Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 160 |
| ensemblid | ENSG00000196961.13 |
| hgncid | 561 |
| symbol | AP2A1 |
| name | adaptor related protein complex 2 subunit alpha 1 |
| refseq_nuc | NM_130787.3 |
| refseq_prot | NP_570603.2 |
| ensembl_nuc | ENST00000354293.10 |
| ensembl_prot | ENSP00000346246.4 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 49767001 |
| end | 49807114 |
| strand | + |
| ver | v1.2 |
| region | chr19:49767001-49807114 |
| region5000 | chr19:49762001-49812114 |
| regionname0 | AP2A1_chr19_49767001_49807114 |
| regionname5000 | AP2A1_chr19_49762001_49812114 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 955 | 341 | 82 | 64 | 133 | 14 | 46 | 101 | AP2A1_chr19_49762001_49812114 | AP2A1 | MPAVS others(950): Show |
chr19 | 49762001 | 49812114 |
| a0002 | 0/0 | 955 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | MPAVS others(950): Show |
chr19 | 49762001 | 49812114 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2865 | 324 | 80 | 61 | 125 | 12 | 44 | AP2A1_chr19_49762001_49812114 | AP2A1 | ATGCC others(2860): Show |
chr19 | 49762001 | 49812114 | ||
| a0001c0002 | 0/0 | 2865 | 4 | 0 | 0 | 3 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | ATGCC others(2860): Show |
chr19 | 49762001 | 49812114 | ||
| a0001c0003 | 0/0 | 2865 | 3 | 0 | 2 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | ATGCC others(2860): Show |
chr19 | 49762001 | 49812114 | ||
| a0001c0004 | 0/0 | 2865 | 2 | 2 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | ATGCC others(2860): Show |
chr19 | 49762001 | 49812114 | ||
| a0001c0005 | 0/0 | 2865 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | ATGCC others(2860): Show |
chr19 | 49762001 | 49812114 | ||
| a0001c0006 | 0/0 | 2865 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | ATGCC others(2860): Show |
chr19 | 49762001 | 49812114 | ||
| a0001c0007 | 0/0 | 2865 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | ATGCC others(2860): Show |
chr19 | 49762001 | 49812114 | ||
| a0001c0009 | 0/0 | 2865 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | ATGCC others(2860): Show |
chr19 | 49762001 | 49812114 | ||
| a0001c0010 | 0/0 | 2865 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | ATGCC others(2860): Show |
chr19 | 49762001 | 49812114 | ||
| a0001c0011 | 0/0 | 2865 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | ATGCC others(2860): Show |
chr19 | 49762001 | 49812114 | ||
| a0001c0012 | 0/0 | 2865 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | ATGCC others(2860): Show |
chr19 | 49762001 | 49812114 | ||
| a0002c0008 | 0/0 | 2865 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | ATGCC others(2860): Show |
chr19 | 49762001 | 49812114 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3357 | 262 | 62 | 52 | 100 | 11 | 35 | AP2A1_chr19_49762001_49812114 | AP2A1 | GCCAG others(3352): Show |
chr19 | 49762001 | 49812114 |
| a0001c0001t0002 | 0/0 | 3361 | 42 | 8 | 7 | 17 | 1 | 9 | AP2A1_chr19_49762001_49812114 | AP2A1 | GCCAG others(3356): Show |
chr19 | 49762001 | 49812114 |
| a0001c0001t0003 | 0/0 | 3357 | 13 | 3 | 2 | 8 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | GCCAG others(3352): Show |
chr19 | 49762001 | 49812114 |
| a0001c0001t0004 | 0/0 | 3357 | 5 | 5 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | GCCAG others(3352): Show |
chr19 | 49762001 | 49812114 |
| a0001c0001t0005 | 0/0 | 3357 | 2 | 2 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | GCCAG others(3352): Show |
chr19 | 49762001 | 49812114 |
| a0001c0002t0001 | 0/0 | 3357 | 4 | 0 | 0 | 3 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | GCCAG others(3352): Show |
chr19 | 49762001 | 49812114 |
| a0001c0003t0001 | 0/0 | 3357 | 3 | 0 | 2 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | GCCAG others(3352): Show |
chr19 | 49762001 | 49812114 |
| a0001c0004t0001 | 0/0 | 3357 | 2 | 2 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | GCCAG others(3352): Show |
chr19 | 49762001 | 49812114 |
| a0001c0005t0001 | 0/0 | 3357 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | GCCAG others(3352): Show |
chr19 | 49762001 | 49812114 |
| a0001c0006t0002 | 0/0 | 3361 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | GCCAG others(3356): Show |
chr19 | 49762001 | 49812114 |
| a0001c0007t0002 | 0/0 | 3361 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | GCCAG others(3356): Show |
chr19 | 49762001 | 49812114 |
| a0001c0009t0001 | 0/0 | 3357 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | GCCAG others(3352): Show |
chr19 | 49762001 | 49812114 |
| a0001c0010t0001 | 0/0 | 3357 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | GCCAG others(3352): Show |
chr19 | 49762001 | 49812114 |
| a0001c0011t0001 | 0/0 | 3357 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | GCCAG others(3352): Show |
chr19 | 49762001 | 49812114 |
| a0001c0012t0002 | 0/0 | 3361 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | GCCAG others(3356): Show |
chr19 | 49762001 | 49812114 |
| a0002c0008t0001 | 0/0 | 3357 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | GCCAG others(3352): Show |
chr19 | 49762001 | 49812114 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 5 | 4 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 1 | 3 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0070 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0175 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0003g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0001t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0003t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0003t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0004t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0004t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0005t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0005t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0006t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0007t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0009t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0010t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0011t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0001c0012t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| a0002c0008t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | GBR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | GBR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | FIN | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0047 | EUR | FIN | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0271 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0216 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01256 | hp2 | a0001 | c0011 | t0001 | g0212 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0270 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | IBS | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | IBS | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0217 | EUR | IBS | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0073 | EUR | IBS | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0086 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02083 | hp2 | a0001 | c0009 | t0001 | g0265 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CDX | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CDX | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0222 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0197 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0241 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0198 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0205 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0204 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0223 | AFR | MSL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | MSL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03453 | hp2 | a0001 | c0004 | t0001 | g0209 | AFR | MSL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | STU | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | STU | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | BEB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | STU | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | STU | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | BEB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | STU | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | STU | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | STU | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | YRI | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | YRI | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | YRI | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18959 | hp1 | a0001 | c0012 | t0002 | g0053 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18963 | hp2 | a0001 | c0010 | t0001 | g0123 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19030 | hp2 | a0001 | c0004 | t0001 | g0302 | AFR | LWK | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | LWK | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19065 | hp1 | a0002 | c0008 | t0001 | g0020 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19068 | hp2 | a0001 | c0005 | t0001 | g0182 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19087 | hp1 | a0001 | c0005 | t0001 | g0188 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | YRI | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | YRI | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | TSI | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | TSI | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | TSI | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA20805 | hp2 | a0001 | c0007 | t0002 | g0039 | EUR | TSI | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA20905 | hp1 | a0001 | c0006 | t0002 | g0043 | SAS | GIH | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | GIH | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0196 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | USA | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | USA | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | USA | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | LWK | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0175 | REF | REF | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0070 | REF | REF | AP2A1_chr19_49762001_49812114 | AP2A1 | chr19 | 49762001 | 49812114 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:49803322 | G | A | 1 | a0002 | 1 | NA19065.hp1 | missense_variant | MODERATE | c.2290G>A | p.Val764Met | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/23 | 2423/3357 | 2290/2868 | 764/955 | chr19 | 49803322 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:49782552 | C | T | 1 | a0001c0003 | 3 | HG01169.hp2 HG01192.hp1 HG01517.hp1 |
synonymous_variant | LOW | c.301C>T | p.Leu101Leu | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/23 | 434/3357 | 301/2868 | 101/955 | chr19 | 49782552 | |||
| chr19:49782683 | C | T | 1 | a0001c0012 | 1 | NA18959.hp1 | synonymous_variant | LOW | c.432C>T | p.Gly144Gly | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/23 | 565/3357 | 432/2868 | 144/955 | chr19 | 49782683 | |||
| chr19:49792031 | G | A | 1 | a0001c0006 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.570G>A | p.Ala190Ala | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/23 | 703/3357 | 570/2868 | 190/955 | chr19 | 49792031 | |||
| chr19:49799456 | C | T | 1 | a0001c0011 | 1 | HG01256.hp2 | synonymous_variant | LOW | c.1095C>T | p.Ala365Ala | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 9/23 | 1228/3357 | 1095/2868 | 365/955 | chr19 | 49799456 | |||
| chr19:49799640 | C | T | 1 | a0001c0002 | 4 | HG00438.hp2 HG02071.hp1 HG02683.hp2 others(1): Show |
synonymous_variant | LOW | c.1146C>T | p.Asp382Asp | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 10/23 | 1279/3357 | 1146/2868 | 382/955 | chr19 | 49799640 | |||
| chr19:49799742 | A | G | 1 | a0001c0005 | 2 | NA19068.hp2 NA19087.hp1 |
synonymous_variant | LOW | c.1248A>G | p.Ala416Ala | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 10/23 | 1381/3357 | 1248/2868 | 416/955 | chr19 | 49799742 | |||
| chr19:49800054 | G | T | 1 | a0001c0010 | 1 | NA18963.hp2 | synonymous_variant | LOW | c.1359G>T | p.Ala453Ala | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 11/23 | 1492/3357 | 1359/2868 | 453/955 | chr19 | 49800054 | |||
| chr19:49801582 | G | A | 1 | a0001c0007 | 1 | NA20805.hp2 | synonymous_variant | LOW | c.1746G>A | p.Glu582Glu | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 13/23 | 1879/3357 | 1746/2868 | 582/955 | chr19 | 49801582 | |||
| chr19:49805661 | G | A | 1 | a0001c0004 | 2 | HG03453.hp2 NA19030.hp2 |
splice_region_variant&synonymous_variant | LOW | c.2469G>A | p.Arg823Arg | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 20/23 | 2602/3357 | 2469/2868 | 823/955 | chr19 | 49805661 | |||
| chr19:49806729 | C | T | 1 | a0001c0009 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.2839C>T | p.Leu947Leu | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 23/23 | 2972/3357 | 2839/2868 | 947/955 | chr19 | 49806729 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:49767008 | A | AGCCC | 4 | a0001c0001t0002 a0001c0006t0002 a0001c0007t0002 others(1): Show |
45 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(42): Show |
5_prime_UTR_variant | MODIFIER | c.-125_-122dupGCCC | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/23 | 121 | INFO_REALIGN_3_PRIME | chr19 | 49767008 | |||||
| chr19:49767028 | C | G | 1 | a0001c0001t0005 | 2 | HG02258.hp2 HG03098.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-106C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/23 | chr19 | 49767028 | |||||||
| chr19:49806760 | C | T | 1 | a0001c0001t0004 | 5 | HG02486.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 23/23 | 2 | chr19 | 49806760 | ||||||
| chr19:49807074 | C | T | 1 | a0001c0001t0003 | 13 | HG00438.hp1 HG01433.hp2 HG01952.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*316C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 23/23 | 316 | chr19 | 49807074 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:49767238 | A | AG | 8 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 others(5): Show |
8 | HG00621.hp1 HG00741.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+44dupG | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49767238 | ||||||
| chr19:49767452 | T | TG | 23 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(20): Show |
27 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(24): Show |
intron_variant | MODIFIER | c.67+253dupG | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49767452 | ||||||
| chr19:49767529 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.67+329T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49767529 | |||||||
| chr19:49767830 | G | A | 43 | a0001c0001t0002g0006 a0001c0001t0002g0023 a0001c0001t0002g0024 others(40): Show |
44 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.67+630G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49767830 | |||||||
| chr19:49767853 | C | T | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(291): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.67+653C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49767853 | |||||||
| chr19:49767906 | A | C | 1 | a0001c0001t0001g0281 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.67+706A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49767906 | |||||||
| chr19:49768062 | T | C | 291 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(288): Show |
324 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.67+862T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49768062 | |||||||
