Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 29915 |
| ensemblid | ENSG00000111727.12 |
| hgncid | 24972 |
| symbol | HCFC2 |
| name | host cell factor C2 |
| refseq_nuc | NM_013320.3 |
| refseq_prot | NP_037452.1 |
| ensembl_nuc | ENST00000229330.9 |
| ensembl_prot | ENSP00000229330.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 104064531 |
| end | 104106524 |
| strand | + |
| ver | v1.2 |
| region | chr12:104064531-104106524 |
| region5000 | chr12:104059531-104111524 |
| regionname0 | HCFC2_chr12_104064531_104106524 |
| regionname5000 | HCFC2_chr12_104059531_104111524 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 792 | 375 | 91 | 62 | 168 | 14 | 38 | 132 | HCFC2_chr12_104059531_104111524 | HCFC2 | MAAPS others(787): Show |
chr12 | 104059531 | 104111524 |
| a0002 | 0/0 | 792 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | MAAPS others(787): Show |
chr12 | 104059531 | 104111524 |
| a0003 | 0/0 | 792 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | MAAPS others(787): Show |
chr12 | 104059531 | 104111524 |
| a0004 | 0/0 | 792 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | MAAPS others(787): Show |
chr12 | 104059531 | 104111524 |
| a0005 | 0/0 | 792 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | MAAPS others(787): Show |
chr12 | 104059531 | 104111524 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2376 | 372 | 89 | 62 | 167 | 14 | 38 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATGGC others(2371): Show |
chr12 | 104059531 | 104111524 | ||
| a0001c0002 | 0/0 | 2376 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATGGC others(2371): Show |
chr12 | 104059531 | 104111524 | ||
| a0001c0006 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATGGC others(2371): Show |
chr12 | 104059531 | 104111524 | ||
| a0002c0003 | 0/0 | 2376 | 2 | 1 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATGGC others(2371): Show |
chr12 | 104059531 | 104111524 | ||
| a0003c0004 | 0/0 | 2376 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATGGC others(2371): Show |
chr12 | 104059531 | 104111524 | ||
| a0004c0005 | 0/0 | 2376 | 2 | 0 | 0 | 0 | 0 | 2 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATGGC others(2371): Show |
chr12 | 104059531 | 104111524 | ||
| a0005c0007 | 0/0 | 2376 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATGGC others(2371): Show |
chr12 | 104059531 | 104111524 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5660 | 148 | 49 | 44 | 32 | 8 | 14 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5655): Show |
chr12 | 104059531 | 104111524 |
| a0001c0001t0002 | 0/0 | 5660 | 58 | 1 | 4 | 47 | 0 | 6 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5655): Show |
chr12 | 104059531 | 104111524 |
| a0001c0001t0003 | 0/0 | 5660 | 56 | 13 | 3 | 35 | 1 | 4 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5655): Show |
chr12 | 104059531 | 104111524 |
| a0001c0001t0004 | 0/0 | 5661 | 52 | 14 | 7 | 22 | 3 | 6 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5656): Show |
chr12 | 104059531 | 104111524 |
| a0001c0001t0005 | 0/0 | 5660 | 11 | 0 | 0 | 11 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5655): Show |
chr12 | 104059531 | 104111524 |
| a0001c0001t0006 | 0/0 | 5661 | 10 | 0 | 2 | 8 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5656): Show |
chr12 | 104059531 | 104111524 |
| a0001c0001t0007 | 0/1 | 5662 | 7 | 0 | 1 | 0 | 2 | 3 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5657): Show |
chr12 | 104059531 | 104111524 |
| a0001c0001t0008 | 0/0 | 5662 | 4 | 1 | 0 | 1 | 0 | 2 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5657): Show |
chr12 | 104059531 | 104111524 |
| a0001c0001t0009 | 0/0 | 5660 | 5 | 5 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5655): Show |
chr12 | 104059531 | 104111524 |
| a0001c0001t0010 | 0/0 | 5659 | 4 | 2 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5654): Show |
chr12 | 104059531 | 104111524 |
| a0001c0001t0011 | 0/0 | 5660 | 4 | 0 | 0 | 4 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5655): Show |
chr12 | 104059531 | 104111524 |
| a0001c0001t0012 | 0/0 | 5659 | 3 | 0 | 0 | 3 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5654): Show |
chr12 | 104059531 | 104111524 |
| a0001c0001t0013 | 0/0 | 5660 | 2 | 0 | 0 | 0 | 0 | 2 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5655): Show |
chr12 | 104059531 | 104111524 |
| a0001c0001t0014 | 0/0 | 5661 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5656): Show |
chr12 | 104059531 | 104111524 |
| a0001c0001t0016 | 0/0 | 5660 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5655): Show |
chr12 | 104059531 | 104111524 |
| a0001c0001t0017 | 0/0 | 5661 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5656): Show |
chr12 | 104059531 | 104111524 |
| a0001c0001t0018 | 0/0 | 5660 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5655): Show |
chr12 | 104059531 | 104111524 |
| a0001c0001t0019 | 0/0 | 5659 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5654): Show |
chr12 | 104059531 | 104111524 |
| a0001c0001t0020 | 0/0 | 5661 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5656): Show |
chr12 | 104059531 | 104111524 |
| a0001c0001t0021 | 0/0 | 5662 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5657): Show |
chr12 | 104059531 | 104111524 |
| a0001c0001t0022 | 0/0 | 5660 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5655): Show |
chr12 | 104059531 | 104111524 |
| a0001c0002t0001 | 0/0 | 5660 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5655): Show |
chr12 | 104059531 | 104111524 |
| a0001c0006t0008 | 0/0 | 5662 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5657): Show |
chr12 | 104059531 | 104111524 |
| a0002c0003t0001 | 0/0 | 5660 | 2 | 1 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5655): Show |
chr12 | 104059531 | 104111524 |
| a0003c0004t0001 | 0/0 | 5660 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5655): Show |
chr12 | 104059531 | 104111524 |
| a0004c0005t0007 | 0/0 | 5662 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5657): Show |
chr12 | 104059531 | 104111524 |
| a0004c0005t0015 | 0/0 | 5663 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5658): Show |
chr12 | 104059531 | 104111524 |
| a0005c0007t0006 | 0/0 | 5661 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | ATTGT others(5656): Show |
chr12 | 104059531 | 104111524 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0003 | 0/0 | 14 | 1 | 7 | 4 | 1 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0006 | 0/0 | 6 | 1 | 4 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 3 | 0 | 2 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0009 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0014 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0004 | 0/0 | 12 | 1 | 2 | 9 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0002 | 0/0 | 14 | 0 | 0 | 14 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0012 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0023 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0001 | 0/0 | 14 | 3 | 0 | 11 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0005g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0006g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0006g0005 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0007g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0007g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0007g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0007g0138 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0008g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0008g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0008g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0009g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0010g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0010g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0010g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0011g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0011g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0011g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0012g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0012g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0012g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0013g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0014g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0016g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0017g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0018g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0019g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0020g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0021g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0001t0022g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0002t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0001c0006t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0002c0003t0001g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0003c0004t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0004c0005t0007g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0004c0005t0015g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| a0005c0007t0006g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0017 | EUR | GBR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0195 | EUR | FIN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | FIN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0188 | EUR | FIN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0181 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0158 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0177 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00673 | hp1 | a0001 | c0001 | t0012 | g0079 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0194 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01081 | hp2 | a0002 | c0003 | t0001 | g0037 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01168 | hp1 | a0001 | c0001 | t0022 | g0159 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0172 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0017 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0197 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0196 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | IBS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | IBS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01516 | hp2 | a0001 | c0001 | t0007 | g0026 | EUR | IBS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01517 | hp2 | a0001 | c0001 | t0007 | g0026 | EUR | IBS | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01884 | hp2 | a0001 | c0001 | t0010 | g0058 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01928 | hp1 | a0005 | c0007 | t0006 | g0005 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0174 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02004 | hp1 | a0001 | c0001 | t0007 | g0135 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02055 | hp1 | a0001 | c0001 | t0018 | g0067 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02074 | hp1 | a0001 | c0001 | t0012 | g0080 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0198 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02080 | hp1 | a0001 | c0006 | t0008 | g0001 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02129 | hp2 | a0001 | c0001 | t0017 | g0004 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0192 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02148 | hp2 | a0001 | c0001 | t0006 | g0005 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | CDX | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CDX | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02257 | hp1 | a0001 | c0001 | t0021 | g0052 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02257 | hp2 | a0001 | c0001 | t0020 | g0193 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02523 | hp1 | a0001 | c0001 | t0016 | g0033 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | KHV | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0008 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0044 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02647 | hp1 | a0002 | c0003 | t0001 | g0037 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0023 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02683 | hp2 | a0001 | c0001 | t0019 | g0075 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02698 | hp1 | a0001 | c0001 | t0007 | g0134 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02698 | hp2 | a0001 | c0001 | t0013 | g0038 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0008 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0190 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0023 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02738 | hp2 | a0004 | c0005 | t0015 | g0137 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0008 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0008 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0179 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02897 | hp1 | a0001 | c0001 | t0009 | g0008 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0189 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03130 | hp2 | a0003 | c0004 | t0001 | g0035 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0166 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03209 | hp2 | a0001 | c0001 | t0014 | g0131 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0187 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0046 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0173 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0162 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0045 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0199 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03491 | hp1 | a0001 | c0001 | t0008 | g0185 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0175 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03492 | hp1 | a0001 | c0001 | t0008 | g0017 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0183 | AFR | ESN | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0163 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0164 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | MSL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0044 | SAS | STU | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0041 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0171 | SAS | PJL | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0160 | SAS | BEB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03834 | hp2 | a0004 | c0005 | t0007 | g0136 | SAS | BEB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | BEB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG04184 | hp1 | a0001 | c0001 | t0007 | g0133 | SAS | BEB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0029 | SAS | BEB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG04204 | hp1 | a0001 | c0001 | t0007 | g0132 | SAS | STU | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG04204 | hp2 | a0001 | c0001 | t0013 | g0038 | SAS | STU | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | STU | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | YRI | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0180 | AFR | YRI | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18612 | hp1 | a0001 | c0001 | t0011 | g0021 | EAS | CHB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0182 | EAS | CHB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18945 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18950 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0217 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0203 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18962 | hp1 | a0001 | c0001 | t0006 | g0165 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18965 | hp2 | a0001 | c0001 | t0010 | g0054 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18967 | hp1 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18981 | hp2 | a0001 | c0001 | t0005 | g0209 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18984 | hp1 | a0001 | c0001 | t0006 | g0141 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18985 | hp1 | a0001 | c0001 | t0010 | g0108 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18989 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18991 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18998 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA18999 | hp2 | a0001 | c0001 | t0006 | g0142 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19000 | hp2 | a0001 | c0001 | t0011 | g0117 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19001 | hp1 | a0001 | c0001 | t0005 | g0206 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19002 | hp1 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19007 | hp2 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | LWK | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | LWK | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19059 | hp1 | a0001 | c0001 | t0005 | g0208 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19059 | hp2 | a0001 | c0001 | t0012 | g0081 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19065 | hp2 | a0001 | c0001 | t0011 | g0113 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19076 | hp1 | a0001 | c0001 | t0011 | g0021 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19078 | hp1 | a0001 | c0001 | t0005 | g0204 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0191 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19083 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | YRI | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0046 | AFR | ASW | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ASW | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0041 | EUR | TSI | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0005 | AMR | CLM | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02486 | hp1 | a0003 | c0004 | t0001 | g0035 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | USA | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0055 | AFR | USA | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0178 | AFR | USA | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA21309 | hp1 | a0001 | c0001 | t0010 | g0019 | AFR | LWK | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0233 | AFR | LWK | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0007 | g0138 | REF | REF | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0119 | REF | REF | HCFC2_chr12_104059531_104111524 | HCFC2 | chr12 | 104059531 | 104111524 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:104067989 | C | T | 1 | a0004 | 2 | HG02738.hp2 HG03834.hp2 |
missense_variant | MODERATE | c.355C>T | p.Pro119Ser | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/15 | 385/5660 | 355/2379 | 119/792 | chr12 | 104067989 | |||
| chr12:104082535 | G | C | 1 | a0002 | 2 | HG01081.hp2 HG02647.hp1 |
missense_variant | MODERATE | c.803G>C | p.Gly268Ala | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 6/15 | 833/5660 | 803/2379 | 268/792 | chr12 | 104082535 | |||
| chr12:104093474 | C | T | 1 | a0005 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.1373C>T | p.Thr458Met | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/15 | 1403/5660 | 1373/2379 | 458/792 | chr12 | 104093474 | |||
| chr12:104093484 | T | A | 1 | a0003 | 2 | HG02486.hp1 HG03130.hp2 |
missense_variant | MODERATE | c.1383T>A | p.Asn461Lys | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/15 | 1413/5660 | 1383/2379 | 461/792 | chr12 | 104093484 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:104066276 | T | G | 1 | a0001c0002 | 2 | HG03225.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.273T>G | p.Val91Val | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/15 | 303/5660 | 273/2379 | 91/792 | chr12 | 104066276 | |||
| chr12:104098363 | A | G | 1 | a0001c0006 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.1761A>G | p.Pro587Pro | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/15 | 1791/5660 | 1761/2379 | 587/792 | chr12 | 104098363 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:104103823 | A | T | 1 | a0001c0001t0009 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*550A>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 550 | chr12 | 104103823 | ||||||
| chr12:104103885 | G | T | 1 | a0001c0001t0022 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*612G>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 612 | chr12 | 104103885 | ||||||
| chr12:104104591 | A | G | 5 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0021 others(2): Show |
69 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*1318A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 1318 | chr12 | 104104591 | ||||||
| chr12:104105195 | T | TA | 5 | a0001c0001t0007 a0001c0001t0014 a0001c0001t0021 others(2): Show |
10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1926dupA | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 1927 | INFO_REALIGN_3_PRIME | chr12 | 104105195 | |||||
| chr12:104105299 | T | C | 4 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0016 others(1): Show |
63 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2026T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 2026 | chr12 | 104105299 | ||||||
| chr12:104105545 | A | G | 1 | a0001c0001t0020 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2272A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 2272 | chr12 | 104105545 | ||||||
| chr12:104105579 | A | AT | 8 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(5): Show |
73 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*2322dupT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 2323 | INFO_REALIGN_3_PRIME | chr12 | 104105579 | |||||
| chr12:104105579 | A | ATT | 3 | a0001c0001t0008 a0001c0006t0008 a0004c0005t0015 |
6 | HG02080.hp1 HG02738.hp2 HG03486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2321_*2322dupTT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 2323 | INFO_REALIGN_3_PRIME | chr12 | 104105579 | |||||
| chr12:104105579 | AT | A | 3 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0019 |
8 | HG00673.hp1 HG01884.hp2 HG02074.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2322delT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 2322 | INFO_REALIGN_3_PRIME | chr12 | 104105579 | |||||
| chr12:104105583 | T | A | 1 | a0001c0001t0018 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2310T>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 2310 | chr12 | 104105583 | ||||||
| chr12:104106107 | A | T | 2 | a0001c0001t0013 a0001c0001t0019 |
3 | HG02683.hp2 HG02698.hp2 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2834A>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 2834 | chr12 | 104106107 | ||||||
| chr12:104106113 | T | C | 1 | a0001c0001t0011 | 4 | NA18612.hp1 NA19000.hp2 NA19065.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2840T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 2840 | chr12 | 104106113 | ||||||
| chr12:104106361 | T | C | 1 | a0001c0001t0005 | 11 | NA18945.hp2 NA18954.hp2 NA18959.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3088T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 3088 | chr12 | 104106361 | ||||||
| chr12:104106432 | T | A | 1 | a0001c0001t0016 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3159T>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 15/15 | 3159 | chr12 | 104106432 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:104064742 | C | T | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG01109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.163+19C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104064742 | |||||||
| chr12:104064776 | G | T | 1 | a0001c0001t0004g0233 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.163+53G>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104064776 | |||||||
| chr12:104064919 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.163+196C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104064919 | |||||||
| chr12:104064965 | C | A | 1 | a0001c0001t0001g0048 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.163+242C>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104064965 | |||||||
| chr12:104065300 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.163+577G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104065300 | |||||||
| chr12:104065382 | G | T | 9 | a0001c0001t0001g0047 a0001c0001t0001g0225 a0001c0001t0001g0226 others(6): Show |
11 | HG02486.hp2 HG02615.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.163+659G>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104065382 | |||||||
| chr12:104065386 | G | C | 1 | a0001c0001t0001g0018 | 3 | HG02723.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.163+663G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104065386 | |||||||
| chr12:104065446 | T | C | 3 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0001c0001t0007g0026 |
