Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57136 |
| ensemblid | ENSG00000101474.12 |
| hgncid | 13238 |
| symbol | APMAP |
| name | adipocyte plasma membrane associated protein |
| refseq_nuc | NM_020531.3 |
| refseq_prot | NP_065392.1 |
| ensembl_nuc | ENST00000217456.3 |
| ensembl_prot | ENSP00000217456.2 |
| mane_status | MANE Select |
| chr | chr20 |
| start | 24962925 |
| end | 24992751 |
| strand | - |
| ver | v1.2 |
| region | chr20:24962925-24992751 |
| region5000 | chr20:24957925-24997751 |
| regionname0 | APMAP_chr20_24962925_24992751 |
| regionname5000 | APMAP_chr20_24957925_24997751 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 416 | 259 | 76 | 60 | 73 | 12 | 36 | 59 | APMAP_chr20_24957925_24997751 | APMAP | MSEAD others(411): Show |
chr20 | 24957925 | 24997751 |
| a0002 | 0/0 | 416 | 7 | 1 | 0 | 5 | 0 | 1 | 5 | APMAP_chr20_24957925_24997751 | APMAP | MSEAD others(411): Show |
chr20 | 24957925 | 24997751 |
| a0003 | 0/0 | 416 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | MSEAD others(411): Show |
chr20 | 24957925 | 24997751 |
| a0004 | 0/0 | 416 | 5 | 1 | 2 | 2 | 0 | 0 | 2 | APMAP_chr20_24957925_24997751 | APMAP | MSEAD others(411): Show |
chr20 | 24957925 | 24997751 |
| a0005 | 0/0 | 416 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | MSEAD others(411): Show |
chr20 | 24957925 | 24997751 |
| a0006 | 0/0 | 416 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | APMAP_chr20_24957925_24997751 | APMAP | MSEAD others(411): Show |
chr20 | 24957925 | 24997751 |
| a0007 | 0/0 | 416 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | APMAP_chr20_24957925_24997751 | APMAP | MSEAD others(411): Show |
chr20 | 24957925 | 24997751 |
| a0008 | 0/0 | 416 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | MSEAD others(411): Show |
chr20 | 24957925 | 24997751 |
| a0009 | 0/0 | 416 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | MSEAD others(411): Show |
chr20 | 24957925 | 24997751 |
| a0010 | 0/0 | 416 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | MSEAD others(411): Show |
chr20 | 24957925 | 24997751 |
| a0011 | 0/0 | 416 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | MSEAD others(411): Show |
chr20 | 24957925 | 24997751 |
| a0012 | 0/0 | 416 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | APMAP_chr20_24957925_24997751 | APMAP | MSEAD others(411): Show |
chr20 | 24957925 | 24997751 |
| a0013 | 0/0 | 416 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | MSEAD others(411): Show |
chr20 | 24957925 | 24997751 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1248 | 223 | 52 | 52 | 73 | 9 | 35 | APMAP_chr20_24957925_24997751 | APMAP | ATGAG others(1243): Show |
chr20 | 24957925 | 24997751 | ||
| a0001c0002 | 0/0 | 1248 | 19 | 8 | 7 | 0 | 3 | 1 | APMAP_chr20_24957925_24997751 | APMAP | ATGAG others(1243): Show |
chr20 | 24957925 | 24997751 | ||
| a0001c0003 | 0/0 | 1248 | 12 | 11 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | ATGAG others(1243): Show |
chr20 | 24957925 | 24997751 | ||
| a0001c0008 | 0/0 | 1248 | 2 | 2 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | ATGAG others(1243): Show |
chr20 | 24957925 | 24997751 | ||
| a0001c0009 | 0/0 | 1248 | 2 | 2 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | ATGAG others(1243): Show |
chr20 | 24957925 | 24997751 | ||
| a0001c0018 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | ATGAG others(1243): Show |
chr20 | 24957925 | 24997751 | ||
| a0002c0004 | 0/0 | 1248 | 7 | 1 | 0 | 5 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | ATGAG others(1243): Show |
chr20 | 24957925 | 24997751 | ||
| a0003c0005 | 0/0 | 1248 | 6 | 6 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | ATGAG others(1243): Show |
chr20 | 24957925 | 24997751 | ||
| a0004c0007 | 0/0 | 1248 | 3 | 1 | 2 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | ATGAG others(1243): Show |
chr20 | 24957925 | 24997751 | ||
| a0004c0012 | 0/0 | 1248 | 2 | 0 | 0 | 2 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | ATGAG others(1243): Show |
chr20 | 24957925 | 24997751 | ||
| a0005c0006 | 0/0 | 1248 | 3 | 3 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | ATGAG others(1243): Show |
chr20 | 24957925 | 24997751 | ||
| a0006c0010 | 0/0 | 1248 | 2 | 0 | 0 | 0 | 0 | 2 | APMAP_chr20_24957925_24997751 | APMAP | ATGAG others(1243): Show |
chr20 | 24957925 | 24997751 | ||
| a0007c0011 | 0/0 | 1248 | 2 | 0 | 0 | 2 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | ATGAG others(1243): Show |
chr20 | 24957925 | 24997751 | ||
| a0008c0015 | 0/0 | 1248 | 1 | 0 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | ATGAG others(1243): Show |
chr20 | 24957925 | 24997751 | ||
| a0009c0014 | 0/0 | 1248 | 1 | 0 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | ATGAG others(1243): Show |
chr20 | 24957925 | 24997751 | ||
| a0010c0013 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | ATGAG others(1243): Show |
chr20 | 24957925 | 24997751 | ||
| a0011c0019 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | ATGAG others(1243): Show |
chr20 | 24957925 | 24997751 | ||
| a0012c0016 | 0/0 | 1248 | 1 | 0 | 0 | 0 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | ATGAG others(1243): Show |
chr20 | 24957925 | 24997751 | ||
| a0013c0017 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | ATGAG others(1243): Show |
chr20 | 24957925 | 24997751 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2202 | 176 | 46 | 40 | 50 | 8 | 31 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0001c0001t0002 | 0/1 | 2202 | 37 | 4 | 8 | 20 | 1 | 3 | APMAP_chr20_24957925_24997751 | APMAP | GGAGC others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0001c0001t0003 | 0/0 | 2202 | 4 | 0 | 4 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0001c0001t0007 | 0/0 | 2202 | 1 | 0 | 0 | 0 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | GGAGC others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0001c0001t0008 | 0/0 | 2202 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0001c0001t0009 | 0/0 | 2202 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0001c0001t0010 | 0/0 | 2202 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0001c0001t0011 | 0/0 | 2202 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0001c0001t0012 | 0/0 | 2202 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0001c0002t0003 | 0/0 | 2202 | 19 | 8 | 7 | 0 | 3 | 1 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0001c0003t0004 | 0/0 | 2202 | 8 | 8 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0001c0003t0005 | 0/0 | 2202 | 4 | 3 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0001c0008t0003 | 0/0 | 2202 | 2 | 2 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0001c0009t0006 | 0/0 | 2202 | 2 | 2 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | GGAGC others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0001c0018t0001 | 0/0 | 2202 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0002c0004t0001 | 0/0 | 2202 | 7 | 1 | 0 | 5 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0003c0005t0001 | 0/0 | 2202 | 6 | 6 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0004c0007t0001 | 0/0 | 2202 | 3 | 1 | 2 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0004c0012t0001 | 0/0 | 2202 | 2 | 0 | 0 | 2 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0005c0006t0001 | 0/0 | 2202 | 3 | 3 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0006c0010t0001 | 0/0 | 2202 | 2 | 0 | 0 | 0 | 0 | 2 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0007c0011t0001 | 0/0 | 2202 | 2 | 0 | 0 | 2 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0008c0015t0001 | 0/0 | 2202 | 1 | 0 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0009c0014t0001 | 0/0 | 2202 | 1 | 0 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0010c0013t0013 | 0/0 | 2202 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0011c0019t0001 | 0/0 | 2202 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0012c0016t0001 | 0/0 | 2202 | 1 | 0 | 0 | 0 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| a0013c0017t0001 | 0/0 | 2202 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | GGAGT others(2197): Show |
chr20 | 24957925 | 24997751 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 17 | 3 | 7 | 0 | 2 | 4 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0002 | 0/0 | 15 | 0 | 0 | 13 | 1 | 1 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0003 | 0/0 | 15 | 1 | 1 | 7 | 1 | 5 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0004 | 0/0 | 13 | 0 | 6 | 0 | 3 | 4 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0006 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0002g0005 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0002g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0002g0010 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0002g0011 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0002g0015 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0002g0056 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0003g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0007g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0008g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0009g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0010g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0011g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0001t0012g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0002t0003g0007 | 0/0 | 6 | 0 | 3 | 0 | 3 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0002t0003g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0002t0003g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0002t0003g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0002t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0002t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0002t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0002t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0003t0004g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0003t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0003t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0003t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0003t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0003t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0003t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0003t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0003t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0003t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0003t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0008t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0008t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0009t0006g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0001c0018t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0002c0004t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0002c0004t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0002c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0002c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0002c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0002c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0003c0005t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0003c0005t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0003c0005t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0004c0007t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0004c0007t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0004c0012t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0005c0006t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0005c0006t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0006c0010t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0007c0011t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0007c0011t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0008c0015t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0009c0014t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0010c0013t0013g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0011c0019t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0012c0016t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| a0013c0017t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG00639 | hp1 | a0008 | c0015 | t0001 | g0098 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0060 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG00735 | hp2 | a0001 | c0002 | t0003 | g0007 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG00738 | hp1 | a0001 | c0002 | t0003 | g0007 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01069 | hp1 | a0004 | c0007 | t0001 | g0033 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01069 | hp2 | a0001 | c0002 | t0003 | g0025 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01071 | hp2 | a0004 | c0007 | t0001 | g0033 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01074 | hp2 | a0001 | c0002 | t0003 | g0007 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01081 | hp2 | a0001 | c0002 | t0003 | g0026 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01109 | hp2 | a0001 | c0003 | t0005 | g0074 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | CLM | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | CLM | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0026 | AMR | CLM | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01515 | hp1 | a0001 | c0002 | t0003 | g0007 | EUR | IBS | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01516 | hp2 | a0001 | c0002 | t0003 | g0007 | EUR | IBS | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01517 | hp2 | a0001 | c0002 | t0003 | g0007 | EUR | IBS | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | ACB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01975 | hp1 | a0009 | c0014 | t0001 | g0135 | AMR | PEL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02055 | hp2 | a0001 | c0002 | t0003 | g0012 | AFR | ACB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02145 | hp1 | a0005 | c0006 | t0001 | g0037 | AFR | ACB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02145 | hp2 | a0001 | c0002 | t0003 | g0063 | AFR | ACB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CDX | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02258 | hp1 | a0001 | c0003 | t0004 | g0066 | AFR | ACB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02300 | hp2 | a0001 | c0002 | t0003 | g0025 | AMR | PEL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02572 | hp2 | a0001 | c0009 | t0006 | g0022 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02630 | hp1 | a0001 | c0002 | t0003 | g0012 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02647 | hp2 | a0001 | c0003 | t0004 | g0069 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0062 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02723 | hp2 | a0003 | c0005 | t0001 | g0046 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0012 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02809 | hp2 | a0001 | c0003 | t0004 | g0070 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02818 | hp2 | a0001 | c0003 | t0005 | g0073 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02896 | hp2 | a0003 | c0005 | t0001 | g0021 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02897 | hp2 | a0003 | c0005 | t0001 | g0021 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02965 | hp1 | a0001 | c0009 | t0006 | g0022 | AFR | ESN | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02965 | hp2 | a0001 | c0018 | t0001 | g0151 | AFR | ESN | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0099 | AFR | ESN | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03098 | hp1 | a0010 | c0013 | t0013 | g0100 | AFR | MSL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03098 | hp2 | a0001 | c0003 | t0004 | g0068 | AFR | MSL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03130 | hp1 | a0003 | c0005 | t0001 | g0021 | AFR | ESN | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03195 | hp1 | a0003 | c0005 | t0001 | g0046 | AFR | ESN | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03195 | hp2 | a0001 | c0003 | t0004 | g0027 | AFR | ESN | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03225 | hp1 | a0001 | c0003 | t0004 | g0071 | AFR | MSL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | MSL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03453 | hp2 | a0001 | c0003 | t0004 | g0067 | AFR | MSL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03486 | hp2 | a0001 | c0003 | t0004 | g0027 | AFR | MSL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03491 | hp2 | a0006 | c0010 | t0001 | g0045 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03492 | hp1 | a0006 | c0010 | t0001 | g0045 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0085 | AFR | ESN | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03579 | hp1 | a0001 | c0008 | t0003 | g0059 | AFR | MSL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03579 | hp2 | a0011 | c0019 | t0001 | g0115 | AFR | MSL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03669 | hp2 | a0001 | c0002 | t0003 | g0064 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | STU | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03927 | hp1 | a0012 | c0016 | t0001 | g0108 | SAS | BEB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03927 | hp2 | a0001 | c0001 | t0007 | g0053 | SAS | BEB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03942 | hp1 | a0002 | c0004 | t0001 | g0139 | SAS | BEB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18522 | hp1 | a0005 | c0006 | t0001 | g0037 | AFR | YRI | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18612 | hp2 | a0001 | c0001 | t0012 | g0142 | EAS | CHB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18906 | hp1 | a0001 | c0002 | t0003 | g0065 | AFR | YRI | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | YRI | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18944 | hp1 | a0007 | c0011 | t0001 | g0143 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18944 | hp2 | a0004 | c0012 | t0001 | g0032 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18957 | hp2 | a0002 | c0004 | t0001 | g0040 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18963 | hp2 | a0007 | c0011 | t0001 | g0144 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18998 | hp1 | a0002 | c0004 | t0001 | g0138 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19002 | hp2 | a0004 | c0012 | t0001 | g0032 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19004 | hp1 | a0002 | c0004 | t0001 | g0040 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19030 | hp1 | a0001 | c0003 | t0005 | g0072 | AFR | LWK | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19043 | hp2 | a0005 | c0006 | t0001 | g0101 | AFR | LWK | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19059 | hp1 | a0001 | c0001 | t0008 | g0136 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19080 | hp1 | a0002 | c0004 | t0001 | g0149 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19081 | hp1 | a0001 | c0001 | t0009 | g0141 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0061 | AFR | ASW | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA20129 | hp2 | a0004 | c0007 | t0001 | g0090 | AFR | ASW | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | TSI | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | GIH | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | GIH | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | ACB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02109 | hp2 | a0002 | c0004 | t0001 | g0127 | AFR | ACB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02486 | hp2 | a0001 | c0002 | t0003 | g0012 | AFR | ACB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03471 | hp1 | a0003 | c0005 | t0001 | g0150 | AFR | MSL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG06807 | hp1 | a0001 | c0008 | t0003 | g0058 | AFR | USA | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | USA | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18955 | hp1 | a0002 | c0004 | t0001 | g0137 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | USA | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | USA | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA21309 | hp1 | a0013 | c0017 | t0001 | g0120 | AFR | LWK | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| NA21309 | hp2 | a0001 | c0003 | t0005 | g0075 | AFR | LWK | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0056 | REF | REF | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | APMAP_chr20_24957925_24997751 | APMAP | chr20 | 24957925 | 24997751 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:24963847 | G | A | 1 | a0008 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.1217C>T | p.Pro406Leu | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 9/9 | 1280/2202 | 1217/1251 | 406/416 | chr20 | 24963847 | |||
| chr20:24963887 | C | T | 1 | a0009 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.1177G>A | p.Glu393Lys | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 9/9 | 1240/2202 | 1177/1251 | 393/416 | chr20 | 24963887 | |||
| chr20:24963944 | G | A | 1 | a0003 | 6 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
missense_variant | MODERATE | c.1120C>T | p.Arg374Trp | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 9/9 | 1183/2202 | 1120/1251 | 374/416 | chr20 | 24963944 | |||
| chr20:24963986 | G | A | 1 | a0012 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.1078C>T | p.Arg360Trp | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 9/9 | 1141/2202 | 1078/1251 | 360/416 | chr20 | 24963986 | |||
| chr20:24964006 | G | A | 1 | a0006 | 2 | HG03491.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.1058C>T | p.Thr353Met | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 9/9 | 1121/2202 | 1058/1251 | 353/416 | chr20 | 24964006 | |||
| chr20:24969545 | T | C | 1 | a0013 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.829A>G | p.Thr277Ala | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 7/9 | 892/2202 | 829/1251 | 277/416 | chr20 | 24969545 | |||
| chr20:24971511 | G | A | 2 | a0002 a0007 |
9 | HG02109.hp2 HG03942.hp1 NA18944.hp1 others(6): Show |
missense_variant | MODERATE | c.487C>T | p.Leu163Phe | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 5/9 | 550/2202 | 487/1251 | 163/416 | chr20 | 24971511 | |||
| chr20:24973707 | C | A | 1 | a0010 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.359G>T | p.Arg120Leu | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/9 | 422/2202 | 359/1251 | 120/416 | chr20 | 24973707 | |||
| chr20:24978772 | A | G | 1 | a0005 | 3 | HG02145.hp1 NA18522.hp1 NA19043.hp2 |
missense_variant | MODERATE | c.323T>C | p.Ile108Thr | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/9 | 386/2202 | 323/1251 | 108/416 | chr20 | 24978772 | |||
| chr20:24978790 | G | A | 1 | a0007 | 2 | NA18944.hp1 NA18963.hp2 |
missense_variant | MODERATE | c.305C>T | p.Pro102Leu | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/9 | 368/2202 | 305/1251 | 102/416 | chr20 | 24978790 | |||
| chr20:24978868 | G | A | 1 | a0011 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.227C>T | p.Pro76Leu | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/9 | 290/2202 | 227/1251 | 76/416 | chr20 | 24978868 | |||
| chr20:24983920 | T | C | 1 | a0004 | 2 | NA18944.hp2 NA19002.hp2 |
missense_variant | MODERATE | c.195A>G | p.Ile65Met | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/9 | 258/2202 | 195/1251 | 65/416 | chr20 | 24983920 | |||
| chr20:24983922 | T | C | 1 | a0004 | 3 | HG01069.hp1 HG01071.hp2 NA20129.hp2 |
missense_variant | MODERATE | c.193A>G | p.Ile65Val | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/9 | 256/2202 | 193/1251 | 65/416 | chr20 | 24983922 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:24964005 | C | A | 2 | a0001c0009 a0010c0013 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
synonymous_variant | LOW | c.1059G>T | p.Thr353Thr | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 9/9 | 1122/2202 | 1059/1251 | 353/416 | chr20 | 24964005 | |||
| chr20:24969645 | A | G | 1 | a0001c0009 | 2 | HG02572.hp2 HG02965.hp1 |
synonymous_variant | LOW | c.729T>C | p.Asp243Asp | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 7/9 | 792/2202 | 729/1251 | 243/416 | chr20 | 24969645 | |||
| chr20:24970199 | C | T | 1 | a0001c0003 | 12 | HG01109.hp2 HG02258.hp1 HG02647.hp2 others(9): Show |
splice_region_variant&synonymous_variant | LOW | c.711G>A | p.Gly237Gly | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 6/9 | 774/2202 | 711/1251 | 237/416 | chr20 | 24970199 | |||
| chr20:24970238 | T | C | 2 | a0001c0018 a0003c0005 |
7 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
synonymous_variant | LOW | c.672A>G | p.Arg224Arg | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 6/9 | 735/2202 | 672/1251 | 224/416 | chr20 | 24970238 | |||
| chr20:24983911 | C | T | 3 | a0001c0003 a0001c0009 a0010c0013 |
15 | HG01109.hp2 HG02258.hp1 HG02572.hp2 others(12): Show |
synonymous_variant | LOW | c.204G>A | p.Gln68Gln | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/9 | 267/2202 | 204/1251 | 68/416 | chr20 | 24983911 | |||
| chr20:24992611 | C | A | 2 | a0001c0002 a0001c0008 |
21 | HG00735.hp2 HG00738.hp1 HG01069.hp2 others(18): Show |
synonymous_variant | LOW | c.78G>T | p.Pro26Pro | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/9 | 141/2202 | 78/1251 | 26/416 | chr20 | 24992611 | |||
| chr20:24992677 | C | T | 1 | a0001c0008 | 2 | HG03579.hp1 HG06807.hp1 |
synonymous_variant | LOW | c.12G>A | p.Ala4Ala | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/9 | 75/2202 | 12/1251 | 4/416 | chr20 | 24992677 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:24962954 | G | A | 2 | a0001c0009t0006 a0010c0013t0013 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*859C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 9/9 | 859 | chr20 | 24962954 | ||||||
| chr20:24963081 | G | A | 1 | a0010c0013t0013 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*732C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 9/9 | 732 | chr20 | 24963081 | ||||||
| chr20:24963118 | C | T | 1 | a0001c0001t0011 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*695G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 9/9 | 695 | chr20 | 24963118 | ||||||
| chr20:24963308 | C | T | 1 | a0001c0009t0006 | 2 | HG02572.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*505G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 9/9 | 505 | chr20 | 24963308 | ||||||
| chr20:24963439 | G | A | 2 | a0001c0009t0006 a0010c0013t0013 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*374C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 9/9 | 374 | chr20 | 24963439 | ||||||
| chr20:24963465 | C | A | 1 | a0001c0001t0012 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*348G>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 9/9 | 348 | chr20 | 24963465 | ||||||
| chr20:24963510 | T | C | 1 | a0001c0001t0007 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*303A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 9/9 | 303 | chr20 | 24963510 | ||||||
| chr20:24963530 | C | T | 8 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(5): Show |
66 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*283G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 9/9 | 283 | chr20 | 24963530 | ||||||
| chr20:24963544 | T | C | 2 | a0001c0009t0006 a0010c0013t0013 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*269A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 9/9 | 269 | chr20 | 24963544 | ||||||
| chr20:24963612 | C | T | 1 | a0001c0001t0009 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*201G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 9/9 | 201 | chr20 | 24963612 | ||||||
| chr20:24963761 | C | A | 2 | a0001c0009t0006 a0010c0013t0013 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*52G>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 9/9 | 52 | chr20 | 24963761 | ||||||
| chr20:24963774 | A | G | 1 | a0001c0001t0008 | 1 | NA19059.hp1 | 3_prime_UTR_variant | MODIFIER | c.*39T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 9/9 | 39 | chr20 | 24963774 | ||||||
| chr20:24963811 | G | A | 3 | a0001c0001t0003 a0001c0002t0003 a0001c0008t0003 |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 9/9 | 2 | chr20 | 24963811 | ||||||
| chr20:24992697 | C | T | 2 | a0001c0003t0004 a0001c0003t0005 |
12 | HG01109.hp2 HG02258.hp1 HG02647.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-9G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/9 | 9 | chr20 | 24992697 | ||||||
| chr20:24992710 | C | G | 1 | a0001c0003t0004 | 8 | HG02258.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-22G>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/9 | 22 | chr20 | 24992710 | ||||||
| chr20:24992727 | A | G | 3 | a0001c0001t0003 a0001c0002t0003 a0001c0008t0003 |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-39T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/9 | 39 | chr20 | 24992727 | ||||||
| chr20:24992747 | A | G | 3 | a0001c0001t0002 a0001c0001t0007 a0001c0009t0006 |
39 | HG00639.hp2 HG01123.hp2 HG01168.hp1 others(36): Show |
5_prime_UTR_variant | MODIFIER | c.-59T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/9 | 59 | chr20 | 24992747 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:24964028 | G | A | 2 | a0001c0009t0006g0022 a0010c0013t0013g0100 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
splice_region_variant&intron_variant | LOW | c.1042-6C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24964028 | |||||||
| chr20:24964068 | A | T | 1 | a0006c0010t0001g0045 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1042-46T>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24964068 | |||||||
| chr20:24964297 | T | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1042-275A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24964297 | |||||||
| chr20:24964298 | G | A | 1 | a0001c0001t0010g0099 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1042-276C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24964298 | |||||||
| chr20:24964390 | G | A | 1 | a0002c0004t0001g0139 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1042-368C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24964390 | |||||||
| chr20:24964443 | AGGC | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.1042-424_1042-422d others(5): Show |
APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24964443 | |||||||
| chr20:24964588 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1042-566C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24964588 | |||||||
| chr20:24964764 | T | C | 3 | a0001c0003t0005g0072 a0001c0003t0005g0073 a0001c0003t0005g0075 |
3 | HG02818.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1042-742A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24964764 | |||||||
| chr20:24964840 | C | G | 1 | a0001c0003t0005g0073 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1042-818G>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24964840 | |||||||
| chr20:24964866 | G | A | 11 | a0001c0003t0004g0027 a0001c0003t0004g0066 a0001c0003t0004g0067 others(8): Show |
12 | HG01109.hp2 HG02258.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1042-844C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24964866 | |||||||
| chr20:24964891 | C | T | 1 | a0001c0009t0006g0022 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1042-869G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24964891 | |||||||
| chr20:24964945 | G | C | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(75): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.1042-923C>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24964945 | |||||||
| chr20:24964971 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1042-949G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24964971 | |||||||
| chr20:24965274 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1042-1252G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24965274 | |||||||
| chr20:24965465 | G | T | 1 | a0001c0009t0006g0022 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1042-1443C>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24965465 | |||||||
| chr20:24965466 | G | A | 1 | a0001c0001t0001g0044 | 2 | HG01934.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1042-1444C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24965466 | |||||||
| chr20:24965470 | G | A | 2 | a0001c0009t0006g0022 a0010c0013t0013g0100 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1042-1448C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24965470 | |||||||
| chr20:24965491 | C | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0094 |
3 | HG01361.hp2 HG01993.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1042-1469G>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24965491 | |||||||
| chr20:24965736 | A | C | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.1042-1714T>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24965736 | |||||||
| chr20:24965944 | G | A | 1 | a0010c0013t0013g0100 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1042-1922C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24965944 | |||||||
| chr20:24965981 | G | A | 1 | a0001c0003t0005g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1042-1959C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24965981 | |||||||
| chr20:24965983 | G | A | 2 | a0001c0009t0006g0022 a0010c0013t0013g0100 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1042-1961C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24965983 | |||||||
| chr20:24966027 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1042-2005C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24966027 | |||||||
| chr20:24966042 | C | T | 2 | a0001c0009t0006g0022 a0010c0013t0013g0100 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1042-2020G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24966042 | |||||||
| chr20:24966166 | C | G | 1 | a0007c0011t0001g0143 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1042-2144G>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24966166 | |||||||
| chr20:24966185 | G | A | 11 | a0001c0003t0004g0027 a0001c0003t0004g0066 a0001c0003t0004g0067 others(8): Show |
12 | HG01109.hp2 HG02258.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1042-2163C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24966185 | |||||||
| chr20:24966218 | A | G | 1 | a0002c0004t0001g0137 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1042-2196T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24966218 | |||||||
| chr20:24966219 | T | C | 15 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(12): Show |
28 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1042-2197A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24966219 | |||||||
| chr20:24966225 | A | T | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.1042-2203T>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24966225 | |||||||
| chr20:24966261 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1042-2239G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24966261 | |||||||
| chr20:24966334 | A | G | 1 | a0001c0001t0001g0034 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1042-2312T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24966334 | |||||||
| chr20:24966468 | C | G | 1 | a0001c0001t0002g0015 | 3 | HG01192.hp1 HG01515.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1041+2424G>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24966468 | |||||||
| chr20:24966537 | C | T | 1 | a0001c0001t0002g0052 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1041+2355G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24966537 | |||||||
| chr20:24966562 | G | C | 2 | a0001c0009t0006g0022 a0010c0013t0013g0100 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1041+2330C>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24966562 | |||||||
| chr20:24966592 | C | T | 1 | a0001c0001t0001g0030 | 2 | HG01070.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1041+2300G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24966592 | |||||||
| chr20:24966606 | T | C | 1 | a0001c0001t0002g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1041+2286A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24966606 | |||||||
| chr20:24966764 | G | A | 1 | a0001c0009t0006g0022 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1041+2128C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24966764 | |||||||
| chr20:24966800 | C | T | 1 | a0001c0003t0005g0074 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1041+2092G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24966800 | |||||||
| chr20:24966834 | G | A | 2 | a0001c0009t0006g0022 a0010c0013t0013g0100 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1041+2058C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24966834 | |||||||
| chr20:24966840 | C | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1041+2052G>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24966840 | |||||||
| chr20:24966874 | T | C | 2 | a0001c0009t0006g0022 a0010c0013t0013g0100 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1041+2018A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24966874 | |||||||
| chr20:24966884 | T | A | 1 | a0001c0001t0001g0086 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1041+2008A>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24966884 | |||||||
| chr20:24966903 | C | T | 1 | a0001c0003t0005g0073 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1041+1989G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24966903 | |||||||
| chr20:24966917 | C | T | 1 | a0001c0003t0004g0070 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1041+1975G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24966917 | |||||||
| chr20:24967045 | G | C | 2 | a0001c0009t0006g0022 a0010c0013t0013g0100 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1041+1847C>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24967045 | |||||||
| chr20:24967107 | A | T | 1 | a0001c0001t0001g0082 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1041+1785T>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24967107 | |||||||
| chr20:24967110 | A | G | 2 | a0001c0009t0006g0022 a0010c0013t0013g0100 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1041+1782T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24967110 | |||||||
| chr20:24967217 | C | T | 2 | a0001c0009t0006g0022 a0010c0013t0013g0100 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1041+1675G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24967217 | |||||||
| chr20:24967539 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1041+1353T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24967539 | |||||||
| chr20:24967693 | C | A | 1 | a0001c0001t0001g0128 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1041+1199G>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24967693 | |||||||
| chr20:24967696 | T | A | 1 | a0001c0001t0001g0128 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1041+1196A>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24967696 | |||||||
| chr20:24967711 | C | A | 1 | a0004c0007t0001g0033 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1041+1181G>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24967711 | |||||||
| chr20:24967841 | G | C | 2 | a0001c0009t0006g0022 a0010c0013t0013g0100 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1041+1051C>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24967841 | |||||||
| chr20:24967848 | T | A | 1 | a0001c0001t0002g0049 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1041+1044A>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24967848 | |||||||
| chr20:24967887 | C | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0042 |
5 | HG00738.hp2 HG00741.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1041+1005G>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24967887 | |||||||
| chr20:24967958 | C | T | 1 | a0001c0001t0001g0019 | 3 | HG02451.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1041+934G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24967958 | |||||||
| chr20:24967994 | A | G | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1041+898T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24967994 | |||||||
| chr20:24968215 | T | C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.1041+677A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24968215 | |||||||
| chr20:24968251 | G | C | 2 | a0001c0009t0006g0022 a0010c0013t0013g0100 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1041+641C>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24968251 | |||||||
| chr20:24968309 | A | T | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.1041+583T>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24968309 | |||||||
| chr20:24968508 | G | A | 15 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(12): Show |
28 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1041+384C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24968508 | |||||||
| chr20:24968523 | G | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.1041+369C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24968523 | |||||||
| chr20:24968572 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0081 |
2 | HG00609.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1041+320C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24968572 | |||||||
| chr20:24968616 | C | CCAGAAA | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(72): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.1041+270_1041+275d others(8): Show |
APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24968616 | |||||||
| chr20:24968838 | T | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0102 a0001c0001t0001g0117 |
4 | HG02818.hp1 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1041+54A>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 8/8 | chr20 | 24968838 | |||||||
| chr20:24969185 | G | A | 1 | a0001c0001t0001g0014 | 4 | HG02559.hp2 HG02615.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.849-101C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 7/8 | chr20 | 24969185 | |||||||
| chr20:24969228 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.849-144T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 7/8 | chr20 | 24969228 | |||||||
| chr20:24969289 | C | G | 2 | a0001c0001t0001g0018 a0012c0016t0001g0108 |
4 | HG01981.hp2 HG03927.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.849-205G>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 7/8 | chr20 | 24969289 | |||||||
| chr20:24969308 | G | C | 14 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0010 others(11): Show |
35 | HG00639.hp2 HG01123.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.848+218C>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 7/8 | chr20 | 24969308 | |||||||
| chr20:24969327 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.848+199G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 7/8 | chr20 | 24969327 | |||||||
| chr20:24969359 | G | A | 1 | a0001c0009t0006g0022 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.848+167C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 7/8 | chr20 | 24969359 | |||||||
| chr20:24969472 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.848+54G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 7/8 | chr20 | 24969472 | |||||||
| chr20:24969718 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.714-58G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 6/8 | chr20 | 24969718 | |||||||
| chr20:24969737 | A | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.714-77T>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 6/8 | chr20 | 24969737 | |||||||
| chr20:24969947 | T | C | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.713+250A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 6/8 | chr20 | 24969947 | |||||||
| chr20:24970012 | C | T | 1 | a0001c0003t0004g0070 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.713+185G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 6/8 | chr20 | 24970012 | |||||||
| chr20:24970030 | T | C | 1 | a0010c0013t0013g0100 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.713+167A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 6/8 | chr20 | 24970030 | |||||||
| chr20:24970145 | A | G | 15 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(12): Show |
28 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.713+52T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 6/8 | chr20 | 24970145 | |||||||
| chr20:24970192 | C | T | 1 | a0001c0003t0004g0066 | 1 | HG02258.hp1 | splice_region_variant&intron_variant | LOW | c.713+5G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 6/8 | chr20 | 24970192 | |||||||
| chr20:24970445 | C | T | 6 | a0001c0018t0001g0151 a0003c0005t0001g0021 a0003c0005t0001g0046 others(3): Show |
10 | HG02145.hp1 HG02723.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.539-74G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 5/8 | chr20 | 24970445 | |||||||
| chr20:24970506 | T | C | 1 | a0001c0001t0001g0039 | 2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.539-135A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 5/8 | chr20 | 24970506 | |||||||
| chr20:24970739 | A | C | 1 | a0001c0018t0001g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.539-368T>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 5/8 | chr20 | 24970739 | |||||||
| chr20:24970850 | G | A | 14 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0010 others(11): Show |
35 | HG00639.hp2 HG01123.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.539-479C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 5/8 | chr20 | 24970850 | |||||||
| chr20:24970876 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.539-505C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 5/8 | chr20 | 24970876 | |||||||
| chr20:24970942 | T | C | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.538+518A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 5/8 | chr20 | 24970942 | |||||||
| chr20:24970956 | C | T | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.538+504G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 5/8 | chr20 | 24970956 | |||||||
| chr20:24970976 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.538+484A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 5/8 | chr20 | 24970976 | |||||||
| chr20:24971219 | C | T | 1 | a0002c0004t0001g0137 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.538+241G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 5/8 | chr20 | 24971219 | |||||||
| chr20:24971266 | T | C | 1 | a0001c0003t0005g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.538+194A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 5/8 | chr20 | 24971266 | |||||||
| chr20:24971401 | C | T | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.538+59G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 5/8 | chr20 | 24971401 | |||||||
| chr20:24971624 | A | G | 2 | a0001c0009t0006g0022 a0010c0013t0013g0100 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.422-48T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24971624 | |||||||
| chr20:24971728 | G | A | 6 | a0001c0018t0001g0151 a0003c0005t0001g0021 a0003c0005t0001g0046 others(3): Show |
10 | HG02145.hp1 HG02723.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.422-152C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24971728 | |||||||
| chr20:24971892 | G | A | 1 | a0001c0003t0004g0069 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.422-316C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24971892 | |||||||
| chr20:24972064 | TAGGGTGT others(34): Show |
T | 1 | a0001c0009t0006g0022 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.422-529_422-489del others(41): Show |
APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24972064 | |||||||
| chr20:24972111 | G | A | 1 | a0001c0009t0006g0022 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.422-535C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24972111 | |||||||
| chr20:24972123 | G | A | 3 | a0001c0001t0002g0008 a0001c0001t0002g0051 a0001c0001t0002g0055 |
7 | HG02293.hp1 NA18948.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.422-547C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24972123 | |||||||
| chr20:24972135 | G | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0111 a0001c0001t0001g0113 |
3 | HG02451.hp2 HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.422-559C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24972135 | |||||||
| chr20:24972150 | G | GTGTTCAC others(169): Show |
1 | a0001c0001t0001g0125 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.422-750_422-575dup others(176): Show |
APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24972150 | |||||||
| chr20:24972256 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.422-680T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24972256 | |||||||
| chr20:24972258 | G | A | 1 | a0001c0003t0005g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.422-682C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24972258 | |||||||
| chr20:24972435 | C | T | 2 | a0001c0009t0006g0022 a0010c0013t0013g0100 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.422-859G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24972435 | |||||||
| chr20:24972436 | G | A | 1 | a0001c0001t0002g0055 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.422-860C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24972436 | |||||||
| chr20:24972483 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.422-907G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24972483 | |||||||
| chr20:24972495 | C | T | 15 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(12): Show |
28 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.422-919G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24972495 | |||||||
| chr20:24972564 | C | G | 2 | a0001c0008t0003g0058 a0001c0008t0003g0059 |
2 | HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.422-988G>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24972564 | |||||||
| chr20:24972641 | C | T | 1 | a0001c0003t0005g0074 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.421+1004G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24972641 | |||||||
| chr20:24972702 | G | A | 1 | a0001c0001t0001g0043 | 2 | NA19080.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.421+943C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24972702 | |||||||
| chr20:24972730 | T | G | 1 | a0001c0001t0001g0087 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.421+915A>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24972730 | |||||||
| chr20:24972920 | G | A | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.421+725C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24972920 | |||||||
| chr20:24972960 | G | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.421+685C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24972960 | |||||||
| chr20:24973193 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.421+452A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24973193 | |||||||
| chr20:24973358 | C | T | 5 | a0001c0002t0003g0012 a0001c0002t0003g0062 a0001c0002t0003g0063 others(2): Show |
8 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.421+287G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24973358 | |||||||
| chr20:24973359 | G | A | 1 | a0001c0002t0003g0065 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.421+286C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24973359 | |||||||
| chr20:24973486 | G | A | 1 | a0001c0009t0006g0022 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.421+159C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24973486 | |||||||
| chr20:24973526 | AG | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.421+118delC | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 4/8 | chr20 | 24973526 | |||||||
| chr20:24973936 | G | C | 1 | a0001c0001t0001g0013 | 4 | HG01261.hp1 HG02257.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.329-199C>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24973936 | |||||||
| chr20:24974001 | G | A | 4 | a0001c0018t0001g0151 a0003c0005t0001g0021 a0003c0005t0001g0046 others(1): Show |
7 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.329-264C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24974001 | |||||||
| chr20:24974115 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.329-378G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24974115 | |||||||
| chr20:24974251 | A | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.329-514T>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24974251 | |||||||
| chr20:24974322 | T | C | 7 | a0001c0003t0004g0027 a0001c0003t0004g0066 a0001c0003t0004g0067 others(4): Show |
8 | HG02258.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.329-585A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24974322 | |||||||
| chr20:24974349 | TAAGA | T | 1 | a0001c0001t0002g0015 | 3 | HG01192.hp1 HG01515.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.329-616_329-613del others(4): Show |
APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24974349 | |||||||
| chr20:24974374 | T | C | 4 | a0001c0003t0005g0072 a0001c0003t0005g0073 a0001c0009t0006g0022 others(1): Show |
5 | HG02572.hp2 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.329-637A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24974374 | |||||||
| chr20:24974550 | T | C | 2 | a0001c0002t0003g0062 a0001c0002t0003g0063 |
2 | HG02145.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.329-813A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24974550 | |||||||
| chr20:24974718 | A | G | 2 | a0001c0009t0006g0022 a0010c0013t0013g0100 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.329-981T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24974718 | |||||||
| chr20:24975138 | T | A | 1 | a0001c0003t0005g0074 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.329-1401A>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24975138 | |||||||
| chr20:24975262 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.329-1525A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24975262 | |||||||
| chr20:24975345 | T | C | 14 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0010 others(11): Show |
35 | HG00639.hp2 HG01123.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.329-1608A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24975345 | |||||||
| chr20:24975425 | T | G | 13 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0010 others(10): Show |
34 | HG00639.hp2 HG01123.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.329-1688A>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24975425 | |||||||
| chr20:24975497 | T | C | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.329-1760A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24975497 | |||||||
| chr20:24975502 | T | A | 2 | a0001c0009t0006g0022 a0010c0013t0013g0100 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.329-1765A>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24975502 | |||||||
| chr20:24975550 | A | G | 2 | a0005c0006t0001g0037 a0005c0006t0001g0101 |
3 | HG02145.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.329-1813T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24975550 | |||||||
| chr20:24975570 | T | C | 6 | a0001c0018t0001g0151 a0003c0005t0001g0021 a0003c0005t0001g0046 others(3): Show |
10 | HG02145.hp1 HG02723.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.329-1833A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24975570 | |||||||
| chr20:24975685 | T | C | 7 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0104 others(4): Show |
16 | HG01109.hp1 HG01884.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.329-1948A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24975685 | |||||||
| chr20:24975770 | G | C | 4 | a0001c0003t0004g0027 a0001c0003t0004g0068 a0001c0003t0004g0069 others(1): Show |
5 | HG02647.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.329-2033C>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24975770 | |||||||
| chr20:24976017 | C | T | 1 | a0010c0013t0013g0100 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.329-2280G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24976017 | |||||||
| chr20:24976059 | A | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.329-2322T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24976059 | |||||||
| chr20:24976145 | T | C | 7 | a0001c0003t0004g0027 a0001c0003t0004g0066 a0001c0003t0004g0067 others(4): Show |
8 | HG02258.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.329-2408A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24976145 | |||||||
| chr20:24976376 | T | C | 1 | a0005c0006t0001g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.328+2391A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24976376 | |||||||
| chr20:24976528 | C | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.328+2239G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24976528 | |||||||
| chr20:24976622 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.328+2145C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24976622 | |||||||
| chr20:24976643 | C | T | 1 | a0001c0009t0006g0022 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.328+2124G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24976643 | |||||||
| chr20:24976762 | G | A | 2 | a0001c0009t0006g0022 a0010c0013t0013g0100 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.328+2005C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24976762 | |||||||
| chr20:24976819 | C | T | 14 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0010 others(11): Show |
35 | HG00639.hp2 HG01123.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.328+1948G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24976819 | |||||||
| chr20:24977101 | A | G | 15 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(12): Show |
28 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.328+1666T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24977101 | |||||||
| chr20:24977162 | G | A | 1 | a0001c0001t0010g0099 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.328+1605C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24977162 | |||||||
| chr20:24977255 | G | A | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.328+1512C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24977255 | |||||||
| chr20:24977270 | C | A | 2 | a0001c0009t0006g0022 a0010c0013t0013g0100 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.328+1497G>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24977270 | |||||||
| chr20:24977370 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.328+1397G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24977370 | |||||||
| chr20:24977751 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.328+1016A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24977751 | |||||||
| chr20:24977785 | A | C | 7 | a0001c0003t0004g0027 a0001c0003t0004g0066 a0001c0003t0004g0067 others(4): Show |
8 | HG02258.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.328+982T>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24977785 | |||||||
| chr20:24977831 | T | G | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.328+936A>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24977831 | |||||||
| chr20:24977904 | A | C | 2 | a0005c0006t0001g0037 a0005c0006t0001g0101 |
3 | HG02145.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.328+863T>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24977904 | |||||||
| chr20:24978033 | T | C | 6 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0094 others(3): Show |
8 | HG01192.hp2 HG01243.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.328+734A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24978033 | |||||||
| chr20:24978094 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG02071.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.328+673C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24978094 | |||||||
| chr20:24978097 | A | T | 1 | a0001c0001t0001g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.328+670T>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24978097 | |||||||
| chr20:24978201 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.328+566G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24978201 | |||||||
| chr20:24978311 | C | T | 1 | a0001c0002t0003g0061 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.328+456G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24978311 | |||||||
| chr20:24978388 | C | G | 1 | a0001c0001t0001g0013 | 4 | HG01261.hp1 HG02257.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.328+379G>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24978388 | |||||||
| chr20:24978583 | G | A | 2 | a0001c0009t0006g0022 a0010c0013t0013g0100 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.328+184C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24978583 | |||||||
| chr20:24978639 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.328+128C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24978639 | |||||||
| chr20:24978663 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.328+104G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24978663 | |||||||
| chr20:24978679 | C | T | 2 | a0001c0009t0006g0022 a0010c0013t0013g0100 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.328+88G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24978679 | |||||||
| chr20:24978709 | G | A | 3 | a0001c0001t0001g0152 a0001c0001t0009g0141 a0001c0001t0012g0142 |
3 | NA18612.hp2 NA18984.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.328+58C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24978709 | |||||||
| chr20:24978738 | G | GCC | 9 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(6): Show |
20 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.328+28_328+29insGG | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24978738 | |||||||
| chr20:24978738 | G | GCCC | 2 | a0001c0002t0003g0025 a0001c0002t0003g0063 |
3 | HG01069.hp2 HG02145.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.328+28_328+29insGG others(1): Show |
APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24978738 | |||||||
| chr20:24978740 | T | C | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.328+27A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24978740 | |||||||
| chr20:24978745 | C | A | 11 | a0001c0003t0004g0027 a0001c0003t0004g0066 a0001c0003t0004g0067 others(8): Show |
12 | HG01109.hp2 HG02258.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.328+22G>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24978745 | |||||||
| chr20:24978746 | C | G | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.328+21G>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24978746 | |||||||
| chr20:24978748 | C | T | 6 | a0001c0018t0001g0151 a0003c0005t0001g0021 a0003c0005t0001g0046 others(3): Show |
10 | HG02145.hp1 HG02723.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.328+19G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24978748 | |||||||
| chr20:24978748 | CA | C | 3 | a0001c0001t0002g0050 a0001c0001t0002g0057 a0001c0001t0010g0099 |
3 | HG01884.hp1 HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.328+18delT | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24978748 | |||||||
| chr20:24978749 | A | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(80): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.328+18T>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24978749 | |||||||
| chr20:24978750 | C | A | 27 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0010 others(24): Show |
60 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.328+17G>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 3/8 | chr20 | 24978750 | |||||||
| chr20:24978937 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.213-55A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24978937 | |||||||
| chr20:24978972 | AGATGGCA others(125): Show |
A | 1 | a0001c0009t0006g0022 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.213-222_213-91del | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24978972 | |||||||
| chr20:24978983 | T | G | 1 | a0001c0001t0001g0081 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.213-101A>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24978983 | |||||||
| chr20:24979167 | C | A | 1 | a0001c0001t0001g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.213-285G>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24979167 | |||||||
| chr20:24979273 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.213-391C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24979273 | |||||||
| chr20:24979292 | G | A | 2 | a0001c0002t0003g0062 a0001c0002t0003g0063 |
2 | HG02145.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.213-410C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24979292 | |||||||
| chr20:24979335 | C | T | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.213-453G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24979335 | |||||||
| chr20:24979379 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.213-497G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24979379 | |||||||
| chr20:24979402 | G | A | 14 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0010 others(11): Show |
35 | HG00639.hp2 HG01123.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.213-520C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24979402 | |||||||
| chr20:24979449 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.213-567C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24979449 | |||||||
| chr20:24979460 | C | G | 1 | a0001c0001t0001g0043 | 2 | NA19080.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.213-578G>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24979460 | |||||||
| chr20:24979609 | C | A | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.213-727G>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24979609 | |||||||
| chr20:24979677 | A | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.213-795T>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24979677 | |||||||
| chr20:24979680 | C | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.213-798G>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24979680 | |||||||
| chr20:24979681 | C | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.213-799G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24979681 | |||||||
| chr20:24979973 | G | A | 2 | a0001c0001t0001g0009 a0011c0019t0001g0115 |
6 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.213-1091C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24979973 | |||||||
| chr20:24979978 | C | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.213-1096G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24979978 | |||||||
| chr20:24979984 | C | G | 1 | a0001c0001t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.213-1102G>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24979984 | |||||||
| chr20:24980107 | G | A | 2 | a0001c0009t0006g0022 a0010c0013t0013g0100 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.213-1225C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24980107 | |||||||
| chr20:24980113 | G | T | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.213-1231C>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24980113 | |||||||
| chr20:24980152 | T | C | 15 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(12): Show |
28 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.213-1270A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24980152 | |||||||
| chr20:24980213 | A | G | 15 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(12): Show |
28 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.213-1331T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24980213 | |||||||
| chr20:24980357 | G | A | 1 | a0001c0009t0006g0022 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.213-1475C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24980357 | |||||||
| chr20:24980399 | C | T | 1 | a0001c0009t0006g0022 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.213-1517G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24980399 | |||||||
| chr20:24980429 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.213-1547C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24980429 | |||||||
| chr20:24980489 | C | T | 1 | a0010c0013t0013g0100 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.213-1607G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24980489 | |||||||
| chr20:24980606 | G | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0013c0017t0001g0120 |
3 | HG01243.hp2 HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.213-1724C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24980606 | |||||||
| chr20:24980632 | G | T | 1 | a0001c0001t0001g0029 | 2 | NA18963.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.213-1750C>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24980632 | |||||||
| chr20:24980646 | A | G | 2 | a0001c0009t0006g0022 a0010c0013t0013g0100 |
3 | HG02572.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.213-1764T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24980646 | |||||||
| chr20:24980661 | C | T | 4 | a0001c0003t0004g0027 a0001c0003t0004g0068 a0001c0003t0004g0069 others(1): Show |
5 | HG02647.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.213-1779G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24980661 | |||||||
| chr20:24980710 | C | T | 1 | a0001c0002t0003g0025 | 2 | HG01069.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.213-1828G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24980710 | |||||||
| chr20:24980728 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.213-1846C>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24980728 | |||||||
| chr20:24980739 | A | G | 1 | a0001c0001t0001g0042 | 2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.213-1857T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24980739 | |||||||
| chr20:24980775 | G | A | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.213-1893C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24980775 | |||||||
| chr20:24980877 | C | A | 1 | a0001c0001t0001g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.213-1995G>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24980877 | |||||||
| chr20:24980914 | T | C | 1 | a0001c0001t0002g0024 | 2 | HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.213-2032A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24980914 | |||||||
| chr20:24981001 | G | A | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.213-2119C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24981001 | |||||||
| chr20:24981071 | G | C | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.213-2189C>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24981071 | |||||||
| chr20:24981103 | T | C | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.213-2221A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24981103 | |||||||
| chr20:24981111 | C | T | 1 | a0001c0002t0003g0025 | 2 | HG01069.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.213-2229G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24981111 | |||||||
| chr20:24981125 | T | A | 1 | a0001c0001t0001g0110 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.213-2243A>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24981125 | |||||||
| chr20:24981452 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.212+2451T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24981452 | |||||||
| chr20:24981467 | C | T | 1 | a0001c0001t0001g0029 | 2 | NA18963.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.212+2436G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24981467 | |||||||
| chr20:24981651 | T | C | 1 | a0001c0003t0005g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.212+2252A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24981651 | |||||||
| chr20:24981745 | T | C | 1 | a0010c0013t0013g0100 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.212+2158A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24981745 | |||||||
| chr20:24981763 | T | A | 1 | a0001c0001t0001g0146 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.212+2140A>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24981763 | |||||||
| chr20:24981912 | G | A | 1 | a0001c0001t0010g0099 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.212+1991C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24981912 | |||||||
| chr20:24981977 | A | G | 1 | a0001c0003t0005g0074 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.212+1926T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24981977 | |||||||
| chr20:24982021 | C | T | 1 | a0001c0001t0001g0028 | 2 | NA18968.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.212+1882G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24982021 | |||||||
| chr20:24982234 | AAAAGCTG others(50): Show |
A | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.212+1612_212+1668d others(59): Show |
APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24982234 | |||||||
| chr20:24982273 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.212+1630A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24982273 | |||||||
| chr20:24982441 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.212+1462T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24982441 | |||||||
| chr20:24982593 | A | G | 7 | a0001c0003t0004g0027 a0001c0003t0004g0066 a0001c0003t0004g0067 others(4): Show |
8 | HG02258.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.212+1310T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24982593 | |||||||
| chr20:24982831 | A | AC | 27 | a0001c0001t0001g0017 a0001c0001t0001g0038 a0001c0001t0001g0041 others(24): Show |
39 | HG00609.hp2 HG00735.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.212+1071dupG | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24982831 | |||||||
| chr20:24982831 | A | ACC | 8 | a0001c0001t0003g0016 a0001c0002t0003g0012 a0001c0002t0003g0025 others(5): Show |
15 | HG01069.hp2 HG01081.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.212+1070_212+1071d others(4): Show |
APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24982831 | |||||||
| chr20:24983004 | G | A | 1 | a0001c0009t0006g0022 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.212+899C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24983004 | |||||||
| chr20:24983355 | T | C | 1 | a0001c0001t0002g0055 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.212+548A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24983355 | |||||||
| chr20:24983374 | C | T | 13 | a0001c0003t0004g0027 a0001c0003t0004g0066 a0001c0003t0004g0067 others(10): Show |
15 | HG01109.hp2 HG02258.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.212+529G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24983374 | |||||||
| chr20:24983566 | T | C | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(72): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.212+337A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24983566 | |||||||
| chr20:24983599 | T | C | 1 | a0006c0010t0001g0045 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.212+304A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24983599 | |||||||
| chr20:24983712 | T | C | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.212+191A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24983712 | |||||||
| chr20:24983830 | C | T | 13 | a0001c0003t0004g0027 a0001c0003t0004g0066 a0001c0003t0004g0067 others(10): Show |
15 | HG01109.hp2 HG02258.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.212+73G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 2/8 | chr20 | 24983830 | |||||||
| chr20:24984086 | G | A | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.96-67C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24984086 | |||||||
| chr20:24984136 | A | T | 1 | a0010c0013t0013g0100 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.96-117T>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24984136 | |||||||
| chr20:24984181 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.96-162A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24984181 | |||||||
| chr20:24984212 | C | CT | 13 | a0001c0003t0004g0027 a0001c0003t0004g0066 a0001c0003t0004g0067 others(10): Show |
15 | HG01109.hp2 HG02258.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.96-194dupA | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24984212 | |||||||
| chr20:24984251 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.96-232C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24984251 | |||||||
| chr20:24984300 | G | T | 2 | a0003c0005t0001g0021 a0003c0005t0001g0150 |
4 | HG02896.hp2 HG02897.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.96-281C>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24984300 | |||||||
| chr20:24984490 | G | A | 1 | a0001c0003t0005g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.96-471C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24984490 | |||||||
| chr20:24984837 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.96-818T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24984837 | |||||||
| chr20:24985205 | G | A | 1 | a0001c0009t0006g0022 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.96-1186C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24985205 | |||||||
| chr20:24985269 | G | A | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.96-1250C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24985269 | |||||||
| chr20:24985454 | C | G | 4 | a0001c0018t0001g0151 a0003c0005t0001g0021 a0003c0005t0001g0046 others(1): Show |
7 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.96-1435G>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24985454 | |||||||
| chr20:24985526 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.96-1507T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24985526 | |||||||
| chr20:24985664 | T | C | 1 | a0001c0009t0006g0022 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.96-1645A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24985664 | |||||||
| chr20:24985721 | T | G | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.96-1702A>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24985721 | |||||||
| chr20:24985764 | T | G | 26 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(23): Show |
40 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.96-1745A>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24985764 | |||||||
| chr20:24985768 | T | G | 13 | a0001c0003t0004g0027 a0001c0003t0004g0066 a0001c0003t0004g0067 others(10): Show |
15 | HG01109.hp2 HG02258.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.96-1749A>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24985768 | |||||||
| chr20:24985783 | T | TA | 13 | a0001c0003t0004g0027 a0001c0003t0004g0066 a0001c0003t0004g0067 others(10): Show |
15 | HG01109.hp2 HG02258.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.96-1765dupT | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24985783 | |||||||
| chr20:24985810 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.96-1791T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24985810 | |||||||
| chr20:24985829 | C | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0041 a0001c0001t0001g0123 others(4): Show |
20 | HG00099.hp1 HG01106.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.96-1810G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24985829 | |||||||
| chr20:24985832 | GA | G | 26 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(23): Show |
40 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.96-1814delT | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24985832 | |||||||
| chr20:24985882 | G | C | 1 | a0001c0001t0001g0091 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.96-1863C>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24985882 | |||||||
| chr20:24985914 | C | T | 1 | a0001c0001t0002g0051 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.96-1895G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24985914 | |||||||
| chr20:24985915 | G | A | 4 | a0001c0001t0001g0092 a0001c0003t0005g0072 a0001c0003t0005g0073 others(1): Show |
4 | HG02818.hp2 NA19000.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.96-1896C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24985915 | |||||||
| chr20:24985951 | G | A | 1 | a0001c0003t0005g0074 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.96-1932C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24985951 | |||||||
| chr20:24985983 | C | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.96-1964G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24985983 | |||||||
| chr20:24986115 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96-2096G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24986115 | |||||||
| chr20:24986118 | G | A | 1 | a0001c0009t0006g0022 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.96-2099C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24986118 | |||||||
| chr20:24986294 | T | C | 2 | a0005c0006t0001g0037 a0005c0006t0001g0101 |
3 | HG02145.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.96-2275A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24986294 | |||||||
| chr20:24986324 | G | A | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.96-2305C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24986324 | |||||||
| chr20:24986341 | A | G | 26 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(23): Show |
40 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.96-2322T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24986341 | |||||||
