Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 219899 |
| ensemblid | ENSG00000154114.13 |
| hgncid | 28115 |
| symbol | TBCEL |
| name | tubulin folding cofactor E like |
| refseq_nuc | NM_001363644.2 |
| refseq_prot | NP_001350573.1 |
| ensembl_nuc | ENST00000683345.1 |
| ensembl_prot | ENSP00000507873.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 121024102 |
| end | 121090776 |
| strand | + |
| ver | v1.2 |
| region | chr11:121024102-121090776 |
| region5000 | chr11:121019102-121095776 |
| regionname0 | TBCEL_chr11_121024102_121090776 |
| regionname5000 | TBCEL_chr11_121019102_121095776 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 424 | 262 | 80 | 56 | 92 | 10 | 22 | 68 | TBCEL_chr11_121019102_121095776 | TBCEL | MDQPS others(419): Show |
chr11 | 121019102 | 121095776 |
| a0002 | 0/0 | 424 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | MDQPS others(419): Show |
chr11 | 121019102 | 121095776 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1272 | 258 | 78 | 54 | 92 | 10 | 22 | TBCEL_chr11_121019102_121095776 | TBCEL | ATGGA others(1267): Show |
chr11 | 121019102 | 121095776 | ||
| a0001c0002 | 0/0 | 1272 | 3 | 2 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | ATGGA others(1267): Show |
chr11 | 121019102 | 121095776 | ||
| a0001c0004 | 0/0 | 1272 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | ATGGA others(1267): Show |
chr11 | 121019102 | 121095776 | ||
| a0002c0003 | 0/0 | 1272 | 2 | 0 | 2 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | ATGGA others(1267): Show |
chr11 | 121019102 | 121095776 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5270 | 120 | 28 | 29 | 47 | 3 | 12 | TBCEL_chr11_121019102_121095776 | TBCEL | GCTTC others(5265): Show |
chr11 | 121019102 | 121095776 |
| a0001c0001t0002 | 0/0 | 5270 | 75 | 5 | 15 | 43 | 4 | 8 | TBCEL_chr11_121019102_121095776 | TBCEL | GCTTC others(5265): Show |
chr11 | 121019102 | 121095776 |
| a0001c0001t0003 | 0/1 | 5270 | 28 | 17 | 9 | 0 | 0 | 1 | TBCEL_chr11_121019102_121095776 | TBCEL | GCTTC others(5265): Show |
chr11 | 121019102 | 121095776 |
| a0001c0001t0004 | 0/0 | 5270 | 7 | 7 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | GCTTC others(5265): Show |
chr11 | 121019102 | 121095776 |
| a0001c0001t0005 | 0/0 | 5270 | 4 | 4 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | GCTTC others(5265): Show |
chr11 | 121019102 | 121095776 |
| a0001c0001t0006 | 0/0 | 5271 | 4 | 4 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | GCTTC others(5266): Show |
chr11 | 121019102 | 121095776 |
| a0001c0001t0007 | 0/0 | 5272 | 3 | 3 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | GCTTC others(5267): Show |
chr11 | 121019102 | 121095776 |
| a0001c0001t0008 | 0/0 | 5270 | 1 | 0 | 0 | 0 | 1 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | GCTTC others(5265): Show |
chr11 | 121019102 | 121095776 |
| a0001c0001t0009 | 0/0 | 5270 | 3 | 1 | 1 | 0 | 1 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | GCTTC others(5265): Show |
chr11 | 121019102 | 121095776 |
| a0001c0001t0010 | 0/0 | 5270 | 3 | 3 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | GCTTC others(5265): Show |
chr11 | 121019102 | 121095776 |
| a0001c0001t0012 | 0/0 | 5270 | 2 | 2 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | GCTTC others(5265): Show |
chr11 | 121019102 | 121095776 |
| a0001c0001t0013 | 0/0 | 5270 | 2 | 2 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | GCTTC others(5265): Show |
chr11 | 121019102 | 121095776 |
| a0001c0001t0014 | 0/0 | 5270 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | GCTTC others(5265): Show |
chr11 | 121019102 | 121095776 |
| a0001c0001t0016 | 0/0 | 5270 | 1 | 0 | 0 | 0 | 1 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | GCTTC others(5265): Show |
chr11 | 121019102 | 121095776 |
| a0001c0001t0017 | 0/0 | 5270 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | GCTTC others(5265): Show |
chr11 | 121019102 | 121095776 |
| a0001c0001t0018 | 0/0 | 5270 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | GCTTC others(5265): Show |
chr11 | 121019102 | 121095776 |
| a0001c0001t0019 | 0/0 | 5272 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | GCTTC others(5267): Show |
chr11 | 121019102 | 121095776 |
| a0001c0001t0021 | 0/0 | 5270 | 1 | 0 | 0 | 0 | 0 | 1 | TBCEL_chr11_121019102_121095776 | TBCEL | GCTTC others(5265): Show |
chr11 | 121019102 | 121095776 |
| a0001c0002t0011 | 0/0 | 5272 | 2 | 2 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | GCTTC others(5267): Show |
chr11 | 121019102 | 121095776 |
| a0001c0002t0020 | 0/0 | 5270 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | GCTTC others(5265): Show |
chr11 | 121019102 | 121095776 |
| a0001c0004t0015 | 0/0 | 5270 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | GCTTC others(5265): Show |
chr11 | 121019102 | 121095776 |
| a0002c0003t0008 | 0/0 | 5270 | 2 | 0 | 2 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | GCTTC others(5265): Show |
chr11 | 121019102 | 121095776 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 14 | 1 | 1 | 8 | 0 | 3 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0003 | 0/0 | 9 | 0 | 2 | 3 | 1 | 3 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0002 | 0/0 | 10 | 0 | 1 | 7 | 0 | 2 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0003g0008 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0003g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0003g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0003g0184 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0004g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0006g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0007g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0008g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0009g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0009g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0009g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0010g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0010g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0010g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0012g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0012g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0013g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0013g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0014g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0016g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0017g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0018g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0019g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0001t0021g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0002t0011g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0002t0011g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0002t0020g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0001c0004t0015g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| a0002c0003t0008g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0018 | EUR | GBR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG00280 | hp1 | a0001 | c0001 | t0016 | g0101 | EUR | FIN | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | FIN | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | CHS | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG00735 | hp1 | a0001 | c0004 | t0015 | g0104 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG00741 | hp1 | a0001 | c0002 | t0020 | g0176 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01070 | hp2 | a0002 | c0003 | t0008 | g0026 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01071 | hp2 | a0002 | c0003 | t0008 | g0026 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | CLM | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | CLM | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01496 | hp2 | a0001 | c0001 | t0009 | g0119 | AMR | CLM | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0083 | EUR | IBS | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0138 | AFR | ACB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | ACB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PEL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | ACB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0076 | AFR | ACB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | CDX | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CDX | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0183 | AFR | ACB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02258 | hp2 | a0001 | c0002 | t0011 | g0198 | AFR | ACB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0196 | AFR | ACB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | KHV | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02572 | hp2 | a0001 | c0001 | t0013 | g0158 | AFR | GWD | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | GWD | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0037 | AFR | GWD | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0078 | AFR | GWD | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0178 | AFR | GWD | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02818 | hp1 | a0001 | c0001 | t0019 | g0188 | AFR | GWD | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02896 | hp2 | a0001 | c0001 | t0010 | g0190 | AFR | GWD | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0194 | AFR | ESN | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ESN | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03041 | hp2 | a0001 | c0001 | t0012 | g0001 | AFR | GWD | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0195 | AFR | ESN | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0075 | AFR | ESN | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | ESN | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03209 | hp1 | a0001 | c0001 | t0010 | g0187 | AFR | MSL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | MSL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0193 | AFR | MSL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03453 | hp2 | a0001 | c0002 | t0011 | g0197 | AFR | MSL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03486 | hp1 | a0001 | c0001 | t0014 | g0182 | AFR | MSL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | ESN | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | ESN | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03540 | hp2 | a0001 | c0001 | t0010 | g0189 | AFR | GWD | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03927 | hp1 | a0001 | c0001 | t0021 | g0124 | SAS | BEB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | BEB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | STU | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | YRI | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18747 | hp2 | a0001 | c0001 | t0018 | g0014 | EAS | CHB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18906 | hp1 | a0001 | c0001 | t0013 | g0157 | AFR | YRI | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0039 | AFR | YRI | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18984 | hp2 | a0001 | c0001 | t0017 | g0003 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0180 | AFR | LWK | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | YRI | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | YRI | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ASW | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | ASW | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA20752 | hp1 | a0001 | c0001 | t0008 | g0106 | EUR | TSI | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0073 | EUR | TSI | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA20805 | hp1 | a0001 | c0001 | t0009 | g0120 | EUR | TSI | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0051 | EUR | TSI | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | GIH | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0186 | AMR | CLM | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | ACB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02486 | hp1 | a0001 | c0001 | t0012 | g0116 | AFR | ACB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | ACB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | MSL | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | USA | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0200 | AFR | USA | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0013 | AFR | USA | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | USA | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0184 | REF | REF | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | TBCEL_chr11_121019102_121095776 | TBCEL | chr11 | 121019102 | 121095776 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:121053712 | G | T | 1 | a0002 | 2 | HG01070.hp2 HG01071.hp2 |
missense_variant | MODERATE | c.435G>T | p.Met145Ile | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 5/9 | 750/5270 | 435/1275 | 145/424 | chr11 | 121053712 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:121047616 | T | C | 1 | a0001c0004 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.222T>C | p.Ala74Ala | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/9 | 537/5270 | 222/1275 | 74/424 | chr11 | 121047616 | |||
| chr11:121058442 | C | G | 1 | a0001c0002 | 3 | HG00741.hp1 HG02258.hp2 HG03453.hp2 |
synonymous_variant | LOW | c.810C>G | p.Thr270Thr | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 7/9 | 1125/5270 | 810/1275 | 270/424 | chr11 | 121058442 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:121024174 | G | A | 1 | a0001c0002t0011 | 2 | HG02258.hp2 HG03453.hp2 |
5_prime_UTR_variant | MODIFIER | c.-243G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/9 | 21517 | chr11 | 121024174 | ||||||
| chr11:121036588 | G | A | 1 | a0001c0001t0014 | 1 | HG03486.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-42G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/9 | chr11 | 121036588 | |||||||
| chr11:121087175 | G | A | 1 | a0001c0002t0011 | 2 | HG02258.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*79G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 79 | chr11 | 121087175 | ||||||
| chr11:121087544 | C | T | 1 | a0001c0001t0021 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*448C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 448 | chr11 | 121087544 | ||||||
| chr11:121087580 | C | CG | 1 | a0001c0001t0006 | 4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*484_*485insG | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 485 | chr11 | 121087580 | ||||||
| chr11:121087581 | A | G | 2 | a0001c0002t0011 a0001c0002t0020 |
3 | HG00741.hp1 HG02258.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*485A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 485 | chr11 | 121087581 | ||||||
| chr11:121087581 | A | T | 1 | a0001c0001t0006 | 4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*485A>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 485 | chr11 | 121087581 | ||||||
| chr11:121087808 | A | G | 1 | a0001c0001t0013 | 2 | HG02572.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*712A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 712 | chr11 | 121087808 | ||||||
| chr11:121087976 | T | C | 1 | a0001c0004t0015 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*880T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 880 | chr11 | 121087976 | ||||||
| chr11:121088092 | G | A | 2 | a0001c0001t0004 a0001c0001t0007 |
10 | HG01891.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*996G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 996 | chr11 | 121088092 | ||||||