| chr19:49768099 | G | A | 43 | a0001c0001t0002g0006 a0001c0001t0002g0023 a0001c0001t0002g0024 others(40): Show |
44 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.67+899G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49768099 | |||||||
| chr19:49768129 | A | G | 1 | a0001c0001t0001g0297 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.67+929A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49768129 | |||||||
| chr19:49768245 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(109): Show |
133 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.67+1045T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49768245 | |||||||
| chr19:49768601 | T | A | 21 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0176 others(18): Show |
23 | HG01074.hp2 HG01934.hp1 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.67+1401T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49768601 | |||||||
| chr19:49768667 | G | T | 80 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(77): Show |
85 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.67+1467G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49768667 | |||||||
| chr19:49768801 | C | T | 3 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 |
3 | HG02622.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.67+1601C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49768801 | |||||||
| chr19:49769194 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.67+1994G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769194 | |||||||
| chr19:49769243 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.67+2043C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769243 | |||||||
| chr19:49769258 | TA | T | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(283): Show |
319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.67+2067delA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49769258 | ||||||
| chr19:49769264 | AAAAG | A | 7 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0210 others(4): Show |
7 | HG02055.hp2 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+2068_67+2071del others(4): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49769264 | ||||||
| chr19:49769283 | G | C | 6 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(3): Show |
6 | HG00609.hp1 HG00621.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+2083G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769283 | |||||||
| chr19:49769435 | C | T | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG01255.hp1 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.67+2235C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769435 | |||||||
| chr19:49769555 | G | A | 1 | a0001c0011t0001g0212 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.67+2355G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769555 | |||||||
| chr19:49769595 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.67+2395A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769595 | |||||||
| chr19:49769719 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.67+2519T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769719 | |||||||
| chr19:49769741 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.67+2541C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769741 | |||||||
| chr19:49769869 | G | A | 42 | a0001c0001t0002g0006 a0001c0001t0002g0023 a0001c0001t0002g0024 others(39): Show |
43 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.67+2669G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769869 | |||||||
| chr19:49769892 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.67+2692C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769892 | |||||||
| chr19:49769951 | C | G | 1 | a0001c0001t0001g0296 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.67+2751C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769951 | |||||||
| chr19:49769994 | C | T | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG01255.hp1 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.67+2794C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49769994 | |||||||
| chr19:49770029 | T | C | 1 | a0001c0001t0003g0086 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.67+2829T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49770029 | |||||||
| chr19:49770308 | C | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0281 |
2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.67+3108C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49770308 | |||||||
| chr19:49770344 | A | AGAATCAG others(1597): Show |
1 | a0001c0001t0001g0192 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.67+3163_67+3164ins others(1604): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49770344 | ||||||
| chr19:49770863 | A | G | 44 | a0001c0001t0001g0174 a0001c0001t0002g0006 a0001c0001t0002g0023 others(41): Show |
45 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.67+3663A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49770863 | |||||||
| chr19:49771228 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.67+4028G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49771228 | |||||||
| chr19:49771265 | C | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.67+4065C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49771265 | |||||||
| chr19:49771277 | G | A | 22 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(19): Show |
26 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(23): Show |
intron_variant | MODIFIER | c.67+4077G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49771277 | |||||||
| chr19:49771303 | T | TA | 28 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(25): Show |
32 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.67+4126dupA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49771303 | ||||||
| chr19:49771303 | T | TAA | 38 | a0001c0001t0001g0174 a0001c0001t0001g0283 a0001c0001t0001g0304 others(35): Show |
39 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.67+4125_67+4126dup others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49771303 | ||||||
| chr19:49771303 | TA | T | 23 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0167 others(20): Show |
25 | HG00280.hp1 HG01169.hp2 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.67+4126delA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49771303 | ||||||
| chr19:49771303 | TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0001g0275 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.67+4116_67+4126del others(11): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49771303 | ||||||
| chr19:49771448 | TTG | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(102): Show |
126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.67+4251_67+4252del others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49771448 | ||||||
| chr19:49771581 | G | A | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG01255.hp1 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.67+4381G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49771581 | |||||||
| chr19:49771704 | T | C | 64 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0174 others(61): Show |
67 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.67+4504T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49771704 | |||||||
| chr19:49771921 | G | A | 45 | a0001c0001t0001g0174 a0001c0001t0001g0177 a0001c0001t0001g0297 others(42): Show |
46 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.67+4721G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49771921 | |||||||
| chr19:49771925 | C | A | 1 | a0001c0001t0001g0215 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.67+4725C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49771925 | |||||||
| chr19:49772023 | A | C | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.67+4823A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772023 | |||||||
| chr19:49772069 | C | A | 1 | a0001c0001t0001g0301 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.67+4869C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772069 | |||||||
| chr19:49772101 | C | T | 65 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(62): Show |
70 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.67+4901C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772101 | |||||||
| chr19:49772121 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0218 a0001c0001t0001g0219 others(1): Show |
5 | HG02723.hp1 HG03195.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+4921G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772121 | |||||||
| chr19:49772195 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.67+4995C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772195 | |||||||
| chr19:49772246 | G | GT | 12 | a0001c0001t0001g0065 a0001c0001t0001g0074 a0001c0001t0001g0075 others(9): Show |
12 | HG00741.hp2 HG01257.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.67+5077dupT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49772246 | ||||||
| chr19:49772246 | GT | G | 72 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(69): Show |
79 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.67+5077delT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49772246 | ||||||
| chr19:49772246 | GTT | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(98): Show |
123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.67+5076_67+5077del others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49772246 | ||||||
| chr19:49772253 | T | TTTTTGTT others(3): Show |
1 | a0001c0001t0001g0189 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.67+5057_67+5058ins others(10): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49772253 | ||||||
| chr19:49772254 | T | C | 1 | a0001c0001t0003g0019 | 2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.67+5054T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772254 | |||||||
| chr19:49772254 | T | TTTTGTTT others(2): Show |
11 | a0001c0001t0001g0176 a0001c0001t0001g0187 a0001c0001t0002g0048 others(8): Show |
11 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.67+5057_67+5058ins others(9): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49772254 | ||||||
| chr19:49772255 | T | TTTGTTTT others(1): Show |
51 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0174 others(48): Show |
54 | HG00280.hp2 HG00621.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.67+5057_67+5058ins others(8): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49772255 | ||||||
| chr19:49772256 | T | G | 6 | a0001c0001t0001g0089 a0001c0001t0001g0269 a0001c0001t0003g0270 others(3): Show |
6 | HG01192.hp1 HG01256.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+5056T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772256 | |||||||
| chr19:49772260 | T | G | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG00621.hp2 HG02155.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+5060T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772260 | |||||||
| chr19:49772388 | G | A | 1 | a0001c0001t0003g0090 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.67+5188G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772388 | |||||||
| chr19:49772534 | C | G | 2 | a0001c0001t0001g0276 a0001c0001t0001g0281 |
2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.67+5334C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772534 | |||||||
| chr19:49772640 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.67+5440C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772640 | |||||||
| chr19:49772790 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.67+5590G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772790 | |||||||
| chr19:49772875 | G | A | 89 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(86): Show |
94 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.67+5675G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772875 | |||||||
| chr19:49772881 | A | G | 4 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0004t0001g0209 others(1): Show |
4 | HG02486.hp1 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+5681A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772881 | |||||||
| chr19:49772898 | C | CT | 20 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0176 others(17): Show |
22 | HG01074.hp2 HG01934.hp1 HG01978.hp2 others(19): Show |
intron_variant | MODIFIER | c.67+5699dupT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49772898 | ||||||
| chr19:49772924 | G | T | 67 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0174 others(64): Show |
70 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.67+5724G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49772924 | |||||||
| chr19:49773157 | G | C | 67 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0092 others(64): Show |
70 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.67+5957G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49773157 | |||||||
| chr19:49773408 | C | T | 2 | a0001c0001t0001g0214 a0001c0001t0001g0238 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.67+6208C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49773408 | |||||||
| chr19:49773411 | C | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG01099.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.67+6211C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49773411 | |||||||
| chr19:49773599 | A | G | 68 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0092 others(65): Show |
71 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.67+6399A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49773599 | |||||||
| chr19:49773611 | T | C | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG01255.hp1 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.67+6411T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49773611 | |||||||
| chr19:49773785 | TCTAA | T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(19): Show |
25 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(22): Show |
intron_variant | MODIFIER | c.67+6590_67+6593del others(4): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49773785 | ||||||
| chr19:49773884 | T | G | 1 | a0001c0001t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.67+6684T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49773884 | |||||||
| chr19:49774026 | AG | A | 303 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(300): Show |
336 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.67+6830delG | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49774026 | ||||||
| chr19:49774435 | G | C | 1 | a0001c0001t0001g0301 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.67+7235G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49774435 | |||||||
| chr19:49774704 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.68-7053C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49774704 | |||||||
| chr19:49774918 | C | CA | 10 | a0001c0001t0001g0071 a0001c0001t0001g0095 a0001c0001t0001g0137 others(7): Show |
10 | HG00621.hp1 HG01175.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.68-6824dupA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49774918 | ||||||
| chr19:49774918 | CA | C | 164 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(161): Show |
176 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.68-6824delA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49774918 | ||||||
| chr19:49774918 | CAA | C | 12 | a0001c0001t0001g0068 a0001c0001t0002g0044 a0001c0001t0002g0045 others(9): Show |
12 | HG00280.hp2 HG00642.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.68-6825_68-6824del others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49774918 | ||||||