| chr20:24986400 | C | T | 6 | a0001c0018t0001g0151 a0003c0005t0001g0021 a0003c0005t0001g0046 others(3): Show |
10 | HG02145.hp1 HG02723.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.96-2381G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24986400 | |||||||
| chr20:24986428 | G | C | 13 | a0001c0003t0004g0027 a0001c0003t0004g0066 a0001c0003t0004g0067 others(10): Show |
15 | HG01109.hp2 HG02258.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.96-2409C>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24986428 | |||||||
| chr20:24986579 | T | C | 1 | a0001c0001t0001g0038 | 2 | HG01256.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.96-2560A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24986579 | |||||||
| chr20:24986582 | C | T | 3 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 |
10 | NA18965.hp2 NA18973.hp2 NA18977.hp1 others(7): Show |
intron_variant | MODIFIER | c.96-2563G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24986582 | |||||||
| chr20:24986623 | G | A | 14 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0010 others(11): Show |
35 | HG00639.hp2 HG01123.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.96-2604C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24986623 | |||||||
| chr20:24986779 | A | G | 1 | a0010c0013t0013g0100 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.96-2760T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24986779 | |||||||
| chr20:24986984 | A | C | 26 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(23): Show |
40 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.96-2965T>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24986984 | |||||||
| chr20:24987056 | T | C | 1 | a0001c0003t0005g0074 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.96-3037A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24987056 | |||||||
| chr20:24987167 | G | C | 4 | a0001c0018t0001g0151 a0003c0005t0001g0021 a0003c0005t0001g0046 others(1): Show |
7 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.96-3148C>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24987167 | |||||||
| chr20:24987190 | A | C | 7 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(4): Show |
10 | HG01168.hp2 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.96-3171T>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24987190 | |||||||
| chr20:24987308 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.96-3289C>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24987308 | |||||||
| chr20:24987381 | T | C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(127): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.96-3362A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24987381 | |||||||
| chr20:24987653 | A | T | 1 | a0001c0001t0001g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.96-3634T>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24987653 | |||||||
| chr20:24988107 | A | G | 1 | a0010c0013t0013g0100 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.96-4088T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24988107 | |||||||
| chr20:24988213 | C | T | 2 | a0001c0001t0001g0103 a0001c0002t0003g0061 |
2 | HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.96-4194G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24988213 | |||||||
| chr20:24988383 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.95+4211G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24988383 | |||||||
| chr20:24988551 | A | G | 1 | a0010c0013t0013g0100 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.95+4043T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24988551 | |||||||
| chr20:24988722 | C | T | 3 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 |
10 | NA18965.hp2 NA18973.hp2 NA18977.hp1 others(7): Show |
intron_variant | MODIFIER | c.95+3872G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24988722 | |||||||
| chr20:24988956 | A | G | 1 | a0002c0004t0001g0040 | 2 | NA18957.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.95+3638T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24988956 | |||||||
| chr20:24989028 | C | A | 1 | a0001c0001t0001g0047 | 2 | HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.95+3566G>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24989028 | |||||||
| chr20:24989170 | T | C | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.95+3424A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24989170 | |||||||
| chr20:24989265 | C | A | 1 | a0001c0001t0001g0038 | 2 | HG01256.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.95+3329G>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24989265 | |||||||
| chr20:24989405 | T | C | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
11 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.95+3189A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24989405 | |||||||
| chr20:24989564 | C | G | 3 | a0001c0001t0001g0102 a0001c0003t0004g0066 a0001c0003t0004g0067 |
3 | HG02258.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.95+3030G>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24989564 | |||||||
| chr20:24989575 | G | T | 1 | a0001c0001t0010g0099 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.95+3019C>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24989575 | |||||||
| chr20:24989628 | T | C | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.95+2966A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24989628 | |||||||
| chr20:24989673 | AT | A | 13 | a0001c0003t0004g0027 a0001c0003t0004g0066 a0001c0003t0004g0067 others(10): Show |
15 | HG01109.hp2 HG02258.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.95+2920delA | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24989673 | |||||||
| chr20:24990147 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.95+2447A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24990147 | |||||||
| chr20:24990420 | T | G | 2 | a0001c0001t0002g0011 a0001c0001t0002g0024 |
6 | HG00639.hp2 HG01123.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.95+2174A>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24990420 | |||||||
| chr20:24990759 | G | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.95+1835C>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24990759 | |||||||
| chr20:24990767 | C | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0117 |
3 | HG02818.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.95+1827G>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24990767 | |||||||
| chr20:24990781 | G | A | 1 | a0013c0017t0001g0120 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.95+1813C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24990781 | |||||||
| chr20:24990791 | T | C | 1 | a0001c0001t0002g0057 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.95+1803A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24990791 | |||||||
| chr20:24990813 | C | T | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.95+1781G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24990813 | |||||||
| chr20:24990939 | A | C | 1 | a0001c0003t0005g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.95+1655T>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24990939 | |||||||
| chr20:24990987 | G | C | 7 | a0001c0003t0004g0027 a0001c0003t0004g0066 a0001c0003t0004g0067 others(4): Show |
8 | HG02258.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.95+1607C>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24990987 | |||||||
| chr20:24991109 | A | G | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.95+1485T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24991109 | |||||||
| chr20:24991257 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.95+1337A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24991257 | |||||||
| chr20:24991311 | T | G | 2 | a0001c0001t0001g0119 a0013c0017t0001g0120 |
2 | HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.95+1283A>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24991311 | |||||||
| chr20:24991334 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.95+1260A>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24991334 | |||||||
| chr20:24991382 | C | G | 1 | a0001c0001t0001g0078 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.95+1212G>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24991382 | |||||||
| chr20:24991544 | C | T | 1 | a0001c0003t0005g0074 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.95+1050G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24991544 | |||||||
| chr20:24991626 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.95+968G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24991626 | |||||||
| chr20:24991697 | C | T | 43 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0010 others(40): Show |
78 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.95+897G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24991697 | |||||||
| chr20:24991703 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.95+891T>C | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24991703 | |||||||
| chr20:24991744 | A | C | 2 | a0001c0003t0005g0072 a0001c0003t0005g0073 |
2 | HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.95+850T>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24991744 | |||||||
| chr20:24991775 | T | A | 11 | a0001c0003t0004g0027 a0001c0003t0004g0066 a0001c0003t0004g0067 others(8): Show |
12 | HG01109.hp2 HG02258.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.95+819A>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24991775 | |||||||
| chr20:24991906 | T | C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.95+688A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24991906 | |||||||
| chr20:24992063 | G | T | 13 | a0001c0001t0003g0016 a0001c0001t0003g0060 a0001c0002t0003g0007 others(10): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.95+531C>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24992063 | |||||||
| chr20:24992082 | T | C | 1 | a0002c0004t0001g0149 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.95+512A>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24992082 | |||||||
| chr20:24992110 | G | A | 4 | a0001c0018t0001g0151 a0003c0005t0001g0021 a0003c0005t0001g0046 others(1): Show |
7 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.95+484C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24992110 | |||||||
| chr20:24992163 | G | C | 16 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0010 others(13): Show |
37 | HG00639.hp2 HG01123.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.95+431C>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24992163 | |||||||
| chr20:24992212 | G | C | 1 | a0001c0001t0002g0057 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.95+382C>G | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24992212 | |||||||
| chr20:24992263 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.95+331C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24992263 | |||||||
| chr20:24992292 | G | A | 1 | a0001c0003t0004g0071 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.95+302C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24992292 | |||||||
| chr20:24992369 | C | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0028 others(31): Show |
59 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.95+225G>A | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24992369 | |||||||
| chr20:24992570 | G | A | 1 | a0001c0001t0001g0047 | 2 | HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.95+24C>T | APMAP | ENSG00000101474.12 | transcript | ENST00000217456.3 | protein_coding | 1/8 | chr20 | 24992570 |