Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7072 |
| ensemblid | ENSG00000116001.17 |
| hgncid | 11802 |
| symbol | TIA1 |
| name | TIA1 cytotoxic granule associated RNA binding protein |
| refseq_nuc | NM_022173.4 |
| refseq_prot | NP_071505.2 |
| ensembl_nuc | ENST00000433529.7 |
| ensembl_prot | ENSP00000401371.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 70209444 |
| end | 70248628 |
| strand | - |
| ver | v1.2 |
| region | chr2:70209444-70248628 |
| region5000 | chr2:70204444-70253628 |
| regionname0 | TIA1_chr2_70209444_70248628 |
| regionname5000 | TIA1_chr2_70204444_70253628 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 386 | 389 | 96 | 66 | 176 | 10 | 39 | 136 | TIA1_chr2_70204444_70253628 | TIA1 | MEDEM others(381): Show |
chr2 | 70204444 | 70253628 |
| a0002 | 0/0 | 386 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | MEDEM others(381): Show |
chr2 | 70204444 | 70253628 |
| a0003 | 0/0 | 386 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | MEDEM others(381): Show |
chr2 | 70204444 | 70253628 |
| a0004 | 0/0 | 386 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | MEDEM others(381): Show |
chr2 | 70204444 | 70253628 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1158 | 379 | 87 | 66 | 175 | 10 | 39 | TIA1_chr2_70204444_70253628 | TIA1 | ATGGA others(1153): Show |
chr2 | 70204444 | 70253628 | ||
| a0001c0002 | 0/0 | 1158 | 4 | 4 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | ATGGA others(1153): Show |
chr2 | 70204444 | 70253628 | ||
| a0001c0003 | 0/0 | 1158 | 3 | 3 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | ATGGA others(1153): Show |
chr2 | 70204444 | 70253628 | ||
| a0001c0005 | 0/0 | 1158 | 2 | 2 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | ATGGA others(1153): Show |
chr2 | 70204444 | 70253628 | ||
| a0001c0008 | 0/0 | 1158 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | ATGGA others(1153): Show |
chr2 | 70204444 | 70253628 | ||
| a0002c0004 | 0/0 | 1158 | 3 | 2 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | ATGGA others(1153): Show |
chr2 | 70204444 | 70253628 | ||
| a0003c0006 | 0/0 | 1158 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | ATGGA others(1153): Show |
chr2 | 70204444 | 70253628 | ||
| a0004c0007 | 0/0 | 1158 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | ATGGA others(1153): Show |
chr2 | 70204444 | 70253628 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4634 | 255 | 59 | 33 | 118 | 9 | 34 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4629): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0002 | 0/0 | 4634 | 41 | 1 | 7 | 30 | 1 | 2 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4629): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0003 | 0/0 | 4635 | 37 | 0 | 18 | 17 | 0 | 2 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4630): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0004 | 0/0 | 4634 | 10 | 8 | 2 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4629): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0005 | 0/0 | 4636 | 5 | 5 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4631): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0006 | 0/0 | 4635 | 4 | 1 | 1 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4630): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0008 | 0/0 | 4636 | 4 | 4 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4631): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0009 | 0/0 | 4634 | 3 | 3 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4629): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0010 | 0/0 | 4634 | 3 | 0 | 3 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4629): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0011 | 0/0 | 4634 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4629): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0013 | 0/0 | 4634 | 2 | 1 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4629): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0014 | 0/0 | 4634 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4629): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0015 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4630): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0016 | 0/0 | 4636 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4631): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0017 | 0/0 | 4634 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4629): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0018 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4630): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0019 | 0/0 | 4634 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4629): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0020 | 0/0 | 4633 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4628): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0021 | 0/0 | 4634 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4629): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0022 | 0/0 | 4634 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4629): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0023 | 0/0 | 4634 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4629): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0024 | 0/0 | 4634 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4629): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0025 | 0/0 | 4634 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4629): Show |
chr2 | 70204444 | 70253628 |
| a0001c0001t0026 | 0/0 | 4634 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4629): Show |
chr2 | 70204444 | 70253628 |
| a0001c0002t0007 | 0/0 | 4635 | 4 | 4 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4630): Show |
chr2 | 70204444 | 70253628 |
| a0001c0003t0001 | 0/0 | 4634 | 3 | 3 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4629): Show |
chr2 | 70204444 | 70253628 |
| a0001c0005t0012 | 0/0 | 4634 | 2 | 2 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4629): Show |
chr2 | 70204444 | 70253628 |
| a0001c0008t0001 | 0/0 | 4634 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4629): Show |
chr2 | 70204444 | 70253628 |
| a0002c0004t0001 | 0/0 | 4634 | 3 | 2 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4629): Show |
chr2 | 70204444 | 70253628 |
| a0003c0006t0001 | 0/0 | 4634 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4629): Show |
chr2 | 70204444 | 70253628 |
| a0004c0007t0001 | 0/0 | 4634 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | GCCGC others(4629): Show |
chr2 | 70204444 | 70253628 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 1 | 2 | 3 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0283 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0004g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0004g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0004g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0004g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0004g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0005g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0005g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0005g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0005g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0006g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0006g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0006g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0008g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0008g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0008g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0008g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0009g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0009g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0009g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0010g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0010g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0011g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0011g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0013g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0013g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0014g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0015g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0016g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0017g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0018g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0019g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0020g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0021g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0022g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0023g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0024g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0025g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0001t0026g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0002t0007g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0002t0007g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0002t0007g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0002t0007g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0003t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0003t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0005t0012g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0005t0012g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0001c0008t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0002c0004t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0002c0004t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0002c0004t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0003c0006t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| a0004c0007t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0231 | EUR | GBR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0285 | EUR | FIN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0178 | EUR | FIN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0341 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG00642 | hp1 | a0001 | c0001 | t0010 | g0359 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0316 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0330 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01099 | hp1 | a0001 | c0001 | t0023 | g0228 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0039 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01167 | hp2 | a0001 | c0001 | t0026 | g0360 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0352 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01243 | hp1 | a0002 | c0004 | t0001 | g0091 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0079 | AMR | PUR | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0065 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0073 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0287 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0224 | EUR | IBS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | IBS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0242 | EUR | IBS | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0083 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0353 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0071 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0314 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01943 | hp1 | a0001 | c0001 | t0010 | g0021 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0339 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01952 | hp2 | a0003 | c0006 | t0001 | g0133 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0063 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0066 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0067 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG01993 | hp2 | a0001 | c0001 | t0010 | g0021 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0334 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0367 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0070 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02083 | hp2 | a0001 | c0008 | t0001 | g0235 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0364 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CDX | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CDX | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CDX | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | CDX | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02258 | hp1 | a0002 | c0004 | t0001 | g0094 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0337 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02280 | hp1 | a0001 | c0005 | t0012 | g0104 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0338 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0068 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0049 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0365 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0363 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02622 | hp1 | a0001 | c0001 | t0019 | g0215 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02630 | hp2 | a0001 | c0001 | t0013 | g0099 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0288 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02717 | hp2 | a0001 | c0001 | t0009 | g0085 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02723 | hp2 | a0001 | c0002 | t0007 | g0301 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0356 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02738 | hp2 | a0004 | c0007 | t0001 | g0202 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0366 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0345 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0354 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03017 | hp2 | a0001 | c0001 | t0014 | g0023 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03041 | hp1 | a0002 | c0004 | t0001 | g0098 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0092 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0096 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03195 | hp1 | a0001 | c0001 | t0022 | g0102 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03225 | hp1 | a0001 | c0001 | t0018 | g0303 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0286 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03453 | hp2 | a0001 | c0002 | t0007 | g0349 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0088 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03486 | hp2 | a0001 | c0002 | t0007 | g0305 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0361 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03540 | hp2 | a0001 | c0001 | t0009 | g0081 | AFR | GWD | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0350 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0040 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0038 | SAS | STU | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | STU | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0323 | SAS | PJL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | BEB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0336 | SAS | STU | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | YRI | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | CHB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0332 | EAS | CHB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | YRI | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0357 | AFR | YRI | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18940 | hp1 | a0001 | c0001 | t0006 | g0125 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18948 | hp2 | a0001 | c0001 | t0011 | g0347 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18952 | hp2 | a0001 | c0001 | t0013 | g0254 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18959 | hp2 | a0001 | c0001 | t0021 | g0123 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18975 | hp1 | a0001 | c0001 | t0025 | g0321 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18983 | hp2 | a0001 | c0001 | t0017 | g0312 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18985 | hp1 | a0001 | c0001 | t0016 | g0074 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0343 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | LWK | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19030 | hp2 | a0001 | c0005 | t0012 | g0117 | AFR | LWK | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19043 | hp1 | a0001 | c0001 | t0024 | g0084 | AFR | LWK | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0344 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19067 | hp2 | a0001 | c0001 | t0015 | g0342 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19084 | hp1 | a0001 | c0001 | t0011 | g0346 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0348 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19086 | hp2 | a0001 | c0001 | t0006 | g0236 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19240 | hp1 | a0001 | c0002 | t0007 | g0304 | AFR | YRI | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ASW | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ASW | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0320 | EUR | TSI | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | TSI | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | GIH | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | GIH | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0362 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | USA | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | USA | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0351 | AFR | USA | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | USA | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA21309 | hp1 | a0001 | c0001 | t0020 | g0219 | AFR | LWK | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | LWK | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0283 | REF | REF | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0227 | REF | REF | TIA1_chr2_70204444_70253628 | TIA1 | chr2 | 70204444 | 70253628 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:70212756 | G | T | 1 | a0003 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.1124C>A | p.Pro375His | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 1322/4634 | 1124/1161 | 375/386 | chr2 | 70212756 | |||
| chr2:70214430 | T | C | 1 | a0004 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.953A>G | p.Gln318Arg | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/13 | 1151/4634 | 953/1161 | 318/386 | chr2 | 70214430 | |||
| chr2:70214436 | G | C | 1 | a0002 | 3 | HG01243.hp1 HG02258.hp1 HG03041.hp1 |
missense_variant | MODERATE | c.947C>G | p.Ala316Gly | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/13 | 1145/4634 | 947/1161 | 316/386 | chr2 | 70214436 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:70212758 | C | T | 1 | a0001c0003 | 3 | HG03098.hp1 HG03139.hp2 HG03486.hp1 |
synonymous_variant | LOW | c.1122G>A | p.Gln374Gln | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 1320/4634 | 1122/1161 | 374/386 | chr2 | 70212758 | |||
