4 | 2 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0001c0003t0003 | 0/0 | 8558 | 33 | 22 | 5 | 0 | 3 | 3 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0001c0003t0005 | 0/0 | 8557 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0001c0003t0009 | 0/0 | 8558 | 3 | 3 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0001c0003t0022 | 0/0 | 8558 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0001c0005t0005 | 0/0 | 8557 | 5 | 3 | 2 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0001c0009t0002 | 0/0 | 8557 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0001c0009t0008 | 0/0 | 8558 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0001c0009t0016 | 0/0 | 8557 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0001c0012t0015 | 0/0 | 8557 | 2 | 2 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0001c0015t0003 | 0/0 | 8558 | 2 | 0 | 2 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0001c0019t0014 | 0/0 | 8558 | 2 | 1 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0001c0025t0003 | 0/0 | 8558 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0001c0029t0001 | 0/0 | 8558 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0001c0031t0005 | 0/0 | 8557 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0001c0034t0007 | 0/0 | 8559 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8554): Show |
chr12 | 121799009 | 121837656 |
a0001c0037t0002 | 0/0 | 8557 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0001c0041t0002 | 0/0 | 8557 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0001c0045t0002 | 0/0 | 8557 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0001c0048t0004 | 0/0 | 8556 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8551): Show |
chr12 | 121799009 | 121837656 |
a0001c0051t0004 | 0/0 | 8556 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8551): Show |
chr12 | 121799009 | 121837656 |
a0001c0053t0004 | 0/0 | 8556 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8551): Show |
chr12 | 121799009 | 121837656 |
a0002c0004t0002 | 0/0 | 8558 | 5 | 4 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0002c0004t0004 | 0/0 | 8557 | 4 | 0 | 0 | 3 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0002c0006t0001 | 0/0 | 8559 | 5 | 0 | 1 | 3 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8554): Show |
chr12 | 121799009 | 121837656 |
a0002c0007t0001 | 0/0 | 8559 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8554): Show |
chr12 | 121799009 | 121837656 |
a0002c0007t0006 | 0/0 | 8558 | 2 | 0 | 0 | 1 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0002c0007t0017 | 0/0 | 8558 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0002c0013t0002 | 0/0 | 8558 | 2 | 2 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0002c0032t0012 | 0/0 | 8560 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8555): Show |
chr12 | 121799009 | 121837656 |
a0002c0050t0001 | 0/0 | 8559 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8554): Show |
chr12 | 121799009 | 121837656 |
a0003c0010t0002 | 0/0 | 8557 | 3 | 3 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0003c0011t0006 | 0/0 | 8557 | 2 | 0 | 0 | 1 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0003c0023t0008 | 0/0 | 8558 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0003c0028t0019 | 0/0 | 8558 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0003c0040t0001 | 0/0 | 8558 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0004c0008t0003 | 0/0 | 8559 | 3 | 1 | 2 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8554): Show |
chr12 | 121799009 | 121837656 |
a0004c0020t0001 | 0/0 | 8559 | 2 | 0 | 0 | 2 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8554): Show |
chr12 | 121799009 | 121837656 |
a0004c0021t0002 | 0/0 | 8558 | 2 | 2 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0005c0014t0008 | 0/0 | 8560 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8555): Show |
chr12 | 121799009 | 121837656 |
a0005c0014t0016 | 0/0 | 8559 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8554): Show |
chr12 | 121799009 | 121837656 |
a0005c0027t0005 | 0/0 | 8559 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8554): Show |
chr12 | 121799009 | 121837656 |
a0005c0036t0001 | 0/0 | 8560 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8555): Show |
chr12 | 121799009 | 121837656 |
a0006c0016t0005 | 0/0 | 8557 | 2 | 2 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0006c0030t0005 | 0/0 | 8557 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0007c0017t0005 | 0/0 | 8557 | 2 | 2 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0008c0022t0001 | 0/0 | 8558 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0008c0022t0002 | 0/0 | 8557 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0009c0018t0003 | 0/0 | 8558 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0009c0018t0013 | 0/0 | 8558 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0010c0042t0001 | 0/0 | 8558 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0011c0043t0002 | 0/0 | 8557 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0012c0038t0002 | 0/0 | 8557 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0013c0039t0001 | 0/0 | 8558 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0014c0052t0001 | 0/0 | 8558 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0015c0033t0023 | 0/0 | 8558 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0016c0026t0013 | 0/0 | 8558 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0017c0046t0005 | 0/0 | 8557 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0018c0035t0004 | 0/0 | 8557 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0019c0049t0001 | 0/0 | 8558 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
a0020c0047t0002 | 0/0 | 8557 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0021c0024t0002 | 0/0 | 8557 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8552): Show |
chr12 | 121799009 | 121837656 |
a0022c0044t0001 | 0/0 | 8558 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | GTATT others(8553): Show |
chr12 | 121799009 | 121837656 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0005 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0004g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0008g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0010g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0010g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0011g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0011g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0020g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0021g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0025g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0001t0026g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0001 | 0/0 | 10 | 0 | 3 | 3 | 1 | 3 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0007g0001 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0007g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0012g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0018g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0002t0024g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0002g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0002g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0003 | 0/0 | 7 | 1 | 3 | 0 | 1 | 2 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0009g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0003t0022g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0005t0005g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0005t0005g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0009t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0009t0008g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0009t0016g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0012t0015g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0012t0015g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0015t0003g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0019t0014g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0019t0014g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0025t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0029t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0031t0005g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0034t0007g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0037t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0041t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0045t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0048t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0051t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0001c0053t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0002c0004t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0002c0004t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0002c0004t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0002c0004t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0002c0004t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0002c0004t0004g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0002c0004t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0002c0004t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0002c0006t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0002c0006t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0002c0006t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0002c0006t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0002c0006t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0002c0007t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0002c0007t0006g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0002c0007t0006g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0002c0007t0017g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0002c0013t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0002c0013t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0002c0032t0012g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0002c0050t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0003c0010t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0003c0010t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0003c0010t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0003c0011t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0003c0011t0006g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0003c0023t0008g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0003c0028t0019g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0003c0040t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0004c0008t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0004c0008t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0004c0008t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0004c0020t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0004c0020t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0004c0021t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0004c0021t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0005c0014t0008g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0005c0014t0016g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0005c0027t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0005c0036t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0006c0016t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0006c0016t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0006c0030t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0007c0017t0005g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0008c0022t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0008c0022t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0009c0018t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0009c0018t0013g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0010c0042t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0011c0043t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0012c0038t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0013c0039t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0014c0052t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0015c0033t0023g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0016c0026t0013g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0017c0046t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0018c0035t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0019c0049t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0020c0047t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0021c0024t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
