Item | Value |
---|---|
geneid | 3892 |
ensemblid | ENSG00000170442.12 |
hgncid | 6463 |
symbol | KRT86 |
name | keratin 86 |
refseq_nuc | NM_001320198.2 |
refseq_prot | NP_001307127.1 |
ensembl_nuc | ENST00000423955.7 |
ensembl_prot | ENSP00000444533.1 |
mane_status | MANE Select |
chr | chr12 |
start | 52274645 |
end | 52309163 |
strand | + |
ver | v1.2 |
region | chr12:52274645-52309163 |
region5000 | chr12:52269645-52314163 |
regionname0 | KRT86_chr12_52274645_52309163 |
regionname5000 | KRT86_chr12_52269645_52314163 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 486 | 396 | 88 | 79 | 172 | 16 | 40 | 136 | KRT86_chr12_52269645_52314163 | KRT86 | MTCGS others(481): Show |
chr12 | 52269645 | 52314163 |
a0002 | 0/0 | 486 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | MTCGS others(481): Show |
chr12 | 52269645 | 52314163 |
a0003 | 0/0 | 486 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | KRT86_chr12_52269645_52314163 | KRT86 | MTCGS others(481): Show |
chr12 | 52269645 | 52314163 |
a0004 | 0/0 | 486 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | MTCGS others(481): Show |
chr12 | 52269645 | 52314163 |
a0005 | 0/0 | 486 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | MTCGS others(481): Show |
chr12 | 52269645 | 52314163 |
a0006 | 0/0 | 486 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | MTCGS others(481): Show |
chr12 | 52269645 | 52314163 |
a0007 | 0/0 | 486 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | MTCGS others(481): Show |
chr12 | 52269645 | 52314163 |
a0008 | 0/0 | 486 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | MTCGS others(481): Show |
chr12 | 52269645 | 52314163 |
a0009 | 0/0 | 486 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | MTCGS others(481): Show |
chr12 | 52269645 | 52314163 |
a0010 | 0/0 | 486 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | MTCGS others(481): Show |
chr12 | 52269645 | 52314163 |
a0011 | 0/0 | 486 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | MTCGS others(481): Show |
chr12 | 52269645 | 52314163 |
a0012 | 0/0 | 486 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | MTCGS others(481): Show |
chr12 | 52269645 | 52314163 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1458 | 160 | 16 | 40 | 78 | 7 | 18 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0001c0002 | 0/0 | 1458 | 141 | 40 | 21 | 68 | 4 | 8 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0001c0003 | 0/0 | 1458 | 47 | 10 | 7 | 17 | 1 | 12 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0001c0004 | 0/0 | 1458 | 9 | 0 | 5 | 0 | 3 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0001c0005 | 0/0 | 1458 | 8 | 7 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0001c0006 | 0/0 | 1458 | 6 | 4 | 2 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0001c0007 | 0/0 | 1458 | 6 | 3 | 0 | 3 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0001c0008 | 0/0 | 1458 | 4 | 0 | 0 | 4 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0001c0010 | 0/0 | 1458 | 3 | 0 | 2 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0001c0014 | 0/0 | 1458 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0001c0015 | 0/0 | 1458 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0001c0016 | 0/0 | 1458 | 2 | 1 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0001c0017 | 0/0 | 1458 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0001c0020 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0001c0021 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0001c0023 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0001c0027 | 0/0 | 1458 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0002c0009 | 0/0 | 1458 | 4 | 4 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0003c0011 | 0/0 | 1458 | 3 | 0 | 0 | 3 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0004c0012 | 0/0 | 1458 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0005c0013 | 0/0 | 1458 | 2 | 0 | 0 | 0 | 0 | 2 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0006c0018 | 0/0 | 1458 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0007c0019 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0008c0025 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0009c0022 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0010c0024 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0011c0028 | 0/0 | 1458 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 | ||
a0012c0026 | 0/0 | 1458 | 1 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATGAC others(1453): Show |
chr12 | 52269645 | 52314163 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2242): Show |
chr12 | 52269645 | 52314163 |
a0001c0001t0002 | 0/0 | 2247 | 98 | 1 | 28 | 51 | 3 | 14 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2242): Show |
chr12 | 52269645 | 52314163 |
a0001c0001t0004 | 0/0 | 2249 | 2 | 1 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2244): Show |
chr12 | 52269645 | 52314163 |
a0001c0001t0005 | 0/0 | 2249 | 51 | 13 | 12 | 19 | 4 | 3 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2244): Show |
chr12 | 52269645 | 52314163 |
a0001c0001t0007 | 0/0 | 2247 | 4 | 0 | 0 | 4 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2242): Show |
chr12 | 52269645 | 52314163 |
a0001c0001t0009 | 0/0 | 2249 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2244): Show |
chr12 | 52269645 | 52314163 |
a0001c0001t0011 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2244): Show |
chr12 | 52269645 | 52314163 |
a0001c0001t0015 | 0/0 | 2249 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2244): Show |
chr12 | 52269645 | 52314163 |
a0001c0002t0001 | 0/0 | 2247 | 89 | 1 | 17 | 62 | 4 | 5 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2242): Show |
chr12 | 52269645 | 52314163 |
a0001c0002t0003 | 0/0 | 2248 | 44 | 32 | 4 | 5 | 0 | 3 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2243): Show |
chr12 | 52269645 | 52314163 |
a0001c0002t0004 | 0/0 | 2249 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2244): Show |
chr12 | 52269645 | 52314163 |
a0001c0002t0008 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2242): Show |
chr12 | 52269645 | 52314163 |
a0001c0002t0011 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2244): Show |
chr12 | 52269645 | 52314163 |
a0001c0002t0013 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2242): Show |
chr12 | 52269645 | 52314163 |
a0001c0002t0018 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2244): Show |
chr12 | 52269645 | 52314163 |
a0001c0002t0020 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2242): Show |
chr12 | 52269645 | 52314163 |
a0001c0002t0021 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2242): Show |
chr12 | 52269645 | 52314163 |
a0001c0003t0004 | 0/0 | 2249 | 45 | 10 | 7 | 15 | 1 | 12 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2244): Show |
chr12 | 52269645 | 52314163 |
a0001c0003t0016 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2242): Show |
chr12 | 52269645 | 52314163 |
a0001c0003t0019 | 0/0 | 2249 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2244): Show |
chr12 | 52269645 | 52314163 |
a0001c0004t0003 | 0/0 | 2248 | 9 | 0 | 5 | 0 | 3 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2243): Show |
chr12 | 52269645 | 52314163 |
a0001c0005t0004 | 0/0 | 2249 | 5 | 5 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2244): Show |
chr12 | 52269645 | 52314163 |
a0001c0005t0006 | 0/0 | 2247 | 3 | 2 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2242): Show |
chr12 | 52269645 | 52314163 |
a0001c0006t0006 | 0/0 | 2247 | 6 | 4 | 2 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2242): Show |
chr12 | 52269645 | 52314163 |
a0001c0007t0003 | 0/0 | 2248 | 3 | 0 | 0 | 3 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2243): Show |
chr12 | 52269645 | 52314163 |
a0001c0007t0005 | 0/0 | 2249 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2244): Show |
chr12 | 52269645 | 52314163 |
a0001c0007t0012 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2244): Show |
chr12 | 52269645 | 52314163 |
a0001c0008t0001 | 0/0 | 2247 | 4 | 0 | 0 | 4 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2242): Show |
chr12 | 52269645 | 52314163 |
a0001c0010t0010 | 0/0 | 2247 | 2 | 0 | 2 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2242): Show |
chr12 | 52269645 | 52314163 |
a0001c0010t0022 | 0/0 | 2247 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTTT others(2242): Show |
chr12 | 52269645 | 52314163 |
a0001c0014t0008 | 0/0 | 2247 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2242): Show |
chr12 | 52269645 | 52314163 |
a0001c0015t0001 | 0/0 | 2247 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2242): Show |
chr12 | 52269645 | 52314163 |
a0001c0016t0003 | 0/0 | 2248 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2243): Show |
chr12 | 52269645 | 52314163 |
a0001c0016t0005 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2244): Show |
chr12 | 52269645 | 52314163 |
a0001c0017t0004 | 0/0 | 2249 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2244): Show |
chr12 | 52269645 | 52314163 |
a0001c0020t0005 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2244): Show |
chr12 | 52269645 | 52314163 |
a0001c0021t0003 | 0/0 | 2248 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2243): Show |
chr12 | 52269645 | 52314163 |
a0001c0023t0001 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2242): Show |
chr12 | 52269645 | 52314163 |
a0001c0027t0004 | 0/0 | 2249 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2244): Show |
chr12 | 52269645 | 52314163 |
a0002c0009t0001 | 0/0 | 2247 | 4 | 4 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2242): Show |
chr12 | 52269645 | 52314163 |
a0003c0011t0001 | 0/0 | 2247 | 3 | 0 | 0 | 3 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2242): Show |
chr12 | 52269645 | 52314163 |
a0004c0012t0003 | 0/0 | 2248 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2243): Show |
chr12 | 52269645 | 52314163 |
a0004c0012t0014 | 0/0 | 2248 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2243): Show |
chr12 | 52269645 | 52314163 |
a0005c0013t0001 | 0/0 | 2247 | 2 | 0 | 0 | 0 | 0 | 2 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2242): Show |
chr12 | 52269645 | 52314163 |
a0006c0018t0005 | 0/0 | 2249 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2244): Show |
chr12 | 52269645 | 52314163 |
a0007c0019t0003 | 0/0 | 2248 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2243): Show |
chr12 | 52269645 | 52314163 |
a0008c0025t0001 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2242): Show |
chr12 | 52269645 | 52314163 |
a0009c0022t0017 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2242): Show |
chr12 | 52269645 | 52314163 |
a0010c0024t0005 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2244): Show |
chr12 | 52269645 | 52314163 |
a0011c0028t0004 | 0/0 | 2249 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2244): Show |
chr12 | 52269645 | 52314163 |
a0012c0026t0001 | 0/0 | 2247 | 1 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | ATTCT others(2242): Show |
chr12 | 52269645 | 52314163 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0001 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0003 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0005g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0007g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0007g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0007g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0009g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0009g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0011g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0001t0015g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0004 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0004g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0008g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0011g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0013g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0018g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0020g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0002t0021g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0007 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0004g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0016g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0003t0019g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0004t0003g0006 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0004t0003g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0004t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0004t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0004t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0005t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0005t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0005t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0005t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0005t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0005t0006g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0005t0006g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0006t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0006t0006g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0006t0006g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0006t0006g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0006t0006g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0006t0006g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0007t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0007t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0007t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0007t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0007t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0007t0012g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0008t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0008t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0008t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0010t0010g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0010t0010g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0010t0022g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0014t0008g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0014t0008g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0015t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0015t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0016t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0016t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0017t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0017t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0020t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0021t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0023t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0001c0027t0004g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0002c0009t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0002c0009t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0002c0009t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0003c0011t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0003c0011t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0003c0011t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0004c0012t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0004c0012t0014g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0005c0013t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0005c0013t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0006c0018t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0007c0019t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0008c0025t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0009c0022t0017g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0010c0024t0005g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0011c0028t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
a0012c0026t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 0 | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0004 | g0309 | EUR | GBR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00099 | hp2 | a0001 | c0010 | t0022 | g0030 | EUR | GBR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00140 | hp1 | a0001 | c0001 | t0005 | g0117 | EUR | GBR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00140 | hp2 | a0001 | c0004 | t0003 | g0285 | EUR | GBR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00280 | hp1 | a0001 | c0001 | t0005 | g0204 | EUR | FIN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0192 | EUR | FIN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0190 | EUR | FIN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00323 | hp2 | a0001 | c0004 | t0003 | g0006 | EUR | FIN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00408 | hp1 | a0001 | c0008 | t0001 | g0087 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00423 | hp1 | a0001 | c0001 | t0005 | g0120 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00423 | hp2 | a0001 | c0003 | t0004 | g0287 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00438 | hp1 | a0001 | c0001 | t0005 | g0128 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00558 | hp1 | a0001 | c0001 | t0005 | g0123 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00621 | hp1 | a0001 | c0002 | t0003 | g0145 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00621 | hp2 | a0001 | c0001 | t0005 | g0055 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0189 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0303 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00642 | hp1 | a0001 | c0003 | t0004 | g0324 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00673 | hp1 | a0001 | c0001 | t0009 | g0109 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00673 | hp2 | a0001 | c0001 | t0015 | g0094 | EAS | CHS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00733 | hp1 | a0001 | c0001 | t0005 | g0027 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00733 | hp2 | a0001 | c0003 | t0004 | g0293 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00738 | hp2 | a0001 | c0003 | t0004 | g0258 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG00741 | hp2 | a0001 | c0004 | t0003 | g0277 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01069 | hp1 | a0001 | c0004 | t0003 | g0039 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0141 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0191 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01071 | hp1 | a0001 | c0004 | t0003 | g0039 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01074 | hp1 | a0001 | c0016 | t0003 | g0041 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01099 | hp1 | a0001 | c0003 | t0004 | g0276 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01099 | hp2 | a0001 | c0001 | t0005 | g0125 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0165 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01106 | hp2 | a0001 | c0004 | t0003 | g0278 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01109 | hp2 | a0001 | c0005 | t0006 | g0166 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01167 | hp1 | a0001 | c0006 | t0006 | g0305 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01168 | hp1 | a0001 | c0002 | t0003 | g0256 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01169 | hp2 | a0001 | c0006 | t0006 | g0281 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01192 | hp2 | a0001 | c0001 | t0005 | g0126 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0115 | AMR | PUR | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01255 | hp1 | a0001 | c0002 | t0003 | g0101 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01255 | hp2 | a0001 | c0003 | t0004 | g0280 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01256 | hp1 | a0001 | c0001 | t0005 | g0147 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0179 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0196 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01261 | hp2 | a0001 | c0001 | t0005 | g0012 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01346 | hp1 | a0006 | c0018 | t0005 | g0025 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01358 | hp1 | a0001 | c0004 | t0003 | g0006 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01358 | hp2 | a0001 | c0002 | t0003 | g0015 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0225 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01433 | hp1 | a0001 | c0002 | t0003 | g0015 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01433 | hp2 | a0001 | c0001 | t0005 | g0124 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0226 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01496 | hp2 | a0001 | c0010 | t0010 | g0030 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0193 | EUR | IBS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0054 | EUR | IBS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01517 | hp1 | a0001 | c0001 | t0005 | g0026 | EUR | IBS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0187 | EUR | IBS | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01884 | hp1 | a0001 | c0002 | t0003 | g0044 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0330 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01891 | hp1 | a0001 | c0017 | t0004 | g0130 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01891 | hp2 | a0001 | c0002 | t0003 | g0231 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0180 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0140 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01978 | hp1 | a0001 | c0003 | t0004 | g0286 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0313 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01993 | hp2 | a0001 | c0001 | t0005 | g0027 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0079 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02027 | hp2 | a0001 | c0001 | t0005 | g0119 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02055 | hp1 | a0001 | c0002 | t0008 | g0156 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02055 | hp2 | a0001 | c0002 | t0003 | g0259 