Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 128989 |
| ensemblid | ENSG00000183597.16 |
| hgncid | 25439 |
| symbol | TANGO2 |
| name | transport and golgi organization 2 homolog |
| refseq_nuc | NM_152906.7 |
| refseq_prot | NP_690870.3 |
| ensembl_nuc | ENST00000327374.9 |
| ensembl_prot | ENSP00000332721.4 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 20021110 |
| end | 20067164 |
| strand | + |
| ver | v1.2 |
| region | chr22:20021110-20067164 |
| region5000 | chr22:20016110-20072164 |
| regionname0 | TANGO2_chr22_20021110_20067164 |
| regionname5000 | TANGO2_chr22_20016110_20072164 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 276 | 375 | 86 | 65 | 158 | 18 | 46 | 116 | TANGO2_chr22_20016110_20072164 | TANGO2 | MCIIF others(271): Show |
chr22 | 20016110 | 20072164 |
| a0002 | 0/0 | 276 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | MCIIF others(271): Show |
chr22 | 20016110 | 20072164 |
| a0003 | 0/0 | 276 | 5 | 3 | 2 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | MCIIF others(271): Show |
chr22 | 20016110 | 20072164 |
| a0004 | 0/0 | 276 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | MCIIF others(271): Show |
chr22 | 20016110 | 20072164 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 828 | 358 | 71 | 65 | 157 | 18 | 45 | TANGO2_chr22_20016110_20072164 | TANGO2 | ATGTG others(823): Show |
chr22 | 20016110 | 20072164 | ||
| a0001c0002 | 0/0 | 828 | 14 | 14 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | ATGTG others(823): Show |
chr22 | 20016110 | 20072164 | ||
| a0001c0005 | 0/0 | 828 | 2 | 1 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | ATGTG others(823): Show |
chr22 | 20016110 | 20072164 | ||
| a0001c0008 | 0/0 | 828 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | ATGTG others(823): Show |
chr22 | 20016110 | 20072164 | ||
| a0002c0003 | 0/0 | 828 | 10 | 10 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | ATGTG others(823): Show |
chr22 | 20016110 | 20072164 | ||
| a0002c0007 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | ATGTG others(823): Show |
chr22 | 20016110 | 20072164 | ||
| a0003c0004 | 0/0 | 828 | 5 | 3 | 2 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | ATGTG others(823): Show |
chr22 | 20016110 | 20072164 | ||
| a0004c0006 | 0/0 | 828 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | ATGTG others(823): Show |
chr22 | 20016110 | 20072164 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3509 | 87 | 19 | 17 | 34 | 7 | 9 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0002 | 0/0 | 3509 | 75 | 27 | 9 | 26 | 3 | 10 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0003 | 0/0 | 3509 | 58 | 0 | 13 | 38 | 3 | 4 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0004 | 0/1 | 3508 | 25 | 0 | 8 | 6 | 2 | 8 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3503): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0005 | 0/0 | 3509 | 19 | 0 | 1 | 18 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0006 | 0/0 | 3509 | 17 | 3 | 3 | 11 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0007 | 0/0 | 3509 | 14 | 1 | 1 | 12 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0008 | 0/0 | 3509 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0009 | 0/0 | 3509 | 10 | 3 | 1 | 3 | 0 | 3 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0011 | 0/0 | 3509 | 6 | 0 | 0 | 1 | 1 | 4 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0012 | 0/0 | 3508 | 6 | 0 | 3 | 2 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3503): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0013 | 0/0 | 3509 | 5 | 5 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0015 | 0/0 | 3509 | 5 | 1 | 2 | 1 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0016 | 0/0 | 3509 | 4 | 0 | 4 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0017 | 0/0 | 3509 | 3 | 0 | 1 | 0 | 2 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0019 | 0/0 | 3509 | 3 | 3 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0020 | 0/0 | 3509 | 2 | 0 | 2 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0021 | 0/0 | 3509 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0022 | 0/0 | 3509 | 2 | 0 | 0 | 0 | 0 | 2 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0023 | 0/0 | 3509 | 2 | 2 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0025 | 0/0 | 3509 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0026 | 0/0 | 3509 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0027 | 0/0 | 3509 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0028 | 0/0 | 3509 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0030 | 0/0 | 3537 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3532): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0031 | 0/0 | 3509 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0032 | 0/0 | 3509 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0033 | 0/0 | 3509 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0034 | 0/0 | 3509 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0036 | 0/0 | 3509 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0037 | 0/0 | 3509 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0038 | 0/0 | 3509 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0001t0039 | 0/0 | 3509 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0002t0008 | 0/0 | 3509 | 10 | 10 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0002t0021 | 0/0 | 3509 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0002t0024 | 0/0 | 3509 | 2 | 2 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0002t0029 | 0/0 | 3509 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0005t0001 | 0/0 | 3509 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0005t0002 | 0/0 | 3509 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0001c0008t0001 | 0/0 | 3509 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0002c0003t0010 | 0/0 | 3509 | 7 | 7 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0002c0003t0018 | 0/0 | 3509 | 3 | 3 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0002c0007t0035 | 0/0 | 3509 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0003c0004t0014 | 0/0 | 3509 | 5 | 3 | 2 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3504): Show |
chr22 | 20016110 | 20072164 |
| a0004c0006t0004 | 0/0 | 3508 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | GAAGT others(3503): Show |
chr22 | 20016110 | 20072164 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 2 | 0 | 3 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0128 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0001 | 0/0 | 11 | 0 | 2 | 7 | 1 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0320 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0005g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0005g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0005g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0005g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0005g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0005g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0006g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0006g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0006g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0006g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0007g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0007g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0007g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0007g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0007g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0007g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0007g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0007g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0007g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0007g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0008g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0009g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0009g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0009g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0009g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0009g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0009g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0009g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0009g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0009g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0009g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0011g0005 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0011g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0011g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0011g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0012g0009 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0012g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0012g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0012g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0013g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0013g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0013g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0013g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0013g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0015g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0015g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0015g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0015g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0016g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0016g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0016g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0017g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0017g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0017g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0019g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0019g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0019g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0020g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0020g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0021g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0022g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0022g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0023g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0023g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0025g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0026g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0027g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0028g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0030g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0031g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0032g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0033g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0034g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0036g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0037g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0038g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0001t0039g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0002t0008g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0002t0008g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0002t0008g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0002t0008g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0002t0008g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0002t0008g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0002t0008g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0002t0008g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0002t0008g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0002t0021g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0002t0024g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0002t0024g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0002t0029g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0005t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0005t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0001c0008t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0002c0003t0010g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0002c0003t0010g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0002c0003t0010g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0002c0003t0010g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0002c0003t0010g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0002c0003t0010g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0002c0003t0010g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0002c0003t0018g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0002c0003t0018g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0002c0003t0018g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0002c0007t0035g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0003c0004t0014g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0003c0004t0014g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0003c0004t0014g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0003c0004t0014g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| a0004c0006t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0271 | EUR | GBR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0028 | EUR | GBR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0072 | EUR | GBR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | FIN | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0120 | EUR | FIN | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00423 | hp1 | a0001 | c0001 | t0011 | g0101 | EAS | CHS | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | CHS | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00438 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | CHS | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00544 | hp1 | a0001 | c0001 | t0038 | g0244 | EAS | CHS | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | CHS | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00597 | hp1 | a0001 | c0001 | t0037 | g0293 | EAS | CHS | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | CHS | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | CHS | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00609 | hp2 | a0001 | c0001 | t0006 | g0133 | EAS | CHS | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00621 | hp1 | a0001 | c0001 | t0005 | g0243 | EAS | CHS | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | CHS | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0058 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0330 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0029 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00673 | hp1 | a0001 | c0001 | t0034 | g0285 | EAS | CHS | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00673 | hp2 | a0001 | c0001 | t0005 | g0303 | EAS | CHS | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0065 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0061 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0191 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0273 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00741 | hp1 | a0001 | c0001 | t0017 | g0232 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0328 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0069 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01069 | hp2 | a0001 | c0001 | t0007 | g0223 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0325 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0326 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0070 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01074 | hp1 | a0001 | c0001 | t0020 | g0087 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01081 | hp1 | a0001 | c0001 | t0016 | g0018 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0327 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0323 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01168 | hp2 | a0001 | c0001 | t0012 | g0009 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01169 | hp1 | a0001 | c0001 | t0012 | g0009 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01175 | hp2 | a0001 | c0001 | t0020 | g0090 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0332 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0288 | AMR | CLM | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | CLM | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01256 | hp1 | a0001 | c0001 | t0012 | g0207 | AMR | CLM | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01256 | hp2 | a0001 | c0001 | t0016 | g0184 | AMR | CLM | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01257 | hp1 | a0004 | c0006 | t0004 | g0071 | AMR | CLM | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01257 | hp2 | a0003 | c0004 | t0014 | g0306 | AMR | CLM | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01258 | hp1 | a0001 | c0001 | t0016 | g0018 | AMR | CLM | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01258 | hp2 | a0003 | c0004 | t0014 | g0307 | AMR | CLM | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | CLM | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01496 | hp2 | a0001 | c0001 | t0016 | g0190 | AMR | CLM | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0123 | EUR | IBS | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0319 | EUR | IBS | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01516 | hp1 | a0001 | c0001 | t0017 | g0001 | EUR | IBS | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0178 | EUR | IBS | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0166 | EUR | IBS | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01517 | hp2 | a0001 | c0001 | t0017 | g0236 | EUR | IBS | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01884 | hp1 | a0001 | c0001 | t0015 | g0200 | AFR | ACB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01884 | hp2 | a0001 | c0002 | t0008 | g0317 | AFR | ACB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | ACB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | ACB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0155 | AMR | PEL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01928 | hp2 | a0001 | c0001 | t0009 | g0189 | AMR | PEL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PEL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | PEL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01952 | hp2 | a0001 | c0001 | t0015 | g0021 | AMR | PEL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01975 | hp1 | a0001 | c0001 | t0006 | g0032 | AMR | PEL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01978 | hp1 | a0001 | c0001 | t0015 | g0021 | AMR | PEL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0318 | AMR | PEL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01993 | hp1 | a0001 | c0001 | t0005 | g0247 | AMR | PEL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01993 | hp2 | a0001 | c0001 | t0006 | g0003 | AMR | PEL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0003 | AMR | PEL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02015 | hp1 | a0001 | c0001 | t0007 | g0287 | EAS | KHV | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | KHV | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02027 | hp1 | a0001 | c0001 | t0026 | g0003 | EAS | KHV | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02027 | hp2 | a0001 | c0001 | t0009 | g0057 | EAS | KHV | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02040 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | KHV | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | KHV | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | ACB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | KHV | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | KHV | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02071 | hp1 | a0001 | c0001 | t0006 | g0036 | EAS | KHV | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0284 | EAS | KHV | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | KHV | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | KHV | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02129 | hp2 | a0001 | c0001 | t0009 | g0129 | EAS | KHV | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | KHV | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | KHV | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0144 | EAS | KHV | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | KHV | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02145 | hp1 | a0002 | c0003 | t0010 | g0110 | AFR | ACB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02145 | hp2 | a0001 | c0001 | t0031 | g0316 | AFR | ACB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0152 | AMR | PEL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0060 | AMR | PEL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02155 | hp1 | a0001 | c0001 | t0005 | g0275 | EAS | CDX | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02155 | hp2 | a0001 | c0001 | t0007 | g0279 | EAS | CDX | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02165 | hp1 | a0001 | c0001 | t0007 | g0007 | EAS | CDX | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | CDX | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | ACB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02257 | hp2 | a0003 | c0004 | t0014 | g0027 | AFR | ACB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02258 | hp1 | a0001 | c0001 | t0009 | g0180 | AFR | ACB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | ACB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02280 | hp1 | a0001 | c0001 | t0036 | g0219 | AFR | ACB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0254 | AFR | ACB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02451 | hp1 | a0002 | c0003 | t0018 | g0253 | AFR | ACB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0263 | AFR | ACB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | KHV | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02523 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | KHV | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02572 | hp1 | a0001 | c0002 | t0029 | g0312 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0222 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02622 | hp1 | a0001 | c0002 | t0008 | g0023 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02622 | hp2 | a0001 | c0001 | t0019 | g0107 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02630 | hp1 | a0001 | c0001 | t0013 | g0114 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02630 | hp2 | a0001 | c0002 | t0021 | g0305 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02647 | hp1 | a0001 | c0002 | t0024 | g0199 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02683 | hp2 | a0001 | c0001 | t0011 | g0005 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02717 | hp1 | a0003 | c0004 | t0014 | g0313 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0264 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0042 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0183 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02735 | hp2 | a0001 | c0001 | t0025 | g0038 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02738 | hp2 | a0001 | c0001 | t0011 | g0099 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02809 | hp1 | a0002 | c0003 | t0010 | g0309 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02809 | hp2 | a0001 | c0002 | t0008 | g0023 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02818 | hp1 | a0001 | c0002 | t0008 | g0203 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02886 | hp1 | a0001 | c0002 | t0008 | g0281 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0198 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02896 | hp1 | a0002 | c0003 | t0010 | g0308 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02965 | hp1 | a0001 | c0001 | t0032 | g0217 | AFR | ESN | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02965 | hp2 | a0001 | c0001 | t0008 | g0256 | AFR | ESN | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | ESN | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02976 | hp1 | a0001 | c0001 | t0028 | g0014 | AFR | ESN | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02976 | hp2 | a0003 | c0004 | t0014 | g0027 | AFR | ESN | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03017 | hp2 | a0001 | c0001 | t0009 | g0324 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03098 | hp1 | a0001 | c0001 | t0023 | g0193 | AFR | MSL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03130 | hp1 | a0001 | c0001 | t0013 | g0116 | AFR | ESN | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03130 | hp2 | a0001 | c0002 | t0008 | g0260 | AFR | ESN | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03139 | hp2 | a0001 | c0001 | t0009 | g0181 | AFR | ESN | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | ESN | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03209 | hp1 | a0002 | c0003 | t0018 | g0197 | AFR | MSL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03209 | hp2 | a0001 | c0001 | t0021 | g0314 | AFR | MSL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03225 | hp1 | a0001 | c0001 | t0023 | g0194 | AFR | MSL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03225 | hp2 | a0001 | c0001 | t0013 | g0111 | AFR | MSL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03239 | hp2 | a0001 | c0001 | t0012 | g0009 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03453 | hp1 | a0002 | c0003 | t0010 | g0047 | AFR | MSL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03453 | hp2 | a0001 | c0001 | t0019 | g0109 | AFR | MSL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03486 | hp2 | a0001 | c0002 | t0008 | g0201 | AFR | MSL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0172 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03491 | hp1 | a0001 | c0001 | t0022 | g0174 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0173 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03492 | hp2 | a0001 | c0001 | t0022 | g0175 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03516 | hp1 | a0002 | c0003 | t0010 | g0311 | AFR | ESN | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03516 | hp2 | a0001 | c0001 | t0013 | g0034 | AFR | ESN | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03540 | hp1 | a0001 | c0001 | t0019 | g0108 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | GWD | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03579 | hp2 | a0001 | c0002 | t0008 | g0280 | AFR | MSL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0233 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0029 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0297 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03688 | hp1 | a0001 | c0001 | t0009 | g0182 | SAS | STU | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0329 | SAS | STU | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0321 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03704 | hp2 | a0001 | c0001 | t0015 | g0246 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03710 | hp2 | a0001 | c0008 | t0001 | g0086 | SAS | PJL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03831 | hp1 | a0001 | c0001 | t0011 | g0100 | SAS | BEB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03831 | hp2 | a0001 | c0001 | t0027 | g0078 | SAS | BEB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0334 | SAS | BEB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0234 | SAS | BEB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0171 | SAS | BEB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0228 | SAS | BEB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0333 | SAS | STU | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG04115 | hp2 | a0001 | c0001 | t0011 | g0005 | SAS | STU | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG04184 | hp1 | a0001 | c0001 | t0009 | g0188 | SAS | BEB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | STU | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | STU | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0028 | SAS | STU | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | STU | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG04228 | hp1 | a0001 | c0001 | t0033 | g0294 | SAS | STU | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0331 | SAS | STU | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18522 | hp1 | a0001 | c0002 | t0008 | g0259 | AFR | YRI | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | YRI | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18612 | hp1 | a0001 | c0001 | t0009 | g0186 | EAS | CHB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18612 | hp2 | a0001 | c0001 | t0005 | g0292 | EAS | CHB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18747 | hp1 | a0001 | c0001 | t0005 | g0248 | EAS | CHB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0252 | AFR | YRI | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18943 | hp1 | a0001 | c0001 | t0012 | g0300 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18944 | hp1 | a0001 | c0001 | t0007 | g0026 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18944 | hp2 | a0001 | c0001 | t0006 | g0031 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18945 | hp1 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18951 | hp1 | a0001 | c0001 | t0030 | g0210 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18956 | hp2 | a0001 | c0001 | t0007 | g0295 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18959 | hp2 | a0001 | c0001 | t0007 | g0282 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0227 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18960 | hp2 | a0001 | c0001 | t0007 | g0278 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18965 | hp1 | a0001 | c0001 | t0006 | g0043 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18968 | hp1 | a0001 | c0005 | t0002 | g0251 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18971 | hp1 | a0001 | c0001 | t0006 | g0121 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18973 | hp1 | a0001 | c0001 | t0005 | g0283 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18973 | hp2 | a0001 | c0001 | t0006 | g0037 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18975 | hp1 | a0001 | c0001 | t0006 | g0049 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0299 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0220 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18980 | hp2 | a0001 | c0001 | t0012 | g0276 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18981 | hp1 | a0001 | c0001 | t0005 | g0242 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18986 | hp1 | a0001 | c0001 | t0015 | g0206 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0298 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18992 | hp2 | a0001 | c0001 | t0005 | g0221 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18998 | hp1 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0250 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19011 | hp2 | a0001 | c0001 | t0007 | g0286 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19012 | hp2 | a0001 | c0001 | t0007 | g0277 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0268 | AFR | LWK | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19030 | hp2 | a0002 | c0003 | t0018 | g0195 | AFR | LWK | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19043 | hp2 | a0001 | c0002 | t0024 | g0205 | AFR | LWK | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19068 | hp1 | a0001 | c0001 | t0005 | g0301 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19070 | hp1 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19070 | hp2 | a0001 | c0001 | t0006 | g0030 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19080 | hp2 | a0001 | c0001 | t0007 | g0026 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19087 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19240 | hp1 | a0001 | c0002 | t0008 | g0261 | AFR | YRI | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | ASW | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA20129 | hp2 | a0002 | c0003 | t0010 | g0046 | AFR | ASW | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA20752 | hp1 | a0001 | c0001 | t0011 | g0005 | EUR | TSI | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0272 | EUR | TSI | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0165 | AMR | CLM | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0265 | AFR | ACB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02109 | hp2 | a0001 | c0001 | t0039 | g0258 | AFR | ACB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0289 | AFR | ACB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | ACB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG02559 | hp2 | a0002 | c0007 | t0035 | g0267 | AFR | ACB | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03471 | hp1 | a0002 | c0003 | t0010 | g0310 | AFR | MSL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG03471 | hp2 | a0001 | c0001 | t0013 | g0113 | AFR | MSL | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG06807 | hp1 | a0001 | c0005 | t0001 | g0337 | AFR | USA | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | USA | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA20300 | hp1 | a0001 | c0001 | t0009 | g0185 | AFR | USA | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0045 | AFR | USA | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | LWK | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0044 | AFR | LWK | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0320 | REF | REF | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0128 | REF | REF | TANGO2_chr22_20016110_20072164 | TANGO2 | chr22 | 20016110 | 20072164 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:20055981 | G | A | 1 | a0004 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.419G>A | p.Arg140Gln | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/9 | 595/3509 | 419/831 | 140/276 | chr22 | 20055981 | |||
| chr22:20063360 | G | A | 1 | a0003 | 5 | HG01257.hp2 HG01258.hp2 HG02257.hp2 others(2): Show |
missense_variant | MODERATE | c.628G>A | p.Glu210Lys | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 8/9 | 804/3509 | 628/831 | 210/276 | chr22 | 20063360 | |||
| chr22:20064566 | T | G | 1 | a0002 | 11 | HG02145.hp1 HG02451.hp1 HG02559.hp2 others(8): Show |
missense_variant | MODERATE | c.735T>G | p.Asp245Glu | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 911/3509 | 735/831 | 245/276 | chr22 | 20064566 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:20061537 | C | T | 1 | a0001c0008 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.459C>T | p.Tyr153Tyr | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/9 | 635/3509 | 459/831 | 153/276 | chr22 | 20061537 | |||
| chr22:20063434 | C | T | 1 | a0001c0002 | 14 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(11): Show |
synonymous_variant | LOW | c.702C>T | p.Tyr234Tyr | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 8/9 | 878/3509 | 702/831 | 234/276 | chr22 | 20063434 | |||
| chr22:20064569 | G | A | 1 | a0001c0005 | 2 | HG06807.hp1 NA18968.hp1 |
synonymous_variant | LOW | c.738G>A | p.Ala246Ala | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 914/3509 | 738/831 | 246/276 | chr22 | 20064569 | |||
| chr22:20064620 | C | T | 1 | a0002c0007 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.789C>T | p.Ser263Ser | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 965/3509 | 789/831 | 263/276 | chr22 | 20064620 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:20021160 | C | T | 1 | a0001c0001t0019 | 3 | HG02622.hp2 HG03453.hp2 HG03540.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-126C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/9 | chr22 | 20021160 | |||||||
| chr22:20021188 | G | T | 22 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(19): Show |
151 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(148): Show |
5_prime_UTR_variant | MODIFIER | c.-98G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/9 | 15611 | chr22 | 20021188 | ||||||
| chr22:20064778 | C | T | 1 | a0001c0001t0039 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*116C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 116 | chr22 | 20064778 | ||||||
| chr22:20064779 | C | A | 4 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0025 others(1): Show |
24 | HG00609.hp2 HG01884.hp1 HG01952.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*117C>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 117 | chr22 | 20064779 | ||||||
| chr22:20064782 | C | T | 1 | a0001c0001t0038 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*120C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 120 | chr22 | 20064782 | ||||||
| chr22:20064808 | T | C | 1 | a0001c0001t0025 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*146T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 146 | chr22 | 20064808 | ||||||
| chr22:20064897 | G | A | 5 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0030 others(2): Show |
33 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*235G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 235 | chr22 | 20064897 | ||||||
| chr22:20064919 | A | G | 4 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0022 others(1): Show |
80 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*257A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 257 | chr22 | 20064919 | ||||||
| chr22:20064958 | C | A | 11 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(8): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*296C>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 296 | chr22 | 20064958 | ||||||
| chr22:20065009 | C | G | 29 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(26): Show |
200 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*347C>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 347 | chr22 | 20065009 | ||||||
| chr22:20065040 | T | TACATGCA others(22): Show |
1 | a0001c0001t0030 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*380_*381insATGCAC others(23): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 381 | INFO_REALIGN_3_PRIME | chr22 | 20065040 | |||||
| chr22:20065043 | G | A | 28 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(25): Show |
199 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*381G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 381 | chr22 | 20065043 | ||||||
| chr22:20065259 | C | T | 30 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(27): Show |
204 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*597C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 597 | chr22 | 20065259 | ||||||
| chr22:20065261 | C | T | 3 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0016 |
28 | HG01069.hp2 HG01081.hp1 HG01256.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*599C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 599 | chr22 | 20065261 | ||||||
| chr22:20065341 | C | T | 1 | a0001c0001t0028 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*679C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 679 | chr22 | 20065341 | ||||||
| chr22:20065456 | C | T | 1 | a0001c0001t0026 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*794C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 794 | chr22 | 20065456 | ||||||
| chr22:20065486 | C | T | 3 | a0001c0001t0011 a0001c0002t0024 a0001c0002t0029 |
9 | HG00423.hp1 HG02572.hp1 HG02647.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*824C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 824 | chr22 | 20065486 | ||||||
| chr22:20065631 | C | T | 12 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0015 others(9): Show |
48 | HG00609.hp2 HG01257.hp2 HG01258.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*969C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 969 | chr22 | 20065631 | ||||||
| chr22:20065691 | C | T | 1 | a0001c0001t0037 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1029C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 1029 | chr22 | 20065691 | ||||||
| chr22:20065930 | C | T | 1 | a0001c0001t0034 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1268C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 1268 | chr22 | 20065930 | ||||||
| chr22:20065972 | A | G | 1 | a0001c0001t0022 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1310A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 1310 | chr22 | 20065972 | ||||||
| chr22:20066031 | C | T | 12 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0015 others(9): Show |
48 | HG00609.hp2 HG01257.hp2 HG01258.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1369C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 1369 | chr22 | 20066031 | ||||||
| chr22:20066057 | G | T | 2 | a0002c0003t0010 a0002c0003t0018 |
10 | HG02145.hp1 HG02451.hp1 HG02809.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1395G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 1395 | chr22 | 20066057 | ||||||
| chr22:20066149 | C | T | 1 | a0002c0007t0035 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1487C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 1487 | chr22 | 20066149 | ||||||
| chr22:20066194 | G | A | 1 | a0001c0001t0032 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1532G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 1532 | chr22 | 20066194 | ||||||
| chr22:20066206 | G | A | 1 | a0001c0001t0036 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1544G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 1544 | chr22 | 20066206 | ||||||
| chr22:20066338 | C | T | 2 | a0001c0001t0017 a0001c0001t0020 |
5 | HG00741.hp1 HG01074.hp1 HG01175.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1676C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 1676 | chr22 | 20066338 | ||||||
| chr22:20066363 | C | T | 1 | a0003c0004t0014 | 5 | HG01257.hp2 HG01258.hp2 HG02257.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1701C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 1701 | chr22 | 20066363 | ||||||
| chr22:20066608 | C | T | 1 | a0002c0007t0035 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1946C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 1946 | chr22 | 20066608 | ||||||
| chr22:20066654 | A | G | 12 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0015 others(9): Show |
48 | HG00609.hp2 HG01257.hp2 HG01258.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1992A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 1992 | chr22 | 20066654 | ||||||
| chr22:20066685 | AG | A | 4 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0030 others(1): Show |
32 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2025delG | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 2025 | INFO_REALIGN_3_PRIME | chr22 | 20066685 | |||||
| chr22:20066935 | A | C | 12 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0015 others(9): Show |
