Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 162 |
| ensemblid | ENSG00000100280.17 |
| hgncid | 554 |
| symbol | AP1B1 |
| name | adaptor related protein complex 1 subunit beta 1 |
| refseq_nuc | NM_001127.4 |
| refseq_prot | NP_001118.3 |
| ensembl_nuc | ENST00000357586.7 |
| ensembl_prot | ENSP00000350199.2 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 29327680 |
| end | 29388570 |
| strand | - |
| ver | v1.2 |
| region | chr22:29327680-29388570 |
| region5000 | chr22:29322680-29393570 |
| regionname0 | AP1B1_chr22_29327680_29388570 |
| regionname5000 | AP1B1_chr22_29322680_29393570 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 949 | 368 | 92 | 60 | 164 | 14 | 36 | 129 | AP1B1_chr22_29322680_29393570 | AP1B1 | MTDSK others(944): Show |
chr22 | 29322680 | 29393570 |
| a0002 | 0/0 | 949 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | MTDSK others(944): Show |
chr22 | 29322680 | 29393570 |
| a0003 | 0/0 | 949 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | MTDSK others(944): Show |
chr22 | 29322680 | 29393570 |
| a0004 | 0/0 | 949 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | MTDSK others(944): Show |
chr22 | 29322680 | 29393570 |
| a0005 | 0/0 | 949 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | MTDSK others(944): Show |
chr22 | 29322680 | 29393570 |
| a0006 | 0/0 | 949 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | MTDSK others(944): Show |
chr22 | 29322680 | 29393570 |
| a0007 | 0/0 | 949 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | MTDSK others(944): Show |
chr22 | 29322680 | 29393570 |
| a0008 | 0/0 | 949 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | MTDSK others(944): Show |
chr22 | 29322680 | 29393570 |
| a0009 | 0/0 | 949 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | MTDSK others(944): Show |
chr22 | 29322680 | 29393570 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2847 | 199 | 41 | 29 | 103 | 6 | 20 | AP1B1_chr22_29322680_29393570 | AP1B1 | ATGAC others(2842): Show |
chr22 | 29322680 | 29393570 | ||
| a0001c0002 | 1/1 | 2847 | 103 | 12 | 24 | 49 | 6 | 10 | AP1B1_chr22_29322680_29393570 | AP1B1 | ATGAC others(2842): Show |
chr22 | 29322680 | 29393570 | ||
| a0001c0003 | 0/0 | 2847 | 47 | 25 | 7 | 11 | 1 | 3 | AP1B1_chr22_29322680_29393570 | AP1B1 | ATGAC others(2842): Show |
chr22 | 29322680 | 29393570 | ||
| a0001c0004 | 0/0 | 2847 | 11 | 11 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | ATGAC others(2842): Show |
chr22 | 29322680 | 29393570 | ||
| a0001c0005 | 0/0 | 2847 | 4 | 1 | 0 | 0 | 1 | 2 | AP1B1_chr22_29322680_29393570 | AP1B1 | ATGAC others(2842): Show |
chr22 | 29322680 | 29393570 | ||
| a0001c0009 | 0/0 | 2847 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | ATGAC others(2842): Show |
chr22 | 29322680 | 29393570 | ||
| a0001c0010 | 0/0 | 2847 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | ATGAC others(2842): Show |
chr22 | 29322680 | 29393570 | ||
| a0001c0014 | 0/0 | 2847 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | ATGAC others(2842): Show |
chr22 | 29322680 | 29393570 | ||
| a0001c0017 | 0/0 | 2847 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | ATGAC others(2842): Show |
chr22 | 29322680 | 29393570 | ||
| a0002c0007 | 0/0 | 2847 | 2 | 0 | 0 | 0 | 0 | 2 | AP1B1_chr22_29322680_29393570 | AP1B1 | ATGAC others(2842): Show |
chr22 | 29322680 | 29393570 | ||
| a0003c0006 | 0/0 | 2847 | 2 | 0 | 0 | 0 | 0 | 2 | AP1B1_chr22_29322680_29393570 | AP1B1 | ATGAC others(2842): Show |
chr22 | 29322680 | 29393570 | ||
| a0004c0013 | 0/0 | 2847 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | ATGAC others(2842): Show |
chr22 | 29322680 | 29393570 | ||
| a0005c0011 | 0/0 | 2847 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | ATGAC others(2842): Show |
chr22 | 29322680 | 29393570 | ||
| a0006c0015 | 0/0 | 2847 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | ATGAC others(2842): Show |
chr22 | 29322680 | 29393570 | ||
| a0007c0016 | 0/0 | 2847 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | ATGAC others(2842): Show |
chr22 | 29322680 | 29393570 | ||
| a0008c0012 | 0/0 | 2847 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | ATGAC others(2842): Show |
chr22 | 29322680 | 29393570 | ||
| a0009c0008 | 0/0 | 2847 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | ATGAC others(2842): Show |
chr22 | 29322680 | 29393570 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4165 | 186 | 32 | 28 | 101 | 5 | 20 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0001c0001t0006 | 0/0 | 4165 | 5 | 5 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0001c0001t0007 | 0/0 | 4165 | 4 | 3 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0001c0001t0008 | 0/0 | 4165 | 2 | 0 | 0 | 2 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0001c0001t0010 | 0/0 | 4165 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0001c0001t0015 | 0/0 | 4165 | 1 | 0 | 0 | 0 | 1 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0001c0002t0001 | 1/1 | 4165 | 97 | 8 | 24 | 47 | 6 | 10 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0001c0002t0005 | 0/0 | 4165 | 6 | 4 | 0 | 2 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0001c0003t0001 | 0/0 | 4165 | 18 | 7 | 3 | 7 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0001c0003t0002 | 0/0 | 4165 | 6 | 1 | 0 | 2 | 1 | 2 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0001c0003t0003 | 0/0 | 4165 | 9 | 6 | 3 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0001c0003t0004 | 0/0 | 4165 | 9 | 8 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0001c0003t0009 | 0/0 | 4165 | 2 | 0 | 0 | 2 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0001c0003t0011 | 0/0 | 4165 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0001c0003t0012 | 0/0 | 4165 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0001c0003t0014 | 0/0 | 4165 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0001c0004t0002 | 0/0 | 4165 | 10 | 10 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0001c0004t0013 | 0/0 | 4165 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0001c0005t0001 | 0/0 | 4165 | 4 | 1 | 0 | 0 | 1 | 2 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0001c0009t0001 | 0/0 | 4165 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0001c0010t0003 | 0/0 | 4165 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0001c0014t0001 | 0/0 | 4165 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0001c0017t0001 | 0/0 | 4165 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0002c0007t0001 | 0/0 | 4165 | 2 | 0 | 0 | 0 | 0 | 2 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0003c0006t0005 | 0/0 | 4165 | 2 | 0 | 0 | 0 | 0 | 2 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0004c0013t0001 | 0/0 | 4165 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0005c0011t0001 | 0/0 | 4165 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0006c0015t0001 | 0/0 | 4165 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0007c0016t0001 | 0/0 | 4165 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0008c0012t0001 | 0/0 | 4165 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| a0009c0008t0001 | 0/0 | 4165 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | AGCTC others(4160): Show |
chr22 | 29322680 | 29393570 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0007g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0007g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0008g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0008g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0010g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0001t0015g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0011 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0242 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0005g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0005g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0005g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0002t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0004g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0004g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0004g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0004g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0004g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0004g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0004g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0004g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0009g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0009g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0011g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0012g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0003t0014g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0004t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0004t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0004t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0004t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0004t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0004t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0004t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0004t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0004t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0004t0002g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0004t0013g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0005t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0005t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0005t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0005t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0009t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0010t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0014t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0001c0017t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0002c0007t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0003c0006t0005g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0003c0006t0005g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0004c0013t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0005c0011t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0006c0015t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0007c0016t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0008c0012t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| a0009c0008t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | GBR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0300 | EUR | GBR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | GBR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0273 | EUR | GBR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00280 | hp1 | a0001 | c0001 | t0015 | g0357 | EUR | FIN | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0299 | EUR | FIN | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0318 | EUR | FIN | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00323 | hp2 | a0001 | c0003 | t0002 | g0097 | EUR | FIN | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0278 | EAS | CHS | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0297 | EAS | CHS | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | CHS | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0319 | EAS | CHS | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0243 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0310 | EAS | CHS | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0311 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0354 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0272 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0291 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0244 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0323 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01099 | hp2 | a0001 | c0003 | t0003 | g0091 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0332 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0095 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0254 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0331 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01192 | hp1 | a0001 | c0001 | t0007 | g0005 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0301 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01243 | hp1 | a0001 | c0003 | t0003 | g0235 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01243 | hp2 | a0001 | c0003 | t0004 | g0337 | AMR | PUR | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0261 | AMR | CLM | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0093 | AMR | CLM | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0288 | AMR | CLM | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0054 | AMR | CLM | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0240 | AMR | CLM | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01496 | hp2 | a0001 | c0003 | t0003 | g0236 | AMR | CLM | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01515 | hp2 | a0001 | c0005 | t0001 | g0265 | EUR | IBS | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0258 | EUR | IBS | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0249 | AMR | PEL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0269 | AMR | PEL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PEL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0251 | AMR | PEL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0196 | AMR | PEL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0250 | AMR | PEL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0282 | AMR | PEL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02015 | hp1 | a0004 | c0013 | t0001 | g0129 | EAS | KHV | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0296 | EAS | KHV | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0052 | AFR | ACB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02055 | hp2 | a0001 | c0003 | t0004 | g0346 | AFR | ACB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02056 | hp2 | a0001 | c0003 | t0002 | g0101 | EAS | KHV | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02071 | hp1 | a0001 | c0003 | t0002 | g0100 | EAS | KHV | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0292 | EAS | KHV | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02080 | hp1 | a0001 | c0002 | t0005 | g0259 | EAS | KHV | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02080 | hp2 | a0005 | c0011 | t0001 | g0168 | EAS | KHV | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | KHV | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02145 | hp1 | a0001 | c0003 | t0002 | g0037 | AFR | ACB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02165 | hp1 | a0006 | c0015 | t0001 | g0170 | EAS | CDX | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CDX | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02257 | hp1 | a0001 | c0003 | t0003 | g0092 | AFR | ACB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0252 | AFR | ACB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02258 | hp2 | a0001 | c0003 | t0004 | g0339 | AFR | ACB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02280 | hp1 | a0001 | c0003 | t0004 | g0345 | AFR | ACB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02451 | hp1 | a0001 | c0003 | t0003 | g0231 | AFR | ACB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02572 | hp2 | a0001 | c0002 | t0005 | g0328 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0257 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02622 | hp2 | a0001 | c0002 | t0005 | g0327 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0307 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02647 | hp1 | a0007 | c0016 | t0001 | g0073 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02647 | hp2 | a0001 | c0004 | t0002 | g0026 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0246 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02717 | hp1 | a0001 | c0004 | t0002 | g0025 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0056 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02723 | hp2 | a0001 | c0002 | t0005 | g0294 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0262 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02738 | hp1 | a0001 | c0003 | t0002 | g0036 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0071 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02809 | hp2 | a0001 | c0004 | t0002 | g0349 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0014 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02818 | hp2 | a0001 | c0003 | t0003 | g0234 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02886 | hp1 | a0008 | c0012 | t0001 | g0015 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0031 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02895 | hp1 | a0001 | c0003 | t0003 | g0232 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02895 | hp2 | a0001 | c0003 | t0004 | g0340 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02897 | hp2 | a0001 | c0003 | t0003 | g0233 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02922 | hp2 | a0001 | c0003 | t0004 | g0335 | AFR | ESN | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02970 | hp1 | a0001 | c0004 | t0002 | g0021 | AFR | ESN | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0356 | AFR | ESN | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0096 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0286 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03041 | hp2 | a0001 | c0004 | t0013 | g0351 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03098 | hp1 | a0001 | c0014 | t0001 | g0191 | AFR | MSL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03098 | hp2 | a0001 | c0004 | t0002 | g0024 | AFR | MSL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | ESN | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03130 | hp2 | a0001 | c0004 | t0002 | g0353 | AFR | ESN | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03209 | hp1 | a0001 | c0010 | t0003 | g0057 | AFR | MSL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0005 | AFR | MSL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03225 | hp2 | a0001 | c0003 | t0011 | g0344 | AFR | MSL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03453 | hp2 | a0001 | c0003 | t0004 | g0343 | AFR | MSL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0330 | AFR | MSL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03486 | hp2 | a0001 | c0003 | t0003 | g0090 | AFR | MSL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03490 | hp1 | a0002 | c0007 | t0001 | g0009 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0280 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0256 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03491 | hp2 | a0003 | c0006 | t0005 | g0304 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03492 | hp1 | a0003 | c0006 | t0005 | g0303 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03492 | hp2 | a0002 | c0007 | t0001 | g0009 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0078 | AFR | ESN | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0032 | AFR | ESN | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0033 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03540 | hp2 | a0001 | c0003 | t0014 | g0098 | AFR | GWD | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0248 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03669 | hp1 | a0001 | c0005 | t0001 | g0266 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03688 | hp1 | a0001 | c0009 | t0001 | g0245 | SAS | STU | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | STU | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0281 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0295 | SAS | BEB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0241 | SAS | BEB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG04115 | hp1 | a0001 | c0003 | t0002 | g0099 | SAS | STU | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG04115 | hp2 | a0001 | c0005 | t0001 | g0312 | SAS | STU | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | STU | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0011 | SAS | STU | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18522 | hp1 | a0001 | c0003 | t0012 | g0347 | AFR | YRI | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | YRI | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | YRI | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18947 | hp2 | a0001 | c0003 | t0001 | g0065 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18948 | hp1 | a0001 | c0002 | t0005 | g0260 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18948 | hp2 | a0001 | c0003 | t0001 | g0186 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18949 | hp2 | a0001 | c0001 | t0008 | g0227 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18950 | hp1 | a0009 | c0008 | t0001 | g0290 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18954 | hp2 | a0001 | c0017 | t0001 | g0158 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0333 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0316 