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02071 | hp2 | a0001 | c0003 | t0004 | g0155 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02074 | hp2 | a0001 | c0003 | t0004 | g0317 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02129 | hp2 | a0001 | c0003 | t0004 | g0298 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02132 | hp2 | a0001 | c0001 | t0005 | g0142 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02135 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02145 | hp1 | a0001 | c0002 | t0003 | g0332 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02145 | hp2 | a0002 | c0009 | t0001 | g0265 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02148 | hp1 | a0001 | c0003 | t0004 | g0300 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0183 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | CDX | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02165 | hp2 | a0001 | c0003 | t0004 | g0288 | EAS | CDX | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02257 | hp1 | a0001 | c0003 | t0004 | g0284 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02257 | hp2 | a0001 | c0002 | t0003 | g0250 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02258 | hp1 | a0001 | c0003 | t0004 | g0290 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02258 | hp2 | a0002 | c0009 | t0001 | g0266 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02280 | hp1 | a0001 | c0002 | t0003 | g0322 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02280 | hp2 | a0001 | c0002 | t0003 | g0043 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02293 | hp2 | a0001 | c0010 | t0010 | g0161 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02300 | hp2 | a0001 | c0001 | t0005 | g0116 | AMR | PEL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02451 | hp1 | a0001 | c0002 | t0003 | g0319 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02451 | hp2 | a0001 | c0002 | t0003 | g0162 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | KHV | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02572 | hp1 | a0001 | c0016 | t0005 | g0333 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02572 | hp2 | a0001 | c0002 | t0003 | g0282 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02602 | hp2 | a0001 | c0003 | t0004 | g0272 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02615 | hp1 | a0001 | c0001 | t0005 | g0310 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02615 | hp2 | a0001 | c0002 | t0003 | g0041 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02622 | hp1 | a0001 | c0005 | t0006 | g0326 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0342 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0042 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02630 | hp2 | a0001 | c0014 | t0008 | g0164 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02647 | hp1 | a0001 | c0005 | t0004 | g0274 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02683 | hp1 | a0001 | c0003 | t0004 | g0320 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02683 | hp2 | a0001 | c0004 | t0003 | g0006 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02698 | hp1 | a0001 | c0003 | t0004 | g0291 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02698 | hp2 | a0001 | c0002 | t0003 | g0244 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02717 | hp1 | a0001 | c0002 | t0003 | g0337 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02717 | hp2 | a0001 | c0002 | t0003 | g0257 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0340 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02723 | hp2 | a0007 | c0019 | t0003 | g0252 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0025 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02809 | hp1 | a0001 | c0001 | t0011 | g0347 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02809 | hp2 | a0001 | c0005 | t0004 | g0151 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02818 | hp1 | a0008 | c0025 | t0001 | g0268 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02818 | hp2 | a0001 | c0007 | t0005 | g0150 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0264 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02886 | hp2 | a0001 | c0002 | t0003 | g0339 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02895 | hp1 | a0001 | c0002 | t0004 | g0029 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02895 | hp2 | a0004 | c0012 | t0003 | g0328 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02896 | hp1 | a0002 | c0009 | t0001 | g0031 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02896 | hp2 | a0001 | c0007 | t0005 | g0152 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02897 | hp1 | a0002 | c0009 | t0001 | g0031 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02897 | hp2 | a0001 | c0002 | t0004 | g0029 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02922 | hp1 | a0001 | c0005 | t0006 | g0139 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02922 | hp2 | a0001 | c0002 | t0018 | g0335 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02965 | hp1 | a0001 | c0002 | t0003 | g0044 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02965 | hp2 | a0004 | c0012 | t0014 | g0160 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0042 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02970 | hp2 | a0001 | c0002 | t0003 | g0229 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02976 | hp1 | a0001 | c0002 | t0003 | g0270 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02976 | hp2 | a0001 | c0002 | t0003 | g0271 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03017 | hp1 | a0005 | c0013 | t0001 | g0185 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03017 | hp2 | a0001 | c0002 | t0003 | g0240 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03041 | hp1 | a0001 | c0002 | t0003 | g0251 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03041 | hp2 | a0001 | c0006 | t0006 | g0273 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03098 | hp1 | a0001 | c0003 | t0004 | g0279 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0253 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03130 | hp1 | a0001 | c0007 | t0012 | g0304 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03130 | hp2 | a0001 | c0020 | t0005 | g0113 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03139 | hp1 | a0001 | c0002 | t0003 | g0306 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03195 | hp1 | a0001 | c0023 | t0001 | g0338 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03195 | hp2 | a0001 | c0002 | t0003 | g0254 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03209 | hp1 | a0001 | c0014 | t0008 | g0163 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03209 | hp2 | a0001 | c0003 | t0004 | g0311 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03225 | hp1 | a0009 | c0022 | t0017 | g0275 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03225 | hp2 | a0001 | c0003 | t0004 | g0334 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0301 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03453 | hp1 | a0001 | c0002 | t0003 | g0249 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03453 | hp2 | a0001 | c0003 | t0004 | g0321 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03486 | hp1 | a0001 | c0006 | t0006 | g0343 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03486 | hp2 | a0001 | c0002 | t0003 | g0327 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03490 | hp1 | a0001 | c0002 | t0003 | g0295 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0033 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0325 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03516 | hp2 | a0001 | c0021 | t0003 | g0261 | AFR | ESN | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03540 | hp1 | a0001 | c0002 | t0021 | g0344 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03540 | hp2 | a0001 | c0002 | t0003 | g0312 | AFR | GWD | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03579 | hp1 | a0001 | c0002 | t0011 | g0346 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0314 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0194 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03669 | hp2 | a0001 | c0003 | t0004 | g0040 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0121 | SAS | STU | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0045 | SAS | STU | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0033 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03704 | hp2 | a0001 | c0003 | t0004 | g0308 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03710 | hp2 | a0001 | c0003 | t0004 | g0040 | SAS | PJL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | BEB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03831 | hp2 | a0001 | c0003 | t0004 | g0323 | SAS | BEB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03834 | hp1 | a0001 | c0027 | t0004 | g0302 | SAS | BEB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03834 | hp2 | a0005 | c0013 | t0001 | g0184 | SAS | BEB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03942 | hp1 | a0001 | c0003 | t0004 | g0007 | SAS | BEB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0112 | SAS | BEB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG04115 | hp1 | a0001 | c0003 | t0004 | g0069 | SAS | STU | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG04115 | hp2 | a0001 | c0001 | t0005 | g0114 | SAS | STU | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | STU | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG04199 | hp2 | a0001 | c0003 | t0004 | g0072 | SAS | STU | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | STU | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG04204 | hp2 | a0001 | c0001 | t0005 | g0103 | SAS | STU | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | STU | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG04228 | hp2 | a0001 | c0003 | t0004 | g0269 | SAS | STU | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18522 | hp1 | a0001 | c0005 | t0004 | g0028 | AFR | YRI | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18522 | hp2 | a0001 | c0002 | t0003 | g0158 | AFR | YRI | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | CHB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | CHB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18906 | hp1 | a0001 | c0002 | t0003 | g0149 | AFR | YRI | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18906 | hp2 | a0010 | c0024 | t0005 | g0331 | AFR | YRI | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18941 | hp1 | a0001 | c0001 | t0007 | g0095 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18942 | hp2 | a0001 | c0001 | t0005 | g0118 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18945 | hp1 | a0001 | c0001 | t0005 | g0199 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18947 | hp2 | a0001 | c0003 | t0004 | g0299 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18957 | hp1 | a0001 | c0008 | t0001 | g0037 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18957 | hp2 | a0001 | c0003 | t0004 | g0318 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18963 | hp1 | a0001 | c0003 | t0004 | g0007 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18963 | hp2 | a0001 | c0002 | t0003 | g0200 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18965 | hp2 | a0001 | c0001 | t0007 | g0056 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18967 | hp1 | a0001 | c0003 | t0004 | g0262 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18968 | hp1 | a0001 | c0003 | t0004 | g0236 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18968 | hp2 | a0003 | c0011 | t0001 | g0122 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18970 | hp1 | a0001 | c0015 | t0001 | g0077 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18971 | hp2 | a0001 | c0002 | t0003 | g0239 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18973 | hp2 | a0011 | c0028 | t0004 | g0315 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18974 | hp1 | a0001 | c0002 | t0003 | g0146 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18977 | hp1 | a0001 | c0002 | t0013 | g0064 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18977 | hp2 | a0001 | c0007 | t0003 | g0067 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18978 | hp1 | a0001 | c0001 | t0005 | g0074 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18981 | hp1 | a0001 | c0003 | t0004 | g0255 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18982 | hp2 | a0001 | c0007 | t0003 | g0289 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18984 | hp2 | a0003 | c0011 | t0001 | g0132 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18986 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18986 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18991 | hp2 | a0001 | c0003 | t0016 | g0263 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18994 | hp2 | a0001 | c0015 | t0001 | g0223 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18997 | hp2 | a0001 | c0001 | t0005 | g0138 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18998 | hp1 | a0001 | c0003 | t0004 | g0242 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA18999 | hp2 | a0001 | c0003 | t0019 | g0144 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19001 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19002 | hp2 | a0001 | c0008 | t0001 | g0198 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19005 | hp1 | a0001 | c0001 | t0005 | g0203 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19006 | hp1 | a0001 | c0003 | t0004 | g0007 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19010 | hp1 | a0003 | c0011 | t0001 | g0133 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19030 | hp1 | a0001 | c0002 | t0003 | g0247 | AFR | LWK | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19030 | hp2 | a0001 | c0006 | t0006 | g0307 | AFR | LWK | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19043 | hp1 | a0001 | c0002 | t0003 | g0329 | AFR | LWK | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19043 | hp2 | a0001 | c0003 | t0004 | g0296 | AFR | LWK | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19056 | hp2 | a0001 | c0008 | t0001 | g0037 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19057 | hp2 | a0001 | c0001 | t0009 | g0078 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19059 | hp1 | a0001 | c0003 | t0004 | g0316 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19059 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19062 | hp2 | a0001 | c0001 | t0005 | g0148 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19063 | hp2 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19065 | hp1 | a0001 | c0001 | t0005 | g0129 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19066 | hp2 | a0001 | c0003 | t0004 | g0007 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19068 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19074 | hp2 | a0001 | c0007 | t0003 | g0292 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19076 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19083 | hp1 | a0001 | c0001 | t0005 | g0143 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19084 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19085 | hp2 | a0001 | c0001 | t0005 | g0127 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19091 | hp2 | a0001 | c0002 | t0003 | g0241 | EAS | JPT | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19240 | hp1 | a0001 | c0002 | t0003 | g0336 | AFR | YRI | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA19240 | hp2 | a0001 | c0005 | t0004 | g0153 | AFR | YRI | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0283 | AFR | ASW | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA20129 | hp2 | a0001 | c0005 | t0004 | g0028 | AFR | ASW | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0188 | EUR | TSI | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA20752 | hp2 | a0001 | c0004 | t0003 | g0006 | EUR | TSI | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA20805 | hp2 | a0001 | c0001 | t0005 | g0134 | EUR | TSI | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | GIH | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA20905 | hp2 | a0001 | c0003 | t0004 | g0154 | SAS | GIH | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG01123 | hp2 | a0001 | c0001 | t0005 | g0026 | AMR | CLM | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0038 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02109 | hp2 | a0001 | c0002 | t0020 | g0345 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02486 | hp1 | a0001 | c0002 | t0003 | g0248 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02486 | hp2 | a0001 | c0002 | t0003 | g0043 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0267 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG02559 | hp2 | a0001 | c0003 | t0004 | g0157 | AFR | ACB | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03471 | hp1 | a0001 | c0003 | t0004 | g0136 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG03471 | hp2 | a0001 | c0002 | t0003 | g0230 | AFR | MSL | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG06807 | hp1 | a0001 | c0006 | t0006 | g0159 | AFR | USA | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
HG06807 | hp2 | a0001 | c0003 | t0004 | g0341 | AFR | USA | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA21309 | hp1 | a0001 | c0017 | t0004 | g0297 | AFR | LWK | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0294 | AFR | LWK | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
homoSapiens_chm13v2 | hp1 | a0012 | c0026 | t0001 | g0131 | REF | REF | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0176 | REF | REF | KRT86_chr12_52269645_52314163 | KRT86 | chr12 | 52269645 | 52314163 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:52302071 | G | A | 1 | a0011 | 1 | NA18973.hp2 | missense_variant | MODERATE | c.155G>A | p.Gly52Glu | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/11 | 363/2247 | 155/1461 | 52/486 | chr12 | 52302071 | |||
chr12:52302113 | G | A | 1 | a0006 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.197G>A | p.Arg66His | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/11 | 405/2247 | 197/1461 | 66/486 | chr12 | 52302113 | |||
chr12:52302220 | G | A | 1 | a0007 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.304G>A | p.Val102Met | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/11 | 512/2247 | 304/1461 | 102/486 | chr12 | 52302220 | |||
chr12:52303146 | A | C | 1 | a0012 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.416A>C | p.Gln139Pro | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/11 | 624/2247 | 416/1461 | 139/486 | chr12 | 52303146 | |||
chr12:52303217 | C | T | 1 | a0008 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.487C>T | p.Arg163Trp | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/11 | 695/2247 | 487/1461 | 163/486 | chr12 | 52303217 | |||
chr12:52304933 | A | G | 2 | a0002 a0008 |
5 | HG02145.hp2 HG02258.hp2 HG02818.hp1 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.641A>G | p.Asp214Gly | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 6/11 | 849/2247 | 641/1461 | 214/486 | chr12 | 52304933 | |||
chr12:52305013 | C | T | 1 | a0003 | 3 | NA18968.hp2 NA18984.hp2 NA19010.hp1 |
missense_variant | MODERATE | c.721C>T | p.Arg241Trp | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 6/11 | 929/2247 | 721/1461 | 241/486 | chr12 | 52305013 | |||
chr12:52305024 | G | C | 1 | a0010 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.732G>C | p.Glu244Asp | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 6/11 | 940/2247 | 732/1461 | 244/486 | chr12 | 52305024 | |||
chr12:52305303 | C | T | 1 | a0005 | 2 | HG03017.hp1 HG03834.hp2 |
missense_variant | MODERATE | c.799C>T | p.Arg267Trp | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 7/11 | 1007/2247 | 799/1461 | 267/486 | chr12 | 52305303 | |||
chr12:52305366 | C | G | 1 | a0009 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.862C>G | p.Arg288Gly | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 7/11 | 1070/2247 | 862/1461 | 288/486 | chr12 | 52305366 | |||
chr12:52305384 | G | A | 1 | a0004 | 2 | HG02895.hp2 HG02965.hp2 |
missense_variant | MODERATE | c.880G>A | p.Glu294Lys | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 7/11 | 1088/2247 | 880/1461 | 294/486 | chr12 | 52305384 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:52301970 | C | T | 4 | a0001c0003 a0001c0017 a0001c0027 others(1): Show |
51 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(48): Show |
synonymous_variant | LOW | c.54C>T | p.Cys18Cys | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/11 | 262/2247 | 54/1461 | 18/486 | chr12 | 52301970 | |||
chr12:52301976 | C | G | 1 | a0001c0016 | 2 | HG01074.hp1 HG02572.hp1 |
synonymous_variant | LOW | c.60C>G | p.Pro20Pro | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/11 | 268/2247 | 60/1461 | 20/486 | chr12 | 52301976 | |||
chr12:52302003 | C | T | 3 | a0001c0003 a0001c0017 a0011c0028 |
50 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(47): Show |
synonymous_variant | LOW | c.87C>T | p.Ala29Ala | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/11 | 295/2247 | 87/1461 | 29/486 | chr12 | 52302003 | |||
chr12:52302117 | C | T | 1 | a0001c0015 | 2 | NA18970.hp1 NA18994.hp2 |
synonymous_variant | LOW | c.201C>T | p.Ser67Ser | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/11 | 409/2247 | 201/1461 | 67/486 | chr12 | 52302117 | |||
chr12:52302204 | C | T | 1 | a0001c0014 | 2 | HG02630.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.288C>T | p.Asp96Asp | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/11 | 496/2247 | 288/1461 | 96/486 | chr12 | 52302204 | |||
chr12:52302213 | G | A | 1 | a0001c0004 | 9 | HG00140.hp2 HG00323.hp2 HG00741.hp2 others(6): Show |
synonymous_variant | LOW | c.297G>A | p.Ala99Ala | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/11 | 505/2247 | 297/1461 | 99/486 | chr12 | 52302213 | |||
chr12:52302264 | G | A | 4 | a0001c0003 a0001c0020 a0001c0027 others(1): Show |
50 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(47): Show |