48 | HG00609.hp2 HG01257.hp2 HG01258.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*2273A>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 2273 | chr22 | 20066935 | ||||||
| chr22:20066957 | A | G | 1 | a0001c0001t0013 | 5 | HG02630.hp1 HG03130.hp1 HG03225.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2295A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 2295 | chr22 | 20066957 | ||||||
| chr22:20066984 | G | A | 12 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0015 others(9): Show |
48 | HG00609.hp2 HG01257.hp2 HG01258.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*2322G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 2322 | chr22 | 20066984 | ||||||
| chr22:20067104 | C | T | 2 | a0001c0001t0027 a0001c0001t0033 |
2 | HG03831.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2442C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 9/9 | 2442 | chr22 | 20067104 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:20021312 | T | C | 29 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0048 others(26): Show |
32 | HG01975.hp1 HG01993.hp2 HG02004.hp1 others(29): Show |
intron_variant | MODIFIER | c.-40+66T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20021312 | |||||||
| chr22:20021365 | C | T | 23 | a0001c0001t0001g0002 a0001c0001t0001g0319 a0001c0001t0001g0322 others(20): Show |
30 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.-40+119C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20021365 | |||||||
| chr22:20021389 | G | T | 1 | a0001c0001t0004g0318 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-40+143G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20021389 | |||||||
| chr22:20021551 | T | C | 1 | a0001c0001t0009g0057 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-40+305T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20021551 | |||||||
| chr22:20021555 | C | T | 168 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0048 others(165): Show |
196 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(193): Show |
intron_variant | MODIFIER | c.-40+309C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20021555 | |||||||
| chr22:20022083 | G | T | 1 | a0001c0001t0003g0192 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-40+837G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20022083 | |||||||
| chr22:20022156 | G | T | 1 | a0001c0002t0008g0317 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-40+910G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20022156 | |||||||
| chr22:20022379 | G | C | 1 | a0001c0001t0001g0319 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-40+1133G>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20022379 | |||||||
| chr22:20022405 | T | C | 69 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(66): Show |
80 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.-40+1159T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20022405 | |||||||
| chr22:20022739 | G | T | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-40+1493G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20022739 | |||||||
| chr22:20023112 | C | T | 1 | a0001c0001t0031g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-40+1866C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20023112 | |||||||
| chr22:20023207 | A | G | 276 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(273): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-40+1961A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20023207 | |||||||
| chr22:20023295 | CT | C | 126 | a0001c0001t0002g0001 a0001c0001t0002g0019 a0001c0001t0002g0020 others(123): Show |
150 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.-40+2058delT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 20023295 | ||||||
| chr22:20023296 | T | C | 24 | a0001c0001t0001g0002 a0001c0001t0001g0178 a0001c0001t0001g0319 others(21): Show |
31 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.-40+2050T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20023296 | |||||||
| chr22:20023302 | T | A | 6 | a0001c0001t0002g0196 a0001c0001t0023g0193 a0001c0001t0023g0194 others(3): Show |
6 | HG01255.hp2 HG02145.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+2056T>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20023302 | |||||||
| chr22:20023327 | G | A | 56 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(53): Show |
65 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.-40+2081G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20023327 | |||||||
| chr22:20023335 | C | T | 34 | a0001c0001t0002g0025 a0001c0001t0002g0288 a0001c0001t0002g0289 others(31): Show |
42 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.-40+2089C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20023335 | |||||||
| chr22:20023400 | G | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0178 a0001c0001t0001g0319 others(21): Show |
31 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.-40+2154G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20023400 | |||||||
| chr22:20023474 | G | T | 1 | a0001c0001t0001g0339 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-40+2228G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20023474 | |||||||
| chr22:20023636 | C | T | 69 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(66): Show |
80 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.-40+2390C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20023636 | |||||||
| chr22:20023755 | G | C | 1 | a0001c0001t0012g0276 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-40+2509G>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20023755 | |||||||
| chr22:20023795 | T | G | 8 | a0001c0001t0002g0202 a0001c0001t0002g0204 a0001c0001t0007g0198 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-40+2549T>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20023795 | |||||||
| chr22:20023855 | C | T | 1 | a0001c0001t0005g0275 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-40+2609C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20023855 | |||||||
| chr22:20023905 | G | A | 1 | a0001c0001t0002g0302 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-40+2659G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20023905 | |||||||
| chr22:20023909 | C | T | 1 | a0001c0001t0031g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-40+2663C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20023909 | |||||||
| chr22:20023951 | A | G | 168 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0048 others(165): Show |
196 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(193): Show |
intron_variant | MODIFIER | c.-40+2705A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20023951 | |||||||
| chr22:20024182 | C | T | 1 | a0001c0001t0003g0177 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-40+2936C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20024182 | |||||||
| chr22:20024314 | T | C | 120 | a0001c0001t0002g0001 a0001c0001t0002g0019 a0001c0001t0002g0020 others(117): Show |
144 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.-40+3068T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20024314 | |||||||
| chr22:20024466 | G | A | 276 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(273): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-40+3220G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20024466 | |||||||
| chr22:20024499 | C | T | 5 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(2): Show |
5 | HG00099.hp1 HG00738.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40+3253C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20024499 | |||||||
| chr22:20024763 | A | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0039 others(204): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.-40+3517A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20024763 | |||||||
| chr22:20024819 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-40+3573C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20024819 | |||||||
| chr22:20024879 | C | T | 1 | a0001c0001t0003g0106 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-40+3633C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20024879 | |||||||
| chr22:20025068 | G | A | 3 | a0001c0001t0023g0193 a0001c0001t0023g0194 a0001c0001t0031g0316 |
3 | HG02145.hp2 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-40+3822G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20025068 | |||||||
| chr22:20025121 | G | A | 2 | a0001c0001t0006g0030 a0001c0001t0006g0031 |
2 | NA18944.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-40+3875G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20025121 | |||||||
| chr22:20025160 | C | T | 1 | a0001c0001t0031g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-40+3914C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20025160 | |||||||
| chr22:20025250 | G | A | 1 | a0001c0001t0007g0277 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-40+4004G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20025250 | |||||||
| chr22:20025341 | C | T | 12 | a0001c0001t0001g0187 a0001c0001t0003g0191 a0001c0001t0004g0183 others(9): Show |
13 | HG00735.hp2 HG01081.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.-40+4095C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20025341 | |||||||
| chr22:20025434 | G | A | 30 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0048 others(27): Show |
33 | HG01975.hp1 HG01993.hp2 HG02004.hp1 others(30): Show |
intron_variant | MODIFIER | c.-40+4188G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20025434 | |||||||
| chr22:20025439 | G | A | 10 | a0001c0001t0001g0059 a0001c0001t0001g0062 a0001c0001t0001g0063 others(7): Show |
11 | HG00639.hp1 HG00733.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.-40+4193G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20025439 | |||||||
| chr22:20025445 | T | C | 207 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0039 others(204): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.-40+4199T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20025445 | |||||||
| chr22:20025476 | G | A | 9 | a0001c0002t0029g0312 a0002c0003t0010g0308 a0002c0003t0010g0309 others(6): Show |
10 | HG01257.hp2 HG01258.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-40+4230G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20025476 | |||||||
| chr22:20025550 | T | A | 2 | a0001c0001t0004g0183 a0001c0001t0009g0182 |
2 | HG02735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-40+4304T>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20025550 | |||||||
| chr22:20025663 | A | G | 2 | a0001c0001t0002g0024 a0001c0001t0002g0269 |
3 | HG02486.hp1 HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-40+4417A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20025663 | |||||||
| chr22:20025699 | A | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0039 others(204): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.-40+4453A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20025699 | |||||||
| chr22:20025766 | G | A | 40 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0048 others(37): Show |
44 | HG01257.hp2 HG01258.hp2 HG01975.hp1 others(41): Show |
intron_variant | MODIFIER | c.-40+4520G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20025766 | |||||||
| chr22:20026125 | C | G | 1 | a0001c0001t0003g0176 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-40+4879C>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20026125 | |||||||
| chr22:20026137 | C | T | 1 | a0001c0001t0005g0303 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-40+4891C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20026137 | |||||||
| chr22:20026159 | G | T | 40 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0048 others(37): Show |
44 | HG01257.hp2 HG01258.hp2 HG01975.hp1 others(41): Show |
intron_variant | MODIFIER | c.-40+4913G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20026159 | |||||||
| chr22:20026170 | C | T | 2 | a0001c0001t0002g0302 a0001c0001t0005g0301 |
2 | HG02132.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-40+4924C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20026170 | |||||||
| chr22:20026229 | C | G | 2 | a0001c0001t0022g0174 a0001c0001t0022g0175 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-40+4983C>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20026229 | |||||||
| chr22:20026254 | C | T | 17 | a0001c0001t0002g0022 a0001c0001t0002g0255 a0001c0001t0002g0257 others(14): Show |
19 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-40+5008C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20026254 | |||||||
| chr22:20026269 | G | A | 40 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0048 others(37): Show |
44 | HG01257.hp2 HG01258.hp2 HG01975.hp1 others(41): Show |
intron_variant | MODIFIER | c.-40+5023G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20026269 | |||||||
| chr22:20026280 | G | C | 276 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(273): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-40+5034G>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20026280 | |||||||
| chr22:20026288 | C | T | 3 | a0001c0001t0002g0252 a0001c0001t0002g0254 a0002c0003t0018g0253 |
3 | HG02280.hp2 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-40+5042C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20026288 | |||||||
| chr22:20026290 | T | C | 201 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0039 others(198): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.-40+5044T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20026290 | |||||||
| chr22:20026388 | A | C | 1 | a0001c0001t0006g0031 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-40+5142A>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20026388 | |||||||
| chr22:20026397 | CA | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(265): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-40+5166delA | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 20026397 | ||||||
| chr22:20026399 | A | G | 4 | a0001c0001t0005g0298 a0001c0001t0005g0299 a0001c0001t0012g0276 others(1): Show |
4 | NA18943.hp1 NA18979.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40+5153A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20026399 | |||||||
| chr22:20026509 | G | C | 120 | a0001c0001t0002g0001 a0001c0001t0002g0019 a0001c0001t0002g0020 others(117): Show |
144 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.-40+5263G>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20026509 | |||||||
| chr22:20026538 | A | G | 44 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0048 others(41): Show |
48 | HG01257.hp2 HG01258.hp2 HG01975.hp1 others(45): Show |
intron_variant | MODIFIER | c.-40+5292A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20026538 | |||||||
| chr22:20026629 | A | G | 127 | a0001c0001t0001g0054 a0001c0001t0002g0001 a0001c0001t0002g0019 others(124): Show |
152 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.-40+5383A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20026629 | |||||||
| chr22:20026675 | A | G | 8 | a0001c0001t0002g0202 a0001c0001t0002g0204 a0001c0001t0007g0198 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-40+5429A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20026675 | |||||||
| chr22:20026751 | TG | T | 3 | a0001c0001t0001g0054 a0001c0001t0002g0022 a0001c0001t0002g0255 |
4 | HG02257.hp1 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40+5510delG | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 20026751 | ||||||
| chr22:20026881 | T | C | 11 | a0001c0001t0001g0179 a0001c0001t0001g0187 a0001c0001t0004g0183 others(8): Show |
11 | HG01928.hp2 HG02027.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-40+5635T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20026881 | |||||||
| chr22:20026913 | G | A | 1 | a0001c0001t0009g0185 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-40+5667G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20026913 | |||||||
| chr22:20026950 | T | C | 182 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0048 others(179): Show |
211 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(208): Show |
intron_variant | MODIFIER | c.-40+5704T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20026950 | |||||||
| chr22:20027063 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-40+5817A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20027063 | |||||||
| chr22:20027202 | G | A | 1 | a0002c0003t0018g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-40+5956G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20027202 | |||||||
| chr22:20027207 | G | C | 1 | a0001c0001t0001g0066 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-40+5961G>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20027207 | |||||||
| chr22:20027395 | C | G | 3 | a0001c0001t0007g0026 a0001c0001t0007g0277 a0001c0001t0007g0295 |
4 | NA18944.hp1 NA18956.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40+6149C>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20027395 | |||||||
| chr22:20027436 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-40+6190T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20027436 | |||||||
| chr22:20027451 | A | G | 2 | a0001c0001t0005g0250 a0001c0005t0002g0251 |
2 | NA18968.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-40+6205A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20027451 | |||||||
| chr22:20027493 | C | T | 126 | a0001c0001t0001g0053 a0001c0001t0001g0117 a0001c0001t0001g0315 others(123): Show |
150 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.-40+6247C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20027493 | |||||||
| chr22:20027596 | G | A | 1 | a0001c0001t0003g0058 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-40+6350G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20027596 | |||||||
| chr22:20027602 | G | A | 1 | a0001c0001t0004g0321 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-40+6356G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20027602 | |||||||
| chr22:20027632 | G | A | 1 | a0001c0001t0001g0322 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-40+6386G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20027632 | |||||||
| chr22:20027705 | T | C | 45 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0048 others(42): Show |
50 | HG01257.hp2 HG01258.hp2 HG01975.hp1 others(47): Show |
intron_variant | MODIFIER | c.-40+6459T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20027705 | |||||||
| chr22:20027868 | G | A | 127 | a0001c0001t0001g0053 a0001c0001t0001g0117 a0001c0001t0001g0315 others(124): Show |
151 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.-40+6622G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20027868 | |||||||
| chr22:20027874 | C | T | 1 | a0001c0001t0002g0254 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-40+6628C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20027874 | |||||||
| chr22:20027890 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-40+6644C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20027890 | |||||||
| chr22:20027915 | C | T | 1 | a0001c0001t0003g0192 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-40+6669C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20027915 | |||||||
| chr22:20027965 | A | G | 1 | a0001c0001t0013g0116 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-40+6719A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20027965 | |||||||
| chr22:20027988 | C | T | 11 | a0001c0001t0001g0179 a0001c0001t0001g0187 a0001c0001t0004g0183 others(8): Show |
11 | HG01928.hp2 HG02027.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-40+6742C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20027988 | |||||||
| chr22:20027999 | G | A | 1 | a0001c0001t0003g0118 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-40+6753G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20027999 | |||||||
| chr22:20028092 | C | A | 5 | a0001c0001t0001g0068 a0001c0001t0004g0069 a0001c0001t0004g0070 others(2): Show |
5 | HG00140.hp2 HG00323.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40+6846C>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20028092 | |||||||
| chr22:20028134 | G | C | 1 | a0001c0001t0007g0198 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-40+6888G>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20028134 | |||||||
| chr22:20028218 | C | T | 97 | a0001c0001t0001g0117 a0001c0001t0002g0001 a0001c0001t0002g0019 others(94): Show |
120 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.-40+6972C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20028218 | |||||||
| chr22:20028336 | A | G | 1 | a0001c0001t0012g0207 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-40+7090A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20028336 | |||||||
| chr22:20028451 | T | C | 233 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(230): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.-40+7205T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20028451 | |||||||
| chr22:20028489 | A | G | 8 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(5): Show |
9 | HG02257.hp1 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-40+7243A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20028489 | |||||||
| chr22:20028497 | T | C | 97 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(94): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.-40+7251T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20028497 | |||||||
| chr22:20028527 | C | T | 1 | a0001c0001t0003g0171 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-40+7281C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20028527 | |||||||
| chr22:20028531 | G | A | 1 | a0001c0001t0002g0208 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-40+7285G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20028531 | |||||||
| chr22:20028631 | C | A | 1 | a0001c0001t0002g0257 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-40+7385C>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20028631 | |||||||
| chr22:20028681 | G | A | 3 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0106 |
3 | NA18961.hp2 NA19002.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-40+7435G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20028681 | |||||||
| chr22:20028969 | G | A | 126 | a0001c0001t0001g0053 a0001c0001t0001g0117 a0001c0001t0001g0315 others(123): Show |
150 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.-40+7723G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20028969 | |||||||
| chr22:20029016 | G | A | 2 | a0001c0001t0023g0193 a0001c0001t0023g0194 |
2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-39-7744G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20029016 | |||||||
| chr22:20029172 | T | C | 1 | a0002c0003t0018g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-39-7588T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20029172 | |||||||
| chr22:20029448 | G | A | 95 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(92): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.-39-7312G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20029448 | |||||||
| chr22:20029536 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-39-7224C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20029536 | |||||||
| chr22:20029596 | G | A | 1 | a0001c0001t0001g0315 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-39-7164G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20029596 | |||||||
| chr22:20029745 | A | G | 244 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(241): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.-39-7015A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20029745 | |||||||
| chr22:20029827 | G | C | 6 | a0001c0001t0039g0258 a0001c0002t0008g0023 a0001c0002t0008g0259 others(3): Show |
7 | HG02109.hp2 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-39-6933G>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20029827 | |||||||
| chr22:20029922 | T | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(103): Show |
124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.-39-6838T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20029922 | |||||||
| chr22:20030030 | G | A | 11 | a0001c0001t0001g0179 a0001c0001t0001g0187 a0001c0001t0004g0183 others(8): Show |
11 | HG01928.hp2 HG02027.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-39-6730G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20030030 | |||||||
| chr22:20030048 | C | T | 1 | a0002c0003t0018g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-39-6712C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20030048 | |||||||
| chr22:20030150 | C | CT | 119 | a0001c0001t0001g0053 a0001c0001t0001g0117 a0001c0001t0001g0179 others(116): Show |
143 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.-39-6591dupT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 20030150 | ||||||
| chr22:20030150 | CT | C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(93): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.-39-6591delT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 20030150 | ||||||
| chr22:20030150 | CTT | C | 8 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(5): Show |
8 | HG01167.hp1 HG01167.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39-6592_-39-6591d others(4): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 20030150 | ||||||
| chr22:20030169 | T | A | 1 | a0001c0001t0002g0262 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-39-6591T>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20030169 | |||||||
| chr22:20030169 | T | TA | 3 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0265 |
3 | HG02109.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-39-6589dupA | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 20030169 | ||||||
| chr22:20030334 | ATTTG | A | 106 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(103): Show |
124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.-39-6402_-39-6399d others(6): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 20030334 | ||||||
| chr22:20030580 | C | T | 126 | a0001c0001t0001g0053 a0001c0001t0001g0117 a0001c0001t0001g0315 others(123): Show |
150 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.-39-6180C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20030580 | |||||||
| chr22:20030608 | GTGC | G | 11 | a0001c0001t0001g0179 a0001c0001t0001g0187 a0001c0001t0004g0183 others(8): Show |
11 | HG01928.hp2 HG02027.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-39-6149_-39-6147d others(5): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 20030608 | ||||||
| chr22:20031023 | C | T | 1 | a0001c0001t0001g0322 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-39-5737C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20031023 | |||||||
| chr22:20031169 | G | A | 8 | a0001c0001t0002g0202 a0001c0001t0002g0204 a0001c0001t0007g0198 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-39-5591G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20031169 | |||||||
| chr22:20031185 | G | A | 8 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(5): Show |
9 | HG02257.hp1 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-39-5575G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20031185 | |||||||
| chr22:20031197 | C | CA | 112 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(109): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.-39-5551dupA | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 20031197 | ||||||
| chr22:20031410 | C | A | 1 | a0001c0001t0027g0078 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39-5350C>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20031410 | |||||||
| chr22:20031533 | G | A | 2 | a0003c0004t0014g0306 a0003c0004t0014g0307 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-39-5227G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20031533 | |||||||
| chr22:20031627 | T | C | 1 | a0001c0002t0024g0199 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-39-5133T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20031627 | |||||||
| chr22:20031652 | C | T | 1 | a0001c0001t0006g0049 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-39-5108C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20031652 | |||||||
| chr22:20031655 | C | T | 95 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(92): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.-39-5105C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20031655 | |||||||
| chr22:20031816 | A | T | 1 | a0002c0003t0018g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-39-4944A>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20031816 | |||||||
| chr22:20031870 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-39-4890G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20031870 | |||||||
| chr22:20032245 | A | G | 106 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(103): Show |
124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.-39-4515A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20032245 | |||||||
| chr22:20032268 | C | T | 1 | a0001c0001t0003g0065 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-39-4492C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20032268 | |||||||
| chr22:20032327 | G | T | 2 | a0003c0004t0014g0306 a0003c0004t0014g0307 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-39-4433G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20032327 | |||||||
| chr22:20032483 | C | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-39-4277C>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20032483 | |||||||
| chr22:20032548 | G | T | 3 | a0001c0001t0002g0209 a0001c0001t0002g0215 a0001c0001t0002g0216 |
3 | HG02572.hp2 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-39-4212G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20032548 | |||||||
| chr22:20032550 | A | G | 137 | a0001c0001t0001g0053 a0001c0001t0001g0117 a0001c0001t0001g0179 others(134): Show |
161 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-39-4210A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20032550 | |||||||
| chr22:20032595 | G | A | 1 | a0001c0001t0027g0078 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39-4165G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20032595 | |||||||
| chr22:20032641 | G | C | 3 | a0001c0002t0008g0280 a0001c0002t0008g0281 a0001c0002t0008g0317 |
3 | HG01884.hp2 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-39-4119G>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20032641 | |||||||
| chr22:20032681 | C | A | 1 | a0001c0001t0001g0079 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-39-4079C>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20032681 | |||||||
| chr22:20032706 | C | T | 126 | a0001c0001t0001g0053 a0001c0001t0001g0117 a0001c0001t0001g0315 others(123): Show |
150 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.-39-4054C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20032706 | |||||||
| chr22:20032860 | G | C | 3 | a0001c0001t0002g0218 a0001c0001t0032g0217 a0001c0001t0036g0219 |
3 | HG01243.hp2 HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-39-3900G>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20032860 | |||||||
| chr22:20032886 | A | G | 8 | a0001c0001t0002g0202 a0001c0001t0002g0204 a0001c0001t0007g0198 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-39-3874A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20032886 | |||||||
| chr22:20032979 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-39-3781G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20032979 | |||||||
| chr22:20033028 | C | G | 1 | a0001c0001t0002g0214 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-39-3732C>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20033028 | |||||||
| chr22:20033073 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-39-3687G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20033073 | |||||||
| chr22:20033227 | G | A | 4 | a0001c0001t0019g0107 a0001c0001t0019g0108 a0001c0001t0019g0109 others(1): Show |
4 | HG02145.hp1 HG02622.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-3533G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20033227 | |||||||
| chr22:20033245 | C | G | 1 | a0001c0001t0009g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-39-3515C>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20033245 | |||||||
| chr22:20033260 | C | T | 5 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0167 others(2): Show |
7 | NA18943.hp2 NA18952.hp1 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.-39-3500C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20033260 | |||||||
| chr22:20033360 | T | C | 11 | a0001c0001t0008g0256 a0001c0001t0021g0314 a0001c0002t0029g0312 others(8): Show |
12 | HG01257.hp2 HG01258.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-39-3400T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20033360 | |||||||
| chr22:20033366 | T | C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(93): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.-39-3394T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20033366 | |||||||
| chr22:20033463 | C | T | 6 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0006g0044 others(3): Show |
6 | HG02922.hp1 HG03453.hp1 NA19240.hp2 others(3): Show |
intron_variant | MODIFIER | c.-39-3297C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20033463 | |||||||
| chr22:20033538 | G | A | 1 | a0001c0001t0003g0073 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-39-3222G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20033538 | |||||||
| chr22:20033658 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-39-3102C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20033658 | |||||||
| chr22:20033707 | C | T | 8 | a0001c0001t0002g0202 a0001c0001t0002g0204 a0001c0001t0007g0198 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-39-3053C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20033707 | |||||||
| chr22:20033956 | A | G | 2 | a0001c0001t0002g0196 a0002c0003t0018g0197 |
2 | HG01255.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-39-2804A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20033956 | |||||||
| chr22:20034137 | G | A | 11 | a0001c0001t0008g0256 a0001c0001t0021g0314 a0001c0002t0029g0312 others(8): Show |
12 | HG01257.hp2 HG01258.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-39-2623G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20034137 | |||||||
| chr22:20034173 | T | G | 106 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(103): Show |
124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.-39-2587T>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20034173 | |||||||
| chr22:20034194 | A | AAAC | 126 | a0001c0001t0001g0053 a0001c0001t0001g0117 a0001c0001t0001g0315 others(123): Show |
150 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.-39-2554_-39-2552d others(5): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 20034194 | ||||||
| chr22:20034206 | C | CA | 9 | a0001c0001t0001g0081 a0001c0001t0003g0126 a0001c0001t0003g0127 others(6): Show |
9 | HG02074.hp1 HG02145.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-39-2545dupA | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr22 | 20034206 | ||||||
| chr22:20034209 | A | C | 137 | a0001c0001t0001g0053 a0001c0001t0001g0117 a0001c0001t0001g0179 others(134): Show |
161 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-39-2551A>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20034209 | |||||||
| chr22:20034212 | A | C | 1 | a0001c0001t0002g0249 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-39-2548A>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20034212 | |||||||
| chr22:20034340 | C | T | 120 | a0001c0001t0001g0053 a0001c0001t0001g0117 a0001c0001t0001g0315 others(117): Show |
144 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.-39-2420C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20034340 | |||||||
| chr22:20034415 | G | T | 96 | a0001c0001t0001g0117 a0001c0001t0002g0001 a0001c0001t0002g0019 others(93): Show |
119 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.-39-2345G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20034415 | |||||||
| chr22:20034442 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0115 |
4 | HG02895.hp2 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-2318C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20034442 | |||||||
| chr22:20034462 | G | A | 8 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(5): Show |
9 | HG02257.hp1 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-39-2298G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20034462 | |||||||
| chr22:20034464 | A | G | 95 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(92): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.-39-2296A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20034464 | |||||||
| chr22:20034571 | G | A | 11 | a0001c0001t0008g0256 a0001c0001t0021g0314 a0001c0002t0029g0312 others(8): Show |
12 | HG01257.hp2 HG01258.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-39-2189G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20034571 | |||||||
| chr22:20034975 | C | G | 278 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-39-1785C>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20034975 | |||||||
| chr22:20034998 | G | A | 1 | a0002c0007t0035g0267 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-39-1762G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20034998 | |||||||
| chr22:20035121 | A | G | 4 | a0001c0001t0019g0107 a0001c0001t0019g0108 a0001c0001t0019g0109 others(1): Show |
4 | HG02145.hp1 HG02622.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-1639A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20035121 | |||||||
| chr22:20035126 | G | C | 1 | a0001c0001t0003g0106 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-39-1634G>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20035126 | |||||||
| chr22:20035223 | C | T | 12 | a0001c0001t0002g0245 a0001c0001t0002g0249 a0001c0001t0002g0270 others(9): Show |
13 | HG00099.hp1 HG00738.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.-39-1537C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20035223 | |||||||
| chr22:20035317 | C | T | 5 | a0001c0001t0003g0123 a0001c0001t0003g0165 a0001c0001t0003g0166 others(2): Show |
5 | HG01123.hp1 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.-39-1443C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20035317 | |||||||
| chr22:20035487 | G | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.-39-1273G>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20035487 | |||||||
| chr22:20035495 | C | T | 2 | a0001c0001t0008g0256 a0001c0001t0021g0314 |
2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-39-1265C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20035495 | |||||||
| chr22:20035564 | C | T | 11 | a0001c0001t0001g0179 a0001c0001t0001g0187 a0001c0001t0004g0183 others(8): Show |
11 | HG01928.hp2 HG02027.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-39-1196C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20035564 | |||||||
| chr22:20035576 | G | A | 95 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(92): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.-39-1184G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20035576 | |||||||
| chr22:20035780 | T | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(235): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-39-980T>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20035780 | |||||||
| chr22:20035818 | G | A | 1 | a0001c0001t0009g0057 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-39-942G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20035818 | |||||||
| chr22:20035921 | C | T | 11 | a0001c0001t0001g0179 a0001c0001t0001g0187 a0001c0001t0004g0183 others(8): Show |
11 | HG01928.hp2 HG02027.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-39-839C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20035921 | |||||||
| chr22:20035968 | C | T | 1 | a0001c0001t0038g0244 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-39-792C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20035968 | |||||||
| chr22:20036023 | C | T | 1 | a0001c0001t0006g0042 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-39-737C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20036023 | |||||||
| chr22:20036167 | A | C | 1 | a0001c0001t0001g0102 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-39-593A>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20036167 | |||||||
| chr22:20036208 | C | T | 11 | a0001c0001t0001g0179 a0001c0001t0001g0187 a0001c0001t0004g0183 others(8): Show |
11 | HG01928.hp2 HG02027.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-39-552C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20036208 | |||||||
| chr22:20036214 | G | A | 1 | a0001c0001t0033g0294 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-39-546G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20036214 | |||||||
| chr22:20036275 | G | A | 1 | a0001c0001t0030g0210 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-39-485G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20036275 | |||||||
| chr22:20036635 | C | G | 1 | a0002c0003t0018g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-39-125C>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20036635 | |||||||
| chr22:20036651 | A | G | 339 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(336): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.-39-109A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 1/8 | chr22 | 20036651 | |||||||
| chr22:20036975 | C | G | 1 | a0001c0001t0001g0164 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.56+121C>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20036975 | |||||||
| chr22:20037002 | C | T | 4 | a0001c0001t0011g0005 a0001c0001t0011g0099 a0001c0001t0011g0100 others(1): Show |
6 | HG00423.hp1 HG02683.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.56+148C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20037002 | |||||||
| chr22:20037081 | G | A | 1 | a0001c0001t0005g0220 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.56+227G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20037081 | |||||||
| chr22:20037109 | T | G | 1 | a0002c0003t0018g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.56+255T>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20037109 | |||||||
| chr22:20037378 | C | T | 8 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(5): Show |
9 | HG02257.hp1 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.56+524C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20037378 | |||||||
| chr22:20037653 | GT | G | 30 | a0001c0001t0001g0033 a0001c0001t0002g0196 a0001c0001t0006g0003 others(27): Show |
34 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(31): Show |
intron_variant | MODIFIER | c.56+803delT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 20037653 | ||||||
| chr22:20037788 | G | T | 14 | a0001c0001t0001g0053 a0001c0001t0001g0315 a0001c0001t0002g0257 others(11): Show |
15 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.56+934G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20037788 | |||||||
| chr22:20037873 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.56+1019G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20037873 | |||||||
| chr22:20038078 | G | GACTGCAT others(8): Show |
1 | a0001c0001t0003g0073 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.56+1226_56+1240dup others(15): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 20038078 | ||||||
| chr22:20038129 | C | T | 71 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0051 others(68): Show |
75 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.56+1275C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20038129 | |||||||
| chr22:20038244 | C | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0117 others(48): Show |
69 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.56+1390C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20038244 | |||||||
| chr22:20038330 | G | A | 12 | a0001c0001t0007g0007 a0001c0001t0007g0026 a0001c0001t0007g0277 others(9): Show |
15 | HG02129.hp2 HG02155.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.56+1476G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20038330 | |||||||
| chr22:20038331 | G | A | 3 | a0001c0001t0003g0126 a0001c0001t0003g0139 a0001c0001t0005g0248 |
3 | HG00621.hp2 HG02074.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.56+1477G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20038331 | |||||||
| chr22:20038428 | C | T | 60 | a0001c0001t0001g0033 a0001c0001t0002g0196 a0001c0001t0002g0249 others(57): Show |
68 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.56+1574C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20038428 | |||||||
| chr22:20038453 | A | G | 1 | a0001c0001t0004g0334 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.56+1599A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20038453 | |||||||
| chr22:20038580 | C | T | 1 | a0001c0001t0003g0163 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.56+1726C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20038580 | |||||||
| chr22:20038581 | G | A | 4 | a0003c0004t0014g0027 a0003c0004t0014g0306 a0003c0004t0014g0307 others(1): Show |
5 | HG01257.hp2 HG01258.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.56+1727G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20038581 | |||||||
| chr22:20038684 | G | A | 9 | a0001c0001t0001g0059 a0001c0001t0003g0010 a0001c0001t0003g0058 others(6): Show |
10 | HG00639.hp1 HG00733.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.56+1830G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20038684 | |||||||
| chr22:20038694 | C | T | 1 | a0001c0002t0021g0305 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.56+1840C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20038694 | |||||||
| chr22:20038706 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.56+1852G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20038706 | |||||||
| chr22:20038721 | C | A | 1 | a0002c0003t0018g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.56+1867C>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20038721 | |||||||
| chr22:20038925 | GT | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(237): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.56+2083delT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 20038925 | ||||||
| chr22:20038929 | T | G | 78 | a0001c0001t0001g0015 a0001c0001t0001g0059 a0001c0001t0001g0143 others(75): Show |
84 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.56+2075T>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20038929 | |||||||
| chr22:20038930 | T | G | 5 | a0001c0001t0003g0124 a0001c0001t0003g0130 a0001c0001t0003g0131 others(2): Show |
5 | HG00597.hp2 HG02056.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.56+2076T>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20038930 | |||||||
| chr22:20038935 | T | A | 8 | a0001c0001t0001g0053 a0001c0001t0002g0202 a0001c0001t0013g0116 others(5): Show |
8 | HG00673.hp1 HG01884.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.56+2081T>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20038935 | |||||||
| chr22:20038937 | TA | T | 78 | a0001c0001t0001g0015 a0001c0001t0001g0059 a0001c0001t0001g0143 others(75): Show |
84 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.56+2084delA | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20038937 | |||||||
| chr22:20038938 | A | T | 1 | a0001c0001t0003g0155 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.56+2084A>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20038938 | |||||||
| chr22:20039002 | A | G | 137 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0059 others(134): Show |
151 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.56+2148A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20039002 | |||||||
| chr22:20039035 | G | A | 11 | a0001c0001t0001g0179 a0001c0001t0002g0024 a0001c0001t0002g0209 others(8): Show |
12 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.56+2181G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20039035 | |||||||
| chr22:20039094 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.56+2240C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20039094 | |||||||
| chr22:20039100 | AT | A | 157 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0059 others(154): Show |
174 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.56+2259delT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 20039100 | ||||||
| chr22:20039154 | G | A | 15 | a0001c0001t0007g0007 a0001c0001t0007g0026 a0001c0001t0007g0198 others(12): Show |
18 | HG01069.hp2 HG02015.hp1 HG02129.hp2 others(15): Show |
intron_variant | MODIFIER | c.56+2300G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20039154 | |||||||
| chr22:20039198 | T | C | 1 | a0001c0001t0031g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.56+2344T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20039198 | |||||||
| chr22:20039235 | C | T | 9 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(6): Show |
9 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.56+2381C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20039235 | |||||||
| chr22:20039350 | C | T | 1 | a0001c0001t0031g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.56+2496C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20039350 | |||||||
| chr22:20039367 | G | A | 2 | a0001c0002t0008g0259 a0001c0002t0021g0305 |
2 | HG02630.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.56+2513G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20039367 | |||||||
| chr22:20039394 | T | C | 168 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0050 others(165): Show |
186 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.56+2540T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20039394 | |||||||
| chr22:20039586 | G | A | 1 | a0001c0001t0002g0228 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.56+2732G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20039586 | |||||||
| chr22:20039659 | C | A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG03017.hp1 HG03491.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.56+2805C>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20039659 | |||||||
| chr22:20039747 | G | A | 10 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(7): Show |
11 | HG02257.hp1 HG02451.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.56+2893G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20039747 | |||||||
| chr22:20039799 | C | T | 9 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(6): Show |
9 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.56+2945C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20039799 | |||||||
| chr22:20039822 | C | G | 1 | a0001c0001t0003g0140 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.56+2968C>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20039822 | |||||||
| chr22:20039865 | A | C | 1 | a0001c0001t0003g0073 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.56+3011A>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20039865 | |||||||
| chr22:20039901 | C | T | 1 | a0001c0001t0002g0226 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.56+3047C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20039901 | |||||||
| chr22:20039934 | A | C | 6 | a0001c0001t0003g0041 a0001c0001t0003g0158 a0001c0001t0003g0159 others(3): Show |
6 | HG00544.hp2 HG00609.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.56+3080A>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20039934 | |||||||
| chr22:20040013 | G | T | 1 | a0001c0001t0002g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.56+3159G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20040013 | |||||||
| chr22:20040016 | G | A | 1 | a0001c0001t0004g0183 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.56+3162G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20040016 | |||||||
| chr22:20040081 | T | C | 6 | a0001c0001t0009g0057 a0001c0001t0009g0182 a0001c0001t0009g0185 others(3): Show |
6 | HG01928.hp2 HG02027.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.56+3227T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20040081 | |||||||
| chr22:20040467 | C | A | 3 | a0001c0001t0019g0107 a0001c0001t0019g0108 a0001c0001t0019g0109 |
3 | HG02622.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.57-2888C>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20040467 | |||||||
| chr22:20040535 | A | G | 1 | a0001c0001t0013g0114 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.57-2820A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20040535 | |||||||
| chr22:20041005 | G | T | 3 | a0001c0001t0019g0107 a0001c0001t0019g0108 a0001c0001t0019g0109 |
3 | HG02622.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.57-2350G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20041005 | |||||||
| chr22:20041018 | C | A | 21 | a0001c0001t0007g0007 a0001c0001t0007g0026 a0001c0001t0007g0198 others(18): Show |
24 | HG01069.hp2 HG01928.hp2 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.57-2337C>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20041018 | |||||||
| chr22:20041151 | G | A | 1 | a0001c0001t0016g0190 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.57-2204G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20041151 | |||||||
| chr22:20041312 | A | AT | 71 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0048 others(68): Show |
89 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.57-2025dupT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 20041312 | ||||||
| chr22:20041312 | AT | A | 30 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0162 others(27): Show |
33 | HG01069.hp2 HG01255.hp1 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.57-2025delT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 20041312 | ||||||
| chr22:20041336 | G | C | 1 | a0001c0001t0006g0121 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.57-2019G>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20041336 | |||||||
| chr22:20041382 | G | A | 2 | a0001c0001t0006g0003 a0001c0001t0006g0032 |
3 | HG01975.hp1 HG01993.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.57-1973G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20041382 | |||||||
| chr22:20041414 | A | G | 1 | a0001c0001t0002g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.57-1941A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20041414 | |||||||
| chr22:20041548 | G | A | 1 | a0001c0001t0002g0230 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.57-1807G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20041548 | |||||||
| chr22:20041560 | C | T | 18 | a0001c0001t0001g0053 a0001c0001t0001g0315 a0001c0001t0002g0202 others(15): Show |
19 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.57-1795C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20041560 | |||||||
| chr22:20041678 | C | T | 2 | a0001c0001t0003g0123 a0001c0001t0003g0166 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.57-1677C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20041678 | |||||||
| chr22:20041736 | G | A | 1 | a0001c0001t0003g0176 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.57-1619G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20041736 | |||||||
| chr22:20041737 | T | C | 186 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0050 others(183): Show |
205 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.57-1618T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20041737 | |||||||
| chr22:20041888 | CT | C | 84 | a0001c0001t0001g0015 a0001c0001t0001g0059 a0001c0001t0001g0143 others(81): Show |
90 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.57-1465delT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 20041888 | ||||||
| chr22:20041985 | C | CT | 6 | a0001c0001t0001g0052 a0001c0001t0001g0079 a0001c0001t0002g0263 others(3): Show |
6 | HG01884.hp2 HG01981.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.57-1355dupT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 20041985 | ||||||
| chr22:20042010 | G | T | 1 | a0001c0001t0031g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.57-1345G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20042010 | |||||||
| chr22:20042016 | C | G | 18 | a0001c0001t0001g0053 a0001c0001t0001g0315 a0001c0001t0002g0202 others(15): Show |
19 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.57-1339C>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20042016 | |||||||
| chr22:20042099 | A | G | 1 | a0001c0001t0031g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.57-1256A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20042099 | |||||||
| chr22:20042156 | A | AT | 30 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(27): Show |
34 | HG01069.hp2 HG01928.hp2 HG02015.hp1 others(31): Show |
intron_variant | MODIFIER | c.57-1189dupT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 20042156 | ||||||
| chr22:20042156 | A | ATT | 139 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0059 others(136): Show |
153 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.57-1190_57-1189dup others(2): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | 20042156 | ||||||
| chr22:20042174 | T | C | 1 | a0003c0004t0014g0313 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.57-1181T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20042174 | |||||||
| chr22:20042276 | T | G | 1 | a0001c0001t0004g0321 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.57-1079T>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20042276 | |||||||
| chr22:20042355 | T | C | 168 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0050 others(165): Show |
186 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.57-1000T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20042355 | |||||||
| chr22:20042422 | A | G | 1 | a0001c0001t0031g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.57-933A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20042422 | |||||||
| chr22:20042431 | C | T | 9 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(6): Show |
9 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.57-924C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20042431 | |||||||
| chr22:20042518 | G | A | 44 | a0001c0001t0001g0033 a0001c0001t0002g0196 a0001c0001t0004g0028 others(41): Show |
52 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.57-837G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20042518 | |||||||
| chr22:20042651 | G | C | 9 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
10 | HG02257.hp1 HG02451.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.57-704G>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20042651 | |||||||
| chr22:20042721 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0077 a0001c0001t0001g0097 others(2): Show |
6 | NA18940.hp2 NA18953.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.57-634C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20042721 | |||||||
| chr22:20042946 | C | T | 1 | a0001c0001t0023g0194 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.57-409C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20042946 | |||||||
| chr22:20043006 | A | G | 1 | a0001c0001t0003g0142 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.57-349A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20043006 | |||||||
| chr22:20043133 | C | T | 1 | a0001c0001t0003g0141 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.57-222C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20043133 | |||||||
| chr22:20043134 | A | T | 5 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(2): Show |
5 | HG00099.hp1 HG00738.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.57-221A>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20043134 | |||||||
| chr22:20043214 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.57-141G>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20043214 | |||||||
| chr22:20043226 | C | A | 21 | a0001c0001t0007g0007 a0001c0001t0007g0026 a0001c0001t0007g0198 others(18): Show |
24 | HG01069.hp2 HG01928.hp2 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.57-129C>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 2/8 | chr22 | 20043226 | |||||||
| chr22:20043457 | C | T | 21 | a0001c0001t0007g0007 a0001c0001t0007g0026 a0001c0001t0007g0198 others(18): Show |
24 | HG01069.hp2 HG01928.hp2 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.145+14C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20043457 | |||||||
| chr22:20043493 | G | C | 12 | a0001c0001t0007g0007 a0001c0001t0007g0026 a0001c0001t0007g0223 others(9): Show |
15 | HG01069.hp2 HG02015.hp1 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.145+50G>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20043493 | |||||||
| chr22:20043553 | G | T | 1 | a0002c0003t0018g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.145+110G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20043553 | |||||||
| chr22:20043579 | G | A | 41 | a0001c0001t0001g0033 a0001c0001t0004g0028 a0001c0001t0004g0029 others(38): Show |
49 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.145+136G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20043579 | |||||||
| chr22:20043603 | G | A | 1 | a0001c0002t0008g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.145+160G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20043603 | |||||||
| chr22:20044055 | T | A | 1 | a0001c0001t0002g0231 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.145+612T>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20044055 | |||||||
| chr22:20044141 | G | A | 83 | a0001c0001t0001g0015 a0001c0001t0001g0059 a0001c0001t0001g0143 others(80): Show |
89 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.145+698G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20044141 | |||||||
| chr22:20044327 | A | G | 85 | a0001c0001t0001g0015 a0001c0001t0001g0059 a0001c0001t0001g0132 others(82): Show |
91 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.145+884A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20044327 | |||||||
| chr22:20044329 | T | C | 1 | a0001c0001t0031g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.145+886T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20044329 | |||||||
| chr22:20044386 | C | T | 20 | a0001c0001t0001g0033 a0001c0001t0005g0247 a0001c0001t0006g0003 others(17): Show |
24 | HG00609.hp2 HG01884.hp1 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.145+943C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20044386 | |||||||
| chr22:20044408 | C | T | 5 | a0001c0001t0003g0124 a0001c0001t0003g0130 a0001c0001t0003g0131 others(2): Show |
5 | HG00597.hp2 HG02056.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.145+965C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20044408 | |||||||
| chr22:20044441 | G | T | 21 | a0001c0001t0007g0007 a0001c0001t0007g0026 a0001c0001t0007g0198 others(18): Show |
24 | HG01069.hp2 HG01928.hp2 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.145+998G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20044441 | |||||||
| chr22:20044451 | G | A | 1 | a0001c0001t0030g0210 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.145+1008G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20044451 | |||||||
| chr22:20044484 | C | G | 83 | a0001c0001t0001g0015 a0001c0001t0001g0059 a0001c0001t0001g0143 others(80): Show |
89 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.145+1041C>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20044484 | |||||||
| chr22:20044531 | ATCAG | A | 15 | a0001c0001t0007g0007 a0001c0001t0007g0026 a0001c0001t0007g0198 others(12): Show |
18 | HG01069.hp2 HG02015.hp1 HG02129.hp2 others(15): Show |
intron_variant | MODIFIER | c.145+1092_145+1095d others(6): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20044531 | ||||||
| chr22:20044535 | G | GTCAA | 17 | a0001c0001t0001g0053 a0001c0001t0001g0315 a0001c0001t0002g0202 others(14): Show |
18 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.145+1105_145+1108d others(6): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20044535 | ||||||
