Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11236 |
| ensemblid | ENSG00000170881.5 |
| hgncid | 17023 |
| symbol | RNF139 |
| name | ring finger protein 139 |
| refseq_nuc | NM_007218.4 |
| refseq_prot | NP_009149.2 |
| ensembl_nuc | ENST00000303545.4 |
| ensembl_prot | ENSP00000304051.4 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 124474880 |
| end | 124488618 |
| strand | + |
| ver | v1.2 |
| region | chr8:124474880-124488618 |
| region5000 | chr8:124469880-124493618 |
| regionname0 | RNF139_chr8_124474880_124488618 |
| regionname5000 | RNF139_chr8_124469880_124493618 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 664 | 403 | 89 | 71 | 185 | 14 | 42 | 146 | RNF139_chr8_124469880_124493618 | RNF139 | MAAVG others(659): Show |
chr8 | 124469880 | 124493618 |
| a0002 | 0/0 | 664 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | MAAVG others(659): Show |
chr8 | 124469880 | 124493618 |
| a0003 | 0/0 | 664 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | MAAVG others(659): Show |
chr8 | 124469880 | 124493618 |
| a0004 | 0/0 | 664 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | MAAVG others(659): Show |
chr8 | 124469880 | 124493618 |
| a0005 | 0/0 | 521 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF139_chr8_124469880_124493618 | RNF139 | MAAVG others(516): Show |
chr8 | 124469880 | 124493618 |
| a0006 | 0/0 | 664 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF139_chr8_124469880_124493618 | RNF139 | MAAVG others(659): Show |
chr8 | 124469880 | 124493618 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1992 | 193 | 28 | 43 | 99 | 9 | 13 | RNF139_chr8_124469880_124493618 | RNF139 | ATGGC others(1987): Show |
chr8 | 124469880 | 124493618 | ||
| a0001c0002 | 0/1 | 1992 | 143 | 49 | 26 | 50 | 4 | 13 | RNF139_chr8_124469880_124493618 | RNF139 | ATGGC others(1987): Show |
chr8 | 124469880 | 124493618 | ||
| a0001c0003 | 0/0 | 1992 | 65 | 11 | 2 | 35 | 1 | 16 | RNF139_chr8_124469880_124493618 | RNF139 | ATGGC others(1987): Show |
chr8 | 124469880 | 124493618 | ||
| a0001c0006 | 0/0 | 1992 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | ATGGC others(1987): Show |
chr8 | 124469880 | 124493618 | ||
| a0001c0007 | 0/0 | 1992 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | ATGGC others(1987): Show |
chr8 | 124469880 | 124493618 | ||
| a0002c0008 | 0/0 | 1992 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | ATGGC others(1987): Show |
chr8 | 124469880 | 124493618 | ||
| a0003c0009 | 0/0 | 1992 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | ATGGC others(1987): Show |
chr8 | 124469880 | 124493618 | ||
| a0004c0010 | 0/0 | 1992 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | ATGGC others(1987): Show |
chr8 | 124469880 | 124493618 | ||
| a0005c0004 | 0/0 | 1952 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | ATGGC others(1947): Show |
chr8 | 124469880 | 124493618 | ||
| a0006c0005 | 0/0 | 1992 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | ATGGC others(1987): Show |
chr8 | 124469880 | 124493618 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3199 | 189 | 27 | 43 | 96 | 9 | 13 | RNF139_chr8_124469880_124493618 | RNF139 | AGAGA others(3194): Show |
chr8 | 124469880 | 124493618 |
| a0001c0001t0003 | 0/0 | 3199 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | AGAGA others(3194): Show |
chr8 | 124469880 | 124493618 |
| a0001c0001t0006 | 0/0 | 3199 | 3 | 0 | 0 | 3 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | AGAGA others(3194): Show |
chr8 | 124469880 | 124493618 |
| a0001c0002t0001 | 0/0 | 3199 | 60 | 25 | 5 | 24 | 0 | 6 | RNF139_chr8_124469880_124493618 | RNF139 | AGAGA others(3194): Show |
chr8 | 124469880 | 124493618 |
| a0001c0002t0002 | 0/1 | 3202 | 38 | 3 | 16 | 13 | 2 | 3 | RNF139_chr8_124469880_124493618 | RNF139 | AGAGA others(3197): Show |
chr8 | 124469880 | 124493618 |
| a0001c0002t0003 | 0/0 | 3199 | 26 | 16 | 3 | 1 | 2 | 4 | RNF139_chr8_124469880_124493618 | RNF139 | AGAGA others(3194): Show |
chr8 | 124469880 | 124493618 |
| a0001c0002t0004 | 0/0 | 3199 | 12 | 0 | 0 | 12 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | AGAGA others(3194): Show |
chr8 | 124469880 | 124493618 |
| a0001c0002t0005 | 0/0 | 3200 | 4 | 2 | 2 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | AGAGA others(3195): Show |
chr8 | 124469880 | 124493618 |
| a0001c0002t0007 | 0/0 | 3199 | 2 | 2 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | AGAGA others(3194): Show |
chr8 | 124469880 | 124493618 |
| a0001c0002t0009 | 0/0 | 3199 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | AGAGA others(3194): Show |
chr8 | 124469880 | 124493618 |
| a0001c0003t0001 | 0/0 | 3199 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | AGAGA others(3194): Show |
chr8 | 124469880 | 124493618 |
| a0001c0003t0002 | 0/0 | 3202 | 64 | 10 | 2 | 35 | 1 | 16 | RNF139_chr8_124469880_124493618 | RNF139 | AGAGA others(3197): Show |
chr8 | 124469880 | 124493618 |
| a0001c0006t0001 | 0/0 | 3199 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | AGAGA others(3194): Show |
chr8 | 124469880 | 124493618 |
| a0001c0007t0001 | 0/0 | 3199 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | AGAGA others(3194): Show |
chr8 | 124469880 | 124493618 |
| a0002c0008t0001 | 0/0 | 3199 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | AGAGA others(3194): Show |
chr8 | 124469880 | 124493618 |
| a0003c0009t0002 | 0/0 | 3202 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | AGAGA others(3197): Show |
chr8 | 124469880 | 124493618 |
| a0004c0010t0008 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | AGAGA others(3195): Show |
chr8 | 124469880 | 124493618 |
| a0005c0004t0001 | 0/0 | 3159 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | AGAGA others(3154): Show |
chr8 | 124469880 | 124493618 |
| a0006c0005t0001 | 0/0 | 3199 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | AGAGA others(3194): Show |
chr8 | 124469880 | 124493618 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 50 | 3 | 10 | 30 | 3 | 4 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0006 | 0/0 | 11 | 5 | 2 | 4 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0008 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 3 | 0 | 3 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 2 | 0 | 3 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0014 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0026 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0001t0006g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0002 | 0/0 | 13 | 13 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0005 | 0/0 | 14 | 0 | 1 | 9 | 0 | 4 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0022 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0030 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0002g0007 | 0/0 | 13 | 2 | 5 | 6 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0002g0011 | 0/0 | 6 | 0 | 2 | 0 | 2 | 2 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0002g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0002g0027 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0002g0111 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0003g0002 | 0/0 | 14 | 14 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0003g0018 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0003g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0004g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0004g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0005g0002 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0007g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0002t0009g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0003t0002g0003 | 0/0 | 22 | 0 | 1 | 16 | 0 | 5 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0003t0002g0004 | 0/0 | 19 | 3 | 0 | 13 | 1 | 2 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0003t0002g0010 | 0/0 | 6 | 0 | 0 | 0 | 0 | 6 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0003t0002g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0003t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0003t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0003t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0003t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0006t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0001c0007t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0002c0008t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0003c0009t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0004c0010t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0005c0004t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| a0006c0005t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00280 | hp1 | a0001 | c0002 | t0003 | g0087 | EUR | FIN | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00280 | hp2 | a0001 | c0003 | t0002 | g0004 | EUR | FIN | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | FIN | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00408 | hp1 | a0001 | c0002 | t0004 | g0140 | EAS | CHS | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | CHS | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00544 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | CHS | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00597 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | CHS | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | CHS | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | CHS | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0128 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00735 | hp1 | a0001 | c0002 | t0003 | g0038 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0045 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0110 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0027 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0027 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0150 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0092 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0146 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01109 | hp1 | a0001 | c0002 | t0005 | g0002 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01167 | hp1 | a0002 | c0008 | t0001 | g0023 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01168 | hp1 | a0001 | c0002 | t0003 | g0018 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0116 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01243 | hp1 | a0001 | c0002 | t0005 | g0002 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | CLM | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | CLM | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | CLM | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0114 | AMR | CLM | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01358 | hp1 | a0001 | c0003 | t0002 | g0079 | AMR | CLM | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01361 | hp1 | a0001 | c0002 | t0003 | g0086 | AMR | CLM | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0115 | AMR | CLM | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | IBS | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0011 | EUR | IBS | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0011 | EUR | IBS | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01884 | hp2 | a0001 | c0002 | t0003 | g0002 | AFR | ACB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01975 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | PEL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02040 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | KHV | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02071 | hp1 | a0001 | c0002 | t0004 | g0148 | EAS | KHV | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | KHV | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | KHV | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0130 | EAS | KHV | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02135 | hp1 | a0001 | c0003 | t0002 | g0074 | EAS | KHV | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02135 | hp2 | a0001 | c0002 | t0003 | g0018 | EAS | KHV | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02145 | hp1 | a0001 | c0003 | t0002 | g0004 | AFR | ACB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0129 | EAS | CDX | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CDX | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02257 | hp2 | a0001 | c0002 | t0005 | g0002 | AFR | ACB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0090 | AFR | ACB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02280 | hp2 | a0001 | c0002 | t0003 | g0106 | AFR | ACB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02451 | hp1 | a0001 | c0003 | t0002 | g0004 | AFR | ACB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02451 | hp2 | a0001 | c0003 | t0002 | g0082 | AFR | ACB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02523 | hp1 | a0003 | c0009 | t0002 | g0004 | EAS | KHV | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02572 | hp2 | a0001 | c0002 | t0003 | g0002 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02602 | hp2 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02615 | hp1 | a0001 | c0002 | t0003 | g0002 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02615 | hp2 | a0001 | c0002 | t0003 | g0002 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0080 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02630 | hp1 | a0001 | c0002 | t0003 | g0002 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0142 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02647 | hp1 | a0001 | c0002 | t0003 | g0002 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0007 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0002 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0023 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02723 | hp1 | a0004 | c0010 | t0008 | g0089 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02735 | hp1 | a0001 | c0003 | t0002 | g0004 | SAS | PJL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02809 | hp2 | a0001 | c0002 | t0003 | g0002 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02818 | hp2 | a0001 | c0002 | t0003 | g0084 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0122 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ESN | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0143 | AFR | ESN | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ESN | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ESN | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02970 | hp2 | a0001 | c0007 | t0001 | g0002 | AFR | ESN | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03017 | hp1 | a0001 | c0003 | t0002 | g0010 | SAS | PJL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0112 | SAS | PJL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03098 | hp1 | a0001 | c0002 | t0003 | g0002 | AFR | MSL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03098 | hp2 | a0001 | c0002 | t0007 | g0044 | AFR | MSL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0144 | AFR | ESN | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03139 | hp1 | a0001 | c0002 | t0003 | g0002 | AFR | ESN | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03139 | hp2 | a0001 | c0003 | t0002 | g0004 | AFR | ESN | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03209 | hp1 | a0001 | c0002 | t0003 | g0002 | AFR | MSL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03225 | hp1 | a0001 | c0003 | t0002 | g0078 | AFR | MSL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03239 | hp2 | a0001 | c0003 | t0002 | g0010 | SAS | PJL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03453 | hp1 | a0001 | c0003 | t0002 | g0017 | AFR | MSL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | MSL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03486 | hp1 | a0001 | c0002 | t0007 | g0044 | AFR | MSL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | MSL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03490 | hp1 | a0001 | c0002 | t0003 | g0018 | SAS | PJL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03490 | hp2 | a0001 | c0003 | t0002 | g0010 | SAS | PJL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0011 | SAS | PJL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03492 | hp1 | a0001 | c0003 | t0002 | g0010 | SAS | PJL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0027 | AFR | ESN | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0121 | AFR | ESN | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03540 | hp1 | a0001 | c0003 | t0002 | g0017 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03540 | hp2 | a0001 | c0002 | t0005 | g0002 | AFR | GWD | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | MSL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03654 | hp1 | a0001 | c0003 | t0002 | g0010 | SAS | PJL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03669 | hp1 | a0001 | c0003 | t0002 | g0010 | SAS | PJL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03669 | hp2 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03688 | hp2 | a0001 | c0003 | t0002 | g0004 | SAS | STU | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03710 | hp1 | a0001 | c0002 | t0003 | g0085 | SAS | PJL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03831 | hp2 | a0001 | c0003 | t0002 | g0071 | SAS | BEB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03834 | hp1 | a0001 | c0003 | t0002 | g0003 | SAS | BEB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03834 | hp2 | a0001 | c0002 | t0003 | g0018 | SAS | BEB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03927 | hp1 | a0001 | c0003 | t0002 | g0003 | SAS | BEB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03942 | hp2 | a0001 | c0002 | t0003 | g0088 | SAS | BEB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0135 | SAS | STU | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0011 | SAS | BEB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0030 | SAS | BEB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG04199 | hp2 | a0001 | c0003 | t0002 | g0076 | SAS | STU | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG04204 | hp1 | a0001 | c0003 | t0002 | g0003 | SAS | STU | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | STU | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG04228 | hp1 | a0001 | c0003 | t0002 | g0073 | SAS | STU | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | STU | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0023 | AFR | YRI | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18906 | hp1 | a0001 | c0002 | t0003 | g0002 | AFR | YRI | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18940 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18946 | hp1 | a0001 | c0002 | t0004 | g0029 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18948 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18949 | hp2 | a0001 | c0002 | t0004 | g0029 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18950 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18951 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18952 | hp1 | a0001 | c0003 | t0002 | g0072 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18959 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18961 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18961 | hp2 | a0005 | c0004 | t0001 | g0008 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18962 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18963 | hp1 | a0001 | c0002 | t0004 | g0005 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18964 | hp1 | a0001 | c0002 | t0004 | g0005 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18964 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18966 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18971 | hp2 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18972 | hp1 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18974 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18975 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18981 | hp1 | a0006 | c0005 | t0001 | g0054 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18981 | hp2 | a0001 | c0002 | t0004 | g0005 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18982 | hp1 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18983 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18990 | hp1 | a0001 | c0003 | t0002 | g0075 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18991 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18992 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18994 | hp2 | a0001 | c0002 | t0004 | g0029 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18998 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18999 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19000 | hp1 | a0001 | c0003 | t0002 | g0070 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19006 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0149 | AFR | LWK | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | LWK | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19057 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19060 | hp1 | a0001 | c0003 | t0002 | g0077 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19060 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19062 | hp2 | a0001 | c0003 | t0002 | g0081 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19064 | hp2 | a0001 | c0002 | t0004 | g0005 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19067 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19072 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19072 | hp2 | a0001 | c0002 | t0004 | g0147 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19074 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19077 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19079 | hp1 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19080 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19081 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19083 | hp1 | a0001 | c0006 | t0001 | g0059 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19087 | hp2 | a0001 | c0002 | t0004 | g0134 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19091 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19240 | hp1 | a0001 | c0002 | t0003 | g0002 | AFR | YRI | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA20129 | hp1 | a0001 | c0003 | t0002 | g0017 | AFR | ASW | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA20129 | hp2 | a0001 | c0002 | t0003 | g0002 | AFR | ASW | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA20752 | hp2 | a0001 | c0002 | t0003 | g0038 | EUR | TSI | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0113 | AMR | CLM | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02109 | hp1 | a0001 | c0003 | t0002 | g0017 | AFR | ACB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | MSL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| HG06807 | hp2 | a0001 | c0002 | t0009 | g0083 | AFR | USA | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18955 | hp1 | a0001 | c0002 | t0004 | g0005 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0145 | AFR | USA | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0007 | AFR | USA | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | LWK | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | LWK | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0111 | REF | REF | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0039 | REF | REF | RNF139_chr8_124469880_124493618 | RNF139 | chr8 | 124469880 | 124493618 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:124475173 | C | T | 1 | a0004 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.64C>T | p.Leu22Phe | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/2 | 294/3199 | 64/1995 | 22/664 | chr8 | 124475173 | |||