| chr19:49774961 | C | T | 4 | a0001c0001t0001g0202 a0001c0001t0001g0210 a0001c0001t0001g0211 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-6796C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49774961 | |||||||
| chr19:49774995 | G | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0218 a0001c0001t0001g0219 others(5): Show |
9 | HG00733.hp2 HG02258.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-6762G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49774995 | |||||||
| chr19:49775008 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.68-6749G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49775008 | |||||||
| chr19:49775029 | G | A | 54 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(51): Show |
59 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.68-6728G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49775029 | |||||||
| chr19:49775180 | A | G | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG00733.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.68-6577A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49775180 | |||||||
| chr19:49775341 | A | G | 1 | a0001c0001t0001g0189 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.68-6416A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49775341 | |||||||
| chr19:49775402 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0300 |
2 | HG02155.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.68-6355C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49775402 | |||||||
| chr19:49775557 | C | T | 3 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 |
3 | HG02622.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.68-6200C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49775557 | |||||||
| chr19:49775576 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.68-6181A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49775576 | |||||||
| chr19:49775669 | C | T | 1 | a0001c0001t0001g0301 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.68-6088C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49775669 | |||||||
| chr19:49775765 | G | A | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0277 |
3 | HG02055.hp2 HG02109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.68-5992G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49775765 | |||||||
| chr19:49775965 | C | A | 8 | a0001c0001t0001g0269 a0001c0001t0001g0276 a0001c0001t0001g0281 others(5): Show |
8 | HG01169.hp2 HG01192.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-5792C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49775965 | |||||||
| chr19:49776080 | C | T | 3 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 |
3 | HG02622.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.68-5677C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776080 | |||||||
| chr19:49776082 | G | A | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG01255.hp1 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.68-5675G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776082 | |||||||
| chr19:49776097 | C | G | 1 | a0001c0001t0001g0259 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.68-5660C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776097 | |||||||
| chr19:49776196 | G | GC | 9 | a0001c0001t0001g0068 a0001c0001t0001g0089 a0001c0001t0001g0142 others(6): Show |
9 | HG00621.hp1 HG01978.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-5556dupC | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49776196 | ||||||
| chr19:49776248 | G | A | 1 | a0001c0001t0002g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.68-5509G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776248 | |||||||
| chr19:49776268 | T | A | 1 | a0001c0001t0001g0282 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.68-5489T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776268 | |||||||
| chr19:49776400 | G | A | 68 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0068 others(65): Show |
71 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.68-5357G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776400 | |||||||
| chr19:49776404 | C | G | 8 | a0001c0001t0001g0269 a0001c0001t0001g0276 a0001c0001t0001g0281 others(5): Show |
8 | HG01169.hp2 HG01192.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-5353C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776404 | |||||||
| chr19:49776501 | G | T | 1 | a0001c0001t0002g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.68-5256G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776501 | |||||||
| chr19:49776631 | CCT | C | 71 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(68): Show |
77 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.68-5125_68-5124del others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776631 | |||||||
| chr19:49776676 | G | T | 6 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0071 others(3): Show |
6 | HG01515.hp1 HG01517.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-5081G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776676 | |||||||
| chr19:49776721 | A | T | 1 | a0001c0001t0001g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.68-5036A>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776721 | |||||||
| chr19:49776809 | G | C | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG01255.hp1 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.68-4948G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776809 | |||||||
| chr19:49776853 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.68-4904C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49776853 | |||||||
| chr19:49777076 | G | GAAA | 6 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 others(3): Show |
6 | HG01255.hp1 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-4671_68-4669dup others(3): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49777076 | ||||||
| chr19:49777076 | G | GAAAA | 56 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0092 others(53): Show |
59 | HG00280.hp2 HG00642.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.68-4672_68-4669dup others(4): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49777076 | ||||||
| chr19:49777076 | G | GAAAAA | 7 | a0001c0001t0001g0068 a0001c0001t0001g0187 a0001c0001t0001g0189 others(4): Show |
7 | HG00621.hp2 HG04199.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-4673_68-4669dup others(5): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49777076 | ||||||
| chr19:49777119 | C | T | 15 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0214 others(12): Show |
17 | HG00423.hp1 HG00738.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.68-4638C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49777119 | |||||||
| chr19:49777219 | A | C | 1 | a0001c0001t0001g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.68-4538A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49777219 | |||||||
| chr19:49777307 | A | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(108): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.68-4450A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49777307 | |||||||
| chr19:49777357 | C | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0281 |
2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.68-4400C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49777357 | |||||||
| chr19:49777392 | T | A | 1 | a0001c0002t0001g0241 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.68-4365T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49777392 | |||||||
| chr19:49777507 | C | T | 5 | a0001c0001t0004g0196 a0001c0001t0004g0197 a0001c0001t0004g0198 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-4250C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49777507 | |||||||
| chr19:49777614 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.68-4143G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49777614 | |||||||
| chr19:49777622 | G | A | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0277 |
3 | HG02055.hp2 HG02109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.68-4135G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49777622 | |||||||
| chr19:49777634 | C | CAA | 59 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0068 others(56): Show |
62 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.68-4109_68-4108dup others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49777634 | ||||||
| chr19:49777634 | C | CAAA | 6 | a0001c0001t0001g0179 a0001c0001t0002g0024 a0001c0001t0002g0025 others(3): Show |
6 | HG02055.hp1 HG03669.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-4110_68-4108dup others(3): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49777634 | ||||||
| chr19:49777799 | C | T | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG01255.hp1 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.68-3958C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49777799 | |||||||
| chr19:49777809 | T | A | 1 | a0001c0001t0001g0224 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.68-3948T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49777809 | |||||||
| chr19:49777833 | TG | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
129 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.68-3921delG | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49777833 | ||||||
| chr19:49778112 | C | G | 68 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0068 others(65): Show |
71 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.68-3645C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778112 | |||||||
| chr19:49778120 | A | C | 1 | a0001c0001t0001g0065 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.68-3637A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778120 | |||||||
| chr19:49778139 | G | A | 4 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(1): Show |
4 | HG02145.hp2 HG02647.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-3618G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778139 | |||||||
| chr19:49778166 | A | G | 1 | a0001c0001t0001g0301 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.68-3591A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778166 | |||||||
| chr19:49778280 | T | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.68-3477T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778280 | |||||||
| chr19:49778303 | C | G | 1 | a0001c0001t0001g0135 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.68-3454C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778303 | |||||||
| chr19:49778335 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.68-3422C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778335 | |||||||
| chr19:49778341 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.68-3416G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778341 | |||||||
| chr19:49778349 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.68-3408G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778349 | |||||||
| chr19:49778379 | T | C | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG01255.hp1 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.68-3378T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778379 | |||||||
| chr19:49778586 | G | T | 1 | a0001c0001t0001g0189 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.68-3171G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778586 | |||||||
| chr19:49778680 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.68-3077C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778680 | |||||||
| chr19:49778796 | G | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
20 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-2961G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49778796 | |||||||
| chr19:49778828 | T | TA | 6 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0290 others(3): Show |
7 | HG02683.hp1 HG02698.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-2926dupA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49778828 | ||||||
| chr19:49778902 | CAT | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
127 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.68-2845_68-2844del others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49778902 | ||||||
| chr19:49779002 | C | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
20 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-2755C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779002 | |||||||
| chr19:49779033 | C | CA | 96 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(93): Show |
102 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.68-2707dupA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49779033 | ||||||
| chr19:49779050 | A | T | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG01255.hp1 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.68-2707A>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779050 | |||||||
| chr19:49779062 | C | T | 69 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0068 others(66): Show |
72 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.68-2695C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779062 | |||||||
| chr19:49779063 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.68-2694G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779063 | |||||||
| chr19:49779240 | G | A | 1 | a0001c0004t0001g0302 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.68-2517G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779240 | |||||||
| chr19:49779305 | C | G | 1 | a0001c0001t0003g0019 | 2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.68-2452C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779305 | |||||||
| chr19:49779332 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.68-2425G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779332 | |||||||
| chr19:49779336 | C | CA | 8 | a0001c0001t0001g0071 a0001c0001t0001g0214 a0001c0001t0001g0215 others(5): Show |
8 | HG03453.hp2 HG03486.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-2400dupA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49779336 | ||||||
| chr19:49779336 | CA | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.68-2400delA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49779336 | ||||||
| chr19:49779336 | CAA | C | 9 | a0001c0001t0001g0134 a0001c0001t0001g0158 a0001c0001t0001g0169 others(6): Show |
9 | HG01515.hp2 HG01884.hp2 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-2401_68-2400del others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49779336 | ||||||
| chr19:49779363 | T | C | 4 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(1): Show |
4 | HG02145.hp2 HG02647.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-2394T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779363 | |||||||
| chr19:49779460 | T | C | 68 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0068 others(65): Show |
71 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.68-2297T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779460 | |||||||
| chr19:49779487 | C | CA | 35 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0078 others(32): Show |
35 | HG00099.hp1 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.68-2246dupA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49779487 | ||||||
| chr19:49779487 | C | CAA | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(65): Show |
87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.68-2247_68-2246dup others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49779487 | ||||||
| chr19:49779487 | C | CAAA | 31 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0088 others(28): Show |
