Item | Value |
---|---|
geneid | 130162 |
ensemblid | ENSG00000162994.16 |
hgncid | 26453 |
symbol | CLHC1 |
name | clathrin heavy chain linker domain containing 1 |
refseq_nuc | NM_152385.4 |
refseq_prot | NP_689598.2 |
ensembl_nuc | ENST00000401408.6 |
ensembl_prot | ENSP00000384869.1 |
mane_status | MANE Select |
chr | chr2 |
start | 55172547 |
end | 55232293 |
strand | - |
ver | v1.2 |
region | chr2:55172547-55232293 |
region5000 | chr2:55167547-55237293 |
regionname0 | CLHC1_chr2_55172547_55232293 |
regionname5000 | CLHC1_chr2_55167547_55237293 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 586 | 140 | 11 | 34 | 75 | 4 | 16 | 61 | CLHC1_chr2_55167547_55237293 | CLHC1 | MSVHQ others(581): Show |
chr2 | 55167547 | 55237293 |
a0002 | 0/1 | 586 | 134 | 36 | 21 | 61 | 4 | 11 | 46 | CLHC1_chr2_55167547_55237293 | CLHC1 | MSVHQ others(581): Show |
chr2 | 55167547 | 55237293 |
a0003 | 0/0 | 586 | 74 | 34 | 8 | 22 | 4 | 6 | 20 | CLHC1_chr2_55167547_55237293 | CLHC1 | MSVHQ others(581): Show |
chr2 | 55167547 | 55237293 |
a0004 | 1/0 | 586 | 21 | 0 | 2 | 11 | 3 | 4 | 9 | CLHC1_chr2_55167547_55237293 | CLHC1 | MSVHQ others(581): Show |
chr2 | 55167547 | 55237293 |
a0005 | 0/0 | 586 | 11 | 2 | 1 | 5 | 1 | 2 | 4 | CLHC1_chr2_55167547_55237293 | CLHC1 | MSVHQ others(581): Show |
chr2 | 55167547 | 55237293 |
a0006 | 0/0 | 586 | 10 | 0 | 0 | 10 | 0 | 0 | 10 | CLHC1_chr2_55167547_55237293 | CLHC1 | MSVHQ others(581): Show |
chr2 | 55167547 | 55237293 |
a0007 | 0/0 | 586 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | MSVHQ others(581): Show |
chr2 | 55167547 | 55237293 |
a0008 | 0/0 | 586 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | MSVHQ others(581): Show |
chr2 | 55167547 | 55237293 |
a0009 | 0/0 | 562 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | MSVHQ others(557): Show |
chr2 | 55167547 | 55237293 |
a0010 | 0/0 | 586 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | MSVHQ others(581): Show |
chr2 | 55167547 | 55237293 |
a0011 | 0/0 | 586 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | MSVHQ others(581): Show |
chr2 | 55167547 | 55237293 |
a0012 | 0/0 | 586 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | MSVHQ others(581): Show |
chr2 | 55167547 | 55237293 |
a0013 | 0/0 | 586 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | MSVHQ others(581): Show |
chr2 | 55167547 | 55237293 |
a0014 | 0/0 | 586 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | MSVHQ others(581): Show |
chr2 | 55167547 | 55237293 |
a0015 | 0/0 | 586 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | MSVHQ others(581): Show |
chr2 | 55167547 | 55237293 |
a0016 | 0/0 | 586 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | MSVHQ others(581): Show |
chr2 | 55167547 | 55237293 |
a0017 | 0/0 | 217 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | MSVHQ others(212): Show |
chr2 | 55167547 | 55237293 |
a0018 | 0/0 | 586 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | MSVHQ others(581): Show |
chr2 | 55167547 | 55237293 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 1758 | 71 | 7 | 9 | 47 | 1 | 7 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0001c0004 | 0/0 | 1758 | 40 | 3 | 20 | 8 | 1 | 8 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0001c0005 | 0/0 | 1758 | 25 | 0 | 3 | 19 | 2 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0001c0012 | 0/0 | 1758 | 2 | 1 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0001c0018 | 0/0 | 1758 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0001c0027 | 0/0 | 1758 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0002c0001 | 0/0 | 1758 | 128 | 34 | 19 | 61 | 4 | 10 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0002c0010 | 0/1 | 1758 | 4 | 0 | 2 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0002c0013 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0002c0016 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0003c0003 | 0/0 | 1758 | 63 | 34 | 8 | 11 | 4 | 6 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0003c0007 | 0/0 | 1758 | 11 | 0 | 0 | 11 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0004c0006 | 1/0 | 1758 | 21 | 0 | 2 | 11 | 3 | 4 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0005c0009 | 0/0 | 1758 | 10 | 2 | 1 | 4 | 1 | 2 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0005c0029 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0006c0008 | 0/0 | 1758 | 10 | 0 | 0 | 10 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0007c0011 | 0/0 | 1758 | 2 | 2 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0008c0014 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0008c0025 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0009c0021 | 0/0 | 1758 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0010c0017 | 0/0 | 1758 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0011c0026 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0012c0024 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0013c0020 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0014c0022 | 0/0 | 1758 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0015c0015 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0016c0028 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0017c0023 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 | ||
a0018c0019 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | ATGTC others(1753): Show |
chr2 | 55167547 | 55237293 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0002 | 0/0 | 5329 | 63 | 4 | 9 | 44 | 0 | 6 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0001c0002t0003 | 0/0 | 5329 | 4 | 3 | 0 | 0 | 1 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0001c0002t0021 | 0/0 | 5329 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0001c0002t0022 | 0/0 | 5330 | 2 | 0 | 0 | 1 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5325): Show |
chr2 | 55167547 | 55237293 |
a0001c0002t0031 | 0/0 | 5329 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0001c0004t0003 | 0/0 | 5329 | 3 | 1 | 0 | 2 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0001c0004t0006 | 0/0 | 5327 | 29 | 1 | 16 | 4 | 1 | 7 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5322): Show |
chr2 | 55167547 | 55237293 |
a0001c0004t0015 | 0/0 | 5327 | 2 | 0 | 0 | 2 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5322): Show |
chr2 | 55167547 | 55237293 |
a0001c0004t0016 | 0/0 | 5327 | 2 | 0 | 2 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5322): Show |
chr2 | 55167547 | 55237293 |
a0001c0004t0019 | 0/0 | 5327 | 2 | 0 | 1 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5322): Show |
chr2 | 55167547 | 55237293 |
a0001c0004t0020 | 0/0 | 5328 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5323): Show |
chr2 | 55167547 | 55237293 |
a0001c0004t0026 | 0/0 | 5328 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5323): Show |
chr2 | 55167547 | 55237293 |
a0001c0005t0003 | 0/0 | 5329 | 25 | 0 | 3 | 19 | 2 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0001c0012t0003 | 0/0 | 5329 | 2 | 1 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0001c0018t0006 | 0/0 | 5327 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5322): Show |
chr2 | 55167547 | 55237293 |
a0001c0027t0003 | 0/0 | 5329 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0002c0001t0001 | 0/0 | 5328 | 90 | 3 | 14 | 60 | 4 | 9 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5323): Show |
chr2 | 55167547 | 55237293 |
a0002c0001t0005 | 0/0 | 5327 | 27 | 25 | 2 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5322): Show |
chr2 | 55167547 | 55237293 |
a0002c0001t0011 | 0/0 | 5328 | 5 | 1 | 3 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5323): Show |
chr2 | 55167547 | 55237293 |
a0002c0001t0012 | 0/0 | 5325 | 3 | 3 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5320): Show |
chr2 | 55167547 | 55237293 |
a0002c0001t0018 | 0/0 | 5329 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0002c0001t0028 | 0/0 | 5325 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5320): Show |
chr2 | 55167547 | 55237293 |
a0002c0001t0029 | 0/0 | 5327 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5322): Show |
chr2 | 55167547 | 55237293 |
a0002c0010t0014 | 0/0 | 5328 | 3 | 0 | 2 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5323): Show |
chr2 | 55167547 | 55237293 |
a0002c0010t0020 | 0/1 | 5328 | 1 | 0 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5323): Show |
chr2 | 55167547 | 55237293 |
a0002c0013t0030 | 0/0 | 5328 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5323): Show |
chr2 | 55167547 | 55237293 |
a0002c0016t0001 | 0/0 | 5328 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5323): Show |
chr2 | 55167547 | 55237293 |
a0003c0003t0004 | 0/0 | 5328 | 35 | 25 | 4 | 0 | 2 | 4 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5323): Show |
chr2 | 55167547 | 55237293 |
a0003c0003t0007 | 0/0 | 5328 | 21 | 5 | 3 | 10 | 2 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5323): Show |
chr2 | 55167547 | 55237293 |
a0003c0003t0017 | 0/0 | 5329 | 2 | 2 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0003c0003t0023 | 0/0 | 5328 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5323): Show |
chr2 | 55167547 | 55237293 |
a0003c0003t0024 | 0/0 | 5328 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5323): Show |
chr2 | 55167547 | 55237293 |
a0003c0003t0025 | 0/0 | 5329 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0003c0003t0027 | 0/0 | 5329 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0003c0003t0033 | 0/0 | 5327 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5322): Show |
chr2 | 55167547 | 55237293 |
a0003c0007t0003 | 0/0 | 5329 | 6 | 0 | 0 | 6 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0003c0007t0010 | 0/0 | 5329 | 5 | 0 | 0 | 5 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0004c0006t0008 | 1/0 | 5330 | 12 | 0 | 2 | 2 | 3 | 4 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5325): Show |
chr2 | 55167547 | 55237293 |
a0004c0006t0009 | 0/0 | 5330 | 9 | 0 | 0 | 9 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5325): Show |
chr2 | 55167547 | 55237293 |
a0005c0009t0002 | 0/0 | 5329 | 7 | 2 | 1 | 1 | 1 | 2 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0005c0009t0013 | 0/0 | 5329 | 3 | 0 | 0 | 3 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0005c0029t0032 | 0/0 | 5329 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0006c0008t0001 | 0/0 | 5328 | 9 | 0 | 0 | 9 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5323): Show |
chr2 | 55167547 | 55237293 |
a0006c0008t0005 | 0/0 | 5327 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5322): Show |
chr2 | 55167547 | 55237293 |
a0007c0011t0005 | 0/0 | 5327 | 2 | 2 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5322): Show |
chr2 | 55167547 | 55237293 |
a0008c0014t0018 | 0/0 | 5329 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0008c0025t0003 | 0/0 | 5329 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0009c0021t0004 | 0/0 | 5328 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5323): Show |
chr2 | 55167547 | 55237293 |
a0010c0017t0001 | 0/0 | 5328 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5323): Show |
chr2 | 55167547 | 55237293 |
a0011c0026t0002 | 0/0 | 5329 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0012c0024t0021 | 0/0 | 5329 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0013c0020t0005 | 0/0 | 5327 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5322): Show |
chr2 | 55167547 | 55237293 |
a0014c0022t0005 | 0/0 | 5327 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5322): Show |
chr2 | 55167547 | 55237293 |
a0015c0015t0001 | 0/0 | 5328 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5323): Show |
chr2 | 55167547 | 55237293 |
a0016c0028t0002 | 0/0 | 5329 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0017c0023t0003 | 0/0 | 5329 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5324): Show |
chr2 | 55167547 | 55237293 |
a0018c0019t0008 | 0/0 | 5330 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | AGATT others(5325): Show |
chr2 | 55167547 | 55237293 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0002g0001 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0005 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0021g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0022g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0022g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0002t0031g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0006g0003 | 0/0 | 7 | 1 | 5 | 0 | 1 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0006g0007 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0006g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0006g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0006g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0006g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0006g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0006g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0006g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0006g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0006g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0006g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0006g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0006g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0006g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0006g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0006g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0015g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0015g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0016g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0016g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0019g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0019g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0020g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0004t0026g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0005t0003g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0005t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0005t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0005t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0005t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0005t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0005t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0005t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0005t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0005t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0005t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0005t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0005t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0005t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0005t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0005t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0012t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0012t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0018t0006g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0001c0027t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0004 | 0/0 | 7 | 0 | 2 | 4 | 1 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0005g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0005g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0005g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0005g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0005g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0011g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0011g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0011g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0011g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0012g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0012g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0018g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0028g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0001t0029g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0010t0014g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0010t0014g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0010t0020g0303 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0013t0030g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0002c0016t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0004g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0007g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0007g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0007g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0007g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0007g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0007g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0007g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0007g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0007g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0007g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0007g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0007g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0007g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0007g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0007g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0017g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0017g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0023g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0024g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0025g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0027g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0003t0033g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0007t0003g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0007t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0007t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0007t0010g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0007t0010g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0007t0010g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0007t0010g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0003c0007t0010g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0004c0006t0008g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0004c0006t0008g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0004c0006t0008g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0004c0006t0008g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0004c0006t0008g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0004c0006t0008g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0004c0006t0008g0263 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0004c0006t0008g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0004c0006t0008g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0004c0006t0008g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0004c0006t0008g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0004c0006t0009g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0004c0006t0009g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0004c0006t0009g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0004c0006t0009g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0004c0006t0009g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0004c0006t0009g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0004c0006t0009g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0004c0006t0009g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0005c0009t0002g0013 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0005c0009t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0005c0009t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0005c0009t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0005c0009t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0005c0009t0013g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0005c0009t0013g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0005c0009t0013g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0005c0029t0032g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0006c0008t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0006c0008t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0006c0008t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0006c0008t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0006c0008t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0006c0008t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0006c0008t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0006c0008t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0007c0011t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0007c0011t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0008c0014t0018g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0008c0025t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0009c0021t0004g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0010c0017t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0011c0026t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0012c0024t0021g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0013c0020t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0014c0022t0005g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0015c0015t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0016c0028t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0017c0023t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
a0018c0019t0008g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0004 | c0006 | t0008 | g0259 | EUR | GBR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00099 | hp2 | a0003 | c0003 | t0007 | g0111 | EUR | GBR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00140 | hp1 | a0002 | c0001 | t0001 | g0004 | EUR | GBR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00140 | hp2 | a0005 | c0009 | t0002 | g0013 | EUR | GBR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00323 | hp1 | a0001 | c0002 | t0003 | g0066 | EUR | FIN | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00323 | hp2 | a0002 | c0001 | t0001 | g0186 | EUR | FIN | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00408 | hp1 | a0002 | c0001 | t0001 | g0182 | EAS | CHS | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00408 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00423 | hp1 | a0002 | c0001 | t0001 | g0027 | EAS | CHS | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00423 | hp2 | a0004 | c0006 | t0008 | g0257 | EAS | CHS | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0288 | EAS | CHS | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00558 | hp1 | a0002 | c0001 | t0001 | g0154 | EAS | CHS | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00558 | hp2 | a0001 | c0002 | t0002 | g0314 | EAS | CHS | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00609 | hp1 | a0004 | c0006 | t0008 | g0258 | EAS | CHS | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00609 | hp2 | a0002 | c0001 | t0001 | g0010 | EAS | CHS | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00621 | hp1 | a0002 | c0001 | t0001 | g0010 | EAS | CHS | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00621 | hp2 | a0002 | c0001 | t0001 | g0168 | EAS | CHS | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00642 | hp1 | a0002 | c0010 | t0014 | g0038 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00642 | hp2 | a0001 | c0004 | t0006 | g0084 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00673 | hp1 | a0002 | c0001 | t0001 | g0167 | EAS | CHS | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00673 | hp2 | a0001 | c0002 | t0002 | g0276 | EAS | CHS | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00735 | hp1 | a0002 | c0001 | t0011 | g0210 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00735 | hp2 | a0001 | c0018 | t0006 | g0086 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00738 | hp1 | a0001 | c0004 | t0006 | g0085 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00738 | hp2 | a0002 | c0001 | t0005 | g0032 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00741 | hp1 | a0004 | c0006 | t0008 | g0260 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG00741 | hp2 | a0002 | c0001 | t0001 | g0004 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01069 | hp1 | a0002 | c0001 | t0001 | g0176 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01069 | hp2 | a0001 | c0004 | t0016 | g0087 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01070 | hp1 | a0001 | c0004 | t0006 | g0095 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01070 | hp2 | a0001 | c0005 | t0003 | g0015 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01071 | hp1 | a0001 | c0004 | t0016 | g0088 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01071 | hp2 | a0001 | c0005 | t0003 | g0015 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01074 | hp1 | a0001 | c0004 | t0006 | g0083 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01074 | hp2 | a0009 | c0021 | t0004 | g0151 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01106 | hp1 | a0003 | c0003 | t0024 | g0110 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01106 | hp2 | a0002 | c0001 | t0001 | g0028 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01109 | hp1 | a0002 | c0001 | t0001 | g0184 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01109 | hp2 | a0003 | c0003 | t0004 | g0122 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0279 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01167 | hp2 | a0001 | c0004 | t0006 | g0003 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01169 | hp1 | a0002 | c0001 | t0001 | g0169 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01169 | hp2 | a0001 | c0004 | t0006 | g0003 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01175 | hp1 | a0001 | c0004 | t0006 | g0003 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01175 | hp2 | a0003 | c0003 | t0007 | g0148 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01192 | hp1 | a0002 | c0001 | t0001 | g0164 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01192 | hp2 | a0005 | c0009 | t0002 | g0013 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01243 | hp1 | a0003 | c0003 | t0004 | g0047 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0297 | AMR | PUR | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01255 | hp1 | a0001 | c0002 | t0002 | g0282 | AMR | CLM | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01255 | hp2 | a0002 | c0001 | t0005 | g0035 | AMR | CLM | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01256 | hp1 | a0002 | c0001 | t0001 | g0022 | AMR | CLM | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01256 | hp2 | a0003 | c0003 | t0007 | g0147 | AMR | CLM | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01257 | hp1 | a0001 | c0004 | t0006 | g0007 | AMR | CLM | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01257 | hp2 | a0002 | c0001 | t0001 | g0185 | AMR | CLM | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01258 | hp1 | a0002 | c0001 | t0001 | g0004 | AMR | CLM | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01258 | hp2 | a0001 | c0004 | t0006 | g0007 | AMR | CLM | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01261 | hp1 | a0003 | c0003 | t0004 | g0139 | AMR | CLM | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01261 | hp2 | a0001 | c0027 | t0003 | g0059 | AMR | CLM | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01346 | hp1 | a0002 | c0001 | t0001 | g0159 | AMR | CLM | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01346 | hp2 | a0003 | c0003 | t0007 | g0017 | AMR | CLM | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | CLM | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01358 | hp2 | a0002 | c0010 | t0014 | g0275 | AMR | CLM | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01361 | hp1 | a0002 | c0001 | t0011 | g0029 | AMR | CLM | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01361 | hp2 | a0001 | c0004 | t0006 | g0003 | AMR | CLM | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01433 | hp1 | a0001 | c0005 | t0003 | g0050 | AMR | CLM | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01433 | hp2 | a0001 | c0004 | t0019 | g0081 | AMR | CLM | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01496 | hp1 | a0001 | c0004 | t0006 | g0079 | AMR | CLM | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01496 | hp2 | a0002 | c0001 | t0001 | g0190 | AMR | CLM | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01515 | hp1 | a0004 | c0006 | t0008 | g0036 | EUR | IBS | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01515 | hp2 | a0001 | c0005 | t0003 | g0063 | EUR | IBS | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01516 | hp1 | a0001 | c0004 | t0006 | g0003 | EUR | IBS | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01516 | hp2 | a0003 | c0003 | t0004 | g0018 | EUR | IBS | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01517 | hp1 | a0004 | c0006 | t0008 | g0036 | EUR | IBS | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01517 | hp2 | a0003 | c0003 | t0004 | g0018 | EUR | IBS | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01884 | hp1 | a0003 | c0003 | t0027 | g0129 | AFR | ACB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01884 | hp2 | a0003 | c0003 | t0004 | g0137 | AFR | ACB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01891 | hp1 | a0002 | c0001 | t0001 | g0242 | AFR | ACB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0301 | AFR | ACB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01928 | hp1 | a0002 | c0001 | t0011 | g0183 | AMR | PEL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0313 | AMR | PEL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0312 | AMR | PEL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01943 | hp2 | a0001 | c0004 | t0006 | g0144 | AMR | PEL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01975 | hp1 | a0001 | c0004 | t0006 | g0080 | AMR | PEL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01975 | hp2 | a0002 | c0001 | t0001 | g0180 | AMR | PEL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01978 | hp1 | a0010 | c0017 | t0001 | g0181 | AMR | PEL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01978 | hp2 | a0001 | c0002 | t0002 | g0316 | AMR | PEL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01981 | hp1 | a0003 | c0003 | t0004 | g0142 | AMR | PEL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01981 | hp2 | a0001 | c0004 | t0006 | g0097 | AMR | PEL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02015 | hp1 | a0011 | c0026 | t0002 | g0281 | EAS | KHV | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02015 | hp2 | a0001 | c0005 | t0003 | g0061 | EAS | KHV | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02040 | hp1 | a0002 | c0001 | t0001 | g0202 | EAS | KHV | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02040 | hp2 | a0003 | c0007 | t0003 | g0044 | EAS | KHV | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02055 | hp1 | a0003 | c0003 | t0004 | g0141 | AFR | ACB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02055 | hp2 | a0003 | c0003 | t0004 | g0048 | AFR | ACB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02056 | hp1 | a0001 | c0004 | t0006 | g0076 | EAS | KHV | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02056 | hp2 | a0003 | c0003 | t0007 | g0123 | EAS | KHV | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02071 | hp1 | a0001 | c0005 | t0003 | g0002 | EAS | KHV | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02071 | hp2 | a0002 | c0001 | t0001 | g0228 | EAS | KHV | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02083 | hp1 | a0012 | c0024 | t0021 | g0290 | EAS | KHV | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02083 | hp2 | a0001 | c0004 | t0003 | g0225 | EAS | KHV | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | KHV | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02132 | hp2 | a0005 | c0009 | t0013 | g0325 | EAS | KHV | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0307 | EAS | KHV | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02135 | hp2 | a0002 | c0001 | t0001 | g0207 | EAS | KHV | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02145 | hp1 | a0003 | c0003 | t0004 | g0136 | AFR | ACB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02145 | hp2 | a0005 | c0009 | t0002 | g0321 | AFR | ACB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02148 | hp1 | a0002 | c0001 | t0001 | g0197 | AMR | PEL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02148 | hp2 | a0001 | c0004 | t0026 | g0082 | AMR | PEL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02155 | hp1 | a0002 | c0001 | t0001 | g0203 | EAS | CDX | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | CDX | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02165 | hp1 | a0002 | c0001 | t0001 | g0172 | EAS | CDX | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02165 | hp2 | a0002 | c0001 | t0001 | g0209 | EAS | CDX | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02257 | hp1 | a0001 | c0004 | t0006 | g0003 | AFR | ACB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02257 | hp2 | a0003 | c0003 | t0004 | g0071 | AFR | ACB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02258 | hp1 | a0003 | c0003 | t0004 | g0115 | AFR | ACB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02258 | hp2 | a0002 | c0001 | t0011 | g0160 | AFR | ACB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02273 | hp1 | a0001 | c0004 | t0006 | g0096 | AMR | PEL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | PEL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02280 | hp1 | a0003 | c0003 | t0007 | g0126 | AFR | ACB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02280 | hp2 | a0008 | c0025 | t0003 | g0058 | AFR | ACB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02300 | hp1 | a0002 | c0001 | t0001 | g0030 | AMR | PEL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02300 | hp2 | a0001 | c0004 | t0006 | g0003 | AMR | PEL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0039 | AFR | ACB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02451 | hp2 | a0007 | c0011 | t0005 | g0042 | AFR | ACB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02523 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | KHV | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02523 | hp2 | a0001 | c0002 | t0021 | g0292 | EAS | KHV | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02602 | hp1 | a0004 | c0006 | t0008 | g0273 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02602 | hp2 | a0002 | c0001 | t0011 | g0029 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02615 | hp1 | a0003 | c0003 | t0033 | g0327 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02615 | hp2 | a0001 | c0012 | t0003 | g0132 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02622 | hp1 | a0003 | c0003 | t0004 | g0119 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02622 | hp2 | a0001 | c0004 | t0003 | g0233 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02630 | hp1 | a0002 | c0001 | t0005 | g0032 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02630 | hp2 | a0002 | c0001 | t0005 | g0153 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02647 | hp1 | a0002 | c0001 | t0005 | g0249 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02647 | hp2 | a0003 | c0003 | t0004 | g0016 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02683 | hp1 | a0003 | c0003 | t0023 | g0133 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02683 | hp2 | a0001 | c0004 | t0006 | g0099 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02698 | hp1 | a0001 | c0004 | t0006 | g0007 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0311 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02717 | hp1 | a0008 | c0014 | t0018 | g0247 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02717 | hp2 | a0013 | c0020 | t0005 | g0043 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02723 | hp1 | a0002 | c0001 | t0018 | g0254 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02723 | hp2 | a0002 | c0001 | t0028 | g0255 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02738 | hp1 | a0003 | c0003 | t0004 | g0140 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02738 | hp2 | a0002 | c0001 | t0001 | g0216 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02809 | hp1 | a0003 | c0003 | t0004 | g0073 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02809 | hp2 | a0002 | c0001 | t0005 | g0034 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02818 | hp1 | a0002 | c0001 | t0005 | g0251 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02818 | hp2 | a0001 | c0002 | t0003 | g0065 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02886 | hp1 | a0002 | c0001 | t0005 | g0238 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02886 | hp2 | a0001 | c0002 | t0003 | g0067 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02896 | hp1 | a0002 | c0001 | t0005 | g0237 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02896 | hp2 | a0003 | c0003 | t0004 | g0106 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02897 | hp1 | a0003 | c0003 | t0004 | g0077 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02897 | hp2 | a0002 | c0001 | t0005 | g0236 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02965 | hp1 | a0002 | c0001 | t0005 | g0245 | AFR | ESN | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02965 | hp2 | a0002 | c0001 | t0005 | g0250 | AFR | ESN | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02970 | hp1 | a0001 | c0004 | t0020 | g0317 | AFR | ESN | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02970 | hp2 | a0003 | c0003 | t0004 | g0134 | AFR | ESN | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02976 | hp1 | a0002 | c0001 | t0005 | g0020 | AFR | ESN | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02976 | hp2 | a0002 | c0001 | t0005 | g0035 | AFR | ESN | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03017 | hp1 | a0002 | c0001 | t0001 | g0161 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03017 | hp2 | a0002 | c0010 | t0014 | g0038 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03041 | hp1 | a0002 | c0001 | t0005 | g0248 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03041 | hp2 | a0003 | c0003 | t0004 | g0107 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03098 | hp1 | a0003 | c0003 | t0004 | g0102 | AFR | MSL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03098 | hp2 | a0002 | c0001 | t0005 | g0100 | AFR | MSL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03130 | hp1 | a0003 | c0003 | t0004 | g0138 | AFR | ESN | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03130 | hp2 | a0002 | c0013 | t0030 | g0235 | AFR | ESN | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03139 | hp1 | a0003 | c0003 | t0004 | g0120 | AFR | ESN | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03139 | hp2 | a0003 | c0003 | t0004 | g0074 | AFR | ESN | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03195 | hp1 | a0002 | c0001 | t0005 | g0243 | AFR | ESN | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03195 | hp2 | a0002 | c0001 | t0005 | g0033 | AFR | ESN | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03209 | hp1 | a0003 | c0003 | t0004 | g0143 | AFR | MSL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03209 | hp2 | a0002 | c0001 | t0001 | g0241 | AFR | MSL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03225 | hp1 | a0002 | c0001 | t0012 | g0021 | AFR | MSL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03225 | hp2 | a0003 | c0003 | t0004 | g0070 | AFR | MSL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03239 | hp1 | a0001 | c0004 | t0006 | g0093 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03239 | hp2 | a0002 | c0001 | t0001 | g0163 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03453 | hp1 | a0003 | c0003 | t0004 | g0072 | AFR | MSL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03453 | hp2 | a0002 | c0001 | t0005 | g0240 | AFR | MSL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03486 | hp1 | a0001 | c0002 | t0003 | g0068 | AFR | MSL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03486 | hp2 | a0002 | c0001 | t0005 | g0034 | AFR | MSL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03491 | hp1 | a0001 | c0004 | t0006 | g0152 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03491 | hp2 | a0002 | c0001 | t0001 | g0199 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03492 | hp1 | a0002 | c0001 | t0001 | g0192 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0284 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03516 | hp1 | a0002 | c0001 | t0005 | g0253 | AFR | ESN | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03516 | hp2 | a0003 | c0003 | t0007 | g0131 | AFR | ESN | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03540 | hp1 | a0003 | c0003 | t0007 | g0017 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03540 | hp2 | a0003 | c0003 | t0017 | g0146 | AFR | GWD | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0286 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03654 | hp2 | a0001 | c0005 | t0003 | g0056 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03669 | hp1 | a0003 | c0003 | t0004 | g0118 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03669 | hp2 | a0004 | c0006 | t0008 | g0270 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03688 | hp1 | a0002 | c0001 | t0001 | g0198 | SAS | STU | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03688 | hp2 | a0001 | c0004 | t0006 | g0092 | SAS | STU | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03704 | hp1 | a0001 | c0002 | t0002 | g0302 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03704 | hp2 | a0001 | c0004 | t0006 | g0007 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03710 | hp1 | a0004 | c0006 | t0008 | g0271 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03710 | hp2 | a0001 | c0002 | t0022 | g0318 | SAS | PJL | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03834 | hp1 | a0005 | c0009 | t0002 | g0013 | SAS | BEB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03834 | hp2 | a0001 | c0004 | t0006 | g0094 | SAS | BEB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03927 | hp1 | a0003 | c0003 | t0004 | g0116 | SAS | BEB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG03927 | hp2 | a0005 | c0009 | t0002 | g0320 | SAS | BEB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG04115 | hp1 | a0002 | c0001 | t0001 | g0191 | SAS | STU | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG04115 | hp2 | a0001 | c0004 | t0019 | g0098 | SAS | STU | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG04184 | hp1 | a0003 | c0003 | t0007 | g0103 | SAS | BEB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG04184 | hp2 | a0002 | c0001 | t0001 | g0101 | SAS | BEB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG04204 | hp1 | a0004 | c0006 | t0008 | g0150 | SAS | STU | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0285 | SAS | STU | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG04228 | hp1 | a0014 | c0022 | t0005 | g0149 | SAS | STU | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG04228 | hp2 | a0003 | c0003 | t0004 | g0145 | SAS | STU | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18522 | hp1 | a0003 | c0003 | t0004 | g0078 | AFR | YRI | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18522 | hp2 | a0002 | c0001 | t0005 | g0239 | AFR | YRI | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18747 | hp1 | a0002 | c0001 | t0001 | g0157 | EAS | CHB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18747 | hp2 | a0002 | c0001 | t0001 | g0232 | EAS | CHB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18906 | hp1 | a0005 | c0009 | t0002 | g0305 | AFR | YRI | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18906 | hp2 | a0003 | c0003 | t0004 | g0117 | AFR | YRI | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18939 | hp2 | a0003 | c0007 | t0010 | g0223 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18940 | hp1 | a0006 | c0008 | t0001 | g0174 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18940 | hp2 | a0001 | c0005 | t0003 | g0054 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18942 | hp1 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18944 | hp1 | a0006 | c0008 | t0001 | g0023 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18944 | hp2 | a0003 | c0003 | t0007 | g0108 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18945 | hp1 | a0001 | c0002 | t0031 | g0293 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18945 | hp2 | a0002 | c0001 | t0001 | g0227 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18946 | hp1 | a0002 | c0001 | t0001 | g0156 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18946 | hp2 | a0002 | c0001 | t0001 | g0175 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18947 | hp2 | a0002 | c0001 | t0001 | g0213 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18948 | hp1 | a0002 | c0001 | t0001 | g0230 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18948 | hp2 | a0001 | c0002 | t0002 | g0299 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18949 | hp1 | a0001 | c0005 | t0003 | g0002 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18949 | hp2 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18951 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18951 | hp2 | a0004 | c0006 | t0009 | g0037 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18952 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18952 | hp2 | a0003 | c0007 | t0003 | g0006 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18953 | hp1 | a0001 | c0002 | t0002 | g0294 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18953 | hp2 | a0002 | c0001 | t0029 | g0226 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18954 | hp1 | a0002 | c0001 | t0001 | g0201 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18954 | hp2 | a0001 | c0005 | t0003 | g0002 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0289 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18957 | hp2 | a0015 | c0015 | t0001 | g0162 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18960 | hp1 | a0002 | c0001 | t0001 | g0193 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18960 | hp2 | a0001 | c0005 | t0003 | g0053 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18961 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18961 | hp2 | a0002 | c0001 | t0001 | g0025 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18963 | hp1 | a0001 | c0002 | t0002 | g0298 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18963 | hp2 | a0006 | c0008 | t0001 | g0023 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18966 | hp1 | a0001 | c0005 | t0003 | g0064 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18966 | hp2 | a0005 | c0009 | t0002 | g0323 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18967 | hp1 | a0002 | c0001 | t0001 | g0206 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0315 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18968 | hp1 | a0016 | c0028 | t0002 | g0296 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18968 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18969 | hp1 | a0001 | c0005 | t0003 | g0049 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18969 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18970 | hp1 | a0001 | c0005 | t0003 | g0014 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18970 | hp2 | a0002 | c0001 | t0001 | g0219 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18971 | hp1 | a0004 | c0006 | t0009 | g0037 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18971 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18972 | hp1 | a0003 | c0003 | t0007 | g0112 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18972 | hp2 | a0004 | c0006 | t0009 | g0269 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18973 | hp1 | a0017 | c0023 | t0003 | g0057 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18973 | hp2 | a0002 | c0001 | t0001 | g0177 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18975 | hp1 | a0005 | c0009 | t0013 | g0326 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18975 | hp2 | a0001 | c0005 | t0003 | g0055 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18978 | hp1 | a0004 | c0006 | t0009 | g0266 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18978 | hp2 | a0003 | c0003 | t0007 | g0128 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18979 | hp1 | a0001 | c0004 | t0015 | g0090 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18979 | hp2 | a0003 | c0007 | t0003 | g0006 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18981 | hp1 | a0003 | c0007 | t0003 | g0046 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18981 | hp2 | a0002 | c0001 | t0001 | g0031 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18982 | hp1 | a0001 | c0004 | t0006 | g0089 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18982 | hp2 | a0004 | c0006 | t0009 | g0262 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18983 | hp1 | a0002 | c0001 | t0001 | g0179 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18983 | hp2 | a0006 | c0008 | t0001 | g0234 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18984 | hp1 | a0002 | c0001 | t0001 | g0217 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0309 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18985 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18985 | hp2 | a0002 | c0001 | t0001 | g0215 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18987 | hp1 | a0001 | c0002 | t0022 | g0308 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18987 | hp2 | a0002 | c0001 | t0001 | g0256 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18988 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18988 | hp2 | a0002 | c0001 | t0001 | g0218 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18989 | hp1 | a0001 | c0002 | t0002 | g0291 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18989 | hp2 | a0004 | c0006 | t0009 | g0267 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18990 | hp1 | a0002 | c0001 | t0001 | g0031 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18990 | hp2 | a0001 | c0005 | t0003 | g0060 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18991 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18991 | hp2 | a0002 | c0001 | t0001 | g0211 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18992 | hp1 | a0001 | c0005 | t0003 | g0002 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18992 | hp2 | a0003 | c0003 | t0007 | g0130 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18993 | hp1 | a0002 | c0001 | t0001 | g0166 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18993 | hp2 | a0003 | c0003 | t0007 | g0135 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18997 | hp1 | a0006 | c0008 | t0005 | g0196 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18997 | hp2 | a0005 | c0009 | t0013 | g0322 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18998 | hp1 | a0001 | c0004 | t0006 | g0019 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0278 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18999 | hp1 | a0004 | c0006 | t0009 | g0264 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18999 | hp2 | a0001 | c0002 | t0002 | g0306 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19000 | hp1 | a0001 | c0005 | t0003 | g0062 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19000 | hp2 | a0006 | c0008 | t0001 | g0214 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19001 | hp1 | a0002 | c0001 | t0001 | g0205 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19001 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19002 | hp1 | a0001 | c0005 | t0003 | g0014 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19002 | hp2 | a0001 | c0004 | t0006 | g0019 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19003 | hp1 | a0003 | c0007 | t0003 | g0006 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19003 | hp2 | a0002 | c0001 | t0001 | g0173 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19004 | hp1 | a0003 | c0003 | t0007 | g0127 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19004 | hp2 | a0003 | c0007 | t0010 | g0224 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19005 | hp2 | a0003 | c0003 | t0007 | g0109 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19006 | hp1 | a0002 | c0001 | t0001 | g0208 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19006 | hp2 | a0002 | c0001 | t0001 | g0231 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19007 | hp1 | a0002 | c0001 | t0001 | g0229 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19007 | hp2 | a0003 | c0007 | t0003 | g0006 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19009 | hp1 | a0002 | c0001 | t0001 | g0026 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19010 | hp1 | a0001 | c0002 | t0002 | g0319 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0287 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19011 | hp1 | a0001 | c0002 | t0002 | g0310 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19011 | hp2 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19012 | hp1 | a0003 | c0007 | t0010 | g0221 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19012 | hp2 | a0002 | c0001 | t0001 | g0200 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19030 | hp1 | a0003 | c0003 | t0017 | g0075 | AFR | LWK | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19030 | hp2 | a0002 | c0001 | t0012 | g0155 | AFR | LWK | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19043 | hp1 | a0002 | c0001 | t0005 | g0020 | AFR | LWK | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19043 | hp2 | a0003 | c0003 | t0004 | g0069 | AFR | LWK | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19054 | hp1 | a0004 | c0006 | t0009 | g0261 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19054 | hp2 | a0002 | c0001 | t0001 | g0026 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19055 | hp1 | a0018 | c0019 | t0008 | g0268 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19055 | hp2 | a0001 | c0002 | t0002 | g0304 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0280 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19056 | hp2 | a0006 | c0008 | t0001 | g0204 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19057 | hp1 | a0002 | c0001 | t0001 | g0212 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19057 | hp2 | a0001 | c0005 | t0003 | g0002 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19058 | hp1 | a0001 | c0005 | t0003 | g0002 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19058 | hp2 | a0001 | c0004 | t0015 | g0091 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19062 | hp1 | a0002 | c0001 | t0001 | g0025 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19062 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19063 | hp1 | a0006 | c0008 | t0001 | g0024 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19063 | hp2 | a0001 | c0004 | t0003 | g0045 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19064 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19064 | hp2 | a0003 | c0003 | t0007 | g0105 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0283 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19065 | hp2 | a0002 | c0001 | t0001 | g0022 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19070 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19070 | hp2 | a0002 | c0001 | t0001 | g0188 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19074 | hp1 | a0002 | c0001 | t0001 | g0178 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19074 | hp2 | a0001 | c0005 | t0003 | g0002 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19075 | hp1 | a0001 | c0002 | t0002 | g0274 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19075 | hp2 | a0001 | c0012 | t0003 | g0195 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19081 | hp1 | a0006 | c0008 | t0001 | g0171 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19081 | hp2 | a0003 | c0007 | t0010 | g0220 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19082 | hp1 | a0003 | c0003 | t0025 | g0125 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19082 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19084 | hp1 | a0001 | c0005 | t0003 | g0052 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19084 | hp2 | a0003 | c0007 | t0010 | g0222 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19085 | hp1 | a0002 | c0001 | t0001 | g0027 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19085 | hp2 | a0003 | c0003 | t0007 | g0124 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19086 | hp1 | a0001 | c0005 | t0003 | g0002 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19087 | hp1 | a0004 | c0006 | t0009 | g0265 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19087 | hp2 | a0002 | c0001 | t0001 | g0030 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19088 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19088 | hp2 | a0002 | c0001 | t0001 | g0010 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19090 | hp2 | a0006 | c0008 | t0001 | g0024 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19091 | hp1 | a0005 | c0029 | t0032 | g0324 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19091 | hp2 | a0002 | c0001 | t0001 | g0165 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19240 | hp1 | a0003 | c0003 | t0007 | g0121 | AFR | YRI | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA19240 | hp2 | a0002 | c0001 | t0012 | g0021 | AFR | YRI | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA20129 | hp1 | a0002 | c0001 | t0005 | g0033 | AFR | ASW | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA20129 | hp2 | a0003 | c0003 | t0004 | g0016 | AFR | ASW | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA20752 | hp1 | a0002 | c0001 | t0001 | g0187 | EUR | TSI | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA20752 | hp2 | a0003 | c0003 | t0007 | g0114 | EUR | TSI | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA20805 | hp1 | a0001 | c0005 | t0003 | g0051 | EUR | TSI | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA20805 | hp2 | a0002 | c0001 | t0001 | g0028 | EUR | TSI | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0005 | SAS | GIH | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA20905 | hp2 | a0002 | c0001 | t0001 | g0170 | SAS | GIH | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | CLM | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG01123 | hp2 | a0004 | c0006 | t0008 | g0272 | AMR | CLM | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02109 | hp1 | a0002 | c0001 | t0005 | g0252 | AFR | ACB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02109 | hp2 | a0007 | c0011 | t0005 | g0041 | AFR | ACB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02486 | hp1 | a0003 | c0003 | t0007 | g0104 | AFR | ACB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0300 | AFR | ACB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02559 | hp1 | a0002 | c0001 | t0005 | g0244 | AFR | ACB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG02559 | hp2 | a0003 | c0003 | t0004 | g0113 | AFR | ACB | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG06807 | hp1 | a0002 | c0001 | t0001 | g0158 | AFR | USA | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