a0022c0044t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0021 | EUR | GBR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | GBR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0056 | EUR | GBR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00140 | hp2 | a0001 | c0003 | t0003 | g0003 | EUR | GBR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0090 | EUR | FIN | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0061 | EUR | FIN | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00323 | hp1 | a0001 | c0002 | t0007 | g0001 | EUR | FIN | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00323 | hp2 | a0001 | c0003 | t0003 | g0135 | EUR | FIN | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | CHS | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | CHS | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00438 | hp1 | a0002 | c0006 | t0001 | g0113 | EAS | CHS | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00438 | hp2 | a0002 | c0004 | t0004 | g0020 | EAS | CHS | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00544 | hp1 | a0002 | c0050 | t0001 | g0075 | EAS | CHS | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00544 | hp2 | a0002 | c0006 | t0001 | g0041 | EAS | CHS | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00597 | hp1 | a0004 | c0020 | t0001 | g0034 | EAS | CHS | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00597 | hp2 | a0001 | c0051 | t0004 | g0002 | EAS | CHS | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00609 | hp2 | a0010 | c0042 | t0001 | g0001 | EAS | CHS | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00639 | hp1 | a0004 | c0008 | t0003 | g0136 | AMR | PUR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00639 | hp2 | a0003 | c0040 | t0001 | g0069 | AMR | PUR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00642 | hp1 | a0001 | c0003 | t0002 | g0013 | AMR | PUR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0074 | AMR | PUR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00735 | hp1 | a0001 | c0003 | t0003 | g0003 | AMR | PUR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG00735 | hp2 | a0002 | c0006 | t0001 | g0104 | AMR | PUR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0181 | AMR | PUR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01074 | hp2 | a0001 | c0003 | t0003 | g0003 | AMR | PUR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0118 | AMR | PUR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01081 | hp2 | a0001 | c0002 | t0003 | g0046 | AMR | PUR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01109 | hp1 | a0001 | c0019 | t0014 | g0159 | AMR | PUR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0059 | AMR | PUR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01168 | hp2 | a0001 | c0015 | t0003 | g0028 | AMR | PUR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01169 | hp2 | a0001 | c0015 | t0003 | g0028 | AMR | PUR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01243 | hp2 | a0001 | c0031 | t0005 | g0142 | AMR | PUR | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | CLM | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | CLM | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01256 | hp2 | a0001 | c0003 | t0003 | g0003 | AMR | CLM | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0070 | AMR | CLM | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01257 | hp2 | a0001 | c0005 | t0005 | g0026 | AMR | CLM | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | CLM | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01258 | hp2 | a0001 | c0005 | t0005 | g0026 | AMR | CLM | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01346 | hp1 | a0001 | c0003 | t0003 | g0168 | AMR | CLM | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01361 | hp1 | a0011 | c0043 | t0002 | g0126 | AMR | CLM | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01361 | hp2 | a0001 | c0002 | t0007 | g0099 | AMR | CLM | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | CLM | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0057 | EUR | IBS | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0015 | EUR | IBS | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01884 | hp1 | a0001 | c0003 | t0003 | g0030 | AFR | ACB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01884 | hp2 | a0006 | c0016 | t0005 | g0184 | AFR | ACB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | PEL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PEL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01934 | hp1 | a0005 | c0036 | t0001 | g0008 | AMR | PEL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01934 | hp2 | a0001 | c0037 | t0002 | g0067 | AMR | PEL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | PEL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01943 | hp2 | a0001 | c0025 | t0003 | g0162 | AMR | PEL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | PEL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01975 | hp1 | a0001 | c0003 | t0003 | g0157 | AMR | PEL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01975 | hp2 | a0012 | c0038 | t0002 | g0109 | AMR | PEL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0077 | AMR | PEL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02015 | hp1 | a0013 | c0039 | t0001 | g0016 | EAS | KHV | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | KHV | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02027 | hp1 | a0001 | c0001 | t0011 | g0068 | EAS | KHV | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | KHV | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02055 | hp1 | a0002 | c0013 | t0002 | g0153 | AFR | ACB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02055 | hp2 | a0002 | c0004 | t0002 | g0011 | AFR | ACB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02056 | hp1 | a0001 | c0002 | t0018 | g0186 | EAS | KHV | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0085 | EAS | KHV | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02071 | hp1 | a0014 | c0052 | t0001 | g0001 | EAS | KHV | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | KHV | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | KHV | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02129 | hp2 | a0008 | c0022 | t0002 | g0079 | EAS | KHV | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | KHV | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02132 | hp2 | a0008 | c0022 | t0001 | g0102 | EAS | KHV | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02145 | hp1 | a0005 | c0014 | t0016 | g0023 | AFR | ACB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02145 | hp2 | a0002 | c0004 | t0002 | g0110 | AFR | ACB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02148 | hp1 | a0002 | c0004 | t0002 | g0106 | AMR | PEL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02148 | hp2 | a0004 | c0008 | t0003 | g0163 | AMR | PEL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | CDX | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CDX | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02258 | hp2 | a0009 | c0018 | t0013 | g0033 | AFR | ACB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | ACB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02280 | hp2 | a0001 | c0003 | t0003 | g0160 | AFR | ACB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | PEL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02451 | hp1 | a0001 | c0003 | t0003 | g0167 | AFR | ACB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02451 | hp2 | a0003 | c0010 | t0002 | g0039 | AFR | ACB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02572 | hp2 | a0001 | c0003 | t0003 | g0193 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02615 | hp1 | a0004 | c0021 | t0002 | g0123 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02615 | hp2 | a0009 | c0018 | t0003 | g0014 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02622 | hp1 | a0015 | c0033 | t0023 | g0141 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02622 | hp2 | a0001 | c0001 | t0026 | g0089 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02630 | hp1 | a0001 | c0003 | t0003 | g0166 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02647 | hp1 | a0004 | c0021 | t0002 | g0010 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02647 | hp2 | a0001 | c0003 | t0003 | g0027 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0086 | SAS | PJL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02683 | hp2 | a0001 | c0003 | t0022 | g0156 | SAS | PJL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02698 | hp1 | a0001 | c0001 | t0020 | g0101 | SAS | PJL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02717 | hp2 | a0003 | c0028 | t0019 | g0140 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02723 | hp2 | a0001 | c0003 | t0003 | g0191 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02738 | hp2 | a0001 | c0001 | t0011 | g0111 | SAS | PJL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02809 | hp1 | a0002 | c0004 | t0002 | g0055 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02809 | hp2 | a0002 | c0004 | t0002 | g0010 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02895 | hp2 | a0001 | c0003 | t0003 | g0164 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02896 | hp2 | a0001 | c0003 | t0003 | g0139 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0178 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02922 | hp1 | a0006 | c0016 | t0005 | g0185 | AFR | ESN | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02922 | hp2 | a0001 | c0003 | t0002 | g0151 | AFR | ESN | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02965 | hp1 | a0016 | c0026 | t0013 | g0014 | AFR | ESN | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | ESN | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | ESN | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02976 | hp2 | a0001 | c0005 | t0005 | g0012 | AFR | ESN | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0066 | SAS | PJL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03041 | hp1 | a0001 | c0003 | t0002 | g0013 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03098 | hp1 | a0004 | c0008 | t0003 | g0154 | AFR | MSL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03098 | hp2 | a0005 | c0027 | t0005 | g0143 | AFR | MSL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03130 | hp1 | a0001 | c0003 | t0003 | g0161 | AFR | ESN | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03130 | hp2 | a0001 | c0003 | t0003 | g0165 | AFR | ESN | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03139 | hp1 | a0001 | c0001 | t0010 | g0078 | AFR | ESN | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03139 | hp2 | a0001 | c0003 | t0003 | g0027 | AFR | ESN | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03195 | hp2 | a0001 | c0003 | t0009 | g0006 | AFR | ESN | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03209 | hp1 | a0001 | c0003 | t0005 | g0030 | AFR | MSL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03209 | hp2 | a0001 | c0005 | t0005 | g0012 | AFR | MSL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03225 | hp1 | a0003 | c0010 | t0002 | g0035 | AFR | MSL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03225 | hp2 | a0001 | c0003 | t0003 | g0137 | AFR | MSL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03239 | hp1 | a0001 | c0003 | t0003 | g0155 | SAS | PJL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0064 | SAS | PJL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03453 | hp1 | a0001 | c0003 | t0003 | g0029 | AFR | MSL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03453 | hp2 | a0017 | c0046 | t0005 | g0040 | AFR | MSL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03486 | hp1 | a0001 | c0012 | t0015 | g0032 | AFR | MSL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | MSL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03490 | hp2 | a0001 | c0003 | t0003 | g0003 | SAS | PJL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03492 | hp2 | a0001 | c0003 | t0003 | g0003 | SAS | PJL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03516 | hp1 | a0001 | c0009 | t0016 | g0023 | AFR | ESN | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03516 | hp2 | a0002 | c0013 | t0002 | g0013 | AFR | ESN | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03579 | hp1 | a0003 | c0010 | t0002 | g0192 | AFR | MSL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03579 | hp2 | a0001 | c0003 | t0003 | g0029 | AFR | MSL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03669 | hp1 | a0002 | c0004 | t0004 | g0002 | SAS | PJL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0071 | SAS | PJL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0087 | SAS | STU | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03688 | hp2 | a0018 | c0035 | t0004 | g0063 | SAS | STU | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03710 | hp2 | a0003 | c0011 | t0006 | g0174 | SAS | PJL | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0114 | SAS | BEB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03831 | hp2 | a0019 | c0049 | t0001 | g0116 | SAS | BEB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03834 | hp1 | a0001 | c0001 | t0008 | g0042 | SAS | BEB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0062 | SAS | BEB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03942 | hp1 | a0002 | c0007 | t0006 | g0171 | SAS | BEB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG03942 | hp2 | a0002 | c0006 | t0001 | g0117 | SAS | BEB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG04184 | hp1 | a0001 | c0001 | t0004 | g0065 | SAS | BEB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0088 | SAS | BEB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG04199 | hp1 | a0002 | c0007 | t0017 | g0172 | SAS | STU | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG04199 | hp2 | a0020 | c0047 | t0002 | g0081 | SAS | STU | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0008 | SAS | STU | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0016 | SAS | STU | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18522 | hp1 | a0001 | c0012 | t0015 | g0175 | AFR | YRI | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18522 | hp2 | a0001 | c0001 | t0010 | g0045 | AFR | YRI | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | YRI | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18906 | hp2 | a0006 | c0030 | t0005 | g0183 | AFR | YRI | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18952 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18954 | hp2 | a0021 | c0024 | t0002 | g0004 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18956 | hp1 | a0001 | c0001 | t0025 | g0037 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18956 | hp2 | a0001 | c0002 | t0007 | g0001 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18959 | hp2 | a0001 | c0001 | t0021 | g0127 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18974 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18975 | hp1 | a0001 | c0002 | t0012 | g0001 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18980 | hp1 | a0022 | c0044 | t0001 | g0049 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0098 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18982 | hp2 | a0001 | c0029 | t0001 | g0145 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18999 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19000 | hp1 | a0004 | c0020 | t0001 | g0190 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19000 | hp2 | a0002 | c0004 | t0004 | g0125 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19004 | hp1 | a0002 | c0004 | t0004 | g0002 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19004 | hp2 | a0003 | c0011 | t0006 | g0173 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19010 | hp1 | a0002 | c0007 | t0001 | g0170 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19011 | hp1 | a0001 | c0048 | t0004 | g0002 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19011 | hp2 | a0001 | c0045 | t0002 | g0054 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19030 | hp1 | a0001 | c0019 | t0014 | g0158 | AFR | LWK | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19030 | hp2 | a0001 | c0003 | t0009 | g0006 | AFR | LWK | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19055 | hp1 | a0002 | c0032 | t0012 | g0147 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19055 | hp2 | a0002 | c0006 | t0001 | g0044 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19056 | hp1 | a0001 | c0041 | t0002 | g0004 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19060 | hp1 | a0001 | c0034 | t0007 | g0130 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19060 | hp2 | a0002 | c0007 | t0006 | g0169 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19082 | hp2 | a0001 | c0009 | t0008 | g0148 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19085 | hp2 | a0001 | c0009 | t0002 | g0144 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19087 | hp1 | a0001 | c0053 | t0004 | g0002 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19087 | hp2 | a0005 | c0014 | t0008 | g0146 | EAS | JPT | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | YRI | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA19240 | hp2 | a0001 | c0003 | t0003 | g0194 | AFR | YRI | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA20129 | hp1 | a0003 | c0023 | t0008 | g0149 | AFR | ASW | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA20129 | hp2 | a0001 | c0003 | t0003 | g0003 | AFR | ASW | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0008 | EUR | TSI | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA20752 | hp2 | a0001 | c0003 | t0003 | g0182 | EUR | TSI | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | TSI | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0017 | EUR | TSI | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | GIH | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0133 | SAS | GIH | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02109 | hp1 | a0007 | c0017 | t0005 | g0025 | AFR | ACB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02109 | hp2 | a0001 | c0003 | t0003 | g0024 | AFR | ACB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02486 | hp1 | a0007 | c0017 | t0005 | g0025 | AFR | ACB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | ACB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG02559 | hp2 | a0001 | c0003 | t0009 | g0006 | AFR | ACB | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG06807 | hp1 | a0001 | c0003 | t0003 | g0138 | AFR | USA | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
HG06807 | hp2 | a0001 | c0005 | t0005 | g0012 | AFR | USA | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | USA | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA20300 | hp2 | a0001 | c0003 | t0003 | g0024 | AFR | USA | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA21309 | hp1 | a0001 | c0003 | t0003 | g0134 | AFR | LWK | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
NA21309 | hp2 | a0001 | c0003 | t0003 | g0150 | AFR | LWK | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
homoSapiens | chm13v2 | a0001 | c0002 | t0024 | g0058 | REF | REF | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
homoSapiens | grch38p0 | a0001 | c0003 | t0002 | g0152 | REF | REF | SETD1B_chr12_121799009_121837656 | SETD1B | chr12 | 121799009 | 121837656 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:121805920 | G | A | 1 | a0021 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.359G>A | p.Arg120Lys | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/17 | 598/8557 | 359/5901 | 120/1966 | chr12 | 121805920 | |||
chr12:121809958 | C | T | 1 | a0009 | 2 | HG02258.hp2 HG02615.hp2 |
missense_variant | MODERATE | c.1013C>T | p.Ala338Val | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/17 | 1252/8557 | 1013/5901 | 338/1966 | chr12 | 121809958 | |||
chr12:121810039 | G | T | 1 | a0008 | 2 | HG02129.hp2 HG02132.hp2 |
missense_variant | MODERATE | c.1094G>T | p.Gly365Val | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/17 | 1333/8557 | 1094/5901 | 365/1966 | chr12 | 121810039 | |||
chr12:121810300 | C | T | 1 | a0014 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.1355C>T | p.Pro452Leu | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/17 | 1594/8557 | 1355/5901 | 452/1966 | chr12 | 121810300 | |||
chr12:121814154 | C | A | 1 | a0018 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.1939C>A | p.Pro647Thr | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/17 | 2178/8557 | 1939/5901 | 647/1966 | chr12 | 121814154 | |||
chr12:121814158 | C | T | 1 | a0015 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.1943C>T | p.Ser648Leu | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/17 | 2182/8557 | 1943/5901 | 648/1966 | chr12 | 121814158 | |||
chr12:121814258 | G | GC | 2 | a0004 a0005 |
11 | HG00597.hp1 HG00639.hp1 HG01934.hp1 others(8): Show |
frameshift_variant | HIGH | c.2048dupC | p.Pro684fs | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/17 | 2288/8557 | 2049/5901 | 683/1966 | INFO_REALIGN_3_PRIME | chr12 | 121814258 | ||
chr12:121814285 | G | GC | 3 | a0002 a0005 a0018 |
27 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(24): Show |
frameshift_variant | HIGH | c.2078dupC | p.Pro694fs | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/17 | 2318/8557 | 2079/5901 | 693/1966 | INFO_REALIGN_3_PRIME | chr12 | 121814285 | ||
chr12:121814920 | G | A | 1 | a0012 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.2705G>A | p.Arg902Gln | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/17 | 2944/8557 | 2705/5901 | 902/1966 | chr12 | 121814920 | |||
chr12:121817082 | C | T | 1 | a0019 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.2765C>T | p.Pro922Leu | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 8/17 | 3004/8557 | 2765/5901 | 922/1966 | chr12 | 121817082 | |||
chr12:121817617 | G | C | 1 | a0013 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.3225G>C | p.Glu1075Asp | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 9/17 | 3464/8557 | 3225/5901 | 1075/1966 | chr12 | 121817617 | |||
chr12:121817849 | C | A | 1 | a0006 | 3 | HG01884.hp2 HG02922.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.3363C>A | p.Asp1121Glu | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 10/17 | 3602/8557 | 3363/5901 | 1121/1966 | chr12 | 121817849 | |||
chr12:121819878 | C | A | 1 | a0002 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.3893C>A | p.Ser1298Tyr | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 11/17 | 4132/8557 | 3893/5901 | 1298/1966 | chr12 | 121819878 | |||
chr12:121822522 | A | G | 2 | a0009 a0016 |
3 | HG02258.hp2 HG02615.hp2 HG02965.hp1 |
missense_variant | MODERATE | c.3943A>G | p.Met1315Val | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/17 | 4182/8557 | 3943/5901 | 1315/1966 | chr12 | 121822522 | |||
chr12:121822580 | C | G | 1 | a0020 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.4001C>G | p.Pro1334Arg | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/17 | 4240/8557 | 4001/5901 | 1334/1966 | chr12 | 121822580 | |||
chr12:121822592 | C | T | 1 | a0008 | 2 | HG02129.hp2 HG02132.hp2 |
missense_variant | MODERATE | c.4013C>T | p.Pro1338Leu | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/17 | 4252/8557 | 4013/5901 | 1338/1966 | chr12 | 121822592 | |||
chr12:121822643 | T | C | 4 | a0002 a0003 a0006 others(1): Show |
16 | HG00639.hp2 HG01884.hp2 HG02451.hp2 others(13): Show |
missense_variant | MODERATE | c.4064T>C | p.Leu1355Pro | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/17 | 4303/8557 | 4064/5901 | 1355/1966 | chr12 | 121822643 | |||
chr12:121822656 | C | A | 1 | a0007 | 2 | HG02109.hp1 HG02486.hp1 |
missense_variant | MODERATE | c.4077C>A | p.His1359Gln | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/17 | 4316/8557 | 4077/5901 | 1359/1966 | chr12 | 121822656 | |||
chr12:121822943 | G | A | 1 | a0010 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.4364G>A | p.Arg1455His | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/17 | 4603/8557 | 4364/5901 | 1455/1966 | chr12 | 121822943 | |||
chr12:121823041 | G | A | 1 | a0011 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.4462G>A | p.Ala1488Thr | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/17 | 4701/8557 | 4462/5901 | 1488/1966 | chr12 | 121823041 | |||
chr12:121823381 | C | T | 1 | a0017 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.4802C>T | p.Pro1601Leu | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/17 | 5041/8557 | 4802/5901 | 1601/1966 | chr12 | 121823381 | |||