| chr11:121088221 | C | T | 2 | a0001c0001t0010 a0001c0001t0019 |
4 | HG02818.hp1 HG02896.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1125C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 1125 | chr11 | 121088221 | ||||||
| chr11:121088329 | G | A | 1 | a0001c0001t0006 | 4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1233G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 1233 | chr11 | 121088329 | ||||||
| chr11:121088516 | A | G | 12 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(9): Show |
129 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*1420A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 1420 | chr11 | 121088516 | ||||||
| chr11:121088754 | A | T | 5 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(2): Show |
90 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1658A>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 1658 | chr11 | 121088754 | ||||||
| chr11:121088874 | C | T | 1 | a0001c0002t0011 | 2 | HG02258.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1778C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 1778 | chr11 | 121088874 | ||||||
| chr11:121089091 | G | A | 4 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(1): Show |
86 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1995G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 1995 | chr11 | 121089091 | ||||||
| chr11:121089249 | A | G | 1 | a0001c0001t0018 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2153A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 2153 | chr11 | 121089249 | ||||||
| chr11:121089345 | G | A | 1 | a0001c0001t0016 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2249G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 2249 | chr11 | 121089345 | ||||||
| chr11:121089696 | T | C | 1 | a0001c0001t0012 | 2 | HG02486.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2600T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 2600 | chr11 | 121089696 | ||||||
| chr11:121090012 | A | G | 1 | a0001c0002t0020 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2916A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 2916 | chr11 | 121090012 | ||||||
| chr11:121090028 | C | G | 1 | a0001c0001t0009 | 3 | HG01496.hp2 HG01891.hp1 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2932C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 2932 | chr11 | 121090028 | ||||||
| chr11:121090056 | T | G | 1 | a0001c0001t0017 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2960T>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 2960 | chr11 | 121090056 | ||||||
| chr11:121090104 | C | T | 1 | a0001c0002t0020 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3008C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 3008 | chr11 | 121090104 | ||||||
| chr11:121090130 | A | C | 1 | a0001c0001t0021 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3034A>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 3034 | chr11 | 121090130 | ||||||
| chr11:121090299 | G | C | 2 | a0001c0001t0008 a0002c0003t0008 |
3 | HG01070.hp2 HG01071.hp2 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3203G>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 3203 | chr11 | 121090299 | ||||||
| chr11:121090657 | A | G | 1 | a0001c0004t0015 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3561A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 3561 | chr11 | 121090657 | ||||||
| chr11:121090660 | C | CAT | 3 | a0001c0001t0007 a0001c0001t0019 a0001c0002t0011 |
6 | HG02109.hp2 HG02258.hp2 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3577_*3578dupAT | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 9/9 | 3579 | INFO_REALIGN_3_PRIME | chr11 | 121090660 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:121024372 | C | G | 2 | a0001c0001t0003g0199 a0001c0001t0003g0200 |
2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-126+81C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121024372 | |||||||
| chr11:121024473 | G | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0029 |
3 | HG00609.hp2 HG00621.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.-126+182G>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121024473 | |||||||
| chr11:121024524 | T | TTGGGC | 73 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(70): Show |
94 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.-126+258_-126+262d others(7): Show |
TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 121024524 | ||||||
| chr11:121024556 | A | G | 100 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(97): Show |
129 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.-126+265A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121024556 | |||||||
| chr11:121024643 | G | A | 73 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(70): Show |
94 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.-126+352G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121024643 | |||||||
| chr11:121025253 | T | C | 1 | a0001c0001t0003g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-126+962T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121025253 | |||||||
| chr11:121025281 | T | TA | 2 | a0001c0001t0002g0012 a0001c0001t0002g0030 |
3 | NA19057.hp2 NA19085.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-126+991dupA | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 121025281 | ||||||
| chr11:121025282 | AC | A | 6 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(3): Show |
6 | HG02258.hp2 HG02451.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-126+992delC | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121025282 | |||||||
| chr11:121025298 | A | G | 1 | a0001c0001t0003g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-126+1007A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121025298 | |||||||
| chr11:121025549 | A | G | 3 | a0001c0001t0003g0191 a0001c0001t0003g0199 a0001c0001t0003g0200 |
3 | HG03471.hp2 HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-126+1258A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121025549 | |||||||
| chr11:121025716 | A | AT | 17 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0174 others(14): Show |
19 | HG00609.hp2 HG00621.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-126+1439dupT | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 121025716 | ||||||
| chr11:121025716 | A | ATT | 55 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(52): Show |
74 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.-126+1438_-126+143 others(6): Show |
TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 121025716 | ||||||
| chr11:121025716 | A | ATTT | 6 | a0001c0001t0001g0088 a0001c0001t0002g0019 a0001c0001t0002g0085 others(3): Show |
7 | HG00621.hp2 HG01109.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.-126+1437_-126+143 others(7): Show |
TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 121025716 | ||||||
| chr11:121025716 | AT | A | 5 | a0001c0001t0003g0178 a0001c0001t0006g0193 a0001c0001t0006g0194 others(2): Show |
5 | HG02451.hp1 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126+1439delT | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 121025716 | ||||||
| chr11:121025731 | A | T | 71 | a0001c0001t0001g0088 a0001c0001t0001g0177 a0001c0001t0002g0002 others(68): Show |
92 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.-126+1440A>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121025731 | |||||||
| chr11:121025736 | A | T | 2 | a0001c0001t0002g0020 a0001c0001t0002g0089 |
3 | NA18964.hp2 NA18999.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.-126+1445A>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121025736 | |||||||
| chr11:121025836 | G | T | 77 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(74): Show |
98 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.-126+1545G>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121025836 | |||||||
| chr11:121025840 | A | G | 70 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(67): Show |
91 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.-126+1549A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121025840 | |||||||
| chr11:121025891 | AT | A | 70 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(67): Show |
91 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.-126+1606delT | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 121025891 | ||||||
| chr11:121025982 | C | T | 1 | a0001c0001t0003g0010 | 3 | HG02258.hp1 HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-126+1691C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121025982 | |||||||
| chr11:121026260 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-126+1969C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121026260 | |||||||
| chr11:121026262 | A | G | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-126+1971A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121026262 | |||||||
| chr11:121026399 | C | A | 1 | a0001c0001t0003g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-126+2108C>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121026399 | |||||||
| chr11:121026586 | C | T | 76 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(73): Show |
97 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.-126+2295C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121026586 | |||||||
| chr11:121026648 | A | G | 1 | a0002c0003t0008g0026 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-126+2357A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121026648 | |||||||
| chr11:121026797 | T | TGTG | 76 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(73): Show |
97 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.-126+2508_-126+250 others(7): Show |
TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 121026797 | ||||||
| chr11:121026993 | T | C | 2 | a0001c0001t0002g0043 a0001c0001t0002g0044 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-126+2702T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121026993 | |||||||
| chr11:121027278 | T | C | 50 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(47): Show |
66 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.-126+2987T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121027278 | |||||||
| chr11:121027432 | C | T | 1 | a0001c0001t0002g0074 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-126+3141C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121027432 | |||||||
| chr11:121027487 | G | T | 66 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(63): Show |
87 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.-126+3196G>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121027487 | |||||||
| chr11:121027523 | C | T | 73 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(70): Show |
94 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.-126+3232C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121027523 | |||||||
| chr11:121027544 | C | T | 70 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(67): Show |
91 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.-126+3253C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121027544 | |||||||
| chr11:121027591 | C | G | 1 | a0001c0001t0002g0073 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-126+3300C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121027591 | |||||||
| chr11:121027773 | A | G | 73 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(70): Show |
94 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.-126+3482A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121027773 | |||||||
| chr11:121027906 | T | C | 1 | a0001c0001t0003g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-126+3615T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121027906 | |||||||
| chr11:121028040 | A | G | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-126+3749A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121028040 | |||||||
| chr11:121028052 | A | G | 72 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(69): Show |
93 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.-126+3761A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121028052 | |||||||
| chr11:121028075 | T | C | 72 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(69): Show |
93 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.-126+3784T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121028075 | |||||||
| chr11:121028087 | C | T | 1 | a0001c0001t0002g0074 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-126+3796C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121028087 | |||||||
| chr11:121028121 | C | CTT | 76 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(73): Show |
97 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.-126+3830_-126+383 others(6): Show |
TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121028121 | |||||||
| chr11:121028210 | T | A | 2 | a0001c0001t0001g0090 a0001c0001t0002g0045 |
2 | HG02083.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-126+3919T>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121028210 | |||||||
| chr11:121028222 | TA | T | 66 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(63): Show |
86 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-126+3935delA | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 121028222 | ||||||
| chr11:121028222 | TAAAATA | T | 4 | a0001c0001t0002g0016 a0001c0001t0002g0071 a0001c0001t0002g0072 others(1): Show |
5 | HG01256.hp1 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-126+3935_-126+394 others(10): Show |
TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 121028222 | ||||||
| chr11:121028288 | T | A | 1 | a0001c0001t0002g0074 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-126+3997T>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121028288 | |||||||
| chr11:121028617 | C | T | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-126+4326C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121028617 | |||||||
| chr11:121028749 | C | T | 76 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(73): Show |
97 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.-126+4458C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121028749 | |||||||
| chr11:121028783 | G | T | 70 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(67): Show |
91 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.-126+4492G>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121028783 | |||||||
| chr11:121028894 | G | A | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-126+4603G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121028894 | |||||||
| chr11:121028988 | C | G | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-126+4697C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121028988 | |||||||
| chr11:121029019 | T | G | 1 | a0001c0001t0002g0034 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-126+4728T>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121029019 | |||||||
| chr11:121029027 | C | G | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-126+4736C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121029027 | |||||||
| chr11:121029042 | T | G | 1 | a0001c0001t0003g0179 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-126+4751T>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121029042 | |||||||
| chr11:121029079 | G | C | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-126+4788G>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121029079 | |||||||