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0325 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18981 | hp2 | a0001 | c0003 | t0009 | g0358 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0320 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19000 | hp1 | a0001 | c0003 | t0001 | g0048 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19011 | hp2 | a0001 | c0003 | t0001 | g0062 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0094 | AFR | LWK | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19030 | hp2 | a0001 | c0004 | t0002 | g0350 | AFR | LWK | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19043 | hp1 | a0001 | c0004 | t0002 | g0342 | AFR | LWK | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19043 | hp2 | a0001 | c0005 | t0001 | g0305 | AFR | LWK | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0315 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19063 | hp2 | a0001 | c0003 | t0001 | g0161 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19064 | hp1 | a0001 | c0003 | t0009 | g0359 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0066 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0348 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0322 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19086 | hp1 | a0001 | c0001 | t0008 | g0215 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19091 | hp2 | a0001 | c0003 | t0001 | g0183 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0019 | AFR | YRI | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0239 | AFR | YRI | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ASW | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA20129 | hp2 | a0001 | c0003 | t0004 | g0338 | AFR | ASW | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | TSI | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0247 | EUR | TSI | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | GIH | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | GIH | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0317 | AMR | CLM | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | CLM | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0022 | AFR | ACB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0030 | AFR | ACB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0329 | AFR | ACB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG02559 | hp2 | a0001 | c0003 | t0004 | g0336 | AFR | ACB | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03471 | hp1 | a0001 | c0002 | t0005 | g0306 | AFR | MSL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG03471 | hp2 | a0001 | c0004 | t0002 | g0027 | AFR | MSL | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG06807 | hp1 | a0001 | c0004 | t0002 | g0352 | AFR | USA | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0020 | AFR | USA | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0355 | AFR | LWK | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0011 | REF | REF | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0242 | REF | REF | AP1B1_chr22_29322680_29393570 | AP1B1 | chr22 | 29322680 | 29393570 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29330635 | G | A | 1 | a0006 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.2599C>T | p.Pro867Ser | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 20/23 | 2773/4165 | 2599/2850 | 867/949 | chr22 | 29330635 | |||
| chr22:29330691 | G | A | 1 | a0007 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.2543C>T | p.Ala848Val | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 20/23 | 2717/4165 | 2543/2850 | 848/949 | chr22 | 29330691 | |||
| chr22:29331879 | C | T | 1 | a0004 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.2347G>A | p.Ala783Thr | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 18/23 | 2521/4165 | 2347/2850 | 783/949 | chr22 | 29331879 | |||
| chr22:29339076 | C | T | 1 | a0008 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.2077G>A | p.Ala693Thr | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/23 | 2251/4165 | 2077/2850 | 693/949 | chr22 | 29339076 | |||
| chr22:29339132 | A | T | 1 | a0005 | 1 | HG02080.hp2 | missense_variant&splice_region_variant | MODERATE | c.2021T>A | p.Ile674Asn | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/23 | 2195/4165 | 2021/2850 | 674/949 | chr22 | 29339132 | |||
| chr22:29340775 | C | T | 1 | a0002 | 2 | HG03490.hp1 HG03492.hp2 |
missense_variant | MODERATE | c.1879G>A | p.Asp627Asn | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 14/23 | 2053/4165 | 1879/2850 | 627/949 | chr22 | 29340775 | |||
| chr22:29349319 | C | T | 1 | a0003 | 2 | HG03491.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.1336G>A | p.Ala446Thr | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/23 | 1510/4165 | 1336/2850 | 446/949 | chr22 | 29349319 | |||
| chr22:29358732 | G | T | 1 | a0009 | 1 | NA18950.hp1 | missense_variant | MODERATE | c.519C>A | p.Asn173Lys | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/23 | 693/4165 | 519/2850 | 173/949 | chr22 | 29358732 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29330477 | G | A | 1 | a0001c0014 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.2667C>T | p.Asn889Asn | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 21/23 | 2841/4165 | 2667/2850 | 889/949 | chr22 | 29330477 | |||
| chr22:29331877 | C | T | 10 | a0001c0001 a0001c0005 a0001c0014 others(7): Show |
212 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(209): Show |
synonymous_variant | LOW | c.2349G>A | p.Ala783Ala | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 18/23 | 2523/4165 | 2349/2850 | 783/949 | chr22 | 29331877 | |||
| chr22:29340671 | A | G | 1 | a0001c0004 | 11 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(8): Show |
synonymous_variant | LOW | c.1983T>C | p.Gly661Gly | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 14/23 | 2157/4165 | 1983/2850 | 661/949 | chr22 | 29340671 | |||
| chr22:29350073 | G | A | 1 | a0001c0017 | 1 | NA18954.hp2 | synonymous_variant | LOW | c.1233C>T | p.Ile411Ile | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 10/23 | 1407/4165 | 1233/2850 | 411/949 | chr22 | 29350073 | |||
| chr22:29354768 | A | G | 1 | a0001c0010 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.820T>C | p.Leu274Leu | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/23 | 994/4165 | 820/2850 | 274/949 | chr22 | 29354768 | |||
| chr22:29358951 | G | A | 1 | a0001c0009 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.300C>T | p.Pro100Pro | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/23 | 474/4165 | 300/2850 | 100/949 | chr22 | 29358951 | |||
| chr22:29359899 | T | C | 12 | a0001c0001 a0001c0003 a0001c0004 others(9): Show |
267 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(264): Show |
synonymous_variant | LOW | c.204A>G | p.Leu68Leu | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 4/23 | 378/4165 | 204/2850 | 68/949 | chr22 | 29359899 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29327804 | G | A | 1 | a0001c0003t0014 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1017C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 23/23 | 1017 | chr22 | 29327804 | ||||||
| chr22:29328013 | C | T | 1 | a0001c0004t0013 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*808G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 23/23 | 808 | chr22 | 29328013 | ||||||
| chr22:29328198 | G | A | 2 | a0001c0001t0007 a0001c0003t0012 |
5 | HG01192.hp1 HG02809.hp1 HG03209.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*623C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 23/23 | 623 | chr22 | 29328198 | ||||||
| chr22:29328269 | G | A | 2 | a0001c0003t0003 a0001c0010t0003 |
10 | HG01099.hp2 HG01243.hp1 HG01496.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*552C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 23/23 | 552 | chr22 | 29328269 | ||||||
| chr22:29328465 | A | T | 1 | a0001c0003t0011 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*356T>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 23/23 | 356 | chr22 | 29328465 | ||||||
| chr22:29328494 | C | T | 2 | a0001c0002t0005 a0003c0006t0005 |
8 | HG02080.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*327G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 23/23 | 327 | chr22 | 29328494 | ||||||
| chr22:29328495 | G | A | 1 | a0001c0001t0008 | 2 | NA18949.hp2 NA19086.hp1 |
3_prime_UTR_variant | MODIFIER | c.*326C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 23/23 | 326 | chr22 | 29328495 | ||||||
| chr22:29328570 | C | T | 1 | a0001c0001t0006 | 5 | HG02630.hp1 HG02896.hp2 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*251G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 23/23 | 251 | chr22 | 29328570 | ||||||
| chr22:29328675 | G | A | 3 | a0001c0003t0004 a0001c0003t0011 a0001c0003t0012 |
11 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*146C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 23/23 | 146 | chr22 | 29328675 | ||||||
| chr22:29328803 | T | C | 5 | a0001c0003t0002 a0001c0003t0009 a0001c0003t0014 others(2): Show |
20 | HG00323.hp2 HG02056.hp2 HG02071.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*18A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 23/23 | 18 | chr22 | 29328803 | ||||||
| chr22:29388448 | G | A | 1 | a0001c0001t0015 | 1 | HG00280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-52C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/23 | 21205 | chr22 | 29388448 | ||||||
| chr22:29388523 | C | G | 1 | a0001c0001t0010 | 1 | HG02818.hp1 | 5_prime_UTR_variant | MODIFIER | c.-127G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/23 | 21280 | chr22 | 29388523 | ||||||
| chr22:29388539 | C | A | 1 | a0001c0003t0009 | 2 | NA18981.hp2 NA19064.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-143G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/23 | chr22 | 29388539 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29328927 | C | A | 9 | a0001c0002t0001g0053 a0001c0002t0001g0263 a0001c0002t0001g0278 others(6): Show |
9 | HG00408.hp2 NA18941.hp2 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.2776-32G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 22/22 | chr22 | 29328927 | |||||||
| chr22:29328962 | G | T | 1 | a0001c0004t0002g0027 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2776-67C>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 22/22 | chr22 | 29328962 | |||||||
| chr22:29328992 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2776-97T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 22/22 | chr22 | 29328992 | |||||||
| chr22:29329452 | T | C | 3 | a0001c0001t0007g0005 a0001c0001t0007g0071 a0001c0001t0007g0078 |
4 | HG01192.hp1 HG02809.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2775+260A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 22/22 | chr22 | 29329452 | |||||||
| chr22:29329650 | G | A | 9 | a0001c0003t0002g0036 a0001c0003t0002g0037 a0001c0003t0002g0097 others(6): Show |
9 | HG00323.hp2 HG02056.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.2775+62C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 22/22 | chr22 | 29329650 | |||||||
| chr22:29329904 | T | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(254): Show |
271 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.2767-184A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 21/22 | chr22 | 29329904 | |||||||
| chr22:29329924 | TG | T | 5 | a0001c0004t0002g0349 a0001c0004t0002g0350 a0001c0004t0002g0352 others(2): Show |
5 | HG02809.hp2 HG03041.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2767-205delC | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 21/22 | chr22 | 29329924 | |||||||
| chr22:29329926 | G | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0070 a0001c0001t0001g0106 others(5): Show |
9 | HG02723.hp1 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.2767-206C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 21/22 | chr22 | 29329926 | |||||||
| chr22:29330612 | G | A | 1 | a0001c0003t0002g0037 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2611+11C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 20/22 | chr22 | 29330612 | |||||||
| chr22:29330843 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2525-134C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 19/22 | chr22 | 29330843 | |||||||
| chr22:29330970 | CCTCGGTG others(9): Show |
C | 1 | a0001c0004t0002g0352 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2525-277_2525-262d others(18): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 19/22 | chr22 | 29330970 | |||||||
| chr22:29331204 | A | T | 1 | a0001c0002t0001g0315 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2524+245T>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 19/22 | chr22 | 29331204 | |||||||
| chr22:29331233 | T | C | 1 | a0001c0003t0002g0037 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2524+216A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 19/22 | chr22 | 29331233 | |||||||
| chr22:29331256 | C | A | 1 | a0001c0001t0001g0145 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2524+193G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 19/22 | chr22 | 29331256 | |||||||
| chr22:29331955 | T | G | 8 | a0001c0002t0005g0259 a0001c0002t0005g0260 a0001c0002t0005g0294 others(5): Show |
8 | HG02080.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2310-39A>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 17/22 | chr22 | 29331955 | |||||||
| chr22:29331967 | C | T | 2 | a0001c0002t0005g0294 a0001c0002t0005g0328 |
2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2310-51G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 17/22 | chr22 | 29331967 | |||||||
| chr22:29332309 | C | T | 1 | a0001c0003t0004g0340 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2310-393G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 17/22 | chr22 | 29332309 | |||||||
| chr22:29332369 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2310-453G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 17/22 | chr22 | 29332369 | |||||||
| chr22:29332494 | C | G | 2 | a0001c0002t0001g0011 a0001c0002t0001g0323 |
2 | HG01081.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2310-578G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 17/22 | chr22 | 29332494 | |||||||
| chr22:29332627 | C | T | 9 | a0001c0003t0004g0335 a0001c0003t0004g0336 a0001c0003t0004g0337 others(6): Show |
9 | HG01243.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2310-711G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 17/22 | chr22 | 29332627 | |||||||
| chr22:29332694 | G | A | 11 | a0001c0004t0002g0021 a0001c0004t0002g0024 a0001c0004t0002g0025 others(8): Show |
11 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.2310-778C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 17/22 | chr22 | 29332694 | |||||||
| chr22:29332703 | C | T | 11 | a0001c0002t0001g0241 a0001c0002t0001g0243 a0001c0002t0001g0244 others(8): Show |
11 | HG00639.hp1 HG01069.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.2310-787G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 17/22 | chr22 | 29332703 | |||||||
| chr22:29332794 | T | C | 112 | a0001c0002t0001g0004 a0001c0002t0001g0011 a0001c0002t0001g0012 others(109): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.2310-878A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 17/22 | chr22 | 29332794 | |||||||
| chr22:29332841 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2310-925G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 17/22 | chr22 | 29332841 | |||||||
| chr22:29332865 | A | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0046 others(46): Show |
54 | HG00140.hp1 HG00423.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.2310-949T>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 17/22 | chr22 | 29332865 | |||||||
| chr22:29333174 | C | A | 1 | a0001c0003t0004g0340 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2309+1091G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 17/22 | chr22 | 29333174 | |||||||
| chr22:29333297 | G | A | 1 | a0001c0004t0002g0353 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2309+968C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 17/22 | chr22 | 29333297 | |||||||
| chr22:29333516 | C | T | 1 | a0001c0003t0004g0340 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2309+749G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 17/22 | chr22 | 29333516 | |||||||
| chr22:29333579 | T | C | 1 | a0001c0014t0001g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2309+686A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 17/22 | chr22 | 29333579 | |||||||
| chr22:29333791 | C | A | 1 | a0001c0003t0004g0340 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2309+474G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 17/22 | chr22 | 29333791 | |||||||
| chr22:29333830 | G | A | 9 | a0001c0003t0002g0036 a0001c0003t0002g0037 a0001c0003t0002g0097 others(6): Show |
9 | HG00323.hp2 HG02056.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.2309+435C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 17/22 | chr22 | 29333830 | |||||||
| chr22:29333837 | G | A | 12 | a0001c0002t0001g0286 a0001c0003t0001g0094 a0001c0003t0003g0090 others(9): Show |
12 | HG01099.hp2 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.2309+428C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 17/22 | chr22 | 29333837 | |||||||
| chr22:29333953 | T | C | 1 | a0001c0002t0001g0262 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2309+312A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 17/22 | chr22 | 29333953 | |||||||
| chr22:29334013 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.2309+252G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 17/22 | chr22 | 29334013 | |||||||
| chr22:29334123 | G | C | 1 | a0001c0001t0010g0014 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2309+142C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 17/22 | chr22 | 29334123 | |||||||
| chr22:29334220 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2309+45T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 17/22 | chr22 | 29334220 | |||||||
| chr22:29334514 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2164-104G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29334514 | |||||||
| chr22:29334636 | A | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
261 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.2164-226T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29334636 | |||||||
| chr22:29334724 | GGCCATGA others(42): Show |
G | 2 | a0001c0003t0002g0037 a0001c0003t0002g0097 |
2 | HG00323.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.2164-363_2164-315d others(51): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29334724 | |||||||
| chr22:29334742 | G | A | 1 | a0001c0004t0002g0342 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2164-332C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29334742 | |||||||
| chr22:29334822 | G | A | 5 | a0001c0003t0001g0022 a0001c0003t0001g0030 a0001c0003t0001g0031 others(2): Show |
5 | HG02109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2164-412C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29334822 | |||||||
| chr22:29334868 | C | T | 1 | a0001c0003t0001g0056 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2164-458G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29334868 | |||||||
| chr22:29334936 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2164-526G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29334936 | |||||||
| chr22:29335038 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2164-628C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29335038 | |||||||
| chr22:29335044 | A | G | 9 | a0001c0003t0002g0036 a0001c0003t0002g0037 a0001c0003t0002g0097 others(6): Show |
9 | HG00323.hp2 HG02056.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.2164-634T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29335044 | |||||||
| chr22:29335233 | T | A | 1 | a0001c0003t0001g0196 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2164-823A>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29335233 | |||||||
| chr22:29335397 | C | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0105 a0001c0001t0001g0184 others(2): Show |
6 | HG02027.hp1 HG02083.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.2164-987G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29335397 | |||||||
| chr22:29335423 | A | G | 1 | a0001c0003t0002g0037 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2164-1013T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29335423 | |||||||
| chr22:29335595 | C | G | 1 | a0001c0001t0001g0082 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2164-1185G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29335595 | |||||||
| chr22:29335622 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2164-1212A>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29335622 | |||||||
| chr22:29335672 | G | C | 1 | a0001c0004t0002g0027 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2164-1262C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29335672 | |||||||
| chr22:29336000 | C | T | 8 | a0001c0002t0005g0259 a0001c0002t0005g0260 a0001c0002t0005g0294 others(5): Show |
8 | HG02080.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2164-1590G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29336000 | |||||||
| chr22:29336024 | G | A | 1 | a0001c0003t0014g0098 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2164-1614C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29336024 | |||||||
| chr22:29336042 | A | G | 20 | a0001c0003t0002g0036 a0001c0003t0002g0037 a0001c0003t0002g0097 others(17): Show |
20 | HG00323.hp2 HG02056.hp2 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2164-1632T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29336042 | |||||||
| chr22:29336230 | A | G | 9 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0135 others(6): Show |
9 | NA18944.hp2 NA18985.hp1 NA18989.hp2 others(6): Show |
intron_variant | MODIFIER | c.2164-1820T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29336230 | |||||||
| chr22:29336504 | G | C | 1 | a0001c0004t0002g0342 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2164-2094C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29336504 | |||||||
| chr22:29336515 | C | A | 1 | a0001c0001t0001g0069 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2164-2105G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29336515 | |||||||
| chr22:29336696 | C | T | 1 | a0001c0002t0001g0273 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2164-2286G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29336696 | |||||||
| chr22:29336741 | T | C | 1 | a0001c0002t0001g0269 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2163+2249A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29336741 | |||||||
| chr22:29336804 | C | CA | 24 | a0001c0001t0001g0046 a0001c0001t0001g0134 a0001c0001t0001g0136 others(21): Show |
24 | HG01074.hp2 HG01496.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.2163+2185dupT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29336804 | |||||||
| chr22:29336804 | C | CAA | 6 | a0001c0003t0002g0097 a0001c0003t0002g0099 a0001c0003t0002g0101 others(3): Show |
6 | HG00323.hp2 HG02056.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.2163+2184_2163+218 others(6): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29336804 | |||||||
| chr22:29336804 | CA | C | 20 | a0001c0001t0001g0125 a0001c0001t0001g0131 a0001c0001t0001g0145 others(17): Show |
20 | HG01515.hp2 HG02109.hp2 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.2163+2185delT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29336804 | |||||||
| chr22:29336992 | T | C | 20 | a0001c0003t0002g0036 a0001c0003t0002g0037 a0001c0003t0002g0097 others(17): Show |
20 | HG00323.hp2 HG02056.hp2 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2163+1998A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29336992 | |||||||
| chr22:29336999 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2163+1991C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29336999 | |||||||
| chr22:29337000 | A | G | 11 | a0001c0004t0002g0021 a0001c0004t0002g0024 a0001c0004t0002g0025 others(8): Show |
11 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.2163+1990T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29337000 | |||||||
| chr22:29337002 | T | G | 1 | a0001c0002t0001g0317 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2163+1988A>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29337002 | |||||||
| chr22:29337059 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0113 |
2 | HG00639.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.2163+1931G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29337059 | |||||||
| chr22:29337078 | G | A | 5 | a0001c0004t0002g0021 a0001c0004t0002g0024 a0001c0004t0002g0025 others(2): Show |
5 | HG02647.hp2 HG02717.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2163+1912C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29337078 | |||||||
| chr22:29337236 | G | A | 9 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0135 others(6): Show |
9 | NA18944.hp2 NA18985.hp1 NA18989.hp2 others(6): Show |
intron_variant | MODIFIER | c.2163+1754C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29337236 | |||||||
| chr22:29337369 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2163+1621C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29337369 | |||||||
| chr22:29337465 | C | G | 20 | a0001c0001t0001g0007 a0001c0001t0001g0042 a0001c0001t0001g0045 others(17): Show |
21 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.2163+1525G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29337465 | |||||||
| chr22:29337521 | C | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0038 others(1): Show |
4 | HG00099.hp1 HG00642.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.2163+1469G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29337521 | |||||||
| chr22:29337535 | G | A | 5 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0018 others(2): Show |
5 | HG02630.hp1 HG02896.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2163+1455C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29337535 | |||||||
| chr22:29337716 | A | C | 11 | a0001c0004t0002g0021 a0001c0004t0002g0024 a0001c0004t0002g0025 others(8): Show |
11 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.2163+1274T>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29337716 | |||||||
| chr22:29337719 | T | C | 5 | a0001c0003t0001g0022 a0001c0003t0001g0030 a0001c0003t0001g0031 others(2): Show |
5 | HG02109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2163+1271A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29337719 | |||||||
| chr22:29337749 | C | G | 11 | a0001c0004t0002g0021 a0001c0004t0002g0024 a0001c0004t0002g0025 others(8): Show |
11 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.2163+1241G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29337749 | |||||||
| chr22:29337749 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2163+1241G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29337749 | |||||||
| chr22:29337894 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2163+1096C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29337894 | |||||||
| chr22:29337987 | C | T | 11 | a0001c0004t0002g0021 a0001c0004t0002g0024 a0001c0004t0002g0025 others(8): Show |
11 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.2163+1003G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29337987 | |||||||
| chr22:29338154 | G | A | 11 | a0001c0003t0004g0335 a0001c0003t0004g0336 a0001c0003t0004g0337 others(8): Show |
11 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2163+836C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29338154 | |||||||
| chr22:29338181 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2163+809G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29338181 | |||||||
| chr22:29338463 | C | T | 1 | a0001c0001t0001g0355 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2163+527G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29338463 | |||||||
| chr22:29338485 | A | C | 1 | a0001c0004t0002g0342 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2163+505T>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29338485 | |||||||
| chr22:29338707 | T | G | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
268 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.2163+283A>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29338707 | |||||||
| chr22:29338808 | G | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(227): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.2163+182C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29338808 | |||||||
| chr22:29338864 | GC | G | 10 | a0001c0002t0001g0308 a0001c0003t0002g0036 a0001c0003t0002g0037 others(7): Show |
10 | HG00323.hp2 HG02056.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.2163+125delG | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29338864 | |||||||
| chr22:29338952 | C | G | 1 | a0001c0001t0001g0084 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2163+38G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29338952 | |||||||
| chr22:29338963 | C | T | 11 | a0001c0004t0002g0021 a0001c0004t0002g0024 a0001c0004t0002g0025 others(8): Show |
11 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.2163+27G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 16/22 | chr22 | 29338963 | |||||||
| chr22:29339321 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
96 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.2020-188G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 15/22 | chr22 | 29339321 | |||||||
| chr22:29339399 | T | C | 1 | a0001c0003t0002g0037 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2020-266A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 15/22 | chr22 | 29339399 | |||||||
| chr22:29339428 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0341 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2020-295G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 15/22 | chr22 | 29339428 | |||||||
| chr22:29339512 | G | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0341 a0008c0012t0001g0015 |
3 | HG02886.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2019+242C>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 15/22 | chr22 | 29339512 | |||||||
| chr22:29339513 | C | A | 1 | a0001c0003t0001g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2019+241G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 15/22 | chr22 | 29339513 | |||||||
| chr22:29339658 | C | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0038 others(1): Show |
4 | HG00099.hp1 HG00642.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.2019+96G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 15/22 | chr22 | 29339658 | |||||||
| chr22:29339700 | C | T | 1 | a0001c0004t0002g0342 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2019+54G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 15/22 | chr22 | 29339700 | |||||||
| chr22:29339908 | G | A | 5 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0018 others(2): Show |
5 | HG02630.hp1 HG02896.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1999-134C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 14/22 | chr22 | 29339908 | |||||||
| chr22:29339914 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1999-140A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 14/22 | chr22 | 29339914 | |||||||
| chr22:29339942 | T | C | 1 | a0001c0004t0002g0342 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1999-168A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 14/22 | chr22 | 29339942 | |||||||
| chr22:29339943 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1999-169C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 14/22 | chr22 | 29339943 | |||||||
| chr22:29340113 | T | C | 3 | a0001c0002t0001g0249 a0001c0002t0001g0250 a0001c0002t0001g0251 |
3 | HG01928.hp1 HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1999-339A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 14/22 | chr22 | 29340113 | |||||||
| chr22:29340190 | C | T | 1 | a0001c0003t0001g0032 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1999-416G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 14/22 | chr22 | 29340190 | |||||||
| chr22:29340326 | C | A | 5 | a0001c0004t0002g0349 a0001c0004t0002g0350 a0001c0004t0002g0352 others(2): Show |
5 | HG02809.hp2 HG03041.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1998+330G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 14/22 | chr22 | 29340326 | |||||||
| chr22:29340380 | C | A | 11 | a0001c0003t0004g0335 a0001c0003t0004g0336 a0001c0003t0004g0337 others(8): Show |
11 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1998+276G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 14/22 | chr22 | 29340380 | |||||||
| chr22:29340923 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1797-66G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 13/22 | chr22 | 29340923 | |||||||
| chr22:29341048 | G | A | 1 | a0001c0004t0002g0350 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1797-191C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 13/22 | chr22 | 29341048 | |||||||
| chr22:29341082 | C | T | 3 | a0001c0001t0001g0076 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | HG00642.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1797-225G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 13/22 | chr22 | 29341082 | |||||||
| chr22:29341170 | G | A | 5 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0018 others(2): Show |
5 | HG02630.hp1 HG02896.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1797-313C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 13/22 | chr22 | 29341170 | |||||||
| chr22:29341424 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1796+77G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 13/22 | chr22 | 29341424 | |||||||
| chr22:29341799 | G | C | 11 | a0001c0004t0002g0021 a0001c0004t0002g0024 a0001c0004t0002g0025 others(8): Show |
11 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1537-39C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 12/22 | chr22 | 29341799 | |||||||
| chr22:29341828 | C | T | 2 | a0001c0003t0004g0335 a0001c0003t0012g0347 |
2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1537-68G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 12/22 | chr22 | 29341828 | |||||||
| chr22:29341834 | T | C | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(69): Show |
76 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1537-74A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 12/22 | chr22 | 29341834 | |||||||
| chr22:29341882 | T | C | 1 | a0001c0002t0001g0279 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1537-122A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 12/22 | chr22 | 29341882 | |||||||
| chr22:29341898 | C | T | 1 | a0001c0002t0001g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1537-138G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 12/22 | chr22 | 29341898 | |||||||
| chr22:29342397 | C | T | 1 | a0001c0003t0001g0093 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1438-14G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29342397 | |||||||
| chr22:29342557 | C | T | 43 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(40): Show |
45 | HG00544.hp2 HG00642.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1438-174G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29342557 | |||||||
| chr22:29342678 | G | A | 5 | a0001c0004t0002g0021 a0001c0004t0002g0024 a0001c0004t0002g0025 others(2): Show |
5 | HG02647.hp2 HG02717.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1438-295C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29342678 | |||||||
| chr22:29342782 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1438-399C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29342782 | |||||||
| chr22:29342868 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1438-485G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29342868 | |||||||
| chr22:29343194 | G | A | 8 | a0001c0003t0004g0335 a0001c0003t0004g0336 a0001c0003t0004g0337 others(5): Show |
8 | HG01243.hp2 HG02055.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1438-811C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29343194 | |||||||
| chr22:29343298 | G | C | 1 | a0001c0002t0001g0300 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1438-915C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29343298 | |||||||
| chr22:29343342 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0181 |
2 | NA18969.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1438-959G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29343342 | |||||||
| chr22:29343343 | G | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0142 a0004c0013t0001g0129 |
3 | HG00597.hp2 HG02015.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1438-960C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29343343 | |||||||
| chr22:29343684 | T | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0220 |
2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1438-1301A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29343684 | |||||||
| chr22:29343724 | C | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0341 a0008c0012t0001g0015 |
3 | HG02886.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1438-1341G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29343724 | |||||||
| chr22:29343902 | G | C | 1 | a0001c0001t0001g0228 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1438-1519C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29343902 | |||||||
| chr22:29343982 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1438-1599C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29343982 | |||||||
| chr22:29343993 | C | T | 1 | a0001c0003t0001g0096 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1438-1610G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29343993 | |||||||
| chr22:29344110 | C | CAAAAAAA others(3): Show |
7 | a0001c0004t0002g0021 a0001c0004t0002g0024 a0001c0004t0002g0025 others(4): Show |
7 | HG02717.hp1 HG02809.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1438-1737_1438-172 others(14): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29344110 | |||||||
| chr22:29344110 | C | CAAAAAAA others(4): Show |
2 | a0001c0004t0002g0026 a0001c0004t0002g0353 |
2 | HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1438-1738_1438-172 others(15): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29344110 | |||||||
| chr22:29344110 | CA | C | 14 | a0001c0002t0001g0279 a0001c0003t0001g0093 a0001c0003t0001g0094 others(11): Show |
14 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1438-1728delT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29344110 | |||||||
| chr22:29344379 | C | T | 1 | a0001c0002t0001g0296 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1438-1996G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29344379 | |||||||
| chr22:29344447 | G | T | 1 | a0001c0001t0001g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1438-2064C>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29344447 | |||||||
| chr22:29344514 | A | AT | 102 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0034 others(99): Show |
104 | HG00408.hp1 HG00609.hp2 HG00673.hp1 others(101): Show |
intron_variant | MODIFIER | c.1438-2132dupA | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29344514 | |||||||
| chr22:29344514 | A | ATT | 14 | a0001c0001t0001g0045 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
14 | HG00642.hp2 HG01071.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.1438-2133_1438-213 others(6): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29344514 | |||||||
| chr22:29344514 | AT | A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0130 a0001c0002t0001g0053 others(10): Show |
14 | HG00558.hp2 HG01099.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1438-2132delA | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29344514 | |||||||
| chr22:29344514 | ATT | A | 8 | a0001c0003t0002g0097 a0001c0003t0002g0099 a0001c0003t0002g0100 others(5): Show |
8 | HG00323.hp2 HG02056.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1438-2133_1438-213 others(6): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29344514 | |||||||
| chr22:29344514 | ATTT | A | 8 | a0001c0004t0002g0021 a0001c0004t0002g0024 a0001c0004t0002g0025 others(5): Show |
8 | HG02717.hp1 HG02809.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1438-2134_1438-213 others(7): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29344514 | |||||||
| chr22:29344739 | A | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(264): Show |
281 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.1438-2356T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29344739 | |||||||
| chr22:29344841 | A | G | 3 | a0001c0003t0004g0338 a0001c0003t0004g0339 a0001c0003t0004g0340 |
3 | HG02258.hp2 HG02895.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1438-2458T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29344841 | |||||||
| chr22:29345222 | T | C | 11 | a0001c0004t0002g0021 a0001c0004t0002g0024 a0001c0004t0002g0025 others(8): Show |
11 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1438-2839A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29345222 | |||||||
| chr22:29345225 | AT | A | 6 | a0001c0001t0001g0124 a0001c0001t0001g0152 a0001c0001t0001g0153 others(3): Show |
6 | HG02257.hp2 HG02572.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1438-2843delA | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29345225 | |||||||
| chr22:29345278 | G | A | 11 | a0001c0004t0002g0021 a0001c0004t0002g0024 a0001c0004t0002g0025 others(8): Show |
11 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1438-2895C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29345278 | |||||||
| chr22:29345337 | A | G | 11 | a0001c0004t0002g0021 a0001c0004t0002g0024 a0001c0004t0002g0025 others(8): Show |
11 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1438-2954T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29345337 | |||||||
| chr22:29345372 | G | GT | 6 | a0001c0001t0001g0118 a0001c0004t0002g0021 a0001c0004t0002g0024 others(3): Show |
6 | HG02647.hp2 HG02717.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1438-2990dupA | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29345372 | |||||||
| chr22:29345506 | G | T | 1 | a0001c0001t0001g0166 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1438-3123C>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29345506 | |||||||
| chr22:29345515 | G | A | 2 | a0001c0002t0001g0307 a0001c0002t0001g0330 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1438-3132C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29345515 | |||||||
| chr22:29345525 | C | T | 2 | a0003c0006t0005g0303 a0003c0006t0005g0304 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1438-3142G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29345525 | |||||||
| chr22:29345538 | A | AT | 92 | a0001c0001t0001g0229 a0001c0002t0001g0004 a0001c0002t0001g0011 others(89): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1438-3156dupA | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29345538 | |||||||
| chr22:29345538 | AT | A | 9 | a0001c0003t0002g0036 a0001c0003t0002g0037 a0001c0003t0002g0097 others(6): Show |
9 | HG00323.hp2 HG02056.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1438-3156delA | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29345538 | |||||||
| chr22:29345650 | G | A | 2 | a0001c0002t0001g0301 a0001c0009t0001g0245 |
2 | HG01192.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1438-3267C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29345650 | |||||||
| chr22:29345650 | G | GT | 5 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0018 others(2): Show |
5 | HG02630.hp1 HG02896.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1438-3268dupA | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29345650 | |||||||
| chr22:29345685 | G | T | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1438-3302C>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29345685 | |||||||
| chr22:29345788 | G | A | 1 | a0001c0004t0002g0027 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1438-3405C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29345788 | |||||||
| chr22:29346083 | G | T | 11 | a0001c0004t0002g0021 a0001c0004t0002g0024 a0001c0004t0002g0025 others(8): Show |
11 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1437+3135C>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29346083 | |||||||
| chr22:29346142 | A | G | 1 | a0001c0002t0001g0300 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1437+3076T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29346142 | |||||||
| chr22:29346236 | A | T | 1 | a0001c0002t0001g0295 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1437+2982T>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29346236 | |||||||
| chr22:29346403 | G | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0079 a0007c0016t0001g0073 |
3 | HG01891.hp2 HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1437+2815C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29346403 | |||||||
| chr22:29346445 | T | G | 1 | a0001c0005t0001g0305 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1437+2773A>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29346445 | |||||||
| chr22:29346528 | A | T | 9 | a0001c0003t0002g0036 a0001c0003t0002g0037 a0001c0003t0002g0097 others(6): Show |
9 | HG00323.hp2 HG02056.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1437+2690T>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29346528 | |||||||
| chr22:29346538 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1437+2680C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29346538 | |||||||
| chr22:29346567 | G | A | 1 | a0001c0004t0002g0021 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1437+2651C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29346567 | |||||||
| chr22:29346587 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1437+2631G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29346587 | |||||||
| chr22:29346794 | T | TG | 27 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0081 others(24): Show |
27 | HG00323.hp2 HG00597.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1437+2423dupC | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29346794 | |||||||
| chr22:29346795 | G | C | 1 | a0001c0002t0001g0284 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1437+2423C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29346795 | |||||||
| chr22:29346800 | G | C | 1 | a0001c0003t0004g0340 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1437+2418C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29346800 | |||||||
| chr22:29346852 | T | C | 27 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0058 others(24): Show |
27 | HG00544.hp2 HG00642.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1437+2366A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29346852 | |||||||
| chr22:29346914 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1437+2304G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29346914 | |||||||
| chr22:29346985 | C | A | 1 | a0001c0003t0002g0099 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1437+2233G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29346985 | |||||||
| chr22:29347120 | T | G | 1 | a0001c0001t0006g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1437+2098A>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29347120 | |||||||
| chr22:29347229 | C | T | 4 | a0001c0002t0001g0269 a0001c0002t0001g0282 a0001c0002t0001g0288 others(1): Show |
4 | HG00280.hp2 HG01358.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1437+1989G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29347229 | |||||||
| chr22:29347358 | C | A | 1 | a0001c0002t0001g0300 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1437+1860G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29347358 | |||||||
| chr22:29347493 | T | C | 112 | a0001c0002t0001g0004 a0001c0002t0001g0011 a0001c0002t0001g0012 others(109): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.1437+1725A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29347493 | |||||||
| chr22:29347582 | C | G | 11 | a0001c0004t0002g0021 a0001c0004t0002g0024 a0001c0004t0002g0025 others(8): Show |
11 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1437+1636G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29347582 | |||||||
| chr22:29347790 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(84): Show |
95 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1437+1428G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29347790 | |||||||
| chr22:29347792 | G | C | 1 | a0001c0001t0001g0058 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1437+1426C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29347792 | |||||||
| chr22:29347880 | C | G | 11 | a0001c0004t0002g0021 a0001c0004t0002g0024 a0001c0004t0002g0025 others(8): Show |
11 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1437+1338G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29347880 | |||||||
| chr22:29348133 | C | T | 1 | a0001c0003t0003g0236 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1437+1085G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29348133 | |||||||
| chr22:29348279 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1437+939T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29348279 | |||||||
| chr22:29348333 | C | T | 1 | a0001c0001t0001g0354 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1437+885G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29348333 | |||||||
| chr22:29348753 | G | T | 1 | a0001c0002t0001g0263 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1437+465C>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29348753 | |||||||
| chr22:29348887 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1437+331C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29348887 | |||||||
| chr22:29349043 | T | G | 11 | a0001c0004t0002g0021 a0001c0004t0002g0024 a0001c0004t0002g0025 others(8): Show |
11 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1437+175A>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29349043 | |||||||
| chr22:29349083 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1437+135A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29349083 | |||||||
| chr22:29349088 | C | T | 5 | a0001c0004t0002g0349 a0001c0004t0002g0350 a0001c0004t0002g0352 others(2): Show |
5 | HG02809.hp2 HG03041.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1437+130G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29349088 | |||||||
| chr22:29349123 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1437+95C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29349123 | |||||||
| chr22:29349136 | G | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0079 a0007c0016t0001g0073 |
3 | HG01891.hp2 HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1437+82C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 11/22 | chr22 | 29349136 | |||||||
| chr22:29349520 | G | GT | 7 | a0001c0002t0001g0053 a0001c0002t0001g0241 a0001c0002t0001g0270 others(4): Show |
7 | HG00544.hp1 HG02258.hp2 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.1272-138dupA | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 10/22 | chr22 | 29349520 | |||||||
| chr22:29349586 | T | A | 1 | a0001c0002t0001g0302 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1272-203A>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 10/22 | chr22 | 29349586 | |||||||
| chr22:29349587 | C | G | 1 | a0001c0002t0001g0302 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1272-204G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 10/22 | chr22 | 29349587 | |||||||
| chr22:29349588 | A | C | 1 | a0001c0002t0001g0302 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1272-205T>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 10/22 | chr22 | 29349588 | |||||||
| chr22:29349589 | C | CTGGGCAA others(18): Show |
1 | a0001c0002t0001g0302 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1272-207_1272-206i others(27): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 10/22 | chr22 | 29349589 | |||||||
| chr22:29349876 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0173 |
2 | NA18950.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1271+159C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 10/22 | chr22 | 29349876 | |||||||
| chr22:29350264 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1156-114A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 9/22 | chr22 | 29350264 | |||||||
| chr22:29350366 | A | G | 1 | a0001c0001t0015g0357 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1156-216T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 9/22 | chr22 | 29350366 | |||||||
| chr22:29350407 | G | A | 1 | a0001c0002t0001g0257 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1156-257C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 9/22 | chr22 | 29350407 | |||||||
| chr22:29350476 | C | T | 1 | a0001c0001t0007g0071 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1156-326G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 9/22 | chr22 | 29350476 | |||||||
| chr22:29350525 | T | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0212 |
3 | HG03139.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1156-375A>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 9/22 | chr22 | 29350525 | |||||||
| chr22:29350591 | C | T | 1 | a0001c0002t0001g0289 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1156-441G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 9/22 | chr22 | 29350591 | |||||||
| chr22:29350716 | T | C | 1 | a0001c0003t0001g0056 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1155+455A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 9/22 | chr22 | 29350716 | |||||||
| chr22:29350737 | C | T | 8 | a0001c0003t0004g0335 a0001c0003t0004g0336 a0001c0003t0004g0337 others(5): Show |
8 | HG01243.hp2 HG02055.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1155+434G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 9/22 | chr22 | 29350737 | |||||||
| chr22:29350847 | G | A | 6 | a0001c0002t0001g0325 a0001c0003t0001g0048 a0001c0003t0001g0161 others(3): Show |
6 | HG01978.hp2 NA18948.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.1155+324C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 9/22 | chr22 | 29350847 | |||||||
| chr22:29351100 | G | C | 1 | a0001c0001t0006g0018 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1155+71C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 9/22 | chr22 | 29351100 | |||||||
| chr22:29351277 | A | G | 9 | a0001c0001t0001g0041 a0001c0001t0001g0122 a0001c0001t0001g0138 others(6): Show |
9 | HG00280.hp1 HG02129.hp2 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.1060-11T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 8/22 | chr22 | 29351277 | |||||||
| chr22:29351314 | T | C | 1 | a0001c0003t0002g0036 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1060-48A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 8/22 | chr22 | 29351314 | |||||||
| chr22:29351361 | G | T | 1 | a0001c0003t0004g0339 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1060-95C>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 8/22 | chr22 | 29351361 | |||||||
| chr22:29351423 | A | C | 11 | a0001c0004t0002g0021 a0001c0004t0002g0024 a0001c0004t0002g0025 others(8): Show |
11 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1060-157T>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 8/22 | chr22 | 29351423 | |||||||
| chr22:29351695 | C | T | 5 | a0001c0004t0002g0021 a0001c0004t0002g0024 a0001c0004t0002g0025 others(2): Show |
5 | HG02647.hp2 HG02717.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+10G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 8/22 | chr22 | 29351695 | |||||||
| chr22:29351925 | G | GGCACAGA others(2): Show |
14 | a0001c0002t0001g0256 a0001c0002t0001g0271 a0001c0002t0001g0274 others(11): Show |
14 | HG00558.hp1 HG00673.hp2 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.939-101_939-100ins others(9): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29351925 | |||||||
| chr22:29352119 | A | G | 11 | a0001c0004t0002g0021 a0001c0004t0002g0024 a0001c0004t0002g0025 others(8): Show |
11 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.939-294T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29352119 | |||||||
| chr22:29352220 | G | A | 1 | a0001c0002t0001g0293 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.939-395C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29352220 | |||||||
| chr22:29352221 | T | A | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG00408.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.939-396A>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29352221 | |||||||
| chr22:29352316 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.939-491G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29352316 | |||||||
| chr22:29352366 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.939-541T>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29352366 | |||||||
| chr22:29352408 | T | A | 2 | a0001c0001t0001g0182 a0001c0001t0001g0224 |
2 | NA18612.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.939-583A>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29352408 | |||||||
| chr22:29352507 | T | C | 1 | a0001c0002t0001g0268 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.939-682A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29352507 | |||||||
| chr22:29352560 | G | A | 1 | a0001c0004t0002g0342 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.939-735C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29352560 | |||||||
| chr22:29352666 | T | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.939-841A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29352666 | |||||||
| chr22:29352707 | T | C | 1 | a0001c0002t0001g0257 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.939-882A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29352707 | |||||||
| chr22:29352731 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.939-906G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29352731 | |||||||
| chr22:29352842 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0181 |
2 | NA18969.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.939-1017C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29352842 | |||||||
| chr22:29352870 | G | A | 51 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
53 | HG00544.hp2 HG00642.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.939-1045C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29352870 | |||||||
| chr22:29352891 | G | A | 1 | a0006c0015t0001g0170 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.939-1066C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29352891 | |||||||
| chr22:29352905 | A | G | 3 | a0001c0001t0001g0106 a0001c0001t0001g0341 a0008c0012t0001g0015 |
3 | HG02886.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.939-1080T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29352905 | |||||||
| chr22:29353015 | C | T | 1 | a0001c0003t0002g0036 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.939-1190G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29353015 | |||||||
| chr22:29353149 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.939-1324A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29353149 | |||||||
| chr22:29353187 | C | T | 10 | a0001c0001t0001g0041 a0001c0001t0001g0138 a0001c0001t0001g0144 others(7): Show |
10 | HG00280.hp1 HG02809.hp2 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.939-1362G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29353187 | |||||||
| chr22:29353234 | G | C | 4 | a0001c0002t0005g0294 a0001c0002t0005g0306 a0001c0002t0005g0327 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.939-1409C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29353234 | |||||||
| chr22:29353240 | T | C | 3 | a0001c0003t0001g0048 a0001c0003t0001g0161 a0001c0003t0001g0186 |
3 | NA18948.hp2 NA19000.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.938+1410A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29353240 | |||||||
| chr22:29353269 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.938+1381C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29353269 | |||||||
| chr22:29353287 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0192 a0001c0001t0001g0197 others(1): Show |
5 | HG02145.hp2 HG02965.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.938+1363G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29353287 | |||||||
| chr22:29353301 | C | T | 2 | a0001c0003t0009g0358 a0001c0003t0009g0359 |
2 | NA18981.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.938+1349G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29353301 | |||||||
| chr22:29353818 | C | T | 1 | a0001c0002t0001g0316 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.938+832G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29353818 | |||||||
| chr22:29353965 | T | C | 1 | a0001c0001t0001g0354 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.938+685A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29353965 | |||||||
| chr22:29354014 | G | A | 1 | a0001c0003t0004g0340 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.938+636C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29354014 | |||||||
| chr22:29354116 | G | A | 1 | a0001c0001t0010g0014 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.938+534C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29354116 | |||||||
| chr22:29354127 | C | T | 1 | a0001c0004t0002g0342 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.938+523G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29354127 | |||||||
| chr22:29354197 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
187 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.938+453A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29354197 | |||||||
| chr22:29354240 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.938+410C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29354240 | |||||||
| chr22:29354418 | C | T | 1 | a0001c0003t0001g0093 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.938+232G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29354418 | |||||||
| chr22:29354431 | G | A | 1 | a0001c0002t0001g0249 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.938+219C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29354431 | |||||||
| chr22:29354607 | C | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0341 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.938+43G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29354607 | |||||||
| chr22:29354613 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.938+37C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29354613 | |||||||
| chr22:29354631 | C | T | 5 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0018 others(2): Show |
5 | HG02630.hp1 HG02896.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.938+19G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 7/22 | chr22 | 29354631 | |||||||
| chr22:29355001 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.717-130G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 6/22 | chr22 | 29355001 | |||||||
| chr22:29355041 | G | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.717-170C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 6/22 | chr22 | 29355041 | |||||||
| chr22:29355192 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.717-321C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 6/22 | chr22 | 29355192 | |||||||
| chr22:29355237 | G | GA | 17 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0135 others(14): Show |
17 | HG02080.hp1 HG02572.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.717-367dupT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 6/22 | chr22 | 29355237 | |||||||
| chr22:29355398 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.717-527G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 6/22 | chr22 | 29355398 | |||||||
| chr22:29355460 | T | TAAAC | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0225 |
3 | HG00609.hp2 NA18975.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.717-593_717-590dup others(4): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 6/22 | chr22 | 29355460 | |||||||
| chr22:29355460 | TAAACAAA others(5): Show |
T | 1 | a0001c0002t0001g0302 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.717-601_717-590del others(12): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 6/22 | chr22 | 29355460 | |||||||
| chr22:29355536 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.717-665C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 6/22 | chr22 | 29355536 | |||||||
| chr22:29355759 | G | A | 1 | a0001c0002t0005g0306 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.716+667C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 6/22 | chr22 | 29355759 | |||||||
| chr22:29355765 | A | T | 5 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0018 others(2): Show |
5 | HG02630.hp1 HG02896.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.716+661T>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 6/22 | chr22 | 29355765 | |||||||
| chr22:29355857 | C | CA | 9 | a0001c0001t0001g0113 a0001c0001t0001g0143 a0001c0001t0001g0150 others(6): Show |
9 | HG01175.hp2 HG02647.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.716+568dupT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 6/22 | chr22 | 29355857 | |||||||
| chr22:29355857 | CA | C | 7 | a0001c0001t0001g0035 a0001c0001t0001g0058 a0001c0001t0001g0060 others(4): Show |
7 | HG01167.hp2 HG03041.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.716+568delT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 6/22 | chr22 | 29355857 | |||||||
| chr22:29355931 | C | T | 8 | a0001c0003t0004g0335 a0001c0003t0004g0336 a0001c0003t0004g0337 others(5): Show |
8 | HG01243.hp2 HG02055.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.716+495G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 6/22 | chr22 | 29355931 | |||||||
| chr22:29356057 | A | G | 5 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0018 others(2): Show |
5 | HG02630.hp1 HG02896.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.716+369T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 6/22 | chr22 | 29356057 | |||||||
| chr22:29356191 | C | A | 1 | a0001c0004t0002g0342 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.716+235G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 6/22 | chr22 | 29356191 | |||||||
| chr22:29356191 | C | G | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(315): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.716+235G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 6/22 | chr22 | 29356191 | |||||||
| chr22:29356298 | C | T | 1 | a0001c0003t0002g0037 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.716+128G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 6/22 | chr22 | 29356298 | |||||||
| chr22:29356410 | C | T | 2 | a0001c0003t0003g0090 a0001c0003t0003g0092 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.716+16G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 6/22 | chr22 | 29356410 | |||||||
| chr22:29356632 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.526-16C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29356632 | |||||||
| chr22:29356789 | C | T | 1 | a0001c0003t0001g0183 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.526-173G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29356789 | |||||||
| chr22:29356796 | A | G | 11 | a0001c0001t0001g0211 a0001c0004t0002g0021 a0001c0004t0002g0024 others(8): Show |
11 | HG02559.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.526-180T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29356796 | |||||||
| chr22:29356876 | C | G | 1 | a0001c0001t0007g0071 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.526-260G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29356876 | |||||||
| chr22:29356897 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.526-281G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29356897 | |||||||
| chr22:29357050 | GTGTTTTT others(10): Show |
G | 5 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0018 others(2): Show |
5 | HG02630.hp1 HG02896.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-451_526-435del others(17): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29357050 | |||||||
| chr22:29357062 | GTTTT | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.526-450_526-447del others(4): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29357062 | |||||||
| chr22:29357065 | T | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0222 |
2 | NA18961.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.526-449A>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29357065 | |||||||
| chr22:29357066 | T | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0164 |
3 | HG03942.hp1 NA19001.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.526-450A>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29357066 | |||||||
| chr22:29357068 | T | G | 1 | a0001c0004t0002g0342 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-452A>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29357068 | |||||||
| chr22:29357069 | G | T | 1 | a0001c0004t0002g0342 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-453C>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29357069 | |||||||
| chr22:29357070 | T | G | 1 | a0001c0001t0001g0190 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.526-454A>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29357070 | |||||||
| chr22:29357076 | T | G | 1 | a0001c0003t0014g0098 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.526-460A>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29357076 | |||||||
| chr22:29357221 | C | T | 8 | a0001c0002t0005g0259 a0001c0002t0005g0260 a0001c0002t0005g0294 others(5): Show |
8 | HG02080.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.526-605G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29357221 | |||||||
| chr22:29357250 | T | G | 3 | a0001c0003t0004g0338 a0001c0003t0004g0339 a0001c0003t0004g0340 |
3 | HG02258.hp2 HG02895.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.526-634A>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29357250 | |||||||
| chr22:29357271 | T | C | 1 | a0001c0003t0003g0236 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.526-655A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29357271 | |||||||
| chr22:29357333 | G | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(69): Show |
76 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.526-717C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29357333 | |||||||
| chr22:29357444 | C | T | 1 | a0001c0003t0004g0338 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.526-828G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29357444 | |||||||
| chr22:29357647 | T | A | 4 | a0001c0002t0001g0052 a0001c0002t0001g0239 a0001c0002t0001g0240 others(1): Show |
4 | HG01496.hp1 HG02055.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-1031A>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29357647 | |||||||
| chr22:29357671 | C | T | 1 | a0001c0003t0014g0098 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.525+1055G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29357671 | |||||||
| chr22:29357688 | G | GT | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(170): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.525+1037dupA | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29357688 | |||||||
| chr22:29357688 | G | GTT | 88 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0034 others(85): Show |
90 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.525+1036_525+1037d others(4): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29357688 | |||||||
| chr22:29357763 | T | A | 9 | a0001c0003t0002g0036 a0001c0003t0002g0037 a0001c0003t0002g0097 others(6): Show |
9 | HG00323.hp2 HG02056.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.525+963A>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29357763 | |||||||
| chr22:29357848 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.525+878G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29357848 | |||||||
| chr22:29358278 | T | C | 4 | a0001c0002t0001g0052 a0001c0002t0001g0239 a0001c0002t0001g0240 others(1): Show |
4 | HG01496.hp1 HG02055.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+448A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29358278 | |||||||
| chr22:29358316 | A | C | 1 | a0004c0013t0001g0129 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.525+410T>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29358316 | |||||||
| chr22:29358459 | T | C | 1 | a0001c0002t0001g0054 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.525+267A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 5/22 | chr22 | 29358459 | |||||||
| chr22:29359007 | G | A | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.280-36C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 4/22 | chr22 | 29359007 | |||||||
| chr22:29359480 | GA | G | 12 | a0001c0001t0001g0211 a0001c0004t0002g0021 a0001c0004t0002g0024 others(9): Show |
12 | HG02559.hp1 HG02647.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.279+343delT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 4/22 | chr22 | 29359480 | |||||||
| chr22:29359486 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.279+338C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 4/22 | chr22 | 29359486 | |||||||
| chr22:29359708 | G | A | 1 | a0001c0003t0003g0236 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.279+116C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 4/22 | chr22 | 29359708 | |||||||
| chr22:29359813 | C | T | 2 | a0001c0004t0002g0352 a0001c0004t0002g0353 |
2 | HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.279+11G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 4/22 | chr22 | 29359813 | |||||||
| chr22:29360181 | G | C | 1 | a0001c0003t0012g0347 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.144-222C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29360181 | |||||||
| chr22:29360305 | T | C | 1 | a0001c0003t0001g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.144-346A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29360305 | |||||||
| chr22:29360540 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.144-581G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29360540 | |||||||
| chr22:29360661 | A | G | 1 | a0001c0003t0012g0347 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.144-702T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29360661 | |||||||
| chr22:29360681 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.144-722A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29360681 | |||||||
| chr22:29360725 | C | T | 3 | a0001c0003t0004g0338 a0001c0003t0004g0339 a0001c0003t0004g0340 |
3 | HG02258.hp2 HG02895.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.144-766G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29360725 | |||||||
| chr22:29360737 | C | T | 11 | a0001c0003t0004g0335 a0001c0003t0004g0336 a0001c0003t0004g0337 others(8): Show |
11 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.144-778G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29360737 | |||||||
| chr22:29360847 | C | G | 15 | a0001c0003t0004g0343 a0001c0003t0004g0345 a0001c0003t0004g0346 others(12): Show |
15 | HG02055.hp2 HG02280.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.144-888G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29360847 | |||||||
| chr22:29360858 | T | C | 1 | a0001c0002t0001g0257 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.144-899A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29360858 | |||||||
| chr22:29360866 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG00544.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.144-907C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29360866 | |||||||
| chr22:29360871 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG00544.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.144-912A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29360871 | |||||||
| chr22:29360874 | G | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG00544.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.144-915C>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29360874 | |||||||
| chr22:29360875 | A | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG00544.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.144-916T>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29360875 | |||||||
| chr22:29360926 | C | T | 2 | a0001c0002t0001g0280 a0001c0002t0001g0281 |
2 | HG03490.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.144-967G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29360926 | |||||||
| chr22:29360993 | G | C | 8 | a0001c0002t0005g0259 a0001c0002t0005g0260 a0001c0002t0005g0294 others(5): Show |
8 | HG02080.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.144-1034C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29360993 | |||||||
| chr22:29361038 | G | A | 10 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(7): Show |
10 | HG00544.hp2 NA18747.hp2 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.144-1079C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29361038 | |||||||
| chr22:29361050 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0069 |
3 | HG01257.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.144-1091A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29361050 | |||||||
| chr22:29361051 | T | C | 18 | a0001c0003t0001g0022 a0001c0003t0001g0030 a0001c0003t0001g0031 others(15): Show |
18 | HG01243.hp2 HG02109.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.144-1092A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29361051 | |||||||
| chr22:29361052 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0069 |
3 | HG01257.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.144-1093T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29361052 | |||||||
| chr22:29361101 | C | T | 95 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(92): Show |
97 | HG00323.hp2 HG00544.hp2 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.144-1142G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29361101 | |||||||
| chr22:29361129 | G | T | 2 | a0001c0002t0001g0307 a0001c0002t0001g0330 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.144-1170C>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29361129 | |||||||
| chr22:29361158 | G | A | 3 | a0001c0002t0001g0052 a0001c0002t0001g0239 a0001c0002t0001g0240 |
3 | HG01496.hp1 HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.144-1199C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29361158 | |||||||
| chr22:29361253 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0046 others(42): Show |
50 | HG00140.hp1 HG00423.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.144-1294G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29361253 | |||||||
| chr22:29361273 | C | A | 1 | a0001c0002t0001g0332 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.144-1314G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29361273 | |||||||
| chr22:29361288 | C | T | 3 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0003t0001g0096 |
3 | HG03017.hp1 HG03942.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.144-1329G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29361288 | |||||||
| chr22:29361349 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.144-1390G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29361349 | |||||||
| chr22:29361391 | G | A | 8 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0135 others(5): Show |
8 | NA18944.hp2 NA18985.hp1 NA18989.hp2 others(5): Show |
intron_variant | MODIFIER | c.144-1432C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29361391 | |||||||
| chr22:29361428 | G | C | 1 | a0001c0002t0001g0310 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.144-1469C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29361428 | |||||||
| chr22:29361511 | AAAACTGT others(10): Show |
A | 1 | a0001c0001t0001g0104 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.143+1473_143+1489d others(19): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29361511 | |||||||
| chr22:29361569 | A | C | 9 | a0001c0003t0002g0036 a0001c0003t0002g0037 a0001c0003t0002g0097 others(6): Show |
9 | HG00323.hp2 HG02056.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.143+1432T>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29361569 | |||||||
| chr22:29361749 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.143+1252T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29361749 | |||||||
| chr22:29361800 | G | GT | 6 | a0001c0001t0001g0059 a0001c0001t0001g0106 a0001c0001t0001g0221 others(3): Show |
6 | HG02056.hp1 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.143+1200dupA | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29361800 | |||||||
| chr22:29361874 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0069 a0001c0001t0001g0077 |
4 | HG01257.hp2 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.143+1127T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29361874 | |||||||
| chr22:29361945 | C | G | 1 | a0001c0001t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.143+1056G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29361945 | |||||||
| chr22:29362038 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.143+963G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29362038 | |||||||
| chr22:29362039 | G | T | 13 | a0001c0003t0001g0093 a0001c0003t0001g0094 a0001c0003t0001g0095 others(10): Show |
13 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.143+962C>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29362039 | |||||||
| chr22:29362189 | C | T | 12 | a0001c0002t0001g0012 a0001c0002t0001g0253 a0001c0002t0001g0264 others(9): Show |
13 | HG00544.hp1 NA18944.hp1 NA18955.hp2 others(10): Show |
intron_variant | MODIFIER | c.143+812G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29362189 | |||||||
| chr22:29362225 | C | T | 38 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(35): Show |
40 | HG00544.hp2 HG00642.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.143+776G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29362225 | |||||||
| chr22:29362246 | C | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
190 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.143+755G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29362246 | |||||||
| chr22:29362376 | T | G | 1 | a0001c0001t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.143+625A>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29362376 | |||||||
| chr22:29362402 | A | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
190 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.143+599T>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29362402 | |||||||
| chr22:29362423 | TGCACCCT others(18): Show |
T | 1 | a0001c0001t0001g0143 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.143+553_143+577del others(25): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29362423 | |||||||
| chr22:29362431 | G | C | 13 | a0001c0003t0001g0093 a0001c0003t0001g0094 a0001c0003t0001g0095 others(10): Show |
13 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.143+570C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29362431 | |||||||
| chr22:29362499 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.143+502T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29362499 | |||||||
| chr22:29362591 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.143+410G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29362591 | |||||||