chr12:121830133 | A | C | 1 | a0022 | 1 | NA18980.hp1 | missense_variant | MODERATE | c.5795A>C | p.His1932Pro | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 6034/8557 | 5795/5901 | 1932/1966 | chr12 | 121830133 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:121805168 | G | A | 1 | a0003c0023 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.225G>A | p.Gly75Gly | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 3/17 | 464/8557 | 225/5901 | 75/1966 | chr12 | 121805168 | |||
chr12:121805999 | C | T | 29 | a0001c0001 a0001c0002 a0001c0034 others(26): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
synonymous_variant | LOW | c.438C>T | p.Ile146Ile | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/17 | 677/8557 | 438/5901 | 146/1966 | chr12 | 121805999 | |||
chr12:121808230 | T | C | 3 | a0002c0007 a0003c0011 a0003c0023 |
7 | HG03710.hp2 HG03942.hp1 HG04199.hp1 others(4): Show |
synonymous_variant | LOW | c.567T>C | p.Tyr189Tyr | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 5/17 | 806/8557 | 567/5901 | 189/1966 | chr12 | 121808230 | |||
chr12:121808287 | C | T | 1 | a0001c0019 | 2 | HG01109.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.624C>T | p.Asp208Asp | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 5/17 | 863/8557 | 624/5901 | 208/1966 | chr12 | 121808287 | |||
chr12:121809947 | C | T | 3 | a0002c0007 a0003c0011 a0003c0023 |
7 | HG03710.hp2 HG03942.hp1 HG04199.hp1 others(4): Show |
synonymous_variant | LOW | c.1002C>T | p.Pro334Pro | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/17 | 1241/8557 | 1002/5901 | 334/1966 | chr12 | 121809947 | |||
chr12:121810208 | G | A | 1 | a0001c0025 | 1 | HG01943.hp2 | synonymous_variant | LOW | c.1263G>A | p.Gly421Gly | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/17 | 1502/8557 | 1263/5901 | 421/1966 | chr12 | 121810208 | |||
chr12:121810250 | A | C | 1 | a0001c0053 | 1 | NA19087.hp1 | synonymous_variant | LOW | c.1305A>C | p.Pro435Pro | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/17 | 1544/8557 | 1305/5901 | 435/1966 | chr12 | 121810250 | |||
chr12:121810406 | G | A | 1 | a0001c0034 | 1 | NA19060.hp1 | synonymous_variant | LOW | c.1461G>A | p.Ser487Ser | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/17 | 1700/8557 | 1461/5901 | 487/1966 | chr12 | 121810406 | |||
chr12:121810440 | C | T | 1 | a0001c0051 | 1 | HG00597.hp2 | synonymous_variant | LOW | c.1495C>T | p.Leu499Leu | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/17 | 1734/8557 | 1495/5901 | 499/1966 | chr12 | 121810440 | |||
chr12:121810676 | C | G | 45 | a0001c0001 a0001c0002 a0001c0005 others(42): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
synonymous_variant | LOW | c.1731C>G | p.Leu577Leu | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/17 | 1970/8557 | 1731/5901 | 577/1966 | chr12 | 121810676 | |||
chr12:121814213 | G | A | 1 | a0001c0012 | 2 | HG03486.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.1998G>A | p.Ala666Ala | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/17 | 2237/8557 | 1998/5901 | 666/1966 | chr12 | 121814213 | |||
chr12:121814291 | C | A | 1 | a0001c0037 | 1 | HG01934.hp2 | synonymous_variant | LOW | c.2076C>A | p.Pro692Pro | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/17 | 2315/8557 | 2076/5901 | 692/1966 | chr12 | 121814291 | |||
chr12:121814603 | C | T | 4 | a0001c0005 a0001c0031 a0005c0027 others(1): Show |
9 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(6): Show |
synonymous_variant | LOW | c.2388C>T | p.Pro796Pro | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/17 | 2627/8557 | 2388/5901 | 796/1966 | chr12 | 121814603 | |||
chr12:121814693 | C | T | 2 | a0006c0016 a0006c0030 |
3 | HG01884.hp2 HG02922.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.2478C>T | p.Ser826Ser | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/17 | 2717/8557 | 2478/5901 | 826/1966 | chr12 | 121814693 | |||
chr12:121817245 | C | T | 1 | a0015c0033 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.2928C>T | p.Gly976Gly | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 8/17 | 3167/8557 | 2928/5901 | 976/1966 | chr12 | 121817245 | |||
chr12:121817566 | C | T | 1 | a0001c0048 | 1 | NA19011.hp1 | synonymous_variant | LOW | c.3174C>T | p.Thr1058Thr | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 9/17 | 3413/8557 | 3174/5901 | 1058/1966 | chr12 | 121817566 | |||
chr12:121819621 | C | T | 1 | a0001c0015 | 2 | HG01168.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.3636C>T | p.Asp1212Asp | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 11/17 | 3875/8557 | 3636/5901 | 1212/1966 | chr12 | 121819621 | |||
chr12:121822641 | C | T | 5 | a0001c0005 a0001c0031 a0005c0027 others(2): Show |
10 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
synonymous_variant | LOW | c.4062C>T | p.Pro1354Pro | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/17 | 4301/8557 | 4062/5901 | 1354/1966 | chr12 | 121822641 | |||
chr12:121822791 | C | A | 1 | a0001c0041 | 1 | NA19056.hp1 | synonymous_variant | LOW | c.4212C>A | p.Pro1404Pro | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/17 | 4451/8557 | 4212/5901 | 1404/1966 | chr12 | 121822791 | |||
chr12:121822899 | C | T | 4 | a0001c0005 a0005c0027 a0007c0017 others(1): Show |
9 | HG01257.hp2 HG01258.hp2 HG02109.hp1 others(6): Show |
synonymous_variant | LOW | c.4320C>T | p.Ser1440Ser | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/17 | 4559/8557 | 4320/5901 | 1440/1966 | chr12 | 121822899 | |||
chr12:121823227 | C | T | 1 | a0015c0033 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.4648C>T | p.Leu1550Leu | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/17 | 4887/8557 | 4648/5901 | 1550/1966 | chr12 | 121823227 | |||
chr12:121823550 | G | A | 12 | a0001c0002 a0001c0029 a0001c0034 others(9): Show |
75 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
synonymous_variant | LOW | c.4971G>A | p.Ala1657Ala | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/17 | 5210/8557 | 4971/5901 | 1657/1966 | chr12 | 121823550 | |||
chr12:121823562 | A | G | 1 | a0006c0030 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.4983A>G | p.Glu1661Glu | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/17 | 5222/8557 | 4983/5901 | 1661/1966 | chr12 | 121823562 | |||
chr12:121825342 | C | T | 1 | a0001c0045 | 1 | NA19011.hp2 | synonymous_variant | LOW | c.5313C>T | p.Thr1771Thr | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/17 | 5552/8557 | 5313/5901 | 1771/1966 | chr12 | 121825342 | |||
chr12:121827611 | C | T | 2 | a0002c0007 a0003c0011 |
6 | HG03710.hp2 HG03942.hp1 HG04199.hp1 others(3): Show |
synonymous_variant | LOW | c.5430C>T | p.Gly1810Gly | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 14/17 | 5669/8557 | 5430/5901 | 1810/1966 | chr12 | 121827611 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:121804077 | A | G | 1 | a0001c0001t0026 | 1 | HG02622.hp2 | 5_prime_UTR_variant | MODIFIER | c.-171A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 1/17 | 661 | chr12 | 121804077 | ||||||
chr12:121804136 | C | T | 1 | a0001c0001t0025 | 1 | NA18956.hp1 | 5_prime_UTR_variant | MODIFIER | c.-112C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 1/17 | 602 | chr12 | 121804136 | ||||||
chr12:121830244 | C | T | 2 | a0001c0009t0016 a0005c0014t0016 |
2 | HG02145.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 5 | chr12 | 121830244 | ||||||
chr12:121830362 | G | T | 1 | a0001c0003t0009 | 3 | HG02559.hp2 HG03195.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*123G>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 123 | chr12 | 121830362 | ||||||
chr12:121830415 | C | T | 1 | a0015c0033t0023 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*176C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 176 | chr12 | 121830415 | ||||||
chr12:121830517 | C | A | 3 | a0002c0007t0006 a0002c0007t0017 a0003c0011t0006 |
5 | HG03710.hp2 HG03942.hp1 HG04199.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*278C>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 278 | chr12 | 121830517 | ||||||
chr12:121830530 | C | CT | 9 | a0001c0001t0003 a0001c0002t0003 a0001c0003t0003 others(6): Show |
46 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*292dupT | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 293 | INFO_REALIGN_3_PRIME | chr12 | 121830530 | |||||
chr12:121830532 | C | T | 1 | a0001c0012t0015 | 2 | HG03486.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*293C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 293 | chr12 | 121830532 | ||||||
chr12:121830545 | T | C | 1 | a0001c0012t0015 | 2 | HG03486.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*306T>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 306 | chr12 | 121830545 | ||||||
chr12:121830578 | G | A | 1 | a0001c0002t0018 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*339G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 339 | chr12 | 121830578 | ||||||
chr12:121830723 | C | T | 1 | a0001c0001t0026 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*484C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 484 | chr12 | 121830723 | ||||||
chr12:121830736 | C | T | 1 | a0001c0003t0022 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*497C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 497 | chr12 | 121830736 | ||||||
chr12:121830759 | G | A | 1 | a0001c0019t0014 | 2 | HG01109.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*520G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 520 | chr12 | 121830759 | ||||||
chr12:121830772 | C | T | 1 | a0001c0001t0021 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*533C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 533 | chr12 | 121830772 | ||||||
chr12:121830790 | C | G | 25 | a0001c0001t0003 a0001c0002t0003 a0001c0003t0003 others(22): Show |
73 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*551C>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 551 | chr12 | 121830790 | ||||||
chr12:121831040 | C | T | 1 | a0002c0007t0017 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*801C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 801 | chr12 | 121831040 | ||||||
chr12:121831276 | G | A | 18 | a0001c0001t0001 a0001c0002t0001 a0001c0002t0007 others(15): Show |
79 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1037G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 1037 | chr12 | 121831276 | ||||||
chr12:121831397 | G | GT | 6 | a0001c0001t0011 a0001c0002t0007 a0001c0002t0012 others(3): Show |
9 | HG00323.hp1 HG01361.hp2 HG02027.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1167dupT | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 1168 | INFO_REALIGN_3_PRIME | chr12 | 121831397 | |||||
chr12:121831451 | CT | C | 8 | a0001c0001t0004 a0001c0001t0021 a0001c0001t0025 others(5): Show |
22 | HG00438.hp2 HG00597.hp2 HG02056.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1222delT | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 1222 | INFO_REALIGN_3_PRIME | chr12 | 121831451 | |||||
chr12:121831682 | G | A | 1 | a0003c0028t0019 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1443G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 1443 | chr12 | 121831682 | ||||||
chr12:121831773 | C | T | 3 | a0001c0003t0009 a0009c0018t0013 a0016c0026t0013 |
5 | HG02258.hp2 HG02559.hp2 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1534C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 1534 | chr12 | 121831773 | ||||||
chr12:121831896 | G | GT | 28 | a0001c0001t0001 a0001c0001t0008 a0001c0002t0001 others(25): Show |
91 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*1667dupT | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 1668 | INFO_REALIGN_3_PRIME | chr12 | 121831896 | |||||
chr12:121831949 | C | T | 1 | a0001c0001t0020 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1710C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 1710 | chr12 | 121831949 | ||||||
chr12:121832012 | G | A | 1 | a0001c0001t0010 | 2 | HG03139.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1773G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 17/17 | 1773 | chr12 | 121832012 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:121804307 | CCGAGCGG others(1): Show |
C | 5 | a0001c0003t0003g0030 a0001c0003t0003g0193 a0001c0003t0003g0194 others(2): Show |
5 | HG01884.hp1 HG02572.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+85_-15+92delAG others(6): Show |
SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 121804307 | ||||||
chr12:121804321 | G | A | 1 | a0001c0001t0002g0031 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-15+88G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 1/16 | chr12 | 121804321 | |||||||
chr12:121804446 | G | T | 1 | a0001c0003t0003g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-15+213G>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 1/16 | chr12 | 121804446 | |||||||
chr12:121804457 | GC | G | 5 | a0001c0002t0001g0187 a0001c0002t0001g0188 a0001c0002t0001g0189 others(2): Show |
5 | HG02027.hp2 HG02056.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+228delC | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 121804457 | ||||||
chr12:121804659 | C | T | 3 | a0006c0016t0005g0184 a0006c0016t0005g0185 a0006c0030t0005g0183 |
3 | HG01884.hp2 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-14-65C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 1/16 | chr12 | 121804659 | |||||||
chr12:121804664 | G | C | 2 | a0001c0002t0001g0187 a0001c0002t0018g0186 |
2 | HG02027.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.-14-60G>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 1/16 | chr12 | 121804664 | |||||||
chr12:121804935 | A | G | 1 | a0001c0003t0003g0182 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.174+24A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 2/16 | chr12 | 121804935 | |||||||
chr12:121805005 | A | C | 1 | a0001c0002t0001g0181 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.174+94A>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 2/16 | chr12 | 121805005 | |||||||
chr12:121805063 | C | T | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG02559.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-55C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 2/16 | chr12 | 121805063 | |||||||
chr12:121805066 | A | G | 1 | a0001c0002t0001g0176 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.175-52A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 2/16 | chr12 | 121805066 | |||||||
chr12:121805105 | T | C | 1 | a0001c0012t0015g0032 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.175-13T>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 2/16 | chr12 | 121805105 | |||||||
chr12:121805261 | C | T | 1 | a0001c0012t0015g0175 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.273+45C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 3/16 | chr12 | 121805261 | |||||||
chr12:121805301 | G | T | 6 | a0002c0007t0001g0170 a0002c0007t0006g0169 a0002c0007t0006g0171 others(3): Show |
6 | HG03710.hp2 HG03942.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+85G>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 3/16 | chr12 | 121805301 | |||||||
chr12:121805535 | G | C | 4 | a0001c0003t0009g0006 a0009c0018t0003g0014 a0009c0018t0013g0033 others(1): Show |
6 | HG02258.hp2 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.274-300G>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 3/16 | chr12 | 121805535 | |||||||
chr12:121805689 | AT | A | 39 | a0001c0003t0003g0024 a0001c0003t0003g0030 a0001c0003t0003g0134 others(36): Show |
46 | HG00323.hp2 HG00639.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.274-130delT | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 121805689 | ||||||
chr12:121805689 | ATT | A | 141 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0050 others(138): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.274-131_274-130del others(2): Show |
SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 121805689 | ||||||
chr12:121805689 | ATTT | A | 6 | a0001c0001t0002g0036 a0001c0001t0002g0177 a0001c0001t0025g0037 others(3): Show |
6 | HG02895.hp1 HG02896.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-132_274-130del others(3): Show |
SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 121805689 | ||||||
chr12:121805692 | T | A | 1 | a0004c0020t0001g0034 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.274-143T>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 3/16 | chr12 | 121805692 | |||||||
chr12:121805785 | C | T | 1 | a0001c0002t0001g0133 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.274-50C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 3/16 | chr12 | 121805785 | |||||||
chr12:121806237 | C | A | 4 | a0003c0010t0002g0035 a0003c0010t0002g0039 a0003c0010t0002g0192 others(1): Show |
4 | HG02451.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.544+132C>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/16 | chr12 | 121806237 | |||||||
chr12:121806340 | A | G | 1 | a0001c0001t0002g0132 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.544+235A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/16 | chr12 | 121806340 | |||||||
chr12:121806598 | G | A | 1 | a0001c0003t0003g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.544+493G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/16 | chr12 | 121806598 | |||||||
chr12:121806672 | C | T | 1 | a0001c0002t0001g0131 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.544+567C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/16 | chr12 | 121806672 | |||||||
chr12:121806725 | G | C | 1 | a0002c0006t0001g0041 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.544+620G>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/16 | chr12 | 121806725 | |||||||
chr12:121806862 | C | T | 2 | a0001c0012t0015g0032 a0001c0012t0015g0175 |
2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.544+757C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/16 | chr12 | 121806862 | |||||||
chr12:121806997 | G | A | 1 | a0001c0001t0008g0042 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.544+892G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/16 | chr12 | 121806997 | |||||||
chr12:121807183 | A | G | 170 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0050 others(167): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.545-1025A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/16 | chr12 | 121807183 | |||||||
chr12:121807205 | G | A | 1 | a0001c0002t0001g0043 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.545-1003G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/16 | chr12 | 121807205 | |||||||
chr12:121807311 | G | T | 1 | a0001c0034t0007g0130 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.545-897G>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/16 | chr12 | 121807311 | |||||||
chr12:121807431 | A | C | 1 | a0003c0023t0008g0149 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.545-777A>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/16 | chr12 | 121807431 | |||||||
chr12:121807438 | A | T | 169 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0050 others(166): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.545-770A>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/16 | chr12 | 121807438 | |||||||
chr12:121807444 | TA | T | 146 | a0001c0001t0001g0005 a0001c0001t0002g0004 a0001c0001t0002g0005 others(143): Show |
178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.545-747delA | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr12 | 121807444 | ||||||
chr12:121807456 | AAAAAAG | A | 12 | a0001c0001t0002g0007 a0001c0001t0002g0052 a0001c0001t0002g0053 others(9): Show |
13 | HG00140.hp1 HG00423.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.545-747_545-742del others(6): Show |
SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr12 | 121807456 | ||||||
chr12:121807526 | A | G | 1 | a0001c0003t0003g0166 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.545-682A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/16 | chr12 | 121807526 | |||||||
chr12:121807560 | G | A | 1 | a0015c0033t0023g0141 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.545-648G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/16 | chr12 | 121807560 | |||||||
chr12:121807609 | C | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0129 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.545-599C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/16 | chr12 | 121807609 | |||||||
chr12:121807749 | C | T | 4 | a0001c0003t0003g0029 a0001c0003t0003g0164 a0001c0003t0003g0165 others(1): Show |
6 | HG01168.hp2 HG01169.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.545-459C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/16 | chr12 | 121807749 | |||||||
chr12:121807924 | C | T | 1 | a0004c0008t0003g0163 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.545-284C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/16 | chr12 | 121807924 | |||||||
chr12:121807925 | G | A | 154 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0050 others(151): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.545-283G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/16 | chr12 | 121807925 | |||||||
chr12:121807926 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.545-282C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/16 | chr12 | 121807926 | |||||||
chr12:121808097 | TGGGGTCT others(1): Show |
T | 2 | a0001c0002t0001g0015 a0001c0002t0001g0057 |
3 | HG00642.hp2 HG01515.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.545-107_545-100del others(8): Show |
SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr12 | 121808097 | ||||||
chr12:121808350 | C | T | 3 | a0006c0016t0005g0184 a0006c0016t0005g0185 a0006c0030t0005g0183 |
3 | HG01884.hp2 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.657+30C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 5/16 | chr12 | 121808350 | |||||||
chr12:121808423 | C | G | 1 | a0002c0007t0017g0172 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.657+103C>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 5/16 | chr12 | 121808423 | |||||||
chr12:121808445 | C | A | 5 | a0001c0005t0005g0012 a0001c0005t0005g0026 a0001c0031t0005g0142 others(2): Show |
9 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.657+125C>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 5/16 | chr12 | 121808445 | |||||||
chr12:121808559 | T | C | 5 | a0001c0001t0002g0007 a0001c0001t0002g0052 a0001c0001t0002g0053 others(2): Show |
6 | HG00423.hp2 HG02071.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.657+239T>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 5/16 | chr12 | 121808559 | |||||||
chr12:121808567 | C | T | 7 | a0002c0007t0001g0170 a0002c0007t0006g0169 a0002c0007t0006g0171 others(4): Show |
7 | HG03710.hp2 HG03942.hp1 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.657+247C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 5/16 | chr12 | 121808567 | |||||||
chr12:121808793 | C | T | 3 | a0001c0009t0008g0148 a0002c0032t0012g0147 a0005c0014t0008g0146 |
3 | NA19055.hp1 NA19082.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.657+473C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 5/16 | chr12 | 121808793 | |||||||
chr12:121808794 | G | A | 1 | a0003c0028t0019g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.657+474G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 5/16 | chr12 | 121808794 | |||||||
chr12:121809026 | C | T | 3 | a0006c0016t0005g0184 a0006c0016t0005g0185 a0006c0030t0005g0183 |
3 | HG01884.hp2 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.658-577C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 5/16 | chr12 | 121809026 | |||||||
chr12:121809125 | C | T | 1 | a0001c0001t0021g0127 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.658-478C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 5/16 | chr12 | 121809125 | |||||||
chr12:121809140 | C | T | 4 | a0001c0009t0008g0148 a0002c0032t0012g0147 a0005c0014t0008g0146 others(1): Show |
4 | HG02622.hp1 NA19055.hp1 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.658-463C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 5/16 | chr12 | 121809140 | |||||||
chr12:121809208 | G | A | 3 | a0001c0002t0001g0008 a0001c0002t0001g0059 a0005c0036t0001g0008 |
4 | HG01109.hp2 HG01934.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.658-395G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 5/16 | chr12 | 121809208 | |||||||
chr12:121809500 | C | T | 1 | a0001c0025t0003g0162 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.658-103C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 5/16 | chr12 | 121809500 | |||||||
chr12:121810854 | A | C | 1 | a0011c0043t0002g0126 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1890+19A>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121810854 | |||||||