| chr11:121029166 | C | G | 1 | a0001c0001t0003g0009 | 3 | HG00738.hp2 HG01099.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-126+4875C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121029166 | |||||||
| chr11:121029194 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-126+4903G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121029194 | |||||||
| chr11:121029279 | C | G | 4 | a0001c0001t0010g0187 a0001c0001t0010g0189 a0001c0001t0010g0190 others(1): Show |
4 | HG02818.hp1 HG02896.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-126+4988C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121029279 | |||||||
| chr11:121029329 | A | G | 2 | a0001c0001t0005g0037 a0001c0001t0005g0038 |
2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-126+5038A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121029329 | |||||||
| chr11:121029654 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-126+5363G>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121029654 | |||||||
| chr11:121029707 | G | A | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-126+5416G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121029707 | |||||||
| chr11:121029772 | T | TTTTC | 80 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(77): Show |
101 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-126+5484_-126+548 others(8): Show |
TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 121029772 | ||||||
| chr11:121030051 | A | G | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-126+5760A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121030051 | |||||||
| chr11:121030116 | T | G | 1 | a0001c0001t0002g0012 | 2 | NA19057.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-126+5825T>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121030116 | |||||||
| chr11:121030168 | A | G | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-126+5877A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121030168 | |||||||
| chr11:121030232 | C | T | 3 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 |
3 | HG02071.hp2 HG02132.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.-126+5941C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121030232 | |||||||
| chr11:121030356 | A | C | 1 | a0001c0001t0002g0067 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-126+6065A>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121030356 | |||||||
| chr11:121030368 | G | T | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-126+6077G>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121030368 | |||||||
| chr11:121030464 | C | T | 1 | a0001c0001t0002g0066 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-125-6041C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121030464 | |||||||
| chr11:121030872 | AT | A | 64 | a0001c0001t0001g0021 a0001c0001t0001g0093 a0001c0001t0001g0094 others(61): Show |
83 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.-125-5618delT | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 121030872 | ||||||
| chr11:121030872 | ATT | A | 29 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(26): Show |
37 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.-125-5619_-125-561 others(6): Show |
TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 121030872 | ||||||
| chr11:121030872 | ATTT | A | 7 | a0001c0001t0004g0005 a0001c0001t0004g0040 a0001c0001t0004g0041 others(4): Show |
10 | HG01891.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-125-5620_-125-561 others(7): Show |
TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 121030872 | ||||||
| chr11:121030892 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-125-5613A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121030892 | |||||||
| chr11:121031095 | C | G | 1 | a0001c0001t0002g0064 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-125-5410C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121031095 | |||||||
| chr11:121031272 | T | C | 2 | a0001c0001t0002g0045 a0001c0001t0002g0046 |
2 | HG02083.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-125-5233T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121031272 | |||||||
| chr11:121031426 | A | G | 4 | a0001c0001t0010g0187 a0001c0001t0010g0189 a0001c0001t0010g0190 others(1): Show |
4 | HG02818.hp1 HG02896.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-125-5079A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121031426 | |||||||
| chr11:121031450 | T | C | 1 | a0001c0001t0003g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-125-5055T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121031450 | |||||||
| chr11:121031569 | T | C | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-125-4936T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121031569 | |||||||
| chr11:121031640 | T | C | 7 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
7 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-125-4865T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121031640 | |||||||
| chr11:121031662 | C | CT | 4 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0003g0028 others(1): Show |
5 | HG01361.hp2 HG02055.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.-125-4822dupT | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 121031662 | ||||||
| chr11:121031662 | CT | C | 57 | a0001c0001t0001g0029 a0001c0001t0001g0096 a0001c0001t0001g0097 others(54): Show |
75 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.-125-4822delT | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 121031662 | ||||||
| chr11:121031662 | CTT | C | 5 | a0001c0001t0002g0014 a0001c0001t0002g0047 a0001c0001t0002g0048 others(2): Show |
5 | HG02735.hp1 NA18747.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.-125-4823_-125-482 others(6): Show |
TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 121031662 | ||||||
| chr11:121031856 | C | T | 4 | a0001c0001t0010g0187 a0001c0001t0010g0189 a0001c0001t0010g0190 others(1): Show |
4 | HG02818.hp1 HG02896.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-125-4649C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121031856 | |||||||
| chr11:121031905 | G | T | 1 | a0001c0001t0002g0070 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-125-4600G>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121031905 | |||||||
| chr11:121032089 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-125-4416G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121032089 | |||||||
| chr11:121032185 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-125-4320A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121032185 | |||||||
| chr11:121032221 | G | A | 79 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(76): Show |
100 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.-125-4284G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121032221 | |||||||
| chr11:121032320 | G | C | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-125-4185G>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121032320 | |||||||
| chr11:121032392 | T | C | 1 | a0001c0001t0002g0049 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-125-4113T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121032392 | |||||||
| chr11:121032703 | A | T | 7 | a0001c0001t0002g0012 a0001c0001t0002g0014 a0001c0001t0002g0030 others(4): Show |
8 | HG00423.hp1 HG01993.hp1 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.-125-3802A>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121032703 | |||||||
| chr11:121032754 | T | C | 1 | a0001c0001t0016g0101 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-125-3751T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121032754 | |||||||
| chr11:121032782 | C | T | 1 | a0001c0001t0003g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-125-3723C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121032782 | |||||||
| chr11:121032878 | T | C | 1 | a0001c0001t0003g0179 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-125-3627T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121032878 | |||||||
| chr11:121032906 | A | C | 1 | a0001c0001t0003g0191 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-125-3599A>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121032906 | |||||||
| chr11:121033043 | A | G | 72 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(69): Show |
93 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.-125-3462A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121033043 | |||||||
| chr11:121033116 | C | T | 1 | a0001c0001t0003g0186 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-125-3389C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121033116 | |||||||
| chr11:121033447 | A | G | 72 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(69): Show |
93 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.-125-3058A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121033447 | |||||||
| chr11:121033465 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | NA18942.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-125-3040C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121033465 | |||||||
| chr11:121033540 | A | G | 4 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0185 others(1): Show |
8 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-125-2965A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121033540 | |||||||
| chr11:121033838 | C | A | 6 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(3): Show |
6 | HG02258.hp2 HG02451.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-125-2667C>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121033838 | |||||||
| chr11:121033916 | A | G | 1 | a0001c0002t0011g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-125-2589A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121033916 | |||||||
| chr11:121033930 | CATGTCTT others(2): Show |
C | 6 | a0001c0001t0001g0092 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
6 | HG00735.hp1 HG01071.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.-125-2573_-125-256 others(13): Show |
TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 121033930 | ||||||
| chr11:121034221 | C | G | 1 | a0001c0001t0003g0010 | 3 | HG02258.hp1 HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-125-2284C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121034221 | |||||||
| chr11:121034323 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01975.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-125-2182A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121034323 | |||||||
| chr11:121034491 | T | C | 2 | a0001c0001t0008g0106 a0002c0003t0008g0026 |
3 | HG01070.hp2 HG01071.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-125-2014T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121034491 | |||||||
| chr11:121034522 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-125-1983A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121034522 | |||||||
| chr11:121034523 | T | C | 7 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
7 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-125-1982T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121034523 | |||||||
| chr11:121034728 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-125-1777A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121034728 | |||||||
| chr11:121034842 | G | A | 7 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
7 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-125-1663G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121034842 | |||||||
| chr11:121034867 | G | A | 1 | a0001c0001t0005g0075 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-125-1638G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121034867 | |||||||
| chr11:121034868 | C | T | 1 | a0001c0001t0002g0074 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-125-1637C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121034868 | |||||||
| chr11:121035043 | T | G | 1 | a0001c0001t0002g0071 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-125-1462T>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121035043 | |||||||
| chr11:121035046 | C | G | 7 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
7 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-125-1459C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121035046 | |||||||
| chr11:121035062 | T | C | 59 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(56): Show |
77 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.-125-1443T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121035062 | |||||||
| chr11:121035101 | C | A | 3 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0186 |
7 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.-125-1404C>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121035101 | |||||||
| chr11:121035265 | A | G | 7 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
7 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-125-1240A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121035265 | |||||||
| chr11:121035387 | A | G | 1 | a0001c0001t0003g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-125-1118A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121035387 | |||||||
| chr11:121035412 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-125-1093G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121035412 | |||||||
| chr11:121035439 | G | T | 1 | a0001c0001t0001g0162 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-125-1066G>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121035439 | |||||||
| chr11:121035473 | A | AT | 4 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0003g0027 others(1): Show |
6 | HG01106.hp1 HG01175.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-125-1019dupT | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 121035473 | ||||||
| chr11:121035734 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-125-771G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121035734 | |||||||
| chr11:121035788 | A | T | 7 | a0001c0001t0001g0100 a0001c0001t0001g0154 a0001c0001t0001g0155 others(4): Show |
7 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-125-717A>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121035788 | |||||||
| chr11:121035966 | C | T | 7 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
7 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-125-539C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121035966 | |||||||
| chr11:121036275 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-125-230C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121036275 | |||||||
| chr11:121036477 | T | C | 1 | a0001c0001t0003g0179 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-125-28T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 1/8 | chr11 | 121036477 | |||||||
| chr11:121036752 | G | A | 1 | a0001c0001t0005g0038 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18+140G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121036752 | |||||||
| chr11:121036773 | G | A | 67 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(64): Show |
88 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.-18+161G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121036773 | |||||||
| chr11:121036953 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-18+341A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121036953 | |||||||
| chr11:121037235 | G | A | 1 | a0001c0001t0003g0010 | 3 | HG02258.hp1 HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-18+623G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121037235 | |||||||
| chr11:121037252 | C | G | 11 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(8): Show |
17 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.-18+640C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121037252 | |||||||
| chr11:121037647 | A | G | 9 | a0001c0001t0001g0099 a0001c0001t0001g0146 a0001c0001t0001g0147 others(6): Show |
9 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18+1035A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121037647 | |||||||
| chr11:121037885 | A | G | 1 | a0001c0001t0004g0078 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-18+1273A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121037885 | |||||||
| chr11:121037911 | G | A | 1 | a0001c0001t0003g0181 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18+1299G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121037911 | |||||||
| chr11:121037963 | A | AT | 9 | a0001c0001t0001g0025 a0001c0001t0001g0090 a0001c0001t0001g0095 others(6): Show |
10 | HG01123.hp2 HG02145.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+1366dupT | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 121037963 | ||||||
| chr11:121037983 | G | A | 3 | a0001c0001t0003g0191 a0001c0001t0003g0199 a0001c0001t0003g0200 |
3 | HG03471.hp2 HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-18+1371G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121037983 | |||||||
| chr11:121038135 | G | T | 7 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
7 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+1523G>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121038135 | |||||||
| chr11:121038280 | A | T | 1 | a0001c0001t0003g0200 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-18+1668A>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121038280 | |||||||
| chr11:121038324 | G | A | 1 | a0001c0001t0006g0193 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-18+1712G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121038324 | |||||||
| chr11:121038325 | T | C | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+1713T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121038325 | |||||||
| chr11:121038343 | C | T | 1 | a0001c0001t0006g0196 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-18+1731C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121038343 | |||||||
| chr11:121038351 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-18+1739G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121038351 | |||||||
| chr11:121038401 | T | G | 3 | a0001c0002t0011g0197 a0001c0002t0011g0198 a0001c0002t0020g0176 |
3 | HG00741.hp1 HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-18+1789T>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121038401 | |||||||
| chr11:121038455 | A | C | 1 | a0001c0001t0005g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-18+1843A>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121038455 | |||||||
| chr11:121038521 | G | A | 2 | a0001c0001t0005g0037 a0001c0001t0005g0038 |
2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-18+1909G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121038521 | |||||||
| chr11:121038561 | C | T | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-18+1949C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121038561 | |||||||
| chr11:121038630 | G | A | 14 | a0001c0001t0001g0100 a0001c0001t0001g0154 a0001c0001t0001g0155 others(11): Show |
14 | HG02451.hp2 HG02723.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.-18+2018G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121038630 | |||||||
| chr11:121038708 | C | T | 1 | a0001c0001t0003g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-18+2096C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121038708 | |||||||
| chr11:121038723 | T | G | 1 | a0001c0001t0001g0107 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-18+2111T>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121038723 | |||||||
| chr11:121038724 | C | G | 3 | a0001c0001t0003g0191 a0001c0001t0003g0199 a0001c0001t0003g0200 |
3 | HG03471.hp2 HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-18+2112C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121038724 | |||||||
| chr11:121038852 | A | G | 1 | a0001c0001t0003g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-18+2240A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121038852 | |||||||
| chr11:121038863 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-18+2251G>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121038863 | |||||||
| chr11:121039026 | C | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0110 |
3 | NA18940.hp2 NA18999.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-18+2414C>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121039026 | |||||||
| chr11:121039240 | G | T | 1 | a0001c0001t0002g0060 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-18+2628G>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121039240 | |||||||
| chr11:121039241 | T | C | 7 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
7 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+2629T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121039241 | |||||||
| chr11:121039516 | C | T | 3 | a0001c0001t0002g0018 a0001c0001t0002g0082 a0001c0001t0002g0083 |
4 | HG00099.hp2 HG01243.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+2904C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121039516 | |||||||
| chr11:121039517 | G | A | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+2905G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121039517 | |||||||
| chr11:121039635 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-18+3023A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121039635 | |||||||
| chr11:121039661 | G | T | 1 | a0001c0001t0003g0183 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-18+3049G>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121039661 | |||||||
| chr11:121039822 | T | G | 7 | a0001c0001t0004g0005 a0001c0001t0004g0040 a0001c0001t0004g0041 others(4): Show |
10 | HG01891.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18+3210T>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121039822 | |||||||
| chr11:121039879 | G | GT | 69 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(66): Show |
90 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.-18+3273dupT | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 121039879 | ||||||
| chr11:121039891 | C | T | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+3279C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121039891 | |||||||
| chr11:121040014 | T | C | 7 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
7 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+3402T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121040014 | |||||||
| chr11:121040264 | A | AGAATTTG others(4): Show |
1 | a0001c0001t0001g0140 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-18+3653_-18+3663d others(13): Show |
TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 121040264 | ||||||
| chr11:121040282 | G | C | 1 | a0001c0001t0001g0140 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-18+3670G>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121040282 | |||||||
| chr11:121040375 | C | T | 1 | a0001c0001t0002g0034 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-18+3763C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121040375 | |||||||
| chr11:121040494 | T | C | 101 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(98): Show |
130 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.-18+3882T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121040494 | |||||||
| chr11:121040797 | T | C | 1 | a0001c0001t0003g0179 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-18+4185T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121040797 | |||||||
| chr11:121040880 | T | G | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-18+4268T>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121040880 | |||||||
| chr11:121041012 | G | A | 1 | a0001c0001t0010g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-18+4400G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121041012 | |||||||
| chr11:121041062 | T | A | 77 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(74): Show |
98 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.-18+4450T>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121041062 | |||||||
| chr11:121041453 | C | T | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-4221C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121041453 | |||||||
| chr11:121041740 | A | G | 7 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
7 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-3934A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121041740 | |||||||
| chr11:121041764 | G | C | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-17-3910G>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121041764 | |||||||
| chr11:121041911 | C | CA | 14 | a0001c0001t0001g0102 a0001c0001t0001g0111 a0001c0001t0001g0112 others(11): Show |
14 | HG02040.hp1 HG02071.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-17-3746dupA | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 121041911 | ||||||
| chr11:121041911 | CA | C | 8 | a0001c0001t0001g0139 a0001c0001t0004g0005 a0001c0001t0004g0040 others(5): Show |
11 | HG01891.hp2 HG01943.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17-3746delA | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 121041911 | ||||||
| chr11:121041969 | T | C | 7 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
7 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-3705T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121041969 | |||||||
| chr11:121042048 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-17-3626C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121042048 | |||||||
| chr11:121042226 | G | A | 1 | a0001c0001t0002g0051 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-17-3448G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121042226 | |||||||
| chr11:121042321 | A | G | 4 | a0001c0001t0010g0187 a0001c0001t0010g0189 a0001c0001t0010g0190 others(1): Show |
4 | HG02818.hp1 HG02896.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-3353A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121042321 | |||||||
| chr11:121042479 | T | C | 1 | a0001c0002t0011g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-17-3195T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121042479 | |||||||
| chr11:121042528 | C | A | 2 | a0001c0001t0007g0013 a0001c0001t0007g0039 |
3 | HG02109.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-17-3146C>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121042528 | |||||||
| chr11:121042636 | A | T | 1 | a0001c0001t0014g0182 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-17-3038A>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121042636 | |||||||
| chr11:121042675 | A | C | 4 | a0001c0001t0010g0187 a0001c0001t0010g0189 a0001c0001t0010g0190 others(1): Show |
4 | HG02818.hp1 HG02896.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-2999A>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121042675 | |||||||
| chr11:121043157 | A | T | 1 | a0001c0001t0001g0162 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-17-2517A>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121043157 | |||||||
| chr11:121043164 | T | TG | 7 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
7 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-2507dupG | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 121043164 | ||||||
| chr11:121043228 | C | T | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-17-2446C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121043228 | |||||||
| chr11:121043387 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-17-2287C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121043387 | |||||||
| chr11:121043587 | C | T | 11 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(8): Show |
17 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-2087C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121043587 | |||||||
| chr11:121043661 | T | C | 101 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(98): Show |
130 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.-17-2013T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121043661 | |||||||
| chr11:121043812 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17-1862A>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121043812 | |||||||
| chr11:121043850 | G | A | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-1824G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121043850 | |||||||
| chr11:121043869 | C | T | 3 | a0001c0001t0010g0187 a0001c0001t0010g0189 a0001c0001t0010g0190 |
3 | HG02896.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-17-1805C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121043869 | |||||||
| chr11:121043994 | C | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0095 |
3 | HG02145.hp1 HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-17-1680C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121043994 | |||||||
| chr11:121044242 | T | C | 7 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
7 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-1432T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121044242 | |||||||
| chr11:121044301 | A | G | 2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
4 | HG02055.hp2 HG02630.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-1373A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121044301 | |||||||
| chr11:121044359 | C | T | 1 | a0001c0001t0006g0196 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-17-1315C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121044359 | |||||||
| chr11:121044401 | A | G | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-17-1273A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121044401 | |||||||
| chr11:121044485 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-17-1189T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121044485 | |||||||
| chr11:121044532 | C | G | 1 | a0001c0001t0009g0138 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-17-1142C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121044532 | |||||||
| chr11:121044886 | A | T | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-17-788A>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121044886 | |||||||
| chr11:121045014 | T | C | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-17-660T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121045014 | |||||||
| chr11:121045306 | C | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0082 a0001c0001t0002g0083 |
4 | HG00099.hp2 HG01243.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-368C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121045306 | |||||||
| chr11:121045348 | A | G | 2 | a0001c0001t0003g0199 a0001c0001t0003g0200 |
2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-17-326A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121045348 | |||||||
| chr11:121045356 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-17-318T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121045356 | |||||||
| chr11:121045467 | C | T | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-17-207C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121045467 | |||||||
| chr11:121045478 | T | C | 2 | a0001c0001t0005g0075 a0001c0001t0005g0076 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-17-196T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 2/8 | chr11 | 121045478 | |||||||
| chr11:121046024 | A | G | 4 | a0001c0001t0010g0187 a0001c0001t0010g0189 a0001c0001t0010g0190 others(1): Show |
4 | HG02818.hp1 HG02896.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+201A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 3/8 | chr11 | 121046024 | |||||||
| chr11:121046026 | G | A | 1 | a0001c0001t0003g0179 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.133+203G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 3/8 | chr11 | 121046026 | |||||||
| chr11:121046218 | T | C | 2 | a0001c0001t0005g0075 a0001c0001t0005g0076 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.133+395T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 3/8 | chr11 | 121046218 | |||||||
| chr11:121046430 | C | G | 1 | a0001c0001t0002g0072 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.133+607C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 3/8 | chr11 | 121046430 | |||||||
| chr11:121046449 | A | G | 1 | a0001c0001t0010g0190 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.133+626A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 3/8 | chr11 | 121046449 | |||||||
| chr11:121046579 | A | C | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.133+756A>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 3/8 | chr11 | 121046579 | |||||||
| chr11:121046868 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.134-660A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 3/8 | chr11 | 121046868 | |||||||
| chr11:121046948 | T | A | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.134-580T>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 3/8 | chr11 | 121046948 | |||||||
| chr11:121047233 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.134-295C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 3/8 | chr11 | 121047233 | |||||||
| chr11:121047425 | TCA | T | 1 | a0001c0001t0003g0010 | 3 | HG02258.hp1 HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.134-98_134-97delCA | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 121047425 | ||||||
| chr11:121047430 | C | G | 3 | a0001c0001t0002g0042 a0001c0001t0002g0080 a0001c0001t0002g0081 |
3 | HG02698.hp2 HG03017.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.134-98C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 3/8 | chr11 | 121047430 | |||||||
| chr11:121047934 | T | TAA | 2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
4 | HG02055.hp2 HG02630.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+267_273+268ins others(2): Show |
TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121047934 | |||||||
| chr11:121047935 | T | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0114 a0001c0001t0003g0027 others(1): Show |
8 | HG02055.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.273+268T>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121047935 | |||||||
| chr11:121047935 | T | TA | 33 | a0001c0001t0001g0115 a0001c0001t0001g0151 a0001c0001t0002g0036 others(30): Show |
39 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.273+290dupA | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 121047935 | ||||||
| chr11:121047935 | T | TAA | 62 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(59): Show |
83 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.273+289_273+290dup others(2): Show |
TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 121047935 | ||||||
| chr11:121047935 | TA | T | 6 | a0001c0001t0001g0105 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG01081.hp1 HG01168.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+290delA | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 121047935 | ||||||
| chr11:121047959 | G | A | 1 | a0001c0001t0006g0196 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.273+292G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121047959 | |||||||
| chr11:121048004 | ATTGTTAT others(7): Show |
A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
4 | HG02055.hp2 HG02630.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+349_273+362del others(14): Show |
TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 121048004 | ||||||
| chr11:121048010 | A | C | 1 | a0001c0001t0010g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.273+343A>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121048010 | |||||||
| chr11:121048581 | A | G | 7 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
7 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+914A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121048581 | |||||||
| chr11:121048617 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.273+950T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121048617 | |||||||
| chr11:121048884 | G | C | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.273+1217G>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121048884 | |||||||
| chr11:121049074 | C | T | 1 | a0001c0001t0003g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.273+1407C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121049074 | |||||||
| chr11:121049118 | C | G | 1 | a0001c0001t0003g0179 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.273+1451C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121049118 | |||||||
| chr11:121049224 | C | T | 7 | a0001c0001t0001g0022 a0001c0001t0001g0098 a0001c0001t0001g0110 others(4): Show |
8 | HG02165.hp2 NA18940.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.273+1557C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121049224 | |||||||
| chr11:121049253 | T | G | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.273+1586T>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121049253 | |||||||
| chr11:121049281 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.273+1614A>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121049281 | |||||||
| chr11:121049659 | T | C | 1 | a0001c0001t0003g0181 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.273+1992T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121049659 | |||||||
| chr11:121049721 | C | T | 7 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
7 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+2054C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121049721 | |||||||
| chr11:121049853 | C | A | 1 | a0001c0001t0008g0106 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.273+2186C>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121049853 | |||||||
| chr11:121049940 | A | G | 80 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(77): Show |
101 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.273+2273A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121049940 | |||||||
| chr11:121050206 | G | A | 1 | a0001c0001t0003g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.273+2539G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121050206 | |||||||
| chr11:121050284 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG02165.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.273+2617G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121050284 | |||||||
| chr11:121050400 | T | C | 73 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(70): Show |
94 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.273+2733T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121050400 | |||||||
| chr11:121050484 | A | G | 2 | a0001c0001t0003g0199 a0001c0001t0003g0200 |
2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.273+2817A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121050484 | |||||||
| chr11:121050732 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.274-2819A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121050732 | |||||||
| chr11:121051157 | C | T | 98 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(95): Show |
127 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.274-2394C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121051157 | |||||||
| chr11:121051231 | G | A | 1 | a0001c0001t0007g0039 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.274-2320G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121051231 | |||||||
| chr11:121051253 | A | G | 4 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0185 others(1): Show |
8 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.274-2298A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121051253 | |||||||
| chr11:121051442 | TTCC | T | 2 | a0001c0001t0003g0199 a0001c0001t0003g0200 |
2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.274-2107_274-2105d others(5): Show |
TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 121051442 | ||||||
| chr11:121051453 | C | G | 2 | a0001c0001t0003g0199 a0001c0001t0003g0200 |
2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.274-2098C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121051453 | |||||||
| chr11:121051518 | C | T | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.274-2033C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121051518 | |||||||
| chr11:121051519 | G | T | 69 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(66): Show |
90 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.274-2032G>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121051519 | |||||||
| chr11:121051782 | G | C | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-1769G>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121051782 | |||||||
| chr11:121051829 | C | T | 7 | a0001c0001t0001g0022 a0001c0001t0001g0098 a0001c0001t0001g0110 others(4): Show |
8 | HG02165.hp2 NA18940.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.274-1722C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121051829 | |||||||
| chr11:121051900 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.274-1651A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121051900 | |||||||
| chr11:121052068 | A | G | 2 | a0001c0001t0002g0035 a0001c0001t0002g0057 |
2 | NA18963.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.274-1483A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121052068 | |||||||
| chr11:121052097 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.274-1454A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121052097 | |||||||
| chr11:121052323 | CT | C | 7 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
7 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-1226delT | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 121052323 | ||||||
| chr11:121052348 | G | A | 1 | a0001c0001t0003g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.274-1203G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121052348 | |||||||
| chr11:121052688 | A | T | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.274-863A>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121052688 | |||||||
| chr11:121052712 | A | G | 1 | a0001c0001t0003g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.274-839A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121052712 | |||||||
| chr11:121052743 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0165 a0001c0001t0001g0166 others(1): Show |
5 | HG01496.hp1 HG01934.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-808C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121052743 | |||||||
| chr11:121052786 | G | A | 72 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(69): Show |
93 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.274-765G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121052786 | |||||||
| chr11:121052816 | T | G | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.274-735T>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121052816 | |||||||
| chr11:121052940 | G | A | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.274-611G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121052940 | |||||||
| chr11:121052964 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.274-587G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121052964 | |||||||
| chr11:121052991 | A | AT | 6 | a0001c0001t0001g0006 a0001c0001t0001g0114 a0001c0001t0010g0187 others(3): Show |
8 | HG02717.hp2 HG02818.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.274-550dupT | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 121052991 | ||||||
| chr11:121053190 | C | G | 73 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(70): Show |
94 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.274-361C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121053190 | |||||||
| chr11:121053300 | C | T | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-251C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121053300 | |||||||
| chr11:121053347 | C | G | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.274-204C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121053347 | |||||||
| chr11:121053355 | T | C | 7 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
7 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-196T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121053355 | |||||||
| chr11:121053415 | C | T | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.274-136C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121053415 | |||||||
| chr11:121053491 | T | C | 11 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(8): Show |
17 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.274-60T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 4/8 | chr11 | 121053491 | |||||||
| chr11:121053825 | A | G | 1 | a0001c0001t0003g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.455+93A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 5/8 | chr11 | 121053825 | |||||||
| chr11:121053962 | A | G | 80 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(77): Show |
101 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.455+230A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 5/8 | chr11 | 121053962 | |||||||
| chr11:121054405 | C | T | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.456-647C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 5/8 | chr11 | 121054405 | |||||||
| chr11:121054454 | C | T | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.456-598C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 5/8 | chr11 | 121054454 | |||||||
| chr11:121054542 | C | T | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.456-510C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 5/8 | chr11 | 121054542 | |||||||
| chr11:121054752 | C | T | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.456-300C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 5/8 | chr11 | 121054752 | |||||||
| chr11:121054809 | T | G | 1 | a0001c0001t0003g0183 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.456-243T>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 5/8 | chr11 | 121054809 | |||||||
| chr11:121054816 | A | G | 53 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(50): Show |
69 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.456-236A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 5/8 | chr11 | 121054816 | |||||||
| chr11:121055427 | A | G | 1 | a0001c0001t0003g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.712+119A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121055427 | |||||||
| chr11:121055514 | T | C | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.712+206T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121055514 | |||||||
| chr11:121055758 | T | A | 77 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(74): Show |
98 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.712+450T>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121055758 | |||||||
| chr11:121055909 | A | AAAATGGT others(24): Show |
7 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
7 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.712+619_712+649dup others(31): Show |
TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 121055909 | ||||||
| chr11:121055920 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.712+612T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121055920 | |||||||
| chr11:121056042 | T | A | 1 | a0001c0001t0001g0143 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.712+734T>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121056042 | |||||||
| chr11:121056043 | T | G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.712+735T>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121056043 | |||||||
| chr11:121056074 | G | C | 1 | a0001c0001t0001g0117 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.712+766G>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121056074 | |||||||
| chr11:121056122 | T | C | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.712+814T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121056122 | |||||||
| chr11:121056127 | T | C | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.712+819T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121056127 | |||||||
| chr11:121056272 | G | T | 1 | a0001c0001t0003g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.712+964G>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121056272 | |||||||
| chr11:121056424 | T | C | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.712+1116T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121056424 | |||||||
| chr11:121056494 | A | G | 1 | a0001c0001t0002g0062 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.712+1186A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121056494 | |||||||
| chr11:121056546 | A | C | 1 | a0001c0001t0001g0131 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.712+1238A>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121056546 | |||||||
| chr11:121056654 | A | G | 1 | a0001c0001t0003g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.712+1346A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121056654 | |||||||
| chr11:121056760 | G | T | 69 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(66): Show |
90 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.712+1452G>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121056760 | |||||||
| chr11:121056785 | G | A | 4 | a0001c0001t0010g0187 a0001c0001t0010g0189 a0001c0001t0010g0190 others(1): Show |
4 | HG02818.hp1 HG02896.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.712+1477G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121056785 | |||||||
| chr11:121056883 | C | G | 5 | a0001c0001t0001g0100 a0001c0001t0001g0154 a0001c0001t0001g0155 others(2): Show |
5 | HG02451.hp2 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.713-1462C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121056883 | |||||||
| chr11:121056911 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.713-1434G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121056911 | |||||||
| chr11:121057080 | G | A | 13 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(10): Show |
21 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.713-1265G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121057080 | |||||||
| chr11:121057172 | G | A | 1 | a0001c0001t0014g0182 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.713-1173G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121057172 | |||||||
| chr11:121057247 | T | A | 1 | a0001c0001t0001g0023 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.713-1098T>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121057247 | |||||||
| chr11:121057630 | C | A | 1 | a0001c0001t0001g0118 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.713-715C>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121057630 | |||||||
| chr11:121057764 | T | C | 1 | a0001c0001t0003g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.713-581T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121057764 | |||||||
| chr11:121057795 | A | G | 1 | a0001c0001t0002g0056 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.713-550A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121057795 | |||||||
| chr11:121057828 | GA | G | 78 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(75): Show |
99 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.713-514delA | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 121057828 | ||||||
| chr11:121057843 | T | G | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.713-502T>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121057843 | |||||||
| chr11:121057901 | A | G | 2 | a0001c0001t0005g0075 a0001c0001t0005g0076 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.713-444A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121057901 | |||||||
| chr11:121057911 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.713-434G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121057911 | |||||||
| chr11:121057981 | A | G | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.713-364A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121057981 | |||||||
| chr11:121057998 | C | T | 69 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(66): Show |
90 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.713-347C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121057998 | |||||||
| chr11:121058000 | T | G | 65 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(62): Show |
86 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.713-345T>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121058000 | |||||||
| chr11:121058013 | G | A | 5 | a0001c0001t0008g0106 a0001c0001t0009g0119 a0001c0001t0009g0120 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.713-332G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121058013 | |||||||
| chr11:121058137 | A | G | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.713-208A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121058137 | |||||||
| chr11:121058191 | G | C | 2 | a0001c0001t0002g0012 a0001c0001t0002g0030 |
3 | NA19057.hp2 NA19085.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.713-154G>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121058191 | |||||||
| chr11:121058328 | A | G | 4 | a0001c0001t0004g0040 a0001c0001t0004g0041 a0001c0001t0007g0013 others(1): Show |
5 | HG01891.hp2 HG02109.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.713-17A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 6/8 | chr11 | 121058328 | |||||||
| chr11:121058488 | G | A | 69 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(66): Show |
90 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.839+17G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 7/8 | chr11 | 121058488 | |||||||
| chr11:121058638 | C | T | 1 | a0001c0001t0016g0101 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.839+167C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 7/8 | chr11 | 121058638 | |||||||
| chr11:121058826 | A | G | 1 | a0001c0001t0003g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.839+355A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 7/8 | chr11 | 121058826 | |||||||
| chr11:121058970 | G | T | 3 | a0001c0001t0002g0055 a0001c0001t0002g0060 a0001c0001t0002g0089 |
3 | HG00408.hp1 HG02273.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.839+499G>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 7/8 | chr11 | 121058970 | |||||||
| chr11:121059180 | T | A | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.839+709T>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 7/8 | chr11 | 121059180 | |||||||
| chr11:121059571 | TTATA | T | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.840-394_840-391del others(4): Show |
TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 121059571 | ||||||
| chr11:121060238 | C | A | 69 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(66): Show |
90 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.956+153C>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121060238 | |||||||
| chr11:121060240 | A | G | 1 | a0001c0001t0019g0188 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.956+155A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121060240 | |||||||
| chr11:121060255 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0163 |
2 | HG01243.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.956+170C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121060255 | |||||||
| chr11:121060345 | T | C | 37 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0023 others(34): Show |
48 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.956+260T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121060345 | |||||||
| chr11:121060420 | CT | C | 1 | a0001c0001t0001g0007 | 3 | HG01099.hp2 HG02109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.956+336delT | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121060420 | |||||||
| chr11:121060696 | G | A | 1 | a0001c0001t0003g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.956+611G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121060696 | |||||||
| chr11:121060966 | G | A | 2 | a0001c0001t0005g0037 a0001c0001t0005g0038 |
2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.956+881G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121060966 | |||||||
| chr11:121061006 | A | G | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.956+921A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121061006 | |||||||
| chr11:121061322 | A | G | 1 | a0001c0001t0002g0054 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.956+1237A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121061322 | |||||||
| chr11:121061331 | T | C | 1 | a0001c0001t0003g0031 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.956+1246T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121061331 | |||||||
| chr11:121061392 | T | C | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.956+1307T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121061392 | |||||||
| chr11:121061427 | G | A | 1 | a0001c0001t0001g0007 | 3 | HG01099.hp2 HG02109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.956+1342G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121061427 | |||||||
| chr11:121061575 | A | G | 2 | a0001c0001t0013g0157 a0001c0001t0013g0158 |
2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.956+1490A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121061575 | |||||||
| chr11:121061581 | C | A | 1 | a0001c0001t0001g0154 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.956+1496C>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121061581 | |||||||
| chr11:121061605 | T | C | 2 | a0001c0001t0005g0075 a0001c0001t0005g0076 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.956+1520T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121061605 | |||||||
| chr11:121061632 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.956+1547A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121061632 | |||||||
| chr11:121061748 | G | A | 76 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(73): Show |
97 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.956+1663G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121061748 | |||||||
| chr11:121061878 | T | C | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.956+1793T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121061878 | |||||||
| chr11:121061958 | T | C | 6 | a0001c0001t0001g0092 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
6 | HG00735.hp1 HG01071.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.956+1873T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121061958 | |||||||
| chr11:121062009 | G | A | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.956+1924G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121062009 | |||||||
| chr11:121062198 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.956+2113A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121062198 | |||||||
| chr11:121062342 | G | T | 69 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(66): Show |
90 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.956+2257G>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121062342 | |||||||
| chr11:121062496 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.956+2411C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121062496 | |||||||
| chr11:121063019 | GCAGTTAA others(10): Show |
G | 1 | a0001c0001t0002g0073 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.956+2937_956+2953d others(19): Show |
TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr11 | 121063019 | ||||||
| chr11:121063077 | T | C | 2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
4 | HG02055.hp2 HG02630.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.956+2992T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121063077 | |||||||
| chr11:121063244 | G | C | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.956+3159G>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121063244 | |||||||
| chr11:121063519 | A | G | 3 | a0001c0001t0003g0191 a0001c0001t0003g0199 a0001c0001t0003g0200 |
3 | HG03471.hp2 HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.956+3434A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121063519 | |||||||
| chr11:121063703 | C | T | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.956+3618C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121063703 | |||||||
| chr11:121064325 | A | T | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.956+4240A>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121064325 | |||||||
| chr11:121064540 | T | C | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.956+4455T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121064540 | |||||||
| chr11:121064581 | C | T | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.956+4496C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121064581 | |||||||
| chr11:121064590 | G | A | 4 | a0001c0001t0010g0187 a0001c0001t0010g0189 a0001c0001t0010g0190 others(1): Show |
4 | HG02818.hp1 HG02896.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.956+4505G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121064590 | |||||||
| chr11:121064596 | T | C | 1 | a0001c0002t0011g0198 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.956+4511T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121064596 | |||||||
| chr11:121064649 | A | C | 1 | a0001c0002t0011g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.956+4564A>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121064649 | |||||||
| chr11:121064660 | G | A | 79 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(76): Show |
100 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.956+4575G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121064660 | |||||||
| chr11:121064818 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.956+4733A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121064818 | |||||||
| chr11:121064849 | A | C | 101 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(98): Show |
130 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.956+4764A>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121064849 | |||||||
| chr11:121064915 | C | T | 1 | a0001c0001t0003g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.956+4830C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121064915 | |||||||
| chr11:121064983 | G | A | 1 | a0001c0001t0002g0067 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.956+4898G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121064983 | |||||||
| chr11:121064989 | C | T | 1 | a0001c0001t0003g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.956+4904C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121064989 | |||||||
| chr11:121065008 | A | C | 2 | a0001c0001t0006g0193 a0001c0001t0006g0194 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.956+4923A>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121065008 | |||||||
| chr11:121065009 | G | T | 2 | a0001c0001t0006g0193 a0001c0001t0006g0194 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.956+4924G>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121065009 | |||||||
| chr11:121065061 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.956+4976C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121065061 | |||||||
| chr11:121065122 | G | A | 1 | a0001c0001t0021g0124 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.956+5037G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121065122 | |||||||
| chr11:121065204 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.956+5119C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121065204 | |||||||
| chr11:121065387 | G | T | 72 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(69): Show |
93 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.956+5302G>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121065387 | |||||||
| chr11:121065520 | T | C | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.956+5435T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121065520 | |||||||
| chr11:121065709 | A | G | 1 | a0001c0001t0002g0048 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.956+5624A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121065709 | |||||||
| chr11:121065749 | A | G | 1 | a0001c0001t0021g0124 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.956+5664A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121065749 | |||||||
| chr11:121066019 | C | G | 1 | a0001c0001t0003g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.956+5934C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121066019 | |||||||
| chr11:121066198 | T | C | 80 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(77): Show |
103 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.956+6113T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121066198 | |||||||
| chr11:121066429 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.956+6344G>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121066429 | |||||||
| chr11:121066717 | T | G | 1 | a0001c0001t0019g0188 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.956+6632T>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121066717 | |||||||
| chr11:121066928 | T | C | 101 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(98): Show |
130 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.956+6843T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121066928 | |||||||
| chr11:121067008 | C | T | 1 | a0001c0001t0002g0059 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.956+6923C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121067008 | |||||||
| chr11:121067054 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.956+6969G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121067054 | |||||||
| chr11:121067066 | C | G | 5 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(2): Show |
5 | HG00741.hp1 HG02451.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.956+6981C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121067066 | |||||||
| chr11:121067582 | TG | T | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.956+7499delG | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr11 | 121067582 | ||||||
| chr11:121067682 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.956+7597G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121067682 | |||||||
| chr11:121067868 | G | A | 2 | a0001c0001t0004g0077 a0001c0001t0004g0078 |
2 | HG02630.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.956+7783G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121067868 | |||||||
| chr11:121067918 | A | C | 3 | a0001c0002t0011g0197 a0001c0002t0011g0198 a0001c0002t0020g0176 |
3 | HG00741.hp1 HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.956+7833A>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121067918 | |||||||
| chr11:121068147 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.956+8062C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121068147 | |||||||
| chr11:121068209 | A | T | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.956+8124A>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121068209 | |||||||
| chr11:121068273 | A | G | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.956+8188A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121068273 | |||||||
| chr11:121068351 | G | T | 1 | a0001c0001t0003g0183 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.956+8266G>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121068351 | |||||||
| chr11:121068595 | C | A | 1 | a0001c0001t0001g0095 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.956+8510C>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121068595 | |||||||
| chr11:121068609 | C | T | 1 | a0001c0001t0009g0120 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.956+8524C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121068609 | |||||||
| chr11:121068654 | T | C | 76 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(73): Show |
97 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.956+8569T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121068654 | |||||||
| chr11:121068654 | T | G | 5 | a0001c0001t0003g0183 a0001c0001t0006g0193 a0001c0001t0006g0194 others(2): Show |
5 | HG02257.hp1 HG02451.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.956+8569T>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121068654 | |||||||
| chr11:121068774 | C | G | 1 | a0001c0001t0002g0080 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.956+8689C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121068774 | |||||||
| chr11:121068776 | A | G | 1 | a0001c0001t0004g0077 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.956+8691A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121068776 | |||||||
| chr11:121068819 | G | A | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.956+8734G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121068819 | |||||||
| chr11:121068828 | G | T | 4 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0185 others(1): Show |
8 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.956+8743G>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121068828 | |||||||
| chr11:121068877 | G | C | 1 | a0001c0001t0003g0032 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.956+8792G>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121068877 | |||||||
| chr11:121068886 | C | CA | 8 | a0001c0001t0001g0093 a0001c0001t0001g0153 a0001c0001t0001g0167 others(5): Show |
9 | HG06807.hp1 NA18906.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.956+8817dupA | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr11 | 121068886 | ||||||
| chr11:121068886 | CA | C | 8 | a0001c0001t0001g0111 a0001c0001t0001g0128 a0001c0001t0001g0156 others(5): Show |
8 | HG01106.hp1 HG02071.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.956+8817delA | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr11 | 121068886 | ||||||
| chr11:121068902 | A | C | 1 | a0001c0001t0013g0158 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.956+8817A>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121068902 | |||||||
| chr11:121069200 | G | A | 3 | a0001c0002t0011g0197 a0001c0002t0011g0198 a0001c0002t0020g0176 |
3 | HG00741.hp1 HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.956+9115G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121069200 | |||||||
| chr11:121069390 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.956+9305G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121069390 | |||||||
| chr11:121069452 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.956+9367C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121069452 | |||||||
| chr11:121069523 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.956+9438G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121069523 | |||||||
| chr11:121069752 | G | A | 100 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(97): Show |
129 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.956+9667G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121069752 | |||||||
| chr11:121069893 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.956+9808C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121069893 | |||||||
| chr11:121069957 | A | G | 1 | a0001c0001t0003g0010 | 3 | HG02258.hp1 HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.956+9872A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121069957 | |||||||
| chr11:121070180 | G | A | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.956+10095G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121070180 | |||||||
| chr11:121070275 | C | G | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.956+10190C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121070275 | |||||||
| chr11:121070416 | T | C | 79 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(76): Show |
100 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.956+10331T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121070416 | |||||||
| chr11:121070717 | G | T | 1 | a0001c0001t0001g0091 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.956+10632G>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121070717 | |||||||
| chr11:121070774 | G | A | 1 | a0001c0001t0002g0051 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.956+10689G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121070774 | |||||||
| chr11:121070789 | A | T | 2 | a0001c0001t0006g0193 a0001c0001t0006g0194 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.956+10704A>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121070789 | |||||||
| chr11:121070831 | A | AT | 71 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(68): Show |
92 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.956+10749dupT | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr11 | 121070831 | ||||||
| chr11:121070834 | T | TA | 8 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(5): Show |
8 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.956+10763dupA | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr11 | 121070834 | ||||||
| chr11:121070874 | A | G | 25 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0023 others(22): Show |
36 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.956+10789A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121070874 | |||||||
| chr11:121071141 | C | T | 1 | a0001c0001t0003g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.956+11056C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121071141 | |||||||
| chr11:121071254 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.956+11169C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121071254 | |||||||
| chr11:121071631 | G | A | 3 | a0001c0001t0010g0187 a0001c0001t0010g0189 a0001c0001t0010g0190 |
3 | HG02896.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.956+11546G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121071631 | |||||||
| chr11:121071885 | G | A | 2 | a0001c0001t0005g0075 a0001c0001t0005g0076 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.956+11800G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121071885 | |||||||
| chr11:121071941 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0087 |
3 | HG00621.hp2 NA18956.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.956+11856C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121071941 | |||||||
| chr11:121072050 | G | A | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.956+11965G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121072050 | |||||||
| chr11:121072186 | G | A | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.956+12101G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121072186 | |||||||
| chr11:121072956 | T | C | 2 | a0001c0001t0002g0082 a0001c0001t0002g0083 |
2 | HG01243.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.956+12871T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121072956 | |||||||
| chr11:121073510 | A | G | 68 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0014 others(65): Show |
87 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.957-13268A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121073510 | |||||||
| chr11:121073564 | A | G | 1 | a0001c0001t0006g0196 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.957-13214A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121073564 | |||||||
| chr11:121073625 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.957-13153G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121073625 | |||||||
| chr11:121073676 | A | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | NA18942.hp2 NA18968.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.957-13102A>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121073676 | |||||||
| chr11:121073785 | G | C | 1 | a0001c0001t0002g0036 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.957-12993G>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121073785 | |||||||
| chr11:121074354 | T | C | 1 | a0001c0001t0003g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.957-12424T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121074354 | |||||||
| chr11:121074473 | A | G | 2 | a0001c0001t0001g0149 a0001c0001t0001g0169 |
2 | HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.957-12305A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121074473 | |||||||
| chr11:121074720 | C | G | 4 | a0001c0001t0010g0187 a0001c0001t0010g0189 a0001c0001t0010g0190 others(1): Show |
4 | HG02818.hp1 HG02896.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.957-12058C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121074720 | |||||||
| chr11:121074884 | A | G | 1 | a0001c0001t0003g0179 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.957-11894A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121074884 | |||||||
| chr11:121075017 | T | C | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.957-11761T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121075017 | |||||||
| chr11:121075193 | C | A | 7 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
7 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.957-11585C>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121075193 | |||||||
| chr11:121075261 | T | G | 3 | a0001c0001t0002g0042 a0001c0001t0002g0080 a0001c0001t0002g0081 |
3 | HG02698.hp2 HG03017.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.957-11517T>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121075261 | |||||||
| chr11:121075761 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.957-11017T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121075761 | |||||||
| chr11:121075871 | G | A | 75 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0014 others(72): Show |
94 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.957-10907G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121075871 | |||||||
| chr11:121075907 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.957-10871G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121075907 | |||||||
| chr11:121076183 | A | G | 64 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0014 others(61): Show |
83 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.957-10595A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121076183 | |||||||
| chr11:121076349 | T | A | 9 | a0001c0001t0001g0088 a0001c0001t0002g0004 a0001c0001t0002g0049 others(6): Show |
15 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.957-10429T>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121076349 | |||||||
| chr11:121076498 | A | G | 18 | a0001c0001t0001g0088 a0001c0001t0002g0004 a0001c0001t0002g0049 others(15): Show |
28 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.957-10280A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121076498 | |||||||
| chr11:121076990 | A | G | 78 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0014 others(75): Show |
99 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.957-9788A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121076990 | |||||||
| chr11:121077080 | T | A | 1 | a0001c0001t0003g0179 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.957-9698T>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121077080 | |||||||
| chr11:121077212 | T | C | 3 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG02165.hp2 NA18942.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.957-9566T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121077212 | |||||||
| chr11:121077239 | T | TA | 68 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0014 others(65): Show |
87 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.957-9538dupA | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr11 | 121077239 | ||||||
| chr11:121077542 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.957-9236C>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121077542 | |||||||
| chr11:121077615 | T | C | 1 | a0001c0001t0014g0182 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.957-9163T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121077615 | |||||||
| chr11:121078030 | C | G | 1 | a0001c0001t0001g0134 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.957-8748C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121078030 | |||||||
| chr11:121078123 | T | G | 19 | a0001c0001t0001g0088 a0001c0001t0002g0004 a0001c0001t0002g0049 others(16): Show |
29 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.957-8655T>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121078123 | |||||||
| chr11:121078199 | A | G | 7 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
7 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.957-8579A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121078199 | |||||||
| chr11:121078345 | C | T | 1 | a0001c0001t0002g0060 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.957-8433C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121078345 | |||||||
| chr11:121078409 | G | A | 1 | a0001c0001t0003g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.957-8369G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121078409 | |||||||
| chr11:121078681 | A | G | 1 | a0001c0001t0003g0179 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.957-8097A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121078681 | |||||||
| chr11:121078725 | G | A | 1 | a0001c0001t0003g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.957-8053G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121078725 | |||||||
| chr11:121078796 | A | G | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.957-7982A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121078796 | |||||||
| chr11:121079293 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.957-7485G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121079293 | |||||||
| chr11:121079325 | T | C | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.957-7453T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121079325 | |||||||
| chr11:121079352 | G | C | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.957-7426G>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121079352 | |||||||
| chr11:121079396 | T | C | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.957-7382T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121079396 | |||||||
| chr11:121079544 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0114 |
4 | HG02717.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.957-7234T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121079544 | |||||||
| chr11:121079704 | C | T | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.957-7074C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121079704 | |||||||
| chr11:121079812 | G | A | 98 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(95): Show |
127 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.957-6966G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121079812 | |||||||
| chr11:121079817 | A | G | 1 | a0001c0001t0002g0079 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.957-6961A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121079817 | |||||||
| chr11:121079923 | T | C | 101 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(98): Show |
130 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.957-6855T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121079923 | |||||||
| chr11:121080043 | T | C | 73 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(70): Show |
94 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.957-6735T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121080043 | |||||||
| chr11:121080056 | G | A | 1 | a0001c0001t0003g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.957-6722G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121080056 | |||||||
| chr11:121080117 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.957-6661G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121080117 | |||||||
| chr11:121080274 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0129 |
2 | HG00408.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.957-6504C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121080274 | |||||||
| chr11:121080665 | G | A | 1 | a0001c0001t0003g0179 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.957-6113G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121080665 | |||||||
| chr11:121081022 | A | G | 1 | a0001c0001t0003g0183 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.957-5756A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121081022 | |||||||
| chr11:121081216 | C | T | 2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
4 | HG02055.hp2 HG02630.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.957-5562C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121081216 | |||||||
| chr11:121081333 | C | T | 1 | a0001c0001t0019g0188 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.957-5445C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121081333 | |||||||
| chr11:121081391 | A | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0148 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.957-5387A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121081391 | |||||||
| chr11:121081456 | T | A | 1 | a0001c0001t0001g0110 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.957-5322T>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121081456 | |||||||
| chr11:121082279 | C | T | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.957-4499C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121082279 | |||||||
| chr11:121082516 | A | G | 1 | a0001c0001t0002g0067 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.957-4262A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121082516 | |||||||
| chr11:121082572 | G | C | 4 | a0001c0001t0010g0187 a0001c0001t0010g0189 a0001c0001t0010g0190 others(1): Show |
4 | HG02818.hp1 HG02896.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.957-4206G>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121082572 | |||||||
| chr11:121082657 | G | A | 7 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
7 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.957-4121G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121082657 | |||||||
| chr11:121082946 | G | A | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.957-3832G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121082946 | |||||||
| chr11:121083205 | T | C | 13 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(10): Show |
21 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.957-3573T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121083205 | |||||||
| chr11:121083255 | G | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0164 |
2 | HG01257.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.957-3523G>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121083255 | |||||||
| chr11:121083294 | T | C | 1 | a0001c0001t0002g0087 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.957-3484T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121083294 | |||||||
| chr11:121083719 | T | G | 1 | a0001c0001t0001g0125 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.957-3059T>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121083719 | |||||||
| chr11:121083727 | T | C | 13 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(10): Show |
21 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.957-3051T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121083727 | |||||||
| chr11:121083737 | T | G | 100 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(97): Show |
129 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.957-3041T>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121083737 | |||||||
| chr11:121083779 | A | G | 1 | a0001c0001t0002g0064 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.957-2999A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121083779 | |||||||
| chr11:121083969 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | NA18971.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.957-2809G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121083969 | |||||||
| chr11:121084020 | G | A | 4 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.957-2758G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121084020 | |||||||
| chr11:121084060 | T | C | 97 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(94): Show |
126 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.957-2718T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121084060 | |||||||
| chr11:121084084 | A | G | 4 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0185 others(1): Show |
8 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.957-2694A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121084084 | |||||||
| chr11:121084202 | T | A | 70 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(67): Show |
91 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.957-2576T>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121084202 | |||||||
| chr11:121084240 | C | T | 1 | a0001c0001t0002g0060 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.957-2538C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121084240 | |||||||
| chr11:121084319 | C | T | 70 | a0001c0001t0001g0088 a0001c0001t0002g0002 a0001c0001t0002g0004 others(67): Show |
91 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.957-2459C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121084319 | |||||||
| chr11:121084549 | G | GC | 2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
4 | HG02055.hp2 HG02630.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.957-2228dupC | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr11 | 121084549 | ||||||
| chr11:121084777 | G | A | 2 | a0001c0001t0003g0010 a0001c0001t0003g0181 |
4 | HG02258.hp1 HG02647.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.957-2001G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121084777 | |||||||
| chr11:121084817 | A | T | 1 | a0001c0001t0014g0182 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.957-1961A>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121084817 | |||||||
| chr11:121084943 | T | A | 1 | a0001c0001t0001g0131 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.957-1835T>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121084943 | |||||||
| chr11:121085042 | T | A | 2 | a0001c0001t0005g0075 a0001c0001t0005g0076 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.957-1736T>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121085042 | |||||||
| chr11:121085186 | G | A | 5 | a0001c0001t0001g0126 a0001c0001t0006g0193 a0001c0001t0006g0194 others(2): Show |
5 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.957-1592G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121085186 | |||||||
| chr11:121085191 | A | G | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.957-1587A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121085191 | |||||||
| chr11:121085265 | C | T | 2 | a0001c0002t0011g0197 a0001c0002t0011g0198 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.957-1513C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121085265 | |||||||
| chr11:121085327 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.957-1451C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121085327 | |||||||
| chr11:121085522 | G | A | 1 | a0001c0002t0020g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.957-1256G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121085522 | |||||||
| chr11:121085697 | G | A | 1 | a0001c0001t0005g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.957-1081G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121085697 | |||||||
| chr11:121085758 | G | A | 1 | a0001c0001t0002g0046 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.957-1020G>A | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121085758 | |||||||
| chr11:121085879 | A | C | 1 | a0001c0001t0003g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.957-899A>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121085879 | |||||||
| chr11:121085949 | C | T | 1 | a0001c0001t0003g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.957-829C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121085949 | |||||||
| chr11:121086033 | C | G | 2 | a0001c0001t0005g0075 a0001c0001t0005g0076 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.957-745C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121086033 | |||||||
| chr11:121086157 | C | G | 7 | a0001c0001t0006g0193 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
7 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.957-621C>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121086157 | |||||||
| chr11:121086190 | A | G | 1 | a0001c0001t0006g0196 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.957-588A>G | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121086190 | |||||||
| chr11:121086306 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.957-472T>C | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121086306 | |||||||
| chr11:121086376 | G | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | NA18942.hp2 NA18968.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.957-402G>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121086376 | |||||||
| chr11:121086430 | C | T | 1 | a0001c0001t0003g0183 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.957-348C>T | TBCEL | ENSG00000154114.13 | transcript | ENST00000683345.1 | protein_coding | 8/8 | chr11 | 121086430 |