| chr22:20044594 | G | T | 2 | a0001c0001t0007g0223 a0001c0001t0009g0324 |
2 | HG01069.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.145+1151G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20044594 | |||||||
| chr22:20044650 | G | A | 2 | a0001c0001t0005g0250 a0001c0005t0002g0251 |
2 | NA18968.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.145+1207G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20044650 | |||||||
| chr22:20044804 | T | C | 187 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0050 others(184): Show |
206 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.145+1361T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20044804 | |||||||
| chr22:20044941 | G | T | 1 | a0001c0001t0001g0006 | 3 | HG02895.hp2 HG02897.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.145+1498G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20044941 | |||||||
| chr22:20045038 | C | T | 3 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0274 |
3 | HG00099.hp1 HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.145+1595C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20045038 | |||||||
| chr22:20045053 | G | A | 24 | a0001c0001t0001g0033 a0001c0001t0002g0196 a0001c0001t0005g0247 others(21): Show |
28 | HG00609.hp2 HG01255.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.145+1610G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20045053 | |||||||
| chr22:20045059 | G | A | 21 | a0001c0001t0007g0007 a0001c0001t0007g0026 a0001c0001t0007g0198 others(18): Show |
24 | HG01069.hp2 HG01928.hp2 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.145+1616G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20045059 | |||||||
| chr22:20045111 | C | T | 1 | a0001c0001t0034g0285 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.145+1668C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20045111 | |||||||
| chr22:20045157 | C | G | 83 | a0001c0001t0001g0059 a0001c0001t0001g0143 a0001c0001t0001g0145 others(80): Show |
88 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.145+1714C>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20045157 | |||||||
| chr22:20045215 | C | T | 2 | a0001c0001t0027g0078 a0001c0001t0033g0294 |
2 | HG03831.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.145+1772C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20045215 | |||||||
| chr22:20045272 | C | CA | 66 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0039 others(63): Show |
84 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.145+1846dupA | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20045272 | ||||||
| chr22:20045272 | CA | C | 152 | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0051 others(149): Show |
166 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.145+1846delA | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20045272 | ||||||
| chr22:20045311 | T | C | 17 | a0001c0001t0001g0053 a0001c0001t0001g0315 a0001c0001t0002g0202 others(14): Show |
18 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.145+1868T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20045311 | |||||||
| chr22:20045409 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.145+1966G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20045409 | |||||||
| chr22:20045499 | C | CT | 10 | a0001c0001t0001g0014 a0001c0001t0001g0077 a0001c0001t0001g0105 others(7): Show |
10 | HG00544.hp1 HG00673.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.145+2077dupT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20045499 | ||||||
| chr22:20045499 | CT | C | 23 | a0001c0001t0001g0053 a0001c0001t0001g0081 a0001c0001t0001g0315 others(20): Show |
24 | HG00639.hp2 HG01257.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.145+2077delT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20045499 | ||||||
| chr22:20045499 | CTT | C | 123 | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0051 others(120): Show |
133 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.145+2076_145+2077d others(4): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20045499 | ||||||
| chr22:20045499 | CTTT | C | 19 | a0001c0001t0007g0007 a0001c0001t0007g0026 a0001c0001t0007g0198 others(16): Show |
22 | HG01069.hp2 HG02015.hp1 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.145+2075_145+2077d others(5): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20045499 | ||||||
| chr22:20045581 | G | A | 1 | a0001c0001t0004g0134 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.145+2138G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20045581 | |||||||
| chr22:20045745 | C | T | 1 | a0001c0001t0002g0265 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.145+2302C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20045745 | |||||||
| chr22:20046063 | G | C | 1 | a0001c0001t0004g0331 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.145+2620G>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20046063 | |||||||
| chr22:20046212 | C | A | 9 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(6): Show |
9 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.145+2769C>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20046212 | |||||||
| chr22:20046234 | C | G | 9 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(6): Show |
9 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.145+2791C>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20046234 | |||||||
| chr22:20046252 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.145+2809C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20046252 | |||||||
| chr22:20046342 | C | G | 1 | a0001c0001t0023g0194 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.145+2899C>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20046342 | |||||||
| chr22:20046436 | A | G | 1 | a0001c0001t0012g0207 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.145+2993A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20046436 | |||||||
| chr22:20046460 | A | AT | 6 | a0001c0001t0001g0064 a0001c0001t0001g0080 a0001c0001t0001g0097 others(3): Show |
6 | HG00738.hp1 HG01978.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.145+3039dupT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20046460 | ||||||
| chr22:20046460 | AT | A | 123 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0039 others(120): Show |
152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.145+3039delT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20046460 | ||||||
| chr22:20046460 | ATT | A | 111 | a0001c0001t0001g0033 a0001c0001t0001g0059 a0001c0001t0001g0145 others(108): Show |
120 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.145+3038_145+3039d others(4): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20046460 | ||||||
| chr22:20046460 | ATTT | A | 8 | a0001c0001t0001g0162 a0001c0001t0003g0325 a0001c0001t0005g0292 others(5): Show |
8 | HG01070.hp1 HG02145.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.145+3037_145+3039d others(5): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20046460 | ||||||
| chr22:20046469 | T | C | 1 | a0001c0001t0030g0210 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.145+3026T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20046469 | |||||||
| chr22:20046527 | C | T | 2 | a0001c0001t0003g0124 a0001c0001t0009g0057 |
2 | HG00597.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.145+3084C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20046527 | |||||||
| chr22:20046693 | G | A | 2 | a0001c0001t0008g0256 a0001c0001t0021g0314 |
2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.145+3250G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20046693 | |||||||
| chr22:20046784 | G | A | 1 | a0001c0001t0004g0144 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.145+3341G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20046784 | |||||||
| chr22:20046791 | T | C | 24 | a0001c0001t0001g0033 a0001c0001t0002g0196 a0001c0001t0005g0247 others(21): Show |
28 | HG00609.hp2 HG01255.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.145+3348T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20046791 | |||||||
| chr22:20046868 | C | T | 82 | a0001c0001t0001g0059 a0001c0001t0001g0145 a0001c0001t0001g0146 others(79): Show |
87 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.145+3425C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20046868 | |||||||
| chr22:20047118 | A | T | 1 | a0002c0003t0018g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.145+3675A>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20047118 | |||||||
| chr22:20047224 | G | GTT | 6 | a0002c0003t0010g0046 a0002c0003t0010g0110 a0002c0003t0010g0308 others(3): Show |
6 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+3783_145+3784d others(4): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20047224 | ||||||
| chr22:20047224 | G | GTTT | 3 | a0002c0003t0010g0047 a0002c0003t0010g0311 a0002c0003t0018g0197 |
3 | HG03209.hp1 HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.145+3782_145+3784d others(5): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20047224 | ||||||
| chr22:20047228 | G | GT | 5 | a0001c0001t0001g0080 a0001c0001t0001g0096 a0001c0001t0001g0097 others(2): Show |
5 | HG00423.hp1 HG01106.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.145+3788dupT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20047228 | ||||||
| chr22:20047228 | G | T | 9 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(6): Show |
9 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.145+3785G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20047228 | |||||||
| chr22:20047232 | G | GT | 15 | a0001c0001t0001g0137 a0001c0001t0002g0001 a0001c0001t0002g0291 others(12): Show |
15 | HG00621.hp1 HG00621.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.145+3807dupT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20047232 | ||||||
| chr22:20047232 | G | T | 82 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(79): Show |
94 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.145+3789G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20047232 | |||||||
| chr22:20047232 | GT | G | 10 | a0001c0001t0001g0146 a0001c0001t0001g0162 a0001c0001t0001g0339 others(7): Show |
10 | HG01169.hp2 HG01517.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.145+3807delT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20047232 | ||||||
| chr22:20047238 | T | G | 2 | a0001c0001t0008g0256 a0001c0001t0021g0314 |
2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.145+3795T>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20047238 | |||||||
| chr22:20047296 | C | T | 24 | a0001c0001t0001g0033 a0001c0001t0002g0196 a0001c0001t0005g0247 others(21): Show |
28 | HG00609.hp2 HG01255.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.145+3853C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20047296 | |||||||
| chr22:20047505 | G | T | 3 | a0001c0001t0004g0029 a0001c0001t0004g0329 a0001c0001t0004g0331 |
4 | HG00642.hp1 HG03654.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+4062G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20047505 | |||||||
| chr22:20047628 | C | T | 9 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(6): Show |
9 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.145+4185C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20047628 | |||||||
| chr22:20047741 | C | A | 20 | a0001c0001t0001g0033 a0001c0001t0005g0247 a0001c0001t0006g0003 others(17): Show |
24 | HG00609.hp2 HG01884.hp1 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.145+4298C>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20047741 | |||||||
| chr22:20047923 | G | GT | 21 | a0001c0001t0007g0007 a0001c0001t0007g0026 a0001c0001t0007g0198 others(18): Show |
24 | HG01069.hp2 HG01928.hp2 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.145+4484dupT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20047923 | ||||||
| chr22:20047928 | G | GT | 7 | a0001c0001t0001g0067 a0001c0001t0001g0095 a0001c0001t0001g0098 others(4): Show |
7 | HG00733.hp2 HG02559.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.145+4498dupT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20047928 | ||||||
| chr22:20047928 | G | T | 21 | a0001c0001t0007g0007 a0001c0001t0007g0026 a0001c0001t0007g0198 others(18): Show |
24 | HG01069.hp2 HG01928.hp2 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.145+4485G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20047928 | |||||||
| chr22:20047933 | T | G | 3 | a0001c0001t0001g0059 a0001c0001t0001g0145 a0001c0001t0001g0164 |
3 | HG01975.hp2 HG02004.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.145+4490T>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20047933 | |||||||
| chr22:20047988 | G | A | 1 | a0001c0001t0031g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.146-4477G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20047988 | |||||||
| chr22:20047994 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.146-4471G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20047994 | |||||||
| chr22:20048014 | T | A | 1 | a0001c0001t0005g0292 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.146-4451T>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20048014 | |||||||
| chr22:20048167 | C | T | 113 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(110): Show |
122 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.146-4298C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20048167 | |||||||
| chr22:20048403 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.146-4062C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20048403 | |||||||
| chr22:20048404 | G | A | 1 | a0001c0001t0003g0158 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.146-4061G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20048404 | |||||||
| chr22:20048591 | A | G | 1 | a0001c0001t0004g0333 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.146-3874A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20048591 | |||||||
| chr22:20048605 | T | G | 2 | a0001c0001t0004g0125 a0001c0001t0004g0135 |
2 | NA18995.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.146-3860T>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20048605 | |||||||
| chr22:20048645 | A | AT | 9 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(6): Show |
9 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.146-3808dupT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20048645 | ||||||
| chr22:20048645 | AT | A | 13 | a0001c0001t0001g0179 a0001c0001t0001g0339 a0001c0001t0002g0024 others(10): Show |
14 | HG01069.hp1 HG01169.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.146-3808delT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20048645 | ||||||
| chr22:20048669 | G | A | 1 | a0001c0001t0002g0233 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.146-3796G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20048669 | |||||||
| chr22:20048708 | G | A | 3 | a0001c0001t0019g0107 a0001c0001t0019g0108 a0001c0001t0019g0109 |
3 | HG02622.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.146-3757G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20048708 | |||||||
| chr22:20048924 | C | T | 1 | a0001c0001t0006g0043 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.146-3541C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20048924 | |||||||
| chr22:20048991 | G | A | 8 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(5): Show |
8 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.146-3474G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20048991 | |||||||
| chr22:20049014 | A | G | 1 | a0001c0002t0008g0280 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.146-3451A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20049014 | |||||||
| chr22:20049172 | A | G | 5 | a0001c0001t0003g0123 a0001c0001t0003g0165 a0001c0001t0003g0166 others(2): Show |
5 | HG01123.hp1 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.146-3293A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20049172 | |||||||
| chr22:20049172 | AAT | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0233 |
3 | HG02602.hp2 HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.146-3292_146-3291d others(4): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20049172 | |||||||
| chr22:20049519 | G | A | 4 | a0001c0002t0008g0203 a0001c0002t0008g0280 a0001c0002t0008g0281 others(1): Show |
4 | HG01884.hp2 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-2946G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20049519 | |||||||
| chr22:20049585 | G | A | 9 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(6): Show |
9 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.146-2880G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20049585 | |||||||
| chr22:20049617 | G | A | 1 | a0001c0001t0011g0101 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.146-2848G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20049617 | |||||||
| chr22:20049655 | T | A | 1 | a0001c0001t0002g0241 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.146-2810T>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20049655 | |||||||
| chr22:20049660 | C | CA | 34 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(31): Show |
38 | HG00544.hp2 HG01069.hp2 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.146-2788dupA | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20049660 | ||||||
| chr22:20049660 | CA | C | 33 | a0001c0001t0001g0033 a0001c0001t0002g0196 a0001c0001t0005g0247 others(30): Show |
37 | HG00609.hp2 HG01255.hp2 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.146-2788delA | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20049660 | ||||||
| chr22:20049664 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.146-2801A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20049664 | |||||||
| chr22:20049718 | G | A | 2 | a0001c0001t0006g0035 a0002c0007t0035g0267 |
2 | HG02559.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.146-2747G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20049718 | |||||||
| chr22:20049792 | G | A | 147 | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0051 others(144): Show |
160 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(157): Show |
intron_variant | MODIFIER | c.146-2673G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20049792 | |||||||
| chr22:20049946 | C | T | 9 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0077 others(6): Show |
11 | NA18940.hp2 NA18951.hp2 NA18953.hp1 others(8): Show |
intron_variant | MODIFIER | c.146-2519C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20049946 | |||||||
| chr22:20049984 | C | T | 24 | a0001c0001t0001g0033 a0001c0001t0002g0196 a0001c0001t0005g0247 others(21): Show |
28 | HG00609.hp2 HG01255.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.146-2481C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20049984 | |||||||
| chr22:20049994 | A | G | 24 | a0001c0001t0001g0033 a0001c0001t0002g0196 a0001c0001t0005g0247 others(21): Show |
28 | HG00609.hp2 HG01255.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.146-2471A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20049994 | |||||||
| chr22:20050004 | C | T | 1 | a0001c0001t0031g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.146-2461C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050004 | |||||||
| chr22:20050175 | C | T | 9 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
10 | HG02257.hp1 HG02451.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.146-2290C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050175 | |||||||
| chr22:20050297 | C | T | 24 | a0001c0001t0001g0033 a0001c0001t0002g0196 a0001c0001t0005g0247 others(21): Show |
28 | HG00609.hp2 HG01255.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.146-2168C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050297 | |||||||
| chr22:20050356 | TG | T | 72 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0054 others(69): Show |
78 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.146-2107delG | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20050356 | ||||||
| chr22:20050357 | G | GT | 62 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0064 others(59): Show |
68 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.146-2108_146-2107i others(3): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050357 | |||||||
| chr22:20050357 | G | GTT | 8 | a0001c0001t0001g0015 a0001c0001t0001g0335 a0001c0001t0002g0290 others(5): Show |
8 | HG01175.hp1 HG02135.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.146-2108_146-2107i others(4): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050357 | |||||||
| chr22:20050357 | GGT | G | 20 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0146 others(17): Show |
24 | HG01255.hp2 HG01884.hp1 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.146-2107_146-2106d others(4): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050357 | |||||||
| chr22:20050358 | G | T | 247 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(244): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.146-2107G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050358 | |||||||
| chr22:20050368 | T | G | 20 | a0001c0001t0007g0007 a0001c0001t0007g0026 a0001c0001t0007g0198 others(17): Show |
23 | HG01069.hp2 HG01928.hp2 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.146-2097T>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050368 | |||||||
| chr22:20050425 | G | A | 1 | a0003c0004t0014g0313 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.146-2040G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050425 | |||||||
| chr22:20050430 | C | A | 2 | a0001c0001t0023g0193 a0001c0001t0023g0194 |
2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.146-2035C>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050430 | |||||||
| chr22:20050508 | T | A | 1 | a0001c0001t0003g0016 | 2 | NA18964.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.146-1957T>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050508 | |||||||
| chr22:20050604 | C | T | 4 | a0003c0004t0014g0027 a0003c0004t0014g0306 a0003c0004t0014g0307 others(1): Show |
5 | HG01257.hp2 HG01258.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.146-1861C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050604 | |||||||
| chr22:20050608 | C | T | 1 | a0002c0007t0035g0267 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.146-1857C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050608 | |||||||
| chr22:20050660 | C | CT | 25 | a0001c0001t0001g0033 a0001c0001t0003g0126 a0001c0001t0005g0247 others(22): Show |
29 | HG00609.hp2 HG01884.hp1 HG01952.hp2 others(26): Show |
intron_variant | MODIFIER | c.146-1789dupT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20050660 | ||||||
| chr22:20050660 | CT | C | 6 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0085 others(3): Show |
6 | HG03490.hp2 HG03491.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.146-1789delT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20050660 | ||||||
| chr22:20050680 | C | G | 6 | a0001c0001t0003g0167 a0001c0001t0003g0168 a0001c0001t0005g0008 others(3): Show |
8 | HG00438.hp2 HG00673.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.146-1785C>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050680 | |||||||
| chr22:20050687 | A | G | 1 | a0001c0001t0016g0190 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.146-1778A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050687 | |||||||
| chr22:20050715 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.146-1750T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050715 | |||||||
| chr22:20050759 | T | C | 1 | a0002c0007t0035g0267 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.146-1706T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050759 | |||||||
| chr22:20050769 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.146-1696T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050769 | |||||||
| chr22:20050774 | C | A | 9 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(6): Show |
9 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.146-1691C>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050774 | |||||||
| chr22:20050793 | G | A | 9 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(6): Show |
9 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.146-1672G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050793 | |||||||
| chr22:20050838 | T | G | 1 | a0001c0001t0007g0286 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.146-1627T>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050838 | |||||||
| chr22:20050842 | G | GT | 18 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0117 others(15): Show |
19 | HG01175.hp1 HG01175.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.146-1607dupT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20050842 | ||||||
| chr22:20050842 | GT | G | 126 | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0051 others(123): Show |
136 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.146-1607delT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr22 | 20050842 | ||||||
| chr22:20050863 | C | A | 2 | a0001c0001t0002g0214 a0001c0001t0002g0225 |
2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.146-1602C>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050863 | |||||||
| chr22:20050867 | G | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.146-1598G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050867 | |||||||
| chr22:20050883 | A | T | 1 | a0001c0001t0002g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.146-1582A>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050883 | |||||||
| chr22:20050969 | A | G | 92 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(89): Show |
98 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.146-1496A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20050969 | |||||||
| chr22:20051021 | C | T | 3 | a0001c0001t0002g0237 a0001c0001t0002g0239 a0001c0001t0002g0304 |
3 | NA18975.hp2 NA19062.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.146-1444C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20051021 | |||||||
| chr22:20051199 | T | G | 24 | a0001c0001t0001g0033 a0001c0001t0002g0196 a0001c0001t0005g0247 others(21): Show |
28 | HG00609.hp2 HG01255.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.146-1266T>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20051199 | |||||||
| chr22:20051233 | T | C | 9 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(6): Show |
9 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.146-1232T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20051233 | |||||||
| chr22:20051259 | C | T | 1 | a0001c0001t0006g0133 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.146-1206C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20051259 | |||||||
| chr22:20051303 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.146-1162G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20051303 | |||||||
| chr22:20051306 | C | T | 1 | a0002c0003t0018g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.146-1159C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20051306 | |||||||
| chr22:20051428 | G | A | 2 | a0001c0001t0012g0276 a0001c0001t0012g0300 |
2 | NA18943.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.146-1037G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20051428 | |||||||
| chr22:20051446 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.146-1019G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20051446 | |||||||
| chr22:20051632 | G | A | 2 | a0001c0001t0002g0288 a0001c0001t0002g0289 |
2 | HG01255.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.146-833G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20051632 | |||||||
| chr22:20051665 | A | G | 1 | a0001c0001t0031g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.146-800A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20051665 | |||||||
| chr22:20052108 | C | A | 1 | a0001c0001t0004g0334 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.146-357C>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20052108 | |||||||
| chr22:20052108 | C | T | 1 | a0001c0001t0015g0200 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.146-357C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20052108 | |||||||
| chr22:20052112 | C | T | 2 | a0001c0001t0009g0182 a0001c0001t0009g0188 |
2 | HG03688.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.146-353C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20052112 | |||||||
| chr22:20052195 | G | A | 8 | a0001c0002t0008g0201 a0001c0002t0008g0203 a0001c0002t0008g0280 others(5): Show |
8 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.146-270G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20052195 | |||||||
| chr22:20052259 | C | T | 1 | a0001c0001t0002g0266 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.146-206C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20052259 | |||||||
| chr22:20052344 | C | T | 24 | a0001c0001t0001g0033 a0001c0001t0002g0196 a0001c0001t0005g0247 others(21): Show |
28 | HG00609.hp2 HG01255.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.146-121C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20052344 | |||||||
| chr22:20052413 | G | A | 1 | a0001c0002t0024g0205 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.146-52G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 3/8 | chr22 | 20052413 | |||||||
| chr22:20052629 | G | C | 1 | a0001c0001t0002g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.265+45G>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 4/8 | chr22 | 20052629 | |||||||
| chr22:20052692 | T | C | 1 | a0001c0001t0032g0217 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.265+108T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 4/8 | chr22 | 20052692 | |||||||
| chr22:20052697 | C | T | 9 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
10 | HG02257.hp1 HG02451.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.265+113C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 4/8 | chr22 | 20052697 | |||||||
| chr22:20052718 | A | C | 1 | a0001c0001t0003g0152 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.265+134A>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 4/8 | chr22 | 20052718 | |||||||
| chr22:20052803 | G | A | 1 | a0001c0001t0013g0114 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.265+219G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 4/8 | chr22 | 20052803 | |||||||
| chr22:20052807 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.265+223C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 4/8 | chr22 | 20052807 | |||||||
| chr22:20052858 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.265+274G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 4/8 | chr22 | 20052858 | |||||||
| chr22:20052877 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.265+293C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 4/8 | chr22 | 20052877 | |||||||
| chr22:20052895 | G | A | 1 | a0001c0008t0001g0086 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.265+311G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 4/8 | chr22 | 20052895 | |||||||
| chr22:20052991 | C | T | 3 | a0001c0001t0006g0035 a0001c0001t0006g0037 a0001c0001t0006g0049 |
3 | NA18973.hp2 NA18975.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.265+407C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 4/8 | chr22 | 20052991 | |||||||
| chr22:20053016 | C | T | 1 | a0001c0001t0001g0015 | 2 | NA18952.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.266-421C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 4/8 | chr22 | 20053016 | |||||||
| chr22:20053017 | G | A | 9 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(6): Show |
9 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.266-420G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 4/8 | chr22 | 20053017 | |||||||
| chr22:20053032 | C | T | 1 | a0001c0001t0003g0142 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.266-405C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 4/8 | chr22 | 20053032 | |||||||
| chr22:20053079 | C | T | 82 | a0001c0001t0001g0059 a0001c0001t0001g0145 a0001c0001t0001g0146 others(79): Show |
87 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.266-358C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 4/8 | chr22 | 20053079 | |||||||
| chr22:20053156 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.266-281A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 4/8 | chr22 | 20053156 | |||||||
| chr22:20053187 | A | T | 1 | a0001c0001t0019g0108 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.266-250A>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 4/8 | chr22 | 20053187 | |||||||
| chr22:20053228 | T | G | 1 | a0002c0007t0035g0267 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.266-209T>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 4/8 | chr22 | 20053228 | |||||||
| chr22:20053298 | T | TG | 21 | a0001c0001t0007g0007 a0001c0001t0007g0026 a0001c0001t0007g0198 others(18): Show |
24 | HG01069.hp2 HG01928.hp2 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.266-138dupG | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | 20053298 | ||||||
| chr22:20053308 | A | C | 1 | a0002c0003t0010g0110 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.266-129A>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 4/8 | chr22 | 20053308 | |||||||
| chr22:20053698 | C | T | 1 | a0001c0001t0013g0114 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.380+147C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20053698 | |||||||
| chr22:20053709 | A | G | 9 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(6): Show |
9 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.380+158A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20053709 | |||||||
| chr22:20054004 | C | T | 3 | a0001c0001t0019g0107 a0001c0001t0019g0108 a0001c0001t0019g0109 |
3 | HG02622.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.380+453C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20054004 | |||||||
| chr22:20054075 | C | T | 2 | a0001c0001t0023g0193 a0002c0003t0018g0253 |
2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.380+524C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20054075 | |||||||
| chr22:20054086 | C | T | 21 | a0001c0001t0007g0007 a0001c0001t0007g0026 a0001c0001t0007g0198 others(18): Show |
24 | HG01069.hp2 HG01928.hp2 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.380+535C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20054086 | |||||||
| chr22:20054159 | G | A | 1 | a0001c0001t0003g0127 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.380+608G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20054159 | |||||||
| chr22:20054181 | T | C | 9 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(6): Show |
9 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.380+630T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20054181 | |||||||
| chr22:20054182 | G | A | 9 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(6): Show |
9 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.380+631G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20054182 | |||||||
| chr22:20054213 | T | C | 33 | a0001c0001t0001g0033 a0001c0001t0002g0196 a0001c0001t0005g0247 others(30): Show |
37 | HG00609.hp2 HG01255.hp2 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.380+662T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20054213 | |||||||
| chr22:20054218 | C | T | 83 | a0001c0001t0001g0059 a0001c0001t0001g0145 a0001c0001t0001g0146 others(80): Show |
88 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.380+667C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20054218 | |||||||
| chr22:20054221 | A | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG03017.hp1 HG03491.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.380+670A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20054221 | |||||||
| chr22:20054310 | G | A | 1 | a0001c0001t0002g0196 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.380+759G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20054310 | |||||||
| chr22:20054343 | C | G | 1 | a0001c0001t0023g0194 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.380+792C>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20054343 | |||||||
| chr22:20054455 | G | A | 1 | a0001c0001t0031g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.380+904G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20054455 | |||||||
| chr22:20054552 | T | G | 148 | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0051 others(145): Show |
161 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(158): Show |
intron_variant | MODIFIER | c.380+1001T>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20054552 | |||||||
| chr22:20054553 | TG | T | 9 | a0001c0001t0002g0025 a0001c0001t0002g0226 a0001c0001t0002g0245 others(6): Show |
10 | HG00673.hp1 HG01255.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.380+1007delG | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | 20054553 | ||||||
| chr22:20054590 | C | T | 1 | a0001c0001t0013g0114 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.380+1039C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20054590 | |||||||
| chr22:20054591 | G | A | 24 | a0001c0001t0001g0033 a0001c0001t0002g0196 a0001c0001t0005g0247 others(21): Show |
28 | HG00609.hp2 HG01255.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.380+1040G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20054591 | |||||||
| chr22:20054757 | G | A | 1 | a0001c0001t0011g0100 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.381-1186G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20054757 | |||||||
| chr22:20054819 | C | G | 1 | a0001c0001t0001g0082 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.381-1124C>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20054819 | |||||||
| chr22:20054872 | T | C | 1 | a0001c0001t0003g0142 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.381-1071T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20054872 | |||||||
| chr22:20055004 | C | T | 1 | a0001c0001t0023g0194 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.381-939C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20055004 | |||||||
| chr22:20055010 | G | C | 1 | a0001c0001t0002g0226 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.381-933G>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20055010 | |||||||
| chr22:20055040 | G | A | 9 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
10 | HG02257.hp1 HG02451.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.381-903G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20055040 | |||||||
| chr22:20055041 | T | G | 9 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
10 | HG02257.hp1 HG02451.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.381-902T>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20055041 | |||||||
| chr22:20055067 | G | A | 1 | a0001c0001t0002g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.381-876G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20055067 | |||||||
| chr22:20055325 | A | G | 20 | a0001c0001t0001g0033 a0001c0001t0005g0247 a0001c0001t0006g0003 others(17): Show |
24 | HG00609.hp2 HG01884.hp1 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.381-618A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20055325 | |||||||
| chr22:20055578 | T | G | 9 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
10 | HG02257.hp1 HG02451.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.381-365T>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20055578 | |||||||
| chr22:20055666 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0112 a0001c0001t0028g0014 |
3 | HG02976.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.381-277C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20055666 | |||||||
| chr22:20055744 | A | C | 2 | a0001c0002t0008g0260 a0001c0002t0008g0261 |
2 | HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.381-199A>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20055744 | |||||||
| chr22:20055836 | A | C | 9 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(6): Show |
9 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.381-107A>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20055836 | |||||||
| chr22:20055847 | C | T | 10 | a0001c0001t0002g0025 a0001c0001t0002g0226 a0001c0001t0002g0245 others(7): Show |
11 | HG00673.hp1 HG01255.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.381-96C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20055847 | |||||||
| chr22:20055848 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.381-95G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20055848 | |||||||
| chr22:20055900 | G | A | 2 | a0001c0001t0004g0069 a0001c0001t0004g0070 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.381-43G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 5/8 | chr22 | 20055900 | |||||||
| chr22:20056047 | G | A | 1 | a0001c0001t0002g0196 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.451+34G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20056047 | |||||||
| chr22:20056059 | G | A | 1 | a0002c0003t0018g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.451+46G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20056059 | |||||||
| chr22:20056177 | A | G | 24 | a0001c0001t0001g0033 a0001c0001t0005g0247 a0001c0001t0006g0003 others(21): Show |
28 | HG00609.hp2 HG01884.hp1 HG01952.hp2 others(25): Show |
intron_variant | MODIFIER | c.451+164A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20056177 | |||||||
| chr22:20056196 | C | A | 1 | a0001c0001t0039g0258 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.451+183C>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20056196 | |||||||
| chr22:20056245 | C | T | 1 | a0001c0001t0001g0006 | 3 | HG02895.hp2 HG02897.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.451+232C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20056245 | |||||||
| chr22:20056428 | A | G | 1 | a0002c0003t0018g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.451+415A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20056428 | |||||||
| chr22:20056448 | C | T | 1 | a0001c0001t0002g0269 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.451+435C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20056448 | |||||||
| chr22:20056518 | G | A | 9 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(6): Show |
9 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.451+505G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20056518 | |||||||
| chr22:20056606 | C | T | 1 | a0001c0001t0033g0294 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.451+593C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20056606 | |||||||