32 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.68-2248_68-2246dup others(3): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49779487 | ||||||
| chr19:49779487 | C | CAAAAAAA others(1365): Show |
1 | a0001c0001t0001g0178 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.68-2118_68-2117ins others(1372): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49779487 | ||||||
| chr19:49779487 | C | CAAAAAAA others(2737): Show |
1 | a0001c0001t0001g0185 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.68-2247_68-2246ins others(2744): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49779487 | ||||||
| chr19:49779487 | CA | C | 51 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0068 others(48): Show |
54 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.68-2246delA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49779487 | ||||||
| chr19:49779500 | A | C | 17 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
20 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-2257A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779500 | |||||||
| chr19:49779511 | A | AAAC | 10 | a0001c0001t0001g0011 a0001c0001t0001g0087 a0001c0001t0001g0095 others(7): Show |
11 | HG01109.hp1 HG01109.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.68-2246_68-2245ins others(3): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779511 | |||||||
| chr19:49779511 | A | AAC | 6 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-2246_68-2245ins others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779511 | |||||||
| chr19:49779640 | G | A | 64 | a0001c0001t0001g0012 a0001c0001t0001g0068 a0001c0001t0001g0092 others(61): Show |
66 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.68-2117G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49779640 | |||||||
| chr19:49780080 | A | G | 8 | a0001c0001t0001g0014 a0001c0001t0001g0218 a0001c0001t0001g0219 others(5): Show |
9 | HG00733.hp2 HG02258.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-1677A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49780080 | |||||||
| chr19:49780122 | C | G | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(292): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.68-1635C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49780122 | |||||||
| chr19:49780188 | C | T | 1 | a0001c0001t0002g0042 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.68-1569C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49780188 | |||||||
| chr19:49780215 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.68-1542G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49780215 | |||||||
| chr19:49780378 | C | A | 1 | a0001c0001t0001g0098 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.68-1379C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49780378 | |||||||
| chr19:49780382 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.68-1375G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49780382 | |||||||
| chr19:49780467 | G | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0147 |
2 | NA18947.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.68-1290G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49780467 | |||||||
| chr19:49780910 | C | T | 5 | a0001c0001t0001g0237 a0001c0001t0001g0257 a0001c0001t0001g0266 others(2): Show |
5 | HG00738.hp1 HG01074.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-847C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49780910 | |||||||
| chr19:49780933 | TGGA | T | 8 | a0001c0001t0001g0069 a0001c0001t0001g0075 a0001c0001t0001g0269 others(5): Show |
8 | HG01169.hp2 HG01192.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-819_68-817delGA others(1): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr19 | 49780933 | ||||||
| chr19:49780950 | C | T | 1 | a0001c0001t0002g0030 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.68-807C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49780950 | |||||||
| chr19:49781312 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.68-445T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49781312 | |||||||
| chr19:49781440 | G | C | 1 | a0001c0001t0001g0261 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.68-317G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49781440 | |||||||
| chr19:49781675 | G | C | 3 | a0001c0001t0001g0242 a0001c0001t0001g0248 a0001c0001t0002g0206 |
3 | NA18961.hp1 NA18969.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.68-82G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 1/22 | chr19 | 49781675 | |||||||
| chr19:49781834 | G | C | 2 | a0001c0001t0002g0034 a0001c0001t0002g0035 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.136+9G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 2/22 | chr19 | 49781834 | |||||||
| chr19:49781839 | C | T | 4 | a0001c0001t0004g0196 a0001c0001t0004g0197 a0001c0001t0004g0198 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+14C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 2/22 | chr19 | 49781839 | |||||||
| chr19:49782135 | C | T | 1 | a0001c0001t0003g0090 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.279+46C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 3/22 | chr19 | 49782135 | |||||||
| chr19:49782136 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.279+47G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 3/22 | chr19 | 49782136 | |||||||
| chr19:49782217 | G | A | 1 | a0001c0005t0001g0188 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.279+128G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 3/22 | chr19 | 49782217 | |||||||
| chr19:49782252 | G | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
20 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.279+163G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 3/22 | chr19 | 49782252 | |||||||
| chr19:49782388 | T | C | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.280-143T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 3/22 | chr19 | 49782388 | |||||||
| chr19:49782479 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.280-52G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 3/22 | chr19 | 49782479 | |||||||
| chr19:49782742 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.473+18C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49782742 | |||||||
| chr19:49782743 | G | A | 4 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0004t0001g0209 others(1): Show |
4 | HG02486.hp1 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.473+19G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49782743 | |||||||
| chr19:49782970 | T | A | 1 | a0001c0001t0001g0111 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.473+246T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49782970 | |||||||
| chr19:49782971 | T | G | 1 | a0001c0001t0001g0111 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.473+247T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49782971 | |||||||
| chr19:49783081 | C | T | 83 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(80): Show |
87 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.473+357C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49783081 | |||||||
| chr19:49783125 | T | C | 78 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(75): Show |
82 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.473+401T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49783125 | |||||||
| chr19:49783517 | C | T | 1 | a0001c0001t0002g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.473+793C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49783517 | |||||||
| chr19:49783593 | A | T | 2 | a0001c0001t0002g0030 a0001c0001t0002g0031 |
2 | HG03704.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.473+869A>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49783593 | |||||||
| chr19:49783679 | G | C | 24 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0176 others(21): Show |
26 | HG01074.hp2 HG01934.hp1 HG01978.hp2 others(23): Show |
intron_variant | MODIFIER | c.473+955G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49783679 | |||||||
| chr19:49783736 | C | G | 18 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0128 others(15): Show |
20 | HG00733.hp2 HG01346.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.473+1012C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49783736 | |||||||
| chr19:49783840 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.473+1116G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49783840 | |||||||
| chr19:49783922 | A | G | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.473+1198A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49783922 | |||||||
| chr19:49783943 | T | C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0128 a0001c0001t0001g0129 others(6): Show |
10 | HG01346.hp2 HG02257.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.473+1219T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49783943 | |||||||
| chr19:49783998 | A | G | 77 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(74): Show |
81 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.473+1274A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49783998 | |||||||
| chr19:49784062 | A | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.473+1338A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784062 | |||||||
| chr19:49784145 | A | C | 1 | a0001c0001t0002g0041 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.473+1421A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784145 | |||||||
| chr19:49784340 | G | T | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1616G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784340 | |||||||
| chr19:49784346 | C | G | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1622C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784346 | |||||||
| chr19:49784347 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1623A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784347 | |||||||
| chr19:49784348 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1624C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784348 | |||||||
| chr19:49784351 | G | C | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1627G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784351 | |||||||
| chr19:49784352 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1628A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784352 | |||||||
| chr19:49784353 | A | C | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1629A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784353 | |||||||
| chr19:49784355 | C | A | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1631C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784355 | |||||||
| chr19:49784356 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1632C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784356 | |||||||
| chr19:49784364 | A | T | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1640A>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784364 | |||||||
| chr19:49784366 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1642A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784366 | |||||||
| chr19:49784367 | G | T | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1643G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784367 | |||||||
| chr19:49784368 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.473+1644G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784368 | |||||||
| chr19:49784368 | G | C | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1644G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784368 | |||||||
| chr19:49784368 | G | T | 1 | a0001c0001t0001g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.473+1644G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784368 | |||||||
| chr19:49784370 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1646T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784370 | |||||||
| chr19:49784372 | C | A | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1648C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784372 | |||||||
| chr19:49784374 | G | C | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1650G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784374 | |||||||
| chr19:49784378 | G | C | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1654G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784378 | |||||||
| chr19:49784381 | G | T | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1657G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784381 | |||||||
| chr19:49784384 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1660A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784384 | |||||||
| chr19:49784386 | C | G | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1662C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784386 | |||||||
| chr19:49784387 | A | G | 206 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0011 others(203): Show |
219 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.473+1663A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784387 | |||||||
| chr19:49784389 | G | C | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1665G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784389 | |||||||
| chr19:49784390 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1666C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784390 | |||||||
| chr19:49784391 | C | G | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1667C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784391 | |||||||
| chr19:49784392 | A | C | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1668A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784392 | |||||||
| chr19:49784397 | A | T | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1673A>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784397 | |||||||
| chr19:49784406 | T | TCCCAAAG others(5): Show |
1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1682_473+1683i others(14): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784406 | |||||||
| chr19:49784409 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1685G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784409 | |||||||
| chr19:49784411 | G | T | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1687G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784411 | |||||||
| chr19:49784420 | A | C | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1696A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784420 | |||||||
| chr19:49784421 | G | C | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1697G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784421 | |||||||
| chr19:49784429 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1705C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784429 | |||||||
| chr19:49784431 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1707C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784431 | |||||||
| chr19:49784431 | CA | C | 95 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(92): Show |
99 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.473+1719delA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49784431 | ||||||
| chr19:49784432 | AAAAAAAA others(26): Show |
A | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1709_473+1741d others(35): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784432 | |||||||
| chr19:49784469 | G | C | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1745G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784469 | |||||||
| chr19:49784470 | G | T | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1746G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784470 | |||||||
| chr19:49784471 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1747A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784471 | |||||||
| chr19:49784472 | A | C | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1748A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784472 | |||||||
| chr19:49784481 | A | C | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1757A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784481 | |||||||
| chr19:49784483 | A | C | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1759A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784483 | |||||||
| chr19:49784486 | G | T | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1762G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784486 | |||||||
| chr19:49784498 | A | T | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1774A>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784498 | |||||||
| chr19:49784499 | G | C | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1775G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784499 | |||||||
| chr19:49784501 | A | T | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1777A>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784501 | |||||||
| chr19:49784502 | T | A | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1778T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784502 | |||||||
| chr19:49784503 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1779A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784503 | |||||||
| chr19:49784505 | T | G | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1781T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784505 | |||||||
| chr19:49784510 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.473+1786A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784510 | |||||||
| chr19:49784544 | T | C | 94 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(91): Show |
98 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.473+1820T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784544 | |||||||
| chr19:49784817 | A | G | 94 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(91): Show |
98 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.473+2093A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784817 | |||||||
| chr19:49784882 | A | C | 1 | a0001c0001t0001g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.473+2158A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784882 | |||||||
| chr19:49784887 | C | A | 11 | a0001c0001t0001g0153 a0001c0001t0001g0195 a0001c0001t0001g0210 others(8): Show |
11 | HG02486.hp2 HG02622.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.473+2163C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784887 | |||||||
| chr19:49784902 | A | G | 6 | a0001c0001t0001g0195 a0001c0001t0004g0196 a0001c0001t0004g0197 others(3): Show |
6 | HG02486.hp2 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+2178A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49784902 | |||||||
| chr19:49785550 | A | C | 6 | a0001c0001t0001g0195 a0001c0001t0004g0196 a0001c0001t0004g0197 others(3): Show |
6 | HG02486.hp2 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+2826A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49785550 | |||||||
| chr19:49785636 | G | T | 1 | a0001c0001t0001g0236 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.473+2912G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49785636 | |||||||
| chr19:49786054 | C | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0281 |
2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.473+3330C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49786054 | |||||||
| chr19:49786160 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.473+3436T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49786160 | |||||||
| chr19:49786171 | C | CAAGAGGC others(13): Show |
83 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(80): Show |
87 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.473+3459_473+3460i others(22): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49786171 | ||||||
| chr19:49786338 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.473+3614G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49786338 | |||||||
| chr19:49786393 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.473+3669T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49786393 | |||||||
| chr19:49786497 | G | C | 1 | a0001c0006t0002g0043 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.473+3773G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49786497 | |||||||
| chr19:49786599 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.473+3875G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49786599 | |||||||
| chr19:49786602 | G | A | 201 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(198): Show |
213 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.473+3878G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49786602 | |||||||
| chr19:49786691 | A | G | 73 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(70): Show |
77 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.473+3967A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49786691 | |||||||
| chr19:49786749 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.473+4025G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49786749 | |||||||
| chr19:49787329 | TTTTTGTT others(18): Show |
T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0218 a0001c0001t0001g0219 others(1): Show |
5 | HG02723.hp1 HG03195.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.474-4601_474-4577d others(27): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49787329 | ||||||
| chr19:49787331 | TTTGTTTG others(9): Show |
T | 3 | a0001c0001t0002g0028 a0001c0001t0002g0031 a0001c0001t0002g0059 |
3 | HG03704.hp1 NA18955.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.474-4601_474-4586d others(18): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49787331 | ||||||
| chr19:49787332 | TTGTTTGT others(8): Show |
T | 71 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(68): Show |
75 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.474-4601_474-4587d others(17): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49787332 | ||||||
| chr19:49787333 | TGTTTGTT others(7): Show |
T | 4 | a0001c0001t0001g0189 a0001c0001t0002g0033 a0001c0001t0002g0040 others(1): Show |
4 | HG02083.hp2 NA18990.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-4601_474-4588d others(16): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787333 | |||||||
| chr19:49787334 | G | T | 115 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0016 others(112): Show |
122 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.474-4601G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787334 | |||||||
| chr19:49787338 | G | GT | 26 | a0001c0001t0001g0011 a0001c0001t0001g0084 a0001c0001t0001g0124 others(23): Show |
26 | HG00438.hp2 HG00738.hp1 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.474-4589dupT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49787338 | ||||||
| chr19:49787338 | G | T | 8 | a0001c0001t0001g0194 a0001c0001t0001g0199 a0001c0001t0001g0200 others(5): Show |
8 | HG01891.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.474-4597G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787338 | |||||||
| chr19:49787341 | T | G | 1 | a0001c0001t0001g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.474-4594T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787341 | |||||||
| chr19:49787342 | T | G | 5 | a0001c0001t0001g0194 a0001c0001t0001g0199 a0001c0001t0001g0200 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.474-4593T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787342 | |||||||
| chr19:49787346 | T | G | 1 | a0001c0001t0001g0211 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.474-4589T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787346 | |||||||
| chr19:49787346 | TG | T | 3 | a0001c0001t0001g0165 a0001c0001t0005g0222 a0001c0001t0005g0223 |
3 | HG02258.hp2 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.474-4588delG | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787346 | |||||||
| chr19:49787347 | G | GT | 17 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
20 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.474-4582dupT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49787347 | ||||||
| chr19:49787347 | G | GTT | 12 | a0001c0001t0001g0269 a0001c0001t0001g0276 a0001c0001t0001g0281 others(9): Show |
12 | HG01169.hp2 HG01256.hp2 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.474-4583_474-4582d others(4): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49787347 | ||||||
| chr19:49787347 | G | T | 69 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(66): Show |
72 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.474-4588G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787347 | |||||||
| chr19:49787353 | T | G | 2 | a0001c0001t0001g0254 a0001c0001t0001g0255 |
2 | HG01346.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.474-4582T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787353 | |||||||
| chr19:49787354 | G | T | 191 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(188): Show |
202 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.474-4581G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787354 | |||||||
| chr19:49787356 | T | G | 14 | a0001c0001t0001g0016 a0001c0001t0001g0066 a0001c0001t0001g0067 others(11): Show |
15 | HG00099.hp1 HG00423.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.474-4579T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787356 | |||||||
| chr19:49787513 | A | AT | 9 | a0001c0001t0001g0161 a0001c0001t0001g0207 a0001c0001t0001g0208 others(6): Show |
9 | HG02109.hp1 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.474-4406dupT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49787513 | ||||||
| chr19:49787513 | AT | A | 96 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(93): Show |
101 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.474-4406delT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49787513 | ||||||
| chr19:49787592 | A | G | 201 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(198): Show |
213 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.474-4343A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787592 | |||||||
| chr19:49787644 | C | T | 6 | a0001c0001t0001g0195 a0001c0001t0004g0196 a0001c0001t0004g0197 others(3): Show |
6 | HG02486.hp2 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-4291C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787644 | |||||||
| chr19:49787796 | C | T | 3 | a0001c0001t0001g0285 a0001c0001t0001g0290 a0001c0001t0001g0294 |
3 | HG02683.hp1 HG02698.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.474-4139C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787796 | |||||||
| chr19:49787876 | A | G | 4 | a0001c0001t0001g0153 a0001c0001t0002g0062 a0001c0001t0002g0063 others(1): Show |
4 | HG02622.hp2 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-4059A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787876 | |||||||
| chr19:49787889 | C | G | 12 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(9): Show |
12 | HG00099.hp1 HG00741.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.474-4046C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787889 | |||||||
| chr19:49787925 | C | T | 4 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0004t0001g0209 others(1): Show |
4 | HG02486.hp1 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.474-4010C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787925 | |||||||
| chr19:49787983 | G | A | 1 | a0001c0001t0002g0059 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.474-3952G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787983 | |||||||
| chr19:49787992 | G | A | 1 | a0001c0001t0002g0059 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.474-3943G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49787992 | |||||||
| chr19:49788009 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.474-3926T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788009 | |||||||
| chr19:49788238 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.474-3697C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788238 | |||||||
| chr19:49788240 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.474-3695C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788240 | |||||||
| chr19:49788260 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0113 |
3 | HG01257.hp2 HG01258.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.474-3675T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788260 | |||||||
| chr19:49788301 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.474-3634C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788301 | |||||||
| chr19:49788416 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.474-3519A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788416 | |||||||
| chr19:49788424 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.474-3511G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788424 | |||||||
| chr19:49788449 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.474-3486G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788449 | |||||||
| chr19:49788521 | C | T | 10 | a0001c0001t0001g0153 a0001c0001t0001g0195 a0001c0001t0002g0062 others(7): Show |
10 | HG02486.hp2 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.474-3414C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788521 | |||||||
| chr19:49788550 | T | A | 22 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(19): Show |
22 | HG00099.hp1 HG00741.hp2 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.474-3385T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788550 | |||||||
| chr19:49788578 | A | G | 73 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(70): Show |
77 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.474-3357A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788578 | |||||||
| chr19:49788707 | C | T | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0005g0222 others(1): Show |
4 | HG00733.hp2 HG02258.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.474-3228C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788707 | |||||||
| chr19:49788798 | G | A | 2 | a0001c0001t0001g0286 a0001c0001t0001g0289 |
2 | HG00597.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.474-3137G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49788798 | |||||||
| chr19:49789086 | C | A | 10 | a0001c0001t0001g0153 a0001c0001t0001g0195 a0001c0001t0002g0062 others(7): Show |
10 | HG02486.hp2 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.474-2849C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49789086 | |||||||
| chr19:49789400 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.474-2535C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49789400 | |||||||
| chr19:49789590 | C | CT | 54 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(51): Show |
63 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.474-2326dupT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49789590 | ||||||
| chr19:49789590 | CT | C | 126 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(123): Show |
136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.474-2326delT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49789590 | ||||||
| chr19:49789590 | CTT | C | 6 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0072 others(3): Show |
6 | HG01515.hp1 HG01517.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.474-2327_474-2326d others(4): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr19 | 49789590 | ||||||
| chr19:49789607 | T | G | 4 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(1): Show |
4 | HG02145.hp2 HG02647.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.474-2328T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49789607 | |||||||
| chr19:49789753 | C | G | 7 | a0001c0001t0001g0004 a0001c0001t0001g0108 a0001c0001t0001g0124 others(4): Show |
9 | HG00609.hp2 HG00673.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.474-2182C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49789753 | |||||||
| chr19:49789826 | C | A | 1 | a0001c0001t0002g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.474-2109C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49789826 | |||||||
| chr19:49789853 | T | G | 95 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(92): Show |
99 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.474-2082T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49789853 | |||||||
| chr19:49789968 | C | T | 2 | a0001c0001t0002g0027 a0001c0001t0002g0048 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.474-1967C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49789968 | |||||||
| chr19:49789972 | C | A | 1 | a0001c0001t0001g0159 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.474-1963C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49789972 | |||||||
| chr19:49790154 | C | T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.474-1781C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49790154 | |||||||
| chr19:49790171 | A | T | 12 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(9): Show |
12 | HG00099.hp1 HG00741.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.474-1764A>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49790171 | |||||||
| chr19:49790178 | G | A | 83 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(80): Show |
87 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.474-1757G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49790178 | |||||||
| chr19:49790361 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.474-1574C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49790361 | |||||||
| chr19:49790443 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.474-1492T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49790443 | |||||||
| chr19:49790484 | C | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0218 a0001c0001t0001g0219 others(1): Show |
5 | HG02723.hp1 HG03195.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.474-1451C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49790484 | |||||||
| chr19:49790495 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.474-1440C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49790495 | |||||||
| chr19:49790647 | A | G | 22 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(19): Show |
22 | HG00099.hp1 HG00741.hp2 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.474-1288A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49790647 | |||||||
| chr19:49790755 | C | A | 8 | a0001c0001t0001g0269 a0001c0001t0001g0276 a0001c0001t0001g0281 others(5): Show |
8 | HG01169.hp2 HG01192.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.474-1180C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49790755 | |||||||
| chr19:49790837 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.474-1098A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49790837 | |||||||
| chr19:49790893 | G | A | 106 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0014 others(103): Show |
114 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.474-1042G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49790893 | |||||||
| chr19:49791110 | A | G | 101 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(98): Show |
105 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.474-825A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49791110 | |||||||
| chr19:49791200 | T | G | 73 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(70): Show |
77 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.474-735T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49791200 | |||||||
| chr19:49791258 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.474-677C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49791258 | |||||||
| chr19:49791353 | C | T | 1 | a0001c0002t0001g0245 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.474-582C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49791353 | |||||||
| chr19:49791384 | C | T | 73 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0016 others(70): Show |
78 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.474-551C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49791384 | |||||||
| chr19:49791453 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.474-482A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49791453 | |||||||
| chr19:49791502 | T | C | 99 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(96): Show |
103 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.474-433T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49791502 | |||||||
| chr19:49791806 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.474-129G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49791806 | |||||||
| chr19:49791808 | C | G | 1 | a0001c0001t0001g0263 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.474-127C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49791808 | |||||||
| chr19:49791891 | G | A | 2 | a0001c0001t0001g0276 a0001c0001t0001g0281 |
2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.474-44G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 4/22 | chr19 | 49791891 | |||||||
| chr19:49792169 | C | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0135 others(1): Show |
5 | HG01243.hp2 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.603+105C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792169 | |||||||
| chr19:49792198 | C | T | 6 | a0001c0001t0001g0195 a0001c0001t0004g0196 a0001c0001t0004g0197 others(3): Show |
6 | HG02486.hp2 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.603+134C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792198 | |||||||
| chr19:49792210 | GGGGCTCC others(105): Show |
G | 3 | a0001c0001t0001g0155 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG02055.hp2 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.603+220_603+331del | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr19 | 49792210 | ||||||
| chr19:49792232 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0004g0197 a0001c0001t0004g0198 |
3 | HG02622.hp1 HG02717.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.603+168C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792232 | |||||||
| chr19:49792233 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.603+169G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792233 | |||||||
| chr19:49792239 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.603+175G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792239 | |||||||
| chr19:49792281 | G | A | 1 | a0001c0001t0001g0292 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.603+217G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792281 | |||||||
| chr19:49792303 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.603+239C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792303 | |||||||
| chr19:49792307 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.603+243C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792307 | |||||||
| chr19:49792350 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.603+286C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792350 | |||||||
| chr19:49792448 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.603+384G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792448 | |||||||
| chr19:49792451 | G | C | 87 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(84): Show |
91 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.603+387G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792451 | |||||||
| chr19:49792540 | C | G | 1 | a0001c0001t0001g0085 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.604-451C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792540 | |||||||
| chr19:49792640 | C | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0113 |
3 | HG01257.hp2 HG01258.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.604-351C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792640 | |||||||
| chr19:49792838 | C | T | 4 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0241 others(1): Show |
4 | HG00438.hp2 HG02071.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.604-153C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792838 | |||||||
| chr19:49792878 | A | G | 4 | a0001c0001t0001g0174 a0001c0001t0002g0006 a0001c0001t0002g0040 others(1): Show |
5 | NA18960.hp2 NA18961.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.604-113A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792878 | |||||||
| chr19:49792888 | T | C | 87 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(84): Show |
91 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.604-103T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792888 | |||||||
| chr19:49792892 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.604-99C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792892 | |||||||
| chr19:49792976 | C | T | 3 | a0001c0001t0001g0213 a0001c0001t0001g0230 a0001c0001t0001g0246 |
3 | HG03834.hp1 NA18989.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.604-15C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 5/22 | chr19 | 49792976 | |||||||
| chr19:49793134 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.705+42C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49793134 | |||||||
| chr19:49793186 | C | T | 4 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0004t0001g0209 others(1): Show |
4 | HG02486.hp1 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.705+94C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49793186 | |||||||
| chr19:49793236 | C | T | 4 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0004t0001g0209 others(1): Show |
4 | HG02486.hp1 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.705+144C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49793236 | |||||||
| chr19:49793291 | G | C | 4 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0004t0001g0209 others(1): Show |
4 | HG02486.hp1 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.705+199G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49793291 | |||||||
| chr19:49793393 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.705+301G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49793393 | |||||||
| chr19:49793403 | C | T | 2 | a0001c0001t0003g0086 a0001c0001t0003g0166 |
2 | HG01952.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.705+311C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49793403 | |||||||
| chr19:49793461 | T | C | 1 | a0001c0011t0001g0212 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.705+369T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49793461 | |||||||
| chr19:49793636 | A | C | 3 | a0001c0001t0001g0134 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG01884.hp2 HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.705+544A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49793636 | |||||||
| chr19:49793747 | A | C | 87 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(84): Show |
91 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.705+655A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49793747 | |||||||
| chr19:49793898 | C | CT | 100 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(97): Show |
105 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.705+833dupT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr19 | 49793898 | ||||||
| chr19:49793898 | C | CTT | 20 | a0001c0001t0001g0074 a0001c0001t0001g0137 a0001c0001t0001g0184 others(17): Show |
20 | HG00642.hp2 HG00741.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.705+832_705+833dup others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr19 | 49793898 | ||||||
| chr19:49793898 | CT | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0020 others(23): Show |
29 | HG00280.hp1 HG00597.hp1 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.705+833delT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr19 | 49793898 | ||||||
| chr19:49794012 | A | T | 4 | a0001c0001t0001g0099 a0001c0001t0001g0109 a0001c0001t0001g0158 others(1): Show |
4 | HG02559.hp1 HG02602.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.705+920A>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794012 | |||||||
| chr19:49794017 | T | C | 4 | a0001c0001t0001g0099 a0001c0001t0001g0109 a0001c0001t0001g0158 others(1): Show |
4 | HG02559.hp1 HG02602.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.705+925T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794017 | |||||||
| chr19:49794026 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0108 a0001c0001t0001g0124 others(2): Show |
7 | HG00609.hp2 HG00738.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.705+934G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794026 | |||||||
| chr19:49794133 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.705+1041C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794133 | |||||||
| chr19:49794135 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.705+1043C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794135 | |||||||
| chr19:49794143 | ACCCGCCT others(295): Show |
A | 1 | a0001c0001t0001g0249 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.705+1060_706-1177d others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr19 | 49794143 | ||||||
| chr19:49794179 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.705+1087C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794179 | |||||||
| chr19:49794221 | G | GT | 97 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(94): Show |
101 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.705+1143dupT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr19 | 49794221 | ||||||
| chr19:49794255 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.705+1163G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794255 | |||||||
| chr19:49794263 | T | C | 17 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
20 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.705+1171T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794263 | |||||||
| chr19:49794297 | C | A | 73 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(70): Show |
77 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.705+1205C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794297 | |||||||
| chr19:49794357 | G | A | 73 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(70): Show |
77 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.705+1265G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794357 | |||||||
| chr19:49794407 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.706-1223G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794407 | |||||||
| chr19:49794412 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.706-1218C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794412 | |||||||
| chr19:49794557 | G | A | 1 | a0001c0001t0001g0292 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.706-1073G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794557 | |||||||