| chr8:124480507 | ATGAATTA others(7632): Show |
A | 1 | a0001 | 1 | HG02622.hp1 | stop_lost&conservative_inframe_deletion&splice_region_variant | HIGH | c.181+5221_*505del | p.Gly61_Ter665delins others(3): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 2/2 | 182/1995 | 61/664 | INFO_REALIGN_3_PRIME | chr8 | 124480507 | |||
| chr8:124486431 | A | G | 1 | a0003 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.782A>G | p.Asn261Ser | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 2/2 | 1012/3199 | 782/1995 | 261/664 | chr8 | 124486431 | |||
| chr8:124487207 | ATGAATCG others(33): Show |
A | 1 | a0005 | 1 | NA18961.hp2 | frameshift_variant | HIGH | c.1563_1602delTCGTAG others(34): Show |
p.Asn521fs | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 2/2 | 1793/3199 | 1563/1995 | 521/664 | INFO_REALIGN_3_PRIME | chr8 | 124487207 | ||
| chr8:124487595 | T | C | 1 | a0002 | 1 | HG01167.hp1 | missense_variant | MODERATE | c.1946T>C | p.Ile649Thr | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 2/2 | 2176/3199 | 1946/1995 | 649/664 | chr8 | 124487595 | |||
| chr8:124487598 | A | G | 1 | a0006 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.1949A>G | p.Gln650Arg | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 2/2 | 2179/3199 | 1949/1995 | 650/664 | chr8 | 124487598 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:124486306 | C | T | 6 | a0001c0002 a0001c0003 a0001c0007 others(3): Show |
211 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(208): Show |
synonymous_variant | LOW | c.657C>T | p.Tyr219Tyr | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 2/2 | 887/3199 | 657/1995 | 219/664 | chr8 | 124486306 | |||
| chr8:124486975 | G | A | 1 | a0001c0007 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.1326G>A | p.Thr442Thr | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 2/2 | 1556/3199 | 1326/1995 | 442/664 | chr8 | 124486975 | |||
| chr8:124487122 | G | A | 2 | a0001c0003 a0003c0009 |
66 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(63): Show |
synonymous_variant | LOW | c.1473G>A | p.Ser491Ser | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 2/2 | 1703/3199 | 1473/1995 | 491/664 | chr8 | 124487122 | |||
| chr8:124487137 | G | T | 1 | a0001c0006 | 1 | NA19083.hp1 | synonymous_variant | LOW | c.1488G>T | p.Arg496Arg | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 2/2 | 1718/3199 | 1488/1995 | 496/664 | chr8 | 124487137 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:124474895 | A | AGCC | 3 | a0001c0002t0002 a0001c0003t0002 a0003c0009t0002 |
102 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(99): Show |
5_prime_UTR_variant | MODIFIER | c.-202_-200dupGCC | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/2 | 199 | INFO_REALIGN_3_PRIME | chr8 | 124474895 | |||||
| chr8:124475034 | C | A | 1 | a0001c0002t0007 | 2 | HG03098.hp2 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-76C>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/2 | 76 | chr8 | 124475034 | ||||||
| chr8:124488151 | G | A | 1 | a0001c0002t0004 | 12 | HG00408.hp1 HG02071.hp1 NA18946.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*507G>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 2/2 | 507 | chr8 | 124488151 | ||||||
| chr8:124488231 | A | G | 1 | a0001c0001t0006 | 3 | HG02040.hp1 NA18961.hp1 NA18971.hp2 |
3_prime_UTR_variant | MODIFIER | c.*587A>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 2/2 | 587 | chr8 | 124488231 | ||||||
| chr8:124488277 | A | G | 3 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0005 |
31 | HG00280.hp1 HG00735.hp1 HG01109.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*633A>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 2/2 | 633 | chr8 | 124488277 | ||||||
| chr8:124488364 | T | C | 1 | a0004c0010t0008 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*720T>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 2/2 | 720 | chr8 | 124488364 | ||||||
| chr8:124488380 | G | GT | 2 | a0001c0002t0005 a0004c0010t0008 |
5 | HG01109.hp1 HG01243.hp1 HG02257.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*744dupT | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 2/2 | 745 | INFO_REALIGN_3_PRIME | chr8 | 124488380 | |||||
| chr8:124488389 | A | T | 1 | a0001c0002t0009 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*745A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 2/2 | 745 | chr8 | 124488389 | ||||||
| chr8:124488482 | C | A | 1 | a0004c0010t0008 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*838C>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 2/2 | 838 | chr8 | 124488482 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:124475322 | C | G | 1 | a0001c0002t0002g0150 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.181+32C>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124475322 | |||||||
| chr8:124475452 | G | T | 27 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(24): Show |
56 | HG00408.hp1 HG00423.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.181+162G>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124475452 | |||||||
| chr8:124475487 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.181+197C>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124475487 | |||||||
| chr8:124475525 | G | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(35): Show |
115 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.181+235G>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124475525 | |||||||
| chr8:124475589 | C | G | 1 | a0001c0002t0001g0149 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.181+299C>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124475589 | |||||||
| chr8:124476031 | A | T | 1 | a0001c0002t0004g0148 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.181+741A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124476031 | |||||||
| chr8:124476086 | C | A | 18 | a0001c0003t0002g0003 a0001c0003t0002g0004 a0001c0003t0002g0010 others(15): Show |
65 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.181+796C>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124476086 | |||||||
| chr8:124476125 | A | G | 2 | a0001c0002t0002g0129 a0001c0002t0002g0130 |
2 | HG02080.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.181+835A>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124476125 | |||||||
| chr8:124476190 | C | G | 1 | a0001c0002t0001g0128 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.181+900C>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124476190 | |||||||
| chr8:124476294 | T | C | 1 | a0001c0002t0001g0132 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.181+1004T>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124476294 | |||||||
| chr8:124476307 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.181+1017C>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124476307 | |||||||
| chr8:124476321 | T | G | 1 | a0001c0002t0009g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.181+1031T>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124476321 | |||||||
| chr8:124476463 | A | C | 1 | a0001c0003t0002g0082 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.181+1173A>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124476463 | |||||||
| chr8:124476646 | A | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
8 | HG01257.hp1 HG01361.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.181+1356A>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124476646 | |||||||
| chr8:124476666 | C | T | 28 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(25): Show |
60 | HG00408.hp1 HG00423.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.181+1376C>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124476666 | |||||||
| chr8:124476747 | ATATTCTT others(13): Show |
A | 1 | a0001c0001t0001g0124 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.181+1459_181+1478d others(22): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124476747 | ||||||
| chr8:124476868 | A | G | 1 | a0001c0002t0007g0044 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.181+1578A>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124476868 | |||||||
| chr8:124476974 | G | T | 1 | a0001c0002t0001g0128 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.181+1684G>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124476974 | |||||||
| chr8:124477060 | T | C | 2 | a0001c0002t0001g0128 a0001c0002t0009g0083 |
2 | HG00639.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.181+1770T>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124477060 | |||||||
| chr8:124477326 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.181+2036A>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124477326 | |||||||
| chr8:124477497 | T | C | 1 | a0001c0001t0001g0024 | 3 | NA18956.hp1 NA19007.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.181+2207T>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124477497 | |||||||
| chr8:124477779 | A | C | 1 | a0001c0002t0004g0147 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.181+2489A>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124477779 | |||||||
| chr8:124477797 | A | G | 2 | a0001c0002t0001g0121 a0001c0002t0001g0122 |
2 | HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.181+2507A>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124477797 | |||||||
| chr8:124477859 | G | A | 7 | a0001c0002t0003g0018 a0001c0002t0003g0038 a0001c0002t0003g0084 others(4): Show |
11 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.181+2569G>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124477859 | |||||||
| chr8:124478091 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.181+2801C>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124478091 | |||||||
| chr8:124478291 | A | G | 3 | a0001c0002t0001g0128 a0001c0002t0002g0021 a0001c0002t0007g0044 |
4 | HG00639.hp2 HG03098.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.181+3001A>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124478291 | |||||||
| chr8:124478310 | C | G | 27 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(24): Show |
59 | HG00408.hp1 HG00423.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.181+3020C>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124478310 | |||||||
| chr8:124478402 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.181+3112A>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124478402 | |||||||
| chr8:124478543 | G | T | 6 | a0001c0002t0003g0018 a0001c0002t0003g0038 a0001c0002t0003g0085 others(3): Show |
10 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.181+3253G>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124478543 | |||||||
| chr8:124478562 | C | G | 1 | a0001c0001t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.181+3272C>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124478562 | |||||||
| chr8:124478605 | C | CA | 22 | a0001c0001t0001g0091 a0001c0002t0001g0028 a0001c0002t0001g0133 others(19): Show |
71 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.181+3330dupA | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124478605 | ||||||
| chr8:124478605 | C | CAA | 7 | a0001c0002t0003g0018 a0001c0002t0003g0038 a0001c0002t0003g0085 others(4): Show |
11 | HG00735.hp1 HG01168.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.181+3329_181+3330d others(4): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124478605 | ||||||
| chr8:124478640 | A | G | 1 | a0001c0002t0007g0044 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.181+3350A>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124478640 | |||||||