| chr2:70212794 | C | T | 1 | a0001c0002 | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
synonymous_variant | LOW | c.1086G>A | p.Pro362Pro | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 1284/4634 | 1086/1161 | 362/386 | chr2 | 70212794 | |||
| chr2:70214459 | C | T | 1 | a0001c0005 | 2 | HG02280.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.924G>A | p.Gln308Gln | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/13 | 1122/4634 | 924/1161 | 308/386 | chr2 | 70214459 | |||
| chr2:70236127 | T | C | 1 | a0001c0008 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.75A>G | p.Gln25Gln | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/13 | 273/4634 | 75/1161 | 25/386 | chr2 | 70236127 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:70209672 | A | G | 1 | a0001c0002t0007 | 4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3047T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 3047 | chr2 | 70209672 | ||||||
| chr2:70209686 | C | T | 9 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(6): Show |
60 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*3033G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 3033 | chr2 | 70209686 | ||||||
| chr2:70209791 | C | A | 1 | a0001c0005t0012 | 2 | HG02280.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2928G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 2928 | chr2 | 70209791 | ||||||
| chr2:70210109 | TA | T | 6 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0015 others(3): Show |
47 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*2609delT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 2609 | chr2 | 70210109 | ||||||
| chr2:70210203 | G | C | 1 | a0001c0001t0021 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2516C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 2516 | chr2 | 70210203 | ||||||
| chr2:70210283 | T | C | 1 | a0001c0001t0011 | 2 | NA18948.hp2 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2436A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 2436 | chr2 | 70210283 | ||||||
| chr2:70210411 | A | G | 1 | a0001c0001t0019 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2308T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 2308 | chr2 | 70210411 | ||||||
| chr2:70210496 | T | A | 1 | a0001c0001t0022 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2223A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 2223 | chr2 | 70210496 | ||||||
| chr2:70210910 | A | G | 2 | a0001c0001t0009 a0001c0001t0024 |
4 | HG01884.hp1 HG02717.hp2 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1809T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 1809 | chr2 | 70210910 | ||||||
| chr2:70211140 | T | C | 1 | a0001c0001t0023 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1579A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 1579 | chr2 | 70211140 | ||||||
| chr2:70211420 | G | GT | 9 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0011 others(6): Show |
89 | HG00544.hp2 HG00609.hp2 HG00621.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*1298dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 1298 | chr2 | 70211420 | ||||||
| chr2:70211420 | G | GTT | 2 | a0001c0001t0005 a0001c0001t0008 |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1297_*1298dupAA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 1298 | chr2 | 70211420 | ||||||
| chr2:70211421 | T | G | 1 | a0001c0001t0013 | 2 | HG02630.hp2 NA18952.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1298A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 1298 | chr2 | 70211421 | ||||||
| chr2:70211474 | G | A | 1 | a0001c0001t0024 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1245C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 1245 | chr2 | 70211474 | ||||||
| chr2:70211892 | C | T | 1 | a0001c0001t0008 | 4 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*827G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 827 | chr2 | 70211892 | ||||||
| chr2:70211926 | G | C | 1 | a0001c0001t0017 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*793C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 793 | chr2 | 70211926 | ||||||
| chr2:70212272 | C | T | 5 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0015 others(2): Show |
46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*447G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 447 | chr2 | 70212272 | ||||||
| chr2:70212316 | G | GT | 3 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0016 |
6 | HG01243.hp2 HG02055.hp2 NA18940.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*402dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 402 | chr2 | 70212316 | ||||||
| chr2:70212327 | T | A | 1 | a0001c0001t0004 | 10 | HG01192.hp1 HG01433.hp1 HG01884.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*392A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 392 | chr2 | 70212327 | ||||||
| chr2:70212394 | T | C | 1 | a0001c0001t0025 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*325A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 13/13 | 325 | chr2 | 70212394 | ||||||
| chr2:70248443 | C | T | 1 | a0001c0001t0014 | 1 | HG03017.hp2 | 5_prime_UTR_variant | MODIFIER | c.-13G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/13 | 13 | chr2 | 70248443 | ||||||
| chr2:70248567 | G | A | 1 | a0001c0001t0010 | 3 | HG00642.hp1 HG01943.hp1 HG01993.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-137C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/13 | chr2 | 70248567 | |||||||
| chr2:70248586 | C | A | 1 | a0001c0001t0026 | 1 | HG01167.hp2 | 5_prime_UTR_variant | MODIFIER | c.-156G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/13 | 156 | chr2 | 70248586 | ||||||
| chr2:70248596 | G | A | 2 | a0001c0001t0005 a0001c0001t0008 |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-166C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/13 | chr2 | 70248596 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:70212873 | G | A | 1 | a0001c0001t0006g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1035-28C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70212873 | |||||||
| chr2:70212978 | T | C | 2 | a0001c0001t0003g0048 a0001c0001t0003g0053 |
2 | HG02129.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1035-133A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70212978 | |||||||
| chr2:70213035 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1035-190A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213035 | |||||||
| chr2:70213077 | T | G | 1 | a0001c0001t0004g0352 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1035-232A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213077 | |||||||
| chr2:70213122 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1035-277C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213122 | |||||||
| chr2:70213212 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1035-367G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213212 | |||||||
| chr2:70213230 | T | G | 1 | a0001c0001t0001g0111 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1035-385A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213230 | |||||||
| chr2:70213257 | T | C | 1 | a0001c0001t0002g0320 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1035-412A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213257 | |||||||
| chr2:70213280 | A | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1035-435T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213280 | |||||||
| chr2:70213316 | C | A | 45 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1035-471G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213316 | |||||||
| chr2:70213345 | C | CT | 10 | a0001c0001t0001g0121 a0001c0001t0001g0126 a0001c0001t0001g0130 others(7): Show |
10 | HG02922.hp2 NA18964.hp1 NA18982.hp1 others(7): Show |
intron_variant | MODIFIER | c.1035-501dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213345 | |||||||
| chr2:70213345 | CT | C | 10 | a0001c0001t0001g0031 a0001c0001t0001g0203 a0001c0001t0001g0226 others(7): Show |
10 | HG01169.hp2 HG01257.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1035-501delA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213345 | |||||||
| chr2:70213350 | T | C | 9 | a0001c0001t0001g0151 a0001c0001t0001g0195 a0001c0001t0001g0196 others(6): Show |
9 | HG02004.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1035-505A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213350 | |||||||
| chr2:70213374 | C | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(84): Show |
99 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1035-529G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213374 | |||||||
| chr2:70213485 | T | C | 1 | a0001c0001t0018g0303 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1035-640A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213485 | |||||||
| chr2:70213599 | T | G | 1 | a0001c0001t0003g0055 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1034+750A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213599 | |||||||
| chr2:70213657 | CT | C | 45 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1034+691delA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213657 | |||||||
| chr2:70213801 | A | G | 1 | a0001c0001t0018g0303 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1034+548T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70213801 | |||||||
| chr2:70214042 | G | A | 1 | a0001c0001t0018g0303 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1034+307C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70214042 | |||||||