synonymous_variant | LOW | c.348G>A | p.Arg116Arg | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/11 | 556/2247 | 348/1461 | 116/486 | chr12 | 52302264 | |||
chr12:52304168 | G | A | 16 | a0001c0002 a0001c0004 a0001c0006 others(13): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(178): Show |
synonymous_variant | LOW | c.636G>A | p.Lys212Lys | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/11 | 844/2247 | 636/1461 | 212/486 | chr12 | 52304168 | |||
chr12:52304976 | T | C | 3 | a0001c0005 a0001c0006 a0001c0021 |
15 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
synonymous_variant | LOW | c.684T>C | p.Asn228Asn | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 6/11 | 892/2247 | 684/1461 | 228/486 | chr12 | 52304976 | |||
chr12:52305248 | C | T | 3 | a0001c0008 a0002c0009 a0008c0025 |
9 | HG00408.hp1 HG02145.hp2 HG02258.hp2 others(6): Show |
synonymous_variant | LOW | c.744C>T | p.Arg248Arg | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 7/11 | 952/2247 | 744/1461 | 248/486 | chr12 | 52305248 | |||
chr12:52305275 | C | G | 1 | a0001c0023 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.771C>G | p.Thr257Thr | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 7/11 | 979/2247 | 771/1461 | 257/486 | chr12 | 52305275 | |||
chr12:52305377 | T | C | 1 | a0001c0006 | 6 | HG01167.hp1 HG01169.hp2 HG03041.hp2 others(3): Show |
synonymous_variant | LOW | c.873T>C | p.Ala291Ala | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 7/11 | 1081/2247 | 873/1461 | 291/486 | chr12 | 52305377 | |||
chr12:52305764 | T | C | 20 | a0001c0002 a0001c0004 a0001c0005 others(17): Show |
200 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(197): Show |
synonymous_variant | LOW | c.1002T>C | p.Ala334Ala | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 8/11 | 1210/2247 | 1002/1461 | 334/486 | chr12 | 52305764 | |||
chr12:52306069 | C | T | 1 | a0001c0014 | 2 | HG02630.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.1036C>T | p.Leu346Leu | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/11 | 1244/2247 | 1036/1461 | 346/486 | chr12 | 52306069 | |||
chr12:52306077 | T | C | 2 | a0001c0005 a0001c0010 |
11 | HG00099.hp2 HG01109.hp2 HG01496.hp2 others(8): Show |
synonymous_variant | LOW | c.1044T>C | p.Ala348Ala | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/11 | 1252/2247 | 1044/1461 | 348/486 | chr12 | 52306077 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:52274648 | C | T | 1 | a0001c0010t0022 | 1 | HG00099.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-205C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 1/11 | chr12 | 52274648 | |||||||
chr12:52274666 | A | G | 4 | a0001c0001t0011 a0001c0002t0011 a0001c0002t0020 others(1): Show |
4 | HG02109.hp2 HG02809.hp1 HG03540.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-187A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 1/11 | 27251 | chr12 | 52274666 | ||||||
chr12:52274716 | C | T | 1 | a0001c0003t0019 | 1 | NA18999.hp2 | 5_prime_UTR_variant | MODIFIER | c.-137C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 1/11 | 27201 | chr12 | 52274716 | ||||||
chr12:52275841 | T | C | 1 | a0001c0007t0012 | 1 | HG03130.hp1 | 5_prime_UTR_variant | MODIFIER | c.-110T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/11 | 26076 | chr12 | 52275841 | ||||||
chr12:52275919 | G | C | 3 | a0001c0001t0011 a0001c0002t0011 a0001c0002t0020 |
3 | HG02109.hp2 HG02809.hp1 HG03579.hp1 |
5_prime_UTR_variant | MODIFIER | c.-32G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/11 | 25998 | chr12 | 52275919 | ||||||
chr12:52275920 | G | A | 3 | a0001c0001t0011 a0001c0002t0011 a0001c0002t0020 |
3 | HG02109.hp2 HG02809.hp1 HG03579.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-31G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/11 | chr12 | 52275920 | |||||||
chr12:52275940 | G | A | 2 | a0001c0001t0007 a0001c0002t0013 |
5 | HG02135.hp2 NA18941.hp1 NA18965.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-11G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/11 | 25977 | chr12 | 52275940 | ||||||
chr12:52308588 | G | A | 1 | a0001c0002t0020 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 3 | chr12 | 52308588 | ||||||
chr12:52308631 | A | C | 2 | a0001c0002t0008 a0001c0014t0008 |
3 | HG02055.hp1 HG02630.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*46A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 46 | chr12 | 52308631 | ||||||
chr12:52308679 | A | G | 13 | a0001c0001t0001 a0001c0002t0001 a0001c0002t0013 others(10): Show |
111 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*94A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 94 | chr12 | 52308679 | ||||||
chr12:52308685 | G | A | 1 | a0004c0012t0014 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*100G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 100 | chr12 | 52308685 | ||||||
chr12:52308712 | C | T | 29 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0011 others(26): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*127C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 127 | chr12 | 52308712 | ||||||
chr12:52308805 | G | A | 1 | a0001c0001t0015 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*220G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 220 | chr12 | 52308805 | ||||||
chr12:52308849 | G | A | 20 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(17): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*264G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 264 | chr12 | 52308849 | ||||||
chr12:52308856 | G | GT | 8 | a0001c0002t0003 a0001c0004t0003 a0001c0007t0003 others(5): Show |
61 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*279dupT | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 280 | INFO_REALIGN_3_PRIME | chr12 | 52308856 | |||||
chr12:52308856 | G | GTT | 20 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(17): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*278_*279dupTT | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 280 | INFO_REALIGN_3_PRIME | chr12 | 52308856 | |||||
chr12:52308872 | A | G | 49 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(46): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
3_prime_UTR_variant | MODIFIER | c.*287A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 287 | chr12 | 52308872 | ||||||
chr12:52308897 | C | T | 10 | a0001c0001t0004 a0001c0001t0009 a0001c0002t0004 others(7): Show |
62 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*312C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 312 | chr12 | 52308897 | ||||||
chr12:52308943 | A | G | 2 | a0001c0005t0006 a0001c0006t0006 |
9 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*358A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 11/11 | 358 | chr12 | 52308943 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:52274798 | A | G | 1 | a0001c0001t0011g0347 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-131+76A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 1/10 | chr12 | 52274798 | |||||||
chr12:52274834 | A | G | 4 | a0001c0001t0011g0347 a0001c0002t0011g0346 a0001c0002t0020g0345 others(1): Show |
4 | HG02109.hp2 HG02809.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-131+112A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 1/10 | chr12 | 52274834 | |||||||
chr12:52274932 | T | G | 86 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0011 others(83): Show |
108 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.-131+210T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 1/10 | chr12 | 52274932 | |||||||
chr12:52275202 | T | C | 5 | a0001c0001t0011g0347 a0001c0002t0011g0346 a0001c0002t0020g0345 others(2): Show |
5 | HG02109.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131+480T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 1/10 | chr12 | 52275202 | |||||||
chr12:52275436 | AT | A | 41 | a0001c0001t0002g0135 a0001c0001t0005g0008 a0001c0001t0005g0025 others(38): Show |
45 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.-130-377delT | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 52275436 | ||||||
chr12:52275627 | A | G | 4 | a0001c0001t0011g0347 a0001c0002t0011g0346 a0001c0002t0020g0345 others(1): Show |
4 | HG02109.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-130-194A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 1/10 | chr12 | 52275627 | |||||||
chr12:52275628 | T | A | 5 | a0001c0005t0004g0028 a0001c0005t0004g0151 a0001c0005t0004g0153 others(2): Show |
6 | HG02809.hp2 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-130-193T>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 1/10 | chr12 | 52275628 | |||||||
chr12:52276029 | C | A | 1 | a0001c0003t0004g0154 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-5+83C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276029 | |||||||
chr12:52276043 | T | A | 1 | a0001c0003t0004g0155 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-5+97T>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276043 | |||||||
chr12:52276170 | G | A | 5 | a0001c0005t0004g0028 a0001c0005t0004g0151 a0001c0005t0004g0153 others(2): Show |
6 | HG02809.hp2 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+224G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276170 | |||||||
chr12:52276247 | C | T | 85 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0011 others(82): Show |
107 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.-5+301C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276247 | |||||||
chr12:52276394 | C | T | 2 | a0001c0001t0005g0342 a0001c0006t0006g0343 |
2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-5+448C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276394 | |||||||
chr12:52276496 | T | C | 103 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0011 others(100): Show |
127 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.-5+550T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276496 | |||||||
chr12:52276568 | C | T | 246 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0011 others(243): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.-5+622C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276568 | |||||||
chr12:52276580 | AG | A | 99 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0011 others(96): Show |
123 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-5+635delG | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276580 | |||||||
chr12:52276792 | A | C | 103 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0011 others(100): Show |
127 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.-5+846A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276792 | |||||||
chr12:52276812 | T | A | 5 | a0001c0001t0002g0011 a0001c0001t0002g0046 a0001c0001t0002g0047 others(2): Show |
6 | HG02523.hp1 NA18944.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+866T>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276812 | |||||||
chr12:52276845 | T | C | 1 | a0001c0002t0001g0165 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-5+899T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276845 | |||||||
chr12:52276887 | C | A | 1 | a0001c0005t0006g0166 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-5+941C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52276887 | |||||||
chr12:52277042 | G | C | 100 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0011 others(97): Show |
124 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.-5+1096G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277042 | |||||||
chr12:52277272 | A | T | 31 | a0001c0001t0002g0245 a0001c0001t0002g0246 a0001c0001t0004g0253 others(28): Show |
33 | HG01168.hp1 HG01891.hp2 HG02027.hp1 others(30): Show |
intron_variant | MODIFIER | c.-5+1326A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277272 | |||||||
chr12:52277277 | G | T | 4 | a0001c0001t0011g0347 a0001c0002t0011g0346 a0001c0002t0020g0345 others(1): Show |
4 | HG02109.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+1331G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277277 | |||||||
chr12:52277319 | G | A | 1 | a0001c0003t0004g0258 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-5+1373G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277319 | |||||||
chr12:52277343 | CA | C | 3 | a0001c0014t0008g0163 a0001c0014t0008g0164 a0002c0009t0001g0031 |
4 | HG02630.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+1400delA | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52277343 | ||||||
chr12:52277470 | T | G | 107 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0011 others(104): Show |
131 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.-5+1524T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277470 | |||||||
chr12:52277505 | C | T | 86 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0011 others(83): Show |
108 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.-5+1559C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277505 | |||||||
chr12:52277654 | G | C | 86 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0011 others(83): Show |
108 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.-5+1708G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277654 | |||||||
chr12:52277694 | T | C | 5 | a0001c0001t0011g0347 a0001c0002t0011g0346 a0001c0002t0020g0345 others(2): Show |
5 | HG02109.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+1748T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277694 | |||||||
chr12:52277699 | G | A | 5 | a0001c0001t0011g0347 a0001c0002t0011g0346 a0001c0002t0020g0345 others(2): Show |
5 | HG02109.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+1753G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277699 | |||||||
chr12:52277768 | A | C | 5 | a0001c0001t0011g0347 a0001c0002t0011g0346 a0001c0002t0020g0345 others(2): Show |
5 | HG02109.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+1822A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277768 | |||||||
chr12:52277794 | G | GC | 5 | a0001c0001t0011g0347 a0001c0002t0011g0346 a0001c0002t0020g0345 others(2): Show |
5 | HG02109.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+1849dupC | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52277794 | ||||||
chr12:52277802 | C | T | 1 | a0001c0003t0004g0341 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-5+1856C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277802 | |||||||
chr12:52277859 | C | G | 1 | a0001c0001t0011g0347 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-5+1913C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277859 | |||||||
chr12:52277882 | T | G | 1 | a0001c0020t0005g0113 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-5+1936T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277882 | |||||||
chr12:52277982 | C | T | 5 | a0001c0001t0011g0347 a0001c0002t0011g0346 a0001c0002t0020g0345 others(2): Show |
5 | HG02109.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+2036C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52277982 | |||||||
chr12:52278041 | C | G | 18 | a0001c0001t0005g0330 a0001c0001t0005g0340 a0001c0002t0003g0044 others(15): Show |
20 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.-5+2095C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278041 | |||||||
chr12:52278231 | TA | T | 5 | a0001c0001t0011g0347 a0001c0002t0011g0346 a0001c0002t0020g0345 others(2): Show |
5 | HG02109.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+2287delA | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52278231 | ||||||
chr12:52278252 | C | T | 1 | a0001c0001t0002g0228 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-5+2306C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278252 | |||||||
chr12:52278358 | C | T | 3 | a0001c0002t0001g0225 a0001c0002t0001g0226 a0001c0002t0001g0227 |
3 | HG01361.hp2 HG01496.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-5+2412C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278358 | |||||||
chr12:52278385 | A | G | 1 | a0001c0001t0005g0148 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-5+2439A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278385 | |||||||
chr12:52278438 | G | GT | 58 | a0001c0001t0002g0224 a0001c0001t0002g0245 a0001c0001t0002g0246 others(55): Show |
62 | HG00140.hp1 HG01109.hp2 HG01884.hp1 others(59): Show |
intron_variant | MODIFIER | c.-5+2511dupT | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52278438 | ||||||
chr12:52278438 | G | GTT | 110 | a0001c0001t0002g0135 a0001c0001t0002g0301 a0001c0001t0005g0008 others(107): Show |
124 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-5+2510_-5+2511dup others(2): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52278438 | ||||||
chr12:52278438 | GT | G | 88 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0011 others(85): Show |
110 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.-5+2511delT | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52278438 | ||||||
chr12:52278438 | GTT | G | 6 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0001c0001t0002g0052 others(3): Show |
6 | HG01070.hp2 HG01169.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+2510_-5+2511del others(2): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52278438 | ||||||
chr12:52278598 | G | A | 2 | a0001c0002t0011g0346 a0001c0002t0020g0345 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-5+2652G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278598 | |||||||
chr12:52278682 | T | C | 1 | a0001c0002t0003g0231 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-5+2736T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278682 | |||||||
chr12:52278802 | T | C | 1 | a0001c0003t0004g0269 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-5+2856T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278802 | |||||||
chr12:52278841 | T | C | 89 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(86): Show |
111 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.-5+2895T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278841 | |||||||
chr12:52278852 | G | C | 160 | a0001c0001t0002g0135 a0001c0001t0002g0245 a0001c0001t0002g0246 others(157): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.-5+2906G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278852 | |||||||
chr12:52278873 | G | A | 42 | a0001c0001t0002g0135 a0001c0001t0005g0008 a0001c0001t0005g0025 others(39): Show |
46 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.-5+2927G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278873 | |||||||
chr12:52278909 | G | A | 1 | a0001c0002t0008g0156 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-5+2963G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278909 | |||||||
chr12:52278921 | C | T | 89 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(86): Show |
111 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.-5+2975C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278921 | |||||||
chr12:52278969 | G | A | 1 | a0001c0002t0003g0270 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-5+3023G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52278969 | |||||||
chr12:52279041 | G | C | 11 | a0001c0001t0005g0330 a0001c0002t0003g0158 a0001c0002t0003g0162 others(8): Show |
12 | HG00099.hp2 HG01496.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-5+3095G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279041 | |||||||
chr12:52279087 | G | GCCGGGCC others(5): Show |
98 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(95): Show |
122 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.-5+3147_-5+3148ins others(12): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52279087 | ||||||
chr12:52279102 | C | T | 77 | a0001c0001t0002g0260 a0001c0001t0002g0301 a0001c0001t0005g0038 others(74): Show |
88 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.-5+3156C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279102 | |||||||
chr12:52279115 | C | T | 2 | a0001c0001t0002g0106 a0001c0001t0002g0107 |
2 | NA18971.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-5+3169C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279115 | |||||||
chr12:52279166 | C | T | 6 | a0001c0001t0005g0264 a0001c0001t0005g0267 a0002c0009t0001g0031 others(3): Show |
7 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5+3220C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279166 | |||||||
chr12:52279206 | A | C | 1 | a0001c0005t0006g0166 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-5+3260A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279206 | |||||||
chr12:52279211 | T | A | 1 | a0001c0003t0004g0272 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-5+3265T>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279211 | |||||||
chr12:52279252 | A | T | 1 | a0001c0001t0002g0023 | 2 | NA18939.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-5+3306A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279252 | |||||||
chr12:52279305 | C | T | 89 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(86): Show |
111 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.-5+3359C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279305 | |||||||
chr12:52279349 | C | T | 1 | a0001c0001t0002g0105 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-5+3403C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279349 | |||||||
chr12:52279409 | G | A | 2 | a0001c0001t0002g0050 a0001c0001t0002g0053 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-5+3463G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279409 | |||||||
chr12:52279461 | G | A | 88 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(85): Show |
110 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.-5+3515G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279461 | |||||||
chr12:52279476 | C | A | 119 | a0001c0001t0002g0135 a0001c0001t0002g0260 a0001c0001t0002g0301 others(116): Show |
134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.-5+3530C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279476 | |||||||
chr12:52279579 | C | A | 1 | a0001c0001t0005g0148 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-5+3633C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279579 | |||||||