| chr8:124478673 | C | T | 1 | a0001c0002t0001g0118 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.181+3383C>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124478673 | |||||||
| chr8:124478723 | C | CT | 19 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0002t0002g0117 others(16): Show |
63 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.181+3447dupT | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124478723 | ||||||
| chr8:124478752 | T | C | 1 | a0001c0002t0002g0092 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.181+3462T>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124478752 | |||||||
| chr8:124478776 | A | G | 1 | a0001c0003t0002g0081 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.181+3486A>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124478776 | |||||||
| chr8:124478916 | G | T | 13 | a0001c0002t0002g0007 a0001c0002t0002g0011 a0001c0002t0002g0092 others(10): Show |
30 | HG00621.hp1 HG00733.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.181+3626G>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124478916 | |||||||
| chr8:124478964 | A | T | 1 | a0001c0002t0003g0084 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.181+3674A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124478964 | |||||||
| chr8:124478966 | C | T | 1 | a0001c0003t0002g0080 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.181+3676C>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124478966 | |||||||
| chr8:124479014 | C | A | 19 | a0001c0003t0001g0090 a0001c0003t0002g0003 a0001c0003t0002g0004 others(16): Show |
66 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.181+3724C>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124479014 | |||||||
| chr8:124479107 | T | C | 1 | a0001c0002t0007g0044 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.181+3817T>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124479107 | |||||||
| chr8:124479322 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.181+4032G>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124479322 | |||||||
| chr8:124479354 | T | A | 1 | a0001c0002t0001g0135 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.181+4064T>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124479354 | |||||||
| chr8:124479679 | G | A | 1 | a0001c0002t0002g0110 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.181+4389G>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124479679 | |||||||
| chr8:124479759 | A | G | 1 | a0001c0002t0007g0044 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.181+4469A>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124479759 | |||||||
| chr8:124479840 | G | T | 1 | a0001c0001t0001g0020 | 4 | NA18941.hp2 NA19005.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.181+4550G>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124479840 | |||||||
| chr8:124480139 | TA | T | 29 | a0001c0001t0001g0109 a0001c0002t0001g0005 a0001c0002t0001g0022 others(26): Show |
61 | HG00408.hp1 HG00423.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.181+4861delA | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124480139 | ||||||
| chr8:124480141 | AAAAAAAA others(2894): Show |
A | 1 | a0001c0001t0001g0066 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.181+4857_182-2784d others(2): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124480141 | ||||||
| chr8:124480280 | A | C | 1 | a0001c0002t0001g0128 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.181+4990A>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124480280 | |||||||
| chr8:124480404 | T | A | 1 | a0001c0002t0003g0084 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.181+5114T>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124480404 | |||||||
| chr8:124480404 | T | TA | 29 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0002t0001g0005 others(26): Show |
58 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.181+5136dupA | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124480404 | ||||||
| chr8:124480404 | TA | T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(30): Show |
84 | HG00280.hp1 HG00323.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.181+5136delA | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124480404 | ||||||
| chr8:124480404 | TAA | T | 10 | a0001c0002t0001g0121 a0001c0002t0001g0122 a0001c0002t0002g0027 others(7): Show |
15 | HG01070.hp1 HG01081.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.181+5135_181+5136d others(4): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124480404 | ||||||
| chr8:124480428 | G | T | 1 | a0001c0003t0002g0017 | 4 | HG02109.hp1 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.181+5138G>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124480428 | |||||||
| chr8:124480429 | A | C | 1 | a0001c0003t0002g0017 | 4 | HG02109.hp1 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.181+5139A>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124480429 | |||||||
| chr8:124480571 | G | A | 1 | a0001c0002t0007g0044 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.182-5260G>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124480571 | |||||||
| chr8:124480786 | CCCCATCC others(4146): Show |
C | 1 | a0001c0001t0001g0032 | 2 | NA18612.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.182-5041_182-889de others(1): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124480786 | ||||||
| chr8:124480917 | A | T | 1 | a0001c0001t0001g0049 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.182-4914A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124480917 | |||||||
| chr8:124480928 | G | T | 1 | a0001c0002t0003g0084 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.182-4903G>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124480928 | |||||||
| chr8:124481103 | A | G | 1 | a0001c0002t0004g0134 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.182-4728A>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124481103 | |||||||
| chr8:124481298 | T | C | 13 | a0001c0002t0002g0007 a0001c0002t0002g0011 a0001c0002t0002g0092 others(10): Show |
30 | HG00621.hp1 HG00733.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.182-4533T>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124481298 | |||||||
| chr8:124481333 | G | A | 1 | a0001c0003t0002g0004 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.182-4498G>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124481333 | |||||||
| chr8:124481369 | C | T | 2 | a0001c0002t0001g0128 a0001c0002t0009g0083 |
2 | HG00639.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.182-4462C>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124481369 | |||||||
| chr8:124481374 | T | C | 12 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0028 others(9): Show |
35 | HG00423.hp2 HG00609.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.182-4457T>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124481374 | |||||||
| chr8:124481403 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.182-4428A>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124481403 | |||||||
| chr8:124481406 | G | C | 2 | a0001c0002t0001g0121 a0001c0002t0001g0122 |
2 | HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.182-4425G>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124481406 | |||||||
| chr8:124481418 | C | T | 2 | a0001c0002t0003g0018 a0001c0002t0003g0085 |
2 | HG03710.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.182-4413C>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124481418 | |||||||
| chr8:124481423 | C | T | 1 | a0004c0010t0008g0089 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.182-4408C>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124481423 | |||||||
| chr8:124481701 | A | G | 13 | a0001c0002t0002g0007 a0001c0002t0002g0011 a0001c0002t0002g0092 others(10): Show |
30 | HG00621.hp1 HG00733.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.182-4130A>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124481701 | |||||||
| chr8:124481778 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.182-4053T>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124481778 | |||||||
| chr8:124482031 | A | G | 1 | a0001c0001t0001g0006 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.182-3800A>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482031 | |||||||
| chr8:124482114 | C | A | 1 | a0001c0003t0002g0003 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.182-3717C>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482114 | |||||||
| chr8:124482377 | G | T | 1 | a0001c0002t0003g0018 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.182-3454G>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482377 | |||||||
| chr8:124482403 | T | G | 1 | a0001c0001t0001g0001 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.182-3428T>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482403 | |||||||
| chr8:124482556 | A | G | 1 | a0006c0005t0001g0054 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.182-3275A>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482556 | |||||||
| chr8:124482620 | G | A | 6 | a0001c0002t0002g0007 a0001c0002t0002g0113 a0001c0002t0002g0114 others(3): Show |
14 | HG00621.hp1 HG01074.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.182-3211G>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482620 | |||||||
| chr8:124482644 | G | C | 1 | a0001c0003t0002g0003 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.182-3187G>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482644 | |||||||
| chr8:124482681 | G | C | 19 | a0001c0003t0001g0090 a0001c0003t0002g0003 a0001c0003t0002g0004 others(16): Show |
66 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.182-3150G>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482681 | |||||||
| chr8:124482693 | G | A | 1 | a0002c0008t0001g0023 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.182-3138G>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482693 | |||||||
| chr8:124482762 | A | T | 1 | a0001c0001t0001g0009 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.182-3069A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482762 | |||||||
| chr8:124482848 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.182-2983C>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482848 | |||||||
| chr8:124482909 | G | A | 21 | a0001c0002t0001g0121 a0001c0002t0001g0122 a0001c0003t0001g0090 others(18): Show |
68 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.182-2922G>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482909 | |||||||
| chr8:124482916 | A | ATATATAT others(568): Show |
1 | a0001c0002t0009g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.182-2915_182-2914i others(577): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482916 | |||||||
| chr8:124482920 | C | A | 1 | a0001c0002t0009g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.182-2911C>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482920 | |||||||
| chr8:124482921 | C | T | 1 | a0001c0002t0009g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.182-2910C>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482921 | |||||||
| chr8:124482925 | A | T | 1 | a0001c0002t0009g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.182-2906A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482925 | |||||||
| chr8:124482931 | A | T | 1 | a0001c0002t0009g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.182-2900A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482931 | |||||||
| chr8:124482934 | AT | A | 2 | a0001c0003t0001g0090 a0001c0003t0002g0017 |
4 | HG02109.hp1 HG02258.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.182-2896delT | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482934 | |||||||
| chr8:124482935 | T | A | 18 | a0001c0002t0003g0002 a0001c0003t0002g0003 a0001c0003t0002g0004 others(15): Show |
62 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.182-2896T>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482935 | |||||||
| chr8:124482937 | A | T | 1 | a0001c0002t0009g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.182-2894A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482937 | |||||||
| chr8:124482939 | A | AAT | 6 | a0001c0002t0003g0018 a0001c0002t0003g0038 a0001c0002t0003g0085 others(3): Show |
9 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.182-2891_182-2890i others(4): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124482939 | ||||||
| chr8:124482939 | A | T | 2 | a0001c0002t0003g0018 a0001c0002t0009g0083 |
2 | HG03490.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.182-2892A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482939 | |||||||
| chr8:124482939 | AAAAAATA others(5): Show |
A | 1 | a0001c0002t0001g0005 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.182-2890_182-2879d others(14): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124482939 | ||||||
| chr8:124482940 | A | T | 1 | a0001c0002t0009g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.182-2891A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482940 | |||||||
| chr8:124482941 | A | T | 9 | a0001c0002t0001g0143 a0001c0002t0003g0018 a0001c0002t0003g0038 others(6): Show |
13 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.182-2890A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482941 | |||||||
| chr8:124482943 | A | T | 44 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0024 others(41): Show |
76 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.182-2888A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482943 | |||||||
| chr8:124482944 | AT | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0055 |
4 | NA18946.hp2 NA18998.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-2886delT | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482944 | |||||||
| chr8:124482945 | T | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0061 others(20): Show |
77 | HG00323.hp1 HG00597.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.182-2886T>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482945 | |||||||
| chr8:124482947 | T | A | 3 | a0001c0002t0005g0002 a0001c0003t0002g0003 a0001c0003t0002g0017 |
9 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.182-2884T>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482947 | |||||||
| chr8:124482948 | A | T | 1 | a0001c0002t0001g0132 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.182-2883A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482948 | |||||||
| chr8:124482949 | T | A | 1 | a0001c0003t0002g0017 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.182-2882T>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482949 | |||||||
| chr8:124482949 | TATATATA others(157): Show |
T | 1 | a0001c0002t0001g0132 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.182-2872_182-2709d others(2): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124482949 | ||||||
| chr8:124482954 | A | T | 1 | a0001c0002t0009g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.182-2877A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482954 | |||||||
| chr8:124482956 | A | T | 1 | a0001c0002t0009g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.182-2875A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482956 | |||||||
| chr8:124482958 | A | AATATATA others(25): Show |
1 | a0001c0001t0001g0049 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.182-2872_182-2841d others(34): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124482958 | ||||||
| chr8:124482958 | A | T | 27 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(24): Show |
58 | HG00408.hp1 HG00423.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.182-2873A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482958 | |||||||
| chr8:124482958 | AAT | A | 13 | a0001c0001t0001g0031 a0001c0002t0002g0007 a0001c0002t0002g0011 others(10): Show |
31 | HG00621.hp1 HG00733.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.182-2862_182-2861d others(4): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124482958 | ||||||
| chr8:124482971 | TA | T | 4 | a0001c0001t0001g0001 a0001c0002t0001g0121 a0001c0002t0001g0122 others(1): Show |
4 | HG00639.hp2 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-2859delA | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482971 | |||||||
| chr8:124482972 | A | T | 1 | a0004c0010t0008g0089 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.182-2859A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482972 | |||||||
| chr8:124482974 | T | A | 1 | a0001c0002t0001g0128 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.182-2857T>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482974 | |||||||
| chr8:124482975 | T | A | 2 | a0001c0002t0001g0128 a0004c0010t0008g0089 |
2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.182-2856T>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482975 | |||||||
| chr8:124482976 | A | T | 1 | a0001c0002t0002g0116 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.182-2855A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482976 | |||||||
| chr8:124482977 | A | AAT | 19 | a0001c0002t0007g0044 a0001c0003t0002g0003 a0001c0003t0002g0004 others(16): Show |
66 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.182-2843_182-2842d others(4): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124482977 | ||||||
| chr8:124482977 | A | AATATATA others(28): Show |
7 | a0001c0002t0001g0135 a0001c0002t0004g0005 a0001c0002t0004g0029 others(4): Show |
13 | HG00408.hp1 HG02071.hp1 HG04115.hp1 others(10): Show |
intron_variant | MODIFIER | c.182-2836_182-2802d others(37): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124482977 | ||||||
| chr8:124482977 | A | T | 2 | a0001c0002t0001g0128 a0001c0002t0002g0116 |
2 | HG00639.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.182-2854A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482977 | |||||||
| chr8:124482988 | A | T | 1 | a0001c0002t0009g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.182-2843A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482988 | |||||||
| chr8:124482990 | T | A | 1 | a0001c0002t0002g0027 | 3 | HG01070.hp1 HG01071.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.182-2841T>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482990 | |||||||
| chr8:124482991 | T | A | 2 | a0001c0002t0001g0121 a0001c0002t0001g0122 |
2 | HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.182-2840T>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482991 | |||||||
| chr8:124482992 | A | T | 1 | a0001c0002t0002g0027 | 3 | HG01070.hp1 HG01071.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.182-2839A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482992 | |||||||
| chr8:124482993 | A | T | 1 | a0001c0002t0002g0116 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.182-2838A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482993 | |||||||
| chr8:124482995 | A | AAT | 3 | a0001c0001t0001g0014 a0001c0001t0001g0125 a0001c0001t0001g0127 |
6 | HG01257.hp1 HG01361.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.182-2827_182-2826d others(4): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124482995 | ||||||
| chr8:124482995 | A | T | 6 | a0001c0002t0001g0121 a0001c0002t0001g0122 a0001c0002t0002g0116 others(3): Show |
6 | HG01192.hp1 HG02896.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.182-2836A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482995 | |||||||
| chr8:124482997 | T | A | 1 | a0001c0001t0001g0024 | 3 | NA18956.hp1 NA19007.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.182-2834T>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124482997 | |||||||
| chr8:124483007 | A | T | 2 | a0001c0002t0002g0116 a0001c0002t0009g0083 |
2 | HG01192.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.182-2824A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483007 | |||||||
| chr8:124483008 | A | T | 4 | a0001c0002t0001g0121 a0001c0002t0001g0122 a0001c0002t0002g0116 others(1): Show |
4 | HG01192.hp1 HG02896.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-2823A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483008 | |||||||
| chr8:124483009 | A | T | 3 | a0001c0002t0001g0121 a0001c0002t0001g0122 a0001c0002t0009g0083 |
3 | HG02896.hp2 HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.182-2822A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483009 | |||||||
| chr8:124483010 | A | AT | 1 | a0001c0002t0002g0027 | 3 | HG01070.hp1 HG01071.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.182-2821_182-2820i others(3): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483010 | |||||||
| chr8:124483010 | A | T | 2 | a0001c0002t0001g0121 a0001c0002t0001g0122 |
2 | HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.182-2821A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483010 | |||||||
| chr8:124483010 | AAT | A | 8 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0020 others(5): Show |
23 | HG01069.hp2 HG01071.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.182-2808_182-2807d others(4): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483010 | ||||||
| chr8:124483012 | T | A | 2 | a0001c0002t0001g0121 a0001c0002t0001g0122 |
2 | HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.182-2819T>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483012 | |||||||
| chr8:124483012 | T | TGTATATT others(282): Show |
1 | a0001c0002t0002g0027 | 3 | HG01070.hp1 HG01071.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.182-2819_182-2818i others(291): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483012 | |||||||
| chr8:124483013 | A | ATATATAT others(46): Show |
1 | a0001c0002t0003g0084 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.182-2811_182-2810i others(55): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483013 | ||||||
| chr8:124483023 | A | T | 22 | a0001c0002t0001g0128 a0001c0002t0002g0027 a0001c0002t0003g0084 others(19): Show |
71 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.182-2808A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483023 | |||||||
| chr8:124483025 | T | A | 1 | a0001c0002t0001g0128 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.182-2806T>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483025 | |||||||
| chr8:124483026 | T | A | 1 | a0001c0002t0001g0128 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.182-2805T>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483026 | |||||||
| chr8:124483026 | T | TAAAAATA others(10): Show |
2 | a0001c0002t0001g0121 a0001c0002t0001g0122 |
2 | HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.182-2802_182-2801i others(19): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483026 | ||||||
| chr8:124483026 | TAAATATA others(80): Show |
T | 1 | a0001c0002t0002g0116 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.182-2803_182-2717d others(89): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483026 | ||||||
| chr8:124483027 | A | T | 1 | a0001c0001t0001g0126 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.182-2804A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483027 | |||||||
| chr8:124483028 | A | T | 2 | a0001c0001t0001g0126 a0001c0002t0001g0128 |
2 | HG00639.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.182-2803A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483028 | |||||||
| chr8:124483039 | A | T | 1 | a0001c0002t0009g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.182-2792A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483039 | |||||||
| chr8:124483040 | TTTAAAAA others(8): Show |
T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0051 others(1): Show |
9 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.182-2778_182-2764d others(17): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483040 | ||||||
| chr8:124483044 | A | T | 4 | a0001c0001t0001g0126 a0001c0002t0002g0027 a0001c0002t0003g0084 others(1): Show |
6 | HG01070.hp1 HG01071.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.182-2787A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483044 | |||||||
| chr8:124483046 | A | T | 5 | a0001c0001t0001g0126 a0001c0002t0002g0021 a0001c0002t0002g0027 others(2): Show |
10 | HG01070.hp1 HG01071.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.182-2785A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483046 | |||||||
| chr8:124483053 | C | A | 71 | a0001c0001t0001g0031 a0001c0001t0001g0066 a0001c0002t0001g0005 others(68): Show |
173 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.182-2778C>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483053 | |||||||
| chr8:124483053 | C | T | 3 | a0001c0001t0001g0126 a0001c0002t0002g0027 a0001c0002t0009g0083 |
5 | HG01070.hp1 HG01071.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.182-2778C>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483053 | |||||||
| chr8:124483055 | A | T | 3 | a0001c0001t0001g0126 a0001c0002t0002g0027 a0001c0002t0003g0084 |
5 | HG01070.hp1 HG01071.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.182-2776A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483055 | |||||||
| chr8:124483056 | T | TA | 2 | a0001c0002t0002g0027 a0001c0002t0009g0083 |
4 | HG01070.hp1 HG01071.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.182-2775_182-2774i others(3): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483056 | |||||||
| chr8:124483059 | A | T | 2 | a0001c0002t0002g0027 a0001c0002t0009g0083 |
4 | HG01070.hp1 HG01071.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.182-2772A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483059 | |||||||
| chr8:124483061 | A | T | 5 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0002g0027 others(2): Show |
7 | HG01070.hp1 HG01071.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.182-2770A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483061 | |||||||
| chr8:124483062 | A | T | 1 | a0001c0001t0001g0066 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.182-2769A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483062 | |||||||
| chr8:124483064 | A | T | 1 | a0001c0002t0009g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.182-2767A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483064 | |||||||
| chr8:124483066 | A | T | 1 | a0001c0002t0002g0027 | 3 | HG01070.hp1 HG01071.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.182-2765A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483066 | |||||||
| chr8:124483072 | A | T | 1 | a0004c0010t0008g0089 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.182-2759A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483072 | |||||||
| chr8:124483072 | AT | A | 6 | a0001c0001t0001g0066 a0001c0001t0001g0107 a0001c0002t0001g0005 others(3): Show |
10 | HG00639.hp2 HG02165.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.182-2757delT | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483072 | ||||||
| chr8:124483073 | T | TA | 4 | a0001c0002t0001g0045 a0001c0002t0002g0027 a0001c0002t0009g0083 others(1): Show |
7 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.182-2758_182-2757i others(3): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483073 | |||||||
| chr8:124483073 | T | TAAATATA others(403): Show |
1 | a0004c0010t0008g0089 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.182-2758_182-2757i others(412): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483073 | |||||||
| chr8:124483074 | TA | T | 8 | a0001c0001t0001g0108 a0001c0002t0001g0023 a0001c0002t0001g0143 others(5): Show |
10 | HG01099.hp2 HG01167.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.182-2756delA | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483074 | |||||||
| chr8:124483077 | T | A | 1 | a0001c0001t0001g0093 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.182-2754T>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483077 | |||||||
| chr8:124483078 | TAA | T | 4 | a0001c0001t0001g0066 a0001c0002t0003g0084 a0001c0002t0009g0083 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-2751_182-2750d others(4): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483078 | ||||||
| chr8:124483079 | A | T | 1 | a0001c0002t0002g0027 | 3 | HG01070.hp1 HG01071.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.182-2752A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483079 | |||||||
| chr8:124483080 | A | T | 2 | a0001c0001t0001g0126 a0001c0002t0002g0027 |
4 | HG01070.hp1 HG01071.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.182-2751A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483080 | |||||||
| chr8:124483080 | AAT | A | 19 | a0001c0001t0001g0024 a0001c0001t0001g0094 a0001c0003t0002g0003 others(16): Show |
63 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.182-2740_182-2739d others(4): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483080 | ||||||
| chr8:124483082 | T | A | 16 | a0001c0001t0001g0031 a0001c0001t0001g0093 a0001c0002t0002g0007 others(13): Show |
39 | HG00621.hp1 HG00733.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.182-2749T>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483082 | |||||||
| chr8:124483088 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.182-2743T>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483088 | |||||||
| chr8:124483089 | A | T | 1 | a0001c0002t0009g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.182-2742A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483089 | |||||||
| chr8:124483091 | A | T | 5 | a0001c0001t0001g0066 a0001c0001t0001g0126 a0001c0002t0003g0084 others(2): Show |
5 | HG02723.hp1 HG02818.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.182-2740A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483091 | |||||||
| chr8:124483094 | T | A | 1 | a0001c0003t0002g0010 | 6 | HG03017.hp1 HG03239.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.182-2737T>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483094 | |||||||
| chr8:124483095 | A | ATATATAT others(5): Show |
1 | a0001c0002t0002g0027 | 3 | HG01070.hp1 HG01071.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.182-2736_182-2735i others(14): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483095 | |||||||
| chr8:124483096 | A | T | 1 | a0001c0002t0002g0027 | 3 | HG01070.hp1 HG01071.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.182-2735A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483096 | |||||||
| chr8:124483098 | A | AT | 1 | a0001c0003t0002g0010 | 6 | HG03017.hp1 HG03239.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.182-2733_182-2732i others(3): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483098 | |||||||
| chr8:124483098 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.182-2733A>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483098 | |||||||
| chr8:124483098 | A | T | 11 | a0001c0001t0001g0066 a0001c0001t0001g0126 a0001c0002t0003g0018 others(8): Show |
15 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.182-2733A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483098 | |||||||
| chr8:124483105 | A | C | 1 | a0001c0001t0001g0107 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.182-2726A>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483105 | |||||||
| chr8:124483107 | AT | A | 4 | a0001c0001t0001g0066 a0001c0001t0001g0126 a0001c0002t0003g0084 others(1): Show |
4 | HG02818.hp2 HG06807.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.182-2722delT | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483107 | ||||||
| chr8:124483108 | T | TA | 1 | a0001c0002t0002g0027 | 3 | HG01070.hp1 HG01071.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.182-2723_182-2722i others(3): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTA others(382): Show |
1 | a0001c0002t0003g0002 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.182-2723_182-2722i others(391): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTA others(374): Show |
1 | a0001c0002t0003g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.182-2723_182-2722i others(383): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(363): Show |
2 | a0001c0001t0001g0002 a0001c0001t0001g0065 |
2 | HG02273.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.182-2723_182-2722i others(372): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(385): Show |
1 | a0001c0001t0001g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.182-2723_182-2722i others(394): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(413): Show |
1 | a0001c0002t0003g0002 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.182-2723_182-2722i others(422): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(227): Show |
1 | a0001c0002t0003g0002 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.182-2723_182-2722i others(236): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(392): Show |
1 | a0001c0002t0005g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.182-2723_182-2722i others(401): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(392): Show |
1 | a0001c0002t0005g0002 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.182-2723_182-2722i others(401): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(392): Show |
1 | a0001c0002t0005g0002 | 2 | HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.182-2723_182-2722i others(401): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(418): Show |
1 | a0001c0002t0003g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.182-2723_182-2722i others(427): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(390): Show |
1 | a0001c0002t0003g0002 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.182-2723_182-2722i others(399): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(390): Show |
1 | a0001c0002t0003g0002 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.182-2723_182-2722i others(399): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(364): Show |
1 | a0001c0002t0003g0106 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.182-2723_182-2722i others(373): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(427): Show |
1 | a0001c0007t0001g0002 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.182-2723_182-2722i others(436): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(437): Show |
1 | a0001c0002t0001g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.182-2723_182-2722i others(446): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(381): Show |
1 | a0001c0002t0003g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.182-2723_182-2722i others(390): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(383): Show |
1 | a0001c0002t0003g0002 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.182-2723_182-2722i others(392): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(383): Show |
1 | a0001c0002t0003g0002 | 2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.182-2723_182-2722i others(392): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(383): Show |
1 | a0001c0002t0003g0002 | 2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.182-2723_182-2722i others(392): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(406): Show |
1 | a0001c0002t0002g0021 | 4 | NA18939.hp2 NA18947.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.182-2723_182-2722i others(415): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(431): Show |
1 | a0001c0002t0001g0002 | 3 | HG02886.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.182-2723_182-2722i others(440): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(431): Show |