HG06807 | hp2 | a0001 | c0002 | t0002 | g0039 | AFR | USA | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0277 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA18955 | hp2 | a0002 | c0001 | t0001 | g0194 | EAS | JPT | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA20300 | hp1 | a0002 | c0016 | t0001 | g0189 | AFR | USA | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
NA20300 | hp2 | a0002 | c0001 | t0005 | g0246 | AFR | USA | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
homoSapiens | chm13v2 | a0002 | c0010 | t0020 | g0303 | REF | REF | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
homoSapiens | grch38p0 | a0004 | c0006 | t0008 | g0263 | REF | REF | CLHC1_chr2_55167547_55237293 | CLHC1 | chr2 | 55167547 | 55237293 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:55175863 | C | T | 1 | a0011 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.1688G>A | p.Arg563Gln | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 2014/5330 | 1688/1761 | 563/586 | chr2 | 55175863 | |||
chr2:55175864 | G | A | 1 | a0009 | 1 | HG01074.hp2 | stop_gained | HIGH | c.1687C>T | p.Arg563* | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 2013/5330 | 1687/1761 | 563/586 | chr2 | 55175864 | |||
chr2:55177616 | T | C | 1 | a0015 | 1 | NA18957.hp2 | missense_variant | MODERATE | c.1550A>G | p.Asn517Ser | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 12/13 | 1876/5330 | 1550/1761 | 517/586 | chr2 | 55177616 | |||
chr2:55177658 | G | A | 7 | a0002 a0006 a0007 others(4): Show |
149 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(146): Show |
missense_variant | MODERATE | c.1508C>T | p.Ala503Val | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 12/13 | 1834/5330 | 1508/1761 | 503/586 | chr2 | 55177658 | |||
chr2:55180574 | C | G | 1 | a0008 | 2 | HG02280.hp2 HG02717.hp1 |
missense_variant | MODERATE | c.1320G>C | p.Leu440Phe | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/13 | 1646/5330 | 1320/1761 | 440/586 | chr2 | 55180574 | |||
chr2:55180618 | C | T | 16 | a0001 a0002 a0003 others(13): Show |
381 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(378): Show |
missense_variant | MODERATE | c.1276G>A | p.Val426Ile | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/13 | 1602/5330 | 1276/1761 | 426/586 | chr2 | 55180618 | |||
chr2:55180656 | G | A | 1 | a0006 | 10 | NA18940.hp1 NA18944.hp1 NA18963.hp2 others(7): Show |
missense_variant | MODERATE | c.1238C>T | p.Thr413Ile | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/13 | 1564/5330 | 1238/1761 | 413/586 | chr2 | 55180656 | |||
chr2:55181640 | G | T | 1 | a0007 | 2 | HG02109.hp2 HG02451.hp2 |
missense_variant | MODERATE | c.1111C>A | p.Leu371Met | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 10/13 | 1437/5330 | 1111/1761 | 371/586 | chr2 | 55181640 | |||
chr2:55181649 | C | T | 1 | a0007 | 2 | HG02109.hp2 HG02451.hp2 |
missense_variant | MODERATE | c.1102G>A | p.Ala368Thr | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 10/13 | 1428/5330 | 1102/1761 | 368/586 | chr2 | 55181649 | |||
chr2:55206307 | T | G | 1 | a0010 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.969A>C | p.Arg323Ser | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/13 | 1295/5330 | 969/1761 | 323/586 | chr2 | 55206307 | |||
chr2:55206356 | A | C | 1 | a0012 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.920T>G | p.Leu307Arg | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/13 | 1246/5330 | 920/1761 | 307/586 | chr2 | 55206356 | |||
chr2:55208669 | G | A | 1 | a0016 | 1 | NA18968.hp1 | missense_variant | MODERATE | c.856C>T | p.Arg286Cys | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/13 | 1182/5330 | 856/1761 | 286/586 | chr2 | 55208669 | |||
chr2:55209673 | G | A | 1 | a0018 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.658C>T | p.Arg220Trp | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 6/13 | 984/5330 | 658/1761 | 220/586 | chr2 | 55209673 | |||
chr2:55209678 | A | T | 1 | a0017 | 1 | NA18973.hp1 | stop_gained | HIGH | c.653T>A | p.Leu218* | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 6/13 | 979/5330 | 653/1761 | 218/586 | chr2 | 55209678 | |||
chr2:55209740 | C | A | 1 | a0013 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.591G>T | p.Met197Ile | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 6/13 | 917/5330 | 591/1761 | 197/586 | chr2 | 55209740 | |||
chr2:55209798 | G | A | 2 | a0003 a0009 |
75 | HG00099.hp2 HG01074.hp2 HG01106.hp1 others(72): Show |
missense_variant | MODERATE | c.533C>T | p.Ala178Val | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 6/13 | 859/5330 | 533/1761 | 178/586 | chr2 | 55209798 | |||
chr2:55209801 | T | C | 1 | a0014 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.530A>G | p.Asp177Gly | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 6/13 | 856/5330 | 530/1761 | 177/586 | chr2 | 55209801 | |||
chr2:55222276 | C | A | 1 | a0005 | 11 | HG00140.hp2 HG01192.hp2 HG02132.hp2 others(8): Show |
missense_variant | MODERATE | c.136G>T | p.Ala46Ser | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/13 | 462/5330 | 136/1761 | 46/586 | chr2 | 55222276 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:55175874 | C | T | 1 | a0001c0027 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.1677G>A | p.Thr559Thr | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 2003/5330 | 1677/1761 | 559/586 | chr2 | 55175874 | |||
chr2:55177618 | G | A | 1 | a0002c0016 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.1548C>T | p.Ile516Ile | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 12/13 | 1874/5330 | 1548/1761 | 516/586 | chr2 | 55177618 | |||
chr2:55177747 | T | C | 8 | a0001c0005 a0001c0012 a0001c0027 others(5): Show |
43 | HG01070.hp2 HG01071.hp2 HG01261.hp2 others(40): Show |
synonymous_variant | LOW | c.1419A>G | p.Gln473Gln | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 12/13 | 1745/5330 | 1419/1761 | 473/586 | chr2 | 55177747 | |||
chr2:55209477 | T | C | 1 | a0001c0018 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.741A>G | p.Ser247Ser | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 7/13 | 1067/5330 | 741/1761 | 247/586 | chr2 | 55209477 | |||
chr2:55222259 | G | T | 1 | a0002c0013 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.153C>A | p.Ile51Ile | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/13 | 479/5330 | 153/1761 | 51/586 | chr2 | 55222259 | |||
chr2:55222328 | T | C | 11 | a0001c0002 a0001c0005 a0001c0027 others(8): Show |
116 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
synonymous_variant | LOW | c.84A>G | p.Gln28Gln | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/13 | 410/5330 | 84/1761 | 28/586 | chr2 | 55222328 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:55172554 | T | A | 1 | a0005c0029t0032 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3236A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 3236 | chr2 | 55172554 | ||||||
chr2:55172701 | TA | T | 23 | a0001c0004t0006 a0001c0004t0015 a0001c0004t0016 others(20): Show |
212 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*3088delT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 3088 | chr2 | 55172701 | ||||||
chr2:55172701 | TAA | T | 9 | a0002c0001t0005 a0002c0001t0012 a0002c0001t0028 others(6): Show |
38 | HG00738.hp2 HG01255.hp2 HG02109.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*3087_*3088delTT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 3087 | chr2 | 55172701 | ||||||
chr2:55172763 | C | T | 1 | a0003c0003t0024 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3027G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 3027 | chr2 | 55172763 | ||||||
chr2:55172901 | G | C | 2 | a0001c0002t0021 a0012c0024t0021 |
2 | HG02083.hp1 HG02523.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2889C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 2889 | chr2 | 55172901 | ||||||
chr2:55173306 | T | G | 1 | a0001c0004t0015 | 2 | NA18979.hp1 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2484A>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 2484 | chr2 | 55173306 | ||||||
chr2:55173326 | T | C | 53 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0021 others(50): Show |
381 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(378): Show |
3_prime_UTR_variant | MODIFIER | c.*2464A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 2464 | chr2 | 55173326 | ||||||
chr2:55173604 | G | A | 1 | a0002c0001t0011 | 5 | HG00735.hp1 HG01361.hp1 HG01928.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2186C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 2186 | chr2 | 55173604 | ||||||
chr2:55173726 | T | C | 1 | a0001c0004t0016 | 2 | HG01069.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2064A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 2064 | chr2 | 55173726 | ||||||
chr2:55173841 | T | A | 1 | a0003c0003t0027 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1949A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 1949 | chr2 | 55173841 | ||||||
chr2:55174012 | GA | G | 42 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0021 others(39): Show |
337 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(334): Show |
3_prime_UTR_variant | MODIFIER | c.*1777delT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 1777 | chr2 | 55174012 | ||||||
chr2:55174012 | GAA | G | 6 | a0001c0004t0006 a0001c0004t0015 a0001c0004t0016 others(3): Show |
37 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1776_*1777delTT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 1776 | chr2 | 55174012 | ||||||
chr2:55174159 | G | T | 1 | a0003c0003t0023 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1631C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 1631 | chr2 | 55174159 | ||||||
chr2:55174173 | T | G | 1 | a0001c0002t0031 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1617A>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 1617 | chr2 | 55174173 | ||||||
chr2:55174232 | A | G | 1 | a0003c0007t0010 | 5 | NA18939.hp2 NA19004.hp2 NA19012.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1558T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 1558 | chr2 | 55174232 | ||||||
chr2:55174426 | G | A | 53 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0021 others(50): Show |
381 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(378): Show |
3_prime_UTR_variant | MODIFIER | c.*1364C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 1364 | chr2 | 55174426 | ||||||
chr2:55174638 | T | C | 1 | a0004c0006t0009 | 9 | NA18951.hp2 NA18971.hp1 NA18972.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1152A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 1152 | chr2 | 55174638 | ||||||
chr2:55174920 | C | A | 2 | a0005c0009t0013 a0005c0029t0032 |
4 | HG02132.hp2 NA18975.hp1 NA18997.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*870G>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 870 | chr2 | 55174920 | ||||||
chr2:55175041 | T | C | 2 | a0002c0001t0012 a0002c0001t0028 |
4 | HG02723.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*749A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 749 | chr2 | 55175041 | ||||||
chr2:55175061 | T | A | 9 | a0003c0003t0004 a0003c0003t0007 a0003c0003t0017 others(6): Show |
64 | HG00099.hp2 HG01074.hp2 HG01106.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*729A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 729 | chr2 | 55175061 | ||||||
chr2:55175089 | C | T | 18 | a0002c0001t0001 a0002c0001t0005 a0002c0001t0011 others(15): Show |
150 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*701G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 701 | chr2 | 55175089 | ||||||
chr2:55175093 | CAG | C | 2 | a0002c0001t0012 a0002c0001t0028 |
4 | HG02723.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*695_*696delCT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 695 | chr2 | 55175093 | ||||||
chr2:55175136 | C | A | 17 | a0002c0001t0001 a0002c0001t0005 a0002c0001t0011 others(14): Show |
149 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*654G>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 654 | chr2 | 55175136 | ||||||
chr2:55175374 | C | T | 4 | a0003c0003t0007 a0003c0003t0023 a0003c0003t0024 others(1): Show |
24 | HG00099.hp2 HG01106.hp1 HG01175.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*416G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 416 | chr2 | 55175374 | ||||||
chr2:55175655 | T | C | 1 | a0001c0004t0019 | 2 | HG01433.hp2 HG04115.hp2 |
3_prime_UTR_variant | MODIFIER | c.*135A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 13/13 | 135 | chr2 | 55175655 | ||||||
chr2:55232237 | T | G | 12 | a0001c0002t0002 a0001c0002t0021 a0001c0002t0022 others(9): Show |
85 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(82): Show |
5_prime_UTR_variant | MODIFIER | c.-270A>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/13 | 9826 | chr2 | 55232237 | ||||||
chr2:55232267 | T | A | 1 | a0003c0003t0033 | 1 | HG02615.hp1 | 5_prime_UTR_variant | MODIFIER | c.-300A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/13 | 9856 | chr2 | 55232267 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:55176148 | C | CTCA | 95 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(92): Show |
130 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1565-165_1565-163d others(5): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 12/12 | chr2 | 55176148 | |||||||
chr2:55176365 | T | G | 1 | a0003c0003t0004g0122 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1565-379A>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 12/12 | chr2 | 55176365 | |||||||
chr2:55176499 | T | C | 114 | a0002c0001t0001g0004 a0002c0001t0001g0009 a0002c0001t0001g0010 others(111): Show |
139 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1565-513A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 12/12 | chr2 | 55176499 | |||||||
chr2:55176530 | T | C | 28 | a0001c0002t0002g0313 a0001c0004t0006g0003 a0001c0004t0006g0007 others(25): Show |
38 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1565-544A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 12/12 | chr2 | 55176530 | |||||||
chr2:55176546 | T | A | 6 | a0001c0002t0002g0008 a0001c0002t0002g0283 a0001c0002t0002g0287 others(3): Show |
9 | HG00544.hp1 HG00558.hp2 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.1565-560A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 12/12 | chr2 | 55176546 | |||||||
chr2:55176665 | G | A | 1 | a0003c0003t0007g0121 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1565-679C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 12/12 | chr2 | 55176665 | |||||||
chr2:55176882 | T | C | 2 | a0003c0003t0004g0071 a0003c0003t0004g0074 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1564+720A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 12/12 | chr2 | 55176882 | |||||||
chr2:55177138 | G | T | 1 | a0003c0003t0007g0109 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1564+464C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 12/12 | chr2 | 55177138 | |||||||
chr2:55177421 | T | C | 1 | a0002c0001t0012g0155 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1564+181A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 12/12 | chr2 | 55177421 | |||||||
chr2:55177789 | C | T | 61 | a0003c0003t0004g0016 a0003c0003t0004g0018 a0003c0003t0004g0047 others(58): Show |
64 | HG00099.hp2 HG01074.hp2 HG01106.hp1 others(61): Show |
splice_region_variant&intron_variant | LOW | c.1385-8G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55177789 | |||||||
chr2:55177901 | T | A | 63 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(60): Show |
86 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1385-120A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55177901 | |||||||
chr2:55177952 | C | CA | 113 | a0002c0001t0001g0004 a0002c0001t0001g0009 a0002c0001t0001g0010 others(110): Show |
138 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.1385-172dupT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55177952 | |||||||
chr2:55178096 | A | G | 21 | a0002c0001t0005g0032 a0002c0001t0005g0033 a0002c0001t0005g0034 others(18): Show |
25 | HG00738.hp2 HG01255.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1385-315T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55178096 | |||||||
chr2:55178278 | T | G | 1 | a0001c0004t0020g0317 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1385-497A>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55178278 | |||||||
chr2:55178332 | G | A | 113 | a0002c0001t0001g0004 a0002c0001t0001g0009 a0002c0001t0001g0010 others(110): Show |
138 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.1385-551C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55178332 | |||||||
chr2:55178380 | T | C | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1385-599A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55178380 | |||||||
chr2:55178403 | A | G | 1 | a0014c0022t0005g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1385-622T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55178403 | |||||||
chr2:55178428 | G | T | 1 | a0001c0002t0002g0311 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1385-647C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55178428 | |||||||
chr2:55178439 | T | G | 7 | a0002c0001t0001g0172 a0002c0001t0001g0173 a0002c0001t0001g0193 others(4): Show |
7 | HG02071.hp2 HG02165.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.1385-658A>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55178439 | |||||||
chr2:55178531 | G | A | 9 | a0001c0012t0003g0195 a0003c0007t0003g0006 a0003c0007t0003g0044 others(6): Show |
12 | HG02040.hp2 NA18939.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.1385-750C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55178531 | |||||||
chr2:55178556 | G | T | 112 | a0002c0001t0001g0004 a0002c0001t0001g0009 a0002c0001t0001g0010 others(109): Show |
137 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.1385-775C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55178556 | |||||||
chr2:55178599 | C | T | 1 | a0011c0026t0002g0281 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1385-818G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55178599 | |||||||
chr2:55178607 | G | C | 1 | a0002c0001t0001g0180 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1385-826C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55178607 | |||||||
chr2:55178711 | C | A | 114 | a0002c0001t0001g0004 a0002c0001t0001g0009 a0002c0001t0001g0010 others(111): Show |
139 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1385-930G>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55178711 | |||||||
chr2:55178780 | G | C | 28 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(25): Show |
38 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1385-999C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55178780 | |||||||
chr2:55178912 | T | A | 1 | a0006c0008t0001g0174 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1385-1131A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55178912 | |||||||
chr2:55178917 | A | AATT | 3 | a0001c0002t0002g0282 a0004c0006t0008g0270 a0014c0022t0005g0149 |
3 | HG01255.hp1 HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1385-1139_1385-113 others(7): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55178917 | |||||||
chr2:55178917 | AATT | A | 121 | a0002c0001t0001g0004 a0002c0001t0001g0009 a0002c0001t0001g0010 others(118): Show |
148 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.1385-1139_1385-113 others(7): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55178917 | |||||||
chr2:55178993 | A | G | 1 | a0001c0004t0006g0152 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1385-1212T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55178993 | |||||||
chr2:55179069 | C | T | 1 | a0002c0001t0001g0194 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1385-1288G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55179069 | |||||||
chr2:55179090 | TAAATTCT others(3): Show |
T | 1 | a0014c0022t0005g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1385-1319_1385-131 others(14): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55179090 | |||||||
chr2:55179101 | A | T | 1 | a0014c0022t0005g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1385-1320T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55179101 | |||||||
chr2:55179288 | G | C | 113 | a0002c0001t0001g0004 a0002c0001t0001g0009 a0002c0001t0001g0010 others(110): Show |
138 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.1384+1222C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55179288 | |||||||
chr2:55179354 | G | A | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1384+1156C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55179354 | |||||||
chr2:55179354 | G | C | 1 | a0003c0003t0004g0118 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1384+1156C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55179354 | |||||||
chr2:55179466 | A | C | 96 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(93): Show |
131 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.1384+1044T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55179466 | |||||||
chr2:55179526 | T | C | 89 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(86): Show |
102 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1384+984A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55179526 | |||||||
chr2:55179625 | A | G | 65 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(62): Show |
88 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1384+885T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55179625 | |||||||
chr2:55179645 | G | T | 3 | a0004c0006t0009g0037 a0004c0006t0009g0265 a0004c0006t0009g0266 |
4 | NA18951.hp2 NA18971.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1384+865C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55179645 | |||||||
chr2:55179646 | G | A | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1384+864C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55179646 | |||||||
chr2:55179736 | A | G | 7 | a0002c0001t0005g0032 a0002c0001t0005g0033 a0002c0001t0005g0100 others(4): Show |
9 | HG00738.hp2 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1384+774T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55179736 | |||||||
chr2:55179738 | G | A | 4 | a0001c0002t0002g0012 a0001c0002t0002g0312 a0001c0002t0002g0313 others(1): Show |
6 | HG01123.hp1 HG01358.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.1384+772C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55179738 | |||||||
chr2:55179818 | T | G | 165 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(162): Show |
204 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.1384+692A>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55179818 | |||||||
chr2:55179851 | G | A | 10 | a0003c0003t0004g0069 a0003c0003t0004g0070 a0003c0003t0004g0071 others(7): Show |
10 | HG01109.hp2 HG02257.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1384+659C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55179851 | |||||||
chr2:55180152 | C | CA | 98 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(95): Show |
134 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1384+357dupT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55180152 | |||||||
chr2:55180160 | A | T | 3 | a0007c0011t0005g0041 a0007c0011t0005g0042 a0013c0020t0005g0043 |
3 | HG02109.hp2 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1384+350T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55180160 | |||||||
chr2:55180162 | T | A | 167 | a0002c0001t0001g0004 a0002c0001t0001g0009 a0002c0001t0001g0010 others(164): Show |
197 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.1384+348A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55180162 | |||||||
chr2:55180164 | T | A | 1 | a0002c0001t0001g0212 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1384+346A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55180164 | |||||||
chr2:55180171 | A | G | 61 | a0003c0003t0004g0016 a0003c0003t0004g0018 a0003c0003t0004g0047 others(58): Show |
64 | HG00099.hp2 HG01074.hp2 HG01106.hp1 others(61): Show |
intron_variant | MODIFIER | c.1384+339T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55180171 | |||||||
chr2:55180252 | G | A | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1384+258C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55180252 | |||||||
chr2:55180323 | C | T | 303 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(300): Show |
378 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(375): Show |
intron_variant | MODIFIER | c.1384+187G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55180323 | |||||||
chr2:55180343 | T | C | 1 | a0002c0001t0001g0256 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1384+167A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55180343 | |||||||
chr2:55180418 | C | T | 1 | a0014c0022t0005g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1384+92G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55180418 | |||||||
chr2:55180474 | T | A | 30 | a0001c0005t0003g0002 a0001c0005t0003g0014 a0001c0005t0003g0015 others(27): Show |
42 | HG01070.hp2 HG01071.hp2 HG01261.hp2 others(39): Show |
intron_variant | MODIFIER | c.1384+36A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 11/12 | chr2 | 55180474 | |||||||
chr2:55180772 | G | A | 1 | a0002c0001t0005g0250 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1182-60C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 10/12 | chr2 | 55180772 | |||||||
chr2:55180793 | C | T | 1 | a0002c0001t0001g0161 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1182-81G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 10/12 | chr2 | 55180793 | |||||||
chr2:55180799 | G | A | 300 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(297): Show |
374 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(371): Show |
intron_variant | MODIFIER | c.1182-87C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 10/12 | chr2 | 55180799 | |||||||
chr2:55180909 | A | G | 1 | a0013c0020t0005g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1182-197T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 10/12 | chr2 | 55180909 | |||||||
chr2:55181083 | C | A | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1182-371G>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 10/12 | chr2 | 55181083 | |||||||