chr12:121811041 | C | G | 1 | a0002c0004t0004g0125 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1890+206C>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121811041 | |||||||
chr12:121811142 | G | T | 167 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0050 others(164): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1890+307G>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121811142 | |||||||
chr12:121811185 | G | A | 154 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0050 others(151): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1890+350G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121811185 | |||||||
chr12:121811195 | C | G | 1 | a0001c0002t0001g0022 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1890+360C>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121811195 | |||||||
chr12:121811292 | G | C | 7 | a0002c0007t0001g0170 a0002c0007t0006g0169 a0002c0007t0006g0171 others(4): Show |
7 | HG03710.hp2 HG03942.hp1 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.1890+457G>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121811292 | |||||||
chr12:121811399 | C | T | 1 | a0001c0002t0001g0021 | 2 | HG00099.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.1890+564C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121811399 | |||||||
chr12:121811633 | C | T | 7 | a0002c0007t0001g0170 a0002c0007t0006g0169 a0002c0007t0006g0171 others(4): Show |
7 | HG03710.hp2 HG03942.hp1 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.1890+798C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121811633 | |||||||
chr12:121811652 | G | A | 1 | a0001c0001t0004g0060 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1890+817G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121811652 | |||||||
chr12:121811847 | A | G | 2 | a0001c0001t0002g0011 a0002c0004t0002g0011 |
3 | HG02055.hp2 HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1890+1012A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121811847 | |||||||
chr12:121811927 | T | C | 4 | a0001c0003t0009g0006 a0009c0018t0003g0014 a0009c0018t0013g0033 others(1): Show |
6 | HG02258.hp2 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1890+1092T>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121811927 | |||||||
chr12:121812004 | C | G | 1 | a0001c0002t0001g0133 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1890+1169C>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121812004 | |||||||
chr12:121812072 | G | A | 1 | a0001c0045t0002g0054 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1890+1237G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121812072 | |||||||
chr12:121812076 | G | C | 1 | a0001c0045t0002g0054 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1890+1241G>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121812076 | |||||||
chr12:121812077 | T | G | 1 | a0001c0045t0002g0054 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1890+1242T>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121812077 | |||||||
chr12:121812090 | G | A | 1 | a0001c0045t0002g0054 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1890+1255G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121812090 | |||||||
chr12:121812092 | C | G | 1 | a0001c0045t0002g0054 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1890+1257C>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121812092 | |||||||
chr12:121812130 | G | A | 1 | a0001c0002t0001g0061 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1890+1295G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121812130 | |||||||
chr12:121812200 | G | A | 4 | a0001c0001t0004g0062 a0001c0001t0004g0064 a0001c0001t0004g0065 others(1): Show |
4 | HG03239.hp2 HG03688.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1890+1365G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121812200 | |||||||
chr12:121812208 | C | T | 1 | a0003c0028t0019g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1890+1373C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121812208 | |||||||
chr12:121812430 | AGCACAGG others(22): Show |
A | 12 | a0001c0001t0002g0010 a0001c0001t0002g0119 a0001c0001t0002g0120 others(9): Show |
12 | HG01243.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1890+1604_1890+163 others(33): Show |
SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr12 | 121812430 | ||||||
chr12:121812496 | C | T | 1 | a0015c0033t0023g0141 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1891-1610C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121812496 | |||||||
chr12:121812582 | A | C | 1 | a0001c0002t0001g0118 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1891-1524A>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121812582 | |||||||
chr12:121812585 | A | T | 154 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0050 others(151): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1891-1521A>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121812585 | |||||||
chr12:121812643 | G | T | 2 | a0002c0006t0001g0117 a0019c0049t0001g0116 |
2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1891-1463G>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121812643 | |||||||
chr12:121812711 | T | C | 175 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0050 others(172): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1891-1395T>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121812711 | |||||||
chr12:121812759 | C | T | 3 | a0001c0009t0008g0148 a0002c0032t0012g0147 a0005c0014t0008g0146 |
3 | NA19055.hp1 NA19082.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1891-1347C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121812759 | |||||||
chr12:121812878 | C | T | 5 | a0001c0005t0005g0012 a0001c0005t0005g0026 a0001c0031t0005g0142 others(2): Show |
9 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1891-1228C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121812878 | |||||||
chr12:121812977 | C | G | 2 | a0001c0009t0016g0023 a0005c0014t0016g0023 |
2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1891-1129C>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121812977 | |||||||
chr12:121813069 | C | G | 2 | a0002c0007t0006g0171 a0003c0011t0006g0174 |
2 | HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1891-1037C>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121813069 | |||||||
chr12:121813290 | C | T | 1 | a0004c0020t0001g0190 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1891-816C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121813290 | |||||||
chr12:121813322 | TAAC | T | 154 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0050 others(151): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1891-779_1891-777d others(5): Show |
SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr12 | 121813322 | ||||||
chr12:121813714 | C | T | 1 | a0022c0044t0001g0049 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1891-392C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121813714 | |||||||
chr12:121813750 | G | A | 168 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0050 others(165): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1891-356G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 6/16 | chr12 | 121813750 | |||||||
chr12:121814965 | TGTGGAGG others(6): Show |
T | 4 | a0003c0010t0002g0035 a0003c0010t0002g0039 a0003c0010t0002g0192 others(1): Show |
4 | HG02451.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2715+37_2715+49del others(13): Show |
SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 121814965 | ||||||
chr12:121815011 | G | T | 3 | a0001c0009t0008g0148 a0002c0032t0012g0147 a0005c0014t0008g0146 |
3 | NA19055.hp1 NA19082.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.2715+81G>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121815011 | |||||||
chr12:121815120 | C | A | 1 | a0001c0002t0001g0066 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2715+190C>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121815120 | |||||||
chr12:121815161 | G | A | 2 | a0001c0009t0016g0023 a0005c0014t0016g0023 |
2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2715+231G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121815161 | |||||||
chr12:121815262 | A | G | 1 | a0001c0001t0002g0115 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2715+332A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121815262 | |||||||
chr12:121815278 | A | G | 2 | a0001c0012t0015g0032 a0001c0012t0015g0175 |
2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2715+348A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121815278 | |||||||
chr12:121815346 | C | T | 4 | a0001c0003t0003g0139 a0001c0003t0003g0160 a0001c0003t0003g0161 others(1): Show |
4 | HG02280.hp2 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2715+416C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121815346 | |||||||
chr12:121815398 | G | GC | 141 | a0001c0001t0001g0005 a0001c0001t0001g0050 a0001c0001t0002g0004 others(138): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.2715+476dupC | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 121815398 | ||||||
chr12:121815406 | C | G | 2 | a0001c0009t0016g0023 a0005c0014t0016g0023 |
2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2715+476C>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121815406 | |||||||
chr12:121815431 | G | A | 3 | a0003c0010t0002g0035 a0003c0010t0002g0039 a0003c0010t0002g0192 |
3 | HG02451.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2715+501G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121815431 | |||||||
chr12:121815473 | C | T | 1 | a0001c0003t0003g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2715+543C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121815473 | |||||||
chr12:121815555 | G | A | 2 | a0001c0001t0002g0115 a0001c0037t0002g0067 |
2 | HG01928.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.2715+625G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121815555 | |||||||
chr12:121815726 | G | A | 1 | a0001c0003t0003g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2715+796G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121815726 | |||||||
chr12:121815781 | G | A | 1 | a0006c0030t0005g0183 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2715+851G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121815781 | |||||||
chr12:121815823 | C | CT | 7 | a0001c0001t0002g0105 a0001c0002t0001g0103 a0001c0009t0008g0148 others(4): Show |
7 | HG00735.hp2 HG02132.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.2715+913dupT | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 121815823 | ||||||
chr12:121815823 | CT | C | 9 | a0001c0001t0002g0036 a0001c0001t0011g0068 a0001c0002t0001g0070 others(6): Show |
9 | HG00323.hp2 HG00639.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2715+913delT | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 121815823 | ||||||
chr12:121815844 | C | T | 5 | a0001c0001t0002g0107 a0001c0001t0002g0108 a0001c0001t0002g0115 others(2): Show |
5 | HG01928.hp2 HG01934.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2715+914C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121815844 | |||||||
chr12:121816172 | C | CA | 3 | a0001c0009t0008g0148 a0002c0032t0012g0147 a0005c0014t0008g0146 |
3 | NA19055.hp1 NA19082.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.2716-860dupA | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 121816172 | ||||||
chr12:121816279 | C | T | 2 | a0001c0019t0014g0158 a0001c0019t0014g0159 |
2 | HG01109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2716-754C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121816279 | |||||||
chr12:121816416 | G | A | 1 | a0001c0002t0001g0071 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2716-617G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121816416 | |||||||
chr12:121816534 | G | A | 1 | a0001c0031t0005g0142 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2716-499G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121816534 | |||||||
chr12:121816549 | A | G | 1 | a0001c0001t0020g0101 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2716-484A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121816549 | |||||||
chr12:121816803 | A | T | 1 | a0004c0021t0002g0123 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2716-230A>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121816803 | |||||||