| chr2:70214050 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1034+299C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70214050 | |||||||
| chr2:70214199 | T | TA | 45 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1034+149dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70214199 | |||||||
| chr2:70214218 | G | A | 4 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0113 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1034+131C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70214218 | |||||||
| chr2:70214229 | G | A | 58 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(55): Show |
60 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.1034+120C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 12/12 | chr2 | 70214229 | |||||||
| chr2:70214632 | TAAAAAAA others(1): Show |
T | 6 | a0001c0001t0001g0025 a0001c0001t0001g0120 a0001c0001t0001g0141 others(3): Show |
6 | HG02602.hp2 HG02698.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.889-146_889-139del others(8): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 11/12 | chr2 | 70214632 | |||||||
| chr2:70214643 | A | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
206 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.889-149T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 11/12 | chr2 | 70214643 | |||||||
| chr2:70214651 | A | AC | 42 | a0001c0001t0001g0075 a0001c0001t0001g0209 a0001c0001t0001g0218 others(39): Show |
43 | HG00609.hp2 HG00735.hp2 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.889-158_889-157ins others(1): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 11/12 | chr2 | 70214651 | |||||||
| chr2:70214651 | A | C | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(306): Show |
333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.889-157T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 11/12 | chr2 | 70214651 | |||||||
| chr2:70214668 | A | G | 1 | a0001c0001t0018g0303 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.889-174T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 11/12 | chr2 | 70214668 | |||||||
| chr2:70214720 | G | C | 19 | a0001c0001t0001g0014 a0001c0001t0001g0203 a0001c0001t0001g0206 others(16): Show |
20 | HG02074.hp1 HG02083.hp2 NA18747.hp1 others(17): Show |
intron_variant | MODIFIER | c.889-226C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 11/12 | chr2 | 70214720 | |||||||
| chr2:70214811 | T | C | 1 | a0001c0001t0002g0335 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.889-317A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 11/12 | chr2 | 70214811 | |||||||
| chr2:70214864 | T | G | 38 | a0001c0001t0001g0075 a0001c0001t0003g0004 a0001c0001t0003g0027 others(35): Show |
39 | HG00609.hp2 HG00735.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.889-370A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 11/12 | chr2 | 70214864 | |||||||
| chr2:70215047 | A | G | 4 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(1): Show |
5 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.888+324T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 11/12 | chr2 | 70215047 | |||||||
| chr2:70215184 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0197 |
3 | HG03704.hp2 NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.888+187C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 11/12 | chr2 | 70215184 | |||||||
| chr2:70215590 | ACAGTTTG | A | 17 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0090 others(14): Show |
17 | HG01243.hp1 HG01884.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.765-103_765-97delC others(6): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70215590 | |||||||
| chr2:70215598 | C | T | 1 | a0001c0001t0018g0303 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.765-104G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70215598 | |||||||
| chr2:70215660 | T | C | 58 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(55): Show |
60 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.765-166A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70215660 | |||||||
| chr2:70215706 | G | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0175 |
2 | HG00609.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.765-212C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70215706 | |||||||
| chr2:70215720 | G | C | 3 | a0001c0001t0002g0322 a0001c0001t0002g0326 a0001c0001t0002g0327 |
3 | NA18959.hp1 NA18965.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.765-226C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70215720 | |||||||
| chr2:70215753 | A | T | 1 | a0001c0001t0006g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.765-259T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70215753 | |||||||
| chr2:70215822 | C | A | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0265 |
3 | NA18943.hp1 NA18962.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.765-328G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70215822 | |||||||
| chr2:70215880 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.764+328G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70215880 | |||||||
| chr2:70215900 | C | T | 15 | a0001c0001t0001g0295 a0001c0001t0003g0045 a0001c0001t0003g0049 others(12): Show |
15 | HG01257.hp2 HG01258.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.764+308G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70215900 | |||||||
| chr2:70215998 | C | T | 1 | a0001c0001t0002g0348 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.764+210G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70215998 | |||||||
| chr2:70216003 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | NA18945.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.764+205G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70216003 | |||||||
| chr2:70216033 | T | C | 17 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0090 others(14): Show |
17 | HG01243.hp1 HG01884.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.764+175A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70216033 | |||||||
| chr2:70216115 | T | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.764+93A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70216115 | |||||||
| chr2:70216191 | T | A | 1 | a0001c0001t0001g0232 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.764+17A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 10/12 | chr2 | 70216191 | |||||||
| chr2:70216596 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.584-97G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 8/12 | chr2 | 70216596 | |||||||
| chr2:70217184 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.475-190A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217184 | |||||||
| chr2:70217202 | C | T | 1 | a0001c0001t0020g0219 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.475-208G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217202 | |||||||
| chr2:70217303 | C | T | 3 | a0001c0001t0009g0083 a0001c0001t0009g0085 a0001c0001t0024g0084 |
3 | HG01884.hp1 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.475-309G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217303 | |||||||
| chr2:70217304 | G | T | 60 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0002g0019 others(57): Show |
62 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.475-310C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217304 | |||||||
| chr2:70217369 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0022g0102 |
2 | HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.475-375C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217369 | |||||||
| chr2:70217404 | CTTT | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(87): Show |
103 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.475-413_475-411del others(3): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217404 | |||||||
| chr2:70217558 | T | C | 38 | a0001c0001t0001g0075 a0001c0001t0003g0004 a0001c0001t0003g0027 others(35): Show |
39 | HG00609.hp2 HG00735.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.475-564A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217558 | |||||||
| chr2:70217562 | T | TCATTTTT others(329): Show |
1 | a0001c0001t0002g0330 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.475-569_475-568ins others(336): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217562 | |||||||
| chr2:70217651 | C | A | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-657G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217651 | |||||||
| chr2:70217656 | C | G | 3 | a0001c0001t0001g0224 a0001c0001t0001g0246 a0001c0001t0001g0273 |
3 | HG01106.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.475-662G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217656 | |||||||
| chr2:70217716 | C | A | 3 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0248 |
3 | HG01070.hp1 HG01175.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.475-722G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217716 | |||||||
| chr2:70217866 | G | A | 58 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(55): Show |
60 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.475-872C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217866 | |||||||
| chr2:70217888 | T | C | 49 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(46): Show |
50 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.475-894A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217888 | |||||||
