Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51101 |
| ensemblid | ENSG00000104427.13 |
| hgncid | 24277 |
| symbol | ZC2HC1A |
| name | zinc finger C2HC-type containing 1A |
| refseq_nuc | NM_016010.3 |
| refseq_prot | NP_057094.2 |
| ensembl_nuc | ENST00000263849.9 |
| ensembl_prot | ENSP00000263849.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 78666089 |
| end | 78719765 |
| strand | + |
| ver | v1.2 |
| region | chr8:78666089-78719765 |
| region5000 | chr8:78661089-78724765 |
| regionname0 | ZC2HC1A_chr8_78666089_78719765 |
| regionname5000 | ZC2HC1A_chr8_78661089_78724765 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 325 | 259 | 83 | 55 | 80 | 16 | 23 | 58 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | MEGLE others(320): Show |
chr8 | 78661089 | 78724765 |
| a0002 | 0/0 | 325 | 3 | 1 | 1 | 0 | 0 | 1 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | MEGME others(320): Show |
chr8 | 78661089 | 78724765 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 975 | 162 | 41 | 40 | 55 | 9 | 17 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | ATGGA others(970): Show |
chr8 | 78661089 | 78724765 | ||
| a0001c0002 | 1/0 | 975 | 87 | 37 | 13 | 24 | 6 | 6 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | ATGGA others(970): Show |
chr8 | 78661089 | 78724765 | ||
| a0001c0003 | 0/1 | 975 | 8 | 5 | 1 | 0 | 1 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | ATGGA others(970): Show |
chr8 | 78661089 | 78724765 | ||
| a0001c0005 | 0/0 | 975 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | ATGGA others(970): Show |
chr8 | 78661089 | 78724765 | ||
| a0001c0006 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | ATGGA others(970): Show |
chr8 | 78661089 | 78724765 | ||
| a0002c0004 | 0/0 | 975 | 3 | 1 | 1 | 0 | 0 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | ATGGA others(970): Show |
chr8 | 78661089 | 78724765 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3310 | 142 | 28 | 37 | 51 | 9 | 17 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | AGAGC others(3305): Show |
chr8 | 78661089 | 78724765 |
| a0001c0001t0003 | 0/0 | 3309 | 12 | 9 | 2 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | AGAGC others(3304): Show |
chr8 | 78661089 | 78724765 |
| a0001c0001t0004 | 0/0 | 3310 | 5 | 4 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | AGAGC others(3305): Show |
chr8 | 78661089 | 78724765 |
| a0001c0001t0011 | 0/0 | 3310 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | AGAGC others(3305): Show |
chr8 | 78661089 | 78724765 |
| a0001c0001t0012 | 0/0 | 3310 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | AGAGC others(3305): Show |
chr8 | 78661089 | 78724765 |
| a0001c0001t0013 | 0/0 | 3310 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | AGAGC others(3305): Show |
chr8 | 78661089 | 78724765 |
| a0001c0002t0002 | 1/0 | 3310 | 75 | 30 | 8 | 24 | 6 | 6 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | AGAGC others(3305): Show |
chr8 | 78661089 | 78724765 |
| a0001c0002t0006 | 0/0 | 3309 | 5 | 4 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | AGAGC others(3304): Show |
chr8 | 78661089 | 78724765 |
| a0001c0002t0007 | 0/0 | 3310 | 4 | 2 | 2 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | AGAGC others(3305): Show |
chr8 | 78661089 | 78724765 |
| a0001c0002t0009 | 0/0 | 3310 | 2 | 0 | 2 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | AGAGC others(3305): Show |
chr8 | 78661089 | 78724765 |
| a0001c0002t0014 | 0/0 | 3311 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | AGAGC others(3306): Show |
chr8 | 78661089 | 78724765 |
| a0001c0003t0005 | 0/0 | 3310 | 5 | 5 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | AGAGC others(3305): Show |
chr8 | 78661089 | 78724765 |
| a0001c0003t0008 | 0/1 | 3310 | 3 | 0 | 1 | 0 | 1 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | AGAGC others(3305): Show |
chr8 | 78661089 | 78724765 |
| a0001c0005t0010 | 0/0 | 3310 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | AGAGC others(3305): Show |
chr8 | 78661089 | 78724765 |
| a0001c0006t0001 | 0/0 | 3310 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | AGAGC others(3305): Show |
chr8 | 78661089 | 78724765 |
| a0002c0004t0003 | 0/0 | 3309 | 3 | 1 | 1 | 0 | 0 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | AGAGC others(3304): Show |
chr8 | 78661089 | 78724765 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 10 | 0 | 7 | 2 | 0 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 0 | 6 | 1 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 2 | 2 | 2 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0005 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0003g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0003g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0011g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0012g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0001t0013g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0004 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0006 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0011 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0030 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0006g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0006g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0007g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0007g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0009g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0009g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0002t0014g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0003t0005g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0003t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0003t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0003t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0003t0008g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0003t0008g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0003t0008g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0005t0010g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0001c0006t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0002c0004t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0002c0004t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| a0002c0004t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | GBR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0030 | EUR | GBR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0011 | EUR | GBR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0164 | EUR | FIN | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0159 | EAS | CHS | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG00738 | hp2 | a0001 | c0003 | t0008 | g0151 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0166 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01069 | hp1 | a0001 | c0002 | t0006 | g0183 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01070 | hp1 | a0001 | c0002 | t0009 | g0177 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01071 | hp2 | a0001 | c0002 | t0009 | g0176 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01081 | hp2 | a0001 | c0002 | t0007 | g0013 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0157 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0041 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0167 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0156 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01243 | hp2 | a0001 | c0002 | t0007 | g0013 | AMR | PUR | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | CLM | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0139 | AMR | CLM | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01346 | hp2 | a0001 | c0005 | t0010 | g0070 | AMR | CLM | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0165 | AMR | CLM | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | IBS | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0031 | EUR | IBS | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0006 | EUR | IBS | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0031 | EUR | IBS | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0057 | AFR | ACB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | ACB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0033 | AFR | ACB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0049 | AFR | ACB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01943 | hp2 | a0002 | c0004 | t0003 | g0186 | AMR | PEL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0171 | EAS | KHV | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02040 | hp2 | a0001 | c0001 | t0011 | g0073 | EAS | KHV | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | ACB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02145 | hp1 | a0001 | c0002 | t0006 | g0184 | AFR | ACB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0030 | AFR | ACB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02258 | hp1 | a0001 | c0003 | t0005 | g0179 | AFR | ACB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02615 | hp2 | a0001 | c0002 | t0006 | g0035 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0029 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02630 | hp1 | a0001 | c0002 | t0014 | g0018 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0037 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02647 | hp2 | a0001 | c0003 | t0005 | g0034 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02717 | hp2 | a0002 | c0004 | t0003 | g0188 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0036 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02738 | hp2 | a0002 | c0004 | t0003 | g0187 | SAS | PJL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02818 | hp1 | a0001 | c0003 | t0005 | g0034 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0042 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0055 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0039 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | ESN | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0122 | AFR | ESN | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0028 | AFR | ESN | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0120 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0028 | AFR | MSL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | MSL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0018 | AFR | ESN | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0045 | AFR | ESN | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03195 | hp1 | a0001 | c0002 | t0006 | g0185 | AFR | ESN | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | ESN | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0175 | AFR | MSL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | MSL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0097 | AFR | MSL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03486 | hp2 | a0001 | c0003 | t0005 | g0180 | AFR | MSL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0048 | AFR | ESN | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | ESN | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03540 | hp1 | a0001 | c0003 | t0005 | g0178 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03579 | hp1 | a0001 | c0002 | t0007 | g0182 | AFR | MSL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0192 | SAS | STU | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0158 | SAS | PJL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0191 | SAS | BEB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0173 | SAS | BEB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | STU | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0193 | SAS | STU | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18522 | hp1 | a0001 | c0002 | t0006 | g0035 | AFR | YRI | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | CHB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0152 | AFR | YRI | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18959 | hp2 | a0001 | c0002 | t0002 | g0160 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18985 | hp2 | a0001 | c0001 | t0012 | g0129 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19001 | hp2 | a0001 | c0006 | t0001 | g0119 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0153 | AFR | LWK | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0029 | AFR | LWK | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0038 | AFR | LWK | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19059 | hp1 | a0001 | c0001 | t0013 | g0131 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0172 | AFR | YRI | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ASW | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0047 | AFR | ASW | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | TSI | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | TSI | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA20805 | hp2 | a0001 | c0003 | t0008 | g0150 | EUR | TSI | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0033 | AFR | ACB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02109 | hp2 | a0001 | c0002 | t0007 | g0181 | AFR | ACB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0046 | AFR | ACB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | ACB | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0140 | AFR | MSL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0058 | AFR | MSL | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0138 | AFR | LWK | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0168 | AFR | LWK | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0008 | g0149 | REF | REF | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0011 | REF | REF | ZC2HC1A_chr8_78661089_78724765 | ZC2HC1A | chr8 | 78661089 | 78724765 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:78666158 | C | A | 1 | a0002 | 3 | HG01943.hp2 HG02717.hp2 HG02738.hp2 |
missense_variant | MODERATE | c.10C>A | p.Leu4Met | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/9 | 70/3310 | 10/978 | 4/325 | chr8 | 78666158 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:78678616 | T | C | 1 | a0001c0005 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.147T>C | p.Phe49Phe | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/9 | 207/3310 | 147/978 | 49/325 | chr8 | 78678616 | |||
| chr8:78689343 | C | A | 1 | a0001c0006 | 1 | NA19001.hp2 | synonymous_variant | LOW | c.474C>A | p.Thr158Thr | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/9 | 534/3310 | 474/978 | 158/325 | chr8 | 78689343 | |||
| chr8:78697412 | G | A | 1 | a0001c0003 | 7 | HG00738.hp2 HG02258.hp1 HG02647.hp2 others(4): Show |
synonymous_variant | LOW | c.510G>A | p.Lys170Lys | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 6/9 | 570/3310 | 510/978 | 170/325 | chr8 | 78697412 | |||
| chr8:78698475 | A | G | 4 | a0001c0001 a0001c0005 a0001c0006 others(1): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
synonymous_variant | LOW | c.666A>G | p.Leu222Leu | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/9 | 726/3310 | 666/978 | 222/325 | chr8 | 78698475 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:78666135 | G | A | 1 | a0001c0005t0010 | 1 | HG01346.hp2 | 5_prime_UTR_variant | MODIFIER | c.-14G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/9 | 14 | chr8 | 78666135 | ||||||
| chr8:78717503 | C | CA | 8 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0011 others(5): Show |
153 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*24dupA | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 9/9 | 25 | INFO_REALIGN_3_PRIME | chr8 | 78717503 | |||||
| chr8:78717944 | G | A | 1 | a0001c0003t0005 | 5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*451G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 9/9 | 451 | chr8 | 78717944 | ||||||
| chr8:78718036 | C | T | 1 | a0001c0003t0005 | 5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*543C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 9/9 | 543 | chr8 | 78718036 | ||||||
| chr8:78718106 | G | A | 11 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(8): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*613G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 9/9 | 613 | chr8 | 78718106 | ||||||
| chr8:78718180 | T | G | 1 | a0001c0001t0011 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*687T>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 9/9 | 687 | chr8 | 78718180 | ||||||
| chr8:78718332 | A | G | 1 | a0001c0001t0013 | 1 | NA19059.hp1 | 3_prime_UTR_variant | MODIFIER | c.*839A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 9/9 | 839 | chr8 | 78718332 | ||||||
| chr8:78718373 | A | C | 9 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(6): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*880A>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 9/9 | 880 | chr8 | 78718373 | ||||||
| chr8:78718449 | A | G | 1 | a0001c0001t0012 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*956A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 9/9 | 956 | chr8 | 78718449 | ||||||
| chr8:78718550 | C | G | 1 | a0001c0002t0009 | 2 | HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1057C>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 9/9 | 1057 | chr8 | 78718550 | ||||||
| chr8:78718662 | A | T | 1 | a0001c0001t0004 | 5 | HG01256.hp1 HG02717.hp1 HG03453.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1169A>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 9/9 | 1169 | chr8 | 78718662 | ||||||
| chr8:78719008 | C | T | 1 | a0001c0002t0006 | 5 | HG01069.hp1 HG02145.hp1 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1515C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 9/9 | 1515 | chr8 | 78719008 | ||||||
| chr8:78719234 | AT | A | 9 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(6): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*1748delT | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 9/9 | 1748 | INFO_REALIGN_3_PRIME | chr8 | 78719234 | |||||
| chr8:78719515 | TA | T | 1 | a0001c0002t0006 | 5 | HG01069.hp1 HG02145.hp1 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2030delA | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 9/9 | 2030 | INFO_REALIGN_3_PRIME | chr8 | 78719515 | |||||
| chr8:78719672 | G | T | 1 | a0001c0002t0007 | 4 | HG01081.hp2 HG01243.hp2 HG02109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2179G>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 9/9 | 2179 | chr8 | 78719672 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:78666371 | C | T | 1 | a0001c0001t0003g0195 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.16+207C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78666371 | |||||||
| chr8:78666391 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.16+227C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78666391 | |||||||
| chr8:78666564 | C | G | 3 | a0001c0002t0002g0191 a0001c0002t0002g0192 a0001c0002t0002g0193 |
3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.16+400C>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78666564 | |||||||
| chr8:78666657 | A | T | 1 | a0001c0001t0001g0190 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.16+493A>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78666657 | |||||||
| chr8:78666738 | A | T | 1 | a0001c0001t0001g0189 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.16+574A>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78666738 | |||||||
| chr8:78666834 | C | T | 3 | a0002c0004t0003g0186 a0002c0004t0003g0187 a0002c0004t0003g0188 |
3 | HG01943.hp2 HG02717.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.16+670C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78666834 | |||||||
| chr8:78666893 | T | A | 5 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(2): Show |
6 | HG02055.hp2 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.16+729T>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78666893 | |||||||
| chr8:78666929 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.16+765G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78666929 | |||||||
| chr8:78667060 | C | G | 9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.16+896C>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78667060 | |||||||
| chr8:78667205 | C | T | 2 | a0001c0002t0007g0181 a0001c0002t0007g0182 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.16+1041C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78667205 | |||||||
| chr8:78667297 | A | C | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.16+1133A>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78667297 | |||||||
| chr8:78667474 | A | G | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.16+1310A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78667474 | |||||||
| chr8:78667607 | C | T | 35 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0009 others(32): Show |
52 | HG00099.hp2 HG00280.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.16+1443C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78667607 | |||||||
| chr8:78667736 | G | A | 1 | a0002c0004t0003g0186 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.16+1572G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78667736 | |||||||
| chr8:78667830 | A | G | 2 | a0001c0003t0008g0150 a0001c0003t0008g0151 |
2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.16+1666A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78667830 | |||||||
| chr8:78667959 | A | AT | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(110): Show |
153 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.16+1807dupT | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 78667959 | ||||||
| chr8:78669078 | TTC | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(71): Show |
100 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.16+2916_16+2917del others(2): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 78669078 | ||||||
| chr8:78669087 | G | A | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG01261.hp2 HG01928.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.16+2923G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78669087 | |||||||
| chr8:78669132 | TTCTTTA | T | 4 | a0001c0002t0002g0018 a0001c0002t0002g0057 a0001c0002t0002g0058 others(1): Show |
4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+2976_16+2981del others(6): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 78669132 | ||||||
| chr8:78669277 | C | T | 3 | a0001c0001t0003g0017 a0001c0001t0003g0055 a0001c0001t0003g0056 |
4 | HG01167.hp2 HG01169.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.16+3113C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78669277 | |||||||
| chr8:78669300 | C | T | 6 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(3): Show |
7 | HG00738.hp2 HG02258.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.16+3136C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78669300 | |||||||
| chr8:78669305 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.16+3141A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78669305 | |||||||
| chr8:78669386 | G | GCTAAGTA others(69): Show |
9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.16+3223_16+3298dup others(76): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 78669386 | ||||||
| chr8:78669393 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.16+3229A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78669393 | |||||||
| chr8:78669497 | G | A | 9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.16+3333G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78669497 | |||||||
| chr8:78669501 | C | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.16+3337C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78669501 | |||||||
| chr8:78669532 | A | C | 1 | a0001c0003t0005g0034 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.16+3368A>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78669532 | |||||||
| chr8:78669549 | G | T | 1 | a0001c0002t0002g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.16+3385G>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78669549 | |||||||
| chr8:78669608 | A | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.16+3444A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78669608 | |||||||
| chr8:78669679 | TAAAC | T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG03239.hp2 HG04184.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.16+3520_16+3523del others(4): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 78669679 | ||||||
| chr8:78669746 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.16+3582C>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78669746 | |||||||
| chr8:78669913 | T | A | 2 | a0001c0003t0008g0150 a0001c0003t0008g0151 |
2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.16+3749T>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78669913 | |||||||
| chr8:78669964 | TTTC | T | 10 | a0001c0001t0003g0016 a0001c0001t0003g0195 a0001c0002t0002g0010 others(7): Show |
13 | HG02055.hp2 HG02145.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.16+3803_16+3805del others(3): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 78669964 | ||||||
| chr8:78669967 | C | CT | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(119): Show |
164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.16+3806dupT | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | 78669967 | ||||||
| chr8:78669971 | C | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(139): Show |
189 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.16+3807C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78669971 | |||||||
| chr8:78670054 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.16+3890G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78670054 | |||||||
| chr8:78670063 | G | A | 2 | a0001c0001t0003g0016 a0001c0001t0003g0195 |
3 | HG02818.hp2 HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.16+3899G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78670063 | |||||||
| chr8:78670261 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.16+4097T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78670261 | |||||||
| chr8:78670265 | C | T | 4 | a0001c0002t0002g0018 a0001c0002t0002g0057 a0001c0002t0002g0058 others(1): Show |
4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+4101C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78670265 | |||||||
| chr8:78670419 | T | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.16+4255T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78670419 | |||||||
| chr8:78670622 | A | G | 1 | a0002c0004t0003g0188 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.16+4458A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78670622 | |||||||
| chr8:78670653 | T | C | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG02004.hp1 HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.16+4489T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78670653 | |||||||
| chr8:78670685 | A | G | 2 | a0001c0002t0009g0176 a0001c0002t0009g0177 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.16+4521A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78670685 | |||||||
| chr8:78670828 | T | C | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.16+4664T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78670828 | |||||||
| chr8:78670845 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG00738.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.16+4681G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78670845 | |||||||
| chr8:78671202 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.17-4585T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78671202 | |||||||
| chr8:78671417 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.17-4370A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78671417 | |||||||
| chr8:78671489 | A | G | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.17-4298A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78671489 | |||||||
| chr8:78671530 | T | A | 1 | a0001c0003t0005g0034 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.17-4257T>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78671530 | |||||||
| chr8:78671641 | C | G | 1 | a0001c0001t0001g0144 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.17-4146C>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78671641 | |||||||
| chr8:78671672 | A | AG | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.17-4115_17-4114ins others(1): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78671672 | |||||||
| chr8:78671793 | T | G | 1 | a0001c0003t0005g0178 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.17-3994T>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78671793 | |||||||
| chr8:78671850 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0094 |
3 | HG00673.hp2 HG02080.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.17-3937T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78671850 | |||||||
| chr8:78671940 | C | T | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.17-3847C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78671940 | |||||||
| chr8:78672225 | T | A | 5 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0055 others(2): Show |
7 | HG01167.hp2 HG01169.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.17-3562T>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78672225 | |||||||
| chr8:78672327 | A | G | 3 | a0001c0002t0002g0191 a0001c0002t0002g0192 a0001c0002t0002g0193 |
3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.17-3460A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78672327 | |||||||
| chr8:78672345 | C | G | 2 | a0001c0003t0008g0150 a0001c0003t0008g0151 |
2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.17-3442C>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78672345 | |||||||
| chr8:78672397 | C | G | 5 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(2): Show |
6 | HG02055.hp2 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.17-3390C>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78672397 | |||||||
| chr8:78672404 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.17-3383T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78672404 | |||||||
| chr8:78672480 | C | T | 1 | a0001c0002t0002g0048 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.17-3307C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78672480 | |||||||
| chr8:78672573 | T | C | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG01261.hp2 HG01928.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.17-3214T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78672573 | |||||||
| chr8:78672794 | T | A | 6 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(3): Show |
7 | HG00738.hp2 HG02258.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.17-2993T>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78672794 | |||||||
| chr8:78672909 | T | A | 3 | a0002c0004t0003g0186 a0002c0004t0003g0187 a0002c0004t0003g0188 |
3 | HG01943.hp2 HG02717.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.17-2878T>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78672909 | |||||||
| chr8:78672967 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0052 |
3 | HG03209.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.17-2820A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78672967 | |||||||
| chr8:78673013 | G | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(107): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.17-2774G>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78673013 | |||||||
| chr8:78673435 | A | G | 4 | a0001c0002t0002g0018 a0001c0002t0002g0057 a0001c0002t0002g0058 others(1): Show |
4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-2352A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78673435 | |||||||
| chr8:78673515 | A | C | 9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.17-2272A>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78673515 | |||||||
| chr8:78673577 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.17-2210G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78673577 | |||||||
| chr8:78673589 | C | A | 1 | a0001c0001t0004g0097 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.17-2198C>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78673589 | |||||||
| chr8:78673649 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.17-2138C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78673649 | |||||||
| chr8:78673700 | C | T | 3 | a0001c0002t0002g0191 a0001c0002t0002g0192 a0001c0002t0002g0193 |
3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.17-2087C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78673700 | |||||||
| chr8:78673842 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.17-1945A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78673842 | |||||||
| chr8:78674198 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0050 others(1): Show |
6 | HG01109.hp1 HG02886.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.17-1589G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78674198 | |||||||
| chr8:78674220 | C | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.17-1567C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78674220 | |||||||
| chr8:78674230 | C | G | 1 | a0002c0004t0003g0187 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.17-1557C>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78674230 | |||||||
| chr8:78674617 | T | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.17-1170T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78674617 | |||||||
| chr8:78674778 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG03831.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.17-1009T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78674778 | |||||||
| chr8:78674911 | A | C | 1 | a0001c0001t0001g0061 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.17-876A>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78674911 | |||||||
| chr8:78675305 | T | C | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.17-482T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78675305 | |||||||
| chr8:78675350 | G | A | 2 | a0001c0003t0008g0150 a0001c0003t0008g0151 |
2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.17-437G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78675350 | |||||||
| chr8:78675521 | A | G | 3 | a0002c0004t0003g0186 a0002c0004t0003g0187 a0002c0004t0003g0188 |
3 | HG01943.hp2 HG02717.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.17-266A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78675521 | |||||||
| chr8:78675593 | T | A | 1 | a0001c0001t0001g0189 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.17-194T>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78675593 | |||||||
| chr8:78675620 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(107): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.17-167A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 1/8 | chr8 | 78675620 | |||||||
| chr8:78675947 | T | C | 2 | a0001c0001t0003g0016 a0001c0001t0003g0195 |
3 | HG02818.hp2 HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.93+84T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78675947 | |||||||
| chr8:78675954 | A | C | 1 | a0001c0001t0001g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.93+91A>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78675954 | |||||||
| chr8:78675977 | G | A | 3 | a0001c0002t0002g0028 a0001c0002t0002g0152 a0001c0002t0002g0153 |
4 | HG02970.hp2 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.93+114G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78675977 | |||||||
| chr8:78676125 | T | TA | 10 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0101 others(7): Show |
11 | HG00738.hp2 HG01243.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.93+275dupA | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr8 | 78676125 | ||||||
| chr8:78676139 | C | A | 1 | a0001c0001t0001g0100 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.93+276C>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78676139 | |||||||
| chr8:78676694 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.93+831T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78676694 | |||||||
| chr8:78676730 | CTT | C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0051 a0001c0001t0001g0066 others(1): Show |
5 | HG01192.hp2 HG01981.hp2 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+870_93+871delTT | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr8 | 78676730 | ||||||
| chr8:78676790 | C | T | 1 | a0001c0002t0002g0175 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.93+927C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78676790 | |||||||
| chr8:78676828 | C | T | 3 | a0002c0004t0003g0186 a0002c0004t0003g0187 a0002c0004t0003g0188 |
3 | HG01943.hp2 HG02717.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.93+965C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78676828 | |||||||
| chr8:78676859 | A | T | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.93+996A>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78676859 | |||||||
| chr8:78676969 | GATAGTCA others(12): Show |
G | 1 | a0001c0001t0001g0091 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.93+1109_93+1127del others(19): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr8 | 78676969 | ||||||
| chr8:78677061 | A | G | 1 | a0001c0003t0008g0151 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.93+1198A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78677061 | |||||||
| chr8:78677132 | G | A | 3 | a0001c0002t0007g0013 a0001c0002t0007g0181 a0001c0002t0007g0182 |
4 | HG01081.hp2 HG01243.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+1269G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78677132 | |||||||
| chr8:78677215 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.94-1348C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78677215 | |||||||
| chr8:78677226 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.94-1337A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78677226 | |||||||
| chr8:78677354 | TA | T | 35 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0009 others(32): Show |
52 | HG00099.hp2 HG00280.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.94-1198delA | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr8 | 78677354 | ||||||
| chr8:78677460 | T | A | 35 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0009 others(32): Show |
52 | HG00099.hp2 HG00280.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.94-1103T>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78677460 | |||||||
| chr8:78677477 | A | G | 1 | a0001c0002t0002g0174 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.94-1086A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78677477 | |||||||
| chr8:78677529 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.94-1034T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78677529 | |||||||
| chr8:78677541 | T | G | 9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.94-1022T>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78677541 | |||||||
| chr8:78677634 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0050 others(1): Show |
6 | HG01109.hp1 HG02886.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.94-929G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78677634 | |||||||
| chr8:78677645 | A | C | 4 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG01074.hp2 HG02056.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-918A>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78677645 | |||||||
| chr8:78677648 | CT | C | 28 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0019 others(25): Show |
41 | HG00408.hp2 HG01167.hp1 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.94-905delT | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr8 | 78677648 | ||||||
| chr8:78677777 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.94-786A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78677777 | |||||||
| chr8:78677948 | T | A | 2 | a0001c0002t0007g0181 a0001c0002t0007g0182 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.94-615T>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78677948 | |||||||
| chr8:78678244 | G | A | 6 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0001g0099 others(3): Show |
6 | HG01074.hp2 HG02056.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.94-319G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78678244 | |||||||
| chr8:78678356 | A | G | 6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0050 others(3): Show |
8 | HG01109.hp1 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.94-207A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78678356 | |||||||
| chr8:78678388 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01243.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.94-175C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78678388 | |||||||
| chr8:78678516 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.94-47C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78678516 | |||||||
| chr8:78678558 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG00738.hp1 | splice_region_variant&intron_variant | LOW | c.94-5A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 2/8 | chr8 | 78678558 | |||||||
| chr8:78678782 | G | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.210+103G>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78678782 | |||||||
| chr8:78678824 | G | A | 2 | a0001c0002t0007g0181 a0001c0002t0007g0182 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.210+145G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78678824 | |||||||
| chr8:78678931 | A | G | 1 | a0001c0003t0005g0034 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.210+252A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78678931 | |||||||
| chr8:78679061 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.210+382C>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78679061 | |||||||
| chr8:78679109 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.210+430G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78679109 | |||||||
| chr8:78679212 | A | AT | 3 | a0002c0004t0003g0186 a0002c0004t0003g0187 a0002c0004t0003g0188 |
3 | HG01943.hp2 HG02717.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.210+537dupT | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 78679212 | ||||||
| chr8:78679275 | A | G | 1 | a0001c0002t0002g0173 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.210+596A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78679275 | |||||||
| chr8:78679287 | T | A | 5 | a0001c0001t0001g0022 a0001c0001t0001g0078 a0001c0001t0001g0088 others(2): Show |
6 | NA18940.hp1 NA18964.hp2 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+608T>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78679287 | |||||||
| chr8:78679438 | A | G | 6 | a0001c0002t0002g0018 a0001c0002t0002g0057 a0001c0002t0002g0058 others(3): Show |
6 | HG00738.hp2 HG01884.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+759A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78679438 | |||||||
| chr8:78679513 | A | C | 4 | a0001c0002t0002g0018 a0001c0002t0002g0057 a0001c0002t0002g0058 others(1): Show |
4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+834A>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78679513 | |||||||
| chr8:78679535 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(137): Show |
186 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.210+856C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78679535 | |||||||
| chr8:78679548 | T | G | 4 | a0001c0002t0002g0018 a0001c0002t0002g0057 a0001c0002t0002g0058 others(1): Show |
4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+869T>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78679548 | |||||||
| chr8:78679888 | C | T | 2 | a0001c0001t0003g0016 a0001c0001t0003g0195 |
3 | HG02818.hp2 HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.210+1209C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78679888 | |||||||
| chr8:78680052 | C | A | 1 | a0001c0001t0001g0107 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.210+1373C>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78680052 | |||||||
| chr8:78680191 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.210+1512T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78680191 | |||||||
| chr8:78680249 | C | T | 8 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0055 others(5): Show |
10 | HG01167.hp2 HG01169.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.210+1570C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78680249 | |||||||
| chr8:78680258 | G | A | 4 | a0001c0002t0002g0018 a0001c0002t0002g0057 a0001c0002t0002g0058 others(1): Show |
4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+1579G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78680258 | |||||||
| chr8:78680286 | C | CA | 8 | a0001c0002t0002g0036 a0001c0002t0002g0037 a0001c0002t0002g0038 others(5): Show |
8 | HG01069.hp1 HG01106.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.210+1636dupA | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 78680286 | ||||||
| chr8:78680286 | CA | C | 31 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0018 others(28): Show |
46 | HG00099.hp2 HG00280.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.210+1636delA | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 78680286 | ||||||
| chr8:78680286 | CAAAAAAA | C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0020 others(8): Show |
14 | HG01109.hp1 HG01175.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.210+1630_210+1636d others(9): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 78680286 | ||||||
| chr8:78680286 | CAAAAAAA others(1): Show |
C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(104): Show |
145 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.210+1629_210+1636d others(10): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 78680286 | ||||||
| chr8:78680286 | CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0001g0076 a0001c0001t0003g0016 a0001c0001t0003g0017 others(3): Show |
8 | HG01167.hp2 HG01169.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.210+1628_210+1636d others(11): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 78680286 | ||||||
| chr8:78680286 | CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0002g0039 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.210+1625_210+1636d others(14): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 78680286 | ||||||
| chr8:78680286 | CAAAAAAA others(8): Show |
C | 3 | a0001c0002t0002g0191 a0001c0002t0002g0192 a0001c0002t0002g0193 |
3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.210+1622_210+1636d others(17): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 78680286 | ||||||
| chr8:78680317 | C | G | 1 | a0001c0001t0001g0075 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.210+1638C>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78680317 | |||||||
| chr8:78680629 | T | C | 1 | a0001c0001t0003g0016 | 2 | HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.210+1950T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78680629 | |||||||
| chr8:78680633 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.210+1954A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78680633 | |||||||
| chr8:78680826 | G | A | 1 | a0001c0002t0002g0161 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.210+2147G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78680826 | |||||||
| chr8:78680898 | G | A | 8 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0055 others(5): Show |
10 | HG01167.hp2 HG01169.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.210+2219G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78680898 | |||||||
| chr8:78681015 | G | C | 2 | a0001c0003t0008g0150 a0001c0003t0008g0151 |
2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.210+2336G>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78681015 | |||||||
| chr8:78681075 | C | CT | 5 | a0001c0002t0002g0012 a0001c0002t0002g0045 a0001c0002t0002g0046 others(2): Show |
6 | HG01884.hp2 HG02559.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+2408dupT | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 78681075 | ||||||
| chr8:78681364 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.210+2685G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78681364 | |||||||
| chr8:78681390 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.210+2711C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78681390 | |||||||
| chr8:78681501 | T | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.210+2822T>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78681501 | |||||||
| chr8:78681513 | G | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0078 others(16): Show |
29 | HG01074.hp2 HG01099.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.210+2834G>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78681513 | |||||||
| chr8:78681524 | C | G | 3 | a0001c0001t0003g0017 a0001c0001t0003g0055 a0001c0001t0003g0056 |
4 | HG01167.hp2 HG01169.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+2845C>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78681524 | |||||||
| chr8:78681589 | A | G | 9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.210+2910A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78681589 | |||||||
| chr8:78681741 | G | T | 9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.210+3062G>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78681741 | |||||||
| chr8:78681851 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.210+3172A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78681851 | |||||||
| chr8:78681901 | CT | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.210+3236delT | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 78681901 | ||||||
| chr8:78682006 | A | G | 2 | a0001c0003t0008g0150 a0001c0003t0008g0151 |
2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.210+3327A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78682006 | |||||||
| chr8:78682030 | G | A | 1 | a0001c0002t0002g0191 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.210+3351G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78682030 | |||||||
| chr8:78682327 | T | TAAGAAAT others(320): Show |
1 | a0001c0001t0001g0023 | 2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.210+3667_210+3668i others(329): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 78682327 | ||||||
| chr8:78682327 | T | TAAGAAAT others(340): Show |
1 | a0001c0001t0001g0118 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.210+3667_210+3668i others(349): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 78682327 | ||||||
| chr8:78682327 | T | TAAGAAAT others(341): Show |
1 | a0001c0001t0001g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.210+3667_210+3668i others(350): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 78682327 | ||||||
| chr8:78682327 | T | TAAGAAAT others(345): Show |
2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG01070.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.210+3667_210+3668i others(354): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 78682327 | ||||||
| chr8:78682327 | T | TAAGAAAT others(347): Show |
1 | a0001c0001t0001g0114 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.210+3667_210+3668i others(356): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 78682327 | ||||||
| chr8:78682338 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.210+3659G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78682338 | |||||||
| chr8:78682423 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0050 others(1): Show |
6 | HG01109.hp1 HG02886.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+3744G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78682423 | |||||||
| chr8:78682471 | G | A | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+3792G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78682471 | |||||||
| chr8:78682679 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.211-3788A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78682679 | |||||||
| chr8:78682709 | C | T | 9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.211-3758C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78682709 | |||||||
| chr8:78682731 | A | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.211-3736A>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78682731 | |||||||
| chr8:78682781 | A | T | 1 | a0001c0003t0008g0151 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.211-3686A>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78682781 | |||||||
| chr8:78682957 | T | A | 1 | a0001c0006t0001g0119 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.211-3510T>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78682957 | |||||||
| chr8:78682962 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0074 |
2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.211-3505C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78682962 | |||||||
| chr8:78682996 | T | G | 1 | a0001c0006t0001g0119 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.211-3471T>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78682996 | |||||||
| chr8:78682997 | G | T | 1 | a0001c0006t0001g0119 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.211-3470G>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78682997 | |||||||
| chr8:78682998 | T | G | 1 | a0001c0006t0001g0119 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.211-3469T>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78682998 | |||||||
| chr8:78683169 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.211-3298A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78683169 | |||||||
| chr8:78683170 | TTCTGGGG | T | 2 | a0001c0003t0008g0150 a0001c0003t0008g0151 |
2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.211-3291_211-3285d others(9): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 78683170 | ||||||
| chr8:78683236 | T | A | 1 | a0001c0006t0001g0119 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.211-3231T>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78683236 | |||||||
| chr8:78683487 | T | C | 1 | a0001c0006t0001g0119 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.211-2980T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78683487 | |||||||
| chr8:78683534 | C | T | 1 | a0001c0002t0002g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.211-2933C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78683534 | |||||||
| chr8:78683535 | G | A | 35 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0009 others(32): Show |
52 | HG00099.hp2 HG00280.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.211-2932G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78683535 | |||||||
| chr8:78683612 | A | T | 1 | a0001c0002t0007g0013 | 2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.211-2855A>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78683612 | |||||||
| chr8:78683682 | A | C | 1 | a0001c0006t0001g0119 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.211-2785A>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78683682 | |||||||
| chr8:78683683 | T | A | 1 | a0001c0006t0001g0119 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.211-2784T>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78683683 | |||||||
| chr8:78683822 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.211-2645G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78683822 | |||||||
| chr8:78683880 | C | A | 1 | a0001c0006t0001g0119 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.211-2587C>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78683880 | |||||||
| chr8:78684011 | A | G | 1 | a0001c0002t0002g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.211-2456A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78684011 | |||||||
| chr8:78684049 | G | T | 4 | a0001c0002t0002g0018 a0001c0002t0002g0057 a0001c0002t0002g0058 others(1): Show |
4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-2418G>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78684049 | |||||||
| chr8:78684261 | G | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(137): Show |
186 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.211-2206G>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78684261 | |||||||
| chr8:78684647 | C | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.211-1820C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78684647 | |||||||
| chr8:78684785 | G | C | 3 | a0001c0002t0002g0191 a0001c0002t0002g0192 a0001c0002t0002g0193 |
3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.211-1682G>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78684785 | |||||||
| chr8:78684836 | T | G | 1 | a0001c0002t0002g0173 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.211-1631T>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78684836 | |||||||
| chr8:78684901 | C | T | 5 | a0001c0001t0004g0097 a0001c0001t0004g0137 a0001c0001t0004g0138 others(2): Show |
5 | HG01256.hp1 HG02717.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.211-1566C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78684901 | |||||||
| chr8:78684969 | G | C | 4 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(1): Show |
4 | HG02965.hp2 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-1498G>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78684969 | |||||||
| chr8:78685200 | G | T | 1 | a0001c0001t0001g0136 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.211-1267G>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78685200 | |||||||
| chr8:78685223 | G | A | 3 | a0001c0002t0007g0013 a0001c0002t0007g0181 a0001c0002t0007g0182 |
4 | HG01081.hp2 HG01243.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-1244G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78685223 | |||||||
| chr8:78685236 | A | G | 1 | a0001c0001t0004g0097 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.211-1231A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78685236 | |||||||
| chr8:78685252 | GC | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.211-1213delC | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 78685252 | ||||||
| chr8:78685254 | C | A | 3 | a0001c0002t0007g0013 a0001c0002t0007g0181 a0001c0002t0007g0182 |
4 | HG01081.hp2 HG01243.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-1213C>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78685254 | |||||||
| chr8:78685271 | C | T | 5 | a0001c0002t0002g0058 a0001c0002t0006g0035 a0001c0002t0006g0183 others(2): Show |
6 | HG01069.hp1 HG02145.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-1196C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78685271 | |||||||
| chr8:78685349 | A | T | 1 | a0001c0002t0002g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.211-1118A>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78685349 | |||||||
| chr8:78685516 | A | T | 51 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0009 others(48): Show |
70 | HG00099.hp2 HG00280.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.211-951A>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78685516 | |||||||
| chr8:78685934 | C | T | 1 | a0001c0002t0002g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.211-533C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78685934 | |||||||
| chr8:78686073 | C | A | 1 | a0001c0002t0002g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.211-394C>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78686073 | |||||||
| chr8:78686078 | T | G | 4 | a0001c0002t0002g0018 a0001c0002t0002g0057 a0001c0002t0002g0058 others(1): Show |
4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-389T>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78686078 | |||||||
| chr8:78686127 | G | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(71): Show |
100 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.211-340G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78686127 | |||||||
| chr8:78686139 | T | C | 1 | a0001c0002t0002g0162 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.211-328T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78686139 | |||||||
| chr8:78686218 | T | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.211-249T>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78686218 | |||||||
| chr8:78686280 | G | A | 3 | a0001c0002t0002g0191 a0001c0002t0002g0192 a0001c0002t0002g0193 |
3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.211-187G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78686280 | |||||||
| chr8:78686431 | G | GTTTA | 39 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0009 others(36): Show |
56 | HG00099.hp2 HG00280.hp1 HG00673.hp1 others(53): Show |
splice_acceptor_variant&intron_variant | HIGH | c.211-6_211-3dupTTAT | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 78686431 | ||||||
| chr8:78686431 | G | GTTTATTT others(1): Show |
2 | a0001c0002t0002g0033 a0001c0002t0002g0193 |
3 | HG01891.hp1 HG02109.hp1 HG04228.hp2 |
splice_acceptor_variant&intron_variant | HIGH | c.211-10_211-3dupTTA others(5): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 78686431 | ||||||
| chr8:78686431 | GTTTA | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
splice_region_variant&intron_variant | LOW | c.211-6_211-3delTTAT | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 78686431 | ||||||
| chr8:78686431 | GTTTATTT others(5): Show |
G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0147 |
3 | HG02602.hp2 HG03669.hp1 HG04184.hp1 |
splice_region_variant&intron_variant | LOW | c.211-14_211-3delTTA others(9): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr8 | 78686431 | ||||||
| chr8:78686461 | T | A | 1 | a0001c0006t0001g0119 | 1 | NA19001.hp2 | splice_region_variant&intron_variant | LOW | c.211-6T>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 3/8 | chr8 | 78686461 | |||||||
| chr8:78686679 | A | G | 1 | a0001c0002t0002g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.352+71A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78686679 | |||||||
| chr8:78686704 | T | C | 2 | a0001c0002t0009g0176 a0001c0002t0009g0177 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.352+96T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78686704 | |||||||
| chr8:78686786 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.352+178A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78686786 | |||||||
| chr8:78686837 | C | T | 1 | a0001c0001t0004g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.352+229C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78686837 | |||||||
| chr8:78686849 | A | G | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.352+241A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78686849 | |||||||
| chr8:78686869 | T | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(107): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.352+261T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78686869 | |||||||
| chr8:78687132 | G | A | 1 | a0001c0002t0002g0164 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.352+524G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78687132 | |||||||
| chr8:78687203 | C | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.352+595C>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78687203 | |||||||
| chr8:78687263 | T | G | 1 | a0001c0001t0004g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.352+655T>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78687263 | |||||||
| chr8:78687270 | A | G | 9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.352+662A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78687270 | |||||||
| chr8:78687490 | A | G | 1 | a0001c0001t0001g0027 | 2 | HG00099.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.352+882A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78687490 | |||||||
| chr8:78687492 | GTTTATAT others(15): Show |
G | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.352+906_352+927del others(22): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 78687492 | ||||||
| chr8:78687518 | A | G | 2 | a0001c0002t0007g0181 a0001c0002t0007g0182 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.352+910A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78687518 | |||||||
| chr8:78687530 | A | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.352+922A>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78687530 | |||||||
| chr8:78687588 | A | C | 1 | a0001c0002t0002g0172 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.352+980A>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78687588 | |||||||
| chr8:78687604 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.352+996A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78687604 | |||||||
| chr8:78687634 | TTA | T | 2 | a0001c0001t0003g0106 a0001c0002t0002g0171 |
2 | HG02015.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.352+1036_352+1037d others(4): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 78687634 | ||||||
| chr8:78687644 | A | C | 2 | a0001c0002t0002g0032 a0001c0002t0002g0160 |
3 | NA18959.hp2 NA18994.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.352+1036A>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78687644 | |||||||
| chr8:78687649 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
161 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.352+1041C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78687649 | |||||||
| chr8:78687680 | TTATATAT others(17): Show |
T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
160 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.352+1104_352+1127d others(26): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 78687680 | ||||||
| chr8:78687680 | TTATATAT others(85): Show |
T | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.352+1104_352+1195d others(94): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 78687680 | ||||||
| chr8:78687702 | TTATATAT others(63): Show |
T | 8 | a0001c0001t0001g0075 a0001c0001t0001g0101 a0001c0001t0001g0146 others(5): Show |
9 | HG01167.hp2 HG01169.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.352+1104_352+1173d others(72): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 78687702 | ||||||
| chr8:78687705 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.352+1097T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78687705 | |||||||
| chr8:78687726 | TTATATAT others(39): Show |
T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
160 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.352+1131_352+1176d others(48): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 78687726 | ||||||
| chr8:78687766 | G | T | 9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.352+1158G>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78687766 | |||||||
| chr8:78687772 | A | ATATATAT others(15): Show |
9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.352+1175_352+1196d others(24): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 78687772 | ||||||
| chr8:78687800 | A | G | 7 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0077 others(4): Show |
9 | HG00408.hp1 HG00544.hp1 HG00621.hp2 others(6): Show |
intron_variant | MODIFIER | c.352+1192A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78687800 | |||||||
| chr8:78687837 | TTA | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.352+1239_352+1240d others(4): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 78687837 | ||||||
| chr8:78687860 | ATATC | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(70): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.352+1256_352+1259d others(6): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 78687860 | ||||||
| chr8:78687883 | T | A | 1 | a0001c0006t0001g0119 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.352+1275T>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78687883 | |||||||
| chr8:78687884 | T | C | 4 | a0001c0002t0002g0018 a0001c0002t0002g0057 a0001c0002t0002g0058 others(1): Show |
4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.352+1276T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78687884 | |||||||
| chr8:78687885 | A | T | 1 | a0001c0006t0001g0119 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.352+1277A>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78687885 | |||||||
| chr8:78687901 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.352+1293A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78687901 | |||||||
| chr8:78687912 | A | AAT | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.353-1304_353-1303d others(4): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 78687912 | ||||||
| chr8:78687920 | ATTAT | A | 1 | a0001c0002t0002g0029 | 2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.353-1297_353-1294d others(6): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 78687920 | ||||||
| chr8:78687986 | T | C | 3 | a0002c0004t0003g0186 a0002c0004t0003g0187 a0002c0004t0003g0188 |
3 | HG01943.hp2 HG02717.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.353-1236T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78687986 | |||||||
| chr8:78688123 | T | C | 1 | a0001c0001t0003g0120 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.353-1099T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78688123 | |||||||
| chr8:78688231 | A | G | 5 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(2): Show |
6 | HG02055.hp2 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.353-991A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78688231 | |||||||
| chr8:78688404 | G | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.353-818G>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78688404 | |||||||
| chr8:78688532 | T | A | 1 | a0001c0006t0001g0119 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.353-690T>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78688532 | |||||||
| chr8:78688754 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.353-468G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78688754 | |||||||
| chr8:78688910 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.353-312G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78688910 | |||||||
| chr8:78689034 | C | CT | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
166 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.353-175dupT | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr8 | 78689034 | ||||||
| chr8:78689185 | T | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(107): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.353-37T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 4/8 | chr8 | 78689185 | |||||||
| chr8:78689652 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(137): Show |
186 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.504+279T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78689652 | |||||||
| chr8:78689911 | G | A | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.504+538G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78689911 | |||||||
| chr8:78690013 | C | G | 2 | a0001c0003t0008g0150 a0001c0003t0008g0151 |
2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.504+640C>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78690013 | |||||||
| chr8:78690040 | C | T | 1 | a0001c0002t0002g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.504+667C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78690040 | |||||||
| chr8:78690182 | C | T | 2 | a0001c0003t0008g0150 a0001c0003t0008g0151 |
2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.504+809C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78690182 | |||||||
| chr8:78690184 | C | A | 2 | a0001c0003t0008g0150 a0001c0003t0008g0151 |
2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.504+811C>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78690184 | |||||||
| chr8:78690249 | C | T | 8 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0055 others(5): Show |
10 | HG01167.hp2 HG01169.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.504+876C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78690249 | |||||||
| chr8:78690270 | T | C | 9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.504+897T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78690270 | |||||||
| chr8:78690281 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.504+908C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78690281 | |||||||
| chr8:78690311 | G | A | 9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.504+938G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78690311 | |||||||
| chr8:78690330 | C | A | 1 | a0001c0002t0002g0029 | 2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.504+957C>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78690330 | |||||||
| chr8:78690559 | C | CA | 6 | a0001c0001t0001g0059 a0001c0001t0001g0066 a0001c0001t0001g0098 others(3): Show |
6 | HG01928.hp1 HG01981.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.504+1202dupA | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 78690559 | ||||||
| chr8:78690559 | CA | C | 19 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0096 others(16): Show |
22 | HG00738.hp2 HG01069.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.504+1202delA | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 78690559 | ||||||
| chr8:78690655 | T | A | 1 | a0001c0006t0001g0119 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.504+1282T>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78690655 | |||||||
| chr8:78690928 | C | A | 6 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(3): Show |
7 | HG00738.hp2 HG02258.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+1555C>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78690928 | |||||||
| chr8:78691021 | T | TA | 3 | a0001c0002t0007g0013 a0001c0002t0007g0181 a0001c0002t0007g0182 |
4 | HG01081.hp2 HG01243.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.504+1651dupA | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 78691021 | ||||||
| chr8:78691071 | C | G | 4 | a0001c0002t0002g0159 a0001c0002t0002g0170 a0001c0002t0002g0171 others(1): Show |
4 | HG00673.hp1 HG02015.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.504+1698C>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78691071 | |||||||
| chr8:78691116 | G | T | 9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.504+1743G>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78691116 | |||||||
| chr8:78691247 | CTTTAGTT others(14): Show |
C | 9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.504+1877_504+1897d others(23): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 78691247 | ||||||
| chr8:78691459 | A | G | 3 | a0001c0002t0007g0013 a0001c0002t0007g0181 a0001c0002t0007g0182 |
4 | HG01081.hp2 HG01243.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.504+2086A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78691459 | |||||||
| chr8:78691470 | A | G | 1 | a0001c0003t0008g0150 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.504+2097A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78691470 | |||||||
| chr8:78691512 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.504+2139T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78691512 | |||||||
| chr8:78691589 | C | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.504+2216C>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78691589 | |||||||
| chr8:78691689 | T | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
166 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.504+2316T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78691689 | |||||||
| chr8:78691702 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(136): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.504+2329G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78691702 | |||||||
| chr8:78691751 | A | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG00738.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.504+2378A>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78691751 | |||||||
| chr8:78691757 | G | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01261.hp2 HG01928.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.504+2384G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78691757 | |||||||
| chr8:78691860 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.504+2487G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78691860 | |||||||
| chr8:78691911 | G | T | 9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.504+2538G>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78691911 | |||||||
| chr8:78692220 | A | G | 8 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0055 others(5): Show |
10 | HG01167.hp2 HG01169.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.504+2847A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78692220 | |||||||
| chr8:78692243 | T | A | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.504+2870T>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78692243 | |||||||
| chr8:78692268 | A | G | 1 | a0001c0001t0004g0139 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.504+2895A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78692268 | |||||||
| chr8:78692494 | C | A | 4 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(1): Show |
4 | HG02965.hp2 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.504+3121C>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78692494 | |||||||
| chr8:78692495 | A | G | 1 | a0001c0002t0002g0169 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.504+3122A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78692495 | |||||||
| chr8:78692652 | C | A | 1 | a0001c0001t0001g0069 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.504+3279C>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78692652 | |||||||
| chr8:78692694 | C | T | 3 | a0001c0001t0003g0017 a0001c0001t0003g0055 a0001c0001t0003g0056 |
4 | HG01167.hp2 HG01169.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.504+3321C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78692694 | |||||||
| chr8:78692838 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.504+3465C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78692838 | |||||||
| chr8:78692888 | C | A | 1 | a0001c0002t0002g0156 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.504+3515C>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78692888 | |||||||
| chr8:78693066 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.504+3693A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78693066 | |||||||
| chr8:78693150 | G | C | 1 | a0001c0002t0002g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.504+3777G>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78693150 | |||||||
| chr8:78693166 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.504+3793A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78693166 | |||||||
| chr8:78693181 | G | A | 4 | a0001c0001t0001g0053 a0001c0002t0007g0013 a0001c0002t0007g0181 others(1): Show |
5 | HG01081.hp2 HG01243.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.504+3808G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78693181 | |||||||
| chr8:78693211 | T | C | 1 | a0001c0002t0002g0173 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.504+3838T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78693211 | |||||||
| chr8:78693280 | A | G | 33 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0019 others(30): Show |
46 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.504+3907A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78693280 | |||||||
| chr8:78693340 | T | C | 1 | a0001c0002t0002g0045 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.504+3967T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78693340 | |||||||
| chr8:78693388 | C | T | 1 | a0001c0003t0008g0150 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.504+4015C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78693388 | |||||||
| chr8:78693494 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.505-3913A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78693494 | |||||||
| chr8:78693516 | C | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.505-3891C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78693516 | |||||||
| chr8:78693605 | G | T | 1 | a0001c0001t0001g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.505-3802G>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78693605 | |||||||
| chr8:78693945 | A | C | 1 | a0001c0001t0001g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.505-3462A>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78693945 | |||||||
| chr8:78693950 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.505-3457T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78693950 | |||||||
| chr8:78693994 | T | G | 4 | a0001c0002t0002g0165 a0001c0002t0002g0166 a0001c0002t0009g0176 others(1): Show |
4 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.505-3413T>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78693994 | |||||||
| chr8:78694286 | G | GT | 5 | a0001c0002t0002g0047 a0001c0003t0005g0034 a0001c0003t0005g0178 others(2): Show |
6 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-3108dupT | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 78694286 | ||||||
| chr8:78694286 | GT | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
166 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.505-3108delT | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr8 | 78694286 | ||||||
| chr8:78694369 | C | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(136): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.505-3038C>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78694369 | |||||||
| chr8:78694373 | A | T | 1 | a0001c0001t0001g0102 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.505-3034A>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78694373 | |||||||
| chr8:78694400 | C | T | 5 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(2): Show |
6 | HG02055.hp2 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-3007C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78694400 | |||||||
| chr8:78694759 | A | G | 9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.505-2648A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78694759 | |||||||
| chr8:78694850 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.505-2557C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78694850 | |||||||
| chr8:78694854 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.505-2553G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78694854 | |||||||
| chr8:78695095 | C | G | 6 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(3): Show |
7 | HG00738.hp2 HG02258.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.505-2312C>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78695095 | |||||||
| chr8:78695461 | G | A | 4 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(1): Show |
4 | HG02965.hp2 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.505-1946G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78695461 | |||||||
| chr8:78695514 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0124 a0001c0001t0001g0125 |
5 | HG01069.hp2 HG01071.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.505-1893G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78695514 | |||||||
| chr8:78695582 | A | G | 3 | a0002c0004t0003g0186 a0002c0004t0003g0187 a0002c0004t0003g0188 |
3 | HG01943.hp2 HG02717.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.505-1825A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78695582 | |||||||
| chr8:78695656 | C | A | 36 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0009 others(33): Show |
52 | HG00099.hp2 HG00280.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.505-1751C>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78695656 | |||||||
| chr8:78695658 | A | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.505-1749A>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78695658 | |||||||
| chr8:78695660 | A | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0113 |
2 | HG00544.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.505-1747A>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78695660 | |||||||
| chr8:78695708 | G | T | 3 | a0001c0002t0002g0191 a0001c0002t0002g0192 a0001c0002t0002g0193 |
3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.505-1699G>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78695708 | |||||||
| chr8:78695736 | T | C | 4 | a0001c0002t0002g0030 a0001c0002t0002g0156 a0001c0002t0002g0157 others(1): Show |
5 | HG00099.hp2 HG01099.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-1671T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78695736 | |||||||
| chr8:78696017 | T | C | 1 | a0001c0003t0005g0179 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.505-1390T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78696017 | |||||||
| chr8:78696019 | A | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(70): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.505-1388A>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78696019 | |||||||
| chr8:78696186 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(136): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.505-1221T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78696186 | |||||||
| chr8:78696236 | G | C | 1 | a0001c0001t0003g0121 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.505-1171G>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78696236 | |||||||
| chr8:78696404 | T | C | 6 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(3): Show |
7 | HG00738.hp2 HG02258.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.505-1003T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78696404 | |||||||
| chr8:78696444 | C | T | 3 | a0002c0004t0003g0186 a0002c0004t0003g0187 a0002c0004t0003g0188 |
3 | HG01943.hp2 HG02717.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.505-963C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78696444 | |||||||
| chr8:78696480 | G | A | 1 | a0001c0002t0002g0168 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.505-927G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78696480 | |||||||
| chr8:78696737 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.505-670G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78696737 | |||||||
| chr8:78696790 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.505-617C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78696790 | |||||||
| chr8:78696994 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.505-413A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78696994 | |||||||
| chr8:78697147 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.505-260A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78697147 | |||||||
| chr8:78697259 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0050 others(1): Show |
6 | HG01109.hp1 HG02886.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-148G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78697259 | |||||||
| chr8:78697348 | A | G | 1 | a0001c0003t0005g0179 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.505-59A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 5/8 | chr8 | 78697348 | |||||||
| chr8:78697577 | G | T | 1 | a0001c0001t0003g0195 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.604+71G>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 6/8 | chr8 | 78697577 | |||||||
| chr8:78697633 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.604+127G>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 6/8 | chr8 | 78697633 | |||||||
| chr8:78697682 | C | CT | 12 | a0001c0001t0001g0025 a0001c0001t0001g0067 a0001c0001t0001g0075 others(9): Show |
14 | HG00408.hp2 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.604+192dupT | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr8 | 78697682 | ||||||
| chr8:78697701 | C | T | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+195C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 6/8 | chr8 | 78697701 | |||||||
| chr8:78697838 | C | G | 1 | a0001c0002t0007g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.604+332C>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 6/8 | chr8 | 78697838 | |||||||
| chr8:78697867 | A | G | 4 | a0001c0002t0002g0018 a0001c0002t0002g0057 a0001c0002t0002g0058 others(1): Show |
4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.604+361A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 6/8 | chr8 | 78697867 | |||||||
| chr8:78697871 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.604+365G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 6/8 | chr8 | 78697871 | |||||||
| chr8:78697901 | A | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0069 a0001c0001t0001g0086 |
7 | HG01167.hp1 HG02922.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.604+395A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 6/8 | chr8 | 78697901 | |||||||
| chr8:78697935 | C | T | 1 | a0001c0001t0004g0139 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.604+429C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 6/8 | chr8 | 78697935 | |||||||
| chr8:78697975 | C | T | 9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.605-439C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 6/8 | chr8 | 78697975 | |||||||
| chr8:78698095 | C | G | 1 | a0001c0002t0006g0184 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.605-319C>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 6/8 | chr8 | 78698095 | |||||||
| chr8:78698178 | T | C | 1 | a0001c0003t0008g0150 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.605-236T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 6/8 | chr8 | 78698178 | |||||||
| chr8:78699133 | T | TAAG | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.704+621_704+622ins others(3): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr8 | 78699133 | ||||||
| chr8:78699236 | A | G | 2 | a0001c0003t0008g0150 a0001c0003t0008g0151 |
2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.704+723A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78699236 | |||||||
| chr8:78699318 | A | G | 5 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(2): Show |
6 | HG02055.hp2 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.704+805A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78699318 | |||||||
| chr8:78699437 | A | G | 1 | a0001c0002t0002g0039 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.704+924A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78699437 | |||||||
| chr8:78699514 | A | G | 3 | a0001c0002t0007g0013 a0001c0002t0007g0181 a0001c0002t0007g0182 |
4 | HG01081.hp2 HG01243.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.704+1001A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78699514 | |||||||
| chr8:78699583 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0050 others(1): Show |
6 | HG01109.hp1 HG02886.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.704+1070C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78699583 | |||||||
| chr8:78699649 | G | A | 1 | a0001c0005t0010g0070 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.704+1136G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78699649 | |||||||
| chr8:78699664 | A | G | 1 | a0001c0002t0002g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.704+1151A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78699664 | |||||||
| chr8:78699861 | G | A | 9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.704+1348G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78699861 | |||||||
| chr8:78699869 | T | C | 3 | a0001c0001t0003g0017 a0001c0001t0003g0055 a0001c0001t0003g0056 |
4 | HG01167.hp2 HG01169.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.704+1356T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78699869 | |||||||
| chr8:78700122 | G | T | 1 | a0001c0001t0003g0121 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.704+1609G>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78700122 | |||||||
| chr8:78700238 | T | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(107): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.704+1725T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78700238 | |||||||
| chr8:78700368 | G | A | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.704+1855G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78700368 | |||||||
| chr8:78700518 | C | A | 4 | a0001c0002t0006g0035 a0001c0002t0006g0183 a0001c0002t0006g0184 others(1): Show |
5 | HG01069.hp1 HG02145.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.704+2005C>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78700518 | |||||||
| chr8:78700554 | G | A | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.704+2041G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78700554 | |||||||
| chr8:78700868 | A | G | 1 | a0001c0002t0002g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.704+2355A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78700868 | |||||||
| chr8:78701192 | T | G | 2 | a0001c0003t0008g0150 a0001c0003t0008g0151 |
2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.704+2679T>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78701192 | |||||||
| chr8:78701476 | G | A | 9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.704+2963G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78701476 | |||||||
| chr8:78701529 | A | G | 4 | a0001c0002t0006g0035 a0001c0002t0006g0183 a0001c0002t0006g0184 others(1): Show |
5 | HG01069.hp1 HG02145.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.704+3016A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78701529 | |||||||
| chr8:78701632 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0013g0131 |
2 | NA19059.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.704+3119C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78701632 | |||||||
| chr8:78701716 | T | C | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.704+3203T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78701716 | |||||||
| chr8:78701732 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0127 |
2 | HG01258.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.704+3219G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78701732 | |||||||
| chr8:78701806 | T | C | 35 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0009 others(32): Show |
52 | HG00099.hp2 HG00280.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.704+3293T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78701806 | |||||||
| chr8:78701809 | G | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(140): Show |
190 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.704+3296G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78701809 | |||||||
| chr8:78701852 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.704+3339G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78701852 | |||||||
| chr8:78702113 | A | G | 1 | a0001c0001t0001g0189 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.704+3600A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78702113 | |||||||
| chr8:78702124 | A | G | 4 | a0001c0002t0002g0018 a0001c0002t0002g0057 a0001c0002t0002g0058 others(1): Show |
4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.704+3611A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78702124 | |||||||
| chr8:78702203 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(107): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.704+3690G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78702203 | |||||||
| chr8:78702251 | T | C | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.704+3738T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78702251 | |||||||
| chr8:78702280 | G | T | 9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.704+3767G>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78702280 | |||||||
| chr8:78702620 | C | T | 1 | a0001c0002t0002g0154 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.704+4107C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78702620 | |||||||
| chr8:78702634 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.704+4121T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78702634 | |||||||
| chr8:78702812 | T | G | 1 | a0002c0004t0003g0186 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.704+4299T>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78702812 | |||||||
| chr8:78702825 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0135 |
4 | HG01106.hp1 HG01255.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.704+4312T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78702825 | |||||||
| chr8:78702834 | T | G | 4 | a0001c0002t0002g0159 a0001c0002t0002g0170 a0001c0002t0002g0171 others(1): Show |
4 | HG00673.hp1 HG02015.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.704+4321T>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78702834 | |||||||
| chr8:78702970 | C | T | 3 | a0001c0001t0001g0072 a0001c0001t0001g0081 a0001c0001t0001g0104 |
3 | HG00621.hp1 HG02083.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.704+4457C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78702970 | |||||||
| chr8:78702971 | G | A | 4 | a0001c0002t0002g0018 a0001c0002t0002g0057 a0001c0002t0002g0058 others(1): Show |
4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.704+4458G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78702971 | |||||||
| chr8:78703016 | C | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(107): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.704+4503C>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78703016 | |||||||
| chr8:78703081 | G | A | 6 | a0001c0002t0002g0006 a0001c0002t0002g0030 a0001c0002t0002g0156 others(3): Show |
10 | HG00099.hp2 HG00280.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.704+4568G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78703081 | |||||||
| chr8:78703187 | G | A | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.704+4674G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78703187 | |||||||
| chr8:78703396 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.704+4883C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78703396 | |||||||
| chr8:78703536 | C | CT | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.704+5039dupT | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr8 | 78703536 | ||||||
| chr8:78703536 | C | CTT | 7 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0050 others(4): Show |
10 | HG01109.hp1 HG02647.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.704+5038_704+5039d others(4): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr8 | 78703536 | ||||||
| chr8:78703536 | CT | C | 14 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(11): Show |
16 | HG01069.hp1 HG01168.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.704+5039delT | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr8 | 78703536 | ||||||
| chr8:78703552 | T | A | 1 | a0001c0002t0002g0043 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.704+5039T>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78703552 | |||||||
| chr8:78703603 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.704+5090C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78703603 | |||||||
| chr8:78703712 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.704+5199G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78703712 | |||||||
| chr8:78704004 | C | A | 1 | a0001c0001t0001g0115 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.704+5491C>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78704004 | |||||||
| chr8:78704006 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.704+5493G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78704006 | |||||||
| chr8:78704063 | A | G | 1 | a0001c0002t0002g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.704+5550A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78704063 | |||||||
| chr8:78704345 | G | A | 9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.704+5832G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78704345 | |||||||
| chr8:78704387 | C | CA | 29 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0050 others(26): Show |
35 | HG00621.hp1 HG01069.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.704+5893dupA | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr8 | 78704387 | ||||||
| chr8:78704533 | C | A | 1 | a0001c0001t0001g0065 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.704+6020C>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78704533 | |||||||
| chr8:78704734 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.704+6221G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78704734 | |||||||
| chr8:78704828 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.704+6315G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78704828 | |||||||
| chr8:78704978 | A | G | 2 | a0001c0002t0007g0181 a0001c0002t0007g0182 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.704+6465A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78704978 | |||||||
| chr8:78705078 | G | A | 41 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0009 others(38): Show |
59 | HG00099.hp2 HG00280.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.704+6565G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78705078 | |||||||
| chr8:78705539 | C | T | 1 | a0001c0003t0005g0178 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.704+7026C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78705539 | |||||||
| chr8:78705604 | C | T | 1 | a0001c0001t0001g0189 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.704+7091C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78705604 | |||||||
| chr8:78705611 | G | T | 2 | a0001c0001t0003g0016 a0001c0001t0003g0195 |
3 | HG02818.hp2 HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.704+7098G>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78705611 | |||||||
| chr8:78705718 | C | G | 3 | a0001c0002t0002g0191 a0001c0002t0002g0192 a0001c0002t0002g0193 |
3 | HG03688.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.704+7205C>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78705718 | |||||||
| chr8:78705743 | T | G | 2 | a0001c0003t0008g0150 a0001c0003t0008g0151 |
2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.704+7230T>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78705743 | |||||||
| chr8:78706179 | C | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | NA19002.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.704+7666C>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78706179 | |||||||
| chr8:78706392 | G | A | 1 | a0001c0002t0007g0013 | 2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.704+7879G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78706392 | |||||||
| chr8:78706621 | T | C | 23 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0009 others(20): Show |
36 | HG00099.hp2 HG00280.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.704+8108T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78706621 | |||||||
| chr8:78706696 | C | A | 1 | a0001c0002t0002g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.704+8183C>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78706696 | |||||||
| chr8:78706900 | A | G | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.705-8321A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78706900 | |||||||
| chr8:78707061 | C | T | 1 | a0001c0002t0002g0038 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.705-8160C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78707061 | |||||||
| chr8:78707067 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.705-8154G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78707067 | |||||||
| chr8:78707086 | A | G | 2 | a0001c0002t0002g0032 a0001c0002t0002g0160 |
3 | NA18959.hp2 NA18994.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.705-8135A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78707086 | |||||||
| chr8:78707386 | A | C | 1 | a0001c0002t0002g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.705-7835A>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78707386 | |||||||
| chr8:78707440 | A | G | 9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.705-7781A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78707440 | |||||||
| chr8:78707653 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.705-7568A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78707653 | |||||||
| chr8:78707786 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.705-7435G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78707786 | |||||||
| chr8:78707855 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.705-7366C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78707855 | |||||||
| chr8:78707855 | CT | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.705-7353delT | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr8 | 78707855 | ||||||
| chr8:78707856 | T | C | 1 | a0001c0001t0001g0194 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.705-7365T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78707856 | |||||||
| chr8:78707931 | C | G | 1 | a0001c0002t0002g0046 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.705-7290C>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78707931 | |||||||
| chr8:78707934 | T | C | 4 | a0001c0002t0002g0018 a0001c0002t0002g0057 a0001c0002t0002g0058 others(1): Show |
4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.705-7287T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78707934 | |||||||
| chr8:78708040 | A | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0050 others(1): Show |
6 | HG01109.hp1 HG02886.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.705-7181A>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78708040 | |||||||
| chr8:78708119 | G | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.705-7102G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78708119 | |||||||
| chr8:78708120 | A | G | 8 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0055 others(5): Show |
10 | HG01167.hp2 HG01169.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.705-7101A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78708120 | |||||||
| chr8:78708218 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.705-7003C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78708218 | |||||||
| chr8:78708413 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.705-6808C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78708413 | |||||||
| chr8:78708672 | CT | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
162 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.705-6539delT | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr8 | 78708672 | ||||||
| chr8:78708682 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.705-6539T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78708682 | |||||||
| chr8:78708683 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.705-6538C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78708683 | |||||||
| chr8:78708683 | CTTTTTTT others(7): Show |
C | 2 | a0001c0002t0002g0043 a0001c0002t0002g0044 |
2 | NA18612.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.705-6537_705-6524d others(16): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78708683 | |||||||
| chr8:78708684 | T | C | 3 | a0001c0001t0003g0017 a0001c0001t0003g0055 a0001c0001t0003g0056 |
4 | HG01167.hp2 HG01169.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.705-6537T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78708684 | |||||||
| chr8:78708776 | A | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.705-6445A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78708776 | |||||||
| chr8:78708831 | C | A | 1 | a0001c0001t0001g0189 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.705-6390C>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78708831 | |||||||
| chr8:78708957 | C | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.705-6264C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78708957 | |||||||
| chr8:78709085 | C | T | 2 | a0001c0001t0004g0138 a0001c0001t0004g0139 |
2 | HG01256.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.705-6136C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78709085 | |||||||
| chr8:78709095 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0050 others(1): Show |
6 | HG01109.hp1 HG02886.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.705-6126G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78709095 | |||||||
| chr8:78709144 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.705-6077A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78709144 | |||||||
| chr8:78709474 | G | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.705-5747G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78709474 | |||||||
| chr8:78709886 | C | T | 1 | a0001c0002t0002g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.705-5335C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78709886 | |||||||
| chr8:78710094 | A | G | 8 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0055 others(5): Show |
10 | HG01167.hp2 HG01169.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.705-5127A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78710094 | |||||||
| chr8:78710128 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(137): Show |
186 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.705-5093T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78710128 | |||||||
| chr8:78710129 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.705-5092G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78710129 | |||||||
| chr8:78710509 | G | C | 1 | a0001c0001t0001g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.705-4712G>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78710509 | |||||||
| chr8:78710777 | T | A | 1 | a0001c0002t0002g0058 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.705-4444T>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78710777 | |||||||
| chr8:78710980 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.705-4241T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78710980 | |||||||
| chr8:78711072 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0050 others(1): Show |
6 | HG01109.hp1 HG02886.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.705-4149A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78711072 | |||||||
| chr8:78711302 | A | G | 2 | a0001c0002t0007g0181 a0001c0002t0007g0182 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.705-3919A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78711302 | |||||||
| chr8:78711382 | A | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
148 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.705-3839A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78711382 | |||||||
| chr8:78711400 | A | T | 4 | a0001c0002t0002g0018 a0001c0002t0002g0057 a0001c0002t0002g0058 others(1): Show |
4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.705-3821A>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78711400 | |||||||
| chr8:78711603 | T | C | 54 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0009 others(51): Show |
73 | HG00099.hp2 HG00280.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.705-3618T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78711603 | |||||||
| chr8:78711824 | C | T | 1 | a0001c0002t0002g0057 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.705-3397C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78711824 | |||||||
| chr8:78712370 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(113): Show |
157 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.705-2851T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78712370 | |||||||
| chr8:78712390 | T | C | 8 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0055 others(5): Show |
10 | HG01167.hp2 HG01169.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.705-2831T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78712390 | |||||||
| chr8:78712402 | G | A | 2 | a0001c0003t0008g0150 a0001c0003t0008g0151 |
2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.705-2819G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78712402 | |||||||
| chr8:78712424 | G | A | 1 | a0001c0002t0002g0152 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.705-2797G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78712424 | |||||||
| chr8:78713045 | C | G | 1 | a0001c0002t0002g0043 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.705-2176C>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78713045 | |||||||
| chr8:78713239 | G | C | 1 | a0001c0003t0008g0150 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.705-1982G>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78713239 | |||||||
| chr8:78713271 | T | C | 1 | a0001c0002t0002g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.705-1950T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78713271 | |||||||
| chr8:78713394 | T | A | 3 | a0002c0004t0003g0186 a0002c0004t0003g0187 a0002c0004t0003g0188 |
3 | HG01943.hp2 HG02717.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.705-1827T>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78713394 | |||||||
| chr8:78713984 | A | G | 2 | a0001c0003t0008g0150 a0001c0003t0008g0151 |
2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.705-1237A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78713984 | |||||||
| chr8:78714040 | T | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0019 others(30): Show |
46 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.705-1181T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78714040 | |||||||
| chr8:78714076 | A | T | 1 | a0001c0001t0001g0053 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.705-1145A>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78714076 | |||||||
| chr8:78714191 | G | A | 1 | a0001c0002t0002g0044 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.705-1030G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78714191 | |||||||
| chr8:78714278 | A | T | 1 | a0001c0001t0001g0100 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.705-943A>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78714278 | |||||||
| chr8:78714279 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.705-942C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78714279 | |||||||
| chr8:78714436 | A | G | 13 | a0001c0001t0001g0024 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
14 | HG00738.hp1 HG01978.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.705-785A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78714436 | |||||||
| chr8:78714570 | G | T | 1 | a0001c0001t0004g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.705-651G>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78714570 | |||||||
| chr8:78714677 | G | A | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.705-544G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78714677 | |||||||
| chr8:78714683 | C | T | 9 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(6): Show |
11 | HG01069.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.705-538C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 7/8 | chr8 | 78714683 | |||||||
| chr8:78715513 | A | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01243.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.812+185A>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 8/8 | chr8 | 78715513 | |||||||
| chr8:78715514 | G | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01243.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.812+186G>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 8/8 | chr8 | 78715514 | |||||||
| chr8:78715667 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.812+339T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 8/8 | chr8 | 78715667 | |||||||
| chr8:78715724 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.812+396A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 8/8 | chr8 | 78715724 | |||||||
| chr8:78715739 | C | T | 35 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0009 others(32): Show |
52 | HG00099.hp2 HG00280.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.812+411C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 8/8 | chr8 | 78715739 | |||||||
| chr8:78715897 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0135 |
4 | HG01106.hp1 HG01255.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.812+569G>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 8/8 | chr8 | 78715897 | |||||||
| chr8:78716039 | C | CA | 8 | a0001c0001t0001g0071 a0001c0001t0001g0094 a0001c0001t0001g0108 others(5): Show |
8 | HG00738.hp2 HG01175.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.812+727dupA | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr8 | 78716039 | ||||||
| chr8:78716039 | C | CAA | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.812+726_812+727dup others(2): Show |
ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr8 | 78716039 | ||||||
| chr8:78716091 | T | C | 1 | a0001c0002t0002g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.812+763T>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 8/8 | chr8 | 78716091 | |||||||
| chr8:78716191 | C | T | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.812+863C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 8/8 | chr8 | 78716191 | |||||||
| chr8:78716370 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
194 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.813-958A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 8/8 | chr8 | 78716370 | |||||||
| chr8:78716492 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.813-836C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 8/8 | chr8 | 78716492 | |||||||
| chr8:78716674 | A | G | 4 | a0001c0002t0002g0018 a0001c0002t0002g0057 a0001c0002t0002g0058 others(1): Show |
4 | HG01884.hp1 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.813-654A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 8/8 | chr8 | 78716674 | |||||||
| chr8:78716693 | A | C | 1 | a0001c0002t0002g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.813-635A>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 8/8 | chr8 | 78716693 | |||||||
| chr8:78716761 | C | A | 2 | a0001c0003t0008g0150 a0001c0003t0008g0151 |
2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.813-567C>A | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 8/8 | chr8 | 78716761 | |||||||
| chr8:78716803 | C | T | 1 | a0001c0001t0004g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.813-525C>T | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 8/8 | chr8 | 78716803 | |||||||
| chr8:78716804 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.813-524A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 8/8 | chr8 | 78716804 | |||||||
| chr8:78717017 | T | TA | 35 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0009 others(32): Show |
52 | HG00099.hp2 HG00280.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.813-308dupA | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr8 | 78717017 | ||||||
| chr8:78717043 | C | G | 1 | a0001c0002t0002g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.813-285C>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 8/8 | chr8 | 78717043 | |||||||
| chr8:78717124 | G | C | 4 | a0001c0003t0005g0034 a0001c0003t0005g0178 a0001c0003t0005g0179 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.813-204G>C | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 8/8 | chr8 | 78717124 | |||||||
| chr8:78717139 | A | G | 4 | a0001c0002t0002g0010 a0001c0002t0002g0036 a0001c0002t0002g0037 others(1): Show |
5 | HG02055.hp2 HG02630.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.813-189A>G | ZC2HC1A | ENSG00000104427.13 | transcript | ENST00000263849.9 | protein_coding | 8/8 | chr8 | 78717139 |