chr2:55181236 | C | T | 3 | a0002c0001t0001g0227 a0002c0001t0029g0226 a0015c0015t0001g0162 |
3 | NA18945.hp2 NA18953.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1181+334G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 10/12 | chr2 | 55181236 | |||||||
chr2:55181420 | C | A | 92 | a0002c0001t0001g0004 a0002c0001t0001g0009 a0002c0001t0001g0010 others(89): Show |
113 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.1181+150G>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 10/12 | chr2 | 55181420 | |||||||
chr2:55181750 | G | A | 1 | a0002c0013t0030g0235 | 1 | HG03130.hp2 | splice_region_variant&intron_variant | LOW | c.1007-6C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55181750 | |||||||
chr2:55181889 | ATAGAT | A | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1007-150_1007-146d others(7): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55181889 | |||||||
chr2:55181943 | G | A | 1 | a0003c0003t0004g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1007-199C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55181943 | |||||||
chr2:55182029 | A | G | 2 | a0001c0005t0003g0060 a0001c0005t0003g0061 |
2 | HG02015.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1007-285T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55182029 | |||||||
chr2:55182105 | C | T | 1 | a0002c0001t0001g0025 | 2 | NA18961.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1007-361G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55182105 | |||||||
chr2:55182106 | G | A | 1 | a0002c0001t0005g0240 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1007-362C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55182106 | |||||||
chr2:55182184 | C | A | 20 | a0002c0001t0005g0032 a0002c0001t0005g0033 a0002c0001t0005g0034 others(17): Show |
24 | HG00738.hp2 HG01255.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1007-440G>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55182184 | |||||||
chr2:55182284 | T | C | 113 | a0002c0001t0001g0004 a0002c0001t0001g0009 a0002c0001t0001g0010 others(110): Show |
138 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.1007-540A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55182284 | |||||||
chr2:55182465 | G | A | 1 | a0002c0013t0030g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1007-721C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55182465 | |||||||
chr2:55182685 | G | A | 1 | a0001c0004t0006g0076 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1007-941C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55182685 | |||||||
chr2:55182714 | A | G | 1 | a0003c0003t0004g0113 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1007-970T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55182714 | |||||||
chr2:55182734 | T | C | 1 | a0003c0007t0003g0046 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1007-990A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55182734 | |||||||
chr2:55182761 | GAAGGAGA others(11384): Show |
G | 1 | a0002c0001t0018g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1006+12118_1007-10 others(5): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55182761 | |||||||
chr2:55182763 | A | C | 4 | a0001c0002t0002g0297 a0001c0002t0003g0065 a0001c0002t0003g0067 others(1): Show |
4 | HG01243.hp2 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-1019T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55182763 | |||||||
chr2:55182785 | T | G | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1007-1041A>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55182785 | |||||||
chr2:55182807 | C | T | 1 | a0005c0009t0013g0325 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1007-1063G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55182807 | |||||||
chr2:55182831 | G | A | 3 | a0002c0001t0012g0021 a0002c0001t0012g0155 a0002c0001t0028g0255 |
4 | HG02723.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-1087C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55182831 | |||||||
chr2:55182853 | G | C | 3 | a0006c0008t0001g0023 a0006c0008t0001g0174 a0006c0008t0001g0204 |
4 | NA18940.hp1 NA18944.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-1109C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55182853 | |||||||
chr2:55183067 | T | C | 3 | a0002c0001t0001g0004 a0002c0001t0001g0022 a0002c0001t0001g0030 |
4 | NA18949.hp2 NA19064.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-1323A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55183067 | |||||||
chr2:55183168 | T | A | 1 | a0002c0001t0001g0004 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1007-1424A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55183168 | |||||||
chr2:55183270 | A | G | 1 | a0013c0020t0005g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1007-1526T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55183270 | |||||||
chr2:55183528 | C | T | 121 | a0002c0001t0001g0004 a0002c0001t0001g0009 a0002c0001t0001g0010 others(118): Show |
148 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.1007-1784G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55183528 | |||||||
chr2:55183672 | G | C | 89 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(86): Show |
102 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1007-1928C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55183672 | |||||||
chr2:55183699 | C | T | 95 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(92): Show |
130 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1007-1955G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55183699 | |||||||
chr2:55183767 | A | T | 1 | a0003c0003t0004g0118 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1007-2023T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55183767 | |||||||
chr2:55183991 | G | C | 2 | a0002c0001t0001g0170 a0002c0001t0001g0190 |
2 | HG01496.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1007-2247C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55183991 | |||||||
chr2:55184020 | C | T | 1 | a0003c0003t0004g0102 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1007-2276G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55184020 | |||||||
chr2:55184058 | C | T | 1 | a0008c0014t0018g0247 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1007-2314G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55184058 | |||||||
chr2:55184104 | T | TTC | 8 | a0001c0002t0002g0297 a0001c0002t0003g0065 a0001c0002t0003g0067 others(5): Show |
8 | HG01243.hp2 HG02723.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1007-2361_1007-236 others(6): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55184104 | |||||||
chr2:55184105 | T | TC | 294 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(291): Show |
368 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(365): Show |
intron_variant | MODIFIER | c.1007-2362_1007-236 others(5): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55184105 | |||||||
chr2:55184106 | A | C | 4 | a0002c0001t0001g0166 a0002c0001t0001g0185 a0003c0003t0004g0077 others(1): Show |
4 | HG01257.hp2 HG02897.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007-2362T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55184106 | |||||||
chr2:55184106 | A | T | 301 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(298): Show |
376 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(373): Show |
intron_variant | MODIFIER | c.1007-2362T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55184106 | |||||||
chr2:55184722 | G | T | 192 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(189): Show |
242 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.1007-2978C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55184722 | |||||||
chr2:55184840 | G | A | 1 | a0002c0001t0001g0175 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1007-3096C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55184840 | |||||||
chr2:55184919 | A | AAC | 66 | a0001c0002t0002g0285 a0001c0002t0002g0298 a0001c0002t0002g0307 others(63): Show |
69 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(66): Show |
intron_variant | MODIFIER | c.1007-3177_1007-317 others(6): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55184919 | |||||||
chr2:55184919 | A | AACAC | 111 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0040 others(108): Show |
137 | HG00323.hp2 HG00544.hp2 HG00609.hp2 others(134): Show |
intron_variant | MODIFIER | c.1007-3179_1007-317 others(8): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55184919 | |||||||
chr2:55184919 | A | AACACAC | 38 | a0001c0002t0002g0001 a0001c0004t0006g0076 a0001c0004t0019g0098 others(35): Show |
41 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1007-3181_1007-317 others(10): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55184919 | |||||||
chr2:55184919 | A | AACACACA others(1): Show |
7 | a0001c0004t0006g0019 a0001c0004t0006g0152 a0002c0001t0001g0026 others(4): Show |
7 | HG02976.hp2 HG03491.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1007-3183_1007-317 others(12): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55184919 | |||||||
chr2:55184919 | A | AACACACA others(3): Show |
5 | a0001c0004t0006g0019 a0002c0001t0001g0026 a0002c0001t0001g0194 others(2): Show |
5 | HG03669.hp1 HG03927.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007-3185_1007-317 others(14): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55184919 | |||||||
chr2:55184919 | AAC | A | 21 | a0001c0002t0002g0012 a0001c0002t0002g0300 a0001c0002t0002g0301 others(18): Show |
24 | HG00323.hp1 HG01123.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.1007-3177_1007-317 others(6): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55184919 | |||||||
chr2:55184919 | AACAC | A | 26 | a0001c0004t0020g0317 a0001c0005t0003g0002 a0001c0005t0003g0015 others(23): Show |
36 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1007-3179_1007-317 others(8): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55184919 | |||||||
chr2:55184919 | AACACAC | A | 3 | a0001c0005t0003g0014 a0003c0003t0004g0048 a0003c0003t0004g0141 |
4 | HG02055.hp1 HG02055.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007-3181_1007-317 others(10): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55184919 | |||||||
chr2:55184959 | CACAA | C | 6 | a0005c0009t0002g0013 a0005c0009t0002g0321 a0005c0009t0013g0322 others(3): Show |
8 | HG00140.hp2 HG01192.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.1007-3219_1007-321 others(8): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55184959 | |||||||
chr2:55184961 | CAA | C | 4 | a0001c0002t0002g0039 a0001c0002t0002g0279 a0005c0009t0002g0305 others(1): Show |
5 | HG01167.hp1 HG02451.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007-3219_1007-321 others(6): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55184961 | |||||||
chr2:55184963 | A | C | 4 | a0001c0002t0002g0297 a0001c0002t0003g0065 a0001c0002t0003g0067 others(1): Show |
4 | HG01243.hp2 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-3219T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55184963 | |||||||
chr2:55185014 | G | T | 1 | a0001c0018t0006g0086 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1007-3270C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55185014 | |||||||
chr2:55185016 | C | G | 65 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(62): Show |
88 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1007-3272G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55185016 | |||||||
chr2:55185263 | A | G | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1007-3519T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55185263 | |||||||
chr2:55185278 | C | T | 2 | a0001c0002t0002g0300 a0001c0002t0002g0301 |
2 | HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1007-3534G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55185278 | |||||||
chr2:55185314 | A | C | 1 | a0005c0009t0002g0320 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1007-3570T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55185314 | |||||||
chr2:55185434 | T | C | 3 | a0007c0011t0005g0041 a0007c0011t0005g0042 a0013c0020t0005g0043 |
3 | HG02109.hp2 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1007-3690A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55185434 | |||||||
chr2:55185479 | T | C | 1 | a0001c0002t0002g0012 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1007-3735A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55185479 | |||||||
chr2:55185533 | C | T | 1 | a0001c0005t0003g0002 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1007-3789G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55185533 | |||||||
chr2:55185620 | G | C | 89 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(86): Show |
102 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1007-3876C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55185620 | |||||||
chr2:55185701 | T | C | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1007-3957A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55185701 | |||||||
chr2:55185808 | T | A | 1 | a0005c0009t0013g0322 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1007-4064A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55185808 | |||||||
chr2:55185809 | A | T | 1 | a0005c0009t0013g0322 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1007-4065T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55185809 | |||||||
chr2:55185811 | T | A | 1 | a0005c0009t0013g0322 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1007-4067A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55185811 | |||||||
chr2:55185842 | C | T | 1 | a0002c0016t0001g0189 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1007-4098G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55185842 | |||||||
chr2:55185927 | A | G | 1 | a0002c0001t0001g0188 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1007-4183T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55185927 | |||||||
chr2:55185963 | A | T | 89 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(86): Show |
102 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1007-4219T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55185963 | |||||||
chr2:55186097 | C | G | 1 | a0004c0006t0008g0150 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1007-4353G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55186097 | |||||||
chr2:55186108 | T | C | 1 | a0001c0002t0002g0306 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1007-4364A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55186108 | |||||||
chr2:55186203 | A | G | 1 | a0002c0010t0014g0038 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1007-4459T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55186203 | |||||||
chr2:55186365 | A | G | 1 | a0003c0003t0004g0138 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1007-4621T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55186365 | |||||||
chr2:55186403 | C | T | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1007-4659G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55186403 | |||||||
chr2:55186417 | T | A | 1 | a0005c0009t0013g0325 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1007-4673A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55186417 | |||||||
chr2:55186508 | C | G | 65 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(62): Show |
88 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1007-4764G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55186508 | |||||||
chr2:55186583 | A | G | 1 | a0001c0002t0002g0001 | 4 | NA18969.hp2 NA18991.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-4839T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55186583 | |||||||
chr2:55186588 | TACA | T | 29 | a0001c0005t0003g0002 a0001c0005t0003g0014 a0001c0005t0003g0015 others(26): Show |
41 | HG01070.hp2 HG01071.hp2 HG01261.hp2 others(38): Show |
intron_variant | MODIFIER | c.1007-4847_1007-484 others(7): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55186588 | |||||||
chr2:55186622 | G | A | 1 | a0001c0002t0022g0318 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1007-4878C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55186622 | |||||||
chr2:55186642 | A | G | 8 | a0001c0002t0002g0005 a0001c0002t0002g0274 a0001c0002t0002g0289 others(5): Show |
9 | NA18942.hp2 NA18945.hp1 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.1007-4898T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55186642 | |||||||
chr2:55186753 | TGACAGAG others(3): Show |
T | 1 | a0002c0001t0005g0245 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1007-5019_1007-501 others(14): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55186753 | |||||||
chr2:55186993 | G | A | 65 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(62): Show |
88 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1007-5249C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55186993 | |||||||
chr2:55186994 | C | T | 1 | a0003c0003t0004g0145 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1007-5250G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55186994 | |||||||
chr2:55187044 | A | G | 1 | a0002c0001t0001g0026 | 2 | NA19009.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1007-5300T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55187044 | |||||||
chr2:55187116 | C | T | 1 | a0002c0001t0005g0249 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1007-5372G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55187116 | |||||||
chr2:55187228 | G | A | 96 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(93): Show |
132 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1007-5484C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55187228 | |||||||
chr2:55187279 | C | CAAATA | 62 | a0001c0002t0002g0005 a0001c0002t0002g0274 a0001c0002t0002g0289 others(59): Show |
74 | HG00642.hp1 HG00738.hp2 HG01074.hp2 others(71): Show |
intron_variant | MODIFIER | c.1007-5540_1007-553 others(9): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55187279 | |||||||
chr2:55187279 | C | CAAATAAA others(3): Show |
41 | a0001c0005t0003g0002 a0001c0005t0003g0014 a0001c0005t0003g0015 others(38): Show |
51 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.1007-5545_1007-553 others(14): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55187279 | |||||||
chr2:55187279 | C | CAAATAAA others(8): Show |
8 | a0001c0005t0003g0060 a0001c0012t0003g0132 a0002c0001t0005g0035 others(5): Show |
8 | HG01255.hp2 HG02615.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1007-5550_1007-553 others(19): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55187279 | |||||||
chr2:55187279 | C | CAAATAAA others(13): Show |
5 | a0002c0001t0005g0035 a0002c0001t0005g0253 a0002c0001t0012g0021 others(2): Show |
6 | HG02723.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1007-5555_1007-553 others(24): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55187279 | |||||||
chr2:55187279 | CAAATA | C | 62 | a0001c0002t0002g0039 a0001c0002t0002g0279 a0001c0002t0002g0284 others(59): Show |
78 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.1007-5540_1007-553 others(9): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55187279 | |||||||
chr2:55187279 | CAAATAAA others(3): Show |
C | 2 | a0002c0001t0001g0241 a0002c0001t0001g0242 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1007-5545_1007-553 others(14): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55187279 | |||||||
chr2:55187330 | G | A | 91 | a0002c0001t0001g0004 a0002c0001t0001g0009 a0002c0001t0001g0010 others(88): Show |
112 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1007-5586C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55187330 | |||||||
chr2:55187474 | G | T | 27 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(24): Show |
37 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1007-5730C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55187474 | |||||||
chr2:55187674 | G | A | 3 | a0002c0001t0012g0021 a0002c0001t0012g0155 a0002c0001t0028g0255 |
4 | HG02723.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-5930C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55187674 | |||||||
chr2:55187674 | G | C | 1 | a0003c0003t0004g0106 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1007-5930C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55187674 | |||||||
chr2:55187998 | C | T | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1007-6254G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55187998 | |||||||
chr2:55188106 | G | C | 2 | a0001c0002t0002g0011 a0001c0002t0002g0276 |
2 | HG00673.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.1007-6362C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55188106 | |||||||
chr2:55188247 | T | C | 3 | a0002c0001t0012g0021 a0002c0001t0012g0155 a0002c0001t0028g0255 |
4 | HG02723.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-6503A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55188247 | |||||||
chr2:55188295 | G | A | 1 | a0005c0009t0013g0325 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1007-6551C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55188295 | |||||||
chr2:55188307 | C | A | 1 | a0002c0001t0001g0256 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1007-6563G>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55188307 | |||||||
chr2:55188340 | T | C | 4 | a0001c0004t0006g0007 a0001c0004t0006g0094 a0001c0004t0006g0095 others(1): Show |
5 | HG01070.hp1 HG02683.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.1007-6596A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55188340 | |||||||
chr2:55188484 | G | T | 88 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(85): Show |
101 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(98): Show |
intron_variant | MODIFIER | c.1007-6740C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55188484 | |||||||
chr2:55188487 | T | C | 1 | a0003c0007t0003g0044 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1007-6743A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55188487 | |||||||
chr2:55188489 | C | T | 1 | a0018c0019t0008g0268 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1007-6745G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55188489 | |||||||
chr2:55188976 | T | C | 1 | a0001c0005t0003g0049 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1007-7232A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55188976 | |||||||
chr2:55189052 | A | C | 1 | a0003c0003t0007g0131 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1007-7308T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55189052 | |||||||
chr2:55189338 | T | G | 1 | a0001c0002t0003g0066 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1007-7594A>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55189338 | |||||||
chr2:55189345 | T | C | 1 | a0003c0003t0007g0104 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1007-7601A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55189345 | |||||||
chr2:55189467 | T | C | 1 | a0002c0001t0001g0154 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1007-7723A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55189467 | |||||||
chr2:55189605 | C | T | 210 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(207): Show |
250 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.1007-7861G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55189605 | |||||||
chr2:55189817 | T | C | 305 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(302): Show |
380 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(377): Show |
intron_variant | MODIFIER | c.1007-8073A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55189817 | |||||||
chr2:55190009 | T | G | 1 | a0001c0002t0022g0308 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1007-8265A>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55190009 | |||||||
chr2:55190084 | G | T | 1 | a0014c0022t0005g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1007-8340C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55190084 | |||||||
chr2:55190085 | C | T | 1 | a0014c0022t0005g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1007-8341G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55190085 | |||||||
chr2:55190106 | G | A | 2 | a0001c0002t0002g0300 a0001c0002t0002g0301 |
2 | HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1007-8362C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55190106 | |||||||
chr2:55190189 | C | T | 1 | a0002c0001t0005g0250 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1007-8445G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55190189 | |||||||
chr2:55190190 | G | A | 9 | a0001c0002t0002g0280 a0006c0008t0001g0023 a0006c0008t0001g0024 others(6): Show |
11 | NA18940.hp1 NA18944.hp1 NA18963.hp2 others(8): Show |
intron_variant | MODIFIER | c.1007-8446C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55190190 | |||||||
chr2:55190194 | A | G | 1 | a0013c0020t0005g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1007-8450T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55190194 | |||||||
chr2:55190218 | T | G | 1 | a0003c0003t0017g0146 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1007-8474A>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55190218 | |||||||
chr2:55190221 | A | AT | 89 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(86): Show |
102 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1007-8478dupA | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55190221 | |||||||
chr2:55190283 | G | A | 4 | a0001c0002t0002g0012 a0001c0002t0002g0312 a0001c0002t0002g0313 others(1): Show |
6 | HG01123.hp1 HG01358.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.1007-8539C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55190283 | |||||||
chr2:55190323 | A | T | 1 | a0001c0004t0006g0019 | 2 | NA18998.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1007-8579T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55190323 | |||||||
chr2:55190352 | T | G | 1 | a0001c0002t0002g0005 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1007-8608A>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55190352 | |||||||
chr2:55190469 | G | A | 1 | a0001c0004t0020g0317 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1007-8725C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55190469 | |||||||
chr2:55190652 | T | C | 12 | a0003c0003t0004g0016 a0003c0003t0004g0106 a0003c0003t0004g0113 others(9): Show |
13 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1007-8908A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55190652 | |||||||
chr2:55190674 | T | C | 4 | a0001c0002t0002g0297 a0001c0002t0003g0065 a0001c0002t0003g0067 others(1): Show |
4 | HG01243.hp2 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-8930A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55190674 | |||||||
chr2:55190722 | A | T | 61 | a0003c0003t0004g0016 a0003c0003t0004g0018 a0003c0003t0004g0047 others(58): Show |
64 | HG00099.hp2 HG01074.hp2 HG01106.hp1 others(61): Show |
intron_variant | MODIFIER | c.1007-8978T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55190722 | |||||||
chr2:55190771 | C | T | 3 | a0003c0003t0007g0130 a0003c0003t0007g0135 a0003c0003t0025g0125 |
3 | NA18992.hp2 NA18993.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1007-9027G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55190771 | |||||||
chr2:55190831 | T | G | 2 | a0002c0001t0001g0192 a0002c0001t0001g0199 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1007-9087A>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55190831 | |||||||
chr2:55190925 | A | G | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1007-9181T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55190925 | |||||||
chr2:55191088 | A | G | 1 | a0011c0026t0002g0281 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1007-9344T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55191088 | |||||||
chr2:55191102 | C | T | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1007-9358G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55191102 | |||||||
chr2:55191177 | C | A | 2 | a0001c0002t0002g0312 a0001c0002t0002g0313 |
2 | HG01928.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1007-9433G>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55191177 | |||||||
chr2:55191273 | T | C | 114 | a0001c0002t0002g0280 a0002c0001t0001g0004 a0002c0001t0001g0009 others(111): Show |
139 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1007-9529A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55191273 | |||||||
chr2:55191424 | C | T | 3 | a0002c0001t0012g0021 a0002c0001t0012g0155 a0002c0001t0028g0255 |
4 | HG02723.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-9680G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55191424 | |||||||
chr2:55191572 | C | T | 1 | a0002c0001t0001g0232 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1007-9828G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55191572 | |||||||
chr2:55191687 | C | T | 1 | a0013c0020t0005g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1007-9943G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55191687 | |||||||
chr2:55191799 | C | A | 305 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(302): Show |
380 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(377): Show |
intron_variant | MODIFIER | c.1007-10055G>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55191799 | |||||||
chr2:55191807 | A | G | 3 | a0003c0003t0004g0119 a0003c0003t0004g0138 a0003c0003t0004g0143 |
3 | HG02622.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1007-10063T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55191807 | |||||||
chr2:55191907 | A | C | 95 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(92): Show |
130 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1007-10163T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55191907 | |||||||
chr2:55192119 | C | CTGT | 30 | a0001c0005t0003g0002 a0001c0005t0003g0014 a0001c0005t0003g0015 others(27): Show |
42 | HG01070.hp2 HG01071.hp2 HG01261.hp2 others(39): Show |
intron_variant | MODIFIER | c.1007-10378_1007-10 others(9): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55192119 | |||||||
chr2:55192201 | C | A | 113 | a0001c0002t0002g0280 a0002c0001t0001g0004 a0002c0001t0001g0009 others(110): Show |
138 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.1007-10457G>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55192201 | |||||||
chr2:55192339 | C | T | 28 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(25): Show |
38 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1007-10595G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55192339 | |||||||
chr2:55192367 | A | T | 1 | a0004c0006t0009g0266 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1007-10623T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55192367 | |||||||
chr2:55192372 | G | A | 1 | a0002c0001t0001g0004 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1007-10628C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55192372 | |||||||
chr2:55192492 | T | C | 2 | a0001c0002t0021g0292 a0012c0024t0021g0290 |
2 | HG02083.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1007-10748A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55192492 | |||||||
chr2:55192558 | C | G | 114 | a0001c0002t0002g0280 a0002c0001t0001g0004 a0002c0001t0001g0009 others(111): Show |
139 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1007-10814G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55192558 | |||||||
chr2:55192618 | C | T | 1 | a0003c0003t0007g0123 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1007-10874G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55192618 | |||||||
chr2:55192643 | G | A | 1 | a0002c0001t0005g0033 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1007-10899C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55192643 | |||||||
chr2:55192766 | T | C | 2 | a0001c0004t0016g0087 a0001c0004t0016g0088 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1007-11022A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55192766 | |||||||
chr2:55192888 | C | CT | 11 | a0001c0002t0002g0274 a0001c0004t0006g0003 a0001c0004t0006g0085 others(8): Show |
12 | HG00738.hp1 HG01069.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1007-11145dupA | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55192888 | |||||||
chr2:55192888 | CT | C | 13 | a0001c0004t0006g0093 a0001c0004t0006g0095 a0002c0001t0001g0004 others(10): Show |
14 | HG00140.hp1 HG01070.hp1 HG02300.hp1 others(11): Show |
intron_variant | MODIFIER | c.1007-11145delA | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55192888 | |||||||
chr2:55192957 | A | C | 1 | a0003c0003t0004g0078 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1007-11213T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55192957 | |||||||
chr2:55192977 | G | A | 3 | a0001c0002t0002g0288 a0002c0001t0005g0020 a0002c0001t0005g0153 |
4 | HG00544.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007-11233C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55192977 | |||||||
chr2:55192986 | G | A | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1007-11242C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55192986 | |||||||
chr2:55192993 | C | T | 1 | a0002c0001t0001g0190 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1007-11249G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55192993 | |||||||
chr2:55193016 | G | A | 1 | a0003c0003t0004g0070 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1007-11272C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55193016 | |||||||
chr2:55193027 | A | T | 2 | a0001c0002t0002g0011 a0001c0002t0002g0276 |
2 | HG00673.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.1007-11283T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55193027 | |||||||
chr2:55193050 | CCGG | C | 92 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(89): Show |
106 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(103): Show |
intron_variant | MODIFIER | c.1007-11309_1007-11 others(9): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55193050 | |||||||
chr2:55193054 | C | T | 1 | a0002c0001t0001g0201 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1007-11310G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55193054 | |||||||
chr2:55193181 | C | T | 89 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(86): Show |
102 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1007-11437G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55193181 | |||||||
chr2:55193182 | G | A | 1 | a0002c0001t0001g0175 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1007-11438C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55193182 | |||||||
chr2:55193275 | G | T | 1 | a0002c0001t0001g0205 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1007-11531C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55193275 | |||||||
chr2:55193371 | G | GA | 3 | a0002c0001t0012g0021 a0002c0001t0012g0155 a0002c0001t0028g0255 |
4 | HG02723.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-11628dupT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55193371 | |||||||
chr2:55193560 | T | C | 1 | a0002c0001t0001g0208 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1007-11816A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55193560 | |||||||
chr2:55193585 | G | C | 1 | a0002c0001t0001g0191 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1007-11841C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55193585 | |||||||
chr2:55193688 | C | T | 1 | a0002c0013t0030g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1007-11944G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55193688 | |||||||
chr2:55193689 | G | A | 88 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(85): Show |
101 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(98): Show |
intron_variant | MODIFIER | c.1007-11945C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55193689 | |||||||
chr2:55193978 | T | G | 2 | a0003c0003t0004g0047 a0003c0003t0004g0048 |
2 | HG01243.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1007-12234A>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55193978 | |||||||
chr2:55194122 | G | C | 1 | a0003c0007t0003g0006 | 4 | NA18952.hp2 NA18979.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006+12148C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55194122 | |||||||
chr2:55194151 | C | G | 2 | a0003c0003t0017g0146 a0003c0003t0027g0129 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1006+12119G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55194151 | |||||||
chr2:55194183 | T | C | 3 | a0002c0001t0012g0021 a0002c0001t0012g0155 a0002c0001t0028g0255 |
4 | HG02723.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006+12087A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55194183 | |||||||
chr2:55194214 | T | A | 1 | a0002c0001t0001g0157 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1006+12056A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55194214 | |||||||
chr2:55194725 | AT | A | 4 | a0005c0009t0013g0322 a0005c0009t0013g0325 a0005c0009t0013g0326 others(1): Show |
4 | HG02132.hp2 NA18975.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006+11544delA | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55194725 | |||||||
chr2:55194814 | C | T | 1 | a0002c0001t0001g0256 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1006+11456G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55194814 | |||||||
chr2:55194877 | G | A | 124 | a0001c0002t0002g0280 a0002c0001t0001g0004 a0002c0001t0001g0009 others(121): Show |
151 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1006+11393C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55194877 | |||||||
chr2:55194933 | T | G | 1 | a0003c0007t0010g0223 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1006+11337A>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55194933 | |||||||
chr2:55194943 | G | C | 1 | a0004c0006t0008g0259 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1006+11327C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55194943 | |||||||
chr2:55194985 | T | C | 1 | a0002c0001t0001g0197 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1006+11285A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55194985 | |||||||
chr2:55195230 | C | T | 1 | a0014c0022t0005g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1006+11040G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55195230 | |||||||
chr2:55195318 | T | C | 92 | a0001c0002t0002g0280 a0002c0001t0001g0004 a0002c0001t0001g0009 others(89): Show |
113 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.1006+10952A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55195318 | |||||||
chr2:55195533 | G | A | 1 | a0003c0003t0007g0147 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1006+10737C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55195533 | |||||||
chr2:55195935 | G | A | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1006+10335C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55195935 | |||||||
chr2:55196061 | C | T | 2 | a0003c0003t0007g0108 a0003c0003t0007g0123 |
2 | HG02056.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.1006+10209G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55196061 | |||||||
chr2:55196093 | C | T | 1 | a0002c0001t0001g0202 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1006+10177G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55196093 | |||||||
chr2:55196173 | G | A | 7 | a0003c0003t0004g0018 a0003c0003t0004g0102 a0003c0003t0004g0139 others(4): Show |
8 | HG01074.hp2 HG01261.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.1006+10097C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55196173 | |||||||
chr2:55196207 | A | C | 1 | a0003c0003t0004g0122 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1006+10063T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55196207 | |||||||
chr2:55196507 | T | C | 1 | a0001c0002t0002g0319 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1006+9763A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55196507 | |||||||
chr2:55196719 | G | C | 63 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(60): Show |
86 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1006+9551C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55196719 | |||||||
chr2:55196962 | C | G | 1 | a0014c0022t0005g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1006+9308G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55196962 | |||||||
chr2:55197027 | T | C | 3 | a0003c0003t0007g0130 a0003c0003t0007g0135 a0003c0003t0025g0125 |
3 | NA18992.hp2 NA18993.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1006+9243A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55197027 | |||||||
chr2:55197075 | C | T | 3 | a0007c0011t0005g0041 a0007c0011t0005g0042 a0013c0020t0005g0043 |
3 | HG02109.hp2 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1006+9195G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55197075 | |||||||
chr2:55197093 | G | A | 63 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(60): Show |
86 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1006+9177C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55197093 | |||||||
chr2:55197098 | G | C | 1 | a0008c0025t0003g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1006+9172C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55197098 | |||||||
chr2:55197279 | T | C | 1 | a0002c0001t0001g0212 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1006+8991A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55197279 | |||||||
chr2:55197338 | C | T | 1 | a0002c0001t0001g0194 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1006+8932G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55197338 | |||||||
chr2:55197343 | A | C | 1 | a0003c0003t0023g0133 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1006+8927T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55197343 | |||||||
chr2:55197527 | C | T | 2 | a0002c0001t0001g0198 a0002c0001t0001g0216 |
2 | HG02738.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1006+8743G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55197527 | |||||||
chr2:55197733 | T | C | 98 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(95): Show |
114 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(111): Show |
intron_variant | MODIFIER | c.1006+8537A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55197733 | |||||||
chr2:55197859 | G | T | 1 | a0002c0001t0001g0193 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1006+8411C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55197859 | |||||||
chr2:55197951 | G | A | 1 | a0002c0013t0030g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1006+8319C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55197951 | |||||||
chr2:55198058 | C | G | 2 | a0002c0010t0014g0038 a0002c0010t0014g0275 |
3 | HG00642.hp1 HG01358.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1006+8212G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55198058 | |||||||
chr2:55198079 | G | T | 1 | a0014c0022t0005g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1006+8191C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55198079 | |||||||
chr2:55198088 | C | G | 1 | a0003c0003t0004g0102 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1006+8182G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55198088 | |||||||
chr2:55198139 | A | T | 2 | a0003c0003t0017g0146 a0003c0003t0027g0129 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1006+8131T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55198139 | |||||||
chr2:55198147 | T | G | 1 | a0005c0009t0013g0325 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1006+8123A>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55198147 | |||||||
chr2:55198230 | A | C | 1 | a0006c0008t0001g0174 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1006+8040T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55198230 | |||||||
chr2:55198390 | G | T | 118 | a0001c0004t0003g0233 a0002c0001t0001g0004 a0002c0001t0001g0009 others(115): Show |
144 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.1006+7880C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55198390 | |||||||
chr2:55198500 | G | A | 3 | a0007c0011t0005g0041 a0007c0011t0005g0042 a0013c0020t0005g0043 |
3 | HG02109.hp2 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1006+7770C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55198500 | |||||||
chr2:55198652 | A | G | 3 | a0007c0011t0005g0041 a0007c0011t0005g0042 a0013c0020t0005g0043 |
3 | HG02109.hp2 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1006+7618T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55198652 | |||||||
chr2:55198754 | C | G | 1 | a0002c0001t0001g0166 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1006+7516G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55198754 | |||||||
chr2:55198796 | C | T | 1 | a0002c0001t0001g0188 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1006+7474G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55198796 | |||||||
chr2:55198895 | A | G | 3 | a0007c0011t0005g0041 a0007c0011t0005g0042 a0013c0020t0005g0043 |
3 | HG02109.hp2 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1006+7375T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55198895 | |||||||
chr2:55198988 | T | C | 16 | a0001c0012t0003g0195 a0003c0003t0004g0018 a0003c0003t0004g0102 others(13): Show |
20 | HG01074.hp2 HG01261.hp1 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.1006+7282A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55198988 | |||||||
chr2:55199053 | T | C | 1 | a0002c0001t0001g0190 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1006+7217A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55199053 | |||||||
chr2:55199091 | G | C | 2 | a0002c0001t0001g0198 a0002c0001t0001g0216 |
2 | HG02738.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1006+7179C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55199091 | |||||||
chr2:55199239 | G | C | 1 | a0005c0009t0013g0325 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1006+7031C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55199239 | |||||||
chr2:55199296 | C | CA | 7 | a0002c0001t0001g0216 a0004c0006t0008g0260 a0004c0006t0008g0272 others(4): Show |
7 | HG00741.hp1 HG01123.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1006+6973dupT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55199296 | |||||||
chr2:55199296 | CA | C | 167 | a0001c0004t0003g0233 a0001c0004t0006g0003 a0001c0004t0006g0019 others(164): Show |
202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.1006+6973delT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55199296 | |||||||
chr2:55199296 | CAA | C | 94 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(91): Show |
127 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1006+6972_1006+697 others(6): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55199296 | |||||||
chr2:55199311 | A | G | 84 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(81): Show |
116 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1006+6959T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55199311 | |||||||
chr2:55199394 | A | C | 1 | a0006c0008t0001g0174 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1006+6876T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55199394 | |||||||
chr2:55199450 | T | G | 98 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(95): Show |
114 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(111): Show |
intron_variant | MODIFIER | c.1006+6820A>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55199450 | |||||||
chr2:55199464 | A | G | 1 | a0003c0003t0004g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1006+6806T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55199464 | |||||||
chr2:55199528 | G | C | 1 | a0002c0001t0001g0166 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1006+6742C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55199528 | |||||||
chr2:55199555 | T | C | 1 | a0003c0003t0023g0133 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1006+6715A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55199555 | |||||||
chr2:55199595 | A | C | 1 | a0006c0008t0001g0174 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1006+6675T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55199595 | |||||||
chr2:55199744 | C | T | 1 | a0001c0002t0002g0304 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1006+6526G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55199744 | |||||||
chr2:55199745 | T | C | 1 | a0001c0002t0002g0304 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1006+6525A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55199745 | |||||||
chr2:55200011 | C | A | 19 | a0002c0001t0001g0009 a0002c0001t0001g0027 a0002c0001t0001g0154 others(16): Show |
22 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.1006+6259G>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55200011 | |||||||
chr2:55200225 | T | TA | 103 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0011 others(100): Show |
130 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.1006+6044dupT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55200225 | |||||||
chr2:55200225 | T | TAA | 91 | a0001c0002t0002g0039 a0001c0002t0002g0279 a0001c0002t0002g0287 others(88): Show |
113 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.1006+6043_1006+604 others(6): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55200225 | |||||||
chr2:55200225 | T | TAAA | 6 | a0002c0001t0001g0165 a0002c0001t0001g0170 a0002c0001t0001g0191 others(3): Show |
7 | HG01516.hp2 HG01517.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1006+6042_1006+604 others(7): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55200225 | |||||||
chr2:55200225 | T | TAAAA | 62 | a0001c0004t0006g0095 a0001c0004t0020g0317 a0001c0012t0003g0195 others(59): Show |
67 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.1006+6041_1006+604 others(8): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55200225 | |||||||
chr2:55200225 | T | TAAAAA | 32 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(29): Show |
42 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1006+6040_1006+604 others(9): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55200225 | |||||||
chr2:55200261 | T | TAA | 97 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(94): Show |
113 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(110): Show |
intron_variant | MODIFIER | c.1006+6007_1006+600 others(6): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55200261 | |||||||
chr2:55200262 | A | T | 86 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(83): Show |
119 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1006+6008T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55200262 | |||||||
chr2:55200334 | C | T | 306 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(303): Show |
381 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(378): Show |
intron_variant | MODIFIER | c.1006+5936G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55200334 | |||||||
chr2:55200400 | A | G | 2 | a0004c0006t0008g0257 a0004c0006t0008g0258 |
2 | HG00423.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.1006+5870T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55200400 | |||||||
chr2:55200478 | T | C | 1 | a0002c0001t0001g0101 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1006+5792A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55200478 | |||||||
chr2:55200567 | A | C | 1 | a0006c0008t0001g0174 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1006+5703T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55200567 | |||||||
chr2:55200626 | G | C | 1 | a0002c0001t0001g0157 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1006+5644C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55200626 | |||||||
chr2:55200654 | C | T | 52 | a0003c0003t0004g0016 a0003c0003t0004g0069 a0003c0003t0004g0070 others(49): Show |
54 | HG00099.hp2 HG01106.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.1006+5616G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55200654 | |||||||
chr2:55200668 | T | C | 1 | a0003c0003t0007g0104 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1006+5602A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55200668 | |||||||
chr2:55200883 | G | T | 1 | a0001c0012t0003g0195 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1006+5387C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55200883 | |||||||
chr2:55201053 | T | C | 3 | a0007c0011t0005g0041 a0007c0011t0005g0042 a0013c0020t0005g0043 |
3 | HG02109.hp2 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1006+5217A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55201053 | |||||||
chr2:55201069 | C | T | 1 | a0002c0001t0005g0238 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1006+5201G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55201069 | |||||||
chr2:55201243 | TAA | T | 28 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(25): Show |
38 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1006+5025_1006+502 others(6): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55201243 | |||||||
chr2:55201367 | G | A | 2 | a0002c0001t0001g0192 a0002c0001t0001g0199 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1006+4903C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55201367 | |||||||
chr2:55201544 | A | T | 20 | a0001c0005t0003g0002 a0001c0005t0003g0014 a0001c0005t0003g0015 others(17): Show |
29 | HG01070.hp2 HG01071.hp2 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.1006+4726T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55201544 | |||||||
chr2:55201601 | T | C | 1 | a0004c0006t0008g0257 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1006+4669A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55201601 | |||||||
chr2:55201602 | A | G | 1 | a0008c0025t0003g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1006+4668T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55201602 | |||||||
chr2:55201804 | C | A | 2 | a0004c0006t0009g0261 a0004c0006t0009g0267 |
2 | NA18989.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1006+4466G>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55201804 | |||||||
chr2:55201878 | T | C | 9 | a0002c0001t0005g0238 a0002c0001t0005g0239 a0002c0001t0005g0240 others(6): Show |
10 | HG02109.hp2 HG02451.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1006+4392A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55201878 | |||||||
chr2:55201882 | T | A | 1 | a0001c0002t0022g0318 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1006+4388A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55201882 | |||||||
chr2:55201903 | G | C | 19 | a0002c0001t0001g0009 a0002c0001t0001g0027 a0002c0001t0001g0154 others(16): Show |
22 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.1006+4367C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55201903 | |||||||
chr2:55202188 | AG | A | 113 | a0001c0004t0003g0233 a0001c0012t0003g0195 a0002c0001t0001g0004 others(110): Show |
138 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.1006+4081delC | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55202188 | |||||||
chr2:55202224 | C | T | 2 | a0007c0011t0005g0041 a0007c0011t0005g0042 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1006+4046G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55202224 | |||||||
chr2:55202255 | G | GA | 100 | a0001c0004t0003g0233 a0001c0012t0003g0195 a0002c0001t0001g0004 others(97): Show |
125 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1006+4014dupT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55202255 | |||||||
chr2:55202255 | G | GAA | 9 | a0002c0001t0001g0200 a0002c0001t0001g0201 a0002c0001t0001g0202 others(6): Show |
9 | HG02040.hp1 HG02071.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1006+4013_1006+401 others(6): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55202255 | |||||||
chr2:55202277 | T | C | 1 | a0003c0003t0027g0129 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1006+3993A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55202277 | |||||||
chr2:55202459 | G | C | 1 | a0005c0009t0013g0325 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1006+3811C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55202459 | |||||||
chr2:55202493 | T | C | 2 | a0007c0011t0005g0041 a0007c0011t0005g0042 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1006+3777A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55202493 | |||||||
chr2:55202512 | C | T | 1 | a0003c0007t0003g0006 | 4 | NA18952.hp2 NA18979.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006+3758G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55202512 | |||||||
chr2:55202556 | C | CA | 10 | a0001c0012t0003g0195 a0002c0001t0005g0249 a0006c0008t0001g0023 others(7): Show |
12 | HG02647.hp1 NA18940.hp1 NA18944.hp1 others(9): Show |
intron_variant | MODIFIER | c.1006+3713dupT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55202556 | |||||||
chr2:55202697 | G | C | 3 | a0002c0001t0001g0010 a0002c0001t0001g0025 a0002c0001t0001g0157 |
6 | HG00609.hp2 HG00621.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.1006+3573C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55202697 | |||||||
chr2:55202880 | C | G | 1 | a0001c0004t0006g0152 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1006+3390G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55202880 | |||||||
chr2:55202897 | C | CA | 6 | a0002c0001t0001g0176 a0002c0001t0001g0198 a0002c0001t0001g0206 others(3): Show |
6 | HG01069.hp1 HG01891.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006+3372dupT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55202897 | |||||||
chr2:55202897 | CA | C | 104 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(101): Show |
123 | HG00099.hp2 HG00735.hp2 HG00738.hp1 others(120): Show |
intron_variant | MODIFIER | c.1006+3372delT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55202897 | |||||||
chr2:55202915 | A | C | 2 | a0003c0003t0007g0121 a0003c0003t0007g0126 |
2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1006+3355T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55202915 | |||||||
chr2:55202915 | A | T | 1 | a0001c0004t0006g0152 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1006+3355T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55202915 | |||||||
chr2:55202933 | C | G | 1 | a0011c0026t0002g0281 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1006+3337G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55202933 | |||||||
chr2:55202951 | T | C | 1 | a0001c0004t0003g0045 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1006+3319A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55202951 | |||||||
chr2:55203115 | G | C | 3 | a0002c0001t0012g0021 a0002c0001t0012g0155 a0002c0001t0028g0255 |
4 | HG02723.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006+3155C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55203115 | |||||||
chr2:55203579 | A | G | 1 | a0013c0020t0005g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1006+2691T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55203579 | |||||||
chr2:55204109 | A | G | 2 | a0001c0002t0002g0312 a0001c0002t0002g0313 |
2 | HG01928.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1006+2161T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55204109 | |||||||
chr2:55204151 | G | A | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1006+2119C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55204151 | |||||||
chr2:55204240 | C | T | 1 | a0001c0002t0002g0294 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1006+2030G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55204240 | |||||||
chr2:55204349 | G | A | 1 | a0003c0003t0007g0114 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1006+1921C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55204349 | |||||||
chr2:55204542 | C | T | 3 | a0002c0001t0001g0178 a0002c0001t0001g0179 a0002c0001t0001g0213 |
3 | NA18947.hp2 NA18983.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1006+1728G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55204542 | |||||||
chr2:55204603 | T | A | 4 | a0003c0003t0007g0017 a0003c0003t0007g0121 a0003c0003t0007g0126 others(1): Show |
5 | HG01346.hp2 HG02280.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+1667A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55204603 | |||||||
chr2:55204704 | T | C | 1 | a0014c0022t0005g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1006+1566A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55204704 | |||||||
chr2:55204838 | A | G | 2 | a0001c0005t0003g0014 a0001c0005t0003g0055 |
3 | NA18970.hp1 NA18975.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1006+1432T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55204838 | |||||||
chr2:55204887 | T | C | 8 | a0001c0002t0002g0008 a0001c0002t0002g0283 a0001c0002t0002g0285 others(5): Show |
11 | HG00544.hp1 HG00558.hp2 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.1006+1383A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55204887 | |||||||
chr2:55204986 | A | T | 1 | a0005c0009t0002g0323 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1006+1284T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55204986 | |||||||
chr2:55205200 | G | C | 64 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(61): Show |
87 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1006+1070C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55205200 | |||||||
chr2:55205400 | T | TAC | 200 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(197): Show |
258 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.1006+868_1006+869d others(4): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55205400 | |||||||
chr2:55205400 | T | TACAC | 5 | a0001c0002t0002g0283 a0001c0002t0002g0304 a0002c0001t0001g0026 others(2): Show |
6 | HG03130.hp2 NA18946.hp2 NA19009.hp1 others(3): Show |
intron_variant | MODIFIER | c.1006+866_1006+869d others(6): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55205400 | |||||||
chr2:55205423 | G | A | 1 | a0014c0022t0005g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1006+847C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55205423 | |||||||
chr2:55205437 | A | G | 3 | a0002c0001t0012g0021 a0002c0001t0012g0155 a0002c0001t0028g0255 |
4 | HG02723.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006+833T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55205437 | |||||||
chr2:55205497 | A | T | 3 | a0007c0011t0005g0041 a0007c0011t0005g0042 a0013c0020t0005g0043 |
3 | HG02109.hp2 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1006+773T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55205497 | |||||||
chr2:55205535 | G | A | 1 | a0002c0001t0005g0153 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1006+735C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55205535 | |||||||
chr2:55205773 | T | C | 1 | a0002c0001t0001g0159 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1006+497A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55205773 | |||||||
chr2:55205894 | C | CA | 138 | a0001c0002t0002g0039 a0001c0002t0002g0279 a0001c0002t0002g0297 others(135): Show |
167 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(164): Show |
intron_variant | MODIFIER | c.1006+375dupT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55205894 | |||||||
chr2:55205951 | T | C | 1 | a0010c0017t0001g0181 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1006+319A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55205951 | |||||||
chr2:55206170 | G | T | 2 | a0002c0001t0001g0185 a0002c0001t0001g0186 |
2 | HG00323.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.1006+100C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55206170 | |||||||
chr2:55206238 | T | C | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1006+32A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 9/12 | chr2 | 55206238 | |||||||
chr2:55206377 | C | CT | 3 | a0002c0001t0001g0178 a0002c0001t0001g0179 a0002c0001t0001g0213 |
3 | NA18947.hp2 NA18983.hp1 NA19074.hp1 |
splice_acceptor_variant&intron_variant | HIGH | c.900-2dupA | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55206377 | |||||||
chr2:55206475 | C | T | 1 | a0002c0001t0001g0185 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.900-99G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55206475 | |||||||
chr2:55206823 | T | TGGGCCGG others(50): Show |
1 | a0001c0002t0002g0274 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.900-504_900-448dup others(57): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55206823 | |||||||
chr2:55206840 | T | C | 94 | a0001c0004t0003g0233 a0001c0012t0003g0195 a0002c0001t0001g0004 others(91): Show |
115 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.900-464A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55206840 | |||||||
chr2:55206950 | C | CA | 74 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0012 others(71): Show |
102 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.900-575dupT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55206950 | |||||||
chr2:55206950 | C | CAA | 15 | a0001c0002t0002g0008 a0001c0002t0002g0011 a0001c0002t0002g0276 others(12): Show |
20 | HG00544.hp1 HG00558.hp2 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.900-576_900-575dup others(2): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55206950 | |||||||
chr2:55207014 | C | T | 1 | a0002c0001t0001g0200 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.900-638G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55207014 | |||||||
chr2:55207104 | G | C | 1 | a0001c0002t0022g0318 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.900-728C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55207104 | |||||||
chr2:55207199 | G | A | 1 | a0001c0005t0003g0060 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.900-823C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55207199 | |||||||
chr2:55207209 | C | T | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.900-833G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55207209 | |||||||
chr2:55207459 | C | G | 300 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(297): Show |
374 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(371): Show |
intron_variant | MODIFIER | c.900-1083G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55207459 | |||||||
chr2:55207763 | T | C | 1 | a0003c0003t0004g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.899+863A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55207763 | |||||||
chr2:55207798 | A | C | 1 | a0002c0001t0005g0244 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.899+828T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55207798 | |||||||
chr2:55207819 | G | A | 1 | a0014c0022t0005g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.899+807C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55207819 | |||||||
chr2:55207824 | A | C | 1 | a0003c0003t0004g0072 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.899+802T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55207824 | |||||||
chr2:55207921 | G | A | 306 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(303): Show |
381 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(378): Show |
intron_variant | MODIFIER | c.899+705C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55207921 | |||||||
chr2:55208028 | T | C | 70 | a0002c0001t0001g0101 a0003c0003t0004g0016 a0003c0003t0004g0018 others(67): Show |
76 | HG00099.hp2 HG01074.hp2 HG01106.hp1 others(73): Show |
intron_variant | MODIFIER | c.899+598A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55208028 | |||||||
chr2:55208048 | A | C | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.899+578T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55208048 | |||||||
chr2:55208259 | G | A | 1 | a0002c0001t0001g0215 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.899+367C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55208259 | |||||||
chr2:55208303 | C | T | 113 | a0001c0004t0003g0233 a0001c0012t0003g0195 a0002c0001t0001g0004 others(110): Show |
137 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.899+323G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55208303 | |||||||
chr2:55208305 | T | C | 2 | a0001c0002t0002g0300 a0001c0002t0002g0301 |
2 | HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.899+321A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55208305 | |||||||
chr2:55208319 | G | A | 1 | a0003c0003t0004g0078 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.899+307C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55208319 | |||||||
chr2:55208429 | A | C | 98 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(95): Show |
114 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(111): Show |
intron_variant | MODIFIER | c.899+197T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55208429 | |||||||
chr2:55208435 | C | T | 1 | a0003c0003t0004g0078 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.899+191G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 8/12 | chr2 | 55208435 | |||||||
chr2:55208865 | CT | C | 55 | a0001c0002t0002g0315 a0001c0002t0022g0308 a0001c0004t0006g0003 others(52): Show |
70 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.815-156delA | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 7/12 | chr2 | 55208865 | |||||||
chr2:55208865 | CTT | C | 189 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(186): Show |
246 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.815-157_815-156del others(2): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 7/12 | chr2 | 55208865 | |||||||
chr2:55208865 | CTTT | C | 6 | a0001c0002t0002g0274 a0001c0002t0002g0289 a0001c0002t0002g0312 others(3): Show |
6 | HG01943.hp1 HG03491.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.815-158_815-156del others(3): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 7/12 | chr2 | 55208865 | |||||||
chr2:55208866 | T | C | 52 | a0002c0001t0001g0101 a0003c0003t0004g0016 a0003c0003t0004g0069 others(49): Show |
54 | HG00099.hp2 HG01106.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.815-156A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 7/12 | chr2 | 55208866 | |||||||
chr2:55208867 | T | C | 17 | a0003c0003t0004g0018 a0003c0003t0004g0047 a0003c0003t0004g0048 others(14): Show |
21 | HG01074.hp2 HG01243.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.815-157A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 7/12 | chr2 | 55208867 | |||||||
chr2:55209031 | C | T | 1 | a0002c0001t0011g0183 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.815-321G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 7/12 | chr2 | 55209031 | |||||||
chr2:55209290 | C | G | 2 | a0001c0002t0002g0039 a0001c0002t0002g0279 |
3 | HG01167.hp1 HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.814+114G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 7/12 | chr2 | 55209290 | |||||||
chr2:55209351 | C | T | 2 | a0001c0002t0002g0300 a0001c0002t0002g0301 |
2 | HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.814+53G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 7/12 | chr2 | 55209351 | |||||||
chr2:55209352 | GA | G | 100 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(97): Show |
117 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(114): Show |
intron_variant | MODIFIER | c.814+51delT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 7/12 | chr2 | 55209352 | |||||||
chr2:55209859 | C | T | 1 | a0001c0002t0002g0285 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.500-28G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55209859 | |||||||
chr2:55209860 | G | A | 21 | a0002c0001t0005g0032 a0002c0001t0005g0033 a0002c0001t0005g0034 others(18): Show |
25 | HG00738.hp2 HG01255.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.500-29C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55209860 | |||||||
chr2:55209878 | C | T | 27 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(24): Show |
37 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.500-47G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55209878 | |||||||
chr2:55209879 | G | A | 1 | a0002c0001t0001g0207 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.500-48C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55209879 | |||||||
chr2:55209879 | G | T | 1 | a0002c0001t0001g0176 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.500-48C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55209879 | |||||||
chr2:55210020 | T | C | 9 | a0005c0009t0002g0013 a0005c0009t0002g0305 a0005c0009t0002g0320 others(6): Show |
11 | HG00140.hp2 HG01192.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.500-189A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55210020 | |||||||
chr2:55210097 | C | T | 1 | a0013c0020t0005g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.500-266G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55210097 | |||||||
chr2:55210206 | A | T | 1 | a0001c0005t0003g0056 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.500-375T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55210206 | |||||||
chr2:55210215 | G | C | 5 | a0001c0004t0006g0007 a0001c0004t0006g0079 a0001c0004t0006g0094 others(2): Show |
8 | HG01070.hp1 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.500-384C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55210215 | |||||||
chr2:55210231 | C | G | 2 | a0003c0003t0017g0146 a0003c0003t0027g0129 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.500-400G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55210231 | |||||||
chr2:55210241 | G | C | 4 | a0001c0004t0020g0317 a0007c0011t0005g0041 a0007c0011t0005g0042 others(1): Show |
4 | HG02109.hp2 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.500-410C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55210241 | |||||||
chr2:55210326 | G | C | 2 | a0001c0002t0002g0039 a0001c0002t0002g0279 |
3 | HG01167.hp1 HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.500-495C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55210326 | |||||||
chr2:55210523 | A | G | 1 | a0001c0005t0003g0055 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.500-692T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55210523 | |||||||
chr2:55210575 | A | T | 22 | a0002c0001t0005g0032 a0002c0001t0005g0033 a0002c0001t0005g0034 others(19): Show |
26 | HG00738.hp2 HG01255.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.500-744T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55210575 | |||||||
chr2:55210637 | G | A | 1 | a0001c0005t0003g0015 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.500-806C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55210637 | |||||||
chr2:55210763 | C | G | 1 | a0002c0001t0001g0241 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.500-932G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55210763 | |||||||
chr2:55210834 | C | T | 1 | a0001c0004t0020g0317 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.500-1003G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55210834 | |||||||
chr2:55210869 | G | T | 201 | a0001c0002t0002g0291 a0001c0002t0002g0312 a0001c0002t0002g0313 others(198): Show |
247 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.500-1038C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55210869 | |||||||
chr2:55210871 | G | T | 29 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(26): Show |
40 | HG00408.hp1 HG00735.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.500-1040C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55210871 | |||||||
chr2:55210873 | G | T | 9 | a0001c0004t0006g0007 a0001c0004t0006g0079 a0001c0004t0006g0092 others(6): Show |
12 | HG01070.hp1 HG01257.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.500-1042C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55210873 | |||||||
chr2:55210972 | G | C | 27 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(24): Show |
37 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.500-1141C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55210972 | |||||||
chr2:55211025 | T | C | 3 | a0002c0001t0005g0251 a0003c0003t0017g0146 a0003c0003t0027g0129 |
3 | HG01884.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.500-1194A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55211025 | |||||||
chr2:55211077 | C | T | 1 | a0001c0004t0020g0317 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.500-1246G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55211077 | |||||||
chr2:55211078 | A | G | 1 | a0003c0003t0007g0148 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.500-1247T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55211078 | |||||||
chr2:55211091 | A | G | 302 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(299): Show |
377 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(374): Show |
intron_variant | MODIFIER | c.500-1260T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55211091 | |||||||
chr2:55211178 | C | T | 306 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(303): Show |
381 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(378): Show |
intron_variant | MODIFIER | c.500-1347G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55211178 | |||||||
chr2:55211212 | T | C | 4 | a0001c0002t0002g0288 a0002c0001t0001g0217 a0002c0001t0001g0218 others(1): Show |
4 | HG00544.hp1 NA18970.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.500-1381A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55211212 | |||||||
chr2:55211328 | C | T | 2 | a0001c0002t0002g0300 a0001c0002t0002g0301 |
2 | HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.499+1345G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55211328 | |||||||
chr2:55211362 | C | A | 1 | a0001c0004t0015g0091 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.499+1311G>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55211362 | |||||||
chr2:55211437 | G | C | 98 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(95): Show |
114 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(111): Show |
intron_variant | MODIFIER | c.499+1236C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55211437 | |||||||
chr2:55211489 | G | C | 1 | a0005c0009t0013g0325 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.499+1184C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55211489 | |||||||
chr2:55211502 | C | CA | 8 | a0001c0002t0002g0297 a0001c0004t0006g0076 a0001c0004t0006g0085 others(5): Show |
8 | HG00735.hp2 HG00738.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.499+1170dupT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55211502 | |||||||
chr2:55211502 | CA | C | 179 | a0001c0002t0002g0286 a0001c0004t0003g0225 a0001c0004t0003g0233 others(176): Show |
211 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.499+1170delT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55211502 | |||||||
chr2:55211594 | T | C | 1 | a0002c0013t0030g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.499+1079A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55211594 | |||||||
chr2:55211764 | T | A | 1 | a0001c0002t0002g0316 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.499+909A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55211764 | |||||||
chr2:55211915 | C | G | 2 | a0002c0010t0014g0038 a0002c0010t0014g0275 |
3 | HG00642.hp1 HG01358.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.499+758G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55211915 | |||||||
chr2:55211996 | G | C | 1 | a0003c0003t0004g0115 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.499+677C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55211996 | |||||||
chr2:55212071 | G | C | 1 | a0004c0006t0008g0150 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.499+602C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55212071 | |||||||
chr2:55212077 | G | C | 1 | a0002c0001t0005g0250 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.499+596C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55212077 | |||||||
chr2:55212155 | T | C | 91 | a0001c0005t0003g0002 a0001c0005t0003g0014 a0001c0005t0003g0015 others(88): Show |
106 | HG00099.hp2 HG01070.hp2 HG01071.hp2 others(103): Show |
intron_variant | MODIFIER | c.499+518A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55212155 | |||||||
chr2:55212348 | G | C | 3 | a0002c0001t0012g0021 a0002c0001t0012g0155 a0002c0001t0028g0255 |
4 | HG02723.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.499+325C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55212348 | |||||||
chr2:55212368 | C | A | 1 | a0002c0001t0005g0250 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.499+305G>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55212368 | |||||||
chr2:55212452 | T | A | 1 | a0001c0002t0002g0298 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.499+221A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55212452 | |||||||
chr2:55212503 | C | A | 1 | a0003c0007t0003g0006 | 4 | NA18952.hp2 NA18979.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+170G>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55212503 | |||||||
chr2:55212531 | C | G | 307 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(304): Show |
382 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(379): Show |
intron_variant | MODIFIER | c.499+142G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55212531 | |||||||
chr2:55212569 | G | A | 20 | a0002c0001t0005g0032 a0002c0001t0005g0033 a0002c0001t0005g0034 others(17): Show |
24 | HG00738.hp2 HG01255.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.499+104C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55212569 | |||||||
chr2:55212649 | A | T | 1 | a0002c0001t0001g0101 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.499+24T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 5/12 | chr2 | 55212649 | |||||||
chr2:55212827 | C | A | 306 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(303): Show |
381 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(378): Show |
intron_variant | MODIFIER | c.366-21G>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55212827 | |||||||
chr2:55212850 | T | C | 1 | a0002c0001t0001g0209 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.366-44A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55212850 | |||||||
chr2:55213605 | AC | A | 122 | a0001c0004t0003g0233 a0001c0004t0020g0317 a0001c0012t0003g0195 others(119): Show |
148 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.366-800delG | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55213605 | |||||||
chr2:55213654 | A | T | 7 | a0002c0001t0001g0156 a0002c0001t0001g0177 a0002c0001t0001g0178 others(4): Show |
7 | HG01975.hp2 HG01978.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.366-848T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55213654 | |||||||
chr2:55213880 | G | A | 1 | a0003c0003t0023g0133 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.366-1074C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55213880 | |||||||
chr2:55213968 | C | G | 1 | a0011c0026t0002g0281 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.366-1162G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55213968 | |||||||
chr2:55214242 | G | A | 92 | a0001c0004t0003g0233 a0001c0012t0003g0195 a0002c0001t0001g0004 others(89): Show |
113 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.366-1436C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55214242 | |||||||
chr2:55214327 | G | C | 4 | a0001c0002t0002g0304 a0001c0004t0006g0089 a0001c0004t0015g0090 others(1): Show |
4 | NA18979.hp1 NA18982.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-1521C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55214327 | |||||||
chr2:55214362 | G | T | 1 | a0002c0001t0001g0175 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.366-1556C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55214362 | |||||||
chr2:55214429 | G | A | 185 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(182): Show |
234 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.366-1623C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55214429 | |||||||
chr2:55214448 | C | T | 1 | a0002c0001t0001g0177 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.366-1642G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55214448 | |||||||
chr2:55215162 | G | T | 3 | a0002c0001t0012g0021 a0002c0001t0012g0155 a0002c0001t0028g0255 |
4 | HG02723.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-2356C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55215162 | |||||||
chr2:55215254 | A | G | 83 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(80): Show |
116 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.366-2448T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55215254 | |||||||
chr2:55215285 | T | C | 2 | a0003c0003t0017g0146 a0003c0003t0027g0129 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.366-2479A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55215285 | |||||||
chr2:55215582 | C | T | 1 | a0004c0006t0008g0150 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.365+2229G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55215582 | |||||||
chr2:55215772 | G | A | 19 | a0002c0001t0001g0241 a0002c0001t0001g0242 a0002c0001t0005g0032 others(16): Show |
23 | HG00738.hp2 HG01255.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.365+2039C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55215772 | |||||||
chr2:55215815 | G | T | 1 | a0003c0003t0004g0106 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.365+1996C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55215815 | |||||||
chr2:55215859 | A | G | 1 | a0004c0006t0008g0272 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.365+1952T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55215859 | |||||||
chr2:55216022 | T | C | 306 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(303): Show |
381 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(378): Show |
intron_variant | MODIFIER | c.365+1789A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55216022 | |||||||
chr2:55216040 | C | T | 1 | a0003c0003t0004g0071 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.365+1771G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55216040 | |||||||
chr2:55216090 | C | A | 3 | a0007c0011t0005g0041 a0007c0011t0005g0042 a0013c0020t0005g0043 |
3 | HG02109.hp2 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.365+1721G>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55216090 | |||||||
chr2:55216112 | TA | T | 89 | a0001c0002t0002g0307 a0001c0002t0002g0315 a0001c0004t0003g0233 others(86): Show |
109 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.365+1698delT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55216112 | |||||||
chr2:55216112 | TAA | T | 208 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(205): Show |
262 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.365+1697_365+1698d others(4): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55216112 | |||||||
chr2:55216112 | TAAA | T | 6 | a0001c0002t0002g0289 a0001c0005t0003g0053 a0002c0001t0005g0035 others(3): Show |
7 | HG01255.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.365+1696_365+1698d others(5): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55216112 | |||||||
chr2:55216291 | C | CA | 8 | a0001c0002t0002g0299 a0002c0001t0005g0100 a0003c0003t0004g0116 others(5): Show |
8 | HG01109.hp2 HG03098.hp2 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.365+1519dupT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55216291 | |||||||
chr2:55216375 | C | G | 1 | a0003c0003t0004g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.365+1436G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55216375 | |||||||
chr2:55216451 | T | C | 2 | a0001c0002t0002g0300 a0001c0002t0002g0301 |
2 | HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.365+1360A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55216451 | |||||||
chr2:55216456 | A | G | 113 | a0001c0004t0003g0233 a0001c0004t0020g0317 a0001c0012t0003g0195 others(110): Show |
137 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.365+1355T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55216456 | |||||||
chr2:55216510 | C | T | 1 | a0001c0002t0003g0066 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.365+1301G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55216510 | |||||||
chr2:55216596 | C | T | 3 | a0007c0011t0005g0041 a0007c0011t0005g0042 a0013c0020t0005g0043 |
3 | HG02109.hp2 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.365+1215G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55216596 | |||||||
chr2:55216697 | C | CT | 83 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(80): Show |
116 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.365+1113dupA | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55216697 | |||||||
chr2:55216832 | A | G | 7 | a0001c0002t0002g0008 a0001c0002t0002g0283 a0001c0002t0002g0285 others(4): Show |
10 | HG00544.hp1 HG00558.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+979T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55216832 | |||||||
chr2:55216920 | T | C | 7 | a0001c0004t0020g0317 a0002c0001t0012g0021 a0002c0001t0012g0155 others(4): Show |
8 | HG02109.hp2 HG02451.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.365+891A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55216920 | |||||||
chr2:55216939 | C | A | 1 | a0002c0001t0018g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.365+872G>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55216939 | |||||||
chr2:55217063 | C | G | 1 | a0001c0002t0002g0285 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.365+748G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217063 | |||||||
chr2:55217270 | C | T | 2 | a0007c0011t0005g0041 a0007c0011t0005g0042 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.365+541G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217270 | |||||||
chr2:55217418 | G | A | 1 | a0001c0002t0002g0302 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.365+393C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217418 | |||||||
chr2:55217523 | C | CA | 8 | a0001c0004t0003g0225 a0003c0003t0004g0141 a0003c0003t0004g0142 others(5): Show |
8 | HG00609.hp1 HG01981.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.365+287dupT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217523 | |||||||
chr2:55217523 | C | CAAA | 17 | a0001c0004t0003g0045 a0002c0001t0001g0101 a0003c0003t0004g0077 others(14): Show |
18 | HG01109.hp2 HG01256.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.365+285_365+287dup others(3): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217523 | |||||||
chr2:55217523 | C | CAAAA | 14 | a0003c0003t0004g0078 a0003c0003t0004g0136 a0003c0003t0004g0143 others(11): Show |
14 | HG01884.hp1 HG02056.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.365+284_365+287dup others(4): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217523 | |||||||
chr2:55217542 | AAAAAAAA others(9): Show |
A | 1 | a0002c0001t0001g0212 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.365+253_365+268del others(16): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217542 | |||||||
chr2:55217542 | AAAAAAAA others(11): Show |
A | 1 | a0013c0020t0005g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.365+251_365+268del others(18): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217542 | |||||||
chr2:55217542 | AAAAAAAA others(13): Show |
A | 1 | a0007c0011t0005g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.365+249_365+268del others(20): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217542 | |||||||
chr2:55217542 | AAAAAAAA others(15): Show |
A | 1 | a0007c0011t0005g0042 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.365+247_365+268del others(22): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217542 | |||||||
chr2:55217545 | AAAAAAAA others(4): Show |
A | 1 | a0003c0003t0004g0016 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.365+255_365+265del others(11): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217545 | |||||||
chr2:55217545 | AAAAAAAA others(6): Show |
A | 1 | a0003c0003t0004g0106 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.365+253_365+265del others(13): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217545 | |||||||
chr2:55217545 | AAAAAAAA others(16): Show |
A | 1 | a0002c0001t0012g0155 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.365+243_365+265del others(23): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217545 | |||||||
chr2:55217546 | A | ATATATAT others(6): Show |
1 | a0001c0002t0002g0314 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.365+264_365+265ins others(13): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217546 | |||||||
chr2:55217546 | AAAAAAAA others(3): Show |
A | 1 | a0001c0002t0022g0318 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.365+255_365+264del others(10): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217546 | |||||||
chr2:55217546 | AAAAAAAA others(5): Show |
A | 3 | a0001c0002t0002g0280 a0001c0002t0002g0282 a0002c0001t0005g0245 |
3 | HG01255.hp1 HG02965.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.365+253_365+264del others(12): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217546 | |||||||
chr2:55217546 | AAAAAAAA others(15): Show |
A | 2 | a0002c0001t0012g0021 a0002c0001t0028g0255 |
3 | HG02723.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.365+243_365+264del others(22): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217546 | |||||||
chr2:55217547 | AAAAAAAT | A | 14 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(11): Show |
21 | HG00544.hp2 HG01358.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.365+257_365+263del others(7): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217547 | |||||||
chr2:55217547 | AAAAAAAT others(4): Show |
A | 5 | a0001c0002t0002g0284 a0001c0002t0002g0311 a0001c0002t0003g0066 others(2): Show |
7 | HG00323.hp1 HG00642.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.365+253_365+263del others(11): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217547 | |||||||
chr2:55217547 | AAAAAAAT others(16): Show |
A | 1 | a0001c0004t0020g0317 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.365+241_365+263del others(23): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217547 | |||||||
chr2:55217548 | A | AATATATA others(7): Show |
1 | a0001c0005t0003g0002 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.365+262_365+263ins others(14): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217548 | |||||||
chr2:55217548 | A | T | 2 | a0001c0002t0002g0011 a0001c0002t0002g0314 |
2 | HG00558.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.365+263T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217548 | |||||||
chr2:55217548 | AAAAAATA others(3): Show |
A | 1 | a0001c0002t0002g0005 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.365+253_365+262del others(10): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217548 | |||||||
chr2:55217548 | AAAAAATA others(5): Show |
A | 5 | a0001c0002t0002g0279 a0001c0002t0002g0300 a0001c0002t0002g0301 others(2): Show |
5 | HG01167.hp1 HG01891.hp2 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.365+251_365+262del others(12): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217548 | |||||||
chr2:55217549 | AAAAATAT | A | 6 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0012 others(3): Show |
8 | HG00408.hp2 HG01123.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.365+255_365+261del others(7): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217549 | |||||||
chr2:55217549 | AAAAATAT others(4): Show |
A | 9 | a0001c0002t0003g0065 a0001c0002t0003g0067 a0001c0002t0003g0068 others(6): Show |
9 | HG01891.hp1 HG02145.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.365+251_365+261del others(11): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217549 | |||||||
chr2:55217549 | AAAAATAT others(6): Show |
A | 1 | a0001c0002t0002g0039 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.365+249_365+261del others(13): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217549 | |||||||
chr2:55217550 | A | AT | 4 | a0004c0006t0008g0036 a0004c0006t0008g0259 a0004c0006t0008g0260 others(1): Show |
5 | HG00099.hp1 HG00741.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.365+260_365+261ins others(1): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217550 | |||||||
chr2:55217550 | A | ATATATAT others(4): Show |
2 | a0002c0001t0001g0216 a0002c0010t0014g0275 |
2 | HG01358.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.365+260_365+261ins others(11): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217550 | |||||||
chr2:55217550 | A | T | 8 | a0001c0002t0002g0008 a0001c0002t0002g0011 a0001c0002t0002g0287 others(5): Show |
9 | HG00558.hp2 HG02071.hp1 NA18984.hp2 others(6): Show |
intron_variant | MODIFIER | c.365+261T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217550 | |||||||
chr2:55217550 | AAAATATA others(3): Show |
A | 6 | a0001c0002t0002g0297 a0002c0001t0001g0241 a0002c0001t0005g0238 others(3): Show |
6 | HG01243.hp2 HG02886.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.365+251_365+260del others(10): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217550 | |||||||
chr2:55217550 | AAAATATA others(5): Show |
A | 5 | a0001c0002t0002g0039 a0002c0001t0005g0035 a0002c0001t0005g0236 others(2): Show |
5 | HG01255.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.365+249_365+260del others(12): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217550 | |||||||
chr2:55217550 | AAAATATA others(9): Show |
A | 5 | a0001c0004t0006g0083 a0001c0004t0006g0084 a0001c0004t0016g0087 others(2): Show |
5 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.365+245_365+260del others(16): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217550 | |||||||
chr2:55217551 | AAATATAT others(4): Show |
A | 13 | a0002c0001t0005g0032 a0002c0001t0005g0033 a0002c0001t0005g0034 others(10): Show |
16 | HG00738.hp2 HG02109.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.365+249_365+259del others(11): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217551 | |||||||
chr2:55217551 | AAATATAT others(8): Show |
A | 2 | a0001c0004t0006g0003 a0001c0004t0006g0076 |
2 | HG01175.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.365+245_365+259del others(15): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217551 | |||||||
chr2:55217551 | AAATATAT others(10): Show |
A | 1 | a0001c0004t0006g0003 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.365+243_365+259del others(17): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217551 | |||||||
chr2:55217552 | A | AAAAAAAA others(12): Show |
1 | a0001c0005t0003g0055 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.365+258_365+259ins others(19): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | A | AAAAAAAT others(18): Show |
1 | a0002c0001t0005g0020 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.365+258_365+259ins others(25): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | A | AAAAAATA others(3): Show |
1 | a0003c0003t0004g0107 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.365+258_365+259ins others(10): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | A | AAAAAATA others(11): Show |
1 | a0001c0005t0003g0050 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.365+258_365+259ins others(18): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | A | AAAAAATA others(13): Show |
1 | a0001c0005t0003g0052 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.365+258_365+259ins others(20): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | A | AAAAATAT others(6): Show |
1 | a0001c0005t0003g0002 | 2 | NA18954.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.365+258_365+259ins others(13): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | A | AAAAATAT others(12): Show |
1 | a0001c0005t0003g0002 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.365+258_365+259ins others(19): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | A | AAAATATA others(7): Show |
1 | a0001c0005t0003g0056 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.365+258_365+259ins others(14): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | A | AAAATATA others(9): Show |
3 | a0001c0005t0003g0054 a0001c0005t0003g0063 a0001c0027t0003g0059 |
3 | HG01261.hp2 HG01515.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.365+258_365+259ins others(16): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | A | AAAATATA others(13): Show |
2 | a0001c0005t0003g0014 a0001c0005t0003g0062 |
2 | NA18970.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.365+258_365+259ins others(20): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | A | AAATATAT others(10): Show |
1 | a0003c0003t0017g0075 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.365+258_365+259ins others(17): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | A | AAATATAT others(16): Show |
1 | a0001c0005t0003g0015 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.365+258_365+259ins others(23): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | A | AATACATA others(9): Show |
1 | a0003c0003t0004g0069 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.365+258_365+259ins others(16): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | A | AATATATA others(5): Show |
1 | a0001c0005t0003g0002 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.365+247_365+258dup others(12): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | A | AATATATA others(7): Show |
4 | a0001c0005t0003g0049 a0001c0005t0003g0064 a0002c0001t0005g0020 others(1): Show |
4 | NA18966.hp1 NA18969.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.365+245_365+258dup others(14): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | A | AATATATA others(9): Show |
2 | a0001c0005t0003g0002 a0001c0005t0003g0014 |
2 | NA18949.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.365+243_365+258dup others(16): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | A | AATATATA others(11): Show |
1 | a0001c0005t0003g0002 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.365+241_365+258dup others(18): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | A | AATATATA others(15): Show |
1 | a0002c0001t0005g0153 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.365+237_365+258dup others(22): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | A | AATATATA others(17): Show |
1 | a0001c0005t0003g0015 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.365+235_365+258dup others(24): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | A | ATAT | 5 | a0004c0006t0009g0037 a0004c0006t0009g0264 a0004c0006t0009g0265 others(2): Show |
6 | NA18951.hp2 NA18971.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.365+258_365+259ins others(3): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | A | ATATATAT others(8): Show |
1 | a0001c0005t0003g0053 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.365+258_365+259ins others(15): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | A | T | 24 | a0001c0002t0002g0008 a0001c0002t0002g0011 a0001c0002t0002g0283 others(21): Show |
26 | HG00099.hp1 HG00558.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.365+259T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | AAT | A | 7 | a0002c0001t0001g0004 a0002c0001t0001g0187 a0002c0001t0001g0211 others(4): Show |
9 | HG00735.hp1 HG01074.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.365+257_365+258del others(2): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | AATAT | A | 11 | a0001c0012t0003g0195 a0002c0001t0001g0010 a0002c0001t0001g0026 others(8): Show |
11 | HG00621.hp1 HG02165.hp1 HG04115.hp1 others(8): Show |
intron_variant | MODIFIER | c.365+255_365+258del others(4): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | AATATAT | A | 25 | a0002c0001t0001g0004 a0002c0001t0001g0009 a0002c0001t0001g0027 others(22): Show |
29 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.365+253_365+258del others(6): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | AATATATA others(3): Show |
A | 2 | a0002c0001t0005g0253 a0005c0009t0013g0326 |
2 | HG03516.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.365+249_365+258del others(10): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | AATATATA others(7): Show |
A | 8 | a0001c0004t0006g0007 a0001c0004t0006g0079 a0001c0004t0006g0093 others(5): Show |
10 | HG01070.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.365+245_365+258del others(14): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217552 | AATATATA others(9): Show |
A | 12 | a0001c0004t0006g0003 a0001c0004t0006g0019 a0001c0004t0006g0080 others(9): Show |
16 | HG00735.hp2 HG00738.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.365+243_365+258del others(16): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217552 | |||||||
chr2:55217553 | AT | A | 7 | a0002c0001t0001g0028 a0002c0001t0001g0184 a0002c0001t0001g0190 others(4): Show |
8 | HG01106.hp2 HG01109.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.365+257delA | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217553 | |||||||
chr2:55217553 | ATAT | A | 19 | a0002c0001t0001g0004 a0002c0001t0001g0010 a0002c0001t0001g0022 others(16): Show |
20 | HG01975.hp2 HG01978.hp1 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.365+255_365+257del others(3): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217553 | |||||||
chr2:55217553 | ATATAT | A | 11 | a0002c0001t0001g0026 a0002c0001t0001g0031 a0002c0001t0001g0163 others(8): Show |
12 | HG00621.hp2 HG01192.hp1 HG03239.hp2 others(9): Show |
intron_variant | MODIFIER | c.365+253_365+257del others(5): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217553 | |||||||
chr2:55217553 | ATATATAT others(4): Show |
A | 1 | a0002c0001t0005g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.365+247_365+257del others(11): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217553 | |||||||
chr2:55217553 | ATATATAT others(6): Show |
A | 1 | a0001c0004t0006g0092 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.365+245_365+257del others(13): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217553 | |||||||
chr2:55217553 | ATATATAT others(8): Show |
A | 2 | a0001c0004t0006g0007 a0001c0004t0026g0082 |
2 | HG02148.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.365+243_365+257del others(15): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217553 | |||||||
chr2:55217554 | T | A | 44 | a0001c0004t0003g0045 a0001c0004t0003g0225 a0002c0001t0001g0010 others(41): Show |
44 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.365+257A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217554 | |||||||
chr2:55217556 | T | A | 26 | a0001c0004t0003g0045 a0001c0004t0003g0225 a0002c0001t0001g0004 others(23): Show |
28 | HG00609.hp1 HG00735.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.365+255A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217556 | |||||||
chr2:55217558 | T | A | 12 | a0001c0004t0003g0045 a0001c0012t0003g0195 a0002c0001t0001g0004 others(9): Show |
15 | HG00621.hp1 HG03540.hp2 NA18940.hp1 others(12): Show |
intron_variant | MODIFIER | c.365+253A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217558 | |||||||
chr2:55217560 | T | A | 11 | a0002c0001t0001g0004 a0002c0001t0001g0026 a0002c0001t0001g0163 others(8): Show |
12 | HG00408.hp1 HG00741.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.365+251A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217560 | |||||||
chr2:55217562 | T | A | 1 | a0002c0001t0001g0175 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.365+249A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217562 | |||||||
chr2:55217563 | A | G | 4 | a0004c0006t0008g0036 a0004c0006t0008g0259 a0004c0006t0008g0260 others(1): Show |
5 | HG00099.hp1 HG00741.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.365+248T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217563 | |||||||
chr2:55217568 | T | A | 6 | a0001c0004t0006g0079 a0001c0004t0006g0092 a0001c0004t0006g0093 others(3): Show |
6 | HG01070.hp1 HG01496.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.365+243A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217568 | |||||||
chr2:55217584 | T | C | 2 | a0002c0013t0030g0235 a0003c0003t0004g0137 |
2 | HG01884.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.365+227A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217584 | |||||||
chr2:55217584 | T | TATATATA others(7): Show |
1 | a0001c0005t0003g0061 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.365+226_365+227ins others(14): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217584 | |||||||
chr2:55217584 | T | TATATATA others(11): Show |
1 | a0001c0005t0003g0060 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.365+226_365+227ins others(18): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217584 | |||||||
chr2:55217603 | C | T | 223 | a0001c0004t0003g0045 a0001c0004t0003g0225 a0001c0004t0003g0233 others(220): Show |
265 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.365+208G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217603 | |||||||
chr2:55217650 | A | G | 1 | a0001c0004t0006g0080 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.365+161T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217650 | |||||||
chr2:55217660 | C | G | 2 | a0007c0011t0005g0041 a0007c0011t0005g0042 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.365+151G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217660 | |||||||
chr2:55217722 | A | C | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.365+89T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217722 | |||||||
chr2:55217769 | G | A | 3 | a0007c0011t0005g0041 a0007c0011t0005g0042 a0013c0020t0005g0043 |
3 | HG02109.hp2 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.365+42C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 4/12 | chr2 | 55217769 | |||||||
chr2:55218051 | G | A | 1 | a0014c0022t0005g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178-53C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55218051 | |||||||
chr2:55218124 | C | T | 1 | a0003c0003t0007g0105 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.178-126G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55218124 | |||||||
chr2:55218175 | C | T | 101 | a0001c0004t0003g0045 a0001c0004t0003g0225 a0001c0004t0006g0003 others(98): Show |
117 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(114): Show |
intron_variant | MODIFIER | c.178-177G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55218175 | |||||||
chr2:55218382 | C | T | 300 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(297): Show |
374 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(371): Show |
intron_variant | MODIFIER | c.178-384G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55218382 | |||||||
chr2:55218592 | G | A | 1 | a0001c0004t0020g0317 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.178-594C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55218592 | |||||||
chr2:55218667 | C | G | 1 | a0003c0003t0033g0327 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.178-669G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55218667 | |||||||
chr2:55219220 | A | G | 191 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(188): Show |
242 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.178-1222T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55219220 | |||||||
chr2:55219467 | A | G | 1 | a0006c0008t0001g0174 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.178-1469T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55219467 | |||||||
chr2:55219487 | C | G | 1 | a0003c0003t0004g0069 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.178-1489G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55219487 | |||||||
chr2:55219643 | C | T | 1 | a0014c0022t0005g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178-1645G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55219643 | |||||||
chr2:55219764 | G | A | 7 | a0003c0003t0004g0018 a0003c0003t0004g0102 a0003c0003t0004g0139 others(4): Show |
8 | HG01074.hp2 HG01261.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.178-1766C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55219764 | |||||||
chr2:55220297 | G | C | 1 | a0002c0001t0018g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.177+1938C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55220297 | |||||||
chr2:55220596 | G | A | 299 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(296): Show |
373 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(370): Show |
intron_variant | MODIFIER | c.177+1639C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55220596 | |||||||
chr2:55221037 | A | G | 2 | a0003c0003t0007g0103 a0003c0003t0007g0104 |
2 | HG02486.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.177+1198T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55221037 | |||||||
chr2:55221151 | T | G | 1 | a0001c0004t0020g0317 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.177+1084A>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55221151 | |||||||
chr2:55221172 | G | C | 1 | a0001c0002t0003g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.177+1063C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55221172 | |||||||
chr2:55221292 | G | A | 3 | a0002c0001t0001g0217 a0002c0001t0001g0218 a0002c0001t0001g0219 |
3 | NA18970.hp2 NA18984.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.177+943C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55221292 | |||||||
chr2:55221332 | T | C | 3 | a0002c0001t0012g0021 a0002c0001t0012g0155 a0002c0001t0028g0255 |
4 | HG02723.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+903A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55221332 | |||||||
chr2:55221337 | G | A | 1 | a0002c0001t0005g0250 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.177+898C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55221337 | |||||||
chr2:55221542 | A | T | 1 | a0002c0001t0001g0173 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.177+693T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55221542 | |||||||
chr2:55221629 | G | T | 1 | a0002c0001t0001g0172 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.177+606C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55221629 | |||||||
chr2:55221713 | C | A | 1 | a0001c0002t0002g0304 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.177+522G>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55221713 | |||||||
chr2:55221760 | T | C | 1 | a0002c0013t0030g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.177+475A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55221760 | |||||||
chr2:55221766 | C | A | 1 | a0001c0004t0006g0096 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.177+469G>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55221766 | |||||||
chr2:55221813 | A | G | 2 | a0002c0001t0001g0241 a0002c0001t0001g0242 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.177+422T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55221813 | |||||||
chr2:55221866 | A | G | 103 | a0001c0004t0003g0045 a0001c0004t0006g0003 a0001c0004t0006g0007 others(100): Show |
120 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.177+369T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55221866 | |||||||
chr2:55222029 | A | G | 1 | a0001c0002t0002g0284 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.177+206T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55222029 | |||||||
chr2:55222112 | C | T | 6 | a0002c0001t0005g0035 a0002c0001t0005g0236 a0002c0001t0005g0237 others(3): Show |
7 | HG01255.hp2 HG02109.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+123G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55222112 | |||||||
chr2:55222120 | G | A | 300 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(297): Show |
374 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(371): Show |
intron_variant | MODIFIER | c.177+115C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55222120 | |||||||
chr2:55222182 | T | C | 83 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(80): Show |
116 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.177+53A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 3/12 | chr2 | 55222182 | |||||||
chr2:55222631 | T | A | 3 | a0002c0001t0012g0021 a0002c0001t0012g0155 a0002c0001t0028g0255 |
4 | HG02723.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-82-138A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55222631 | |||||||
chr2:55222852 | C | T | 1 | a0006c0008t0001g0171 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-82-359G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55222852 | |||||||
chr2:55222858 | T | G | 1 | a0014c0022t0005g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-82-365A>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55222858 | |||||||
chr2:55222876 | C | T | 1 | a0002c0013t0030g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-82-383G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55222876 | |||||||
chr2:55222918 | C | CA | 69 | a0001c0004t0003g0045 a0001c0004t0006g0079 a0001c0004t0006g0144 others(66): Show |
73 | HG00099.hp2 HG00558.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.-82-426dupT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55222918 | |||||||
chr2:55222918 | C | CAA | 37 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(34): Show |
50 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.-82-427_-82-426dup others(2): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55222918 | |||||||
chr2:55222918 | C | CAAA | 9 | a0001c0004t0006g0097 a0001c0004t0006g0099 a0001c0004t0019g0098 others(6): Show |
10 | HG01175.hp2 HG01981.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-82-428_-82-426dup others(3): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55222918 | |||||||
chr2:55222918 | CA | C | 97 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(94): Show |
133 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.-82-426delT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55222918 | |||||||
chr2:55222918 | CAA | C | 8 | a0001c0002t0002g0283 a0001c0002t0002g0310 a0001c0002t0003g0066 others(5): Show |
9 | HG00323.hp1 HG00738.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.-82-427_-82-426del others(2): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55222918 | |||||||
chr2:55222976 | C | T | 101 | a0001c0004t0003g0045 a0001c0004t0006g0003 a0001c0004t0006g0007 others(98): Show |
117 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(114): Show |
intron_variant | MODIFIER | c.-82-483G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55222976 | |||||||
chr2:55223068 | T | C | 6 | a0002c0001t0005g0035 a0002c0001t0005g0236 a0002c0001t0005g0237 others(3): Show |
7 | HG01255.hp2 HG02109.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-82-575A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55223068 | |||||||
chr2:55223181 | A | G | 1 | a0001c0002t0022g0318 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-82-688T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55223181 | |||||||
chr2:55223348 | G | A | 307 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(304): Show |
382 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(379): Show |
intron_variant | MODIFIER | c.-82-855C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55223348 | |||||||
chr2:55223420 | C | T | 1 | a0014c0022t0005g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-82-927G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55223420 | |||||||
chr2:55223500 | C | G | 1 | a0001c0002t0002g0282 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-82-1007G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55223500 | |||||||
chr2:55223592 | C | T | 1 | a0014c0022t0005g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-82-1099G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55223592 | |||||||
chr2:55223627 | G | GGGGCGAG others(3): Show |
1 | a0001c0004t0020g0317 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-82-1144_-82-1135d others(12): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55223627 | |||||||
chr2:55223630 | G | C | 1 | a0003c0003t0004g0138 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-82-1137C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55223630 | |||||||
chr2:55223682 | C | G | 8 | a0001c0004t0020g0317 a0002c0001t0012g0021 a0002c0001t0012g0155 others(5): Show |
9 | HG02109.hp2 HG02451.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-82-1189G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55223682 | |||||||
chr2:55223880 | C | G | 7 | a0001c0004t0020g0317 a0002c0001t0012g0021 a0002c0001t0012g0155 others(4): Show |
8 | HG02109.hp2 HG02451.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-82-1387G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55223880 | |||||||
chr2:55223930 | G | T | 19 | a0001c0005t0003g0002 a0001c0005t0003g0014 a0001c0005t0003g0015 others(16): Show |
28 | HG01070.hp2 HG01071.hp2 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.-82-1437C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55223930 | |||||||
chr2:55224107 | TAA | T | 3 | a0007c0011t0005g0041 a0007c0011t0005g0042 a0013c0020t0005g0043 |
3 | HG02109.hp2 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-82-1616_-82-1615d others(4): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55224107 | |||||||
chr2:55224303 | G | C | 3 | a0002c0001t0001g0217 a0002c0001t0001g0218 a0002c0001t0001g0219 |
3 | NA18970.hp2 NA18984.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.-82-1810C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55224303 | |||||||
chr2:55224497 | C | T | 89 | a0001c0004t0003g0233 a0001c0004t0006g0076 a0001c0004t0020g0317 others(86): Show |
108 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.-82-2004G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55224497 | |||||||
chr2:55224499 | A | C | 1 | a0003c0003t0017g0146 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-82-2006T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55224499 | |||||||
chr2:55224878 | C | T | 86 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(83): Show |
119 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.-82-2385G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55224878 | |||||||
chr2:55224992 | G | A | 1 | a0001c0005t0003g0063 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-82-2499C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55224992 | |||||||
chr2:55225031 | G | T | 1 | a0002c0001t0001g0165 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-82-2538C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55225031 | |||||||
chr2:55225130 | G | T | 2 | a0002c0001t0001g0163 a0002c0001t0001g0164 |
2 | HG01192.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-82-2637C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55225130 | |||||||
chr2:55225149 | G | C | 1 | a0001c0002t0002g0319 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-82-2656C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55225149 | |||||||
chr2:55225239 | G | A | 55 | a0001c0012t0003g0132 a0003c0003t0004g0016 a0003c0003t0004g0047 others(52): Show |
57 | HG00099.hp2 HG01106.hp1 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.-82-2746C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55225239 | |||||||
chr2:55225247 | G | C | 3 | a0001c0002t0002g0040 a0001c0002t0002g0278 a0001c0002t0002g0315 |
4 | NA18947.hp1 NA18967.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.-82-2754C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55225247 | |||||||
chr2:55225558 | G | T | 1 | a0014c0022t0005g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-83+2474C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55225558 | |||||||
chr2:55225712 | G | C | 225 | a0001c0002t0002g0309 a0001c0002t0022g0308 a0001c0004t0003g0045 others(222): Show |
267 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.-83+2320C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55225712 | |||||||
chr2:55225750 | C | A | 1 | a0002c0001t0001g0228 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-83+2282G>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55225750 | |||||||
chr2:55225782 | G | C | 1 | a0001c0002t0002g0310 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-83+2250C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55225782 | |||||||
chr2:55225788 | G | A | 1 | a0002c0001t0001g0229 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-83+2244C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55225788 | |||||||
chr2:55225796 | C | G | 2 | a0002c0001t0001g0163 a0002c0001t0001g0164 |
2 | HG01192.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-83+2236G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55225796 | |||||||
chr2:55225835 | A | G | 96 | a0001c0002t0002g0314 a0001c0004t0003g0225 a0001c0004t0003g0233 others(93): Show |
116 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-83+2197T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55225835 | |||||||
chr2:55225963 | C | T | 205 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(202): Show |
259 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.-83+2069G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55225963 | |||||||
chr2:55226035 | C | T | 26 | a0001c0004t0006g0003 a0001c0004t0006g0007 a0001c0004t0006g0019 others(23): Show |
36 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.-83+1997G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55226035 | |||||||
chr2:55226141 | A | G | 1 | a0003c0003t0004g0078 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-83+1891T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55226141 | |||||||
chr2:55226191 | CA | C | 209 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(206): Show |
264 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.-83+1840delT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55226191 | |||||||
chr2:55226192 | A | AAAAAAAA others(1152): Show |
1 | a0001c0004t0020g0317 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-83+1839_-83+1840i others(1161): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55226192 | |||||||
chr2:55226298 | G | C | 1 | a0001c0002t0002g0319 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-83+1734C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55226298 | |||||||
chr2:55226304 | T | C | 1 | a0002c0001t0005g0243 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-83+1728A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55226304 | |||||||
chr2:55226339 | G | T | 1 | a0002c0001t0011g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-83+1693C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55226339 | |||||||
chr2:55226441 | T | C | 2 | a0002c0001t0001g0230 a0002c0001t0001g0231 |
2 | NA18948.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.-83+1591A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55226441 | |||||||
chr2:55226587 | T | C | 1 | a0002c0001t0001g0232 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-83+1445A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55226587 | |||||||
chr2:55226677 | G | A | 1 | a0001c0004t0003g0233 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-83+1355C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55226677 | |||||||
chr2:55226696 | A | G | 2 | a0002c0001t0001g0158 a0002c0001t0001g0159 |
2 | HG01346.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-83+1336T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55226696 | |||||||
chr2:55226732 | A | G | 1 | a0001c0005t0003g0052 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-83+1300T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55226732 | |||||||
chr2:55227248 | G | T | 1 | a0002c0001t0001g0256 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-83+784C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55227248 | |||||||
chr2:55227315 | A | G | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-83+717T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55227315 | |||||||
chr2:55227362 | C | T | 1 | a0003c0003t0033g0327 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-83+670G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55227362 | |||||||
chr2:55227400 | C | G | 4 | a0001c0004t0003g0045 a0003c0007t0003g0006 a0003c0007t0003g0044 others(1): Show |
7 | HG02040.hp2 NA18952.hp2 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.-83+632G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55227400 | |||||||
chr2:55227592 | C | G | 1 | a0001c0005t0003g0051 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-83+440G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55227592 | |||||||
chr2:55227627 | G | T | 102 | a0001c0004t0003g0225 a0001c0004t0003g0233 a0001c0004t0006g0076 others(99): Show |
123 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.-83+405C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55227627 | |||||||
chr2:55227629 | G | C | 1 | a0001c0002t0002g0311 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-83+403C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55227629 | |||||||
chr2:55227677 | C | CA | 192 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(189): Show |
242 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.-83+354dupT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55227677 | |||||||
chr2:55227677 | C | CAA | 109 | a0001c0004t0003g0045 a0001c0004t0003g0225 a0001c0004t0003g0233 others(106): Show |
134 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.-83+353_-83+354dup others(2): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55227677 | |||||||
chr2:55227723 | C | T | 1 | a0001c0002t0002g0280 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-83+309G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55227723 | |||||||
chr2:55227735 | T | C | 1 | a0001c0004t0006g0144 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-83+297A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55227735 | |||||||
chr2:55227793 | A | C | 1 | a0014c0022t0005g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-83+239T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55227793 | |||||||
chr2:55227835 | G | T | 2 | a0002c0001t0005g0236 a0002c0001t0005g0237 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-83+197C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55227835 | |||||||
chr2:55227848 | CTT | C | 205 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(202): Show |
259 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.-83+182_-83+183del others(2): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 2/12 | chr2 | 55227848 | |||||||
chr2:55228335 | A | G | 24 | a0002c0001t0001g0241 a0002c0001t0001g0242 a0002c0001t0005g0032 others(21): Show |
28 | HG00738.hp2 HG01255.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.-255-131T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55228335 | |||||||
chr2:55228492 | T | C | 5 | a0005c0009t0002g0323 a0005c0009t0013g0322 a0005c0009t0013g0325 others(2): Show |
5 | HG02132.hp2 NA18966.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.-255-288A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55228492 | |||||||
chr2:55228507 | G | T | 1 | a0001c0004t0020g0317 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-255-303C>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55228507 | |||||||
chr2:55228623 | G | C | 1 | a0001c0002t0002g0311 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-255-419C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55228623 | |||||||
chr2:55228649 | G | A | 1 | a0003c0003t0004g0145 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-255-445C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55228649 | |||||||
chr2:55228712 | G | A | 1 | a0003c0003t0017g0146 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-255-508C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55228712 | |||||||
chr2:55228731 | T | C | 307 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(304): Show |
382 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(379): Show |
intron_variant | MODIFIER | c.-255-527A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55228731 | |||||||
chr2:55228749 | C | T | 1 | a0003c0003t0004g0070 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-255-545G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55228749 | |||||||
chr2:55228791 | T | G | 307 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(304): Show |
382 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(379): Show |
intron_variant | MODIFIER | c.-255-587A>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55228791 | |||||||
chr2:55228802 | A | T | 1 | a0014c0022t0005g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-255-598T>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55228802 | |||||||
chr2:55228906 | T | C | 4 | a0001c0002t0002g0012 a0001c0002t0002g0312 a0001c0002t0002g0313 others(1): Show |
6 | HG01123.hp1 HG01358.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.-255-702A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55228906 | |||||||
chr2:55228947 | T | C | 307 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(304): Show |
382 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(379): Show |
intron_variant | MODIFIER | c.-255-743A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55228947 | |||||||
chr2:55228966 | A | G | 1 | a0003c0007t0003g0044 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-255-762T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55228966 | |||||||
chr2:55229130 | G | A | 6 | a0002c0001t0012g0021 a0002c0001t0012g0155 a0002c0001t0028g0255 others(3): Show |
7 | HG02109.hp2 HG02451.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-255-926C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55229130 | |||||||
chr2:55229150 | C | CA | 95 | a0001c0004t0003g0225 a0001c0004t0003g0233 a0001c0004t0020g0317 others(92): Show |
114 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.-255-947dupT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55229150 | |||||||
chr2:55229150 | C | CAA | 49 | a0001c0002t0002g0277 a0001c0002t0002g0278 a0001c0002t0002g0279 others(46): Show |
63 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.-255-948_-255-947d others(4): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55229150 | |||||||
chr2:55229150 | C | CAAA | 61 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(58): Show |
85 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.-255-949_-255-947d others(5): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55229150 | |||||||
chr2:55229150 | CAAAAA | C | 94 | a0001c0004t0003g0045 a0001c0004t0006g0003 a0001c0004t0006g0007 others(91): Show |
110 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(107): Show |
intron_variant | MODIFIER | c.-255-951_-255-947d others(7): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55229150 | |||||||
chr2:55229166 | A | AG | 3 | a0002c0001t0012g0021 a0002c0001t0012g0155 a0002c0001t0028g0255 |
4 | HG02723.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-255-963_-255-962i others(3): Show |
CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55229166 | |||||||
chr2:55229224 | T | C | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-255-1020A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55229224 | |||||||
chr2:55229271 | A | C | 2 | a0004c0006t0008g0257 a0004c0006t0008g0258 |
2 | HG00423.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.-255-1067T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55229271 | |||||||
chr2:55229457 | T | A | 307 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(304): Show |
382 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(379): Show |
intron_variant | MODIFIER | c.-255-1253A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55229457 | |||||||
chr2:55229663 | G | A | 1 | a0004c0006t0008g0150 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-255-1459C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55229663 | |||||||
chr2:55229760 | G | C | 123 | a0001c0004t0003g0045 a0001c0004t0006g0003 a0001c0004t0006g0007 others(120): Show |
144 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(141): Show |
intron_variant | MODIFIER | c.-255-1556C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55229760 | |||||||
chr2:55229861 | G | A | 2 | a0003c0003t0004g0018 a0009c0021t0004g0151 |
3 | HG01074.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-255-1657C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55229861 | |||||||
chr2:55229872 | C | G | 307 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(304): Show |
382 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(379): Show |
intron_variant | MODIFIER | c.-255-1668G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55229872 | |||||||
chr2:55229942 | G | A | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-255-1738C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55229942 | |||||||
chr2:55230013 | G | A | 1 | a0001c0004t0006g0152 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-255-1809C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55230013 | |||||||
chr2:55230059 | C | T | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-255-1855G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55230059 | |||||||
chr2:55230124 | T | C | 1 | a0001c0004t0006g0019 | 2 | NA18998.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-255-1920A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55230124 | |||||||
chr2:55230125 | A | G | 1 | a0002c0010t0014g0275 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-255-1921T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55230125 | |||||||
chr2:55230158 | C | T | 7 | a0003c0003t0004g0069 a0003c0003t0004g0070 a0003c0003t0004g0071 others(4): Show |
7 | HG02257.hp2 HG02809.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-255-1954G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55230158 | |||||||
chr2:55230246 | A | G | 20 | a0001c0005t0003g0002 a0001c0005t0003g0014 a0001c0005t0003g0015 others(17): Show |
29 | HG01070.hp2 HG01071.hp2 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.-256+1977T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55230246 | |||||||
chr2:55230433 | T | C | 98 | a0001c0004t0003g0045 a0001c0004t0006g0003 a0001c0004t0006g0007 others(95): Show |
114 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(111): Show |
intron_variant | MODIFIER | c.-256+1790A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55230433 | |||||||
chr2:55230695 | C | A | 2 | a0002c0001t0005g0020 a0002c0001t0005g0153 |
3 | HG02630.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-256+1528G>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55230695 | |||||||
chr2:55230944 | T | A | 98 | a0001c0004t0003g0225 a0001c0004t0003g0233 a0001c0004t0020g0317 others(95): Show |
119 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.-256+1279A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55230944 | |||||||
chr2:55231086 | C | G | 1 | a0002c0001t0001g0154 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-256+1137G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55231086 | |||||||
chr2:55231189 | A | G | 101 | a0001c0004t0003g0225 a0001c0004t0003g0233 a0001c0004t0020g0317 others(98): Show |
122 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.-256+1034T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55231189 | |||||||
chr2:55231252 | G | GA | 26 | a0001c0002t0002g0314 a0001c0002t0002g0315 a0001c0002t0002g0316 others(23): Show |
30 | HG00558.hp2 HG00738.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.-256+970dupT | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55231252 | |||||||
chr2:55231253 | A | C | 2 | a0003c0003t0004g0047 a0003c0003t0004g0048 |
2 | HG01243.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-256+970T>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55231253 | |||||||
chr2:55231364 | A | G | 3 | a0007c0011t0005g0041 a0007c0011t0005g0042 a0013c0020t0005g0043 |
3 | HG02109.hp2 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-256+859T>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55231364 | |||||||
chr2:55231395 | G | A | 1 | a0002c0001t0018g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-256+828C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55231395 | |||||||
chr2:55231526 | G | C | 101 | a0001c0004t0003g0225 a0001c0004t0003g0233 a0001c0004t0020g0317 others(98): Show |
122 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.-256+697C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55231526 | |||||||
chr2:55231700 | T | C | 25 | a0002c0001t0001g0241 a0002c0001t0001g0242 a0002c0001t0005g0032 others(22): Show |
29 | HG00738.hp2 HG01255.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.-256+523A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55231700 | |||||||
chr2:55231752 | C | G | 4 | a0001c0004t0003g0045 a0003c0007t0003g0006 a0003c0007t0003g0044 others(1): Show |
7 | HG02040.hp2 NA18952.hp2 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.-256+471G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55231752 | |||||||
chr2:55231905 | G | C | 1 | a0001c0002t0022g0318 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-256+318C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55231905 | |||||||
chr2:55231933 | G | A | 1 | a0001c0002t0002g0319 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-256+290C>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55231933 | |||||||
chr2:55231938 | G | C | 1 | a0002c0001t0001g0256 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-256+285C>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55231938 | |||||||
chr2:55231958 | C | G | 307 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0008 others(304): Show |
382 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(379): Show |
intron_variant | MODIFIER | c.-256+265G>C | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55231958 | |||||||
chr2:55232040 | T | A | 1 | a0001c0002t0002g0274 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-256+183A>T | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55232040 | |||||||
chr2:55232044 | T | C | 8 | a0005c0009t0002g0013 a0005c0009t0002g0320 a0005c0009t0002g0321 others(5): Show |
10 | HG00140.hp2 HG01192.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.-256+179A>G | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55232044 | |||||||
chr2:55232135 | C | T | 1 | a0001c0002t0002g0274 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-256+88G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55232135 | |||||||
chr2:55232146 | C | T | 3 | a0007c0011t0005g0041 a0007c0011t0005g0042 a0013c0020t0005g0043 |
3 | HG02109.hp2 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-256+77G>A | CLHC1 | ENSG00000162994.16 | transcript | ENST00000401408.6 | protein_coding | 1/12 | chr2 | 55232146 |