| chr2:70217908 | A | ATC | 3 | a0001c0001t0001g0221 a0001c0001t0001g0245 a0001c0001t0001g0264 |
3 | HG02602.hp1 HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.475-915_475-914ins others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217908 | |||||||
| chr2:70217920 | A | G | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-926T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70217920 | |||||||
| chr2:70218051 | C | A | 1 | a0001c0001t0002g0343 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.475-1057G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70218051 | |||||||
| chr2:70218104 | G | GT | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-1111dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70218104 | |||||||
| chr2:70218114 | T | G | 1 | a0001c0001t0001g0097 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.475-1120A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70218114 | |||||||
| chr2:70218119 | G | C | 50 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(47): Show |
51 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.475-1125C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70218119 | |||||||
| chr2:70218267 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
269 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.475-1273T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70218267 | |||||||
| chr2:70218403 | C | G | 45 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.475-1409G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70218403 | |||||||
| chr2:70218449 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0190 |
2 | NA18979.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.475-1455G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70218449 | |||||||
| chr2:70218530 | C | A | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-1536G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70218530 | |||||||
| chr2:70218804 | T | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.475-1810A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70218804 | |||||||
| chr2:70218832 | A | T | 1 | a0001c0001t0002g0322 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.475-1838T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70218832 | |||||||
| chr2:70218973 | G | C | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-1979C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70218973 | |||||||
| chr2:70219187 | A | T | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-2193T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219187 | |||||||
| chr2:70219193 | A | G | 45 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.475-2199T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219193 | |||||||
| chr2:70219199 | G | C | 1 | a0001c0001t0013g0099 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.475-2205C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219199 | |||||||
| chr2:70219239 | GGGA | G | 45 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.475-2248_475-2246d others(5): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219239 | |||||||
| chr2:70219392 | A | T | 1 | a0001c0001t0020g0219 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.475-2398T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219392 | |||||||
| chr2:70219625 | C | G | 1 | a0001c0001t0004g0353 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.475-2631G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219625 | |||||||
| chr2:70219653 | A | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(80): Show |
96 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.475-2659T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219653 | |||||||
| chr2:70219738 | C | CT | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
210 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(207): Show |
intron_variant | MODIFIER | c.475-2745dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219738 | |||||||
| chr2:70219738 | C | CTT | 5 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
6 | HG02074.hp2 HG02083.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.475-2746_475-2745d others(4): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219738 | |||||||
| chr2:70219738 | CT | C | 7 | a0001c0001t0001g0203 a0001c0001t0001g0218 a0001c0001t0001g0221 others(4): Show |
8 | HG00642.hp1 HG01943.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.475-2745delA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219738 | |||||||
| chr2:70219759 | A | G | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-2765T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219759 | |||||||
| chr2:70219867 | A | G | 2 | a0001c0001t0002g0322 a0001c0001t0002g0327 |
2 | NA18959.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.475-2873T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219867 | |||||||
| chr2:70219891 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.475-2897A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219891 | |||||||
| chr2:70219943 | C | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.475-2949G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219943 | |||||||
| chr2:70219968 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.475-2974A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219968 | |||||||
| chr2:70219984 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.475-2990C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70219984 | |||||||
| chr2:70220023 | CT | C | 37 | a0001c0001t0003g0004 a0001c0001t0003g0027 a0001c0001t0003g0038 others(34): Show |
38 | HG00609.hp2 HG00735.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.475-3030delA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220023 | |||||||
| chr2:70220072 | T | C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG02040.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.475-3078A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220072 | |||||||
| chr2:70220134 | G | C | 1 | a0001c0001t0022g0102 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.475-3140C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220134 | |||||||
| chr2:70220250 | A | T | 1 | a0003c0006t0001g0133 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.475-3256T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220250 | |||||||
| chr2:70220342 | A | G | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-3348T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220342 | |||||||
| chr2:70220453 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.475-3459A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220453 | |||||||
| chr2:70220467 | T | C | 1 | a0001c0001t0001g0010 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.475-3473A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220467 | |||||||
| chr2:70220540 | G | T | 1 | a0001c0001t0001g0253 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.475-3546C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220540 | |||||||
| chr2:70220604 | A | C | 2 | a0001c0001t0001g0171 a0001c0001t0001g0194 |
2 | HG03669.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.475-3610T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220604 | |||||||
| chr2:70220605 | T | C | 2 | a0001c0005t0012g0104 a0001c0005t0012g0117 |
2 | HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.475-3611A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220605 | |||||||
| chr2:70220648 | G | T | 15 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0082 others(12): Show |
16 | HG01192.hp1 HG01433.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.475-3654C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220648 | |||||||
| chr2:70220743 | G | A | 2 | a0001c0001t0001g0243 a0001c0001t0001g0276 |
2 | HG01192.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.475-3749C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220743 | |||||||
| chr2:70220894 | G | T | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+3660C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220894 | |||||||
| chr2:70220964 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.474+3590C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220964 | |||||||
| chr2:70220983 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.474+3571T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70220983 | |||||||
| chr2:70221006 | A | T | 4 | a0001c0001t0001g0289 a0001c0001t0004g0286 a0001c0001t0004g0287 others(1): Show |
4 | HG01433.hp1 HG02257.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+3548T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221006 | |||||||
| chr2:70221008 | T | A | 1 | a0001c0001t0001g0075 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.474+3546A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221008 | |||||||
| chr2:70221030 | G | A | 8 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(5): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.474+3524C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221030 | |||||||
| chr2:70221061 | C | T | 8 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(5): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.474+3493G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221061 | |||||||
| chr2:70221080 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0194 |
2 | HG03669.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.474+3474G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221080 | |||||||
| chr2:70221141 | T | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.474+3413A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221141 | |||||||