chr12:52279726 | T | C | 88 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(85): Show |
110 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.-5+3780T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279726 | |||||||
chr12:52279765 | T | G | 1 | a0001c0001t0002g0054 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-5+3819T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279765 | |||||||
chr12:52279782 | G | C | 1 | a0001c0001t0005g0055 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-5+3836G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279782 | |||||||
chr12:52279828 | C | T | 2 | a0001c0002t0011g0346 a0001c0002t0020g0345 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-5+3882C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279828 | |||||||
chr12:52279849 | C | T | 1 | a0001c0002t0001g0104 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-5+3903C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279849 | |||||||
chr12:52279992 | G | C | 2 | a0001c0002t0008g0156 a0001c0020t0005g0113 |
2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-5+4046G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52279992 | |||||||
chr12:52280086 | C | T | 88 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(85): Show |
110 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.-5+4140C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52280086 | |||||||
chr12:52280287 | T | C | 280 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(277): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-5+4341T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52280287 | |||||||
chr12:52280304 | T | C | 1 | a0001c0006t0006g0273 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-5+4358T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52280304 | |||||||
chr12:52280472 | C | T | 5 | a0001c0005t0004g0028 a0001c0005t0004g0151 a0001c0005t0004g0153 others(2): Show |
6 | HG02809.hp2 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+4526C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52280472 | |||||||
chr12:52280488 | C | T | 5 | a0001c0005t0004g0028 a0001c0005t0004g0151 a0001c0005t0004g0153 others(2): Show |
6 | HG02809.hp2 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+4542C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52280488 | |||||||
chr12:52280638 | C | T | 1 | a0001c0002t0001g0220 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-5+4692C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52280638 | |||||||
chr12:52280813 | A | T | 1 | a0004c0012t0003g0328 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-5+4867A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52280813 | |||||||
chr12:52280925 | C | T | 10 | a0001c0002t0003g0158 a0001c0002t0003g0162 a0001c0002t0003g0271 others(7): Show |
11 | HG00099.hp2 HG01496.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.-5+4979C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52280925 | |||||||
chr12:52280932 | C | T | 1 | a0001c0001t0005g0147 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-5+4986C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52280932 | |||||||
chr12:52280968 | G | A | 1 | a0001c0001t0007g0056 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-5+5022G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52280968 | |||||||
chr12:52281010 | CT | C | 3 | a0001c0001t0005g0342 a0001c0006t0006g0343 a0010c0024t0005g0331 |
3 | HG02622.hp2 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-5+5067delT | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52281010 | ||||||
chr12:52281241 | A | G | 17 | a0001c0002t0003g0158 a0001c0002t0003g0162 a0001c0002t0003g0271 others(14): Show |
19 | HG00099.hp2 HG01496.hp2 HG02293.hp2 others(16): Show |
intron_variant | MODIFIER | c.-5+5295A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281241 | |||||||
chr12:52281250 | C | T | 88 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(85): Show |
110 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.-5+5304C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281250 | |||||||
chr12:52281267 | A | G | 46 | a0001c0001t0002g0034 a0001c0001t0002g0205 a0001c0001t0002g0207 others(43): Show |
61 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.-5+5321A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281267 | |||||||
chr12:52281314 | T | C | 88 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(85): Show |
110 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.-5+5368T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281314 | |||||||
chr12:52281317 | A | G | 1 | a0001c0001t0005g0103 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-5+5371A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281317 | |||||||
chr12:52281410 | C | G | 1 | a0001c0001t0002g0102 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-5+5464C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281410 | |||||||
chr12:52281652 | T | A | 88 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(85): Show |
110 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.-5+5706T>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281652 | |||||||
chr12:52281661 | T | G | 86 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(83): Show |
108 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.-5+5715T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281661 | |||||||
chr12:52281677 | C | T | 2 | a0001c0001t0005g0330 a0001c0001t0005g0340 |
2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-5+5731C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281677 | |||||||
chr12:52281701 | C | G | 1 | a0001c0002t0003g0231 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-5+5755C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281701 | |||||||
chr12:52281773 | C | G | 1 | a0001c0002t0003g0327 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-5+5827C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281773 | |||||||
chr12:52281879 | C | T | 1 | a0001c0001t0002g0107 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-5+5933C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281879 | |||||||
chr12:52281895 | C | T | 103 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(100): Show |
126 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.-5+5949C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281895 | |||||||
chr12:52281896 | G | A | 15 | a0001c0002t0003g0158 a0001c0002t0003g0162 a0001c0002t0003g0271 others(12): Show |
17 | HG00099.hp2 HG01496.hp2 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.-5+5950G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281896 | |||||||
chr12:52281914 | A | C | 76 | a0001c0001t0002g0260 a0001c0001t0002g0301 a0001c0001t0005g0038 others(73): Show |
87 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.-5+5968A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281914 | |||||||
chr12:52281933 | G | A | 10 | a0001c0002t0003g0158 a0001c0002t0003g0162 a0001c0002t0003g0271 others(7): Show |
11 | HG00099.hp2 HG01496.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.-5+5987G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52281933 | |||||||
chr12:52282102 | G | GAAT | 265 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(262): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.-5+6157_-5+6158ins others(3): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52282102 | ||||||
chr12:52282118 | G | A | 15 | a0001c0001t0005g0330 a0001c0001t0005g0340 a0001c0002t0003g0044 others(12): Show |
16 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-5+6172G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282118 | |||||||
chr12:52282133 | G | A | 280 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(277): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-5+6187G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282133 | |||||||
chr12:52282151 | T | A | 1 | a0001c0003t0004g0154 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-5+6205T>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282151 | |||||||
chr12:52282215 | G | A | 87 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(84): Show |
109 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-5+6269G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282215 | |||||||
chr12:52282236 | A | AT | 39 | a0001c0001t0002g0135 a0001c0001t0005g0008 a0001c0001t0005g0025 others(36): Show |
43 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.-5+6304dupT | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52282236 | ||||||
chr12:52282236 | A | ATTT | 83 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(80): Show |
105 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.-5+6302_-5+6304dup others(3): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52282236 | ||||||
chr12:52282257 | A | G | 87 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(84): Show |
109 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-5+6311A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282257 | |||||||
chr12:52282295 | C | A | 87 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(84): Show |
109 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-5+6349C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282295 | |||||||
chr12:52282323 | C | T | 14 | a0001c0001t0004g0253 a0001c0002t0003g0101 a0001c0002t0003g0149 others(11): Show |
14 | HG01168.hp1 HG01255.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-5+6377C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282323 | |||||||
chr12:52282333 | C | T | 76 | a0001c0001t0002g0260 a0001c0001t0002g0301 a0001c0001t0005g0038 others(73): Show |
87 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.-5+6387C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282333 | |||||||
chr12:52282349 | C | T | 85 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(82): Show |
107 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.-5+6403C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282349 | |||||||
chr12:52282417 | T | C | 6 | a0001c0002t0003g0158 a0001c0002t0003g0162 a0001c0002t0003g0271 others(3): Show |
7 | HG02451.hp2 HG02559.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5+6471T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282417 | |||||||
chr12:52282437 | T | C | 87 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(84): Show |
109 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-5+6491T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282437 | |||||||
chr12:52282438 | G | A | 1 | a0001c0002t0008g0156 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-5+6492G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282438 | |||||||
chr12:52282463 | T | C | 87 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(84): Show |
109 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-5+6517T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282463 | |||||||
chr12:52282598 | C | T | 1 | a0001c0005t0006g0326 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-5+6652C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282598 | |||||||
chr12:52282619 | A | G | 87 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(84): Show |
109 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-5+6673A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282619 | |||||||
chr12:52282635 | A | G | 1 | a0001c0001t0002g0100 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-5+6689A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282635 | |||||||
chr12:52282694 | A | G | 15 | a0001c0002t0003g0158 a0001c0002t0003g0162 a0001c0002t0003g0271 others(12): Show |
17 | HG00099.hp2 HG01496.hp2 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.-5+6748A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282694 | |||||||
chr12:52282724 | C | T | 1 | a0001c0021t0003g0261 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-5+6778C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282724 | |||||||
chr12:52282741 | C | T | 87 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(84): Show |
109 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-5+6795C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282741 | |||||||
chr12:52282971 | C | G | 102 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(99): Show |
125 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.-5+7025C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52282971 | |||||||
chr12:52283004 | T | G | 1 | a0001c0005t0004g0274 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-5+7058T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283004 | |||||||
chr12:52283030 | A | G | 1 | a0001c0001t0005g0325 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-5+7084A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283030 | |||||||
chr12:52283060 | C | T | 6 | a0001c0002t0003g0158 a0001c0002t0003g0162 a0001c0002t0003g0271 others(3): Show |
7 | HG02451.hp2 HG02559.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5+7114C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283060 | |||||||
chr12:52283134 | G | A | 3 | a0001c0002t0001g0197 a0001c0002t0001g0222 a0001c0008t0001g0198 |
3 | NA19000.hp2 NA19002.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-5+7188G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283134 | |||||||
chr12:52283134 | G | T | 1 | a0001c0001t0005g0147 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-5+7188G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283134 | |||||||
chr12:52283159 | G | C | 1 | a0009c0022t0017g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-5+7213G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283159 | |||||||
chr12:52283183 | C | G | 2 | a0001c0001t0002g0245 a0001c0001t0002g0246 |
2 | NA18747.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.-5+7237C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283183 | |||||||
chr12:52283193 | A | G | 117 | a0001c0001t0002g0135 a0001c0001t0002g0260 a0001c0001t0002g0301 others(114): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.-5+7247A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283193 | |||||||
chr12:52283205 | A | C | 86 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(83): Show |
108 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.-5+7259A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283205 | |||||||
chr12:52283252 | G | A | 160 | a0001c0001t0002g0135 a0001c0001t0002g0260 a0001c0001t0002g0301 others(157): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.-5+7306G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283252 | |||||||
chr12:52283259 | T | TG | 351 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(348): Show |
413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.-5+7314dupG | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52283259 | ||||||
chr12:52283275 | T | C | 279 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(276): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-5+7329T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283275 | |||||||
chr12:52283377 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-5+7431G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283377 | |||||||
chr12:52283392 | C | CA | 56 | a0001c0001t0002g0059 a0001c0001t0002g0260 a0001c0001t0005g0025 others(53): Show |
63 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.-5+7470dupA | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52283392 | ||||||
chr12:52283392 | C | CAA | 27 | a0001c0001t0002g0245 a0001c0001t0002g0246 a0001c0001t0004g0253 others(24): Show |
28 | HG00423.hp1 HG01109.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.-5+7469_-5+7470dup others(2): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52283392 | ||||||
chr12:52283392 | C | CAAA | 13 | a0001c0002t0001g0232 a0001c0002t0001g0233 a0001c0002t0001g0234 others(10): Show |
13 | HG01255.hp1 HG01891.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.-5+7468_-5+7470dup others(3): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52283392 | ||||||
chr12:52283392 | CA | C | 76 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(73): Show |
98 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.-5+7470delA | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52283392 | ||||||
chr12:52283404 | A | AAAT | 9 | a0001c0002t0003g0158 a0001c0002t0003g0162 a0001c0002t0003g0271 others(6): Show |
10 | HG00099.hp2 HG01496.hp2 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.-5+7460_-5+7461ins others(3): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52283404 | ||||||
chr12:52283409 | A | T | 10 | a0001c0002t0003g0158 a0001c0002t0003g0162 a0001c0002t0003g0271 others(7): Show |
11 | HG00099.hp2 HG01496.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.-5+7463A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283409 | |||||||
chr12:52283425 | G | T | 1 | a0001c0002t0008g0156 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-5+7479G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283425 | |||||||
chr12:52283452 | T | C | 41 | a0001c0001t0002g0245 a0001c0001t0002g0246 a0001c0001t0004g0253 others(38): Show |
43 | HG01109.hp2 HG01168.hp1 HG01255.hp1 others(40): Show |
intron_variant | MODIFIER | c.-5+7506T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283452 | |||||||
chr12:52283470 | A | AT | 11 | a0001c0001t0002g0195 a0001c0001t0005g0128 a0001c0002t0001g0165 others(8): Show |
11 | HG00438.hp1 HG01106.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5+7549dupT | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52283470 | ||||||
chr12:52283470 | AT | A | 117 | a0001c0001t0002g0034 a0001c0001t0002g0135 a0001c0001t0002g0205 others(114): Show |
141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.-5+7549delT | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52283470 | ||||||
chr12:52283470 | ATT | A | 65 | a0001c0001t0002g0260 a0001c0001t0002g0301 a0001c0001t0005g0038 others(62): Show |
73 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.-5+7548_-5+7549del others(2): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52283470 | ||||||
chr12:52283470 | ATTTTTT | A | 14 | a0001c0001t0002g0012 a0001c0001t0002g0022 a0001c0001t0002g0068 others(11): Show |
15 | HG01261.hp1 HG01261.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.-5+7544_-5+7549del others(6): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52283470 | ||||||
chr12:52283470 | ATTTTTTT | A | 74 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(71): Show |
95 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.-5+7543_-5+7549del others(7): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52283470 | ||||||
chr12:52283509 | G | A | 2 | a0001c0003t0004g0284 a0001c0003t0004g0311 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-5+7563G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283509 | |||||||
chr12:52283626 | A | C | 1 | a0001c0001t0004g0253 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-5+7680A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283626 | |||||||
chr12:52283731 | C | T | 1 | a0001c0002t0001g0192 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-5+7785C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283731 | |||||||
chr12:52283759 | C | A | 4 | a0001c0002t0011g0346 a0001c0002t0020g0345 a0001c0014t0008g0163 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+7813C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283759 | |||||||
chr12:52283925 | T | G | 106 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(103): Show |
131 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.-5+7979T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52283925 | |||||||
chr12:52284126 | A | G | 2 | a0001c0001t0011g0347 a0001c0023t0001g0338 |
2 | HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-5+8180A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284126 | |||||||
chr12:52284139 | T | C | 4 | a0001c0002t0011g0346 a0001c0002t0020g0345 a0001c0014t0008g0163 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+8193T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284139 | |||||||
chr12:52284150 | G | A | 5 | a0001c0005t0004g0028 a0001c0005t0004g0151 a0001c0005t0004g0153 others(2): Show |
6 | HG02809.hp2 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+8204G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284150 | |||||||
chr12:52284167 | G | A | 1 | a0001c0001t0005g0342 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-5+8221G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284167 | |||||||
chr12:52284187 | G | C | 1 | a0001c0020t0005g0113 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-5+8241G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284187 | |||||||
chr12:52284190 | T | G | 1 | a0001c0002t0003g0327 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-5+8244T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284190 | |||||||
chr12:52284236 | C | T | 1 | a0001c0003t0004g0320 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-5+8290C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284236 | |||||||
chr12:52284272 | G | A | 1 | a0001c0002t0003g0312 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-5+8326G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284272 | |||||||
chr12:52284338 | C | T | 4 | a0001c0001t0005g0042 a0001c0001t0005g0283 a0001c0001t0005g0310 others(1): Show |
5 | HG02615.hp1 HG02630.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+8392C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284338 | |||||||
chr12:52284343 | C | A | 1 | a0001c0001t0005g0148 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-5+8397C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284343 | |||||||
chr12:52284343 | C | T | 1 | a0001c0020t0005g0113 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-5+8397C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284343 | |||||||
chr12:52284344 | G | A | 1 | a0001c0023t0001g0338 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-5+8398G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284344 | |||||||
chr12:52284351 | A | G | 1 | a0001c0001t0002g0098 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-5+8405A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284351 | |||||||