| chr19:49794684 | T | C | 1 | a0001c0001t0001g0242 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.706-946T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794684 | |||||||
| chr19:49794736 | C | T | 1 | a0001c0001t0002g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.706-894C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794736 | |||||||
| chr19:49794860 | A | G | 201 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(198): Show |
213 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.706-770A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794860 | |||||||
| chr19:49794916 | G | T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(8): Show |
14 | HG00597.hp1 HG02135.hp1 HG04184.hp2 others(11): Show |
intron_variant | MODIFIER | c.706-714G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794916 | |||||||
| chr19:49794965 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.706-665G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794965 | |||||||
| chr19:49794972 | C | T | 1 | a0001c0001t0002g0049 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.706-658C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49794972 | |||||||
| chr19:49795162 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.706-468T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49795162 | |||||||
| chr19:49795368 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.706-262T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49795368 | |||||||
| chr19:49795399 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.706-231G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49795399 | |||||||
| chr19:49795469 | C | T | 1 | a0001c0001t0001g0303 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.706-161C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49795469 | |||||||
| chr19:49795476 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0001g0115 |
2 | HG01934.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.706-154G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49795476 | |||||||
| chr19:49795547 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.706-83C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 6/22 | chr19 | 49795547 | |||||||
| chr19:49795808 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.814+70G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49795808 | |||||||
| chr19:49796063 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.814+325C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796063 | |||||||
| chr19:49796151 | T | G | 166 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(163): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.814+413T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796151 | |||||||
| chr19:49796226 | G | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0075 a0001c0001t0001g0231 |
3 | HG02602.hp1 HG03704.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.814+488G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796226 | |||||||
| chr19:49796349 | C | T | 19 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0108 others(16): Show |
21 | HG01934.hp1 HG01978.hp2 HG01981.hp1 others(18): Show |
intron_variant | MODIFIER | c.814+611C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796349 | |||||||
| chr19:49796456 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.814+718G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796456 | |||||||
| chr19:49796497 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.814+759T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796497 | |||||||
| chr19:49796500 | A | G | 167 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(164): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.814+762A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796500 | |||||||
| chr19:49796608 | C | T | 39 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0068 others(36): Show |
41 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.814+870C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796608 | |||||||
| chr19:49796609 | G | A | 18 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0177 others(15): Show |
21 | HG00597.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.814+871G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796609 | |||||||
| chr19:49796644 | T | C | 4 | a0001c0001t0001g0099 a0001c0001t0001g0109 a0001c0001t0001g0158 others(1): Show |
4 | HG02559.hp1 HG02602.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.814+906T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796644 | |||||||
| chr19:49796659 | CCT | C | 12 | a0001c0001t0001g0004 a0001c0001t0001g0106 a0001c0001t0001g0118 others(9): Show |
14 | HG00609.hp2 HG00673.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.814+922_814+923del others(2): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796659 | |||||||
| chr19:49796769 | A | G | 118 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(115): Show |
122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.814+1031A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796769 | |||||||
| chr19:49796808 | A | G | 1 | a0001c0011t0001g0212 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.814+1070A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796808 | |||||||
| chr19:49796910 | T | C | 1 | a0001c0001t0004g0197 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.814+1172T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49796910 | |||||||
| chr19:49797068 | C | G | 6 | a0001c0001t0001g0194 a0001c0001t0001g0199 a0001c0001t0001g0201 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.814+1330C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49797068 | |||||||
| chr19:49797220 | C | T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(18): Show |
24 | HG00597.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.814+1482C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49797220 | |||||||
| chr19:49797522 | C | T | 12 | a0001c0001t0001g0092 a0001c0001t0001g0174 a0001c0001t0002g0006 others(9): Show |
13 | HG01975.hp1 NA18952.hp1 NA18959.hp1 others(10): Show |
intron_variant | MODIFIER | c.815-1280C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49797522 | |||||||
| chr19:49797851 | CAGA | C | 29 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0120 others(26): Show |
30 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.815-948_815-946del others(3): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr19 | 49797851 | ||||||
| chr19:49797877 | T | G | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.815-925T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49797877 | |||||||
| chr19:49797895 | A | T | 67 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0065 others(64): Show |
69 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.815-907A>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49797895 | |||||||
| chr19:49797913 | CA | C | 116 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(113): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.815-883delA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr19 | 49797913 | ||||||
| chr19:49797961 | C | T | 5 | a0001c0001t0004g0196 a0001c0001t0004g0197 a0001c0001t0004g0198 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.815-841C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49797961 | |||||||
| chr19:49798030 | C | T | 18 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(15): Show |
21 | HG00597.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.815-772C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798030 | |||||||
| chr19:49798151 | T | G | 1 | a0001c0001t0001g0160 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.815-651T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798151 | |||||||
| chr19:49798172 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.815-630C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798172 | |||||||
| chr19:49798178 | A | C | 1 | a0001c0001t0002g0028 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.815-624A>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798178 | |||||||
| chr19:49798287 | G | C | 1 | a0001c0001t0002g0024 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.815-515G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798287 | |||||||
| chr19:49798288 | G | A | 116 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(113): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.815-514G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798288 | |||||||
| chr19:49798338 | C | T | 2 | a0001c0004t0001g0209 a0001c0004t0001g0302 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.815-464C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798338 | |||||||
| chr19:49798396 | A | G | 177 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0011 others(174): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.815-406A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798396 | |||||||
| chr19:49798542 | C | T | 2 | a0001c0004t0001g0209 a0001c0004t0001g0302 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.815-260C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798542 | |||||||
| chr19:49798563 | A | G | 40 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0022 others(37): Show |
42 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.815-239A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798563 | |||||||
| chr19:49798587 | T | G | 116 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(113): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.815-215T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798587 | |||||||
| chr19:49798618 | C | G | 5 | a0001c0001t0004g0196 a0001c0001t0004g0197 a0001c0001t0004g0198 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.815-184C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 7/22 | chr19 | 49798618 | |||||||
| chr19:49799031 | G | C | 1 | a0001c0001t0001g0087 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.965+79G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 8/22 | chr19 | 49799031 | |||||||
| chr19:49799251 | T | C | 1 | a0001c0001t0001g0291 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.966-76T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 8/22 | chr19 | 49799251 | |||||||
| chr19:49799579 | G | C | 1 | a0001c0001t0001g0269 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1135-50G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 9/22 | chr19 | 49799579 | |||||||
| chr19:49799941 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1273-27A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 10/22 | chr19 | 49799941 | |||||||
| chr19:49799943 | T | A | 1 | a0001c0001t0001g0084 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1273-25T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 10/22 | chr19 | 49799943 | |||||||
| chr19:49800202 | G | C | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1455+52G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 11/22 | chr19 | 49800202 | |||||||
| chr19:49800227 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1455+77G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 11/22 | chr19 | 49800227 | |||||||
| chr19:49800267 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1455+117G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 11/22 | chr19 | 49800267 | |||||||
| chr19:49800356 | G | C | 43 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0022 others(40): Show |
45 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1455+206G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 11/22 | chr19 | 49800356 | |||||||
| chr19:49800403 | G | A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(18): Show |
24 | HG00597.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1455+253G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 11/22 | chr19 | 49800403 | |||||||
| chr19:49800410 | T | C | 2 | a0001c0004t0001g0209 a0001c0004t0001g0302 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1455+260T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 11/22 | chr19 | 49800410 | |||||||
| chr19:49800449 | T | TTTTG | 22 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(19): Show |
25 | HG00597.hp1 HG01074.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1455+319_1455+322d others(6): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr19 | 49800449 | ||||||
| chr19:49800482 | G | A | 25 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0092 others(22): Show |
27 | HG01934.hp1 HG01975.hp1 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.1455+332G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 11/22 | chr19 | 49800482 | |||||||
| chr19:49800496 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1455+346T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 11/22 | chr19 | 49800496 | |||||||
| chr19:49800532 | G | A | 6 | a0001c0001t0001g0194 a0001c0001t0001g0199 a0001c0001t0001g0201 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1455+382G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 11/22 | chr19 | 49800532 | |||||||
| chr19:49801079 | A | G | 118 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(115): Show |
122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1553+21A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 12/22 | chr19 | 49801079 | |||||||
| chr19:49801132 | G | GTCCCAGG others(16): Show |
1 | a0001c0001t0001g0259 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1553+76_1553+77ins others(23): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr19 | 49801132 | ||||||
| chr19:49801135 | T | C | 118 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(115): Show |
122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1553+77T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 12/22 | chr19 | 49801135 | |||||||
| chr19:49801182 | T | C | 118 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(115): Show |
122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1553+124T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 12/22 | chr19 | 49801182 | |||||||
| chr19:49801189 | A | G | 1 | a0001c0010t0001g0123 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1553+131A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 12/22 | chr19 | 49801189 | |||||||
| chr19:49801190 | G | C | 1 | a0001c0010t0001g0123 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1553+132G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 12/22 | chr19 | 49801190 | |||||||
| chr19:49801191 | C | G | 1 | a0001c0010t0001g0123 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1553+133C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 12/22 | chr19 | 49801191 | |||||||
| chr19:49801635 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1785+14C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 13/22 | chr19 | 49801635 | |||||||
| chr19:49801664 | C | T | 1 | a0001c0010t0001g0123 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1785+43C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 13/22 | chr19 | 49801664 | |||||||
| chr19:49801694 | C | A | 1 | a0001c0001t0001g0240 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1786-28C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 13/22 | chr19 | 49801694 | |||||||
| chr19:49801909 | CCCTGCCA others(18): Show |
C | 1 | a0001c0001t0001g0117 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1953+27_1954-41del others(25): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr19 | 49801909 | ||||||
| chr19:49801968 | G | A | 2 | a0001c0001t0001g0278 a0001c0001t0001g0280 |
2 | HG01255.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1954-13G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 14/22 | chr19 | 49801968 | |||||||