| chr2:70221151 | C | T | 1 | a0001c0001t0018g0303 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.474+3403G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221151 | |||||||
| chr2:70221198 | G | C | 4 | a0001c0001t0008g0363 a0001c0001t0008g0364 a0001c0001t0008g0366 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+3356C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221198 | |||||||
| chr2:70221202 | T | G | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+3352A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221202 | |||||||
| chr2:70221311 | T | TA | 14 | a0001c0001t0003g0045 a0001c0001t0003g0049 a0001c0001t0003g0050 others(11): Show |
14 | HG01257.hp2 HG01258.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.474+3242dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221311 | |||||||
| chr2:70221470 | C | CA | 46 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(43): Show |
47 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.474+3083dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221470 | |||||||
| chr2:70221474 | A | T | 4 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(1): Show |
5 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.474+3080T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221474 | |||||||
| chr2:70221488 | C | T | 1 | a0001c0001t0002g0335 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.474+3066G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221488 | |||||||
| chr2:70221601 | G | A | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+2953C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221601 | |||||||
| chr2:70221798 | A | AT | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(87): Show |
103 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.474+2755dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221798 | |||||||
| chr2:70221798 | A | T | 3 | a0001c0001t0001g0086 a0001c0001t0001g0289 a0001c0001t0004g0288 |
3 | HG02257.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.474+2756T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221798 | |||||||
| chr2:70221799 | T | A | 1 | a0001c0001t0001g0244 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.474+2755A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221799 | |||||||
| chr2:70221827 | G | A | 5 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.474+2727C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221827 | |||||||
| chr2:70221863 | C | T | 1 | a0001c0001t0004g0350 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.474+2691G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221863 | |||||||
| chr2:70221935 | G | A | 1 | a0001c0001t0019g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.474+2619C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221935 | |||||||
| chr2:70221981 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.474+2573A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221981 | |||||||
| chr2:70221992 | C | G | 1 | a0001c0001t0003g0063 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.474+2562G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70221992 | |||||||
| chr2:70222056 | A | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0105 others(5): Show |
9 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+2498T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222056 | |||||||
| chr2:70222062 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.474+2492C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222062 | |||||||
| chr2:70222136 | AAAAC | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0214 others(5): Show |
9 | HG00423.hp2 NA18941.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.474+2414_474+2417d others(6): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222136 | |||||||
| chr2:70222148 | C | A | 5 | a0001c0001t0001g0069 a0001c0001t0001g0187 a0001c0001t0003g0038 others(2): Show |
5 | HG02055.hp2 HG02257.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.474+2406G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222148 | |||||||
| chr2:70222148 | C | CA | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(84): Show |
100 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.474+2405dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222148 | |||||||
| chr2:70222152 | A | C | 7 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0291 others(4): Show |
7 | HG00544.hp1 HG01884.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.474+2402T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222152 | |||||||
| chr2:70222207 | A | C | 1 | a0001c0002t0007g0305 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.474+2347T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222207 | |||||||
| chr2:70222398 | C | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0198 |
3 | HG02630.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.474+2156G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222398 | |||||||
| chr2:70222470 | G | A | 1 | a0001c0001t0026g0360 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.474+2084C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222470 | |||||||
| chr2:70222557 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.474+1997C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222557 | |||||||
| chr2:70222602 | T | C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0082 |
2 | HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.474+1952A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222602 | |||||||
| chr2:70222644 | A | G | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
272 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.474+1910T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222644 | |||||||
| chr2:70222648 | G | A | 45 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.474+1906C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222648 | |||||||
| chr2:70222731 | T | C | 1 | a0001c0001t0001g0282 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.474+1823A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222731 | |||||||
| chr2:70222863 | G | A | 3 | a0001c0001t0001g0266 a0001c0001t0001g0281 a0001c0001t0001g0284 |
3 | NA18963.hp2 NA19055.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.474+1691C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222863 | |||||||
| chr2:70222873 | C | A | 1 | a0001c0001t0019g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.474+1681G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222873 | |||||||
| chr2:70222876 | T | G | 10 | a0001c0001t0001g0289 a0001c0001t0004g0020 a0001c0001t0004g0286 others(7): Show |
11 | HG01192.hp1 HG01433.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.474+1678A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222876 | |||||||
| chr2:70222878 | C | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0197 a0001c0001t0001g0356 |
3 | HG01257.hp1 HG02735.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.474+1676G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222878 | |||||||
| chr2:70222894 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.474+1660T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222894 | |||||||
| chr2:70222900 | C | T | 1 | a0001c0001t0004g0351 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.474+1654G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222900 | |||||||
| chr2:70222916 | A | G | 4 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0113 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.474+1638T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222916 | |||||||
| chr2:70222926 | ATAT | A | 9 | a0001c0001t0001g0289 a0001c0001t0004g0020 a0001c0001t0004g0286 others(6): Show |
10 | HG01192.hp1 HG01433.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.474+1625_474+1627d others(5): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222926 | |||||||
| chr2:70222929 | T | G | 1 | a0001c0001t0004g0353 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.474+1625A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70222929 | |||||||
| chr2:70223008 | A | G | 1 | a0001c0001t0006g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.474+1546T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70223008 | |||||||
| chr2:70223064 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.474+1490A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70223064 | |||||||
| chr2:70223154 | A | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0251 a0001c0001t0001g0285 |
3 | HG00280.hp1 HG00642.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.474+1400T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70223154 | |||||||
| chr2:70223253 | T | C | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+1301A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70223253 | |||||||
| chr2:70223297 | G | C | 60 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0002g0019 others(57): Show |
62 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.474+1257C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70223297 | |||||||
| chr2:70223315 | CTTAATTT | C | 45 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.474+1232_474+1238d others(9): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70223315 | |||||||
| chr2:70223577 | A | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.474+977T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70223577 | |||||||
| chr2:70223710 | G | A | 1 | a0001c0001t0018g0303 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.474+844C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70223710 | |||||||
| chr2:70224042 | C | T | 8 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(5): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.474+512G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70224042 | |||||||
| chr2:70224075 | G | A | 1 | a0001c0001t0003g0048 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.474+479C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70224075 | |||||||
| chr2:70224164 | C | T | 8 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(5): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.474+390G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70224164 | |||||||
| chr2:70224209 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.474+345G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70224209 | |||||||
| chr2:70224270 | G | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
175 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.474+284C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70224270 | |||||||
| chr2:70224349 | C | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.474+205G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70224349 | |||||||
| chr2:70224349 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.474+205G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70224349 | |||||||
| chr2:70224370 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG02976.hp2 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.474+184C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70224370 | |||||||
| chr2:70224471 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.474+83G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70224471 | |||||||
| chr2:70224472 | GA | G | 29 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0030 others(26): Show |
30 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.474+81delT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70224472 | |||||||
| chr2:70224473 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.474+81T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 7/12 | chr2 | 70224473 | |||||||
| chr2:70224652 | G | A | 17 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0090 others(14): Show |
17 | HG01243.hp1 HG01884.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.399-23C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70224652 | |||||||
| chr2:70225285 | A | C | 1 | a0001c0001t0001g0082 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.399-656T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70225285 | |||||||
| chr2:70225478 | A | C | 1 | a0001c0001t0001g0291 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.399-849T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70225478 | |||||||
| chr2:70226251 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0190 |
2 | NA18979.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.398+1484G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70226251 | |||||||
| chr2:70226252 | G | A | 5 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0296 others(2): Show |
5 | NA18962.hp1 NA18966.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.398+1483C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70226252 | |||||||
| chr2:70226290 | C | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0198 |
3 | HG02630.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.398+1445G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70226290 | |||||||
| chr2:70226348 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.398+1387G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70226348 | |||||||
| chr2:70226351 | G | A | 1 | a0001c0001t0013g0099 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.398+1384C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70226351 | |||||||
| chr2:70226631 | G | A | 8 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(5): Show |
8 | HG02622.hp1 HG02630.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.398+1104C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70226631 | |||||||
| chr2:70226685 | C | T | 1 | a0001c0001t0003g0054 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.398+1050G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70226685 | |||||||
| chr2:70226820 | T | C | 4 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0103 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.398+915A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70226820 | |||||||
| chr2:70226853 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0022g0102 |
2 | HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.398+882G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70226853 | |||||||
| chr2:70226894 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.398+841G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70226894 | |||||||
| chr2:70227073 | T | A | 8 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(5): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.398+662A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70227073 | |||||||
| chr2:70227113 | T | G | 13 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0030 others(10): Show |
14 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.398+622A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70227113 | |||||||
| chr2:70227151 | T | A | 2 | a0001c0001t0001g0289 a0001c0001t0004g0288 |
2 | HG02257.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.398+584A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70227151 | |||||||
| chr2:70227234 | T | C | 37 | a0001c0001t0003g0004 a0001c0001t0003g0027 a0001c0001t0003g0038 others(34): Show |
38 | HG00609.hp2 HG00735.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.398+501A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70227234 | |||||||
| chr2:70227662 | G | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
106 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.398+73C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 6/12 | chr2 | 70227662 | |||||||
| chr2:70228072 | C | T | 46 | a0001c0001t0001g0149 a0001c0001t0002g0019 a0001c0001t0002g0302 others(43): Show |
47 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.311-250G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 5/12 | chr2 | 70228072 | |||||||
| chr2:70228482 | A | AACAGTAA others(5): Show |
1 | a0001c0001t0002g0331 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.310+565_310+576dup others(12): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 5/12 | chr2 | 70228482 | |||||||
| chr2:70228681 | T | A | 1 | a0001c0008t0001g0235 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.310+378A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 5/12 | chr2 | 70228681 | |||||||
| chr2:70228775 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
269 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.310+284T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 5/12 | chr2 | 70228775 | |||||||
| chr2:70228809 | C | T | 1 | a0001c0001t0004g0351 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.310+250G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 5/12 | chr2 | 70228809 | |||||||
| chr2:70229206 | C | T | 30 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0030 others(27): Show |
31 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.277+58G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 4/12 | chr2 | 70229206 | |||||||
| chr2:70229237 | T | C | 8 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(5): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.277+27A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 4/12 | chr2 | 70229237 | |||||||
| chr2:70229352 | C | T | 8 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(5): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.223-34G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229352 | |||||||
| chr2:70229395 | G | C | 1 | a0001c0001t0014g0023 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.223-77C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229395 | |||||||
| chr2:70229400 | A | G | 1 | a0001c0001t0001g0294 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.223-82T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229400 | |||||||
| chr2:70229454 | C | T | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
277 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.223-136G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229454 | |||||||
| chr2:70229565 | T | C | 3 | a0001c0001t0001g0069 a0001c0001t0001g0086 a0001c0001t0006g0070 |
3 | HG02055.hp2 HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.223-247A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229565 | |||||||
| chr2:70229583 | C | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0200 others(4): Show |
9 | HG00558.hp2 HG02015.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.223-265G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229583 | |||||||
| chr2:70229647 | G | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0086 a0001c0001t0006g0070 |
3 | HG02055.hp2 HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.223-329C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229647 | |||||||
| chr2:70229802 | A | G | 1 | a0001c0001t0003g0062 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.223-484T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229802 | |||||||
| chr2:70229937 | C | CA | 18 | a0001c0001t0001g0069 a0001c0001t0001g0176 a0001c0001t0001g0186 others(15): Show |
19 | HG00741.hp2 HG01109.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.223-620dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229937 | |||||||
| chr2:70229945 | A | G | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-627T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229945 | |||||||
| chr2:70229966 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.223-648G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229966 | |||||||
| chr2:70229987 | G | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
269 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.223-669C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70229987 | |||||||
| chr2:70230018 | C | T | 2 | a0001c0001t0003g0048 a0001c0001t0003g0053 |
2 | HG02129.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.223-700G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230018 | |||||||
| chr2:70230059 | C | T | 1 | a0001c0002t0007g0301 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.222+697G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230059 | |||||||
| chr2:70230073 | T | C | 58 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(55): Show |
60 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.222+683A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230073 | |||||||
| chr2:70230083 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.222+673T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230083 | |||||||
| chr2:70230116 | G | A | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(2): Show |
5 | HG02735.hp1 HG02738.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+640C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230116 | |||||||
| chr2:70230170 | A | G | 60 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0002g0019 others(57): Show |
62 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.222+586T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230170 | |||||||
| chr2:70230181 | T | G | 2 | a0001c0001t0003g0048 a0001c0001t0003g0053 |
2 | HG02129.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.222+575A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230181 | |||||||
| chr2:70230198 | G | A | 15 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0082 others(12): Show |
16 | HG01192.hp1 HG01433.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.222+558C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230198 | |||||||
| chr2:70230203 | G | A | 1 | a0001c0001t0002g0331 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.222+553C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230203 | |||||||
| chr2:70230241 | C | CA | 31 | a0001c0001t0001g0033 a0001c0001t0001g0078 a0001c0001t0001g0080 others(28): Show |
32 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.222+514dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230241 | |||||||
| chr2:70230241 | CA | C | 6 | a0001c0001t0001g0030 a0001c0001t0001g0144 a0001c0001t0001g0163 others(3): Show |
6 | HG01167.hp2 HG02129.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.222+514delT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230241 | |||||||
| chr2:70230376 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.222+380G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230376 | |||||||
| chr2:70230477 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0251 a0001c0001t0001g0285 |
3 | HG00280.hp1 HG00642.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.222+279G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230477 | |||||||
| chr2:70230496 | C | T | 4 | a0001c0001t0004g0020 a0001c0001t0004g0350 a0001c0001t0004g0352 others(1): Show |
5 | HG01192.hp1 HG02922.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+260G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230496 | |||||||
| chr2:70230523 | G | A | 1 | a0001c0001t0002g0332 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.222+233C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230523 | |||||||
| chr2:70230608 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(198): Show |
218 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.222+148A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230608 | |||||||
| chr2:70230652 | C | CA | 94 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(91): Show |
96 | HG00544.hp2 HG00609.hp2 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.222+103dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230652 | |||||||
| chr2:70230652 | C | CAA | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
134 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.222+102_222+103dup others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230652 | |||||||
| chr2:70230652 | C | CAAA | 11 | a0001c0001t0001g0009 a0001c0001t0001g0129 a0001c0001t0001g0135 others(8): Show |
12 | HG00621.hp2 HG02155.hp1 NA18953.hp1 others(9): Show |
intron_variant | MODIFIER | c.222+101_222+103dup others(3): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230652 | |||||||
| chr2:70230693 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.222+63G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | 70230693 | |||||||
| chr2:70231135 | T | TA | 5 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0250 others(2): Show |
5 | HG01069.hp2 HG01169.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-282dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70231135 | |||||||
| chr2:70231226 | C | T | 45 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.124-372G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70231226 | |||||||
| chr2:70231234 | G | A | 8 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(5): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.124-380C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70231234 | |||||||
| chr2:70231324 | A | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0261 |
2 | HG02074.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.124-470T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70231324 | |||||||
| chr2:70231448 | T | TA | 47 | a0001c0001t0001g0153 a0001c0001t0002g0019 a0001c0001t0002g0302 others(44): Show |
48 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.124-595dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70231448 | |||||||
| chr2:70231632 | A | T | 4 | a0001c0001t0001g0289 a0001c0001t0004g0286 a0001c0001t0004g0287 others(1): Show |
4 | HG01433.hp1 HG02257.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-778T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70231632 | |||||||
| chr2:70231877 | A | T | 8 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(5): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.124-1023T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70231877 | |||||||
| chr2:70231881 | A | G | 1 | a0001c0001t0001g0010 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.124-1027T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70231881 | |||||||
| chr2:70232018 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0162 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.124-1164G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232018 | |||||||
| chr2:70232030 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.124-1176C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232030 | |||||||
| chr2:70232095 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
269 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.124-1241T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232095 | |||||||
| chr2:70232137 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.124-1283C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232137 | |||||||
| chr2:70232196 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.124-1342C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232196 | |||||||
| chr2:70232208 | C | CA | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(81): Show |
97 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.124-1355dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232208 | |||||||
| chr2:70232208 | CA | C | 7 | a0001c0001t0001g0284 a0001c0001t0002g0340 a0001c0001t0003g0062 others(4): Show |
7 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.124-1355delT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232208 | |||||||
| chr2:70232265 | G | A | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-1411C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232265 | |||||||
| chr2:70232335 | G | GT | 2 | a0001c0001t0001g0010 a0001c0001t0001g0189 |
3 | HG01070.hp2 HG01071.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.124-1482dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232335 | |||||||
| chr2:70232432 | C | A | 45 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.124-1578G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232432 | |||||||
| chr2:70232432 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.124-1578G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232432 | |||||||
| chr2:70232526 | G | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0229 |
5 | HG01256.hp2 HG01258.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-1672C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232526 | |||||||
| chr2:70232540 | C | CA | 15 | a0001c0001t0001g0016 a0001c0001t0001g0204 a0001c0001t0001g0218 others(12): Show |
16 | HG00558.hp2 HG02132.hp2 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.124-1687dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232540 | |||||||
| chr2:70232540 | C | CAAA | 9 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0212 others(6): