Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9917 |
| ensemblid | ENSG00000116199.12 |
| hgncid | 23017 |
| symbol | FAM20B |
| name | FAM20B glycosaminoglycan xylosylkinase |
| refseq_nuc | NM_014864.4 |
| refseq_prot | NP_055679.1 |
| ensembl_nuc | ENST00000263733.5 |
| ensembl_prot | ENSP00000263733.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 179025894 |
| end | 179076567 |
| strand | + |
| ver | v1.2 |
| region | chr1:179025894-179076567 |
| region5000 | chr1:179020894-179081567 |
| regionname0 | FAM20B_chr1_179025894_179076567 |
| regionname5000 | FAM20B_chr1_179020894_179081567 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 409 | 406 | 89 | 78 | 190 | 14 | 33 | 144 | FAM20B_chr1_179020894_179081567 | FAM20B | MKLKQ others(404): Show |
chr1 | 179020894 | 179081567 |
| a0002 | 0/0 | 409 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | MKLKQ others(404): Show |
chr1 | 179020894 | 179081567 |
| a0003 | 0/0 | 409 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | MKLKQ others(404): Show |
chr1 | 179020894 | 179081567 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1227 | 404 | 89 | 76 | 190 | 14 | 33 | FAM20B_chr1_179020894_179081567 | FAM20B | ATGAA others(1222): Show |
chr1 | 179020894 | 179081567 | ||
| a0001c0002 | 0/0 | 1227 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | ATGAA others(1222): Show |
chr1 | 179020894 | 179081567 | ||
| a0002c0003 | 0/0 | 1227 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | ATGAA others(1222): Show |
chr1 | 179020894 | 179081567 | ||
| a0003c0004 | 0/0 | 1227 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | ATGAA others(1222): Show |
chr1 | 179020894 | 179081567 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5990 | 112 | 23 | 22 | 50 | 7 | 9 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5985): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0002 | 1/0 | 5991 | 93 | 2 | 25 | 51 | 3 | 11 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5986): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0003 | 0/0 | 5990 | 65 | 8 | 6 | 47 | 0 | 4 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5985): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0004 | 0/0 | 5991 | 26 | 0 | 10 | 9 | 2 | 5 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5986): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0005 | 0/0 | 5991 | 17 | 2 | 1 | 14 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5986): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0006 | 0/0 | 5990 | 15 | 9 | 2 | 0 | 1 | 3 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5985): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0007 | 0/0 | 5990 | 10 | 9 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5985): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0008 | 0/0 | 5990 | 10 | 9 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5985): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0009 | 0/0 | 5990 | 5 | 5 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5985): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0010 | 0/0 | 5990 | 5 | 0 | 4 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5985): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0011 | 0/0 | 5990 | 4 | 3 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5985): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0012 | 0/0 | 5991 | 4 | 2 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5986): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0013 | 0/0 | 5991 | 3 | 0 | 0 | 3 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5986): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0014 | 0/0 | 5991 | 3 | 0 | 0 | 3 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5986): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0015 | 0/0 | 5990 | 3 | 3 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5985): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0016 | 0/0 | 5990 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5985): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0017 | 0/0 | 5991 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5986): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0018 | 0/0 | 5990 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5985): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0019 | 0/0 | 5990 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5985): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0021 | 0/0 | 5991 | 2 | 0 | 1 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5986): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0022 | 0/0 | 5990 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5985): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0023 | 0/0 | 5990 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5985): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0024 | 0/0 | 5991 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5986): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0025 | 0/0 | 5991 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5986): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0026 | 0/0 | 5974 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5969): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0027 | 0/0 | 5991 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5986): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0028 | 0/0 | 5991 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5986): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0029 | 0/0 | 5990 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5985): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0030 | 0/0 | 5990 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5985): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0031 | 0/0 | 5990 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5985): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0032 | 0/0 | 5991 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5986): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0033 | 0/0 | 5991 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5986): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0034 | 0/0 | 5990 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5985): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0035 | 0/0 | 5990 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5985): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0036 | 0/0 | 5991 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5986): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0037 | 0/0 | 5991 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5986): Show |
chr1 | 179020894 | 179081567 |
| a0001c0001t0038 | 0/0 | 5990 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5985): Show |
chr1 | 179020894 | 179081567 |
| a0001c0002t0020 | 0/0 | 5990 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5985): Show |
chr1 | 179020894 | 179081567 |
| a0002c0003t0005 | 0/0 | 5991 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5986): Show |
chr1 | 179020894 | 179081567 |
| a0003c0004t0006 | 0/0 | 5990 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | GGGTG others(5985): Show |
chr1 | 179020894 | 179081567 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 0 | 0 | 12 | 1 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0046 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0276 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0002 | 0/0 | 13 | 0 | 2 | 11 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0003 | 0/0 | 9 | 0 | 1 | 3 | 0 | 5 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0006 | 0/0 | 6 | 1 | 4 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0008 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0193 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0004g0007 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0004g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0004g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0004g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0004g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0005g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0006g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0006g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0006g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0006g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0006g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0006g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0007g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0007g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0007g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0007g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0007g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0008g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0008g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0008g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0008g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0008g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0008g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0008g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0009g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0009g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0009g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0009g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0010g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0010g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0010g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0010g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0011g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0011g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0011g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0012g0014 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0012g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0013g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0013g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0013g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0014g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0014g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0014g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0015g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0015g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0015g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0016g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0016g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0017g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0017g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0018g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0019g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0019g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0021g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0021g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0022g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0023g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0023g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0024g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0025g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0026g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0027g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0028g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0029g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0030g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0031g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0032g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0033g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0034g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0035g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0036g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0037g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0001t0038g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0002t0020g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0001c0002t0020g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0002c0003t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| a0003c0004t0006g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0201 | EUR | GBR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | GBR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00140 | hp1 | a0001 | c0001 | t0006 | g0092 | EUR | GBR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0031 | EUR | GBR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0279 | EUR | FIN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00544 | hp1 | a0001 | c0001 | t0005 | g0064 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00544 | hp2 | a0001 | c0001 | t0014 | g0198 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0156 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00639 | hp1 | a0001 | c0001 | t0010 | g0024 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00642 | hp1 | a0001 | c0001 | t0021 | g0124 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0130 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00733 | hp2 | a0001 | c0001 | t0006 | g0097 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00735 | hp2 | a0001 | c0002 | t0020 | g0105 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0168 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01069 | hp2 | a0001 | c0001 | t0011 | g0015 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01070 | hp1 | a0001 | c0001 | t0010 | g0096 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01070 | hp2 | a0001 | c0001 | t0012 | g0014 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01071 | hp2 | a0001 | c0001 | t0012 | g0014 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0066 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0129 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0128 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01099 | hp2 | a0001 | c0001 | t0007 | g0108 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0162 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0154 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0032 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01175 | hp1 | a0001 | c0002 | t0020 | g0104 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01175 | hp2 | a0001 | c0001 | t0010 | g0091 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0152 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0032 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01346 | hp2 | a0001 | c0001 | t0008 | g0224 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0169 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01433 | hp1 | a0001 | c0001 | t0010 | g0024 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0165 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0161 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0186 | EUR | IBS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01515 | hp2 | a0001 | c0001 | t0010 | g0095 | EUR | IBS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0006 | EUR | IBS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01891 | hp1 | a0001 | c0001 | t0015 | g0101 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01891 | hp2 | a0001 | c0001 | t0011 | g0102 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0033 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0094 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02015 | hp1 | a0001 | c0001 | t0005 | g0062 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0223 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02056 | hp2 | a0001 | c0001 | t0005 | g0061 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02074 | hp1 | a0001 | c0001 | t0027 | g0008 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0059 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02083 | hp1 | a0001 | c0001 | t0021 | g0116 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02083 | hp2 | a0001 | c0001 | t0035 | g0133 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0071 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0109 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | CDX | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | CDX | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | CDX | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02165 | hp2 | a0001 | c0001 | t0026 | g0157 | EAS | CDX | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0089 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0122 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0043 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02451 | hp2 | a0001 | c0001 | t0019 | g0074 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02572 | hp1 | a0001 | c0001 | t0017 | g0291 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02572 | hp2 | a0001 | c0001 | t0016 | g0225 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0290 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0107 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02630 | hp1 | a0001 | c0001 | t0019 | g0075 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02647 | hp1 | a0001 | c0001 | t0016 | g0226 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0106 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02723 | hp1 | a0001 | c0001 | t0011 | g0015 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0112 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02809 | hp1 | a0001 | c0001 | t0033 | g0015 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0060 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02886 | hp2 | a0002 | c0003 | t0005 | g0063 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02895 | hp2 | a0001 | c0001 | t0018 | g0026 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02897 | hp1 | a0001 | c0001 | t0018 | g0026 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0082 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0150 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0042 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02965 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0025 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02976 | hp1 | a0001 | c0001 | t0030 | g0262 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0042 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0159 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03017 | hp2 | a0001 | c0001 | t0029 | g0280 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03041 | hp1 | a0001 | c0001 | t0015 | g0080 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0285 | AFR | MSL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0084 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0085 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0068 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0111 | AFR | MSL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0086 | AFR | MSL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | MSL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03486 | hp2 | a0001 | c0001 | t0017 | g0292 | AFR | MSL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0160 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0113 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0117 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03516 | hp1 | a0001 | c0001 | t0011 | g0103 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0088 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03540 | hp1 | a0001 | c0001 | t0015 | g0081 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03579 | hp1 | a0001 | c0001 | t0009 | g0222 | AFR | MSL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0027 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03704 | hp1 | a0003 | c0004 | t0006 | g0079 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0087 | SAS | BEB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | BEB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0153 | SAS | BEB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0189 | SAS | BEB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0200 | SAS | BEB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0083 | SAS | BEB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG04115 | hp1 | a0001 | c0001 | t0006 | g0090 | SAS | STU | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0145 | SAS | STU | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0164 | SAS | STU | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | STU | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0031 | SAS | STU | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | YRI | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0250 | AFR | YRI | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | CHB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | YRI | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18942 | hp1 | a0001 | c0001 | t0005 | g0072 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18951 | hp2 | a0001 | c0001 | t0005 | g0065 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18964 | hp2 | a0001 | c0001 | t0013 | g0007 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18974 | hp2 | a0001 | c0001 | t0023 | g0027 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18977 | hp2 | a0001 | c0001 | t0037 | g0010 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18979 | hp2 | a0001 | c0001 | t0034 | g0140 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18993 | hp2 | a0001 | c0001 | t0028 | g0017 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18994 | hp2 | a0001 | c0001 | t0014 | g0213 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18998 | hp1 | a0001 | c0001 | t0013 | g0163 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19000 | hp1 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19001 | hp1 | a0001 | c0001 | t0022 | g0029 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19001 | hp2 | a0001 | c0001 | t0031 | g0252 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19004 | hp1 | a0001 | c0001 | t0005 | g0067 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19006 | hp1 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19006 | hp2 | a0001 | c0001 | t0036 | g0141 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | LWK | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19030 | hp2 | a0001 | c0001 | t0032 | g0100 | AFR | LWK | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19043 | hp1 | a0001 | c0001 | t0025 | g0206 | AFR | LWK | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0098 | AFR | LWK | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19064 | hp1 | a0001 | c0001 | t0005 | g0069 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19076 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19078 | hp1 | a0001 | c0001 | t0014 | g0215 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19086 | hp1 | a0001 | c0001 | t0013 | g0158 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19087 | hp1 | a0001 | c0001 | t0023 | g0125 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0284 | AFR | YRI | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA20129 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | ASW | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | ASW | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | TSI | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0151 | EUR | TSI | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0287 | EUR | TSI | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | GIH | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | GIH | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02109 | hp1 | a0001 | c0001 | t0012 | g0099 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02109 | hp2 | a0001 | c0001 | t0024 | g0073 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0110 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02559 | hp1 | a0001 | c0001 | t0012 | g0014 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0283 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | MSL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0293 | AFR | MSL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG06807 | hp1 | a0001 | c0001 | t0038 | g0057 | AFR | USA | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0093 | AFR | USA | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18955 | hp1 | a0001 | c0001 | t0022 | g0029 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | USA | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | USA | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA21309 | hp1 | a0001 | c0001 | t0009 | g0221 | AFR | LWK | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | LWK | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0276 | REF | REF | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0193 | REF | REF | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:179044186 | A | G | 1 | a0003 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.339A>G | p.Ile113Met | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/8 | 677/5991 | 339/1230 | 113/409 | chr1 | 179044186 | |||
| chr1:179072034 | G | A | 1 | a0002 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.1120G>A | p.Ala374Thr | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 1458/5991 | 1120/1230 | 374/409 | chr1 | 179072034 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:179044069 | G | A | 1 | a0001c0002 | 2 | HG00735.hp2 HG01175.hp1 |
synonymous_variant | LOW | c.222G>A | p.Arg74Arg | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/8 | 560/5991 | 222/1230 | 74/409 | chr1 | 179044069 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:179025943 | G | C | 2 | a0001c0001t0009 a0001c0001t0016 |
7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-289G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/8 | 17905 | chr1 | 179025943 | ||||||
| chr1:179026015 | C | T | 1 | a0001c0001t0038 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-217C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/8 | 17833 | chr1 | 179026015 | ||||||
| chr1:179026033 | G | C | 1 | a0001c0001t0007 | 10 | HG01099.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-199G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/8 | 17815 | chr1 | 179026033 | ||||||
| chr1:179043812 | C | G | 9 | a0001c0001t0003 a0001c0001t0015 a0001c0001t0021 others(6): Show |
78 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
5_prime_UTR_variant | MODIFIER | c.-36C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/8 | 36 | chr1 | 179043812 | ||||||
| chr1:179072164 | G | C | 1 | a0001c0001t0016 | 2 | HG02572.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*20G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 20 | chr1 | 179072164 | ||||||
| chr1:179072175 | T | C | 1 | a0001c0001t0008 | 10 | HG01346.hp2 HG02055.hp1 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*31T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 31 | chr1 | 179072175 | ||||||
| chr1:179072256 | G | A | 4 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0038 others(1): Show |
22 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*112G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 112 | chr1 | 179072256 | ||||||
| chr1:179072263 | A | G | 30 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(27): Show |
275 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*119A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 119 | chr1 | 179072263 | ||||||
| chr1:179072517 | C | T | 1 | a0001c0001t0014 | 3 | HG00544.hp2 NA18994.hp2 NA19078.hp1 |
3_prime_UTR_variant | MODIFIER | c.*373C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 373 | chr1 | 179072517 | ||||||
| chr1:179072557 | CT | C | 26 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(23): Show |
268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*425delT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 425 | INFO_REALIGN_3_PRIME | chr1 | 179072557 | |||||
| chr1:179072682 | G | C | 1 | a0001c0001t0029 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*538G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 538 | chr1 | 179072682 | ||||||
| chr1:179072719 | T | C | 2 | a0001c0001t0009 a0001c0001t0016 |
7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*575T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 575 | chr1 | 179072719 | ||||||
| chr1:179072798 | C | T | 1 | a0001c0001t0023 | 2 | NA18974.hp2 NA19087.hp1 |
3_prime_UTR_variant | MODIFIER | c.*654C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 654 | chr1 | 179072798 | ||||||
| chr1:179072835 | G | T | 8 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0011 others(5): Show |
38 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*691G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 691 | chr1 | 179072835 | ||||||
| chr1:179072955 | C | A | 1 | a0001c0001t0010 | 5 | HG00639.hp1 HG01070.hp1 HG01175.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*811C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 811 | chr1 | 179072955 | ||||||
| chr1:179072957 | A | G | 7 | a0001c0001t0003 a0001c0001t0015 a0001c0001t0022 others(4): Show |
75 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*813A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 813 | chr1 | 179072957 | ||||||
| chr1:179073092 | T | C | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(19): Show |
234 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*948T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 948 | chr1 | 179073092 | ||||||
| chr1:179073135 | T | C | 7 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0011 others(4): Show |
36 | HG00544.hp1 HG01069.hp2 HG01074.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*991T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 991 | chr1 | 179073135 | ||||||
| chr1:179073165 | C | A | 11 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(8): Show |
149 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*1021C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 1021 | chr1 | 179073165 | ||||||
| chr1:179073166 | G | A | 1 | a0001c0001t0035 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1022G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 1022 | chr1 | 179073166 | ||||||
| chr1:179073181 | C | T | 7 | a0001c0001t0003 a0001c0001t0015 a0001c0001t0022 others(4): Show |
75 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1037C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 1037 | chr1 | 179073181 | ||||||
| chr1:179073315 | T | G | 14 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(11): Show |
158 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*1171T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 1171 | chr1 | 179073315 | ||||||
| chr1:179073389 | T | C | 35 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(32): Show |
307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*1245T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 1245 | chr1 | 179073389 | ||||||
| chr1:179073484 | T | C | 1 | a0001c0001t0027 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1340T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 1340 | chr1 | 179073484 | ||||||
| chr1:179073613 | G | A | 1 | a0001c0001t0030 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1469G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 1469 | chr1 | 179073613 | ||||||
| chr1:179073846 | G | C | 7 | a0001c0001t0003 a0001c0001t0015 a0001c0001t0022 others(4): Show |
75 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1702G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 1702 | chr1 | 179073846 | ||||||
| chr1:179073876 | C | A | 2 | a0001c0001t0009 a0001c0001t0016 |
7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1732C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 1732 | chr1 | 179073876 | ||||||
| chr1:179074404 | T | G | 30 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(27): Show |
275 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*2260T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 2260 | chr1 | 179074404 | ||||||
| chr1:179074418 | G | A | 7 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0015 others(4): Show |
77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2274G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 2274 | chr1 | 179074418 | ||||||
| chr1:179074804 | G | A | 8 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0011 others(5): Show |
38 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2660G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 2660 | chr1 | 179074804 | ||||||
| chr1:179074907 | G | A | 1 | a0001c0001t0015 | 3 | HG01891.hp1 HG03041.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2763G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 2763 | chr1 | 179074907 | ||||||
| chr1:179074913 | G | A | 1 | a0001c0001t0019 | 2 | HG02451.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2769G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 2769 | chr1 | 179074913 | ||||||
| chr1:179074980 | A | T | 1 | a0001c0001t0031 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2836A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 2836 | chr1 | 179074980 | ||||||
| chr1:179075065 | G | C | 1 | a0001c0001t0024 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2921G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 2921 | chr1 | 179075065 | ||||||
| chr1:179075167 | G | A | 8 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0015 others(5): Show |
79 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*3023G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 3023 | chr1 | 179075167 | ||||||
| chr1:179075191 | T | TA | 4 | a0001c0001t0005 a0001c0001t0017 a0001c0001t0036 others(1): Show |
21 | HG00544.hp1 HG01074.hp1 HG02015.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3060dupA | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 3061 | INFO_REALIGN_3_PRIME | chr1 | 179075191 | |||||
| chr1:179075194 | AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0026 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3053_*3069delAAAA others(13): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 3053 | INFO_REALIGN_3_PRIME | chr1 | 179075194 | |||||
| chr1:179075246 | T | G | 1 | a0001c0001t0022 | 2 | NA18955.hp1 NA19001.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3102T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 3102 | chr1 | 179075246 | ||||||
| chr1:179075320 | A | G | 1 | a0001c0001t0016 | 2 | HG02572.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3176A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 3176 | chr1 | 179075320 | ||||||
| chr1:179075437 | C | T | 1 | a0001c0001t0012 | 4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3293C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 3293 | chr1 | 179075437 | ||||||
| chr1:179075588 | A | G | 3 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0026 |
30 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3444A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 3444 | chr1 | 179075588 | ||||||
| chr1:179075839 | G | T | 1 | a0001c0001t0028 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3695G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 3695 | chr1 | 179075839 | ||||||
| chr1:179076338 | G | A | 8 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0015 others(5): Show |
79 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*4194G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 4194 | chr1 | 179076338 | ||||||
| chr1:179076347 | A | C | 1 | a0001c0001t0032 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4203A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 4203 | chr1 | 179076347 | ||||||
| chr1:179076358 | A | C | 1 | a0001c0001t0012 | 4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4214A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 4214 | chr1 | 179076358 | ||||||
| chr1:179076365 | C | A | 30 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(27): Show |
273 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*4221C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 4221 | chr1 | 179076365 | ||||||
| chr1:179076477 | A | G | 1 | a0001c0001t0013 | 3 | NA18964.hp2 NA18998.hp1 NA19086.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4333A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 4333 | chr1 | 179076477 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:179026148 | G | A | 10 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0049 others(7): Show |
12 | HG00280.hp1 HG00621.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.-134+50G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026148 | |||||||
| chr1:179026167 | A | G | 1 | a0001c0001t0003g0293 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-134+69A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026167 | |||||||
| chr1:179026365 | G | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(93): Show |
133 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.-134+267G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026365 | |||||||
| chr1:179026386 | G | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(206): Show |
274 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.-134+288G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026386 | |||||||
| chr1:179026390 | C | T | 1 | a0001c0001t0007g0150 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-134+292C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026390 | |||||||
| chr1:179026601 | A | T | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-134+503A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026601 | |||||||
| chr1:179026746 | G | T | 5 | a0001c0001t0003g0030 a0001c0001t0003g0146 a0001c0001t0003g0147 others(2): Show |
6 | NA18953.hp2 NA18959.hp1 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.-134+648G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026746 | |||||||
| chr1:179026753 | C | T | 1 | a0001c0001t0003g0293 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-134+655C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026753 | |||||||
| chr1:179026781 | C | T | 1 | a0001c0001t0009g0290 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-134+683C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026781 | |||||||
| chr1:179026821 | G | A | 1 | a0001c0001t0038g0057 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-134+723G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026821 | |||||||
| chr1:179026901 | G | A | 2 | a0001c0001t0009g0221 a0001c0001t0009g0222 |
2 | HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-134+803G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026901 | |||||||
| chr1:179026948 | T | C | 2 | a0001c0001t0008g0223 a0001c0001t0008g0224 |
2 | HG01346.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-134+850T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026948 | |||||||
| chr1:179026954 | T | G | 2 | a0001c0001t0008g0223 a0001c0001t0008g0224 |
2 | HG01346.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-134+856T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026954 | |||||||
| chr1:179027209 | T | G | 235 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(232): Show |
308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.-134+1111T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179027209 | |||||||
| chr1:179027278 | A | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(87): Show |
126 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.-134+1180A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179027278 | |||||||
| chr1:179027526 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-134+1428G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179027526 | |||||||
| chr1:179027658 | G | A | 16 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(13): Show |
18 | HG00544.hp1 HG01074.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.-134+1560G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179027658 | |||||||
| chr1:179027746 | A | G | 49 | a0001c0001t0001g0131 a0001c0001t0003g0004 a0001c0001t0003g0005 others(46): Show |
68 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-134+1648A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179027746 | |||||||
| chr1:179027763 | G | C | 1 | a0001c0001t0024g0073 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-134+1665G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179027763 | |||||||
| chr1:179027938 | T | C | 8 | a0001c0001t0001g0011 a0001c0001t0001g0227 a0001c0001t0001g0228 others(5): Show |
11 | HG00099.hp2 HG00609.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.-134+1840T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179027938 | |||||||
| chr1:179027958 | C | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0234 others(1): Show |
5 | HG01109.hp1 HG02055.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-134+1860C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179027958 | |||||||
| chr1:179028024 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(93): Show |
133 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.-134+1926C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028024 | |||||||
| chr1:179028040 | A | G | 1 | a0001c0001t0018g0026 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-134+1942A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028040 | |||||||
| chr1:179028105 | G | T | 4 | a0001c0001t0002g0017 a0001c0001t0002g0219 a0001c0001t0002g0220 others(1): Show |
5 | HG00621.hp1 NA18942.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.-134+2007G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028105 | |||||||
| chr1:179028109 | A | G | 1 | a0001c0001t0003g0145 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-134+2011A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028109 | |||||||
| chr1:179028114 | T | C | 2 | a0001c0001t0019g0074 a0001c0001t0019g0075 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-134+2016T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028114 | |||||||
| chr1:179028179 | G | A | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG01123.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.-134+2081G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028179 | |||||||
| chr1:179028420 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-134+2322A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028420 | |||||||
| chr1:179028454 | C | T | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-134+2356C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028454 | |||||||
| chr1:179028477 | G | C | 4 | a0001c0001t0003g0023 a0001c0001t0003g0076 a0001c0001t0003g0077 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-134+2379G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028477 | |||||||
| chr1:179028549 | T | G | 1 | a0001c0001t0018g0026 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-134+2451T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028549 | |||||||
| chr1:179028581 | AAAAC | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0234 others(1): Show |
5 | HG01109.hp1 HG02055.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-134+2498_-134+250 others(8): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179028581 | ||||||
| chr1:179028648 | C | T | 33 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(30): Show |
37 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.-134+2550C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028648 | |||||||
| chr1:179028664 | G | T | 2 | a0001c0001t0003g0148 a0001c0001t0003g0149 |
2 | NA18985.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.-134+2566G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028664 | |||||||
| chr1:179028901 | A | G | 1 | a0001c0001t0015g0101 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-134+2803A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028901 | |||||||
| chr1:179028912 | G | A | 1 | a0001c0001t0018g0026 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-134+2814G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028912 | |||||||
| chr1:179028927 | C | T | 1 | a0001c0001t0007g0112 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-134+2829C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028927 | |||||||
| chr1:179029005 | C | T | 1 | a0001c0001t0004g0168 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-134+2907C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179029005 | |||||||
| chr1:179029014 | G | A | 1 | a0001c0001t0004g0151 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-134+2916G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179029014 | |||||||
| chr1:179029103 | C | T | 1 | a0001c0001t0003g0144 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-134+3005C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179029103 | |||||||
| chr1:179029246 | C | G | 1 | a0001c0001t0003g0167 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-134+3148C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179029246 | |||||||
| chr1:179029281 | A | C | 1 | a0001c0001t0002g0218 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-134+3183A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179029281 | |||||||
| chr1:179029695 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-134+3597G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179029695 | |||||||
| chr1:179029969 | A | C | 1 | a0001c0001t0032g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-134+3871A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179029969 | |||||||
| chr1:179030154 | C | A | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-134+4056C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179030154 | |||||||
| chr1:179030339 | G | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-134+4241G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179030339 | |||||||
| chr1:179030345 | G | T | 1 | a0001c0001t0001g0289 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-134+4247G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179030345 | |||||||
| chr1:179030822 | G | A | 4 | a0001c0001t0011g0015 a0001c0001t0011g0102 a0001c0001t0011g0103 others(1): Show |
5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-134+4724G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179030822 | |||||||
| chr1:179030878 | C | CA | 6 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 others(3): Show |
6 | HG01257.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-134+4795dupA | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179030878 | ||||||
| chr1:179030878 | CA | C | 6 | a0001c0001t0009g0042 a0001c0001t0009g0221 a0001c0001t0009g0222 others(3): Show |
7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-134+4795delA | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179030878 | ||||||
| chr1:179030922 | A | G | 9 | a0001c0001t0007g0025 a0001c0001t0007g0106 a0001c0001t0007g0107 others(6): Show |
10 | HG01099.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-134+4824A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179030922 | |||||||
| chr1:179031008 | G | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(230): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.-134+4910G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179031008 | |||||||
| chr1:179031309 | A | G | 60 | a0001c0001t0003g0023 a0001c0001t0003g0076 a0001c0001t0003g0077 others(57): Show |
68 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.-134+5211A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179031309 | |||||||
| chr1:179031340 | G | A | 38 | a0001c0001t0001g0131 a0001c0001t0003g0005 a0001c0001t0003g0010 others(35): Show |
49 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.-134+5242G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179031340 | |||||||
| chr1:179031563 | G | A | 1 | a0001c0001t0002g0171 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-134+5465G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179031563 | |||||||
| chr1:179031590 | A | C | 58 | a0001c0001t0001g0131 a0001c0001t0003g0004 a0001c0001t0003g0005 others(55): Show |
79 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-134+5492A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179031590 | |||||||
| chr1:179031698 | G | C | 1 | a0001c0001t0032g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-134+5600G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179031698 | |||||||
| chr1:179031764 | T | C | 1 | a0001c0001t0032g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-134+5666T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179031764 | |||||||
| chr1:179031768 | GCTTAT | G | 20 | a0001c0001t0006g0082 a0001c0001t0006g0083 a0001c0001t0006g0084 others(17): Show |
21 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-134+5675_-134+567 others(9): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179031768 | ||||||
| chr1:179032179 | A | G | 1 | a0001c0001t0032g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-134+6081A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179032179 | |||||||
| chr1:179032305 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(107): Show |
147 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-134+6207G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179032305 | |||||||
| chr1:179032313 | C | CT | 13 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0211 others(10): Show |
15 | HG00639.hp2 HG00673.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.-134+6241dupT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179032313 | ||||||
| chr1:179032313 | C | CTTT | 14 | a0001c0001t0005g0013 a0001c0001t0005g0060 a0001c0001t0005g0061 others(11): Show |
16 | HG00544.hp1 HG01074.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.-134+6239_-134+624 others(7): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179032313 | ||||||
| chr1:179032313 | CT | C | 71 | a0001c0001t0002g0036 a0001c0001t0002g0172 a0001c0001t0002g0173 others(68): Show |
98 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.-134+6241delT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179032313 | ||||||
| chr1:179032313 | CTT | C | 13 | a0001c0001t0003g0113 a0001c0001t0003g0114 a0001c0001t0003g0115 others(10): Show |
15 | HG00140.hp2 HG01099.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.-134+6240_-134+624 others(6): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179032313 | ||||||
| chr1:179032313 | CTTTTTTT | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(84): Show |
123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.-134+6235_-134+624 others(11): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179032313 | ||||||
| chr1:179032313 | CTTTTTTT others(1): Show |
C | 23 | a0001c0001t0001g0021 a0001c0001t0001g0240 a0001c0001t0001g0241 others(20): Show |
25 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.-134+6234_-134+624 others(12): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179032313 | ||||||
| chr1:179032313 | CTTTTTTT others(7): Show |
C | 4 | a0001c0001t0011g0015 a0001c0001t0011g0102 a0001c0001t0011g0103 others(1): Show |
5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-134+6228_-134+624 others(18): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179032313 | ||||||
| chr1:179032404 | C | T | 1 | a0001c0001t0002g0208 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-134+6306C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179032404 | |||||||
| chr1:179032441 | A | G | 1 | a0001c0001t0003g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-134+6343A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179032441 | |||||||
| chr1:179032453 | T | TAGGTAAT others(4498): Show |
1 | a0001c0001t0001g0289 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-134+6371_-134+637 others(4509): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179032453 | ||||||
| chr1:179032462 | G | A | 2 | a0001c0001t0019g0074 a0001c0001t0019g0075 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-134+6364G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179032462 | |||||||
| chr1:179032506 | G | T | 8 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(5): Show |
9 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.-134+6408G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179032506 | |||||||
| chr1:179032673 | T | C | 4 | a0001c0001t0003g0023 a0001c0001t0003g0076 a0001c0001t0003g0077 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-134+6575T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179032673 | |||||||
| chr1:179032687 | A | G | 2 | a0001c0001t0012g0014 a0001c0001t0012g0099 |
4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-134+6589A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179032687 | |||||||
| chr1:179032756 | C | T | 6 | a0001c0001t0008g0012 a0001c0001t0008g0223 a0001c0001t0008g0224 others(3): Show |
9 | HG01346.hp2 HG02055.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-134+6658C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179032756 | |||||||
| chr1:179032998 | C | T | 1 | a0001c0001t0024g0073 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-134+6900C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179032998 | |||||||
| chr1:179033081 | C | T | 16 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(13): Show |
18 | HG00544.hp1 HG01074.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.-134+6983C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179033081 | |||||||
| chr1:179033192 | G | A | 1 | a0001c0001t0003g0132 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-134+7094G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179033192 | |||||||
| chr1:179033264 | G | A | 1 | a0001c0001t0001g0286 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-134+7166G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179033264 | |||||||
| chr1:179033335 | T | C | 1 | a0001c0001t0002g0172 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-134+7237T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179033335 | |||||||
| chr1:179033540 | G | A | 1 | a0001c0001t0008g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-134+7442G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179033540 | |||||||
| chr1:179033728 | C | T | 4 | a0001c0001t0011g0015 a0001c0001t0011g0102 a0001c0001t0011g0103 others(1): Show |
5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-134+7630C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179033728 | |||||||
| chr1:179033834 | A | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(119): Show |
167 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.-134+7736A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179033834 | |||||||
| chr1:179034006 | A | G | 1 | a0001c0001t0002g0207 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-134+7908A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179034006 | |||||||
| chr1:179034113 | A | G | 2 | a0001c0001t0024g0073 a0001c0001t0032g0100 |
2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-134+8015A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179034113 | |||||||
| chr1:179034355 | C | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(231): Show |
307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.-134+8257C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179034355 | |||||||
| chr1:179034384 | T | TTC | 5 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0244 others(2): Show |
5 | HG00735.hp2 HG01175.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-134+8304_-134+830 others(6): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179034384 | ||||||
| chr1:179034462 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-134+8364T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179034462 | |||||||
| chr1:179034534 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-134+8436C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179034534 | |||||||
| chr1:179034573 | G | T | 1 | a0001c0001t0002g0217 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-134+8475G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179034573 | |||||||
| chr1:179034631 | A | T | 1 | a0001c0001t0003g0169 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-134+8533A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179034631 | |||||||
| chr1:179035035 | G | C | 1 | a0001c0001t0001g0245 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-133-8680G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035035 | |||||||
| chr1:179035047 | G | C | 20 | a0001c0001t0006g0082 a0001c0001t0006g0083 a0001c0001t0006g0084 others(17): Show |
21 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-133-8668G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035047 | |||||||
| chr1:179035222 | T | C | 2 | a0001c0001t0019g0074 a0001c0001t0019g0075 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-133-8493T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035222 | |||||||
| chr1:179035341 | C | T | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-133-8374C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035341 | |||||||
| chr1:179035356 | C | T | 1 | a0001c0001t0006g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-133-8359C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035356 | |||||||
| chr1:179035441 | G | T | 4 | a0001c0001t0003g0023 a0001c0001t0003g0076 a0001c0001t0003g0077 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-133-8274G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035441 | |||||||
| chr1:179035467 | A | G | 24 | a0001c0001t0003g0023 a0001c0001t0003g0076 a0001c0001t0003g0077 others(21): Show |
26 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.-133-8248A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035467 | |||||||
| chr1:179035500 | C | A | 1 | a0001c0001t0017g0291 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-133-8215C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035500 | |||||||
| chr1:179035523 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(90): Show |
129 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.-133-8192A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035523 | |||||||
| chr1:179035630 | T | C | 1 | a0001c0001t0021g0116 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-133-8085T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035630 | |||||||
| chr1:179035643 | T | A | 16 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(13): Show |
18 | HG00544.hp1 HG01074.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.-133-8072T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035643 | |||||||
| chr1:179035668 | C | T | 1 | a0001c0002t0020g0105 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-133-8047C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035668 | |||||||
| chr1:179035810 | T | TTG | 6 | a0001c0001t0015g0080 a0001c0001t0015g0081 a0001c0001t0015g0101 others(3): Show |
6 | HG01891.hp1 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-133-7889_-133-788 others(6): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179035810 | ||||||
| chr1:179035856 | G | A | 2 | a0001c0002t0020g0104 a0001c0002t0020g0105 |
2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-133-7859G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035856 | |||||||
| chr1:179035946 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(88): Show |
127 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.-133-7769G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035946 | |||||||
| chr1:179035989 | G | C | 1 | a0001c0001t0001g0050 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-133-7726G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035989 | |||||||
| chr1:179036163 | C | G | 1 | a0001c0001t0025g0206 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-133-7552C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179036163 | |||||||
| chr1:179036413 | A | T | 1 | a0001c0001t0001g0231 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-133-7302A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179036413 | |||||||
| chr1:179036484 | A | G | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-133-7231A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179036484 | |||||||
| chr1:179036783 | C | T | 2 | a0001c0001t0012g0014 a0001c0001t0012g0099 |
4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-133-6932C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179036783 | |||||||
| chr1:179036835 | A | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(230): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.-133-6880A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179036835 | |||||||
| chr1:179036878 | G | A | 1 | a0001c0001t0025g0206 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-133-6837G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179036878 | |||||||
| chr1:179036971 | A | G | 2 | a0001c0001t0007g0111 a0001c0001t0007g0150 |
2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-133-6744A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179036971 | |||||||
| chr1:179036994 | C | G | 1 | a0001c0001t0001g0281 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-133-6721C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179036994 | |||||||
| chr1:179037248 | G | T | 6 | a0001c0001t0009g0042 a0001c0001t0009g0221 a0001c0001t0009g0222 others(3): Show |
7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-133-6467G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179037248 | |||||||
| chr1:179037268 | C | T | 1 | a0001c0001t0029g0280 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-133-6447C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179037268 | |||||||
| chr1:179037327 | G | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(204): Show |
272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.-133-6388G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179037327 | |||||||
| chr1:179037358 | C | CT | 204 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(201): Show |
267 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.-133-6348dupT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179037358 | ||||||
| chr1:179037475 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-133-6240C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179037475 | |||||||
| chr1:179037479 | C | CT | 58 | a0001c0001t0002g0176 a0001c0001t0002g0202 a0001c0001t0002g0203 others(55): Show |
78 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.-133-6215dupT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179037479 | ||||||
| chr1:179037479 | C | CTT | 46 | a0001c0001t0001g0227 a0001c0001t0001g0234 a0001c0001t0001g0240 others(43): Show |
56 | HG00544.hp1 HG00597.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.-133-6216_-133-621 others(6): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179037479 | ||||||
| chr1:179037479 | C | CTTT | 75 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(72): Show |
109 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.-133-6217_-133-621 others(7): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179037479 | ||||||
| chr1:179037479 | C | CTTTT | 44 | a0001c0001t0001g0020 a0001c0001t0001g0044 a0001c0001t0001g0047 others(41): Show |
49 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.-133-6218_-133-621 others(8): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179037479 | ||||||
| chr1:179037479 | C | CTTTTT | 8 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0006g0088 others(5): Show |
9 | HG00639.hp1 HG00733.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.-133-6219_-133-621 others(9): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179037479 | ||||||
| chr1:179037766 | C | T | 1 | a0001c0001t0018g0026 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-133-5949C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179037766 | |||||||
| chr1:179038068 | GA | G | 2 | a0001c0001t0012g0014 a0001c0001t0012g0099 |
4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-133-5646delA | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179038068 | |||||||
| chr1:179038142 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(115): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-133-5573C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179038142 | |||||||
| chr1:179038317 | A | C | 1 | a0001c0001t0003g0139 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-133-5398A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179038317 | |||||||
| chr1:179038326 | G | A | 1 | a0001c0001t0032g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-133-5389G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179038326 | |||||||
| chr1:179038357 | G | A | 1 | a0001c0001t0024g0073 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-133-5358G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179038357 | |||||||
| chr1:179038411 | C | CA | 179 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(176): Show |
242 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.-133-5289dupA | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179038411 | ||||||
| chr1:179038411 | C | CAA | 25 | a0001c0001t0001g0265 a0001c0001t0001g0277 a0001c0001t0003g0113 others(22): Show |
26 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.-133-5290_-133-528 others(6): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179038411 | ||||||
| chr1:179038441 | G | A | 6 | a0001c0001t0009g0042 a0001c0001t0009g0221 a0001c0001t0009g0222 others(3): Show |
7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-133-5274G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179038441 | |||||||
| chr1:179038705 | C | T | 48 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(45): Show |
67 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-133-5010C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179038705 | |||||||
| chr1:179038725 | A | T | 3 | a0001c0001t0012g0014 a0001c0001t0012g0099 a0001c0001t0032g0100 |
5 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-133-4990A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179038725 | |||||||
| chr1:179038808 | G | A | 1 | a0001c0001t0005g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-133-4907G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179038808 | |||||||
| chr1:179038965 | A | AT | 4 | a0001c0001t0003g0023 a0001c0001t0003g0076 a0001c0001t0003g0077 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-133-4750_-133-474 others(5): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179038965 | |||||||
| chr1:179039143 | G | A | 2 | a0001c0001t0002g0178 a0001c0001t0002g0207 |
2 | HG04228.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-133-4572G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039143 | |||||||
| chr1:179039190 | T | G | 2 | a0001c0002t0020g0104 a0001c0002t0020g0105 |
2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-133-4525T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039190 | |||||||
| chr1:179039382 | G | A | 48 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(45): Show |
67 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-133-4333G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039382 | |||||||
| chr1:179039568 | G | A | 1 | a0001c0001t0002g0219 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-133-4147G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039568 | |||||||
| chr1:179039612 | A | C | 2 | a0001c0001t0012g0014 a0001c0001t0012g0099 |
4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-133-4103A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039612 | |||||||
| chr1:179039644 | G | C | 1 | a0001c0001t0038g0057 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-133-4071G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039644 | |||||||
| chr1:179039739 | A | T | 3 | a0001c0001t0006g0082 a0001c0001t0006g0088 a0001c0001t0006g0089 |
3 | HG02257.hp2 HG02897.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-133-3976A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039739 | |||||||
| chr1:179039741 | TA | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(86): Show |
121 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.-133-3973delA | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039741 | |||||||
| chr1:179039742 | A | T | 28 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0255 others(25): Show |
30 | HG00140.hp1 HG00597.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.-133-3973A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039742 | |||||||
| chr1:179039743 | T | A | 6 | a0001c0001t0006g0092 a0001c0001t0009g0042 a0001c0001t0009g0221 others(3): Show |
7 | HG00140.hp1 HG02615.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-133-3972T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039743 | |||||||
| chr1:179039744 | T | A | 3 | a0001c0001t0001g0228 a0001c0001t0001g0240 a0001c0001t0001g0247 |
3 | HG00099.hp2 NA18959.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.-133-3971T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039744 | |||||||
| chr1:179039775 | T | C | 37 | a0001c0001t0003g0023 a0001c0001t0003g0076 a0001c0001t0003g0077 others(34): Show |
42 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.-133-3940T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039775 | |||||||
| chr1:179039800 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(126): Show |
170 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.-133-3915T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039800 | |||||||
| chr1:179039886 | G | A | 4 | a0001c0001t0003g0023 a0001c0001t0003g0076 a0001c0001t0003g0077 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-133-3829G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039886 | |||||||
| chr1:179039895 | G | T | 2 | a0001c0001t0012g0014 a0001c0001t0012g0099 |
4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-133-3820G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039895 | |||||||
| chr1:179039957 | A | G | 5 | a0001c0001t0007g0025 a0001c0001t0007g0108 a0001c0001t0007g0109 others(2): Show |
6 | HG01099.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-133-3758A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039957 | |||||||
| chr1:179039986 | C | T | 1 | a0001c0001t0007g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-133-3729C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039986 | |||||||
| chr1:179040105 | A | G | 2 | a0001c0002t0020g0104 a0001c0002t0020g0105 |
2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-133-3610A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040105 | |||||||
| chr1:179040146 | A | C | 1 | a0001c0001t0004g0162 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-133-3569A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040146 | |||||||
| chr1:179040208 | C | T | 1 | a0001c0001t0032g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-133-3507C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040208 | |||||||
| chr1:179040227 | C | T | 1 | a0001c0001t0004g0165 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-133-3488C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040227 | |||||||
| chr1:179040263 | G | A | 1 | a0001c0001t0032g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-133-3452G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040263 | |||||||
| chr1:179040384 | G | A | 1 | a0001c0001t0006g0093 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-133-3331G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040384 | |||||||
| chr1:179040438 | G | C | 1 | a0001c0001t0001g0248 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-133-3277G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040438 | |||||||
| chr1:179040493 | CCCCCCCA others(211): Show |
C | 32 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(29): Show |
36 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.-133-3187_-133-297 others(4): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179040493 | ||||||
| chr1:179040494 | CCCCCCAC others(210): Show |
C | 1 | a0001c0001t0005g0061 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-133-3215_-133-299 others(4): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179040494 | ||||||
| chr1:179040510 | C | T | 54 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(51): Show |
75 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-133-3205C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040510 | |||||||
| chr1:179040511 | G | A | 26 | a0001c0001t0004g0007 a0001c0001t0004g0031 a0001c0001t0004g0032 others(23): Show |
35 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.-133-3204G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040511 | |||||||
| chr1:179040520 | GGCTGGCC others(42): Show |
G | 23 | a0001c0001t0004g0007 a0001c0001t0004g0031 a0001c0001t0004g0032 others(20): Show |
30 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.-133-3183_-133-313 others(53): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179040520 | ||||||
| chr1:179040531 | C | T | 54 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(51): Show |
75 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-133-3184C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040531 | |||||||
| chr1:179040572 | TGGCCGGG others(30): Show |
T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0227 a0001c0001t0001g0228 others(1): Show |
7 | HG00099.hp2 HG00609.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.-133-3129_-133-309 others(41): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179040572 | ||||||
| chr1:179040654 | C | T | 1 | a0001c0001t0003g0114 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-133-3061C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040654 | |||||||
| chr1:179040664 | TCCCCCCA others(40): Show |
T | 7 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0245 others(4): Show |
10 | HG01081.hp2 HG01167.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.-133-2998_-133-295 others(51): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179040664 | ||||||
| chr1:179040665 | C | CCCCCCAC others(39): Show |
1 | a0001c0001t0002g0174 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-133-3044_-133-299 others(50): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179040665 | ||||||
| chr1:179040679 | C | T | 1 | a0001c0001t0018g0026 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-133-3036C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040679 | |||||||
| chr1:179040690 | C | T | 32 | a0001c0001t0003g0005 a0001c0001t0003g0010 a0001c0001t0003g0016 others(29): Show |
44 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.-133-3025C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040690 | |||||||
| chr1:179040691 | G | A | 1 | a0001c0001t0002g0006 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-133-3024G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040691 | |||||||
| chr1:179040703 | G | A | 2 | a0001c0001t0003g0149 a0001c0001t0006g0085 |
2 | HG03195.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.-133-3012G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040703 | |||||||
| chr1:179040740 | C | T | 1 | a0001c0001t0025g0206 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-133-2975C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040740 | |||||||
| chr1:179040779 | G | A | 1 | a0001c0001t0004g0151 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-133-2936G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040779 | |||||||
| chr1:179040948 | G | A | 18 | a0001c0001t0001g0018 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
25 | HG01081.hp2 HG01109.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.-133-2767G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040948 | |||||||
| chr1:179040964 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(114): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-133-2751C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040964 | |||||||
| chr1:179040981 | C | A | 1 | a0001c0001t0006g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-133-2734C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040981 | |||||||
| chr1:179040981 | C | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(149): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-133-2734C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040981 | |||||||
| chr1:179040984 | C | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(204): Show |
272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.-133-2731C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040984 | |||||||
| chr1:179041020 | A | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(204): Show |
272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.-133-2695A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041020 | |||||||
| chr1:179041089 | TGATGGGA others(33): Show |
T | 34 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(31): Show |
38 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.-133-2607_-133-256 others(44): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179041089 | ||||||
| chr1:179041104 | C | T | 2 | a0001c0001t0012g0014 a0001c0001t0012g0099 |
4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-133-2611C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041104 | |||||||
| chr1:179041115 | G | A | 3 | a0001c0001t0015g0080 a0001c0001t0015g0081 a0001c0001t0015g0101 |
3 | HG01891.hp1 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-133-2600G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041115 | |||||||
| chr1:179041144 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-133-2571C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041144 | |||||||
| chr1:179041191 | G | T | 1 | a0001c0001t0032g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-133-2524G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041191 | |||||||
| chr1:179041218 | A | G | 1 | a0001c0001t0003g0137 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-133-2497A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041218 | |||||||
| chr1:179041233 | T | G | 1 | a0001c0001t0018g0026 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-133-2482T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041233 | |||||||
| chr1:179041248 | C | CG | 9 | a0001c0001t0001g0131 a0001c0001t0001g0251 a0001c0001t0002g0179 others(6): Show |
9 | HG01099.hp2 HG01261.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.-133-2463dupG | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179041248 | ||||||
| chr1:179041317 | G | A | 1 | a0001c0001t0024g0073 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-133-2398G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041317 | |||||||
| chr1:179041384 | G | A | 2 | a0001c0001t0002g0037 a0001c0001t0002g0217 |
3 | HG00673.hp2 NA18747.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.-133-2331G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041384 | |||||||
| chr1:179041391 | C | T | 1 | a0001c0001t0004g0161 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-133-2324C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041391 | |||||||
| chr1:179041392 | G | A | 9 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0179 others(6): Show |
11 | HG01106.hp2 HG01255.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.-133-2323G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041392 | |||||||
| chr1:179041409 | G | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(203): Show |
269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-133-2306G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041409 | |||||||
| chr1:179041472 | G | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(230): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.-133-2243G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041472 | |||||||
| chr1:179041590 | C | T | 1 | a0001c0001t0006g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-133-2125C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041590 | |||||||
| chr1:179041601 | C | CAGAGGGA others(69): Show |
20 | a0001c0001t0006g0082 a0001c0001t0006g0083 a0001c0001t0006g0084 others(17): Show |
21 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-133-2086_-133-208 others(80): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179041601 | ||||||
| chr1:179041671 | G | GGAGGGA | 117 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(114): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-133-2029_-133-202 others(10): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179041671 | ||||||
| chr1:179041671 | G | GGAGGGAG others(5): Show |
1 | a0001c0001t0029g0280 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-133-2035_-133-202 others(16): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179041671 | ||||||
| chr1:179041671 | G | GGAGGGAG others(36): Show |
33 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(30): Show |
37 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.-133-2024_-133-202 others(47): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179041671 | ||||||
| chr1:179041683 | AGAGGGAG others(12): Show |
A | 1 | a0001c0001t0004g0031 | 2 | HG00140.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-133-2022_-133-200 others(23): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179041683 | ||||||
| chr1:179041779 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-133-1936C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041779 | |||||||
| chr1:179041811 | A | G | 31 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(28): Show |
35 | HG00544.hp1 HG01069.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.-133-1904A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041811 | |||||||
| chr1:179041927 | G | T | 1 | a0001c0001t0024g0073 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-133-1788G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041927 | |||||||
| chr1:179041967 | A | G | 1 | a0001c0001t0006g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-133-1748A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041967 | |||||||
| chr1:179042174 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0241 |
2 | NA18953.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-133-1541G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042174 | |||||||
| chr1:179042184 | C | T | 1 | a0001c0001t0024g0073 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-133-1531C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042184 | |||||||
| chr1:179042250 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0288 |
3 | NA18956.hp1 NA18961.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.-133-1465G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042250 | |||||||
| chr1:179042289 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-133-1426C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042289 | |||||||
| chr1:179042298 | G | T | 4 | a0001c0001t0011g0015 a0001c0001t0011g0102 a0001c0001t0011g0103 others(1): Show |
5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-133-1417G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042298 | |||||||
| chr1:179042344 | C | A | 6 | a0001c0001t0009g0042 a0001c0001t0009g0221 a0001c0001t0009g0222 others(3): Show |
7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-133-1371C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042344 | |||||||
| chr1:179042349 | C | T | 56 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(53): Show |
77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-133-1366C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042349 | |||||||
| chr1:179042397 | C | T | 1 | a0001c0001t0010g0096 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-133-1318C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042397 | |||||||
| chr1:179042741 | T | C | 1 | a0001c0001t0002g0180 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-133-974T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042741 | |||||||
| chr1:179042762 | T | A | 8 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(5): Show |
9 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.-133-953T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042762 | |||||||
| chr1:179042790 | A | C | 1 | a0001c0001t0036g0141 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-133-925A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042790 | |||||||
| chr1:179042960 | G | A | 16 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(13): Show |
18 | HG00544.hp1 HG01074.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.-133-755G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042960 | |||||||
| chr1:179042978 | G | A | 2 | a0001c0001t0003g0118 a0001c0001t0003g0119 |
2 | HG00423.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-133-737G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042978 | |||||||
| chr1:179043073 | A | G | 57 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(54): Show |
78 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.-133-642A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179043073 | |||||||
| chr1:179043090 | C | A | 56 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(53): Show |
77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-133-625C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179043090 | |||||||
| chr1:179043467 | G | A | 4 | a0001c0001t0011g0015 a0001c0001t0011g0102 a0001c0001t0011g0103 others(1): Show |
5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-133-248G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179043467 | |||||||
| chr1:179043504 | A | G | 2 | a0001c0001t0005g0059 a0001c0001t0005g0071 |
2 | HG02080.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.-133-211A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179043504 | |||||||
| chr1:179043565 | C | T | 2 | a0001c0001t0018g0026 a0001c0001t0030g0262 |
3 | HG02895.hp2 HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-133-150C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179043565 | |||||||
| chr1:179043567 | A | G | 8 | a0001c0001t0001g0011 a0001c0001t0001g0227 a0001c0001t0001g0228 others(5): Show |
11 | HG00099.hp2 HG00609.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.-133-148A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179043567 | |||||||
| chr1:179043582 | A | T | 2 | a0001c0001t0012g0014 a0001c0001t0012g0099 |
4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-133-133A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179043582 | |||||||
| chr1:179044291 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.377+67G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179044291 | |||||||
| chr1:179044397 | A | G | 1 | a0001c0001t0006g0092 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.377+173A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179044397 | |||||||
| chr1:179044851 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.377+627C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179044851 | |||||||
| chr1:179045080 | T | C | 58 | a0001c0001t0001g0131 a0001c0001t0003g0004 a0001c0001t0003g0005 others(55): Show |
79 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.377+856T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179045080 | |||||||
| chr1:179045135 | G | A | 2 | a0001c0002t0020g0104 a0001c0002t0020g0105 |
2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.377+911G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179045135 | |||||||
| chr1:179045277 | C | T | 1 | a0001c0001t0032g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.377+1053C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179045277 | |||||||
| chr1:179045278 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.377+1054G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179045278 | |||||||
| chr1:179045494 | G | T | 1 | a0001c0001t0001g0231 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.377+1270G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179045494 | |||||||
| chr1:179045643 | G | T | 1 | a0001c0001t0001g0050 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.377+1419G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179045643 | |||||||
| chr1:179045670 | C | T | 20 | a0001c0001t0006g0082 a0001c0001t0006g0083 a0001c0001t0006g0084 others(17): Show |
21 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.377+1446C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179045670 | |||||||
| chr1:179045671 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0278 |
4 | HG02258.hp1 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.377+1447G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179045671 | |||||||
| chr1:179045912 | C | CA | 14 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0131 others(11): Show |
14 | HG00735.hp1 HG02056.hp2 HG02738.hp2 others(11): Show |
intron_variant | MODIFIER | c.377+1697dupA | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 179045912 | ||||||
| chr1:179045963 | A | T | 1 | a0001c0001t0003g0167 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.377+1739A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179045963 | |||||||
| chr1:179045993 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.377+1769T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179045993 | |||||||
| chr1:179046188 | C | G | 1 | a0001c0001t0003g0293 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.377+1964C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179046188 | |||||||
| chr1:179046372 | C | T | 1 | a0001c0001t0018g0026 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.377+2148C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179046372 | |||||||
| chr1:179046594 | G | T | 49 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(46): Show |
69 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.377+2370G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179046594 | |||||||
| chr1:179046680 | G | A | 1 | a0001c0001t0002g0184 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.377+2456G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179046680 | |||||||
| chr1:179046778 | G | A | 3 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0144 |
3 | NA18941.hp2 NA18955.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.377+2554G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179046778 | |||||||
| chr1:179046822 | C | G | 34 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(31): Show |
38 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.377+2598C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179046822 | |||||||
| chr1:179046860 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(149): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.377+2636T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179046860 | |||||||
| chr1:179046889 | G | A | 2 | a0001c0001t0019g0074 a0001c0001t0019g0075 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.377+2665G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179046889 | |||||||
| chr1:179046927 | G | A | 2 | a0001c0001t0012g0014 a0001c0001t0012g0099 |
4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.377+2703G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179046927 | |||||||
| chr1:179046951 | C | T | 1 | a0001c0001t0003g0144 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.377+2727C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179046951 | |||||||
| chr1:179047257 | C | T | 4 | a0001c0001t0011g0015 a0001c0001t0011g0102 a0001c0001t0011g0103 others(1): Show |
5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.378-3022C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179047257 | |||||||
| chr1:179047263 | C | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(115): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.378-3016C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179047263 | |||||||
| chr1:179047348 | T | C | 57 | a0001c0001t0001g0131 a0001c0001t0003g0004 a0001c0001t0003g0005 others(54): Show |
78 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.378-2931T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179047348 | |||||||
| chr1:179047422 | C | T | 1 | a0001c0001t0002g0220 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.378-2857C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179047422 | |||||||
| chr1:179047476 | C | T | 9 | a0001c0001t0001g0019 a0001c0001t0001g0237 a0001c0001t0001g0238 others(6): Show |
11 | HG01168.hp1 HG01192.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.378-2803C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179047476 | |||||||
| chr1:179047512 | G | T | 1 | a0001c0001t0006g0097 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.378-2767G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179047512 | |||||||
| chr1:179047637 | G | C | 34 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(31): Show |
38 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.378-2642G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179047637 | |||||||
| chr1:179047795 | T | A | 34 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(31): Show |
38 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.378-2484T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179047795 | |||||||
| chr1:179048052 | T | A | 1 | a0001c0001t0032g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.378-2227T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179048052 | |||||||
| chr1:179048195 | G | A | 6 | a0001c0001t0009g0042 a0001c0001t0009g0221 a0001c0001t0009g0222 others(3): Show |
7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.378-2084G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179048195 | |||||||
| chr1:179048241 | G | A | 4 | a0001c0001t0011g0015 a0001c0001t0011g0102 a0001c0001t0011g0103 others(1): Show |
5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.378-2038G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179048241 | |||||||
| chr1:179048367 | T | C | 6 | a0001c0001t0009g0042 a0001c0001t0009g0221 a0001c0001t0009g0222 others(3): Show |
7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.378-1912T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179048367 | |||||||
| chr1:179048380 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.378-1899C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179048380 | |||||||
| chr1:179048507 | G | A | 4 | a0001c0001t0003g0023 a0001c0001t0003g0076 a0001c0001t0003g0077 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.378-1772G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179048507 | |||||||
| chr1:179048580 | G | GC | 3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG01257.hp2 HG01258.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.378-1697dupC | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 179048580 | ||||||
| chr1:179048586 | A | G | 1 | a0001c0001t0002g0200 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.378-1693A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179048586 | |||||||
| chr1:179049135 | A | C | 7 | a0001c0001t0008g0012 a0001c0001t0008g0223 a0001c0001t0008g0224 others(4): Show |
10 | HG01346.hp2 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.378-1144A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179049135 | |||||||
| chr1:179049177 | C | T | 1 | a0001c0001t0003g0129 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.378-1102C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179049177 | |||||||
| chr1:179049181 | T | C | 1 | a0001c0001t0032g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.378-1098T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179049181 | |||||||
| chr1:179049344 | C | T | 5 | a0001c0001t0002g0039 a0001c0001t0002g0179 a0001c0001t0002g0181 others(2): Show |
6 | NA18962.hp2 NA18989.hp2 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.378-935C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179049344 | |||||||
| chr1:179049389 | A | G | 2 | a0001c0001t0003g0128 a0001c0001t0003g0129 |
2 | HG01081.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.378-890A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179049389 | |||||||
| chr1:179049441 | C | T | 14 | a0001c0001t0003g0005 a0001c0001t0003g0016 a0001c0001t0003g0028 others(11): Show |
24 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.378-838C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179049441 | |||||||
| chr1:179049611 | G | C | 34 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(31): Show |
38 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.378-668G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179049611 | |||||||
| chr1:179049648 | C | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(115): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.378-631C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179049648 | |||||||
| chr1:179049707 | A | T | 6 | a0001c0001t0009g0042 a0001c0001t0009g0221 a0001c0001t0009g0222 others(3): Show |
7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.378-572A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179049707 | |||||||
| chr1:179049790 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(149): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.378-489T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179049790 | |||||||
| chr1:179049884 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(114): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.378-395C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179049884 | |||||||
| chr1:179050051 | A | G | 62 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(59): Show |
92 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.378-228A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179050051 | |||||||
| chr1:179050103 | C | G | 34 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(31): Show |
38 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.378-176C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179050103 | |||||||
| chr1:179050441 | C | G | 16 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(13): Show |
18 | HG00544.hp1 HG01074.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.464+76C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179050441 | |||||||
| chr1:179050479 | G | A | 1 | a0001c0001t0004g0155 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.464+114G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179050479 | |||||||
| chr1:179050525 | T | G | 2 | a0001c0002t0020g0104 a0001c0002t0020g0105 |
2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.464+160T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179050525 | |||||||
| chr1:179051053 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(109): Show |
149 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.464+688C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179051053 | |||||||
| chr1:179051055 | C | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(208): Show |
277 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.464+690C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179051055 | |||||||
| chr1:179051058 | C | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(208): Show |
277 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.464+693C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179051058 | |||||||
| chr1:179051071 | G | A | 2 | a0001c0001t0012g0014 a0001c0001t0012g0099 |
4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.464+706G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179051071 | |||||||
| chr1:179051122 | TA | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(125): Show |
167 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.464+772delA | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 179051122 | ||||||
| chr1:179051242 | C | G | 49 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(46): Show |
69 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.464+877C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179051242 | |||||||
| chr1:179051560 | G | A | 9 | a0001c0001t0007g0025 a0001c0001t0007g0106 a0001c0001t0007g0107 others(6): Show |
10 | HG01099.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.464+1195G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179051560 | |||||||
| chr1:179051840 | G | C | 1 | a0001c0001t0032g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.464+1475G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179051840 | |||||||
| chr1:179051928 | G | A | 2 | a0001c0001t0001g0229 a0001c0001t0001g0263 |
2 | HG00609.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.464+1563G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179051928 | |||||||
| chr1:179052033 | A | G | 9 | a0001c0001t0007g0025 a0001c0001t0007g0106 a0001c0001t0007g0107 others(6): Show |
10 | HG01099.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.464+1668A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052033 | |||||||
| chr1:179052097 | G | A | 201 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(198): Show |
270 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.464+1732G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052097 | |||||||
| chr1:179052123 | C | T | 4 | a0001c0001t0011g0015 a0001c0001t0011g0102 a0001c0001t0011g0103 others(1): Show |
5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.464+1758C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052123 | |||||||
| chr1:179052193 | T | A | 1 | a0001c0001t0001g0256 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.464+1828T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052193 | |||||||
| chr1:179052218 | CAT | C | 4 | a0001c0001t0001g0261 a0001c0001t0015g0080 a0001c0001t0015g0081 others(1): Show |
4 | HG01891.hp1 HG02040.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.464+1856_464+1857d others(4): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 179052218 | ||||||
| chr1:179052442 | T | G | 1 | a0001c0001t0001g0242 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.464+2077T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052442 | |||||||
| chr1:179052516 | G | A | 23 | a0001c0001t0004g0007 a0001c0001t0004g0031 a0001c0001t0004g0032 others(20): Show |
30 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.465-2013G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052516 | |||||||
| chr1:179052601 | T | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(115): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.465-1928T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052601 | |||||||
| chr1:179052611 | T | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(138): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.465-1918T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052611 | |||||||
| chr1:179052676 | A | G | 1 | a0001c0001t0005g0067 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.465-1853A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052676 | |||||||
| chr1:179052823 | C | T | 23 | a0001c0001t0004g0007 a0001c0001t0004g0031 a0001c0001t0004g0032 others(20): Show |
30 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.465-1706C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052823 | |||||||
| chr1:179052940 | A | C | 1 | a0001c0001t0003g0130 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.465-1589A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052940 | |||||||
| chr1:179052946 | A | G | 16 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(13): Show |
18 | HG00544.hp1 HG01074.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.465-1583A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052946 | |||||||
| chr1:179052993 | C | T | 2 | a0001c0002t0020g0104 a0001c0002t0020g0105 |
2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.465-1536C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052993 | |||||||
| chr1:179053101 | G | T | 92 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(89): Show |
119 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.465-1428G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179053101 | |||||||
| chr1:179053232 | T | C | 7 | a0001c0001t0008g0012 a0001c0001t0008g0223 a0001c0001t0008g0224 others(4): Show |
10 | HG01346.hp2 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.465-1297T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179053232 | |||||||
| chr1:179053293 | T | C | 58 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(55): Show |
81 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.465-1236T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179053293 | |||||||
| chr1:179053443 | CCAAA | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(109): Show |
149 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.465-1061_465-1058d others(6): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 179053443 | ||||||
| chr1:179053444 | C | G | 32 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(29): Show |
36 | HG00544.hp1 HG01069.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.465-1085C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179053444 | |||||||
| chr1:179053495 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(116): Show |
158 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.465-1034A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179053495 | |||||||
| chr1:179053515 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(208): Show |
277 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.465-1014T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179053515 | |||||||
| chr1:179053547 | T | G | 3 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
3 | HG02280.hp1 HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.465-982T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179053547 | |||||||
| chr1:179053582 | C | T | 2 | a0001c0002t0020g0104 a0001c0002t0020g0105 |
2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.465-947C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179053582 | |||||||
| chr1:179053933 | G | C | 2 | a0001c0002t0020g0104 a0001c0002t0020g0105 |
2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.465-596G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179053933 | |||||||
| chr1:179054017 | C | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(208): Show |
277 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.465-512C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179054017 | |||||||
| chr1:179054108 | C | CT | 16 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(13): Show |
18 | HG00544.hp1 HG01074.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.465-409dupT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 179054108 | ||||||
| chr1:179054275 | C | T | 1 | a0001c0001t0032g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.465-254C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179054275 | |||||||
| chr1:179054390 | G | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0227 a0001c0001t0001g0228 others(4): Show |
10 | HG00099.hp2 HG00609.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.465-139G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179054390 | |||||||
| chr1:179054466 | G | T | 58 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(55): Show |
81 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.465-63G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179054466 | |||||||
| chr1:179054502 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.465-27C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179054502 | |||||||
| chr1:179054744 | T | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(89): Show |
128 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.574+106T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179054744 | |||||||
| chr1:179054841 | G | A | 3 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0026g0157 |
3 | HG00597.hp2 HG02132.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.574+203G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179054841 | |||||||
| chr1:179055221 | G | C | 2 | a0001c0001t0012g0014 a0001c0001t0012g0099 |
4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.574+583G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179055221 | |||||||
| chr1:179055418 | T | G | 7 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0245 others(4): Show |
10 | HG01081.hp2 HG01167.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.574+780T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179055418 | |||||||
| chr1:179055444 | A | T | 1 | a0001c0001t0001g0261 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.574+806A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179055444 | |||||||
| chr1:179055558 | A | C | 1 | a0001c0001t0001g0288 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.574+920A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179055558 | |||||||
| chr1:179055628 | T | C | 1 | a0001c0001t0038g0057 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.574+990T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179055628 | |||||||
| chr1:179055688 | C | T | 1 | a0001c0001t0006g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.574+1050C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179055688 | |||||||
| chr1:179055697 | A | T | 1 | a0001c0001t0007g0150 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.574+1059A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179055697 | |||||||
| chr1:179055750 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(208): Show |
277 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.574+1112A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179055750 | |||||||
| chr1:179056048 | G | A | 1 | a0001c0001t0002g0185 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.574+1410G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179056048 | |||||||
| chr1:179056234 | A | G | 34 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(31): Show |
38 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.574+1596A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179056234 | |||||||
| chr1:179056314 | A | G | 1 | a0001c0001t0018g0026 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.574+1676A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179056314 | |||||||
| chr1:179056334 | C | G | 56 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(53): Show |
77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.574+1696C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179056334 | |||||||
| chr1:179056463 | A | G | 1 | a0001c0001t0002g0175 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.574+1825A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179056463 | |||||||
| chr1:179056538 | C | G | 2 | a0001c0002t0020g0104 a0001c0002t0020g0105 |
2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.574+1900C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179056538 | |||||||
| chr1:179056661 | G | A | 2 | a0001c0001t0006g0094 a0001c0001t0006g0097 |
2 | HG00733.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.574+2023G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179056661 | |||||||
| chr1:179056805 | A | G | 3 | a0001c0001t0016g0225 a0001c0001t0016g0226 a0001c0001t0018g0026 |
4 | HG02572.hp2 HG02647.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.574+2167A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179056805 | |||||||
| chr1:179056982 | T | G | 1 | a0001c0001t0006g0083 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.574+2344T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179056982 | |||||||
| chr1:179057020 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.574+2382C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057020 | |||||||
| chr1:179057025 | G | A | 1 | a0001c0001t0002g0186 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.574+2387G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057025 | |||||||
| chr1:179057134 | C | T | 3 | a0001c0001t0023g0125 a0001c0002t0020g0104 a0001c0002t0020g0105 |
3 | HG00735.hp2 HG01175.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.574+2496C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057134 | |||||||
| chr1:179057142 | C | G | 2 | a0001c0001t0012g0014 a0001c0001t0012g0099 |
4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.574+2504C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057142 | |||||||
| chr1:179057288 | T | A | 2 | a0001c0001t0016g0225 a0001c0001t0016g0226 |
2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.574+2650T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057288 | |||||||
| chr1:179057354 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(208): Show |
277 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.574+2716A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057354 | |||||||
| chr1:179057392 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(115): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.574+2754C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057392 | |||||||
| chr1:179057432 | C | A | 211 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(208): Show |
277 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.574+2794C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057432 | |||||||
| chr1:179057535 | T | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(116): Show |
158 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.574+2897T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057535 | |||||||
| chr1:179057678 | G | C | 1 | a0001c0001t0002g0218 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.574+3040G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057678 | |||||||
| chr1:179057762 | T | C | 9 | a0001c0001t0007g0025 a0001c0001t0007g0106 a0001c0001t0007g0107 others(6): Show |
10 | HG01099.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.574+3124T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057762 | |||||||
| chr1:179057825 | G | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(116): Show |
158 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.574+3187G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057825 | |||||||
| chr1:179058005 | C | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(116): Show |
158 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.574+3367C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058005 | |||||||
| chr1:179058217 | A | G | 24 | a0001c0001t0003g0129 a0001c0001t0004g0007 a0001c0001t0004g0031 others(21): Show |
31 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.574+3579A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058217 | |||||||
| chr1:179058415 | G | A | 6 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0152 others(3): Show |
8 | HG00140.hp2 HG00738.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.574+3777G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058415 | |||||||
| chr1:179058647 | T | A | 1 | a0001c0001t0001g0270 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.574+4009T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058647 | |||||||
| chr1:179058685 | A | G | 6 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(3): Show |
8 | HG02080.hp1 HG02135.hp1 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.574+4047A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058685 | |||||||
| chr1:179058777 | G | C | 4 | a0001c0001t0003g0114 a0001c0001t0003g0122 a0001c0001t0003g0123 others(1): Show |
4 | HG02280.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.574+4139G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058777 | |||||||
| chr1:179058834 | G | A | 1 | a0001c0001t0002g0178 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.574+4196G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058834 | |||||||
| chr1:179058836 | A | G | 1 | a0001c0001t0018g0026 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.574+4198A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058836 | |||||||
| chr1:179058870 | T | A | 1 | a0001c0001t0002g0187 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.574+4232T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058870 | |||||||
| chr1:179058879 | A | T | 1 | a0001c0001t0003g0293 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.574+4241A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058879 | |||||||
| chr1:179058957 | T | A | 16 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(13): Show |
18 | HG00544.hp1 HG01074.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.574+4319T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058957 | |||||||
| chr1:179058999 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.574+4361A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058999 | |||||||
| chr1:179059003 | T | C | 1 | a0001c0001t0002g0188 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.574+4365T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179059003 | |||||||
| chr1:179059017 | G | C | 1 | a0001c0001t0002g0187 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.574+4379G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179059017 | |||||||
| chr1:179059038 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.574+4400G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179059038 | |||||||
| chr1:179059311 | T | C | 56 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(53): Show |
77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.575-4616T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179059311 | |||||||
| chr1:179059528 | C | G | 1 | a0001c0001t0006g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.575-4399C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179059528 | |||||||
| chr1:179059700 | G | A | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0049 others(8): Show |
13 | HG00280.hp1 HG00621.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.575-4227G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179059700 | |||||||
| chr1:179059801 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(211): Show |
280 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.575-4126A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179059801 | |||||||
| chr1:179059919 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.575-4008C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179059919 | |||||||
| chr1:179059971 | C | CA | 9 | a0001c0001t0001g0131 a0001c0001t0001g0263 a0001c0001t0001g0271 others(6): Show |
9 | HG02922.hp2 HG03927.hp2 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.575-3940dupA | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 179059971 | ||||||
| chr1:179059971 | CA | C | 57 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(54): Show |
78 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.575-3940delA | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 179059971 | ||||||
| chr1:179059990 | C | A | 2 | a0001c0002t0020g0104 a0001c0002t0020g0105 |
2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.575-3937C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179059990 | |||||||
| chr1:179060101 | A | AT | 210 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(207): Show |
282 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.575-3819dupT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 179060101 | ||||||
| chr1:179060101 | A | T | 21 | a0001c0001t0003g0127 a0001c0001t0006g0082 a0001c0001t0006g0083 others(18): Show |
22 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.575-3826A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179060101 | |||||||
| chr1:179060102 | T | TA | 5 | a0001c0001t0001g0263 a0001c0001t0001g0272 a0001c0001t0002g0190 others(2): Show |
5 | HG02083.hp2 HG02922.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.575-3825_575-3824i others(3): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179060102 | |||||||
| chr1:179060304 | T | C | 1 | a0001c0001t0003g0134 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.575-3623T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179060304 | |||||||
| chr1:179060586 | G | C | 4 | a0001c0001t0011g0015 a0001c0001t0011g0102 a0001c0001t0011g0103 others(1): Show |
5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.575-3341G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179060586 | |||||||
| chr1:179061010 | C | A | 1 | a0001c0001t0001g0275 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.575-2917C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179061010 | |||||||
| chr1:179061011 | G | A | 1 | a0001c0001t0025g0206 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.575-2916G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179061011 | |||||||
| chr1:179061076 | A | AT | 123 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(120): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.575-2831dupT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 179061076 | ||||||
| chr1:179061076 | A | ATT | 16 | a0001c0001t0001g0046 a0001c0001t0001g0056 a0001c0001t0001g0233 others(13): Show |
17 | HG01175.hp2 HG01346.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.575-2832_575-2831d others(4): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 179061076 | ||||||
| chr1:179061076 | AT | A | 42 | a0001c0001t0002g0040 a0001c0001t0002g0191 a0001c0001t0002g0192 others(39): Show |
49 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.575-2831delT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 179061076 | ||||||
| chr1:179061076 | ATT | A | 53 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(50): Show |
74 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.575-2832_575-2831d others(4): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 179061076 | ||||||
| chr1:179061166 | C | T | 1 | a0001c0001t0002g0218 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.575-2761C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179061166 | |||||||
| chr1:179061190 | C | T | 56 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(53): Show |
77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.575-2737C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179061190 | |||||||
| chr1:179061234 | G | A | 236 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(233): Show |
309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.575-2693G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179061234 | |||||||
| chr1:179061549 | A | G | 34 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(31): Show |
38 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.575-2378A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179061549 | |||||||
| chr1:179061642 | C | G | 1 | a0001c0001t0003g0293 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.575-2285C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179061642 | |||||||
| chr1:179061648 | A | T | 4 | a0001c0001t0011g0015 a0001c0001t0011g0102 a0001c0001t0011g0103 others(1): Show |
5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.575-2279A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179061648 | |||||||
| chr1:179061807 | C | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(119): Show |
161 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.575-2120C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179061807 | |||||||
| chr1:179061960 | T | C | 32 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(29): Show |
36 | HG00544.hp1 HG01069.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.575-1967T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179061960 | |||||||
| chr1:179062014 | C | CT | 34 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(31): Show |
38 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.575-1903dupT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 179062014 | ||||||
| chr1:179062076 | G | A | 1 | a0001c0001t0018g0026 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.575-1851G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062076 | |||||||
| chr1:179062154 | A | G | 7 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0245 others(4): Show |
10 | HG01081.hp2 HG01167.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.575-1773A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062154 | |||||||
| chr1:179062162 | A | C | 2 | a0001c0001t0019g0074 a0001c0001t0019g0075 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.575-1765A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062162 | |||||||
| chr1:179062170 | A | T | 2 | a0001c0001t0012g0014 a0001c0001t0012g0099 |
4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.575-1757A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062170 | |||||||
| chr1:179062212 | C | G | 2 | a0001c0001t0012g0014 a0001c0001t0012g0099 |
4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.575-1715C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062212 | |||||||
| chr1:179062467 | A | C | 1 | a0001c0001t0006g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.575-1460A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062467 | |||||||
| chr1:179062478 | C | T | 14 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0245 others(11): Show |
20 | HG01081.hp2 HG01167.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.575-1449C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062478 | |||||||
| chr1:179062588 | T | C | 2 | a0001c0001t0012g0014 a0001c0001t0012g0099 |
4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.575-1339T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062588 | |||||||
| chr1:179062669 | A | G | 1 | a0001c0001t0022g0029 | 2 | NA18955.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.575-1258A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062669 | |||||||
| chr1:179062752 | C | A | 23 | a0001c0001t0004g0007 a0001c0001t0004g0031 a0001c0001t0004g0032 others(20): Show |
30 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.575-1175C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062752 | |||||||
| chr1:179062789 | A | G | 1 | a0001c0001t0024g0073 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.575-1138A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062789 | |||||||
| chr1:179062868 | A | G | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0234 others(1): Show |
5 | HG01109.hp1 HG02055.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.575-1059A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062868 | |||||||
| chr1:179062928 | C | G | 1 | a0001c0001t0002g0189 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.575-999C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062928 | |||||||
| chr1:179062948 | A | G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(119): Show |
161 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.575-979A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062948 | |||||||
| chr1:179063013 | A | G | 2 | a0001c0001t0012g0014 a0001c0001t0012g0099 |
4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.575-914A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179063013 | |||||||
| chr1:179063080 | C | T | 16 | a0001c0001t0005g0013 a0001c0001t0005g0058 a0001c0001t0005g0059 others(13): Show |
18 | HG00544.hp1 HG01074.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.575-847C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179063080 | |||||||
| chr1:179063183 | G | A | 1 | a0001c0001t0024g0073 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.575-744G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179063183 | |||||||
| chr1:179063206 | G | A | 6 | a0001c0001t0009g0042 a0001c0001t0009g0221 a0001c0001t0009g0222 others(3): Show |
7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.575-721G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179063206 | |||||||
| chr1:179063217 | C | G | 7 | a0001c0001t0001g0045 a0001c0001t0001g0253 a0001c0001t0001g0254 others(4): Show |
8 | HG02145.hp2 HG02818.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.575-710C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179063217 | |||||||
| chr1:179063448 | C | T | 4 | a0001c0001t0011g0015 a0001c0001t0011g0102 a0001c0001t0011g0103 others(1): Show |
5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.575-479C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179063448 | |||||||
| chr1:179063479 | T | A | 56 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(53): Show |
77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.575-448T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179063479 | |||||||
| chr1:179063845 | T | A | 1 | a0001c0001t0002g0182 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.575-82T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179063845 | |||||||
| chr1:179064649 | T | C | 23 | a0001c0001t0004g0007 a0001c0001t0004g0031 a0001c0001t0004g0032 others(20): Show |
30 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.938+153T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179064649 | |||||||
| chr1:179064852 | G | A | 211 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(208): Show |
277 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.938+356G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179064852 | |||||||
| chr1:179065020 | T | A | 1 | a0001c0001t0002g0171 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.938+524T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179065020 | |||||||
| chr1:179065094 | T | A | 23 | a0001c0001t0004g0007 a0001c0001t0004g0031 a0001c0001t0004g0032 others(20): Show |
30 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.938+598T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179065094 | |||||||
| chr1:179065147 | C | CT | 5 | a0001c0001t0011g0015 a0001c0001t0011g0102 a0001c0001t0011g0103 others(2): Show |
6 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.938+662dupT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 179065147 | ||||||
| chr1:179065174 | G | A | 2 | a0001c0001t0004g0159 a0001c0001t0004g0160 |
2 | HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.938+678G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179065174 | |||||||
| chr1:179065253 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.938+757C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179065253 | |||||||
| chr1:179065346 | A | G | 56 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(53): Show |
77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.938+850A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179065346 | |||||||
| chr1:179065416 | T | C | 3 | a0001c0001t0005g0060 a0001c0001t0005g0068 a0002c0003t0005g0063 |
3 | HG02809.hp2 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.938+920T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179065416 | |||||||
| chr1:179065649 | A | C | 56 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(53): Show |
77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.939-1151A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179065649 | |||||||
| chr1:179065683 | C | G | 1 | a0001c0001t0025g0206 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.939-1117C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179065683 | |||||||
| chr1:179065836 | A | G | 1 | a0001c0001t0002g0220 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.939-964A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179065836 | |||||||
| chr1:179065916 | T | C | 1 | a0001c0001t0024g0073 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.939-884T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179065916 | |||||||
| chr1:179066008 | C | G | 1 | a0001c0001t0032g0100 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.939-792C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179066008 | |||||||
| chr1:179066141 | A | G | 9 | a0001c0001t0007g0025 a0001c0001t0007g0106 a0001c0001t0007g0107 others(6): Show |
10 | HG01099.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.939-659A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179066141 | |||||||
| chr1:179066196 | T | C | 56 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(53): Show |
77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.939-604T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179066196 | |||||||
| chr1:179066294 | T | G | 56 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(53): Show |
77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.939-506T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179066294 | |||||||
| chr1:179066327 | T | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(211): Show |
280 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.939-473T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179066327 | |||||||
| chr1:179066527 | C | G | 9 | a0001c0001t0007g0025 a0001c0001t0007g0106 a0001c0001t0007g0107 others(6): Show |
10 | HG01099.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.939-273C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179066527 | |||||||
| chr1:179067150 | C | A | 1 | a0001c0001t0003g0145 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.998+291C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179067150 | |||||||
| chr1:179067267 | C | A | 1 | a0001c0001t0024g0073 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.998+408C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179067267 | |||||||
| chr1:179067402 | C | T | 1 | a0001c0001t0015g0101 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.998+543C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179067402 | |||||||
| chr1:179067537 | G | C | 2 | a0001c0001t0012g0014 a0001c0001t0012g0099 |
4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.998+678G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179067537 | |||||||
| chr1:179067639 | T | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(210): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.998+780T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179067639 | |||||||
| chr1:179067696 | T | G | 2 | a0001c0002t0020g0104 a0001c0002t0020g0105 |
2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.998+837T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179067696 | |||||||
| chr1:179067854 | T | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(236): Show |
312 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.998+995T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179067854 | |||||||
| chr1:179067895 | C | G | 1 | a0001c0001t0003g0143 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.998+1036C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179067895 | |||||||
| chr1:179067983 | A | G | 289 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(286): Show |
392 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(389): Show |
intron_variant | MODIFIER | c.998+1124A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179067983 | |||||||
| chr1:179068043 | G | A | 56 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(53): Show |
77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.998+1184G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179068043 | |||||||
| chr1:179068085 | C | T | 3 | a0001c0001t0015g0080 a0001c0001t0015g0081 a0001c0001t0015g0101 |
3 | HG01891.hp1 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.998+1226C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179068085 | |||||||
| chr1:179068331 | T | C | 8 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(5): Show |
9 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.998+1472T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179068331 | |||||||
| chr1:179068440 | A | AT | 6 | a0001c0001t0009g0042 a0001c0001t0009g0221 a0001c0001t0009g0222 others(3): Show |
7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.998+1593dupT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 179068440 | ||||||
| chr1:179068456 | G | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(112): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.998+1597G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179068456 | |||||||
| chr1:179068536 | A | G | 1 | a0001c0001t0002g0180 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.998+1677A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179068536 | |||||||
| chr1:179068980 | T | C | 2 | a0001c0001t0019g0074 a0001c0001t0019g0075 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.998+2121T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179068980 | |||||||
| chr1:179069020 | T | C | 40 | a0001c0001t0001g0268 a0001c0001t0005g0013 a0001c0001t0005g0058 others(37): Show |
45 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.998+2161T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069020 | |||||||
| chr1:179069032 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.998+2173G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069032 | |||||||
| chr1:179069061 | T | C | 2 | a0001c0002t0020g0104 a0001c0002t0020g0105 |
2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.998+2202T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069061 | |||||||
| chr1:179069115 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.998+2256G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069115 | |||||||
| chr1:179069143 | C | T | 4 | a0001c0001t0003g0023 a0001c0001t0003g0076 a0001c0001t0003g0077 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.998+2284C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069143 | |||||||
| chr1:179069402 | G | A | 55 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(52): Show |
76 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.999-2511G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069402 | |||||||
| chr1:179069463 | C | T | 1 | a0001c0001t0006g0086 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.999-2450C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069463 | |||||||
| chr1:179069474 | G | A | 56 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0010 others(53): Show |
77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.999-2439G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069474 | |||||||
| chr1:179069591 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01192.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.999-2322C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069591 | |||||||
| chr1:179069904 | A | C | 5 | a0001c0001t0002g0171 a0001c0001t0002g0185 a0001c0001t0002g0196 others(2): Show |
5 | NA18969.hp2 NA18991.hp2 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.999-2009A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069904 | |||||||
| chr1:179069909 | C | T | 113 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0043 others(110): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.999-2004C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069909 | |||||||
| chr1:179069920 | C | T | 24 | a0001c0001t0002g0187 a0001c0001t0006g0082 a0001c0001t0006g0083 others(21): Show |
25 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.999-1993C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069920 | |||||||
| chr1:179069951 | T | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0259 |
2 | NA18995.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.999-1962T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069951 | |||||||
| chr1:179070054 | A | G | 4 | a0001c0001t0011g0015 a0001c0001t0011g0102 a0001c0001t0011g0103 others(1): Show |
5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.999-1859A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179070054 | |||||||
| chr1:179070084 | T | C | 29 | a0001c0001t0004g0007 a0001c0001t0004g0031 a0001c0001t0004g0032 others(26): Show |
37 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.999-1829T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179070084 | |||||||
| chr1:179070109 | G | A | 1 | a0001c0001t0024g0073 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.999-1804G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179070109 | |||||||
| chr1:179070148 | T | C | 17 | a0001c0001t0004g0007 a0001c0001t0004g0033 a0001c0001t0004g0034 others(14): Show |
22 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.999-1765T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179070148 | |||||||
| chr1:179070507 | G | A | 6 | a0001c0001t0009g0042 a0001c0001t0009g0221 a0001c0001t0009g0222 others(3): Show |
7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.999-1406G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179070507 | |||||||
| chr1:179070510 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.999-1403C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179070510 | |||||||
| chr1:179070515 | C | CT | 38 | a0001c0001t0001g0009 a0001c0001t0001g0244 a0001c0001t0001g0248 others(35): Show |
51 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.999-1371dupT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 179070515 | ||||||
| chr1:179070515 | CT | C | 76 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0021 others(73): Show |
94 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.999-1371delT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 179070515 | ||||||
| chr1:179070515 | CTT | C | 59 | a0001c0001t0002g0204 a0001c0001t0003g0004 a0001c0001t0003g0005 others(56): Show |
80 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.999-1372_999-1371d others(4): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 179070515 | ||||||
| chr1:179070515 | CTTT | C | 12 | a0001c0001t0002g0218 a0001c0001t0007g0025 a0001c0001t0007g0106 others(9): Show |
13 | HG00735.hp2 HG01099.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.999-1373_999-1371d others(5): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 179070515 | ||||||
| chr1:179070558 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(208): Show |
277 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.999-1355T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179070558 | |||||||
| chr1:179070738 | T | G | 1 | a0001c0001t0004g0162 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.999-1175T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179070738 | |||||||
| chr1:179070934 | G | A | 1 | a0001c0001t0038g0057 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.999-979G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179070934 | |||||||
| chr1:179070942 | T | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(208): Show |
277 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.999-971T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179070942 | |||||||
| chr1:179071023 | A | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(231): Show |
307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.999-890A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071023 | |||||||
| chr1:179071061 | G | A | 3 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0255 |
3 | HG01192.hp2 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.999-852G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071061 | |||||||
| chr1:179071076 | C | T | 9 | a0001c0001t0007g0025 a0001c0001t0007g0106 a0001c0001t0007g0107 others(6): Show |
10 | HG01099.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.999-837C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071076 | |||||||
| chr1:179071118 | A | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(207): Show |
276 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.999-795A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071118 | |||||||
| chr1:179071212 | C | T | 1 | a0001c0001t0002g0200 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.999-701C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071212 | |||||||
| chr1:179071213 | G | A | 1 | a0001c0001t0006g0082 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.999-700G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071213 | |||||||
| chr1:179071220 | C | T | 1 | a0001c0002t0020g0104 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.999-693C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071220 | |||||||
| chr1:179071274 | C | T | 2 | a0001c0001t0019g0074 a0001c0001t0019g0075 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.999-639C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071274 | |||||||
| chr1:179071303 | A | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(110): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.999-610A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071303 | |||||||
| chr1:179071306 | T | A | 1 | a0001c0001t0002g0205 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.999-607T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071306 | |||||||
| chr1:179071405 | G | A | 22 | a0001c0001t0006g0082 a0001c0001t0006g0083 a0001c0001t0006g0084 others(19): Show |
25 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.999-508G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071405 | |||||||
| chr1:179071442 | A | C | 1 | a0001c0001t0003g0147 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.999-471A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071442 | |||||||
| chr1:179071511 | C | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(206): Show |
275 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.999-402C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071511 | |||||||
| chr1:179071601 | A | G | 1 | a0001c0001t0003g0126 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.999-312A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071601 | |||||||
| chr1:179071679 | C | T | 1 | a0001c0001t0007g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.999-234C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071679 | |||||||
| chr1:179071711 | T | A | 15 | a0001c0001t0007g0025 a0001c0001t0007g0106 a0001c0001t0007g0107 others(12): Show |
17 | HG01069.hp2 HG01099.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.999-202T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071711 | |||||||
| chr1:179071795 | T | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(66): Show |
102 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.999-118T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071795 | |||||||
| chr1:179071876 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(206): Show |
275 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.999-37A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071876 | |||||||
| chr1:179071896 | A | G | 6 | a0001c0001t0009g0042 a0001c0001t0009g0221 a0001c0001t0009g0222 others(3): Show |
7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.999-17A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071896 |