| chr22:29362627 | G | A | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.143+374C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29362627 | |||||||
| chr22:29362703 | G | A | 1 | a0001c0003t0002g0037 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.143+298C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29362703 | |||||||
| chr22:29362828 | A | G | 111 | a0001c0002t0001g0004 a0001c0002t0001g0011 a0001c0002t0001g0012 others(108): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.143+173T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29362828 | |||||||
| chr22:29362972 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.143+29A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29362972 | |||||||
| chr22:29362974 | G | T | 13 | a0001c0003t0001g0093 a0001c0003t0001g0094 a0001c0003t0001g0095 others(10): Show |
13 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.143+27C>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 3/22 | chr22 | 29362974 | |||||||
| chr22:29363199 | C | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.38-93G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29363199 | |||||||
| chr22:29363416 | G | A | 1 | a0001c0003t0002g0037 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.38-310C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29363416 | |||||||
| chr22:29363424 | C | T | 1 | a0001c0002t0001g0274 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.38-318G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29363424 | |||||||
| chr22:29363425 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.38-319C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29363425 | |||||||
| chr22:29363455 | C | G | 112 | a0001c0002t0001g0004 a0001c0002t0001g0011 a0001c0002t0001g0012 others(109): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.38-349G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29363455 | |||||||
| chr22:29363537 | A | G | 33 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0058 others(30): Show |
34 | HG00544.hp2 HG00642.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.38-431T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29363537 | |||||||
| chr22:29363594 | G | A | 2 | a0001c0003t0004g0338 a0001c0003t0004g0339 |
2 | HG02258.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.38-488C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29363594 | |||||||
| chr22:29363767 | T | C | 6 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0018 others(3): Show |
6 | HG02630.hp1 HG02896.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.38-661A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29363767 | |||||||
| chr22:29363777 | G | A | 1 | a0001c0003t0004g0337 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.38-671C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29363777 | |||||||
| chr22:29363897 | A | G | 1 | a0001c0003t0001g0056 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.38-791T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29363897 | |||||||
| chr22:29363938 | G | A | 8 | a0001c0002t0005g0259 a0001c0002t0005g0260 a0001c0002t0005g0294 others(5): Show |
8 | HG02080.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.38-832C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29363938 | |||||||
| chr22:29364150 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.38-1044T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29364150 | |||||||
| chr22:29364434 | T | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0220 |
3 | HG02257.hp2 HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.38-1328A>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29364434 | |||||||
| chr22:29364540 | TA | T | 5 | a0001c0004t0002g0349 a0001c0004t0002g0350 a0001c0004t0002g0352 others(2): Show |
5 | HG02809.hp2 HG03041.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.38-1435delT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29364540 | |||||||
| chr22:29364544 | G | A | 4 | a0001c0002t0001g0309 a0001c0002t0001g0310 a0001c0002t0001g0319 others(1): Show |
4 | HG00558.hp1 HG00673.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-1438C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29364544 | |||||||
| chr22:29364609 | G | T | 8 | a0001c0003t0002g0036 a0001c0003t0002g0097 a0001c0003t0002g0099 others(5): Show |
8 | HG00323.hp2 HG02056.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.38-1503C>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29364609 | |||||||
| chr22:29364660 | C | T | 7 | a0001c0003t0004g0335 a0001c0003t0004g0336 a0001c0003t0004g0337 others(4): Show |
7 | HG01243.hp2 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.38-1554G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29364660 | |||||||
| chr22:29364732 | A | G | 1 | a0001c0002t0001g0356 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.38-1626T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29364732 | |||||||
| chr22:29364733 | T | A | 1 | a0001c0002t0001g0356 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.38-1627A>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29364733 | |||||||
| chr22:29364771 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.38-1665G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29364771 | |||||||
| chr22:29364796 | C | A | 1 | a0001c0002t0001g0251 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.38-1690G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29364796 | |||||||
| chr22:29364835 | A | C | 1 | a0001c0003t0001g0056 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.38-1729T>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29364835 | |||||||
| chr22:29364839 | G | C | 3 | a0001c0001t0001g0106 a0001c0001t0001g0341 a0008c0012t0001g0015 |
3 | HG02886.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.38-1733C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29364839 | |||||||
| chr22:29364964 | C | G | 1 | a0001c0002t0001g0257 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.38-1858G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29364964 | |||||||
| chr22:29365243 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.37+1964G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29365243 | |||||||
| chr22:29365251 | A | C | 4 | a0001c0003t0004g0335 a0001c0003t0004g0336 a0001c0003t0004g0337 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+1956T>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29365251 | |||||||
| chr22:29365253 | C | A | 4 | a0001c0003t0004g0335 a0001c0003t0004g0336 a0001c0003t0004g0337 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+1954G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29365253 | |||||||
| chr22:29365487 | C | CA | 12 | a0001c0001t0001g0044 a0001c0001t0001g0126 a0001c0001t0001g0207 others(9): Show |
12 | HG00323.hp2 HG00741.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.37+1719dupT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29365487 | |||||||
| chr22:29365543 | C | G | 1 | a0001c0002t0001g0299 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.37+1664G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29365543 | |||||||
| chr22:29365589 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(84): Show |
95 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.37+1618G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29365589 | |||||||
| chr22:29365601 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.37+1606T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29365601 | |||||||
| chr22:29365661 | C | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.37+1546G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29365661 | |||||||
| chr22:29365863 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.37+1344C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29365863 | |||||||
| chr22:29365870 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.37+1337A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29365870 | |||||||
| chr22:29365967 | T | C | 1 | a0001c0002t0001g0330 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.37+1240A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29365967 | |||||||
| chr22:29365997 | T | G | 1 | a0001c0002t0001g0241 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.37+1210A>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29365997 | |||||||
| chr22:29366107 | G | T | 9 | a0001c0003t0002g0036 a0001c0003t0002g0037 a0001c0003t0002g0097 others(6): Show |
9 | HG00323.hp2 HG02056.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.37+1100C>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366107 | |||||||
| chr22:29366138 | G | C | 1 | a0001c0001t0001g0081 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.37+1069C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366138 | |||||||
| chr22:29366170 | G | A | 2 | a0001c0003t0001g0093 a0001c0003t0001g0095 |
2 | HG01109.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.37+1037C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366170 | |||||||
| chr22:29366173 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0212 |
3 | HG03139.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.37+1034C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366173 | |||||||
| chr22:29366236 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.37+971C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366236 | |||||||
| chr22:29366251 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.37+956C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366251 | |||||||
| chr22:29366380 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.37+827C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366380 | |||||||
| chr22:29366384 | T | A | 9 | a0001c0004t0002g0024 a0001c0004t0002g0025 a0001c0004t0002g0026 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.37+823A>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366384 | |||||||
| chr22:29366385 | C | T | 4 | a0001c0002t0005g0294 a0001c0002t0005g0306 a0001c0002t0005g0327 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+822G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366385 | |||||||
| chr22:29366410 | G | C | 9 | a0001c0004t0002g0024 a0001c0004t0002g0025 a0001c0004t0002g0026 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.37+797C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366410 | |||||||
| chr22:29366492 | C | T | 5 | a0001c0003t0004g0343 a0001c0003t0004g0345 a0001c0003t0004g0346 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.37+715G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366492 | |||||||
| chr22:29366493 | G | A | 1 | a0001c0003t0002g0037 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.37+714C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366493 | |||||||
| chr22:29366585 | C | T | 1 | a0001c0004t0002g0352 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.37+622G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366585 | |||||||
| chr22:29366703 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.37+504C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366703 | |||||||
| chr22:29366725 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.37+482T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366725 | |||||||
| chr22:29366801 | A | G | 4 | a0001c0003t0004g0343 a0001c0003t0004g0345 a0001c0003t0004g0346 others(1): Show |
4 | HG02055.hp2 HG02280.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+406T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366801 | |||||||
| chr22:29366833 | G | GAC | 54 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0105 others(51): Show |
58 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.37+372_37+373dupGT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366833 | |||||||
| chr22:29366833 | G | GACAC | 24 | a0001c0001t0001g0184 a0001c0001t0001g0198 a0001c0001t0001g0212 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.37+370_37+373dupGT others(2): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366833 | |||||||
| chr22:29366833 | G | GACACAC | 5 | a0001c0001t0001g0185 a0001c0002t0001g0241 a0001c0002t0001g0257 others(2): Show |
5 | HG02622.hp1 HG03017.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.37+368_37+373dupGT others(4): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366833 | |||||||
| chr22:29366833 | G | GACACACA others(1): Show |
4 | a0001c0001t0001g0195 a0001c0003t0002g0097 a0001c0003t0003g0236 others(1): Show |
4 | HG00323.hp2 HG01496.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+366_37+373dupGT others(6): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366833 | |||||||
| chr22:29366833 | GAC | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0023 others(77): Show |
86 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.37+372_37+373delGT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366833 | |||||||
| chr22:29366833 | GACAC | G | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(80): Show |
88 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.37+370_37+373delGT others(2): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366833 | |||||||
| chr22:29366833 | GACACAC | G | 9 | a0001c0001t0001g0159 a0001c0001t0001g0162 a0001c0001t0001g0172 others(6): Show |
9 | HG02015.hp2 HG02080.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.37+368_37+373delGT others(4): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366833 | |||||||
| chr22:29366833 | GACACACA others(1): Show |
G | 10 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0038 others(7): Show |
10 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.37+366_37+373delGT others(6): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366833 | |||||||
| chr22:29366833 | GACACACA others(3): Show |
G | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0237 |
3 | HG02451.hp2 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.37+364_37+373delGT others(8): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366833 | |||||||
| chr22:29366833 | GACACACA others(5): Show |
G | 3 | a0001c0003t0001g0030 a0001c0003t0001g0031 a0001c0003t0001g0033 |
3 | HG02109.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.37+362_37+373delGT others(10): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366833 | |||||||
| chr22:29366833 | GACACACA others(9): Show |
G | 2 | a0001c0001t0001g0122 a0001c0004t0002g0025 |
2 | HG02129.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.37+358_37+373delGT others(14): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366833 | |||||||
| chr22:29366833 | GACACACA others(11): Show |
G | 13 | a0001c0003t0004g0343 a0001c0003t0004g0345 a0001c0003t0004g0346 others(10): Show |
13 | HG02055.hp2 HG02280.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.37+356_37+373delGT others(16): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29366833 | |||||||
| chr22:29367085 | C | T | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0003t0001g0056 |
3 | HG02717.hp2 HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.37+122G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 2/22 | chr22 | 29367085 | |||||||
| chr22:29367338 | G | GGGA | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
261 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.-27-71_-27-69dupTC others(1): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29367338 | |||||||
| chr22:29367460 | AC | A | 3 | a0001c0001t0001g0167 a0001c0001t0001g0212 a0001c0001t0001g0222 |
3 | NA18906.hp1 NA18961.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.-27-191delG | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29367460 | |||||||
| chr22:29367461 | C | CT | 3 | a0001c0001t0001g0171 a0001c0003t0002g0101 a0001c0004t0002g0026 |
3 | HG02056.hp2 HG02647.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.-27-192_-27-191ins others(1): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29367461 | |||||||
| chr22:29367462 | C | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
196 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-27-192G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29367462 | |||||||
| chr22:29367478 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-27-208A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29367478 | |||||||
| chr22:29367597 | A | T | 5 | a0001c0003t0001g0022 a0001c0003t0001g0030 a0001c0003t0001g0031 others(2): Show |
5 | HG02109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-327T>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29367597 | |||||||
| chr22:29367933 | A | G | 4 | a0001c0003t0004g0335 a0001c0003t0004g0336 a0001c0003t0004g0337 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27-663T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29367933 | |||||||
| chr22:29368015 | G | A | 9 | a0001c0003t0002g0036 a0001c0003t0002g0037 a0001c0003t0002g0097 others(6): Show |
9 | HG00323.hp2 HG02056.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-27-745C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29368015 | |||||||
| chr22:29368478 | CTA | C | 8 | a0001c0002t0005g0259 a0001c0002t0005g0260 a0001c0002t0005g0294 others(5): Show |
8 | HG02080.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-27-1210_-27-1209d others(4): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29368478 | |||||||
| chr22:29368594 | C | T | 1 | a0001c0002t0001g0317 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-27-1324G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29368594 | |||||||
| chr22:29368708 | C | G | 8 | a0001c0002t0005g0259 a0001c0002t0005g0260 a0001c0002t0005g0294 others(5): Show |
8 | HG02080.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-27-1438G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29368708 | |||||||
| chr22:29368713 | T | TGACG | 13 | a0001c0003t0001g0093 a0001c0003t0001g0094 a0001c0003t0001g0095 others(10): Show |
13 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.-27-1447_-27-1444d others(6): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29368713 | |||||||
| chr22:29368756 | C | CA | 42 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0049 others(39): Show |
43 | HG00544.hp2 HG00642.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.-27-1487dupT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29368756 | |||||||
| chr22:29368756 | CA | C | 30 | a0001c0001t0001g0046 a0001c0001t0001g0105 a0001c0001t0001g0145 others(27): Show |
30 | HG00323.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.-27-1487delT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29368756 | |||||||
| chr22:29368847 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-27-1577T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29368847 | |||||||
| chr22:29368941 | C | CA | 19 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0063 others(16): Show |
20 | HG00408.hp1 HG00544.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.-27-1672dupT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29368941 | |||||||
| chr22:29369176 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-27-1906C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29369176 | |||||||
| chr22:29369392 | GAAGGAAT others(1): Show |
G | 4 | a0001c0001t0001g0070 a0001c0001t0007g0005 a0001c0001t0007g0071 others(1): Show |
5 | HG01192.hp1 HG02809.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27-2130_-27-2123d others(10): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29369392 | |||||||
| chr22:29369393 | A | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
255 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.-27-2123T>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29369393 | |||||||
| chr22:29369401 | A | T | 4 | a0001c0001t0001g0070 a0001c0001t0007g0005 a0001c0001t0007g0071 others(1): Show |
5 | HG01192.hp1 HG02809.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27-2131T>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29369401 | |||||||
| chr22:29369487 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-27-2217A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29369487 | |||||||
| chr22:29369535 | G | A | 13 | a0001c0003t0001g0093 a0001c0003t0001g0094 a0001c0003t0001g0095 others(10): Show |
13 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.-27-2265C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29369535 | |||||||
| chr22:29369622 | A | G | 1 | a0001c0002t0001g0296 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-27-2352T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29369622 | |||||||
| chr22:29369635 | G | A | 6 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0018 others(3): Show |
6 | HG02630.hp1 HG02896.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-2365C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29369635 | |||||||
| chr22:29369684 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-27-2414G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29369684 | |||||||
| chr22:29369686 | C | G | 5 | a0001c0002t0001g0309 a0001c0002t0001g0310 a0001c0002t0001g0315 others(2): Show |