| chr19:49802230 | C | T | 1 | a0001c0001t0002g0028 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2114+89C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802230 | |||||||
| chr19:49802304 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2114+163C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802304 | |||||||
| chr19:49802346 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2114+205G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802346 | |||||||
| chr19:49802361 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2114+220T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802361 | |||||||
| chr19:49802362 | C | G | 1 | a0001c0001t0001g0162 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2114+221C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802362 | |||||||
| chr19:49802423 | C | T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(8): Show |
14 | HG00597.hp1 HG02135.hp1 HG04184.hp2 others(11): Show |
intron_variant | MODIFIER | c.2114+282C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802423 | |||||||
| chr19:49802431 | G | C | 115 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(112): Show |
119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2114+290G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802431 | |||||||
| chr19:49802463 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2114+322C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802463 | |||||||
| chr19:49802505 | C | G | 1 | a0001c0001t0001g0085 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2114+364C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802505 | |||||||
| chr19:49802557 | A | G | 1 | a0001c0001t0002g0028 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2115-392A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802557 | |||||||
| chr19:49802558 | G | A | 1 | a0001c0001t0002g0028 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2115-391G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802558 | |||||||
| chr19:49802637 | G | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0214 a0001c0001t0001g0235 others(3): Show |
7 | HG02129.hp2 HG02735.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2115-312G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802637 | |||||||
| chr19:49802683 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2115-266G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802683 | |||||||
| chr19:49802924 | A | G | 3 | a0001c0001t0002g0027 a0001c0001t0002g0036 a0001c0001t0002g0048 |
3 | HG02055.hp1 HG02109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2115-25A>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802924 | |||||||
| chr19:49802941 | G | T | 40 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0022 others(37): Show |
42 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(39): Show |
splice_region_variant&intron_variant | LOW | c.2115-8G>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802941 | |||||||
| chr19:49802943 | C | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0281 |
2 | HG02717.hp2 NA19240.hp1 |
splice_region_variant&intron_variant | LOW | c.2115-6C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 15/22 | chr19 | 49802943 | |||||||
| chr19:49803048 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2171+43G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 16/22 | chr19 | 49803048 | |||||||
| chr19:49803059 | C | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0238 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2172-48C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 16/22 | chr19 | 49803059 | |||||||
| chr19:49803277 | C | T | 21 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0108 others(18): Show |
23 | HG01891.hp2 HG01934.hp1 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.2255-10C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 17/22 | chr19 | 49803277 | |||||||
| chr19:49803479 | T | C | 2 | a0001c0004t0001g0209 a0001c0004t0001g0302 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2344+103T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803479 | |||||||
| chr19:49803493 | G | A | 2 | a0001c0001t0002g0034 a0001c0001t0002g0035 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2344+117G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803493 | |||||||
| chr19:49803513 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2344+137T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803513 | |||||||
| chr19:49803602 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
6 | HG02723.hp1 HG03041.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.2344+226C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803602 | |||||||
| chr19:49803681 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0299 |
2 | HG00741.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.2344+305G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803681 | |||||||
| chr19:49803722 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0077 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2344+346C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803722 | |||||||
| chr19:49803756 | AC | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0193 a0001c0001t0001g0234 |
3 | HG00423.hp1 HG02071.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.2344+381delC | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803756 | |||||||
| chr19:49803806 | C | T | 20 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0108 others(17): Show |
22 | HG01934.hp1 HG01978.hp2 HG01981.hp1 others(19): Show |
intron_variant | MODIFIER | c.2344+430C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803806 | |||||||
| chr19:49803811 | C | A | 2 | a0001c0001t0002g0034 a0001c0001t0002g0035 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2344+435C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803811 | |||||||
| chr19:49803812 | T | A | 2 | a0001c0001t0002g0034 a0001c0001t0002g0035 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2344+436T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803812 | |||||||
| chr19:49803813 | T | C | 2 | a0001c0001t0002g0034 a0001c0001t0002g0035 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2344+437T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803813 | |||||||
| chr19:49803814 | CCTCATAG others(3): Show |
C | 2 | a0001c0001t0002g0034 a0001c0001t0002g0035 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2344+439_2344+448d others(12): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803814 | |||||||
| chr19:49803898 | T | G | 21 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(18): Show |
24 | HG00597.hp1 HG01074.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.2344+522T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49803898 | |||||||
| chr19:49804008 | G | A | 2 | a0001c0004t0001g0209 a0001c0004t0001g0302 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2344+632G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804008 | |||||||
| chr19:49804087 | C | T | 175 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0011 others(172): Show |
186 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.2344+711C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804087 | |||||||
| chr19:49804144 | G | A | 44 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0068 others(41): Show |
46 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.2344+768G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804144 | |||||||
| chr19:49804151 | G | A | 112 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(109): Show |
116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.2344+775G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804151 | |||||||
| chr19:49804184 | C | A | 1 | a0001c0001t0001g0162 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2344+808C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804184 | |||||||
| chr19:49804210 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2344+834T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804210 | |||||||
| chr19:49804233 | AAAAAG | A | 20 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(17): Show |
23 | HG00597.hp1 HG01074.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.2344+867_2344+871d others(7): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr19 | 49804233 | ||||||
| chr19:49804323 | C | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0254 |
2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.2344+947C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804323 | |||||||
| chr19:49804337 | C | G | 1 | a0001c0001t0001g0085 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2344+961C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804337 | |||||||
| chr19:49804401 | C | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
20 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.2344+1025C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804401 | |||||||
| chr19:49804457 | C | T | 3 | a0001c0001t0001g0103 a0001c0001t0001g0116 a0001c0001t0001g0169 |
3 | HG00733.hp1 HG01243.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.2345-996C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804457 | |||||||
| chr19:49804500 | G | A | 3 | a0001c0001t0001g0154 a0001c0001t0001g0276 a0001c0001t0001g0281 |
3 | HG02280.hp2 HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2345-953G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804500 | |||||||
| chr19:49804540 | G | GA | 114 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(111): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.2345-896dupA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr19 | 49804540 | ||||||
| chr19:49804540 | G | GAA | 9 | a0001c0001t0001g0244 a0001c0001t0001g0258 a0001c0001t0001g0269 others(6): Show |
9 | HG01175.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2345-897_2345-896d others(4): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr19 | 49804540 | ||||||
| chr19:49804540 | GA | G | 15 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0164 others(12): Show |
18 | HG00597.hp1 HG01074.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.2345-896delA | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr19 | 49804540 | ||||||
| chr19:49804557 | AT | A | 17 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0108 others(14): Show |
19 | HG01934.hp1 HG01978.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.2345-894delT | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr19 | 49804557 | ||||||
| chr19:49804558 | T | A | 2 | a0001c0001t0001g0187 a0001c0001t0001g0202 |
2 | HG01891.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.2345-895T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804558 | |||||||
| chr19:49804825 | C | T | 3 | a0001c0001t0001g0121 a0001c0001t0002g0023 a0001c0001t0002g0026 |
3 | HG00621.hp2 HG02155.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.2345-628C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804825 | |||||||
| chr19:49804860 | C | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
20 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.2345-593C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804860 | |||||||
| chr19:49804877 | G | C | 120 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(117): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.2345-576G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49804877 | |||||||
| chr19:49805285 | C | G | 21 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0108 others(18): Show |
23 | HG01891.hp2 HG01934.hp1 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.2345-168C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49805285 | |||||||
| chr19:49805346 | C | A | 21 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0108 others(18): Show |
23 | HG01891.hp2 HG01934.hp1 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.2345-107C>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49805346 | |||||||
| chr19:49805412 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2345-41C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 18/22 | chr19 | 49805412 | |||||||
| chr19:49805616 | G | A | 7 | a0001c0001t0001g0094 a0001c0001t0001g0102 a0001c0001t0001g0140 others(4): Show |
7 | HG00280.hp1 HG01099.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.2468+40G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 19/22 | chr19 | 49805616 | |||||||
| chr19:49805636 | T | C | 122 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(119): Show |
126 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.2469-25T>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 19/22 | chr19 | 49805636 | |||||||
| chr19:49805794 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2585+17G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 20/22 | chr19 | 49805794 | |||||||
| chr19:49805833 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0254 |
2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.2586-39G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 20/22 | chr19 | 49805833 | |||||||
| chr19:49806018 | G | C | 5 | a0001c0001t0004g0196 a0001c0001t0004g0197 a0001c0001t0004g0198 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2655+77G>C | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 21/22 | chr19 | 49806018 | |||||||
| chr19:49806093 | T | A | 1 | a0001c0001t0001g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2656-26T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 21/22 | chr19 | 49806093 | |||||||
| chr19:49806103 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2656-16C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 21/22 | chr19 | 49806103 | |||||||
| chr19:49806108 | C | G | 1 | a0001c0001t0002g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2656-11C>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 21/22 | chr19 | 49806108 | |||||||
| chr19:49806358 | CCCT | C | 161 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(158): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.2790+113_2790+115d others(5): Show |
AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr19 | 49806358 | ||||||
| chr19:49806383 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2790+130C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 22/22 | chr19 | 49806383 | |||||||
| chr19:49806436 | T | G | 1 | a0001c0002t0001g0226 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2790+183T>G | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 22/22 | chr19 | 49806436 | |||||||
| chr19:49806507 | T | A | 1 | a0001c0001t0001g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2791-174T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 22/22 | chr19 | 49806507 | |||||||
| chr19:49806509 | T | A | 1 | a0001c0001t0001g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2791-172T>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 22/22 | chr19 | 49806509 | |||||||
| chr19:49806531 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2791-150C>T | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 22/22 | chr19 | 49806531 | |||||||
| chr19:49806603 | TC | T | 166 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(163): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.2791-76delC | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr19 | 49806603 | ||||||
| chr19:49806626 | G | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
20 | HG00597.hp1 HG01099.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.2791-55G>A | AP2A1 | ENSG00000196961.13 | transcript | ENST00000354293.10 | protein_coding | 22/22 | chr19 | 49806626 |