chr12:121816804 | G | A | 1 | a0004c0021t0002g0123 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2716-229G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121816804 | |||||||
chr12:121816805 | G | C | 1 | a0004c0021t0002g0123 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2716-228G>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121816805 | |||||||
chr12:121816806 | T | A | 1 | a0004c0021t0002g0123 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2716-227T>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121816806 | |||||||
chr12:121816807 | A | G | 56 | a0001c0003t0003g0003 a0001c0003t0003g0024 a0001c0003t0003g0027 others(53): Show |
68 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.2716-226A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121816807 | |||||||
chr12:121816856 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2716-177C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121816856 | |||||||
chr12:121816994 | G | T | 1 | a0001c0001t0002g0122 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2716-39G>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 7/16 | chr12 | 121816994 | |||||||
chr12:121817329 | G | A | 1 | a0001c0019t0014g0158 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2977+35G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 8/16 | chr12 | 121817329 | |||||||
chr12:121817946 | C | T | 1 | a0015c0033t0023g0141 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3418+42C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 10/16 | chr12 | 121817946 | |||||||
chr12:121817991 | G | A | 4 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0128 others(1): Show |
4 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.3418+87G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 10/16 | chr12 | 121817991 | |||||||
chr12:121818148 | G | C | 4 | a0003c0010t0002g0035 a0003c0010t0002g0039 a0003c0010t0002g0192 others(1): Show |
4 | HG02451.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3418+244G>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 10/16 | chr12 | 121818148 | |||||||
chr12:121818305 | G | A | 1 | a0001c0002t0001g0074 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3418+401G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 10/16 | chr12 | 121818305 | |||||||
chr12:121818370 | C | T | 1 | a0015c0033t0023g0141 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3418+466C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 10/16 | chr12 | 121818370 | |||||||
chr12:121818529 | C | T | 1 | a0001c0003t0009g0006 | 3 | HG02559.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3418+625C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 10/16 | chr12 | 121818529 | |||||||
chr12:121818535 | C | T | 34 | a0001c0003t0003g0003 a0001c0003t0003g0024 a0001c0003t0003g0027 others(31): Show |
43 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.3418+631C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 10/16 | chr12 | 121818535 | |||||||
chr12:121818553 | A | T | 2 | a0001c0001t0002g0120 a0001c0001t0002g0121 |
2 | HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3418+649A>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 10/16 | chr12 | 121818553 | |||||||
chr12:121818562 | C | CA | 41 | a0001c0003t0003g0003 a0001c0003t0003g0024 a0001c0003t0003g0027 others(38): Show |
52 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.3418+666dupA | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 121818562 | ||||||
chr12:121818573 | A | G | 1 | a0002c0013t0002g0153 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3418+669A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 10/16 | chr12 | 121818573 | |||||||
chr12:121818717 | C | T | 1 | a0001c0003t0003g0157 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3419-687C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 10/16 | chr12 | 121818717 | |||||||
chr12:121818762 | T | C | 55 | a0001c0003t0003g0003 a0001c0003t0003g0024 a0001c0003t0003g0027 others(52): Show |
66 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.3419-642T>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 10/16 | chr12 | 121818762 | |||||||
chr12:121818889 | C | CA | 8 | a0001c0001t0002g0036 a0001c0001t0002g0120 a0002c0004t0002g0106 others(5): Show |
8 | HG00544.hp1 HG02148.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.3419-498dupA | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 121818889 | ||||||
chr12:121818889 | CA | C | 5 | a0001c0001t0002g0053 a0001c0001t0002g0129 a0001c0002t0001g0100 others(2): Show |
5 | HG01169.hp1 HG02145.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3419-498delA | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 121818889 | ||||||
chr12:121818963 | G | A | 10 | a0002c0007t0001g0170 a0002c0007t0006g0169 a0002c0007t0006g0171 others(7): Show |
10 | HG01884.hp2 HG02922.hp1 HG03710.hp2 others(7): Show |
intron_variant | MODIFIER | c.3419-441G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 10/16 | chr12 | 121818963 | |||||||
chr12:121818993 | C | A | 1 | a0001c0002t0001g0076 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3419-411C>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 10/16 | chr12 | 121818993 | |||||||
chr12:121819013 | G | C | 3 | a0006c0016t0005g0184 a0006c0016t0005g0185 a0006c0030t0005g0183 |
3 | HG01884.hp2 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3419-391G>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 10/16 | chr12 | 121819013 | |||||||
chr12:121819105 | G | A | 4 | a0001c0009t0008g0148 a0002c0032t0012g0147 a0005c0014t0008g0146 others(1): Show |
4 | HG02622.hp1 NA19055.hp1 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.3419-299G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 10/16 | chr12 | 121819105 | |||||||
chr12:121819192 | C | A | 1 | a0003c0028t0019g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3419-212C>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 10/16 | chr12 | 121819192 | |||||||
chr12:121819192 | C | G | 1 | a0001c0001t0002g0115 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3419-212C>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 10/16 | chr12 | 121819192 | |||||||
chr12:121819365 | G | A | 1 | a0001c0003t0003g0157 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3419-39G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 10/16 | chr12 | 121819365 | |||||||
chr12:121819984 | G | A | 34 | a0001c0003t0003g0003 a0001c0003t0003g0024 a0001c0003t0003g0027 others(31): Show |
43 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.3910+89G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 11/16 | chr12 | 121819984 | |||||||
chr12:121820059 | G | A | 1 | a0003c0010t0002g0039 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3910+164G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 11/16 | chr12 | 121820059 | |||||||
chr12:121820132 | A | G | 4 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0128 others(1): Show |
4 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.3910+237A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 11/16 | chr12 | 121820132 | |||||||
chr12:121820141 | G | A | 40 | a0001c0003t0003g0003 a0001c0003t0003g0024 a0001c0003t0003g0027 others(37): Show |
51 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.3910+246G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 11/16 | chr12 | 121820141 | |||||||
chr12:121820212 | T | C | 3 | a0001c0002t0001g0061 a0001c0002t0001g0077 a0001c0002t0001g0118 |
3 | HG00280.hp2 HG01081.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.3910+317T>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 11/16 | chr12 | 121820212 | |||||||
chr12:121820282 | C | T | 1 | a0006c0030t0005g0183 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3910+387C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 11/16 | chr12 | 121820282 | |||||||
chr12:121820307 | G | A | 1 | a0015c0033t0023g0141 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3910+412G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 11/16 | chr12 | 121820307 | |||||||
chr12:121820355 | C | T | 6 | a0002c0007t0001g0170 a0002c0007t0006g0169 a0002c0007t0006g0171 others(3): Show |
6 | HG03710.hp2 HG03942.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.3910+460C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 11/16 | chr12 | 121820355 | |||||||
chr12:121820387 | C | G | 2 | a0001c0002t0001g0019 a0001c0002t0007g0099 |
3 | HG01361.hp2 HG01928.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.3910+492C>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 11/16 | chr12 | 121820387 | |||||||
chr12:121820628 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3910+733G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 11/16 | chr12 | 121820628 | |||||||
chr12:121820754 | C | T | 1 | a0006c0016t0005g0185 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3910+859C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 11/16 | chr12 | 121820754 | |||||||
chr12:121821019 | A | G | 14 | a0001c0003t0003g0024 a0001c0003t0003g0027 a0001c0003t0003g0030 others(11): Show |
16 | HG01884.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.3910+1124A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 11/16 | chr12 | 121821019 | |||||||
chr12:121821070 | C | A | 1 | a0001c0002t0001g0074 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3910+1175C>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 11/16 | chr12 | 121821070 | |||||||
chr12:121821253 | G | T | 2 | a0001c0003t0003g0182 a0001c0025t0003g0162 |
2 | HG01943.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.3911-1237G>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 11/16 | chr12 | 121821253 | |||||||
chr12:121821436 | T | TA | 25 | a0001c0001t0001g0048 a0001c0001t0002g0007 a0001c0001t0002g0009 others(22): Show |
30 | HG00423.hp2 HG00642.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.3911-1039dupA | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr12 | 121821436 | ||||||
chr12:121821553 | C | G | 1 | a0003c0028t0019g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3911-937C>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 11/16 | chr12 | 121821553 | |||||||
chr12:121821611 | C | T | 1 | a0001c0003t0003g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3911-879C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 11/16 | chr12 | 121821611 | |||||||
chr12:121822068 | A | C | 1 | a0001c0002t0001g0057 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3911-422A>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 11/16 | chr12 | 121822068 | |||||||
chr12:121822270 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3911-220C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 11/16 | chr12 | 121822270 | |||||||
chr12:121822444 | T | G | 1 | a0003c0028t0019g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3911-46T>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 11/16 | chr12 | 121822444 | |||||||
chr12:121823884 | C | A | 1 | a0001c0034t0007g0130 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.5170+135C>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/16 | chr12 | 121823884 | |||||||
chr12:121824090 | G | A | 206 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0050 others(203): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.5170+341G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/16 | chr12 | 121824090 | |||||||
chr12:121824142 | T | C | 2 | a0001c0002t0001g0188 a0004c0020t0001g0190 |
2 | HG02165.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.5170+393T>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/16 | chr12 | 121824142 | |||||||
chr12:121824304 | T | C | 1 | a0001c0001t0004g0062 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.5170+555T>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/16 | chr12 | 121824304 | |||||||
chr12:121824524 | A | G | 1 | a0003c0028t0019g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.5171-676A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/16 | chr12 | 121824524 | |||||||
chr12:121824581 | A | G | 1 | a0015c0033t0023g0141 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5171-619A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/16 | chr12 | 121824581 | |||||||
chr12:121824655 | A | C | 1 | a0003c0023t0008g0149 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.5171-545A>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/16 | chr12 | 121824655 | |||||||