chr12:52284428 | G | C | 274 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(271): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.-5+8482G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284428 | |||||||
chr12:52284440 | T | G | 15 | a0001c0001t0005g0264 a0001c0001t0005g0267 a0001c0002t0003g0044 others(12): Show |
17 | HG01884.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-5+8494T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284440 | |||||||
chr12:52284515 | T | C | 275 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(272): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.-5+8569T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284515 | |||||||
chr12:52284647 | T | A | 4 | a0001c0002t0011g0346 a0001c0002t0020g0345 a0001c0014t0008g0163 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+8701T>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284647 | |||||||
chr12:52284654 | T | C | 4 | a0001c0002t0011g0346 a0001c0002t0020g0345 a0001c0014t0008g0163 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+8708T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284654 | |||||||
chr12:52284784 | C | T | 140 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(137): Show |
167 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(164): Show |
intron_variant | MODIFIER | c.-5+8838C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284784 | |||||||
chr12:52284857 | T | G | 1 | a0001c0023t0001g0338 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-5+8911T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284857 | |||||||
chr12:52284859 | G | A | 140 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(137): Show |
167 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(164): Show |
intron_variant | MODIFIER | c.-5+8913G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52284859 | |||||||
chr12:52285025 | A | C | 1 | a0001c0003t0004g0309 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-5+9079A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285025 | |||||||
chr12:52285069 | A | G | 5 | a0001c0005t0004g0028 a0001c0005t0004g0151 a0001c0005t0004g0153 others(2): Show |
6 | HG02809.hp2 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+9123A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285069 | |||||||
chr12:52285116 | A | G | 128 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(125): Show |
154 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.-5+9170A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285116 | |||||||
chr12:52285134 | C | G | 1 | a0001c0002t0003g0322 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-5+9188C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285134 | |||||||
chr12:52285240 | G | A | 133 | a0001c0001t0002g0135 a0001c0001t0002g0260 a0001c0001t0002g0301 others(130): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.-5+9294G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285240 | |||||||
chr12:52285362 | TA | T | 265 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(262): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.-5+9430delA | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52285362 | ||||||
chr12:52285362 | TAA | T | 5 | a0001c0001t0002g0021 a0001c0001t0005g0125 a0001c0001t0005g0147 others(2): Show |
6 | HG01099.hp2 HG01256.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+9429_-5+9430del others(2): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52285362 | ||||||
chr12:52285481 | C | G | 1 | a0001c0003t0004g0320 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-5+9535C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285481 | |||||||
chr12:52285521 | T | C | 1 | a0001c0002t0001g0121 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-5+9575T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285521 | |||||||
chr12:52285548 | A | G | 2 | a0001c0002t0003g0249 a0007c0019t0003g0252 |
2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-5+9602A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285548 | |||||||
chr12:52285793 | G | A | 280 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(277): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-5+9847G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285793 | |||||||
chr12:52285794 | G | A | 1 | a0001c0001t0002g0099 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-5+9848G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285794 | |||||||
chr12:52285928 | T | C | 1 | a0001c0003t0004g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-5+9982T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285928 | |||||||
chr12:52285930 | T | C | 1 | a0001c0021t0003g0261 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-5+9984T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52285930 | |||||||
chr12:52286119 | G | T | 2 | a0001c0014t0008g0163 a0001c0014t0008g0164 |
2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-5+10173G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286119 | |||||||
chr12:52286153 | C | G | 138 | a0001c0001t0002g0135 a0001c0001t0002g0260 a0001c0001t0002g0301 others(135): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.-5+10207C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286153 | |||||||
chr12:52286224 | T | C | 130 | a0001c0001t0002g0135 a0001c0001t0002g0260 a0001c0001t0002g0301 others(127): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.-5+10278T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286224 | |||||||
chr12:52286320 | C | T | 1 | a0001c0002t0011g0346 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-5+10374C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286320 | |||||||
chr12:52286388 | G | A | 7 | a0001c0001t0005g0264 a0001c0001t0005g0267 a0001c0023t0001g0338 others(4): Show |
8 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5+10442G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286388 | |||||||
chr12:52286406 | G | A | 1 | a0001c0002t0008g0156 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-5+10460G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286406 | |||||||
chr12:52286409 | G | A | 1 | a0001c0001t0005g0138 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-5+10463G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286409 | |||||||
chr12:52286426 | A | G | 1 | a0001c0002t0003g0241 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-5+10480A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286426 | |||||||
chr12:52286619 | G | A | 1 | a0001c0006t0006g0343 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-5+10673G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286619 | |||||||
chr12:52286634 | A | C | 1 | a0001c0001t0002g0099 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-5+10688A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286634 | |||||||
chr12:52286643 | G | A | 1 | a0004c0012t0014g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-5+10697G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286643 | |||||||
chr12:52286733 | T | C | 1 | a0001c0001t0002g0068 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-5+10787T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286733 | |||||||
chr12:52286982 | G | A | 42 | a0001c0001t0002g0245 a0001c0001t0002g0246 a0001c0001t0004g0253 others(39): Show |
44 | HG00621.hp1 HG01168.hp1 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.-5+11036G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52286982 | |||||||
chr12:52287005 | T | C | 3 | a0001c0003t0004g0334 a0001c0003t0004g0341 a0001c0016t0005g0333 |
3 | HG02572.hp1 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-5+11059T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287005 | |||||||
chr12:52287069 | G | A | 1 | a0001c0001t0002g0099 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-5+11123G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287069 | |||||||
chr12:52287272 | C | T | 127 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(124): Show |
153 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.-5+11326C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287272 | |||||||
chr12:52287296 | G | A | 86 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(83): Show |
109 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-5+11350G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287296 | |||||||
chr12:52287348 | A | G | 1 | a0001c0003t0004g0341 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-5+11402A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287348 | |||||||
chr12:52287373 | A | G | 3 | a0001c0002t0001g0179 a0001c0002t0001g0191 a0001c0002t0001g0196 |
3 | HG01070.hp1 HG01256.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.-5+11427A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287373 | |||||||
chr12:52287498 | T | C | 278 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(275): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.-5+11552T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287498 | |||||||
chr12:52287632 | T | C | 139 | a0001c0001t0002g0135 a0001c0001t0002g0260 a0001c0001t0002g0301 others(136): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.-5+11686T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287632 | |||||||
chr12:52287653 | A | G | 139 | a0001c0001t0002g0135 a0001c0001t0002g0260 a0001c0001t0002g0301 others(136): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.-5+11707A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287653 | |||||||
chr12:52287676 | G | A | 1 | a0001c0003t0004g0069 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-5+11730G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287676 | |||||||
chr12:52287701 | C | T | 3 | a0001c0001t0002g0020 a0001c0001t0002g0022 a0001c0007t0003g0067 |
5 | NA18947.hp1 NA18965.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+11755C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287701 | |||||||
chr12:52287749 | T | C | 139 | a0001c0001t0002g0135 a0001c0001t0002g0260 a0001c0001t0002g0301 others(136): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.-5+11803T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287749 | |||||||
chr12:52287848 | C | A | 1 | a0004c0012t0014g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-5+11902C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287848 | |||||||
chr12:52287930 | T | C | 338 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(335): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.-5+11984T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287930 | |||||||
chr12:52287949 | A | C | 147 | a0001c0001t0002g0135 a0001c0001t0002g0260 a0001c0001t0002g0301 others(144): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.-5+12003A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287949 | |||||||
chr12:52287972 | T | C | 5 | a0001c0002t0011g0346 a0001c0002t0020g0345 a0001c0014t0008g0163 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+12026T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52287972 | |||||||
chr12:52288022 | G | A | 1 | a0001c0003t0004g0069 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-5+12076G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288022 | |||||||
chr12:52288038 | A | T | 1 | a0012c0026t0001g0131 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-5+12092A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288038 | |||||||
chr12:52288072 | A | C | 1 | a0001c0008t0001g0198 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-5+12126A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288072 | |||||||
chr12:52288128 | C | T | 1 | a0001c0001t0005g0120 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-5+12182C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288128 | |||||||
chr12:52288141 | A | C | 338 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(335): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.-5+12195A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288141 | |||||||
chr12:52288184 | T | C | 349 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(346): Show |
411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
intron_variant | MODIFIER | c.-5+12238T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288184 | |||||||
chr12:52288310 | A | T | 1 | a0004c0012t0014g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-5+12364A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288310 | |||||||
chr12:52288336 | T | C | 1 | a0004c0012t0014g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-5+12390T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288336 | |||||||
chr12:52288342 | C | G | 3 | a0001c0001t0002g0020 a0001c0001t0002g0022 a0001c0007t0003g0067 |
5 | NA18947.hp1 NA18965.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+12396C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288342 | |||||||
chr12:52288346 | C | T | 1 | a0001c0002t0008g0156 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-5+12400C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288346 | |||||||
chr12:52288350 | T | G | 1 | a0001c0002t0008g0156 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-5+12404T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288350 | |||||||
chr12:52288357 | G | A | 60 | a0001c0001t0002g0260 a0001c0001t0002g0301 a0001c0001t0005g0199 others(57): Show |
68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.-5+12411G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288357 | |||||||
chr12:52288430 | C | T | 1 | a0001c0001t0015g0094 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-5+12484C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288430 | |||||||
chr12:52288434 | C | T | 1 | a0001c0002t0004g0029 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-5+12488C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288434 | |||||||
chr12:52288484 | A | AG | 4 | a0001c0001t0005g0342 a0001c0001t0011g0347 a0001c0006t0006g0343 others(1): Show |
4 | HG02622.hp2 HG02809.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+12538_-5+12539i others(3): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288484 | |||||||
chr12:52288591 | C | T | 1 | a0001c0023t0001g0338 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-5+12645C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288591 | |||||||
chr12:52288658 | G | A | 1 | a0004c0012t0014g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-5+12712G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288658 | |||||||
chr12:52288740 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-5+12794C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288740 | |||||||
chr12:52288778 | A | G | 1 | a0001c0023t0001g0338 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-5+12832A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288778 | |||||||
chr12:52288834 | C | A | 49 | a0001c0001t0002g0245 a0001c0001t0002g0246 a0001c0001t0004g0253 others(46): Show |
51 | HG00621.hp1 HG01168.hp1 HG01255.hp1 others(48): Show |
intron_variant | MODIFIER | c.-5+12888C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288834 | |||||||
chr12:52288925 | G | T | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-5+12979G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288925 | |||||||
chr12:52288934 | G | A | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12979G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288934 | |||||||
chr12:52288935 | C | A | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12978C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288935 | |||||||
chr12:52288940 | G | A | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12973G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288940 | |||||||
chr12:52288942 | A | C | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12971A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288942 | |||||||
chr12:52288944 | T | C | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12969T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288944 | |||||||
chr12:52288946 | G | A | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12967G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288946 | |||||||
chr12:52288997 | C | T | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12916C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52288997 | |||||||
chr12:52289001 | T | C | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12912T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289001 | |||||||
chr12:52289002 | G | A | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12911G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289002 | |||||||
chr12:52289007 | A | G | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12906A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289007 | |||||||
chr12:52289010 | T | C | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12903T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289010 | |||||||
chr12:52289016 | C | T | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12897C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289016 | |||||||
chr12:52289021 | A | G | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12892A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289021 | |||||||
chr12:52289022 | GATATTCC others(59): Show |
G | 1 | a0001c0003t0004g0318 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-4-12890_-4-12825d others(68): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289022 | |||||||
chr12:52289032 | A | G | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12881A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289032 | |||||||
chr12:52289091 | C | G | 6 | a0001c0003t0004g0318 a0001c0005t0004g0028 a0001c0005t0004g0151 others(3): Show |
7 | HG02809.hp2 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4-12822C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289091 | |||||||
chr12:52289094 | A | G | 1 | a0001c0003t0004g0318 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-4-12819A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289094 | |||||||
chr12:52289096 | C | G | 1 | a0001c0003t0004g0318 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-4-12817C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289096 | |||||||
chr12:52289097 | C | G | 1 | a0001c0003t0004g0318 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-4-12816C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289097 | |||||||
chr12:52289117 | T | C | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12796T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289117 | |||||||
chr12:52289118 | G | A | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12795G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289118 | |||||||
chr12:52289125 | G | A | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12788G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289125 | |||||||
chr12:52289156 | G | A | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12757G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289156 | |||||||
chr12:52289161 | A | G | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12752A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289161 | |||||||
chr12:52289162 | T | C | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12751T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289162 | |||||||
chr12:52289163 | C | T | 1 | a0001c0002t0003g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-12750C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289163 | |||||||
chr12:52289218 | C | T | 2 | a0001c0002t0003g0145 a0001c0002t0020g0345 |
2 | HG00621.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-4-12695C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289218 | |||||||
chr12:52289333 | C | T | 1 | a0001c0002t0020g0345 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-4-12580C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289333 | |||||||
chr12:52289361 | C | G | 46 | a0001c0001t0002g0245 a0001c0001t0002g0246 a0001c0001t0004g0253 others(43): Show |
48 | HG00621.hp1 HG01168.hp1 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.-4-12552C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289361 | |||||||
chr12:52289364 | G | A | 46 | a0001c0001t0002g0245 a0001c0001t0002g0246 a0001c0001t0004g0253 others(43): Show |
48 | HG00621.hp1 HG01168.hp1 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.-4-12549G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289364 | |||||||
chr12:52289368 | A | G | 46 | a0001c0001t0002g0245 a0001c0001t0002g0246 a0001c0001t0004g0253 others(43): Show |
48 | HG00621.hp1 HG01168.hp1 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.-4-12545A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289368 | |||||||
chr12:52289419 | G | C | 9 | a0001c0001t0005g0342 a0001c0001t0011g0347 a0001c0002t0003g0145 others(6): Show |
9 | HG00621.hp1 HG02109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4-12494G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289419 | |||||||
chr12:52289422 | T | G | 9 | a0001c0001t0005g0342 a0001c0001t0011g0347 a0001c0002t0003g0145 others(6): Show |
9 | HG00621.hp1 HG02109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4-12491T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289422 | |||||||
chr12:52289426 | A | G | 9 | a0001c0001t0005g0342 a0001c0001t0011g0347 a0001c0002t0003g0145 others(6): Show |
9 | HG00621.hp1 HG02109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4-12487A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289426 | |||||||
chr12:52289634 | C | G | 7 | a0001c0001t0005g0264 a0001c0001t0005g0267 a0001c0002t0003g0327 others(4): Show |
8 | HG02145.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-4-12279C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289634 | |||||||
chr12:52289685 | T | C | 12 | a0001c0001t0005g0026 a0001c0001t0005g0140 a0001c0001t0005g0342 others(9): Show |
13 | HG01123.hp2 HG01517.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.-4-12228T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289685 | |||||||
chr12:52289695 | G | C | 269 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(266): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.-4-12218G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289695 | |||||||
chr12:52289798 | C | T | 1 | a0001c0003t0004g0341 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-4-12115C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289798 | |||||||
chr12:52289900 | C | G | 80 | a0001c0001t0002g0260 a0001c0001t0002g0301 a0001c0001t0005g0042 others(77): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.-4-12013C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52289900 | |||||||
chr12:52290056 | C | A | 1 | a0001c0001t0002g0075 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-4-11857C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290056 | |||||||
chr12:52290169 | G | A | 1 | a0001c0021t0003g0261 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-4-11744G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290169 | |||||||
chr12:52290202 | C | G | 2 | a0001c0001t0005g0330 a0001c0001t0005g0340 |
2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-4-11711C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290202 | |||||||
chr12:52290240 | T | G | 33 | a0001c0001t0002g0135 a0001c0001t0005g0008 a0001c0001t0005g0025 others(30): Show |
37 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.-4-11673T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290240 | |||||||
chr12:52290241 | G | T | 2 | a0001c0001t0005g0115 a0001c0001t0005g0116 |
2 | HG01243.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.-4-11672G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290241 | |||||||
chr12:52290295 | C | T | 2 | a0001c0010t0010g0030 a0001c0010t0022g0030 |
2 | HG00099.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-4-11618C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290295 | |||||||
chr12:52290296 | G | A | 2 | a0001c0001t0002g0076 a0001c0015t0001g0077 |
2 | NA18970.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-4-11617G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290296 | |||||||
chr12:52290386 | C | A | 2 | a0001c0002t0008g0156 a0001c0003t0004g0341 |
2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-4-11527C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290386 | |||||||
chr12:52290534 | A | AC | 34 | a0001c0001t0002g0210 a0001c0001t0002g0212 a0001c0001t0002g0217 others(31): Show |
43 | HG00280.hp2 HG00544.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.-4-11367dupC | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52290534 | ||||||
chr12:52290541 | C | CCCA | 16 | a0001c0001t0002g0014 a0001c0001t0002g0046 a0001c0001t0002g0205 others(13): Show |
18 | HG00558.hp2 HG01168.hp1 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.-4-11370_-4-11369i others(5): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52290541 | ||||||
chr12:52290541 | C | CCCCA | 126 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0011 others(123): Show |
150 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.-4-11369_-4-11368i others(6): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52290541 | ||||||
chr12:52290541 | C | CCCCCA | 90 | a0001c0001t0002g0003 a0001c0001t0002g0018 a0001c0001t0002g0024 others(87): Show |
106 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-4-11368_-4-11367i others(7): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52290541 | ||||||
chr12:52290547 | A | ACCCCCC | 36 | a0001c0001t0002g0012 a0001c0001t0002g0019 a0001c0001t0002g0135 others(33): Show |
37 | HG00099.hp1 HG01074.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.-4-11366_-4-11365i others(8): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290547 | |||||||
chr12:52290547 | A | C | 244 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(241): Show |
286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.-4-11366A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290547 | |||||||
chr12:52290570 | G | A | 111 | a0001c0001t0002g0097 a0001c0001t0002g0205 a0001c0001t0002g0260 others(108): Show |
123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.-4-11343G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290570 | |||||||
chr12:52290787 | G | A | 1 | a0001c0005t0004g0151 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-4-11126G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290787 | |||||||
chr12:52290912 | A | G | 43 | a0001c0001t0002g0245 a0001c0001t0002g0246 a0001c0001t0004g0253 others(40): Show |
45 | HG00099.hp2 HG00621.hp1 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.-4-11001A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290912 | |||||||
chr12:52290975 | C | T | 1 | a0003c0011t0001g0133 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-4-10938C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290975 | |||||||
chr12:52290983 | A | G | 4 | a0001c0001t0005g0038 a0001c0005t0004g0274 a0001c0005t0006g0166 others(1): Show |
5 | HG01109.hp2 HG02109.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-10930A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52290983 | |||||||
chr12:52291027 | C | T | 4 | a0001c0001t0005g0342 a0001c0001t0011g0347 a0001c0006t0006g0343 others(1): Show |
4 | HG02622.hp2 HG02809.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-10886C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291027 | |||||||
chr12:52291041 | G | A | 4 | a0001c0001t0005g0342 a0001c0001t0011g0347 a0001c0006t0006g0343 others(1): Show |
4 | HG02622.hp2 HG02809.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-10872G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291041 | |||||||
chr12:52291087 | G | A | 1 | a0001c0002t0003g0162 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-4-10826G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291087 | |||||||
chr12:52291114 | C | T | 1 | a0001c0002t0001g0222 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-4-10799C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291114 | |||||||
chr12:52291118 | C | T | 1 | a0001c0003t0004g0293 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-4-10795C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291118 | |||||||
chr12:52291169 | C | T | 2 | a0001c0001t0005g0330 a0001c0001t0005g0340 |
2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-4-10744C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291169 | |||||||
chr12:52291312 | C | G | 85 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0003 others(82): Show |
108 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.-4-10601C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291312 | |||||||
chr12:52291332 | A | G | 1 | a0001c0003t0004g0341 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-4-10581A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291332 | |||||||
chr12:52291356 | C | T | 1 | a0001c0003t0004g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-4-10557C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291356 | |||||||
chr12:52291395 | C | T | 1 | a0001c0001t0002g0051 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-4-10518C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291395 | |||||||
chr12:52291404 | C | T | 1 | a0001c0002t0008g0156 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-4-10509C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291404 | |||||||
chr12:52291406 | C | G | 12 | a0001c0001t0002g0017 a0001c0001t0002g0065 a0001c0001t0002g0068 others(9): Show |
14 | HG02809.hp2 HG02818.hp2 HG02896.hp2 others(11): Show |
intron_variant | MODIFIER | c.-4-10507C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291406 | |||||||
chr12:52291418 | C | G | 1 | a0001c0002t0008g0156 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-4-10495C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291418 | |||||||
chr12:52291429 | T | G | 43 | a0001c0001t0002g0245 a0001c0001t0002g0246 a0001c0001t0004g0253 others(40): Show |
45 | HG00621.hp1 HG01168.hp1 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.-4-10484T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291429 | |||||||
chr12:52291465 | T | G | 1 | a0001c0003t0004g0276 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-4-10448T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291465 | |||||||
chr12:52291585 | T | G | 4 | a0001c0001t0005g0342 a0001c0001t0011g0347 a0001c0006t0006g0343 others(1): Show |
4 | HG02622.hp2 HG02809.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-10328T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291585 | |||||||
chr12:52291649 | C | G | 119 | a0001c0001t0002g0135 a0001c0001t0002g0260 a0001c0001t0002g0301 others(116): Show |
134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.-4-10264C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291649 | |||||||
chr12:52291665 | G | A | 1 | a0001c0002t0011g0346 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-4-10248G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291665 | |||||||
chr12:52291701 | T | TAAAAGAT others(307): Show |
3 | a0001c0002t0001g0036 a0001c0002t0001g0233 a0001c0002t0001g0243 |
4 | NA18966.hp1 NA18969.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-10194_-4-10193i others(316): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52291701 | ||||||
chr12:52291701 | T | TAAAAGAT others(309): Show |
9 | a0001c0002t0003g0149 a0001c0002t0003g0229 a0001c0002t0003g0230 others(6): Show |
9 | HG01168.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-4-10194_-4-10193i others(318): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52291701 | ||||||
chr12:52291701 | T | TAAAAGAT others(310): Show |
1 | a0001c0002t0003g0244 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-4-10194_-4-10193i others(319): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52291701 | ||||||
chr12:52291701 | T | TAAAAGAT others(320): Show |
8 | a0001c0001t0002g0246 a0001c0002t0001g0232 a0001c0002t0001g0238 others(5): Show |
9 | HG03017.hp2 NA18747.hp2 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.-4-10194_-4-10193i others(329): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52291701 | ||||||
chr12:52291701 | T | TAAAAGAT others(321): Show |
7 | a0001c0001t0002g0245 a0001c0002t0001g0234 a0001c0002t0001g0237 others(4): Show |
7 | HG00621.hp1 HG02027.hp1 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4-10194_-4-10193i others(330): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52291701 | ||||||
chr12:52291701 | T | TAAAAGAT others(322): Show |
2 | a0001c0002t0001g0235 a0001c0003t0004g0255 |
2 | HG02523.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.-4-10194_-4-10193i others(331): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52291701 | ||||||
chr12:52291701 | T | TAAAAGAT others(327): Show |
2 | a0001c0002t0003g0101 a0001c0002t0003g0254 |
2 | HG01255.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-4-10194_-4-10193i others(336): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52291701 | ||||||
chr12:52291701 | T | TAAAAGAT others(328): Show |
1 | a0001c0002t0003g0231 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-4-10194_-4-10193i others(337): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52291701 | ||||||
chr12:52291701 | T | TAAAAGAT others(329): Show |
2 | a0001c0002t0003g0247 a0001c0002t0003g0282 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-4-10194_-4-10193i others(338): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52291701 | ||||||
chr12:52291701 | T | TAAAAGAT others(330): Show |
1 | a0001c0001t0004g0253 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-4-10194_-4-10193i others(339): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52291701 | ||||||
chr12:52291729 | G | T | 3 | a0001c0010t0010g0030 a0001c0010t0010g0161 a0001c0010t0022g0030 |
3 | HG00099.hp2 HG01496.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-4-10184G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291729 | |||||||
chr12:52291761 | C | T | 33 | a0001c0001t0002g0135 a0001c0001t0005g0008 a0001c0001t0005g0025 others(30): Show |
37 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.-4-10152C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52291761 | |||||||
chr12:52292039 | T | C | 3 | a0001c0002t0003g0162 a0001c0002t0003g0271 a0001c0002t0003g0337 |
3 | HG02451.hp2 HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-4-9874T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52292039 | |||||||
chr12:52292666 | ATTTATT | A | 87 | a0001c0001t0002g0260 a0001c0001t0002g0301 a0001c0001t0005g0042 others(84): Show |
98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.-4-9238_-4-9233del others(6): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52292666 | ||||||
chr12:52292982 | C | T | 1 | a0001c0002t0001g0208 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-4-8931C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52292982 | |||||||
chr12:52293113 | C | A | 8 | a0001c0002t0003g0044 a0001c0002t0003g0257 a0001c0002t0003g0329 others(5): Show |
9 | HG01884.hp1 HG02145.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4-8800C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293113 | |||||||
chr12:52293233 | C | T | 1 | a0001c0003t0004g0286 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-4-8680C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293233 | |||||||
chr12:52293243 | C | T | 4 | a0001c0001t0005g0342 a0001c0001t0011g0347 a0001c0006t0006g0343 others(1): Show |
4 | HG02622.hp2 HG02809.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-8670C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293243 | |||||||
chr12:52293262 | T | C | 1 | a0001c0001t0002g0024 | 2 | HG01074.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-4-8651T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293262 | |||||||
chr12:52293286 | G | A | 266 | a0001c0001t0002g0034 a0001c0001t0002g0060 a0001c0001t0002g0205 others(263): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.-4-8627G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293286 | |||||||
chr12:52293369 | A | G | 1 | a0001c0005t0004g0274 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-4-8544A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293369 | |||||||
chr12:52293487 | T | A | 1 | a0001c0007t0003g0289 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-4-8426T>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293487 | |||||||
chr12:52293581 | C | T | 2 | a0001c0001t0002g0301 a0001c0027t0004g0302 |
2 | HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-4-8332C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293581 | |||||||
chr12:52293632 | A | G | 56 | a0001c0001t0002g0092 a0001c0001t0002g0301 a0001c0001t0005g0330 others(53): Show |
65 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.-4-8281A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293632 | |||||||
chr12:52293704 | G | A | 1 | a0001c0002t0020g0345 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-4-8209G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293704 | |||||||
chr12:52293710 | C | T | 1 | a0001c0002t0021g0344 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-4-8203C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293710 | |||||||
chr12:52293847 | T | C | 1 | a0001c0002t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-4-8066T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293847 | |||||||
chr12:52293863 | G | A | 1 | a0001c0002t0001g0313 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-4-8050G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52293863 | |||||||
chr12:52294175 | G | C | 1 | a0001c0002t0001g0209 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-4-7738G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52294175 | |||||||
chr12:52294201 | C | T | 6 | a0001c0006t0006g0159 a0001c0006t0006g0273 a0001c0006t0006g0281 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4-7712C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52294201 | |||||||
chr12:52294477 | AAGGGAGG others(17): Show |
A | 1 | a0001c0003t0004g0324 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-4-7416_-4-7393del others(24): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52294477 | ||||||
chr12:52294559 | G | A | 3 | a0001c0007t0005g0150 a0001c0007t0005g0152 a0001c0007t0012g0304 |
3 | HG02818.hp2 HG02896.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-7354G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52294559 | |||||||
chr12:52294982 | C | T | 89 | a0001c0001t0002g0301 a0001c0002t0001g0036 a0001c0002t0001g0232 others(86): Show |
101 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.-4-6931C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52294982 | |||||||
chr12:52295071 | C | T | 1 | a0001c0003t0004g0069 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-4-6842C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52295071 | |||||||
chr12:52295125 | A | G | 1 | a0001c0002t0001g0188 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-4-6788A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52295125 | |||||||
chr12:52295384 | A | C | 256 | a0001c0001t0002g0205 a0001c0001t0002g0207 a0001c0001t0002g0210 others(253): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-4-6529A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52295384 | |||||||
chr12:52295498 | A | T | 1 | a0001c0002t0021g0344 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-4-6415A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52295498 | |||||||
chr12:52295537 | C | A | 1 | a0001c0001t0002g0061 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-4-6376C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52295537 | |||||||
chr12:52295693 | T | C | 1 | a0001c0003t0004g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-4-6220T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52295693 | |||||||
chr12:52295755 | A | G | 1 | a0001c0002t0003g0256 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-4-6158A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52295755 | |||||||
chr12:52295977 | G | A | 1 | a0001c0001t0005g0115 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-4-5936G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52295977 | |||||||
chr12:52296076 | G | A | 6 | a0001c0001t0005g0027 a0001c0001t0005g0264 a0002c0009t0001g0031 others(3): Show |
8 | HG00733.hp1 HG01993.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-5837G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52296076 | |||||||
chr12:52296112 | G | C | 1 | a0001c0002t0020g0345 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-4-5801G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52296112 | |||||||
chr12:52296290 | C | A | 5 | a0001c0001t0005g0264 a0002c0009t0001g0031 a0002c0009t0001g0265 others(2): Show |
6 | HG02145.hp2 HG02258.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4-5623C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52296290 | |||||||
chr12:52296304 | G | A | 4 | a0001c0002t0011g0346 a0001c0002t0020g0345 a0001c0016t0005g0333 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-5609G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52296304 | |||||||
chr12:52296369 | C | T | 6 | a0001c0006t0006g0159 a0001c0006t0006g0273 a0001c0006t0006g0281 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4-5544C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52296369 | |||||||
chr12:52296468 | G | A | 3 | a0001c0007t0005g0150 a0001c0007t0005g0152 a0001c0007t0012g0304 |
3 | HG02818.hp2 HG02896.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-5445G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52296468 | |||||||
chr12:52296663 | G | GC | 160 | a0001c0001t0002g0301 a0001c0001t0004g0253 a0001c0001t0005g0008 others(157): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.-4-5249dupC | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52296663 | ||||||
chr12:52296682 | C | T | 5 | a0001c0005t0004g0028 a0001c0005t0004g0151 a0001c0005t0004g0153 others(2): Show |
6 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4-5231C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52296682 | |||||||
chr12:52296853 | G | C | 47 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(44): Show |
52 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.-4-5060G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52296853 | |||||||
chr12:52296863 | C | A | 5 | a0001c0001t0005g0264 a0002c0009t0001g0031 a0002c0009t0001g0265 others(2): Show |
6 | HG02145.hp2 HG02258.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4-5050C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52296863 | |||||||
chr12:52296940 | C | T | 5 | a0001c0001t0005g0264 a0002c0009t0001g0031 a0002c0009t0001g0265 others(2): Show |
6 | HG02145.hp2 HG02258.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4-4973C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52296940 | |||||||
chr12:52296941 | G | A | 2 | a0001c0002t0020g0345 a0001c0023t0001g0338 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-4-4972G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52296941 | |||||||
chr12:52297026 | C | T | 1 | a0001c0002t0001g0183 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-4-4887C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52297026 | |||||||
chr12:52297267 | C | G | 2 | a0001c0001t0002g0073 a0001c0001t0002g0098 |
2 | NA18747.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.-4-4646C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52297267 | |||||||
chr12:52297300 | C | G | 13 | a0001c0002t0003g0044 a0001c0002t0003g0158 a0001c0002t0003g0162 others(10): Show |
15 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.-4-4613C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52297300 | |||||||
chr12:52297319 | T | C | 211 | a0001c0001t0002g0205 a0001c0001t0002g0207 a0001c0001t0002g0210 others(208): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.-4-4594T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52297319 | |||||||
chr12:52297496 | G | A | 3 | a0001c0001t0005g0038 a0001c0001t0005g0330 a0001c0001t0005g0340 |
4 | HG01884.hp2 HG02109.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-4417G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52297496 | |||||||
chr12:52297500 | T | C | 2 | a0001c0003t0004g0296 a0001c0003t0004g0321 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-4-4413T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52297500 | |||||||
chr12:52297536 | C | T | 3 | a0001c0001t0005g0038 a0001c0001t0005g0330 a0001c0001t0005g0340 |
4 | HG01884.hp2 HG02109.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-4377C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52297536 | |||||||
chr12:52297540 | G | C | 78 | a0001c0001t0002g0205 a0001c0001t0002g0207 a0001c0001t0002g0210 others(75): Show |
96 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.-4-4373G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52297540 | |||||||
chr12:52297566 | T | C | 1 | a0001c0002t0003g0162 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-4-4347T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52297566 | |||||||
chr12:52297611 | A | G | 1 | a0001c0002t0001g0194 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-4-4302A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52297611 | |||||||
chr12:52297675 | A | G | 2 | a0001c0002t0011g0346 a0001c0016t0005g0333 |
2 | HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-4-4238A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52297675 | |||||||
chr12:52298164 | G | A | 1 | a0001c0016t0005g0333 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-4-3749G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298164 | |||||||
chr12:52298174 | T | C | 51 | a0001c0002t0001g0036 a0001c0002t0001g0232 a0001c0002t0001g0233 others(48): Show |
59 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.-4-3739T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298174 | |||||||
chr12:52298218 | A | G | 3 | a0001c0007t0005g0150 a0001c0007t0005g0152 a0001c0007t0012g0304 |
3 | HG02818.hp2 HG02896.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-3695A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298218 | |||||||
chr12:52298307 | C | T | 45 | a0001c0001t0002g0301 a0001c0003t0004g0007 a0001c0003t0004g0040 others(42): Show |
49 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.-4-3606C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298307 | |||||||
chr12:52298423 | C | T | 5 | a0001c0004t0003g0006 a0001c0004t0003g0039 a0001c0004t0003g0277 others(2): Show |
9 | HG00140.hp2 HG00323.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4-3490C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298423 | |||||||
chr12:52298447 | T | A | 1 | a0001c0001t0005g0125 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-4-3466T>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298447 | |||||||
chr12:52298500 | G | T | 1 | a0001c0002t0021g0344 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-4-3413G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298500 | |||||||
chr12:52298689 | G | A | 66 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(63): Show |
72 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.-4-3224G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298689 | |||||||
chr12:52298727 | A | G | 1 | a0001c0002t0001g0194 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-4-3186A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298727 | |||||||
chr12:52298729 | G | A | 2 | a0001c0001t0001g0167 a0001c0002t0020g0345 |
2 | HG02040.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-4-3184G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298729 | |||||||
chr12:52298768 | T | C | 9 | a0001c0001t0002g0021 a0001c0001t0002g0034 a0001c0001t0002g0062 others(6): Show |
11 | HG00609.hp2 NA18965.hp2 NA18979.hp1 others(8): Show |
intron_variant | MODIFIER | c.-4-3145T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298768 | |||||||
chr12:52298797 | A | C | 1 | a0004c0012t0014g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-4-3116A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298797 | |||||||
chr12:52298810 | A | T | 274 | a0001c0001t0002g0091 a0001c0001t0002g0099 a0001c0001t0002g0205 others(271): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.-4-3103A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298810 | |||||||
chr12:52298886 | C | G | 252 | a0001c0001t0002g0205 a0001c0001t0002g0207 a0001c0001t0002g0212 others(249): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.-4-3027C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298886 | |||||||
chr12:52298920 | C | T | 49 | a0001c0001t0002g0205 a0001c0001t0002g0207 a0001c0001t0002g0212 others(46): Show |
63 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-4-2993C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298920 | |||||||
chr12:52298921 | C | T | 10 | a0001c0001t0005g0042 a0001c0001t0005g0264 a0001c0001t0005g0267 others(7): Show |
11 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.-4-2992C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52298921 | |||||||
chr12:52298925 | AC | A | 4 | a0002c0009t0001g0031 a0002c0009t0001g0265 a0002c0009t0001g0266 others(1): Show |
5 | HG02145.hp2 HG02258.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-2986delC | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 52298925 | ||||||
chr12:52299015 | G | A | 1 | a0001c0023t0001g0338 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-4-2898G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299015 | |||||||
chr12:52299031 | A | G | 49 | a0001c0003t0004g0007 a0001c0003t0004g0040 a0001c0003t0004g0069 others(46): Show |
53 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.-4-2882A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299031 | |||||||
chr12:52299130 | A | G | 65 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(62): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.-4-2783A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299130 | |||||||
chr12:52299176 | C | T | 1 | a0009c0022t0017g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-4-2737C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299176 | |||||||
chr12:52299177 | G | T | 3 | a0001c0007t0005g0150 a0001c0007t0005g0152 a0001c0007t0012g0304 |
3 | HG02818.hp2 HG02896.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-4-2736G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299177 | |||||||
chr12:52299179 | A | G | 1 | a0001c0021t0003g0261 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-4-2734A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299179 | |||||||
chr12:52299220 | A | G | 3 | a0001c0002t0008g0156 a0001c0014t0008g0163 a0001c0014t0008g0164 |
3 | HG02055.hp1 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-4-2693A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299220 | |||||||
chr12:52299392 | C | T | 42 | a0001c0002t0001g0036 a0001c0002t0001g0215 a0001c0002t0001g0232 others(39): Show |
49 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.-4-2521C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299392 | |||||||
chr12:52299529 | T | C | 3 | a0001c0010t0010g0030 a0001c0010t0010g0161 a0001c0010t0022g0030 |
3 | HG00099.hp2 HG01496.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-4-2384T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299529 | |||||||
chr12:52299548 | C | T | 273 | a0001c0001t0002g0205 a0001c0001t0002g0207 a0001c0001t0002g0212 others(270): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.-4-2365C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299548 | |||||||
chr12:52299723 | G | T | 3 | a0001c0002t0008g0156 a0001c0014t0008g0163 a0001c0014t0008g0164 |
3 | HG02055.hp1 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-4-2190G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299723 | |||||||
chr12:52299757 | T | G | 2 | a0005c0013t0001g0184 a0005c0013t0001g0185 |
2 | HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-4-2156T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299757 | |||||||
chr12:52299779 | A | C | 3 | a0001c0002t0001g0206 a0001c0002t0001g0214 a0001c0002t0001g0219 |
3 | NA18980.hp2 NA19060.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.-4-2134A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299779 | |||||||
chr12:52299852 | C | T | 1 | a0001c0003t0004g0154 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-4-2061C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52299852 | |||||||
chr12:52300083 | T | C | 13 | a0001c0005t0004g0028 a0001c0005t0004g0151 a0001c0005t0004g0153 others(10): Show |
14 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.-4-1830T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52300083 | |||||||
chr12:52300185 | T | C | 6 | a0001c0006t0006g0159 a0001c0006t0006g0273 a0001c0006t0006g0281 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4-1728T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52300185 | |||||||
chr12:52300213 | G | T | 273 | a0001c0001t0002g0205 a0001c0001t0002g0207 a0001c0001t0002g0212 others(270): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.-4-1700G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52300213 | |||||||
chr12:52300372 | A | G | 32 | a0001c0002t0003g0015 a0001c0002t0003g0041 a0001c0002t0003g0101 others(29): Show |
37 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.-4-1541A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52300372 | |||||||
chr12:52300403 | G | A | 6 | a0001c0006t0006g0159 a0001c0006t0006g0273 a0001c0006t0006g0281 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4-1510G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52300403 | |||||||
chr12:52300509 | C | A | 117 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(114): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.-4-1404C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52300509 | |||||||
chr12:52300581 | A | T | 1 | a0001c0001t0002g0085 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-4-1332A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52300581 | |||||||
chr12:52300749 | G | T | 47 | a0001c0003t0004g0007 a0001c0003t0004g0040 a0001c0003t0004g0069 others(44): Show |
51 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.-4-1164G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52300749 | |||||||
chr12:52300825 | G | A | 47 | a0001c0003t0004g0007 a0001c0003t0004g0040 a0001c0003t0004g0069 others(44): Show |
51 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.-4-1088G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52300825 | |||||||
chr12:52300966 | A | C | 1 | a0001c0002t0001g0165 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-4-947A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52300966 | |||||||
chr12:52301165 | GA | G | 6 | a0001c0005t0004g0028 a0001c0005t0004g0151 a0001c0005t0004g0153 others(3): Show |
7 | HG01109.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4-747delA | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301165 | |||||||
chr12:52301166 | A | G | 1 | a0001c0005t0006g0326 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-4-747A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301166 | |||||||
chr12:52301263 | G | A | 69 | a0001c0001t0002g0080 a0001c0001t0002g0088 a0001c0001t0007g0056 others(66): Show |
79 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.-4-650G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301263 | |||||||
chr12:52301334 | G | T | 3 | a0001c0002t0011g0346 a0001c0002t0020g0345 a0001c0016t0005g0333 |
3 | HG02109.hp2 HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-4-579G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301334 | |||||||
chr12:52301377 | C | T | 1 | a0001c0002t0001g0303 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-4-536C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301377 | |||||||
chr12:52301414 | G | C | 31 | a0001c0002t0003g0015 a0001c0002t0003g0041 a0001c0002t0003g0101 others(28): Show |
36 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.-4-499G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301414 | |||||||
chr12:52301420 | C | A | 7 | a0001c0005t0004g0028 a0001c0005t0004g0151 a0001c0005t0004g0153 others(4): Show |
8 | HG01109.hp2 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-4-493C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301420 | |||||||
chr12:52301422 | A | G | 1 | a0001c0002t0001g0226 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-4-491A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301422 | |||||||
chr12:52301603 | G | A | 1 | a0001c0002t0001g0211 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-4-310G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301603 | |||||||
chr12:52301654 | A | T | 1 | a0001c0003t0004g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-4-259A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301654 | |||||||
chr12:52301690 | T | C | 1 | a0001c0002t0001g0215 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-4-223T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301690 | |||||||
chr12:52301832 | T | C | 1 | a0001c0001t0002g0024 | 2 | HG01074.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-4-81T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301832 | |||||||
chr12:52301846 | C | T | 47 | a0001c0003t0004g0007 a0001c0003t0004g0040 a0001c0003t0004g0069 others(44): Show |
51 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.-4-67C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301846 | |||||||
chr12:52301884 | C | A | 2 | a0002c0009t0001g0265 a0002c0009t0001g0266 |
2 | HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-4-29C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 2/10 | chr12 | 52301884 | |||||||
chr12:52302341 | C | T | 42 | a0001c0003t0004g0007 a0001c0003t0004g0040 a0001c0003t0004g0069 others(39): Show |
46 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.369+56C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52302341 | |||||||
chr12:52302483 | G | A | 19 | a0001c0002t0003g0043 a0001c0002t0003g0044 a0001c0002t0003g0158 others(16): Show |
22 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.369+198G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52302483 | |||||||
chr12:52302629 | G | A | 1 | a0001c0002t0001g0189 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.369+344G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52302629 | |||||||
chr12:52302732 | C | T | 1 | a0001c0003t0004g0272 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.370-368C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52302732 | |||||||
chr12:52302812 | T | C | 130 | a0001c0001t0002g0047 a0001c0001t0002g0063 a0001c0001t0002g0092 others(127): Show |
144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.370-288T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52302812 | |||||||
chr12:52302835 | G | T | 4 | a0001c0001t0002g0207 a0001c0002t0001g0180 a0001c0015t0001g0077 others(1): Show |
4 | HG01934.hp1 HG02293.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-265G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52302835 | |||||||
chr12:52302841 | T | TG | 63 | a0001c0001t0002g0016 a0001c0001t0002g0048 a0001c0001t0002g0059 others(60): Show |
68 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.370-249dupG | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 52302841 | ||||||
chr12:52302841 | TG | T | 81 | a0001c0001t0002g0051 a0001c0001t0002g0092 a0001c0001t0002g0205 others(78): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.370-249delG | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 52302841 | ||||||
chr12:52302841 | TGG | T | 24 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0121 others(21): Show |
26 | HG00280.hp2 HG00639.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.370-250_370-249del others(2): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 52302841 | ||||||
chr12:52302844 | G | T | 1 | a0001c0002t0001g0221 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.370-256G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52302844 | |||||||
chr12:52302845 | G | GA | 16 | a0001c0002t0003g0015 a0001c0002t0003g0041 a0001c0002t0003g0145 others(13): Show |
21 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.370-255_370-254ins others(1): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52302845 | |||||||
chr12:52302848 | G | A | 2 | a0001c0002t0003g0239 a0001c0002t0003g0241 |
2 | NA18971.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.370-252G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52302848 | |||||||
chr12:52302871 | G | A | 1 | a0001c0021t0003g0261 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.370-229G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52302871 | |||||||
chr12:52303000 | G | T | 41 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(38): Show |
45 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.370-100G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52303000 | |||||||
chr12:52303091 | G | A | 4 | a0001c0002t0021g0344 a0001c0010t0010g0030 a0001c0010t0010g0161 others(1): Show |
4 | HG00099.hp2 HG01496.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-9G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 3/10 | chr12 | 52303091 | |||||||
chr12:52303348 | G | T | 1 | a0001c0002t0001g0221 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.578+40G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303348 | |||||||
chr12:52303349 | T | C | 1 | a0001c0002t0001g0221 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.578+41T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303349 | |||||||
chr12:52303363 | A | G | 2 | a0001c0002t0003g0229 a0001c0002t0003g0230 |
2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.578+55A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303363 | |||||||
chr12:52303486 | G | C | 12 | a0001c0002t0003g0339 a0001c0003t0004g0069 a0001c0003t0004g0072 others(9): Show |
12 | HG01167.hp1 HG01169.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.578+178G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303486 | |||||||
chr12:52303566 | G | C | 4 | a0002c0009t0001g0031 a0002c0009t0001g0265 a0002c0009t0001g0266 others(1): Show |
5 | HG02145.hp2 HG02258.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.578+258G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303566 | |||||||
chr12:52303569 | G | A | 1 | a0001c0017t0004g0297 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.578+261G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303569 | |||||||
chr12:52303691 | G | C | 180 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(177): Show |
211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.578+383G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303691 | |||||||
chr12:52303701 | A | G | 181 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(178): Show |
212 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.578+393A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303701 | |||||||
chr12:52303724 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.579-387C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303724 | |||||||
chr12:52303823 | G | A | 3 | a0001c0001t0005g0134 a0001c0001t0005g0141 a0001c0001t0005g0147 |
3 | HG01069.hp2 HG01256.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.579-288G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303823 | |||||||
chr12:52303960 | T | C | 261 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(258): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.579-151T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303960 | |||||||
chr12:52303964 | A | C | 261 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(258): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.579-147A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303964 | |||||||
chr12:52303967 | C | G | 261 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(258): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.579-144C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303967 | |||||||
chr12:52303988 | C | T | 1 | a0001c0001t0005g0203 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.579-123C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52303988 | |||||||
chr12:52304018 | T | C | 264 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(261): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.579-93T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52304018 | |||||||
chr12:52304022 | C | T | 264 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(261): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.579-89C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52304022 | |||||||
chr12:52304025 | G | C | 264 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(261): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.579-86G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52304025 | |||||||
chr12:52304053 | G | A | 3 | a0001c0002t0011g0346 a0001c0002t0020g0345 a0001c0016t0005g0333 |
3 | HG02109.hp2 HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.579-58G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52304053 | |||||||
chr12:52304083 | C | T | 1 | a0001c0001t0005g0294 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.579-28C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 4/10 | chr12 | 52304083 | |||||||
chr12:52304223 | G | A | 263 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(260): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.639+52G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304223 | |||||||
chr12:52304224 | A | G | 263 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(260): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.639+53A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304224 | |||||||
chr12:52304225 | T | C | 263 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(260): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.639+54T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304225 | |||||||
chr12:52304230 | C | T | 263 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(260): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.639+59C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304230 | |||||||
chr12:52304261 | C | T | 170 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(167): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.639+90C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304261 | |||||||
chr12:52304268 | C | T | 263 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(260): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.639+97C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304268 | |||||||
chr12:52304269 | A | G | 263 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(260): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.639+98A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304269 | |||||||
chr12:52304340 | C | A | 1 | a0001c0001t0002g0082 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.639+169C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304340 | |||||||
chr12:52304354 | T | C | 264 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(261): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+183T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304354 | |||||||
chr12:52304365 | T | C | 264 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(261): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+194T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304365 | |||||||
chr12:52304370 | G | A | 264 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(261): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+199G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304370 | |||||||
chr12:52304376 | A | C | 1 | a0001c0002t0001g0221 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.639+205A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304376 | |||||||
chr12:52304376 | A | G | 263 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(260): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.639+205A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304376 | |||||||
chr12:52304379 | T | C | 264 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(261): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+208T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304379 | |||||||
chr12:52304384 | C | T | 264 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(261): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+213C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304384 | |||||||
chr12:52304385 | A | G | 264 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(261): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+214A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304385 | |||||||
chr12:52304389 | G | A | 264 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(261): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+218G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304389 | |||||||
chr12:52304440 | C | T | 264 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(261): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+269C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304440 | |||||||
chr12:52304442 | A | G | 264 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(261): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+271A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304442 | |||||||
chr12:52304444 | T | G | 264 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(261): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+273T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304444 | |||||||
chr12:52304446 | C | T | 264 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(261): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+275C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304446 | |||||||
chr12:52304448 | G | T | 7 | a0001c0005t0004g0028 a0001c0005t0004g0151 a0001c0005t0004g0153 others(4): Show |
8 | HG01109.hp2 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.639+277G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304448 | |||||||
chr12:52304451 | G | T | 264 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(261): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+280G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304451 | |||||||
chr12:52304452 | C | T | 264 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(261): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+281C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304452 | |||||||
chr12:52304461 | C | A | 264 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(261): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.639+290C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304461 | |||||||
chr12:52304469 | G | GATTCT | 3 | a0001c0002t0011g0346 a0001c0002t0020g0345 a0001c0016t0005g0333 |
3 | HG02109.hp2 HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.639+300_639+301ins others(5): Show |
KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 52304469 | ||||||
chr12:52304472 | A | G | 3 | a0001c0002t0011g0346 a0001c0002t0020g0345 a0001c0016t0005g0333 |
3 | HG02109.hp2 HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.639+301A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304472 | |||||||
chr12:52304472 | A | T | 261 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(258): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.639+301A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304472 | |||||||
chr12:52304474 | A | T | 3 | a0001c0002t0011g0346 a0001c0002t0020g0345 a0001c0016t0005g0333 |
3 | HG02109.hp2 HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.639+303A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304474 | |||||||
chr12:52304490 | G | C | 7 | a0001c0005t0004g0028 a0001c0005t0004g0151 a0001c0005t0004g0153 others(4): Show |
8 | HG01109.hp2 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.639+319G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304490 | |||||||
chr12:52304552 | T | G | 5 | a0001c0001t0002g0049 a0001c0001t0005g0128 a0001c0007t0003g0067 others(2): Show |
5 | HG00438.hp1 NA18944.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.640-380T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304552 | |||||||
chr12:52304582 | T | C | 5 | a0001c0001t0002g0052 a0001c0001t0002g0090 a0001c0007t0003g0067 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.640-350T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304582 | |||||||
chr12:52304587 | C | A | 5 | a0001c0001t0002g0052 a0001c0001t0002g0090 a0001c0007t0003g0067 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.640-345C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304587 | |||||||
chr12:52304588 | T | C | 5 | a0001c0001t0002g0052 a0001c0001t0002g0090 a0001c0007t0003g0067 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.640-344T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304588 | |||||||
chr12:52304595 | T | C | 6 | a0001c0001t0002g0052 a0001c0001t0002g0083 a0001c0001t0002g0090 others(3): Show |
6 | HG01168.hp2 HG01169.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.640-337T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304595 | |||||||
chr12:52304606 | G | T | 10 | a0001c0001t0002g0052 a0001c0001t0002g0059 a0001c0001t0002g0083 others(7): Show |
10 | HG01074.hp1 HG01168.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.640-326G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304606 | |||||||
chr12:52304607 | C | G | 10 | a0001c0001t0002g0052 a0001c0001t0002g0059 a0001c0001t0002g0083 others(7): Show |
10 | HG01074.hp1 HG01168.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.640-325C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304607 | |||||||
chr12:52304678 | G | T | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-254G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304678 | |||||||
chr12:52304680 | G | A | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-252G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304680 | |||||||
chr12:52304686 | A | G | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-246A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304686 | |||||||
chr12:52304694 | T | C | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-238T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304694 | |||||||
chr12:52304696 | A | G | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-236A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304696 | |||||||
chr12:52304702 | T | C | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-230T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304702 | |||||||
chr12:52304709 | C | G | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-223C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304709 | |||||||
chr12:52304710 | A | G | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-222A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304710 | |||||||
chr12:52304727 | C | G | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-205C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304727 | |||||||
chr12:52304729 | G | A | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-203G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304729 | |||||||
chr12:52304732 | C | G | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-200C>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304732 | |||||||
chr12:52304733 | C | T | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-199C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304733 | |||||||
chr12:52304738 | A | G | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-194A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304738 | |||||||
chr12:52304754 | C | A | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-178C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304754 | |||||||
chr12:52304760 | A | G | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-172A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304760 | |||||||
chr12:52304761 | T | G | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-171T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304761 | |||||||
chr12:52304763 | G | A | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-169G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304763 | |||||||
chr12:52304777 | G | C | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-155G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304777 | |||||||
chr12:52304781 | C | T | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-151C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304781 | |||||||
chr12:52304784 | C | T | 1 | a0001c0002t0001g0189 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.640-148C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304784 | |||||||
chr12:52304785 | G | A | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-147G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304785 | |||||||
chr12:52304787 | G | C | 2 | a0001c0005t0006g0139 a0001c0005t0006g0166 |
2 | HG01109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.640-145G>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304787 | |||||||
chr12:52304792 | GC | G | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-138delC | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 52304792 | ||||||
chr12:52304802 | A | G | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-130A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304802 | |||||||
chr12:52304806 | AG | A | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-125delG | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304806 | |||||||
chr12:52304809 | G | A | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-123G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304809 | |||||||
chr12:52304822 | A | G | 3 | a0001c0007t0003g0067 a0001c0007t0003g0289 a0001c0007t0003g0292 |
3 | NA18977.hp2 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.640-110A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 5/10 | chr12 | 52304822 | |||||||
chr12:52305032 | G | A | 1 | a0001c0002t0008g0156 | 1 | HG02055.hp1 | splice_region_variant&intron_variant | LOW | c.735+5G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 6/10 | chr12 | 52305032 | |||||||
chr12:52305051 | A | C | 4 | a0001c0001t0002g0058 a0001c0001t0002g0085 a0001c0001t0002g0089 others(1): Show |
4 | HG00741.hp1 HG01243.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+24A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 6/10 | chr12 | 52305051 | |||||||
chr12:52305056 | T | C | 3 | a0001c0002t0001g0178 a0001c0002t0001g0181 a0001c0002t0001g0221 |
3 | NA18972.hp2 NA19001.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.735+29T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 6/10 | chr12 | 52305056 | |||||||
chr12:52305066 | CAG | C | 7 | a0001c0005t0004g0028 a0001c0005t0004g0151 a0001c0005t0004g0153 others(4): Show |
8 | HG01109.hp2 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.735+44_735+45delAG | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 52305066 | ||||||
chr12:52305147 | G | T | 2 | a0001c0001t0002g0059 a0001c0001t0002g0301 |
2 | HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.736-93G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 6/10 | chr12 | 52305147 | |||||||
chr12:52305180 | T | C | 7 | a0001c0005t0004g0028 a0001c0005t0004g0151 a0001c0005t0004g0153 others(4): Show |
8 | HG01109.hp2 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.736-60T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 6/10 | chr12 | 52305180 | |||||||
chr12:52305192 | G | A | 1 | a0001c0002t0011g0346 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.736-48G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 6/10 | chr12 | 52305192 | |||||||
chr12:52305429 | G | T | 100 | a0001c0001t0004g0253 a0001c0001t0005g0008 a0001c0001t0005g0025 others(97): Show |
110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.900+25G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 7/10 | chr12 | 52305429 | |||||||
chr12:52305507 | A | G | 1 | a0001c0007t0005g0152 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.900+103A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 7/10 | chr12 | 52305507 | |||||||
chr12:52305518 | C | T | 7 | a0001c0005t0004g0028 a0001c0005t0004g0151 a0001c0005t0004g0153 others(4): Show |
8 | HG01109.hp2 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.900+114C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 7/10 | chr12 | 52305518 | |||||||
chr12:52305573 | A | G | 1 | a0001c0001t0002g0224 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.901-90A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 7/10 | chr12 | 52305573 | |||||||
chr12:52305635 | A | G | 10 | a0001c0005t0004g0028 a0001c0005t0004g0151 a0001c0005t0004g0153 others(7): Show |
11 | HG00099.hp2 HG01109.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.901-28A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 7/10 | chr12 | 52305635 | |||||||
chr12:52305837 | G | T | 3 | a0001c0001t0005g0038 a0001c0001t0005g0330 a0001c0001t0005g0340 |
4 | HG01884.hp2 HG02109.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026+49G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 8/10 | chr12 | 52305837 | |||||||
chr12:52305899 | A | G | 1 | a0001c0001t0002g0018 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1026+111A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 8/10 | chr12 | 52305899 | |||||||
chr12:52305913 | G | A | 2 | a0001c0003t0004g0280 a0001c0003t0004g0300 |
2 | HG01255.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1026+125G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 8/10 | chr12 | 52305913 | |||||||
chr12:52305930 | T | A | 1 | a0001c0003t0004g0323 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1027-130T>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 8/10 | chr12 | 52305930 | |||||||
chr12:52305944 | G | A | 166 | a0001c0001t0004g0045 a0001c0001t0004g0253 a0001c0001t0005g0008 others(163): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.1027-116G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 8/10 | chr12 | 52305944 | |||||||
chr12:52305987 | C | T | 6 | a0001c0006t0006g0159 a0001c0006t0006g0273 a0001c0006t0006g0281 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1027-73C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 8/10 | chr12 | 52305987 | |||||||
chr12:52305988 | A | G | 6 | a0001c0006t0006g0159 a0001c0006t0006g0273 a0001c0006t0006g0281 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1027-72A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 8/10 | chr12 | 52305988 | |||||||
chr12:52306045 | C | T | 2 | a0001c0002t0001g0165 a0001c0002t0001g0188 |
2 | HG01106.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1027-15C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 8/10 | chr12 | 52306045 | |||||||
chr12:52306316 | C | A | 160 | a0001c0001t0004g0045 a0001c0001t0004g0253 a0001c0001t0005g0008 others(157): Show |
178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1247+36C>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52306316 | |||||||
chr12:52306416 | C | T | 1 | a0001c0001t0002g0046 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1247+136C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52306416 | |||||||
chr12:52306573 | G | T | 1 | a0005c0013t0001g0185 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1247+293G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52306573 | |||||||
chr12:52306609 | G | A | 1 | a0001c0023t0001g0338 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1247+329G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52306609 | |||||||
chr12:52306925 | A | G | 1 | a0009c0022t0017g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1247+645A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52306925 | |||||||
chr12:52307047 | C | CT | 47 | a0001c0001t0004g0045 a0001c0003t0004g0007 a0001c0003t0004g0040 others(44): Show |
51 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1247+776dupT | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr12 | 52307047 | ||||||
chr12:52307061 | A | T | 1 | a0001c0003t0004g0321 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1247+781A>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307061 | |||||||
chr12:52307084 | G | A | 1 | a0009c0022t0017g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1247+804G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307084 | |||||||
chr12:52307183 | C | T | 176 | a0001c0001t0004g0045 a0001c0001t0004g0253 a0001c0001t0005g0008 others(173): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1247+903C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307183 | |||||||
chr12:52307420 | T | A | 6 | a0001c0006t0006g0159 a0001c0006t0006g0273 a0001c0006t0006g0281 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1248-813T>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307420 | |||||||
chr12:52307461 | C | T | 1 | a0001c0023t0001g0338 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1248-772C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307461 | |||||||
chr12:52307537 | G | A | 1 | a0001c0002t0003g0240 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1248-696G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307537 | |||||||
chr12:52307609 | C | T | 7 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0027 others(4): Show |
9 | HG00733.hp1 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1248-624C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307609 | |||||||
chr12:52307625 | C | T | 55 | a0001c0002t0003g0015 a0001c0002t0003g0041 a0001c0002t0003g0043 others(52): Show |
62 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1248-608C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307625 | |||||||
chr12:52307739 | A | G | 5 | a0001c0003t0004g0258 a0001c0003t0004g0276 a0001c0003t0004g0286 others(2): Show |
5 | HG00738.hp2 HG01099.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1248-494A>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307739 | |||||||
chr12:52307740 | G | A | 1 | a0001c0002t0003g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1248-493G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307740 | |||||||
chr12:52307776 | C | T | 7 | a0001c0005t0004g0028 a0001c0005t0004g0151 a0001c0005t0004g0153 others(4): Show |
8 | HG01109.hp2 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1248-457C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307776 | |||||||
chr12:52307820 | T | G | 1 | a0001c0002t0001g0222 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1248-413T>G | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307820 | |||||||
chr12:52307874 | G | A | 1 | a0001c0021t0003g0261 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1248-359G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307874 | |||||||
chr12:52307919 | G | A | 1 | a0001c0002t0001g0170 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1248-314G>A | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307919 | |||||||
chr12:52307924 | T | C | 16 | a0001c0005t0004g0028 a0001c0005t0004g0151 a0001c0005t0004g0153 others(13): Show |
17 | HG00099.hp2 HG01109.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1248-309T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307924 | |||||||
chr12:52307926 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1248-307C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307926 | |||||||
chr12:52307962 | T | C | 7 | a0001c0005t0004g0028 a0001c0005t0004g0151 a0001c0005t0004g0153 others(4): Show |
8 | HG01109.hp2 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1248-271T>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52307962 | |||||||
chr12:52308049 | A | C | 1 | a0001c0002t0003g0251 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1248-184A>C | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52308049 | |||||||
chr12:52308050 | G | T | 1 | a0001c0002t0003g0251 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1248-183G>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52308050 | |||||||
chr12:52308081 | C | T | 3 | a0001c0010t0010g0030 a0001c0010t0010g0161 a0001c0010t0022g0030 |
3 | HG00099.hp2 HG01496.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1248-152C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 9/10 | chr12 | 52308081 | |||||||
chr12:52308347 | C | T | 6 | a0001c0006t0006g0159 a0001c0006t0006g0273 a0001c0006t0006g0281 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1280-57C>T | KRT86 | ENSG00000170442.12 | transcript | ENST00000423955.7 | protein_coding | 10/10 | chr12 | 52308347 |