| chr22:20056924 | G | T | 1 | a0001c0001t0009g0182 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.451+911G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20056924 | |||||||
| chr22:20056933 | C | T | 1 | a0002c0003t0018g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.451+920C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20056933 | |||||||
| chr22:20057114 | G | A | 1 | a0001c0001t0015g0200 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.451+1101G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20057114 | |||||||
| chr22:20057135 | G | A | 1 | a0001c0001t0030g0210 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.451+1122G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20057135 | |||||||
| chr22:20057410 | G | A | 90 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(87): Show |
96 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.451+1397G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20057410 | |||||||
| chr22:20057513 | C | T | 1 | a0001c0001t0002g0218 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.451+1500C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20057513 | |||||||
| chr22:20057860 | G | A | 25 | a0001c0001t0001g0033 a0001c0001t0005g0247 a0001c0001t0006g0003 others(22): Show |
29 | HG00609.hp2 HG01884.hp1 HG01952.hp2 others(26): Show |
intron_variant | MODIFIER | c.451+1847G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20057860 | |||||||
| chr22:20057888 | A | G | 171 | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0051 others(168): Show |
188 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.451+1875A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20057888 | |||||||
| chr22:20057893 | G | A | 25 | a0001c0001t0001g0033 a0001c0001t0005g0247 a0001c0001t0006g0003 others(22): Show |
29 | HG00609.hp2 HG01884.hp1 HG01952.hp2 others(26): Show |
intron_variant | MODIFIER | c.451+1880G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20057893 | |||||||
| chr22:20057896 | T | C | 271 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0039 others(268): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.451+1883T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20057896 | |||||||
| chr22:20057897 | C | T | 1 | a0001c0001t0023g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.451+1884C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20057897 | |||||||
| chr22:20058029 | T | TTA | 9 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(6): Show |
9 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.451+2017_451+2018i others(4): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 20058029 | ||||||
| chr22:20058030 | T | TA | 137 | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0051 others(134): Show |
150 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.451+2017_451+2018i others(3): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20058030 | |||||||
| chr22:20058031 | T | A | 1 | a0001c0001t0005g0242 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.451+2018T>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20058031 | |||||||
| chr22:20058042 | A | G | 2 | a0001c0002t0024g0199 a0001c0002t0029g0312 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.451+2029A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20058042 | |||||||
| chr22:20058216 | G | A | 6 | a0001c0001t0004g0125 a0001c0001t0004g0134 a0001c0001t0004g0135 others(3): Show |
6 | NA18951.hp1 NA18953.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.451+2203G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20058216 | |||||||
| chr22:20058360 | T | C | 34 | a0001c0001t0001g0033 a0001c0001t0005g0247 a0001c0001t0006g0003 others(31): Show |
38 | HG00609.hp2 HG01884.hp1 HG01952.hp2 others(35): Show |
intron_variant | MODIFIER | c.451+2347T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20058360 | |||||||
| chr22:20058444 | C | A | 34 | a0001c0001t0001g0033 a0001c0001t0005g0247 a0001c0001t0006g0003 others(31): Show |
38 | HG00609.hp2 HG01884.hp1 HG01952.hp2 others(35): Show |
intron_variant | MODIFIER | c.451+2431C>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20058444 | |||||||
| chr22:20058470 | A | G | 1 | a0001c0001t0003g0150 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.451+2457A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20058470 | |||||||
| chr22:20058503 | G | A | 1 | a0001c0001t0002g0226 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.451+2490G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20058503 | |||||||
| chr22:20058519 | A | G | 20 | a0001c0001t0004g0028 a0001c0001t0004g0029 a0001c0001t0004g0069 others(17): Show |
24 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.451+2506A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20058519 | |||||||
| chr22:20058597 | G | A | 4 | a0001c0001t0004g0069 a0001c0001t0004g0070 a0001c0001t0004g0072 others(1): Show |
4 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+2584G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20058597 | |||||||
| chr22:20058627 | G | A | 9 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(6): Show |
9 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.451+2614G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20058627 | |||||||
| chr22:20058641 | C | CAA | 17 | a0001c0001t0004g0028 a0001c0001t0004g0029 a0001c0001t0004g0069 others(14): Show |
21 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.451+2641_451+2642d others(4): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 20058641 | ||||||
| chr22:20058641 | CA | C | 47 | a0001c0001t0001g0033 a0001c0001t0005g0247 a0001c0001t0006g0003 others(44): Show |
54 | HG00609.hp2 HG01069.hp2 HG01884.hp1 others(51): Show |
intron_variant | MODIFIER | c.451+2642delA | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 20058641 | ||||||
| chr22:20058681 | A | C | 2 | a0001c0001t0007g0278 a0001c0001t0007g0282 |
2 | NA18959.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.451+2668A>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20058681 | |||||||
| chr22:20058821 | A | G | 89 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0048 others(86): Show |
108 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.452-2709A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20058821 | |||||||
| chr22:20058880 | C | T | 1 | a0002c0007t0035g0267 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.452-2650C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20058880 | |||||||
| chr22:20059164 | G | A | 233 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0048 others(230): Show |
264 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.452-2366G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20059164 | |||||||
| chr22:20059421 | G | A | 2 | a0001c0001t0001g0315 a0001c0001t0002g0202 |
2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.452-2109G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20059421 | |||||||
| chr22:20059575 | G | A | 2 | a0001c0001t0003g0127 a0001c0001t0005g0243 |
2 | HG00621.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.452-1955G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20059575 | |||||||
| chr22:20059737 | T | C | 1 | a0001c0001t0036g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.452-1793T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20059737 | |||||||
| chr22:20059891 | A | G | 1 | a0002c0007t0035g0267 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.452-1639A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20059891 | |||||||
| chr22:20059960 | A | AT | 6 | a0001c0001t0002g0252 a0001c0001t0002g0254 a0001c0001t0006g0042 others(3): Show |
6 | HG02280.hp2 HG02723.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.452-1557dupT | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 20059960 | ||||||
| chr22:20059981 | G | T | 1 | a0001c0001t0002g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.452-1549G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20059981 | |||||||
| chr22:20060064 | T | C | 25 | a0001c0001t0001g0033 a0001c0001t0005g0247 a0001c0001t0006g0003 others(22): Show |
29 | HG00609.hp2 HG01884.hp1 HG01952.hp2 others(26): Show |
intron_variant | MODIFIER | c.452-1466T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20060064 | |||||||
| chr22:20060098 | C | CCAGCACT others(6): Show |
1 | a0001c0001t0002g0271 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.452-1431_452-1419d others(15): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 20060098 | ||||||
| chr22:20060243 | G | A | 9 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(6): Show |
9 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.452-1287G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20060243 | |||||||
| chr22:20060292 | T | C | 13 | a0001c0002t0008g0023 a0001c0002t0008g0201 a0001c0002t0008g0203 others(10): Show |
14 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.452-1238T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20060292 | |||||||
| chr22:20060328 | G | T | 21 | a0001c0001t0008g0256 a0001c0001t0021g0314 a0001c0001t0023g0193 others(18): Show |
23 | HG01257.hp2 HG01258.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.452-1202G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20060328 | |||||||
| chr22:20060348 | C | CA | 118 | a0001c0001t0002g0216 a0001c0001t0002g0234 a0001c0001t0002g0238 others(115): Show |
128 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.452-1162dupA | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 20060348 | ||||||
| chr22:20060348 | C | CAA | 26 | a0001c0001t0001g0033 a0001c0001t0005g0247 a0001c0001t0005g0299 others(23): Show |
30 | HG00609.hp2 HG01884.hp1 HG01952.hp2 others(27): Show |
intron_variant | MODIFIER | c.452-1163_452-1162d others(4): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 20060348 | ||||||
| chr22:20060348 | CA | C | 25 | a0001c0001t0001g0062 a0001c0001t0001g0084 a0001c0001t0001g0089 others(22): Show |
29 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(26): Show |
intron_variant | MODIFIER | c.452-1162delA | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr22 | 20060348 | ||||||
| chr22:20060450 | C | T | 25 | a0001c0001t0001g0033 a0001c0001t0005g0247 a0001c0001t0006g0003 others(22): Show |
29 | HG00609.hp2 HG01884.hp1 HG01952.hp2 others(26): Show |
intron_variant | MODIFIER | c.452-1080C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20060450 | |||||||
| chr22:20060525 | G | A | 1 | a0001c0001t0003g0176 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.452-1005G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20060525 | |||||||
| chr22:20060560 | T | C | 25 | a0001c0001t0001g0033 a0001c0001t0005g0247 a0001c0001t0006g0003 others(22): Show |
29 | HG00609.hp2 HG01884.hp1 HG01952.hp2 others(26): Show |
intron_variant | MODIFIER | c.452-970T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20060560 | |||||||
| chr22:20060590 | A | G | 1 | a0001c0001t0036g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.452-940A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20060590 | |||||||
| chr22:20060924 | G | A | 4 | a0001c0001t0004g0028 a0001c0001t0004g0328 a0001c0001t0004g0330 others(1): Show |
5 | HG00099.hp2 HG00639.hp2 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-606G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20060924 | |||||||
| chr22:20061045 | T | G | 1 | a0001c0001t0037g0293 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.452-485T>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20061045 | |||||||
| chr22:20061124 | G | C | 24 | a0001c0001t0003g0060 a0001c0001t0006g0003 a0001c0001t0006g0030 others(21): Show |
28 | HG00609.hp2 HG01884.hp1 HG01952.hp2 others(25): Show |
intron_variant | MODIFIER | c.452-406G>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20061124 | |||||||
| chr22:20061190 | G | T | 1 | a0002c0007t0035g0267 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.452-340G>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20061190 | |||||||
| chr22:20061192 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.452-338G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20061192 | |||||||
| chr22:20061219 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0105 |
2 | NA18941.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.452-311G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20061219 | |||||||
| chr22:20061340 | C | T | 13 | a0001c0002t0008g0023 a0001c0002t0008g0201 a0001c0002t0008g0203 others(10): Show |
14 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.452-190C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20061340 | |||||||
| chr22:20061355 | C | T | 1 | a0001c0001t0002g0019 | 2 | NA18945.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.452-175C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20061355 | |||||||
| chr22:20061505 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.452-25A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 6/8 | chr22 | 20061505 | |||||||
| chr22:20061721 | C | T | 23 | a0001c0001t0006g0003 a0001c0001t0006g0030 a0001c0001t0006g0031 others(20): Show |
27 | HG00609.hp2 HG01884.hp1 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.605+38C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | chr22 | 20061721 | |||||||
| chr22:20061762 | G | A | 28 | a0001c0001t0004g0028 a0001c0001t0004g0029 a0001c0001t0004g0069 others(25): Show |
32 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.605+79G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | chr22 | 20061762 | |||||||
| chr22:20061817 | T | C | 181 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0017 others(178): Show |
199 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.605+134T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | chr22 | 20061817 | |||||||
| chr22:20061891 | G | GGGCCCA | 29 | a0001c0001t0004g0028 a0001c0001t0004g0029 a0001c0001t0004g0069 others(26): Show |
33 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.605+229_605+234dup others(6): Show |
TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 20061891 | ||||||
| chr22:20061931 | A | C | 1 | a0001c0001t0003g0177 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.605+248A>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | chr22 | 20061931 | |||||||
| chr22:20061931 | A | G | 180 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0017 others(177): Show |
198 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.605+248A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | chr22 | 20061931 | |||||||
| chr22:20061942 | T | C | 75 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0017 others(72): Show |
80 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.605+259T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | chr22 | 20061942 | |||||||
| chr22:20061972 | G | A | 75 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0017 others(72): Show |
80 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.605+289G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | chr22 | 20061972 | |||||||
| chr22:20062164 | CG | C | 3 | a0001c0001t0023g0193 a0001c0001t0023g0194 a0001c0001t0039g0258 |
3 | HG02109.hp2 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.605+484delG | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr22 | 20062164 | ||||||
| chr22:20062180 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0002g0235 |
2 | HG00438.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.605+497G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | chr22 | 20062180 | |||||||
| chr22:20062261 | C | G | 1 | a0001c0001t0001g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.605+578C>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | chr22 | 20062261 | |||||||
| chr22:20062334 | C | A | 1 | a0001c0001t0001g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.605+651C>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | chr22 | 20062334 | |||||||
| chr22:20062412 | A | C | 181 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0017 others(178): Show |
199 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.605+729A>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | chr22 | 20062412 | |||||||
| chr22:20062416 | A | G | 5 | a0001c0001t0001g0048 a0001c0001t0002g0214 a0001c0001t0002g0222 others(2): Show |
5 | HG01109.hp1 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.605+733A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | chr22 | 20062416 | |||||||
| chr22:20062496 | C | T | 29 | a0001c0001t0003g0176 a0001c0001t0004g0028 a0001c0001t0004g0029 others(26): Show |
33 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.605+813C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | chr22 | 20062496 | |||||||
| chr22:20062584 | C | A | 1 | a0001c0001t0001g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.606-754C>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | chr22 | 20062584 | |||||||
| chr22:20062641 | C | T | 1 | a0001c0001t0003g0192 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.606-697C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | chr22 | 20062641 | |||||||
| chr22:20062702 | G | A | 1 | a0001c0001t0009g0186 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.606-636G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | chr22 | 20062702 | |||||||
| chr22:20062818 | G | A | 1 | a0001c0001t0005g0283 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.606-520G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | chr22 | 20062818 | |||||||
| chr22:20062878 | T | C | 159 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0017 others(156): Show |
173 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.606-460T>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | chr22 | 20062878 | |||||||
| chr22:20062879 | G | A | 1 | a0001c0001t0003g0159 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.606-459G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | chr22 | 20062879 | |||||||
| chr22:20063023 | G | A | 2 | a0001c0001t0002g0025 a0001c0001t0002g0291 |
3 | HG02698.hp2 NA19066.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.606-315G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | chr22 | 20063023 | |||||||
| chr22:20063177 | A | T | 10 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(7): Show |
10 | HG02145.hp1 HG02451.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.606-161A>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | chr22 | 20063177 | |||||||
| chr22:20063310 | A | C | 1 | a0001c0001t0007g0286 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.606-28A>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 7/8 | chr22 | 20063310 | |||||||
| chr22:20063456 | G | A | 22 | a0001c0001t0008g0256 a0001c0001t0021g0314 a0001c0001t0023g0193 others(19): Show |
24 | HG01257.hp2 HG01258.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.710+14G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 8/8 | chr22 | 20063456 | |||||||
| chr22:20063622 | G | A | 4 | a0002c0003t0010g0308 a0002c0003t0010g0309 a0002c0003t0010g0310 others(1): Show |
4 | HG02809.hp1 HG02896.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.710+180G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 8/8 | chr22 | 20063622 | |||||||
| chr22:20063881 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.710+439A>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 8/8 | chr22 | 20063881 | |||||||
| chr22:20063943 | G | A | 181 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0017 others(178): Show |
199 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.710+501G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 8/8 | chr22 | 20063943 | |||||||
| chr22:20063946 | C | G | 3 | a0003c0004t0014g0306 a0003c0004t0014g0307 a0003c0004t0014g0313 |
3 | HG01257.hp2 HG01258.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.710+504C>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 8/8 | chr22 | 20063946 | |||||||
| chr22:20064264 | C | T | 2 | a0001c0001t0007g0223 a0001c0001t0009g0324 |
2 | HG01069.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.711-278C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 8/8 | chr22 | 20064264 | |||||||
| chr22:20064289 | G | A | 2 | a0001c0001t0008g0256 a0001c0001t0021g0314 |
2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.711-253G>A | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 8/8 | chr22 | 20064289 | |||||||
| chr22:20064356 | C | G | 1 | a0001c0001t0003g0148 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.711-186C>G | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 8/8 | chr22 | 20064356 | |||||||
| chr22:20064405 | C | T | 11 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(8): Show |
11 | HG02145.hp1 HG02451.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.711-137C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 8/8 | chr22 | 20064405 | |||||||
| chr22:20064439 | G | C | 2 | a0001c0001t0004g0028 a0001c0001t0004g0334 |
3 | HG00099.hp2 HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.711-103G>C | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 8/8 | chr22 | 20064439 | |||||||
| chr22:20064527 | C | T | 11 | a0002c0003t0010g0046 a0002c0003t0010g0047 a0002c0003t0010g0110 others(8): Show |
11 | HG02145.hp1 HG02451.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.711-15C>T | TANGO2 | ENSG00000183597.16 | transcript | ENST00000327374.9 | protein_coding | 8/8 | chr22 | 20064527 |