1 | a0001c0002t0001g0002 | 3 | HG02559.hp2 HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.182-2723_182-2722i others(440): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(459): Show |
1 | a0001c0002t0001g0002 | 5 | HG01884.hp1 HG02257.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.182-2723_182-2722i others(468): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(506): Show |
1 | a0001c0002t0001g0002 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.182-2723_182-2722i others(515): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483108 | T | TATTATTT others(375): Show |
1 | a0001c0002t0003g0002 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.182-2723_182-2722i others(384): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483108 | |||||||
| chr8:124483110 | A | ATTT | 2 | a0001c0001t0001g0064 a0001c0003t0002g0010 |
7 | HG03017.hp1 HG03239.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.182-2721_182-2720i others(5): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483110 | |||||||
| chr8:124483110 | A | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0093 a0001c0002t0002g0092 others(1): Show |
4 | HG01081.hp2 HG02258.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.182-2721A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483110 | |||||||
| chr8:124483111 | A | T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0065 a0001c0001t0001g0066 others(10): Show |
47 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.182-2720A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483111 | |||||||
| chr8:124483112 | A | T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0065 a0001c0001t0001g0066 others(10): Show |
47 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.182-2719A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483112 | |||||||
| chr8:124483113 | A | AATATATA others(273): Show |
1 | a0001c0002t0002g0112 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.182-2708_182-2707i others(282): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(473): Show |
1 | a0001c0002t0001g0128 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.182-2708_182-2707i others(482): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(376): Show |
1 | a0001c0001t0001g0107 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.182-2708_182-2707i others(385): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(421): Show |
1 | a0001c0002t0001g0045 | 2 | HG00735.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.182-2708_182-2707i others(430): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(302): Show |
1 | a0001c0001t0001g0012 | 5 | HG00140.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.182-2708_182-2707i others(311): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(92): Show |
1 | a0001c0001t0001g0047 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(101): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(114): Show |
1 | a0001c0001t0001g0019 | 4 | HG02015.hp1 NA18994.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.182-2703_182-2702i others(123): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(196): Show |
3 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0067 |
4 | HG02818.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.182-2703_182-2702i others(205): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(315): Show |
1 | a0001c0001t0001g0013 | 5 | HG02258.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.182-2703_182-2702i others(324): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(348): Show |
1 | a0001c0001t0001g0094 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(357): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(321): Show |
1 | a0001c0001t0001g0015 | 4 | HG01168.hp2 HG01169.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.182-2703_182-2702i others(330): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(318): Show |
1 | a0001c0001t0001g0049 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(327): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(208): Show |
2 | a0001c0001t0001g0025 a0001c0001t0001g0109 |
4 | NA18939.hp1 NA18957.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-2703_182-2702i others(217): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(206): Show |
1 | a0001c0001t0001g0095 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(215): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(302): Show |
1 | a0001c0001t0001g0050 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(311): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(344): Show |
1 | a0001c0001t0001g0040 | 2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.182-2703_182-2702i others(353): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(340): Show |
1 | a0001c0001t0001g0051 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.182-2703_182-2702i others(349): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(326): Show |
1 | a0001c0001t0001g0052 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(335): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(298): Show |
1 | a0001c0001t0001g0053 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.182-2703_182-2702i others(307): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(328): Show |
1 | a0006c0005t0001g0054 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(337): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(326): Show |
12 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(9): Show |
67 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.182-2703_182-2702i others(335): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(324): Show |
1 | a0001c0001t0001g0097 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.182-2703_182-2702i others(333): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(332): Show |
1 | a0001c0001t0001g0098 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(341): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(368): Show |
1 | a0001c0001t0001g0124 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(377): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(350): Show |
1 | a0001c0001t0001g0099 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.182-2703_182-2702i others(359): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(348): Show |
6 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0100 others(3): Show |
20 | HG00408.hp2 HG00639.hp1 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.182-2703_182-2702i others(357): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(376): Show |
2 | a0001c0001t0001g0014 a0001c0001t0001g0101 |
6 | HG01257.hp1 HG01975.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.182-2703_182-2702i others(385): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(346): Show |
1 | a0001c0001t0001g0102 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.182-2703_182-2702i others(355): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(483): Show |
1 | a0001c0001t0001g0041 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.182-2703_182-2702i others(492): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(334): Show |
1 | a0001c0001t0001g0103 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.182-2703_182-2702i others(343): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(317): Show |
1 | a0001c0001t0001g0131 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(326): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(316): Show |
1 | a0001c0001t0001g0009 | 6 | HG02683.hp2 HG03688.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.182-2703_182-2702i others(325): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(300): Show |
1 | a0001c0001t0001g0057 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.182-2703_182-2702i others(309): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(344): Show |
1 | a0001c0001t0001g0058 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(353): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(423): Show |
1 | a0001c0006t0001g0059 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(432): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(312): Show |
1 | a0001c0001t0001g0035 | 2 | HG02004.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.182-2703_182-2702i others(321): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(377): Show |
2 | a0001c0001t0001g0020 a0001c0001t0001g0042 |
6 | NA18941.hp2 NA18991.hp1 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.182-2703_182-2702i others(386): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(323): Show |
1 | a0001c0001t0001g0060 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(332): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(235): Show |
1 | a0001c0001t0001g0061 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(244): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(326): Show |
1 | a0001c0001t0001g0104 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.182-2703_182-2702i others(335): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(357): Show |
1 | a0001c0001t0001g0036 | 2 | NA18960.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.182-2703_182-2702i others(366): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(274): Show |
1 | a0001c0001t0001g0043 | 2 | NA18942.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.182-2703_182-2702i others(283): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(268): Show |
3 | a0001c0001t0001g0008 a0001c0001t0001g0091 a0005c0004t0001g0008 |
12 | NA18955.hp2 NA18961.hp2 NA18962.hp1 others(9): Show |
intron_variant | MODIFIER | c.182-2703_182-2702i others(277): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(394): Show |
1 | a0001c0003t0002g0072 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(403): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(394): Show |
1 | a0001c0003t0002g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(403): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(394): Show |
3 | a0001c0003t0002g0003 a0001c0003t0002g0070 a0001c0003t0002g0081 |
24 | HG00597.hp1 HG01975.hp2 HG02602.hp2 others(21): Show |
intron_variant | MODIFIER | c.182-2703_182-2702i others(403): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(392): Show |
5 | a0001c0003t0002g0004 a0001c0003t0002g0071 a0001c0003t0002g0080 others(2): Show |
23 | HG00280.hp2 HG00544.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.182-2703_182-2702i others(401): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(422): Show |
1 | a0001c0003t0002g0074 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(431): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(380): Show |
1 | a0001c0003t0002g0075 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(389): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(392): Show |
1 | a0001c0003t0002g0076 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.182-2703_182-2702i others(401): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(380): Show |
1 | a0001c0003t0002g0077 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(389): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(180): Show |
1 | a0001c0002t0002g0113 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(189): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(396): Show |
1 | a0001c0002t0003g0085 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(405): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(364): Show |
1 | a0001c0003t0002g0078 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(373): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(392): Show |
1 | a0001c0002t0001g0118 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(401): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(361): Show |