5 | HG00558.hp1 HG00673.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-2416G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29369686 | |||||||
| chr22:29369716 | G | T | 1 | a0001c0001t0001g0204 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-27-2446C>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29369716 | |||||||
| chr22:29369755 | A | AGCCTCAG others(3): Show |
1 | a0001c0001t0001g0143 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-27-2495_-27-2486d others(12): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29369755 | |||||||
| chr22:29369837 | A | AT | 54 | a0001c0001t0001g0040 a0001c0001t0001g0061 a0001c0001t0001g0081 others(51): Show |
54 | HG00423.hp1 HG00544.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.-27-2568dupA | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29369837 | |||||||
| chr22:29369837 | AT | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(61): Show |
70 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.-27-2568delA | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29369837 | |||||||
| chr22:29369837 | ATT | A | 13 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0047 others(10): Show |
14 | HG00140.hp1 HG01074.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.-27-2569_-27-2568d others(4): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29369837 | |||||||
| chr22:29370175 | G | A | 2 | a0001c0001t0001g0082 a0001c0005t0001g0305 |
2 | HG00735.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-27-2905C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29370175 | |||||||
| chr22:29370178 | C | T | 13 | a0001c0003t0001g0093 a0001c0003t0001g0094 a0001c0003t0001g0095 others(10): Show |
13 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.-27-2908G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29370178 | |||||||
| chr22:29370315 | T | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-27-3045A>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29370315 | |||||||
| chr22:29370321 | C | T | 1 | a0001c0003t0001g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-27-3051G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29370321 | |||||||
| chr22:29370345 | C | T | 38 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(35): Show |
40 | HG00544.hp2 HG00642.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-27-3075G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29370345 | |||||||
| chr22:29370452 | C | CA | 70 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0040 others(67): Show |
75 | HG00280.hp1 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.-27-3183dupT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29370452 | |||||||
| chr22:29370452 | CA | C | 6 | a0001c0001t0001g0043 a0001c0001t0001g0167 a0001c0002t0001g0053 others(3): Show |
6 | HG01496.hp1 NA18522.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.-27-3183delT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29370452 | |||||||
| chr22:29370466 | A | AAAAAAGA others(3): Show |
1 | a0001c0003t0002g0101 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-27-3197_-27-3196i others(12): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29370466 | |||||||
| chr22:29370466 | A | AAAAAGAA others(2): Show |
7 | a0001c0003t0002g0037 a0001c0003t0002g0097 a0001c0003t0002g0099 others(4): Show |
7 | HG00323.hp2 HG02071.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-27-3197_-27-3196i others(11): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29370466 | |||||||
| chr22:29370466 | A | AAAAAGAA others(6): Show |
1 | a0001c0003t0002g0036 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-27-3197_-27-3196i others(15): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29370466 | |||||||
| chr22:29370753 | A | C | 7 | a0001c0003t0004g0335 a0001c0003t0004g0336 a0001c0003t0004g0337 others(4): Show |
7 | HG01243.hp2 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-27-3483T>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29370753 | |||||||
| chr22:29370795 | T | C | 2 | a0001c0003t0004g0335 a0001c0003t0012g0347 |
2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-27-3525A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29370795 | |||||||
| chr22:29370906 | C | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
260 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.-27-3636G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29370906 | |||||||
| chr22:29370959 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-27-3689C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29370959 | |||||||
| chr22:29370977 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0042 others(68): Show |
77 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.-27-3707C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29370977 | |||||||
| chr22:29370981 | T | C | 1 | a0001c0004t0002g0350 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-27-3711A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29370981 | |||||||
| chr22:29371045 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
200 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.-27-3775T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29371045 | |||||||
| chr22:29371101 | T | C | 5 | a0001c0003t0004g0343 a0001c0003t0004g0345 a0001c0003t0004g0346 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-3831A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29371101 | |||||||
| chr22:29371573 | TA | T | 8 | a0001c0003t0002g0036 a0001c0003t0002g0097 a0001c0003t0002g0099 others(5): Show |
8 | HG00323.hp2 HG02056.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-27-4304delT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29371573 | |||||||
| chr22:29371901 | G | A | 1 | a0001c0002t0001g0302 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-27-4631C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29371901 | |||||||
| chr22:29371902 | A | T | 1 | a0001c0002t0001g0302 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-27-4632T>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29371902 | |||||||
| chr22:29371903 | T | C | 1 | a0001c0002t0001g0302 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-27-4633A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29371903 | |||||||
| chr22:29371936 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-27-4666T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29371936 | |||||||
| chr22:29372401 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0192 a0001c0001t0001g0193 others(3): Show |
7 | HG02145.hp2 HG02965.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-27-5131C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29372401 | |||||||
| chr22:29372424 | C | CA | 7 | a0001c0001t0010g0014 a0001c0002t0001g0249 a0001c0002t0001g0257 others(4): Show |
7 | HG00741.hp1 HG01928.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-27-5155dupT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29372424 | |||||||
| chr22:29372424 | CA | C | 26 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0058 others(23): Show |
27 | HG01257.hp2 HG01515.hp1 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.-27-5155delT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29372424 | |||||||
| chr22:29372485 | T | C | 1 | a0001c0001t0001g0194 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-27-5215A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29372485 | |||||||
| chr22:29372665 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-27-5395G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29372665 | |||||||
| chr22:29373007 | G | A | 1 | a0001c0002t0001g0257 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-27-5737C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29373007 | |||||||
| chr22:29373100 | A | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.-27-5830T>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29373100 | |||||||
| chr22:29373317 | C | A | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(264): Show |
281 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.-27-6047G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29373317 | |||||||
| chr22:29373340 | T | G | 1 | a0001c0003t0004g0335 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-27-6070A>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29373340 | |||||||
| chr22:29373540 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-27-6270C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29373540 | |||||||
| chr22:29373619 | A | T | 1 | a0001c0004t0002g0024 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-27-6349T>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29373619 | |||||||
| chr22:29373637 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
200 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.-27-6367T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29373637 | |||||||
| chr22:29373700 | C | T | 14 | a0001c0003t0004g0343 a0001c0003t0004g0345 a0001c0003t0004g0346 others(11): Show |
14 | HG02055.hp2 HG02280.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.-27-6430G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29373700 | |||||||
| chr22:29373710 | C | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-27-6440G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29373710 | |||||||
| chr22:29373887 | G | C | 4 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0087 others(1): Show |
4 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27-6617C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29373887 | |||||||
| chr22:29373965 | A | AG | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.-27-6696dupC | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29373965 | |||||||
| chr22:29373975 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-27-6705T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29373975 | |||||||
| chr22:29374230 | C | T | 2 | a0003c0006t0005g0303 a0003c0006t0005g0304 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-27-6960G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29374230 | |||||||
| chr22:29374285 | G | GAAAT | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
261 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.-27-7016_-27-7015i others(6): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29374285 | |||||||
| chr22:29374559 | GA | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.-27-7290delT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29374559 | |||||||
| chr22:29374810 | T | C | 1 | a0001c0002t0001g0295 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-27-7540A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29374810 | |||||||
| chr22:29374984 | C | A | 1 | a0001c0001t0001g0354 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-27-7714G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29374984 | |||||||
| chr22:29374989 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-27-7719G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29374989 | |||||||
| chr22:29374996 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-27-7726G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29374996 | |||||||
| chr22:29375207 | C | CG | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
207 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.-27-7938dupC | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29375207 | |||||||
| chr22:29375339 | G | GATT | 6 | a0001c0003t0002g0036 a0001c0003t0002g0099 a0001c0003t0002g0100 others(3): Show |
6 | HG02056.hp2 HG02071.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-8072_-27-8070d others(5): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29375339 | |||||||
| chr22:29375349 | C | CA | 17 | a0001c0002t0001g0055 a0001c0002t0001g0261 a0001c0002t0001g0296 others(14): Show |
17 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(14): Show |
intron_variant | MODIFIER | c.-27-8080dupT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29375349 | |||||||
| chr22:29375349 | CA | C | 18 | a0001c0001t0001g0082 a0001c0001t0001g0106 a0001c0001t0001g0341 others(15): Show |
18 | HG00735.hp2 HG01169.hp1 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.-27-8080delT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29375349 | |||||||
| chr22:29375349 | CAA | C | 57 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0049 others(54): Show |
59 | HG00597.hp1 HG01099.hp2 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.-27-8081_-27-8080d others(4): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29375349 | |||||||
| chr22:29375349 | CAAA | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
186 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-27-8082_-27-8080d others(5): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29375349 | |||||||
| chr22:29375349 | CAAAA | C | 8 | a0001c0001t0001g0105 a0001c0001t0001g0109 a0001c0001t0001g0110 others(5): Show |
8 | HG00639.hp2 HG01099.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.-27-8083_-27-8080d others(6): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29375349 | |||||||
| chr22:29375568 | G | A | 1 | a0002c0007t0001g0009 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-27-8298C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29375568 | |||||||
| chr22:29375792 | T | C | 5 | a0001c0003t0004g0343 a0001c0003t0004g0345 a0001c0003t0004g0346 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-8522A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29375792 | |||||||
| chr22:29375884 | C | T | 5 | a0001c0003t0004g0343 a0001c0003t0004g0345 a0001c0003t0004g0346 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-8614G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29375884 | |||||||
| chr22:29375891 | T | G | 1 | a0001c0003t0001g0093 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-27-8621A>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29375891 | |||||||
| chr22:29375923 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-27-8653G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29375923 | |||||||
| chr22:29376147 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0198 |
2 | HG00423.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.-27-8877G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29376147 | |||||||
| chr22:29376272 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0218 |
2 | NA19011.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-27-9002T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29376272 | |||||||
| chr22:29376402 | G | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
262 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.-27-9132C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29376402 | |||||||
| chr22:29376434 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-27-9164T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29376434 | |||||||
| chr22:29376492 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-27-9222A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29376492 | |||||||
| chr22:29376656 | TG | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-27-9387delC | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29376656 | |||||||
| chr22:29376665 | A | G | 9 | a0001c0003t0002g0036 a0001c0003t0002g0037 a0001c0003t0002g0097 others(6): Show |
9 | HG00323.hp2 HG02056.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-27-9395T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29376665 | |||||||
| chr22:29376808 | G | A | 3 | a0001c0003t0004g0338 a0001c0003t0004g0339 a0001c0003t0004g0340 |
3 | HG02258.hp2 HG02895.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-27-9538C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29376808 | |||||||
| chr22:29376862 | C | T | 4 | a0001c0002t0001g0052 a0001c0002t0001g0239 a0001c0002t0001g0240 others(1): Show |
4 | HG01496.hp1 HG02055.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27-9592G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29376862 | |||||||
| chr22:29376873 | ACTC | A | 5 | a0001c0003t0001g0022 a0001c0003t0001g0030 a0001c0003t0001g0031 others(2): Show |
5 | HG02109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-9606_-27-9604d others(5): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29376873 | |||||||
| chr22:29377048 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-27-9778A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29377048 | |||||||
| chr22:29377111 | G | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
84 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.-27-9841C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29377111 | |||||||
| chr22:29377195 | C | CA | 17 | a0001c0001t0001g0034 a0001c0001t0001g0079 a0001c0003t0001g0066 others(14): Show |
17 | HG00323.hp2 HG01346.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-27-9926dupT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29377195 | |||||||
| chr22:29377195 | CA | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.-27-9926delT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29377195 | |||||||
| chr22:29377195 | CAA | C | 15 | a0001c0001t0001g0043 a0001c0001t0001g0102 a0001c0001t0001g0105 others(12): Show |
15 | HG01169.hp1 HG01255.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.-27-9927_-27-9926d others(4): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29377195 | |||||||
| chr22:29377336 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-27-10066A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29377336 | |||||||
| chr22:29377351 | G | A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0225 |
3 | HG00609.hp2 NA18975.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.-27-10081C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29377351 | |||||||
| chr22:29377810 | C | CA | 6 | a0001c0001t0001g0080 a0001c0001t0001g0209 a0001c0002t0001g0315 others(3): Show |
6 | HG01255.hp1 HG02109.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-27-10541dupT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29377810 | |||||||
| chr22:29377810 | CA | C | 12 | a0001c0001t0001g0069 a0001c0001t0001g0117 a0001c0001t0001g0159 others(9): Show |
12 | HG01257.hp2 HG02647.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27-10541delT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29377810 | |||||||
| chr22:29377880 | A | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
267 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.-28+10544T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29377880 | |||||||
| chr22:29377957 | C | G | 1 | a0001c0001t0001g0068 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-28+10467G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29377957 | |||||||
| chr22:29378136 | A | AGGGCC | 5 | a0001c0004t0002g0349 a0001c0004t0002g0350 a0001c0004t0002g0352 others(2): Show |
5 | HG02809.hp2 HG03041.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28+10283_-28+1028 others(9): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29378136 | |||||||
| chr22:29378278 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-28+10146G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29378278 | |||||||
| chr22:29378307 | A | C | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG00408.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.-28+10117T>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29378307 | |||||||
| chr22:29378552 | C | CA | 26 | a0001c0001t0001g0034 a0001c0001t0001g0081 a0001c0001t0001g0082 others(23): Show |
26 | HG00323.hp2 HG00673.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.-28+9871dupT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29378552 | |||||||
| chr22:29378552 | C | CAA | 6 | a0001c0001t0001g0083 a0001c0002t0001g0238 a0001c0003t0001g0094 others(3): Show |
6 | HG02056.hp2 HG02071.hp1 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28+9870_-28+9871d others(4): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29378552 | |||||||
| chr22:29378552 | CA | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(84): Show |
95 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.-28+9871delT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29378552 | |||||||
| chr22:29378552 | CAA | C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(73): Show |
80 | HG00280.hp1 HG00558.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.-28+9870_-28+9871d others(4): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29378552 | |||||||
| chr22:29378552 | CAAA | C | 7 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0038 others(4): Show |
7 | HG00099.hp1 HG00642.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.-28+9869_-28+9871d others(5): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29378552 | |||||||
| chr22:29378585 | C | G | 1 | a0001c0001t0001g0042 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-28+9839G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29378585 | |||||||
| chr22:29378630 | C | T | 1 | a0001c0004t0002g0342 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-28+9794G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29378630 | |||||||
| chr22:29378675 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0115 |
2 | HG02165.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-28+9749G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29378675 | |||||||
| chr22:29378747 | T | C | 112 | a0001c0002t0001g0004 a0001c0002t0001g0011 a0001c0002t0001g0012 others(109): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.-28+9677A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29378747 | |||||||
| chr22:29378860 | CA | C | 122 | a0001c0001t0001g0010 a0001c0001t0001g0108 a0001c0001t0001g0146 others(119): Show |
127 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.-28+9563delT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29378860 | |||||||
| chr22:29378860 | CAA | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.-28+9562_-28+9563d others(4): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29378860 | |||||||
| chr22:29378860 | CAAA | C | 14 | a0001c0003t0001g0093 a0001c0003t0001g0094 a0001c0003t0001g0095 others(11): Show |
14 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-28+9561_-28+9563d others(5): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29378860 | |||||||
| chr22:29378899 | A | G | 6 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0018 others(3): Show |
6 | HG02630.hp1 HG02896.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+9525T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29378899 | |||||||
| chr22:29379018 | G | C | 6 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0018 others(3): Show |
6 | HG02630.hp1 HG02896.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+9406C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29379018 | |||||||
| chr22:29379034 | C | A | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.-28+9390G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29379034 | |||||||
| chr22:29379111 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-28+9313A>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29379111 | |||||||
| chr22:29379151 | C | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-28+9273G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29379151 | |||||||
| chr22:29379223 | C | T | 4 | a0001c0002t0001g0052 a0001c0002t0001g0239 a0001c0002t0001g0240 others(1): Show |
4 | HG01496.hp1 HG02055.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28+9201G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29379223 | |||||||
| chr22:29379288 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-28+9136G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29379288 | |||||||
| chr22:29379350 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-28+9074C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29379350 | |||||||
| chr22:29379615 | C | T | 5 | a0001c0004t0002g0349 a0001c0004t0002g0350 a0001c0004t0002g0352 others(2): Show |
5 | HG02809.hp2 HG03041.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28+8809G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29379615 | |||||||
| chr22:29379629 | G | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
84 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.-28+8795C>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29379629 | |||||||
| chr22:29379680 | A | G | 1 | a0001c0002t0001g0241 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-28+8744T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29379680 | |||||||
| chr22:29379760 | A | G | 6 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0018 others(3): Show |
6 | HG02630.hp1 HG02896.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+8664T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29379760 | |||||||
| chr22:29379808 | C | T | 5 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(2): Show |
5 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28+8616G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29379808 | |||||||
| chr22:29379851 | G | A | 13 | a0001c0003t0001g0093 a0001c0003t0001g0094 a0001c0003t0001g0095 others(10): Show |
13 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.-28+8573C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29379851 | |||||||
| chr22:29380047 | G | A | 1 | a0001c0002t0001g0316 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-28+8377C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29380047 | |||||||
| chr22:29380061 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-28+8363A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29380061 | |||||||
| chr22:29380226 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-28+8198G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29380226 | |||||||
| chr22:29380334 | C | G | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0028 others(68): Show |
75 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.-28+8090G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29380334 | |||||||
| chr22:29380353 | G | A | 2 | a0001c0002t0001g0317 a0001c0002t0001g0318 |
2 | HG00323.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.-28+8071C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29380353 | |||||||
| chr22:29380354 | A | C | 13 | a0001c0003t0001g0093 a0001c0003t0001g0094 a0001c0003t0001g0095 others(10): Show |
13 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.-28+8070T>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29380354 | |||||||
| chr22:29380360 | C | T | 4 | a0001c0004t0002g0024 a0001c0004t0002g0025 a0001c0004t0002g0026 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28+8064G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29380360 | |||||||
| chr22:29380414 | CG | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(242): Show |
259 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.-28+8009delC | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29380414 | |||||||
| chr22:29380437 | T | C | 1 | a0001c0003t0001g0095 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-28+7987A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29380437 | |||||||
| chr22:29380510 | G | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0220 |
3 | HG02257.hp2 HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-28+7914C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29380510 | |||||||
| chr22:29380554 | T | A | 1 | a0001c0001t0001g0035 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-28+7870A>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29380554 | |||||||
| chr22:29380587 | C | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG00673.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.-28+7837G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29380587 | |||||||
| chr22:29380673 | G | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | NA18960.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-28+7751C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29380673 | |||||||
| chr22:29380755 | C | A | 1 | a0001c0003t0002g0037 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-28+7669G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29380755 | |||||||
| chr22:29380759 | C | T | 6 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0018 others(3): Show |
6 | HG02630.hp1 HG02896.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+7665G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29380759 | |||||||
| chr22:29380858 | C | A | 1 | a0001c0003t0002g0036 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-28+7566G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29380858 | |||||||
| chr22:29380868 | C | T | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0028 others(68): Show |
75 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.-28+7556G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29380868 | |||||||
| chr22:29380892 | A | T | 10 | a0001c0003t0003g0090 a0001c0003t0003g0091 a0001c0003t0003g0092 others(7): Show |
10 | HG01099.hp2 HG01243.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.-28+7532T>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29380892 | |||||||
| chr22:29380955 | T | C | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-28+7469A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29380955 | |||||||
| chr22:29381021 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-28+7403G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29381021 | |||||||
| chr22:29381302 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-28+7122T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29381302 | |||||||
| chr22:29381515 | C | T | 51 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
53 | HG00544.hp2 HG00642.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.-28+6909G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29381515 | |||||||
| chr22:29381592 | C | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-28+6832G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29381592 | |||||||
| chr22:29381727 | G | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0341 a0008c0012t0001g0015 |
3 | HG02886.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-28+6697C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29381727 | |||||||
| chr22:29381990 | G | T | 1 | a0001c0003t0001g0030 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-28+6434C>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29381990 | |||||||
| chr22:29382007 | C | T | 8 | a0001c0003t0002g0037 a0001c0003t0002g0097 a0001c0003t0002g0099 others(5): Show |
8 | HG00323.hp2 HG02056.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28+6417G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29382007 | |||||||
| chr22:29382029 | A | T | 5 | a0001c0003t0001g0022 a0001c0003t0001g0030 a0001c0003t0001g0031 others(2): Show |
5 | HG02109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28+6395T>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29382029 | |||||||
| chr22:29382081 | T | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
199 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.-28+6343A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29382081 | |||||||
| chr22:29382148 | C | T | 1 | a0001c0003t0002g0037 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-28+6276G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29382148 | |||||||
| chr22:29382391 | C | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0341 a0008c0012t0001g0015 |
3 | HG02886.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-28+6033G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29382391 | |||||||
| chr22:29382426 | C | T | 1 | a0001c0002t0001g0256 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-28+5998G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29382426 | |||||||
| chr22:29382463 | G | C | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(344): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.-28+5961C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29382463 | |||||||
| chr22:29382730 | C | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.-28+5694G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29382730 | |||||||
| chr22:29383128 | G | A | 2 | a0001c0002t0001g0319 a0001c0002t0001g0320 |
2 | HG00558.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-28+5296C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29383128 | |||||||
| chr22:29383217 | G | A | 2 | a0001c0001t0008g0215 a0001c0001t0008g0227 |
2 | NA18949.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-28+5207C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29383217 | |||||||
| chr22:29383297 | G | C | 1 | a0001c0002t0001g0255 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-28+5127C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29383297 | |||||||
| chr22:29383448 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.-28+4976G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29383448 | |||||||
| chr22:29383507 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-28+4917C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29383507 | |||||||
| chr22:29383526 | C | A | 1 | a0001c0001t0001g0216 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-28+4898G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29383526 | |||||||
| chr22:29383570 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-28+4854C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29383570 | |||||||
| chr22:29383633 | T | C | 1 | a0001c0002t0001g0255 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-28+4791A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29383633 | |||||||
| chr22:29383634 | G | T | 1 | a0001c0002t0001g0255 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-28+4790C>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29383634 | |||||||
| chr22:29383686 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-28+4738C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29383686 | |||||||
| chr22:29383690 | C | CA | 15 | a0001c0002t0001g0055 a0001c0002t0001g0238 a0001c0002t0001g0321 others(12): Show |
15 | HG01081.hp1 HG01109.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-28+4733dupT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29383690 | |||||||
| chr22:29383690 | CA | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
238 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.-28+4733delT | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29383690 | |||||||
| chr22:29383690 | CAA | C | 7 | a0001c0001t0001g0038 a0001c0001t0001g0104 a0001c0001t0001g0105 others(4): Show |
7 | HG00099.hp1 HG02735.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-28+4732_-28+4733d others(4): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29383690 | |||||||
| chr22:29383754 | A | G | 1 | a0001c0002t0001g0253 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-28+4670T>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29383754 | |||||||
| chr22:29383895 | T | C | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(344): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.-28+4529A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29383895 | |||||||
| chr22:29384089 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-28+4335C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29384089 | |||||||
| chr22:29384093 | C | A | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG00408.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.-28+4331G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29384093 | |||||||
| chr22:29384266 | G | C | 1 | a0008c0012t0001g0015 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-28+4158C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29384266 | |||||||
| chr22:29384497 | G | A | 8 | a0001c0003t0002g0037 a0001c0003t0002g0097 a0001c0003t0002g0099 others(5): Show |
8 | HG00323.hp2 HG02056.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28+3927C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29384497 | |||||||
| chr22:29384543 | G | A | 1 | a0001c0003t0001g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-28+3881C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29384543 | |||||||
| chr22:29384561 | C | T | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-28+3863G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29384561 | |||||||
| chr22:29384643 | G | C | 4 | a0001c0004t0002g0024 a0001c0004t0002g0025 a0001c0004t0002g0026 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28+3781C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29384643 | |||||||
| chr22:29384666 | G | A | 1 | a0001c0002t0001g0356 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-28+3758C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29384666 | |||||||
| chr22:29384823 | G | A | 38 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(35): Show |
40 | HG00544.hp2 HG00642.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-28+3601C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29384823 | |||||||
| chr22:29384895 | A | T | 38 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(35): Show |
40 | HG00544.hp2 HG00642.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-28+3529T>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29384895 | |||||||
| chr22:29385137 | C | T | 3 | a0001c0002t0001g0052 a0001c0002t0001g0239 a0001c0002t0001g0240 |
3 | HG01496.hp1 HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-28+3287G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29385137 | |||||||
| chr22:29385456 | T | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-28+2968A>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29385456 | |||||||
| chr22:29385624 | C | T | 1 | a0001c0002t0001g0238 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-28+2800G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29385624 | |||||||
| chr22:29385811 | T | C | 7 | a0001c0003t0003g0231 a0001c0003t0003g0232 a0001c0003t0003g0233 others(4): Show |
7 | HG01243.hp1 HG01496.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-28+2613A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29385811 | |||||||
| chr22:29386101 | C | A | 1 | a0001c0003t0001g0056 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-28+2323G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29386101 | |||||||
| chr22:29386350 | G | C | 1 | a0001c0001t0001g0237 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-28+2074C>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29386350 | |||||||
| chr22:29386444 | A | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
267 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.-28+1980T>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29386444 | |||||||
| chr22:29386555 | G | A | 1 | a0001c0003t0001g0056 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-28+1869C>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29386555 | |||||||
| chr22:29386654 | A | T | 10 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(7): Show |
10 | HG00544.hp2 NA18747.hp2 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.-28+1770T>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29386654 | |||||||
| chr22:29386720 | C | T | 1 | a0001c0010t0003g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-28+1704G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29386720 | |||||||
| chr22:29387305 | C | CT | 26 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0034 others(23): Show |
26 | HG00099.hp1 HG00642.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.-28+1118dupA | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29387305 | |||||||
| chr22:29387305 | CT | C | 15 | a0001c0001t0001g0334 a0001c0001t0001g0341 a0001c0002t0001g0348 others(12): Show |
15 | HG01070.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-28+1118delA | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29387305 | |||||||
| chr22:29387456 | C | T | 5 | a0001c0003t0001g0022 a0001c0003t0001g0030 a0001c0003t0001g0031 others(2): Show |
5 | HG02109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28+968G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29387456 | |||||||
| chr22:29387509 | T | C | 10 | a0001c0001t0001g0023 a0001c0004t0002g0024 a0001c0004t0002g0025 others(7): Show |
10 | HG01891.hp1 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-28+915A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29387509 | |||||||
| chr22:29387669 | T | C | 1 | a0001c0001t0015g0357 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-28+755A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29387669 | |||||||
| chr22:29387689 | G | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG00642.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-28+735C>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29387689 | |||||||
| chr22:29387772 | T | C | 1 | a0001c0001t0001g0354 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-28+652A>G | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29387772 | |||||||
| chr22:29388054 | A | AATC | 5 | a0001c0001t0001g0023 a0001c0004t0002g0024 a0001c0004t0002g0025 others(2): Show |
5 | HG01891.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28+369_-28+370ins others(3): Show |
AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29388054 | |||||||
| chr22:29388090 | C | A | 1 | a0001c0001t0001g0355 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-28+334G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29388090 | |||||||
| chr22:29388160 | G | T | 1 | a0001c0003t0001g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-28+264C>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29388160 | |||||||
| chr22:29388181 | C | T | 6 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0018 others(3): Show |
6 | HG02630.hp1 HG02896.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+243G>A | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29388181 | |||||||
| chr22:29388274 | C | A | 1 | a0001c0002t0001g0356 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-28+150G>T | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29388274 | |||||||
| chr22:29388374 | C | G | 1 | a0008c0012t0001g0015 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-28+50G>C | AP1B1 | ENSG00000100280.17 | transcript | ENST00000357586.7 | protein_coding | 1/22 | chr22 | 29388374 |