chr12:121824657 | A | AC | 5 | a0001c0001t0002g0082 a0001c0002t0001g0083 a0003c0010t0002g0035 others(2): Show |
5 | HG02451.hp2 HG03225.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.5171-543_5171-542i others(3): Show |
SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/16 | chr12 | 121824657 | |||||||
chr12:121824657 | A | C | 194 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0050 others(191): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.5171-543A>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/16 | chr12 | 121824657 | |||||||
chr12:121824657 | A | G | 2 | a0006c0016t0005g0184 a0006c0016t0005g0185 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.5171-543A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/16 | chr12 | 121824657 | |||||||
chr12:121824883 | C | T | 4 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0128 others(1): Show |
4 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.5171-317C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/16 | chr12 | 121824883 | |||||||
chr12:121824979 | C | CA | 28 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0084 others(25): Show |
32 | HG01167.hp2 HG01168.hp1 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.5171-200dupA | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr12 | 121824979 | ||||||
chr12:121824979 | CA | C | 10 | a0001c0001t0004g0098 a0001c0002t0001g0114 a0001c0009t0008g0148 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.5171-200delA | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr12 | 121824979 | ||||||
chr12:121825042 | G | A | 2 | a0001c0019t0014g0158 a0001c0019t0014g0159 |
2 | HG01109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.5171-158G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/16 | chr12 | 121825042 | |||||||
chr12:121825190 | C | T | 1 | a0015c0033t0023g0141 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5171-10C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 12/16 | chr12 | 121825190 | |||||||
chr12:121825414 | C | T | 1 | a0001c0001t0004g0018 | 2 | NA18970.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.5337+48C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121825414 | |||||||
chr12:121825542 | G | A | 57 | a0001c0003t0003g0003 a0001c0003t0003g0024 a0001c0003t0003g0027 others(54): Show |
68 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.5337+176G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121825542 | |||||||
chr12:121825627 | A | G | 2 | a0001c0009t0008g0148 a0005c0014t0008g0146 |
2 | NA19082.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.5337+261A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121825627 | |||||||
chr12:121825647 | G | GT | 5 | a0001c0001t0002g0052 a0001c0002t0001g0114 a0001c0003t0003g0193 others(2): Show |
5 | HG00423.hp2 HG02055.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.5337+291dupT | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 121825647 | ||||||
chr12:121825660 | G | T | 2 | a0001c0009t0008g0148 a0005c0014t0008g0146 |
2 | NA19082.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.5337+294G>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121825660 | |||||||
chr12:121825846 | A | G | 2 | a0001c0002t0001g0096 a0001c0002t0001g0097 |
2 | NA19010.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.5337+480A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121825846 | |||||||
chr12:121825909 | C | G | 44 | a0001c0003t0003g0003 a0001c0003t0003g0024 a0001c0003t0003g0027 others(41): Show |
56 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.5337+543C>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121825909 | |||||||
chr12:121825938 | G | A | 1 | a0006c0030t0005g0183 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5337+572G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121825938 | |||||||
chr12:121826040 | C | G | 1 | a0001c0002t0001g0019 | 2 | HG01928.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.5337+674C>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121826040 | |||||||
chr12:121826188 | G | C | 1 | a0003c0023t0008g0149 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.5337+822G>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121826188 | |||||||
chr12:121826226 | A | T | 1 | a0001c0002t0001g0071 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.5337+860A>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121826226 | |||||||
chr12:121826267 | G | GT | 61 | a0001c0001t0001g0048 a0001c0002t0001g0001 a0001c0002t0001g0008 others(58): Show |
77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.5337+902dupT | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr12 | 121826267 | ||||||
chr12:121826332 | G | A | 3 | a0003c0010t0002g0035 a0003c0010t0002g0039 a0003c0010t0002g0192 |
3 | HG02451.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5337+966G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121826332 | |||||||
chr12:121826437 | C | G | 2 | a0001c0009t0016g0023 a0005c0014t0016g0023 |
2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.5337+1071C>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121826437 | |||||||
chr12:121826547 | T | G | 8 | a0001c0003t0003g0024 a0001c0003t0003g0030 a0001c0003t0003g0134 others(5): Show |
9 | HG01884.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.5338-972T>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121826547 | |||||||
chr12:121826558 | C | G | 2 | a0001c0001t0002g0056 a0001c0001t0011g0111 |
2 | HG00140.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.5338-961C>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121826558 | |||||||
chr12:121826590 | G | A | 1 | a0001c0002t0001g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5338-929G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121826590 | |||||||
chr12:121826694 | G | C | 1 | a0001c0001t0026g0089 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5338-825G>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121826694 | |||||||
chr12:121826715 | C | T | 7 | a0002c0007t0001g0170 a0002c0007t0006g0169 a0002c0007t0006g0171 others(4): Show |
7 | HG03710.hp2 HG03942.hp1 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.5338-804C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121826715 | |||||||
chr12:121826725 | G | A | 1 | a0001c0012t0015g0175 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5338-794G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121826725 | |||||||
chr12:121826729 | T | C | 25 | a0001c0001t0001g0005 a0001c0001t0001g0050 a0001c0001t0002g0004 others(22): Show |
30 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.5338-790T>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121826729 | |||||||
chr12:121826740 | G | A | 13 | a0002c0007t0001g0170 a0002c0007t0006g0169 a0002c0007t0006g0171 others(10): Show |
13 | HG01884.hp2 HG02451.hp2 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.5338-779G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121826740 | |||||||
chr12:121826741 | C | T | 61 | a0001c0001t0001g0048 a0001c0002t0001g0001 a0001c0002t0001g0008 others(58): Show |
77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.5338-778C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121826741 | |||||||
chr12:121826857 | C | T | 3 | a0003c0010t0002g0035 a0003c0010t0002g0039 a0003c0010t0002g0192 |
3 | HG02451.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5338-662C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121826857 | |||||||
chr12:121826913 | A | G | 1 | a0001c0001t0002g0092 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.5338-606A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121826913 | |||||||
chr12:121827195 | G | A | 4 | a0001c0003t0009g0006 a0009c0018t0003g0014 a0009c0018t0013g0033 others(1): Show |
6 | HG02258.hp2 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.5338-324G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121827195 | |||||||
chr12:121827200 | T | C | 78 | a0001c0001t0001g0048 a0001c0002t0001g0001 a0001c0002t0001g0008 others(75): Show |
94 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.5338-319T>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121827200 | |||||||
chr12:121827257 | A | G | 61 | a0001c0001t0001g0048 a0001c0002t0001g0001 a0001c0002t0001g0008 others(58): Show |
77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.5338-262A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121827257 | |||||||
chr12:121827500 | C | T | 2 | a0002c0006t0001g0117 a0019c0049t0001g0116 |
2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.5338-19C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 13/16 | chr12 | 121827500 | |||||||
chr12:121827677 | C | CG | 6 | a0001c0001t0020g0101 a0001c0002t0001g0095 a0003c0010t0002g0035 others(3): Show |
6 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(3): Show |
intron_variant | MODIFIER | c.5469+31dupG | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr12 | 121827677 | ||||||
chr12:121827702 | G | A | 1 | a0018c0035t0004g0063 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5470-33G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 14/16 | chr12 | 121827702 | |||||||
chr12:121827864 | G | A | 7 | a0002c0007t0006g0169 a0002c0007t0006g0171 a0002c0007t0017g0172 others(4): Show |
7 | HG02622.hp1 HG03710.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.5589+10G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 15/16 | chr12 | 121827864 | |||||||
chr12:121828210 | G | A | 1 | a0001c0001t0002g0093 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5727+140G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 16/16 | chr12 | 121828210 | |||||||
chr12:121828339 | T | C | 5 | a0001c0005t0005g0012 a0001c0005t0005g0026 a0005c0027t0005g0143 others(2): Show |
9 | HG01257.hp2 HG01258.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.5727+269T>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 16/16 | chr12 | 121828339 | |||||||
chr12:121828388 | A | G | 2 | a0001c0012t0015g0032 a0001c0012t0015g0175 |
2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.5727+318A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 16/16 | chr12 | 121828388 | |||||||
chr12:121828458 | G | A | 1 | a0001c0003t0003g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5727+388G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 16/16 | chr12 | 121828458 | |||||||
chr12:121828482 | A | G | 1 | a0015c0033t0023g0141 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5727+412A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 16/16 | chr12 | 121828482 | |||||||
chr12:121828672 | C | G | 1 | a0001c0001t0002g0122 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5727+602C>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 16/16 | chr12 | 121828672 | |||||||
chr12:121828849 | G | A | 7 | a0001c0003t0022g0156 a0002c0007t0006g0169 a0002c0007t0006g0171 others(4): Show |
7 | HG02683.hp2 HG03710.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.5727+779G>A | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 16/16 | chr12 | 121828849 | |||||||
chr12:121828969 | T | C | 1 | a0001c0003t0003g0155 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5727+899T>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 16/16 | chr12 | 121828969 | |||||||
chr12:121829211 | A | G | 91 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0002g0005 others(88): Show |
115 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.5728-855A>G | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 16/16 | chr12 | 121829211 | |||||||
chr12:121829312 | T | C | 144 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0050 others(141): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.5728-754T>C | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 16/16 | chr12 | 121829312 | |||||||
chr12:121829364 | C | T | 2 | a0002c0006t0001g0117 a0019c0049t0001g0116 |
2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.5728-702C>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 16/16 | chr12 | 121829364 | |||||||
chr12:121829994 | G | T | 3 | a0001c0009t0008g0148 a0002c0032t0012g0147 a0005c0014t0008g0146 |
3 | NA19055.hp1 NA19082.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.5728-72G>T | SETD1B | ENSG00000139718.12 | transcript | ENST00000604567.6 | protein_coding | 16/16 | chr12 | 121829994 |