4 | HG01516.hp2 HG01517.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-721T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104065446 | |||||||
| chr12:104065667 | A | G | 29 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(26): Show |
46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.164-500A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104065667 | |||||||
| chr12:104065828 | G | A | 1 | a0001c0001t0021g0052 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.164-339G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104065828 | |||||||
| chr12:104065947 | G | C | 1 | a0001c0001t0001g0053 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.164-220G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104065947 | |||||||
| chr12:104066033 | A | G | 42 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0045 others(39): Show |
59 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.164-134A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104066033 | |||||||
| chr12:104066124 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.164-43C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104066124 | |||||||
| chr12:104066127 | T | G | 42 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0045 others(39): Show |
59 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.164-40T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 1/14 | chr12 | 104066127 | |||||||
| chr12:104066389 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.312+74A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104066389 | |||||||
| chr12:104066404 | T | C | 1 | a0001c0001t0010g0054 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.312+89T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104066404 | |||||||
| chr12:104066434 | GTATTATT others(9): Show |
G | 42 | a0001c0001t0003g0002 a0001c0001t0003g0012 a0001c0001t0003g0023 others(39): Show |
69 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.312+134_312+149del others(16): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 104066434 | ||||||
| chr12:104066450 | C | G | 38 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(35): Show |
60 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.312+135C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104066450 | |||||||
| chr12:104066502 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.312+187T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104066502 | |||||||
| chr12:104066593 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.312+278T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104066593 | |||||||
| chr12:104066772 | T | C | 2 | a0001c0001t0001g0056 a0001c0001t0004g0055 |
2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.312+457T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104066772 | |||||||
| chr12:104066856 | C | T | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.312+541C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104066856 | |||||||
| chr12:104066873 | C | T | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.312+558C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104066873 | |||||||
| chr12:104067133 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0232 a0001c0001t0010g0019 |
4 | HG00323.hp1 HG00738.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.313-814G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104067133 | |||||||
| chr12:104067156 | T | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(121): Show |
190 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.313-791T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104067156 | |||||||
| chr12:104067459 | C | T | 3 | a0001c0001t0001g0130 a0001c0001t0001g0234 a0001c0001t0001g0235 |
3 | HG01109.hp2 HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.313-488C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104067459 | |||||||
| chr12:104067551 | A | G | 1 | a0001c0001t0003g0168 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.313-396A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104067551 | |||||||
| chr12:104067604 | T | G | 1 | a0001c0001t0014g0131 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.313-343T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104067604 | |||||||
| chr12:104067689 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.313-258A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104067689 | |||||||
| chr12:104067762 | C | G | 6 | a0001c0001t0001g0022 a0001c0001t0001g0039 a0001c0001t0001g0125 others(3): Show |
9 | HG02055.hp2 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.313-185C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 2/14 | chr12 | 104067762 | |||||||
| chr12:104068159 | C | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0045 others(40): Show |
60 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.473+52C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104068159 | |||||||
| chr12:104068402 | T | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0170 |
4 | HG02723.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+295T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104068402 | |||||||
| chr12:104068596 | A | C | 38 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(35): Show |
60 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.473+489A>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104068596 | |||||||
| chr12:104068636 | T | C | 1 | a0001c0001t0002g0059 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.473+529T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104068636 | |||||||
| chr12:104069038 | G | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0049 a0001c0001t0001g0060 others(4): Show |
11 | HG00642.hp2 HG01192.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.473+931G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104069038 | |||||||
| chr12:104069115 | G | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
5 | HG02109.hp2 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.473+1008G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104069115 | |||||||
| chr12:104069525 | TA | T | 43 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(40): Show |
57 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.473+1433delA | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104069525 | ||||||
| chr12:104069604 | G | A | 8 | a0001c0001t0001g0017 a0001c0001t0004g0017 a0001c0001t0004g0171 others(5): Show |
9 | HG00099.hp2 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.473+1497G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104069604 | |||||||
| chr12:104069720 | T | C | 1 | a0001c0001t0004g0176 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.473+1613T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104069720 | |||||||
| chr12:104070027 | A | G | 1 | a0001c0001t0009g0008 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.473+1920A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104070027 | |||||||
| chr12:104070035 | T | A | 1 | a0001c0001t0001g0057 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.473+1928T>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104070035 | |||||||
| chr12:104070093 | T | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(240): Show |
372 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.473+1986T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104070093 | |||||||
| chr12:104070130 | C | T | 29 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(26): Show |
46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.473+2023C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104070130 | |||||||
| chr12:104070260 | CCT | C | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.473+2155_473+2156d others(4): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104070260 | ||||||
| chr12:104070769 | T | A | 1 | a0001c0001t0002g0065 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.473+2662T>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104070769 | |||||||
| chr12:104070801 | C | CT | 50 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(47): Show |
73 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.473+2715dupT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104070801 | ||||||
| chr12:104071007 | C | T | 10 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0109 others(7): Show |
14 | HG01074.hp1 HG01256.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.473+2900C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104071007 | |||||||
| chr12:104071024 | T | A | 1 | a0001c0001t0001g0018 | 3 | HG02723.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.473+2917T>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104071024 | |||||||
| chr12:104071049 | G | A | 1 | a0001c0001t0009g0008 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.473+2942G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104071049 | |||||||
| chr12:104071276 | C | A | 1 | a0001c0001t0002g0066 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.473+3169C>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104071276 | |||||||
| chr12:104071360 | A | G | 1 | a0001c0001t0003g0051 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.473+3253A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104071360 | |||||||
| chr12:104071571 | CCTAA | C | 1 | a0001c0001t0009g0008 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.473+3468_473+3471d others(6): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104071571 | ||||||
| chr12:104071576 | CTATTTTA others(3): Show |
C | 1 | a0001c0001t0001g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.473+3486_473+3495d others(12): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104071576 | ||||||
| chr12:104071679 | C | A | 1 | a0001c0001t0002g0027 | 2 | NA18971.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.473+3572C>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104071679 | |||||||
| chr12:104072046 | A | G | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.473+3939A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072046 | |||||||
| chr12:104072198 | C | T | 1 | a0001c0001t0001g0025 | 3 | NA18612.hp2 NA18950.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.473+4091C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072198 | |||||||
| chr12:104072270 | G | C | 1 | a0001c0001t0003g0139 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.473+4163G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072270 | |||||||
| chr12:104072368 | TA | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(70): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.473+4278delA | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104072368 | ||||||
| chr12:104072443 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.473+4336A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072443 | |||||||
| chr12:104072502 | G | A | 1 | a0001c0001t0004g0196 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.473+4395G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072502 | |||||||
| chr12:104072523 | A | G | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | HG01071.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.473+4416A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072523 | |||||||
| chr12:104072608 | T | C | 27 | a0001c0001t0003g0002 a0001c0001t0003g0040 a0001c0001t0003g0139 others(24): Show |
46 | HG00408.hp2 HG00621.hp2 HG01123.hp2 others(43): Show |
intron_variant | MODIFIER | c.473+4501T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072608 | |||||||
| chr12:104072700 | T | G | 47 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(44): Show |
79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.473+4593T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072700 | |||||||
| chr12:104072733 | C | G | 1 | a0001c0001t0001g0018 | 3 | HG02723.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.473+4626C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072733 | |||||||
| chr12:104072787 | C | T | 6 | a0001c0001t0001g0022 a0001c0001t0001g0039 a0001c0001t0001g0125 others(3): Show |
9 | HG02055.hp2 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.473+4680C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072787 | |||||||
| chr12:104072869 | C | T | 1 | a0001c0001t0009g0008 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.473+4762C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072869 | |||||||
| chr12:104072889 | C | G | 1 | a0001c0001t0001g0169 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.473+4782C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104072889 | |||||||
| chr12:104073109 | T | G | 4 | a0001c0001t0004g0082 a0001c0001t0012g0079 a0001c0001t0012g0080 others(1): Show |
4 | HG00408.hp1 HG00673.hp1 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+5002T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104073109 | |||||||
| chr12:104073110 | C | G | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.473+5003C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104073110 | |||||||
| chr12:104073167 | C | CT | 24 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0021 others(21): Show |
42 | HG00438.hp1 HG00544.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.473+5075dupT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104073167 | ||||||
| chr12:104073167 | CTTT | C | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.473+5073_473+5075d others(5): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104073167 | ||||||
| chr12:104073187 | C | T | 37 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(34): Show |
64 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.473+5080C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104073187 | |||||||
| chr12:104073291 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(169): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.473+5184G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104073291 | |||||||
| chr12:104073405 | C | T | 1 | a0001c0001t0009g0008 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.473+5298C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104073405 | |||||||
| chr12:104073410 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0010g0058 |
2 | HG01884.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.473+5303G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104073410 | |||||||
| chr12:104073417 | C | A | 1 | a0001c0001t0003g0041 | 2 | HG03704.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.473+5310C>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104073417 | |||||||
| chr12:104073723 | C | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0045 others(38): Show |
58 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.473+5616C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104073723 | |||||||
| chr12:104073742 | G | A | 1 | a0001c0001t0002g0020 | 3 | HG00558.hp2 HG04228.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.473+5635G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104073742 | |||||||
| chr12:104073834 | A | G | 1 | a0001c0001t0003g0155 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.474-5611A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104073834 | |||||||
| chr12:104074041 | C | G | 1 | a0001c0001t0011g0113 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.474-5404C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104074041 | |||||||
| chr12:104074278 | G | C | 3 | a0001c0001t0001g0130 a0001c0001t0001g0234 a0001c0001t0001g0235 |
3 | HG01109.hp2 HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.474-5167G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104074278 | |||||||
| chr12:104074529 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.474-4916G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104074529 | |||||||
| chr12:104074791 | A | T | 1 | a0001c0001t0001g0057 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.474-4654A>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104074791 | |||||||
| chr12:104075090 | C | T | 3 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 |
3 | HG02486.hp2 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.474-4355C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104075090 | |||||||
| chr12:104075195 | T | TA | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(174): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.474-4238dupA | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104075195 | ||||||
| chr12:104075195 | T | TAA | 4 | a0001c0001t0003g0023 a0001c0001t0003g0041 a0001c0001t0003g0158 others(1): Show |
7 | HG00639.hp2 HG01168.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.474-4239_474-4238d others(4): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104075195 | ||||||
| chr12:104075289 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.474-4156T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104075289 | |||||||
| chr12:104075298 | C | T | 29 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(26): Show |
46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.474-4147C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104075298 | |||||||
| chr12:104075304 | A | G | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.474-4141A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104075304 | |||||||
| chr12:104075457 | C | CT | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(141): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.474-3970dupT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104075457 | ||||||
| chr12:104075457 | C | CTT | 37 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(34): Show |
55 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.474-3971_474-3970d others(4): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104075457 | ||||||
| chr12:104075584 | G | T | 1 | a0001c0001t0001g0169 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.474-3861G>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104075584 | |||||||
| chr12:104075651 | G | A | 2 | a0001c0001t0004g0177 a0001c0001t0004g0197 |
2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.474-3794G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104075651 | |||||||
| chr12:104075659 | C | A | 1 | a0001c0001t0002g0083 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.474-3786C>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104075659 | |||||||
| chr12:104075826 | AT | A | 5 | a0001c0001t0006g0005 a0001c0001t0006g0141 a0001c0001t0006g0142 others(2): Show |
10 | HG01123.hp2 HG01928.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.474-3610delT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104075826 | ||||||
| chr12:104075835 | T | G | 5 | a0001c0001t0006g0005 a0001c0001t0006g0141 a0001c0001t0006g0142 others(2): Show |
10 | HG01123.hp2 HG01928.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.474-3610T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104075835 | |||||||
| chr12:104075939 | G | T | 1 | a0001c0001t0002g0116 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.474-3506G>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104075939 | |||||||
| chr12:104075940 | C | T | 1 | a0001c0001t0002g0116 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.474-3505C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104075940 | |||||||
| chr12:104076433 | A | AT | 124 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(121): Show |
190 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.474-3010dupT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104076433 | ||||||
| chr12:104076477 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.474-2968G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104076477 | |||||||
| chr12:104076655 | T | C | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.474-2790T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104076655 | |||||||
| chr12:104076693 | TCTGCATT others(85): Show |
T | 10 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0210 others(7): Show |
14 | HG00558.hp1 HG02015.hp1 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.474-2721_474-2630d others(94): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104076693 | ||||||
| chr12:104076879 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.474-2566T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104076879 | |||||||
| chr12:104076944 | A | C | 1 | a0001c0001t0002g0101 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.474-2501A>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104076944 | |||||||
| chr12:104076983 | C | T | 3 | a0001c0001t0002g0100 a0004c0005t0007g0136 a0004c0005t0015g0137 |
3 | HG02738.hp2 HG03834.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.474-2462C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104076983 | |||||||
| chr12:104077074 | A | G | 2 | a0001c0001t0004g0194 a0001c0001t0004g0195 |
2 | HG00280.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.474-2371A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104077074 | |||||||
| chr12:104077103 | G | A | 1 | a0001c0001t0002g0084 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.474-2342G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104077103 | |||||||
| chr12:104077252 | T | G | 29 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(26): Show |
46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.474-2193T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104077252 | |||||||
| chr12:104077263 | G | A | 1 | a0001c0001t0014g0131 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.474-2182G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104077263 | |||||||
| chr12:104077550 | G | GT | 6 | a0001c0001t0001g0062 a0001c0001t0002g0099 a0001c0001t0004g0191 others(3): Show |
6 | HG00438.hp2 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.474-1878dupT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104077550 | ||||||
| chr12:104077550 | G | GTTT | 29 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(26): Show |
46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.474-1880_474-1878d others(5): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104077550 | ||||||
| chr12:104077550 | GT | G | 48 | a0001c0001t0001g0225 a0001c0001t0002g0085 a0001c0001t0002g0086 others(45): Show |
75 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.474-1878delT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 104077550 | ||||||
| chr12:104077567 | T | A | 1 | a0001c0001t0009g0008 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.474-1878T>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104077567 | |||||||
| chr12:104077568 | A | T | 1 | a0001c0001t0010g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.474-1877A>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104077568 | |||||||
| chr12:104077840 | A | T | 1 | a0001c0001t0020g0193 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.474-1605A>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104077840 | |||||||
| chr12:104077885 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(180): Show |
285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.474-1560C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104077885 | |||||||
| chr12:104077939 | G | T | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.474-1506G>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104077939 | |||||||
| chr12:104078067 | T | C | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.474-1378T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078067 | |||||||
| chr12:104078161 | G | A | 5 | a0001c0001t0001g0036 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
7 | HG01081.hp2 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.474-1284G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078161 | |||||||
| chr12:104078281 | G | A | 2 | a0001c0001t0001g0169 a0001c0001t0003g0160 |
2 | HG02818.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.474-1164G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078281 | |||||||
| chr12:104078283 | G | T | 1 | a0001c0001t0001g0170 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.474-1162G>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078283 | |||||||
| chr12:104078339 | G | A | 4 | a0001c0001t0001g0036 a0001c0001t0001g0121 a0001c0001t0001g0122 others(1): Show |
6 | HG01081.hp2 HG02280.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-1106G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078339 | |||||||
| chr12:104078343 | A | G | 29 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(26): Show |
46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.474-1102A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078343 | |||||||
| chr12:104078397 | A | G | 29 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(26): Show |
46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.474-1048A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078397 | |||||||
| chr12:104078554 | A | G | 2 | a0001c0001t0002g0034 a0001c0001t0002g0116 |
3 | HG02523.hp2 NA18978.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.474-891A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078554 | |||||||
| chr12:104078587 | A | G | 29 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(26): Show |
46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.474-858A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078587 | |||||||
| chr12:104078678 | T | A | 1 | a0001c0001t0001g0088 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.474-767T>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078678 | |||||||
| chr12:104078786 | G | A | 5 | a0001c0001t0003g0012 a0001c0001t0003g0050 a0001c0001t0003g0051 others(2): Show |
9 | HG01943.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.474-659G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078786 | |||||||
| chr12:104078855 | C | T | 9 | a0001c0001t0001g0047 a0001c0001t0001g0225 a0001c0001t0001g0226 others(6): Show |
11 | HG02486.hp2 HG02615.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.474-590C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078855 | |||||||
| chr12:104078918 | C | A | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.474-527C>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078918 | |||||||
| chr12:104078995 | C | A | 1 | a0001c0001t0002g0101 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.474-450C>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078995 | |||||||
| chr12:104078996 | A | G | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.474-449A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104078996 | |||||||
| chr12:104079088 | A | C | 1 | a0001c0001t0001g0169 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.474-357A>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104079088 | |||||||
| chr12:104079125 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.474-320G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104079125 | |||||||
| chr12:104079333 | G | A | 1 | a0001c0001t0010g0108 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.474-112G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 3/14 | chr12 | 104079333 | |||||||
| chr12:104079696 | A | G | 9 | a0001c0001t0001g0022 a0001c0001t0001g0039 a0001c0001t0001g0125 others(6): Show |
12 | HG02055.hp2 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.682+43A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 4/14 | chr12 | 104079696 | |||||||
| chr12:104079769 | C | A | 1 | a0001c0001t0001g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.682+116C>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 4/14 | chr12 | 104079769 | |||||||
| chr12:104079941 | A | G | 42 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(39): Show |
71 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.682+288A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 4/14 | chr12 | 104079941 | |||||||
| chr12:104080218 | A | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
5 | HG02109.hp2 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.683-528A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 4/14 | chr12 | 104080218 | |||||||
| chr12:104080221 | T | C | 3 | a0001c0001t0014g0131 a0004c0005t0007g0136 a0004c0005t0015g0137 |
3 | HG02738.hp2 HG03209.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.683-525T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 4/14 | chr12 | 104080221 | |||||||
| chr12:104080392 | G | A | 38 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(35): Show |
60 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.683-354G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 4/14 | chr12 | 104080392 | |||||||
| chr12:104080585 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.683-161G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 4/14 | chr12 | 104080585 | |||||||
| chr12:104080952 | G | T | 1 | a0001c0001t0001g0170 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.767+122G>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | chr12 | 104080952 | |||||||
| chr12:104081067 | G | C | 1 | a0001c0001t0001g0028 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.767+237G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | chr12 | 104081067 | |||||||
| chr12:104081102 | T | G | 1 | a0001c0001t0004g0178 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.767+272T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | chr12 | 104081102 | |||||||
| chr12:104081600 | G | GT | 18 | a0001c0001t0001g0047 a0001c0001t0001g0225 a0001c0001t0001g0226 others(15): Show |
25 | HG01243.hp1 HG01516.hp2 HG01517.hp2 others(22): Show |
intron_variant | MODIFIER | c.767+786dupT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 104081600 | ||||||
| chr12:104081600 | GT | G | 13 | a0001c0001t0001g0022 a0001c0001t0001g0039 a0001c0001t0001g0060 others(10): Show |
16 | HG01257.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.767+786delT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 104081600 | ||||||
| chr12:104081624 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.767+794C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | chr12 | 104081624 | |||||||
| chr12:104081852 | C | T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0045 others(35): Show |
55 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.768-648C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | chr12 | 104081852 | |||||||
| chr12:104081904 | C | CA | 9 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0002g0104 others(6): Show |
9 | HG00621.hp2 HG00673.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.768-575dupA | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 104081904 | ||||||
| chr12:104081904 | CA | C | 36 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(33): Show |
57 | HG00323.hp2 HG00558.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.768-575delA | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 104081904 | ||||||
| chr12:104081904 | CAA | C | 9 | a0001c0001t0004g0221 a0001c0001t0007g0026 a0001c0001t0007g0132 others(6): Show |
10 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.768-576_768-575del others(2): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 104081904 | ||||||
| chr12:104081939 | TA | T | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.768-550delA | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 104081939 | ||||||
| chr12:104082167 | A | G | 1 | a0001c0001t0003g0162 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.768-333A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | chr12 | 104082167 | |||||||
| chr12:104082399 | C | T | 4 | a0001c0001t0004g0188 a0001c0001t0004g0194 a0001c0001t0004g0195 others(1): Show |
4 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.768-101C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | chr12 | 104082399 | |||||||
| chr12:104082477 | G | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0202 a0001c0001t0001g0205 |
8 | HG00735.hp1 HG01192.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.768-23G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | chr12 | 104082477 | |||||||
| chr12:104082486 | T | C | 37 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(34): Show |
64 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.768-14T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 5/14 | chr12 | 104082486 | |||||||
| chr12:104082675 | G | A | 10 | a0001c0001t0003g0012 a0001c0001t0003g0023 a0001c0001t0003g0041 others(7): Show |
17 | HG00639.hp2 HG01168.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.875-38G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 6/14 | chr12 | 104082675 | |||||||
| chr12:104083044 | T | C | 1 | a0001c0001t0009g0008 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+143T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104083044 | |||||||
| chr12:104083291 | G | A | 1 | a0004c0005t0007g0136 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1063+390G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104083291 | |||||||
| chr12:104083497 | C | T | 1 | a0004c0005t0015g0137 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1063+596C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104083497 | |||||||
| chr12:104083554 | T | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0129 |
2 | HG01106.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1063+653T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104083554 | |||||||
| chr12:104083615 | A | G | 42 | a0001c0001t0003g0002 a0001c0001t0003g0012 a0001c0001t0003g0023 others(39): Show |
69 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.1063+714A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104083615 | |||||||
| chr12:104083892 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0004g0045 |
2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1063+991C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104083892 | |||||||
| chr12:104083896 | T | C | 38 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(35): Show |
60 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.1063+995T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104083896 | |||||||
| chr12:104083963 | A | G | 4 | a0001c0001t0004g0188 a0001c0001t0004g0194 a0001c0001t0004g0195 others(1): Show |
4 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063+1062A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104083963 | |||||||
| chr12:104083971 | T | G | 1 | a0001c0001t0002g0090 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1063+1070T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104083971 | |||||||
| chr12:104084036 | G | A | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG01109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1063+1135G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104084036 | |||||||
| chr12:104084103 | G | A | 5 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(2): Show |
6 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1063+1202G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104084103 | |||||||
| chr12:104084178 | T | C | 1 | a0001c0001t0009g0008 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+1277T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104084178 | |||||||
| chr12:104084638 | G | C | 1 | a0001c0001t0004g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1063+1737G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104084638 | |||||||
| chr12:104084965 | A | G | 1 | a0004c0005t0007g0136 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1064-1882A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104084965 | |||||||
| chr12:104085012 | A | G | 42 | a0001c0001t0003g0002 a0001c0001t0003g0012 a0001c0001t0003g0023 others(39): Show |
69 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.1064-1835A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104085012 | |||||||
| chr12:104085122 | A | C | 1 | a0001c0001t0003g0040 | 2 | NA18988.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1064-1725A>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104085122 | |||||||
| chr12:104085287 | A | G | 42 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0045 others(39): Show |
59 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1064-1560A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104085287 | |||||||
| chr12:104085736 | T | TTG | 239 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(236): Show |
368 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.1064-1110_1064-110 others(6): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 104085736 | ||||||
| chr12:104085885 | C | G | 1 | a0001c0001t0004g0187 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1064-962C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104085885 | |||||||
| chr12:104085995 | A | AT | 34 | a0001c0001t0001g0036 a0001c0001t0001g0068 a0001c0001t0001g0077 others(31): Show |
41 | HG00673.hp2 HG01081.hp2 HG01361.hp2 others(38): Show |
intron_variant | MODIFIER | c.1064-832dupT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 104085995 | ||||||
| chr12:104085995 | AT | A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0091 a0001c0001t0004g0173 others(4): Show |
9 | HG01496.hp1 HG01884.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1064-832delT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 104085995 | ||||||
| chr12:104086050 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1064-797T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104086050 | |||||||
| chr12:104086058 | T | TG | 26 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0025 others(23): Show |
38 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1064-788dupG | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 104086058 | ||||||
| chr12:104086127 | A | G | 3 | a0001c0001t0014g0131 a0004c0005t0007g0136 a0004c0005t0015g0137 |
3 | HG02738.hp2 HG03209.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1064-720A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104086127 | |||||||
| chr12:104086484 | C | G | 1 | a0001c0001t0003g0041 | 2 | HG03704.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1064-363C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104086484 | |||||||
| chr12:104086619 | A | AAAAT | 78 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0021 others(75): Show |
115 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1064-194_1064-191d others(6): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 104086619 | ||||||
| chr12:104086619 | A | AAAATAAA others(1): Show |
43 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0073 others(40): Show |
74 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1064-198_1064-191d others(10): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 104086619 | ||||||
| chr12:104086619 | A | AAAATAAA others(5): Show |
5 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0001c0001t0003g0143 others(2): Show |
6 | HG01516.hp2 HG01517.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1064-202_1064-191d others(14): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 104086619 | ||||||
| chr12:104086619 | AAAAT | A | 36 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(33): Show |
53 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1064-194_1064-191d others(6): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 104086619 | ||||||
| chr12:104086619 | AAAATAAA others(5): Show |
A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0001g0076 others(7): Show |
24 | HG00438.hp1 HG00544.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1064-202_1064-191d others(14): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 104086619 | ||||||
| chr12:104086714 | A | G | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.1064-133A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104086714 | |||||||
| chr12:104086716 | C | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0170 |
4 | HG02723.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064-131C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 7/14 | chr12 | 104086716 | |||||||
| chr12:104087121 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1231+107G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087121 | |||||||
| chr12:104087249 | G | A | 1 | a0003c0004t0001g0035 | 2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1231+235G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087249 | |||||||
| chr12:104087352 | TA | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(175): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1231+355delA | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087352 | ||||||
| chr12:104087375 | A | G | 1 | a0001c0001t0009g0008 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231+361A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087375 | |||||||
| chr12:104087402 | C | T | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.1231+388C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087402 | |||||||
| chr12:104087409 | ACGTG | A | 1 | a0001c0001t0009g0008 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231+396_1231+399d others(6): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087409 | |||||||
| chr12:104087410 | CGT | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(86): Show |
127 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.1231+427_1231+428d others(4): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087410 | ||||||
| chr12:104087410 | CGTGT | C | 49 | a0001c0001t0001g0048 a0001c0001t0001g0064 a0001c0001t0001g0088 others(46): Show |
77 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.1231+425_1231+428d others(6): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087410 | ||||||
| chr12:104087410 | CGTGTGT | C | 8 | a0001c0001t0002g0065 a0001c0001t0003g0160 a0001c0001t0003g0162 others(5): Show |
9 | HG00423.hp1 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1231+423_1231+428d others(8): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087410 | ||||||
| chr12:104087410 | CGTGTGTG others(1): Show |
C | 4 | a0001c0001t0003g0139 a0001c0001t0014g0131 a0004c0005t0007g0136 others(1): Show |
4 | HG02738.hp2 HG03209.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231+421_1231+428d others(10): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087410 | ||||||
| chr12:104087410 | CGTGTGTG others(3): Show |
C | 36 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(33): Show |
63 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.1231+419_1231+428d others(12): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087410 | ||||||
| chr12:104087410 | CGTGTGTG others(15): Show |
C | 1 | a0001c0001t0001g0105 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1231+407_1231+428d others(24): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087410 | ||||||
| chr12:104087414 | T | A | 1 | a0001c0001t0009g0008 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231+400T>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087414 | |||||||
| chr12:104087437 | G | A | 2 | a0001c0001t0007g0132 a0001c0001t0007g0133 |
2 | HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1231+423G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087437 | |||||||
| chr12:104087439 | GTGTA | G | 3 | a0001c0001t0001g0216 a0001c0001t0007g0132 a0001c0001t0007g0133 |
3 | HG00673.hp2 HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1231+429_1231+432d others(6): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087439 | ||||||
| chr12:104087443 | A | G | 10 | a0001c0001t0001g0057 a0001c0001t0005g0013 a0001c0001t0005g0203 others(7): Show |
14 | HG01884.hp2 HG02257.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.1231+429A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087443 | |||||||
| chr12:104087443 | ATG | A | 20 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(17): Show |
33 | HG00558.hp1 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1231+439_1231+440d others(4): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087443 | ||||||
| chr12:104087445 | G | A | 10 | a0001c0001t0001g0216 a0001c0001t0001g0223 a0001c0001t0005g0013 others(7): Show |
14 | HG00673.hp2 HG01496.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1231+431G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087445 | |||||||
| chr12:104087447 | G | A | 1 | a0001c0001t0010g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1231+433G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087447 | |||||||
| chr12:104087455 | A | G | 2 | a0001c0001t0001g0057 a0001c0001t0010g0058 |
2 | HG01884.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1231+441A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087455 | |||||||
| chr12:104087457 | A | G | 2 | a0001c0001t0001g0057 a0001c0001t0010g0058 |
2 | HG01884.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1231+443A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087457 | |||||||
| chr12:104087466 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1231+452C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087466 | |||||||
| chr12:104087466 | CAT | C | 58 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0029 others(55): Show |
87 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1231+469_1231+470d others(4): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087466 | ||||||
| chr12:104087466 | CATAT | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(146): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1231+467_1231+470d others(6): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087466 | ||||||
| chr12:104087466 | CATATAT | C | 30 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(27): Show |
47 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.1231+465_1231+470d others(8): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087466 | ||||||
| chr12:104087467 | A | ATG | 1 | a0001c0001t0001g0018 | 3 | HG02723.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1231+454_1231+455i others(4): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087467 | ||||||
| chr12:104087468 | T | TATATATA others(15): Show |
1 | a0001c0001t0002g0032 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1231+468_1231+469i others(24): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087468 | ||||||
| chr12:104087470 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1231+456T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087470 | |||||||
| chr12:104087470 | T | TATATATA others(17): Show |
1 | a0001c0001t0007g0135 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1231+466_1231+467i others(26): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087470 | ||||||
| chr12:104087470 | T | TATATATA others(45): Show |
1 | a0001c0001t0022g0159 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1231+466_1231+467i others(54): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087470 | ||||||
| chr12:104087471 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0009g0008 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231+470_1231+483d others(16): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 104087471 | ||||||
| chr12:104087472 | T | C | 1 | a0001c0001t0010g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1231+458T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087472 | |||||||
| chr12:104087479 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1231+465A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087479 | |||||||
| chr12:104087484 | T | C | 1 | a0001c0001t0002g0032 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1231+470T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087484 | |||||||
| chr12:104087496 | T | C | 1 | a0001c0001t0001g0219 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1231+482T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087496 | |||||||
| chr12:104087652 | T | C | 3 | a0001c0001t0012g0079 a0001c0001t0012g0080 a0001c0001t0012g0081 |
3 | HG00673.hp1 HG02074.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.1232-334T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087652 | |||||||
| chr12:104087716 | G | A | 1 | a0001c0001t0009g0008 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1232-270G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087716 | |||||||
| chr12:104087913 | T | C | 4 | a0001c0001t0004g0188 a0001c0001t0004g0194 a0001c0001t0004g0195 others(1): Show |
4 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1232-73T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 8/14 | chr12 | 104087913 | |||||||
| chr12:104088150 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1284+112C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104088150 | |||||||
| chr12:104088232 | T | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0045 others(36): Show |
56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1284+194T>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104088232 | |||||||
| chr12:104088463 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(76): Show |
118 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1284+425G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104088463 | |||||||
| chr12:104088520 | T | C | 1 | a0001c0001t0020g0193 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1284+482T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104088520 | |||||||
| chr12:104088599 | G | A | 37 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(34): Show |
64 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1284+561G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104088599 | |||||||
| chr12:104088769 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1284+731G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104088769 | |||||||
| chr12:104088919 | G | C | 1 | a0001c0001t0002g0092 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1284+881G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104088919 | |||||||
| chr12:104089015 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1284+977T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089015 | |||||||
| chr12:104089043 | A | C | 1 | a0001c0001t0005g0203 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1284+1005A>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089043 | |||||||
| chr12:104089103 | C | T | 3 | a0001c0001t0014g0131 a0004c0005t0007g0136 a0004c0005t0015g0137 |
3 | HG02738.hp2 HG03209.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1284+1065C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089103 | |||||||
| chr12:104089104 | G | A | 3 | a0001c0001t0001g0130 a0001c0001t0001g0234 a0001c0001t0001g0235 |
3 | HG01109.hp2 HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1284+1066G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089104 | |||||||
| chr12:104089143 | C | A | 1 | a0001c0001t0004g0182 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1284+1105C>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089143 | |||||||
| chr12:104089171 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1284+1133G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089171 | |||||||
| chr12:104089448 | G | A | 2 | a0001c0001t0004g0180 a0001c0001t0004g0183 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1284+1410G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089448 | |||||||
| chr12:104089649 | C | T | 1 | a0001c0001t0014g0131 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1284+1611C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089649 | |||||||
| chr12:104089659 | T | G | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.1284+1621T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089659 | |||||||
| chr12:104089795 | T | C | 2 | a0001c0001t0001g0019 a0001c0001t0010g0019 |
3 | HG00738.hp2 HG03490.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1284+1757T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089795 | |||||||
| chr12:104089816 | C | G | 1 | a0001c0001t0010g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1284+1778C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089816 | |||||||
| chr12:104089837 | C | T | 29 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(26): Show |
46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1284+1799C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089837 | |||||||
| chr12:104089850 | A | T | 1 | a0001c0001t0003g0150 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1284+1812A>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104089850 | |||||||
| chr12:104090022 | G | A | 5 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(2): Show |
6 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1284+1984G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104090022 | |||||||
| chr12:104090164 | T | A | 5 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(2): Show |
6 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1284+2126T>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104090164 | |||||||
| chr12:104090198 | A | G | 1 | a0001c0001t0009g0008 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1284+2160A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104090198 | |||||||
| chr12:104090268 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1284+2230A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104090268 | |||||||
| chr12:104090284 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1284+2246C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104090284 | |||||||
| chr12:104090497 | C | CT | 36 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(33): Show |
54 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.1284+2469dupT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 104090497 | ||||||
| chr12:104090698 | C | CA | 38 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(35): Show |
60 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.1284+2665dupA | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 104090698 | ||||||
| chr12:104090942 | G | T | 2 | a0001c0001t0004g0177 a0001c0001t0004g0197 |
2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1285-2444G>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104090942 | |||||||
| chr12:104090960 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1285-2426T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104090960 | |||||||
| chr12:104090986 | T | G | 39 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0045 others(36): Show |
56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1285-2400T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104090986 | |||||||
| chr12:104091014 | G | A | 1 | a0001c0001t0004g0044 | 2 | HG02602.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1285-2372G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104091014 | |||||||
| chr12:104091026 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0045 others(36): Show |
56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1285-2360G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104091026 | |||||||
| chr12:104091190 | A | G | 3 | a0001c0001t0003g0023 a0001c0001t0003g0158 a0001c0001t0022g0159 |
5 | HG00639.hp2 HG01168.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1285-2196A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104091190 | |||||||
| chr12:104091449 | C | T | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.1285-1937C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104091449 | |||||||
| chr12:104091500 | G | A | 29 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(26): Show |
46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1285-1886G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104091500 | |||||||
| chr12:104091592 | G | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0045 others(38): Show |
58 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1285-1794G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104091592 | |||||||
| chr12:104091744 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1285-1642T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104091744 | |||||||
| chr12:104091984 | A | C | 1 | a0001c0001t0001g0231 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1285-1402A>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104091984 | |||||||
| chr12:104092151 | G | T | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.1285-1235G>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104092151 | |||||||
| chr12:104092185 | C | T | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.1285-1201C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104092185 | |||||||
| chr12:104092255 | C | G | 1 | a0001c0001t0003g0147 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1285-1131C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104092255 | |||||||
| chr12:104093026 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1285-360C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104093026 | |||||||
| chr12:104093270 | G | A | 1 | a0001c0001t0004g0181 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1285-116G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 9/14 | chr12 | 104093270 | |||||||
| chr12:104093621 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1462+58G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104093621 | |||||||
| chr12:104093776 | A | AT | 229 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(226): Show |
358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.1462+227dupT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 104093776 | ||||||
| chr12:104093779 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1462+216T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104093779 | |||||||
| chr12:104093799 | G | GCTGTTAC others(370): Show |
1 | a0001c0001t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1462+237_1462+238i others(379): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 104093799 | ||||||
| chr12:104093827 | A | C | 1 | a0001c0001t0001g0226 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1462+264A>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104093827 | |||||||
| chr12:104093946 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1462+383C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104093946 | |||||||
| chr12:104093968 | C | G | 2 | a0001c0001t0002g0031 a0001c0001t0002g0097 |
3 | NA18947.hp2 NA19004.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1462+405C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104093968 | |||||||
| chr12:104094058 | G | A | 1 | a0001c0001t0003g0145 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1462+495G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104094058 | |||||||
| chr12:104094102 | T | C | 2 | a0001c0001t0004g0178 a0001c0001t0004g0179 |
2 | HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1462+539T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104094102 | |||||||
| chr12:104094172 | A | G | 1 | a0001c0001t0020g0193 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1462+609A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104094172 | |||||||
| chr12:104094200 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1462+637C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104094200 | |||||||
| chr12:104094214 | T | G | 1 | a0001c0001t0001g0057 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1462+651T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104094214 | |||||||
| chr12:104094380 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0004g0055 |
2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1462+817C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104094380 | |||||||
| chr12:104094403 | C | A | 2 | a0001c0001t0001g0057 a0001c0001t0010g0058 |
2 | HG01884.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1462+840C>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104094403 | |||||||
| chr12:104094692 | A | G | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.1463-668A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104094692 | |||||||
| chr12:104095100 | AT | A | 41 | a0001c0001t0003g0002 a0001c0001t0003g0012 a0001c0001t0003g0023 others(38): Show |
68 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.1463-257delT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 104095100 | ||||||
| chr12:104095128 | C | T | 5 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(2): Show |
6 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1463-232C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104095128 | |||||||
| chr12:104095147 | G | A | 6 | a0001c0001t0001g0022 a0001c0001t0001g0039 a0001c0001t0001g0125 others(3): Show |
9 | HG02055.hp2 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1463-213G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104095147 | |||||||
| chr12:104095149 | A | G | 4 | a0001c0001t0003g0023 a0001c0001t0003g0041 a0001c0001t0003g0158 others(1): Show |
7 | HG00639.hp2 HG01168.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.1463-211A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104095149 | |||||||
| chr12:104095187 | C | G | 6 | a0001c0001t0001g0022 a0001c0001t0001g0039 a0001c0001t0001g0125 others(3): Show |
9 | HG02055.hp2 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1463-173C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104095187 | |||||||
| chr12:104095243 | G | C | 1 | a0001c0001t0007g0132 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1463-117G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104095243 | |||||||
| chr12:104095342 | T | C | 42 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0045 others(39): Show |
59 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1463-18T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 10/14 | chr12 | 104095342 | |||||||
| chr12:104095623 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1666+60C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 11/14 | chr12 | 104095623 | |||||||
| chr12:104095884 | C | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0202 a0001c0001t0001g0205 |
8 | HG00735.hp1 HG01192.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1666+321C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 11/14 | chr12 | 104095884 | |||||||
| chr12:104095925 | A | G | 1 | a0001c0001t0004g0044 | 2 | HG02602.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1666+362A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 11/14 | chr12 | 104095925 | |||||||
| chr12:104096267 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1667-93C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 11/14 | chr12 | 104096267 | |||||||
| chr12:104096287 | A | G | 1 | a0002c0003t0001g0037 | 2 | HG01081.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1667-73A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 11/14 | chr12 | 104096287 | |||||||
| chr12:104096563 | A | C | 1 | a0001c0001t0009g0008 | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1740+130A>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104096563 | |||||||
| chr12:104096814 | G | A | 1 | a0001c0001t0003g0164 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1740+381G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104096814 | |||||||
| chr12:104096824 | A | C | 1 | a0001c0001t0001g0205 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1740+391A>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104096824 | |||||||
| chr12:104096875 | G | A | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.1740+442G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104096875 | |||||||
| chr12:104096891 | A | G | 9 | a0001c0001t0001g0022 a0001c0001t0001g0039 a0001c0001t0001g0125 others(6): Show |
12 | HG02055.hp2 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1740+458A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104096891 | |||||||
| chr12:104096929 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0045 others(36): Show |
56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1740+496G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104096929 | |||||||
| chr12:104097014 | A | G | 1 | a0001c0001t0010g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1740+581A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104097014 | |||||||
| chr12:104097130 | T | G | 10 | a0001c0001t0001g0022 a0001c0001t0001g0128 a0001c0001t0007g0026 others(7): Show |
13 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.1740+697T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104097130 | |||||||
| chr12:104097200 | C | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(201): Show |
309 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(306): Show |
intron_variant | MODIFIER | c.1740+767C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104097200 | |||||||
| chr12:104097266 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1740+833C>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104097266 | |||||||
| chr12:104097496 | CT | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0045 others(38): Show |
58 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1741-837delT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 104097496 | ||||||
| chr12:104097512 | TAA | T | 47 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0056 others(44): Show |
74 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1741-829_1741-828d others(4): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 104097512 | ||||||
| chr12:104097770 | G | C | 1 | a0001c0001t0002g0124 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1741-573G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104097770 | |||||||
| chr12:104098070 | A | G | 1 | a0001c0001t0002g0094 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1741-273A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104098070 | |||||||
| chr12:104098169 | C | G | 4 | a0001c0001t0002g0011 a0001c0001t0002g0084 a0001c0001t0002g0087 others(1): Show |
8 | NA18951.hp2 NA18973.hp2 NA18979.hp2 others(5): Show |
intron_variant | MODIFIER | c.1741-174C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104098169 | |||||||
| chr12:104098225 | A | G | 62 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0029 others(59): Show |
94 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1741-118A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | chr12 | 104098225 | |||||||
| chr12:104098321 | AT | A | 5 | a0001c0001t0001g0047 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
6 | HG02615.hp1 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1741-13delT | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 104098321 | ||||||
| chr12:104098682 | G | A | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG01109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1878+202G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104098682 | |||||||
| chr12:104098691 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0091 |
2 | HG01496.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1878+211G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104098691 | |||||||
| chr12:104098857 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(80): Show |
122 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1878+377A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104098857 | |||||||
| chr12:104098860 | C | T | 5 | a0001c0001t0001g0110 a0001c0001t0003g0023 a0001c0001t0003g0041 others(2): Show |
8 | HG00639.hp2 HG01074.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1878+380C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104098860 | |||||||
| chr12:104098935 | G | A | 1 | a0001c0001t0003g0149 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1878+455G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104098935 | |||||||
| chr12:104099161 | T | C | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.1878+681T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104099161 | |||||||
| chr12:104099269 | T | G | 12 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0001t0004g0017 others(9): Show |
13 | HG00099.hp2 HG01168.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.1878+789T>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104099269 | |||||||
| chr12:104099301 | C | T | 62 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0029 others(59): Show |
94 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1878+821C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104099301 | |||||||
| chr12:104099403 | A | C | 8 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(5): Show |
9 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.1878+923A>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104099403 | |||||||
| chr12:104099437 | C | T | 5 | a0001c0001t0001g0036 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
7 | HG01081.hp2 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1878+957C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104099437 | |||||||
| chr12:104099516 | G | A | 1 | a0001c0001t0002g0093 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1878+1036G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104099516 | |||||||
| chr12:104099617 | T | A | 72 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0018 others(69): Show |
108 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1878+1137T>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104099617 | |||||||
| chr12:104099908 | C | T | 1 | a0001c0001t0002g0083 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1878+1428C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104099908 | |||||||
| chr12:104100040 | C | T | 3 | a0001c0001t0014g0131 a0004c0005t0007g0136 a0004c0005t0015g0137 |
3 | HG02738.hp2 HG03209.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1878+1560C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100040 | |||||||
| chr12:104100074 | A | G | 1 | a0001c0001t0002g0100 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1878+1594A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100074 | |||||||
| chr12:104100084 | A | T | 1 | a0001c0001t0001g0018 | 3 | HG02723.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1878+1604A>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100084 | |||||||
| chr12:104100197 | C | T | 1 | a0001c0001t0002g0103 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1878+1717C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100197 | |||||||
| chr12:104100316 | C | G | 1 | a0001c0001t0001g0109 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1879-1652C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100316 | |||||||
| chr12:104100320 | C | T | 1 | a0001c0001t0002g0030 | 2 | NA19066.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1879-1648C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100320 | |||||||
| chr12:104100377 | G | A | 5 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(2): Show |
6 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1879-1591G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100377 | |||||||
| chr12:104100518 | G | T | 2 | a0001c0001t0002g0034 a0001c0001t0002g0116 |
3 | HG02523.hp2 NA18978.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1879-1450G>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100518 | |||||||
| chr12:104100558 | A | C | 29 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(26): Show |
46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1879-1410A>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100558 | |||||||
| chr12:104100593 | T | C | 1 | a0001c0001t0021g0052 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1879-1375T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100593 | |||||||
| chr12:104100648 | C | T | 1 | a0001c0001t0003g0163 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1879-1320C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100648 | |||||||
| chr12:104100757 | G | C | 5 | a0001c0001t0007g0026 a0001c0001t0007g0132 a0001c0001t0007g0133 others(2): Show |
6 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1879-1211G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104100757 | |||||||
| chr12:104101056 | CTCTG | C | 29 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0024 others(26): Show |
46 | HG00558.hp1 HG00673.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1879-908_1879-905d others(6): Show |
HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 104101056 | ||||||
| chr12:104101135 | G | A | 1 | a0001c0001t0011g0117 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1879-833G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104101135 | |||||||
| chr12:104101506 | G | A | 3 | a0001c0001t0014g0131 a0004c0005t0007g0136 a0004c0005t0015g0137 |
3 | HG02738.hp2 HG03209.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1879-462G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 13/14 | chr12 | 104101506 | |||||||
| chr12:104102496 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(74): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.2064+343A>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 14/14 | chr12 | 104102496 | |||||||
| chr12:104102505 | G | C | 3 | a0001c0001t0014g0131 a0004c0005t0007g0136 a0004c0005t0015g0137 |
3 | HG02738.hp2 HG03209.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2064+352G>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 14/14 | chr12 | 104102505 | |||||||
| chr12:104102584 | T | C | 1 | a0004c0005t0007g0136 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2065-375T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 14/14 | chr12 | 104102584 | |||||||
| chr12:104102649 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2065-310G>A | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 14/14 | chr12 | 104102649 | |||||||
| chr12:104102844 | T | C | 5 | a0001c0001t0001g0036 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
7 | HG01081.hp2 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.2065-115T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 14/14 | chr12 | 104102844 | |||||||
| chr12:104102942 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2065-17T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 14/14 | chr12 | 104102942 | |||||||
| chr12:104102943 | T | C | 3 | a0001c0001t0001g0110 a0001c0001t0001g0112 a0001c0001t0001g0169 |
3 | HG01074.hp1 HG02818.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.2065-16T>C | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 14/14 | chr12 | 104102943 | |||||||
| chr12:104102943 | T | TC | 33 | a0001c0001t0001g0039 a0001c0001t0001g0125 a0001c0001t0001g0126 others(30): Show |
53 | HG00408.hp2 HG00621.hp2 HG01123.hp2 others(50): Show |
splice_region_variant&intron_variant | LOW | c.2065-7dupC | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 104102943 | ||||||
| chr12:104102946 | C | T | 39 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0045 others(36): Show |
56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.2065-13C>T | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 14/14 | chr12 | 104102946 | |||||||
| chr12:104102949 | C | G | 1 | a0001c0001t0001g0169 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2065-10C>G | HCFC2 | ENSG00000111727.12 | transcript | ENST00000229330.9 | protein_coding | 14/14 | chr12 | 104102949 |