1 | a0001c0002t0007g0044 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.182-2703_182-2702i others(370): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(345): Show |
1 | a0001c0002t0001g0136 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.182-2703_182-2702i others(354): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(445): Show |
2 | a0001c0002t0001g0022 a0001c0002t0001g0133 |
5 | NA18949.hp1 NA18974.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.182-2703_182-2702i others(454): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(443): Show |
1 | a0001c0002t0001g0137 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.182-2703_182-2702i others(452): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(346): Show |
1 | a0001c0002t0001g0143 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(355): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(359): Show |
1 | a0001c0002t0001g0138 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(368): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(369): Show |
1 | a0001c0002t0004g0147 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.182-2703_182-2702i others(378): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(398): Show |
1 | a0001c0002t0001g0139 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(407): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(371): Show |
1 | a0001c0002t0004g0140 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(380): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(369): Show |
7 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0135 others(4): Show |
28 | HG00423.hp2 HG00741.hp2 HG02071.hp1 others(25): Show |
intron_variant | MODIFIER | c.182-2703_182-2702i others(378): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(401): Show |
2 | a0001c0002t0001g0030 a0001c0002t0004g0134 |
4 | HG04184.hp2 NA19067.hp1 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-2703_182-2702i others(410): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(351): Show |
2 | a0001c0002t0001g0142 a0001c0002t0001g0144 |
2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.182-2703_182-2702i others(360): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(318): Show |
4 | a0001c0002t0002g0007 a0001c0002t0002g0117 a0001c0002t0002g0129 others(1): Show |
16 | HG00621.hp1 HG00733.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.182-2703_182-2702i others(327): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(346): Show |
1 | a0001c0002t0002g0114 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.182-2703_182-2702i others(355): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(360): Show |
1 | a0001c0003t0002g0017 | 4 | HG02109.hp1 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.182-2703_182-2702i others(369): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(362): Show |
1 | a0001c0002t0003g0038 | 2 | HG00735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.182-2703_182-2702i others(371): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(398): Show |
3 | a0001c0002t0003g0018 a0001c0002t0003g0087 a0001c0002t0003g0088 |
6 | HG00280.hp1 HG01168.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.182-2703_182-2702i others(407): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(392): Show |
1 | a0001c0002t0003g0086 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(401): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(311): Show |
1 | a0001c0002t0002g0115 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.182-2703_182-2702i others(320): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(314): Show |
4 | a0001c0001t0001g0031 a0001c0002t0002g0011 a0001c0002t0002g0110 others(1): Show |
10 | HG01069.hp1 HG01081.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.182-2703_182-2702i others(323): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(236): Show |
4 | a0001c0002t0001g0023 a0001c0002t0001g0145 a0001c0002t0001g0149 others(1): Show |
6 | HG01167.hp1 HG02717.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.182-2703_182-2702i others(245): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(268): Show |
1 | a0001c0002t0001g0146 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.182-2703_182-2702i others(277): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(140): Show |
2 | a0001c0001t0001g0125 a0001c0001t0001g0127 |
2 | HG01361.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.182-2703_182-2702i others(149): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(136): Show |
2 | a0001c0002t0001g0121 a0001c0002t0001g0122 |
2 | HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.182-2703_182-2702i others(145): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATA others(220): Show |
1 | a0001c0003t0002g0079 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.182-2710_182-2709i others(229): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATT others(153): Show |
1 | a0001c0001t0001g0062 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.182-2712_182-2711i others(162): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATT others(167): Show |
1 | a0001c0001t0001g0037 | 2 | HG00140.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.182-2712_182-2711i others(176): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AATATATT others(361): Show |
1 | a0001c0001t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.182-2712_182-2711i others(370): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483113 | ||||||
| chr8:124483113 | A | AGATATAT others(193): Show |
1 | a0001c0002t0002g0092 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.182-2718_182-2717i others(202): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483113 | |||||||
| chr8:124483113 | A | AGATATAT others(193): Show |
1 | a0001c0001t0001g0063 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.182-2718_182-2717i others(202): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483113 | |||||||
| chr8:124483113 | A | ATATATAT others(358): Show |
1 | a0001c0001t0001g0064 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.182-2718_182-2717i others(367): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483113 | |||||||
| chr8:124483113 | A | ATATATAT others(422): Show |
1 | a0001c0003t0002g0010 | 6 | HG03017.hp1 HG03239.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.182-2718_182-2717i others(431): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483113 | |||||||
| chr8:124483113 | A | ATATATAT others(347): Show |
1 | a0001c0003t0001g0090 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.182-2718_182-2717i others(356): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483113 | |||||||
| chr8:124483113 | A | ATATATAT others(97): Show |
1 | a0001c0001t0001g0093 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.182-2718_182-2717i others(106): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483113 | |||||||
| chr8:124483113 | A | T | 14 | a0001c0001t0001g0002 a0001c0001t0001g0065 a0001c0001t0001g0066 others(11): Show |
48 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.182-2718A>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483113 | |||||||
| chr8:124483137 | T | C | 1 | a0001c0002t0002g0129 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.182-2694T>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483137 | |||||||
| chr8:124483378 | T | C | 1 | a0001c0002t0002g0112 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.182-2453T>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483378 | |||||||
| chr8:124483436 | ATATT | A | 1 | a0001c0001t0001g0026 | 3 | HG00639.hp1 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.182-2383_182-2380d others(6): Show |
RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124483436 | ||||||
| chr8:124483467 | G | T | 7 | a0001c0002t0003g0018 a0001c0002t0003g0038 a0001c0002t0003g0084 others(4): Show |
11 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.182-2364G>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483467 | |||||||
| chr8:124483502 | G | A | 1 | a0001c0001t0001g0013 | 5 | HG02258.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.182-2329G>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483502 | |||||||
| chr8:124483609 | T | G | 27 | a0001c0002t0001g0005 a0001c0002t0001g0022 a0001c0002t0001g0023 others(24): Show |
59 | HG00408.hp1 HG00423.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.182-2222T>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483609 | |||||||
| chr8:124483724 | C | T | 1 | a0001c0002t0003g0084 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.182-2107C>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483724 | |||||||
| chr8:124483983 | T | C | 19 | a0001c0003t0001g0090 a0001c0003t0002g0003 a0001c0003t0002g0004 others(16): Show |
66 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.182-1848T>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124483983 | |||||||
| chr8:124484072 | C | G | 1 | a0001c0001t0001g0056 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.182-1759C>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124484072 | |||||||
| chr8:124484167 | C | T | 1 | a0001c0001t0001g0016 | 4 | HG01069.hp2 HG01071.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-1664C>T | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124484167 | |||||||
| chr8:124484245 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.182-1586A>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124484245 | |||||||
| chr8:124484255 | A | G | 1 | a0001c0001t0001g0034 | 2 | NA18940.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.182-1576A>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124484255 | |||||||
| chr8:124484613 | C | A | 1 | a0001c0002t0002g0027 | 3 | HG01070.hp1 HG01071.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.182-1218C>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124484613 | |||||||
| chr8:124484724 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.182-1107T>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124484724 | |||||||
| chr8:124484892 | G | A | 1 | a0001c0002t0003g0084 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.182-939G>A | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124484892 | |||||||
| chr8:124484920 | A | G | 1 | a0001c0002t0003g0106 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.182-911A>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124484920 | |||||||
| chr8:124485102 | C | G | 1 | a0001c0002t0001g0141 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.182-729C>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124485102 | |||||||
| chr8:124485180 | A | G | 1 | a0001c0002t0007g0044 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.182-651A>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124485180 | |||||||
| chr8:124485288 | T | TG | 2 | a0001c0002t0004g0029 a0001c0002t0004g0147 |
4 | NA18946.hp1 NA18949.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-540dupG | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr8 | 124485288 | ||||||
| chr8:124485329 | A | G | 2 | a0001c0001t0001g0048 a0001c0001t0001g0067 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.182-502A>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124485329 | |||||||
| chr8:124485515 | G | C | 1 | a0001c0002t0001g0145 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.182-316G>C | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124485515 | |||||||
| chr8:124485551 | A | G | 5 | a0001c0002t0001g0023 a0001c0002t0001g0145 a0001c0002t0001g0146 others(2): Show |
7 | HG01099.hp2 HG01167.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.182-280A>G | RNF139 | ENSG00000170881.5 | transcript | ENST00000303545.4 | protein_coding | 1/1 | chr8 | 124485551 |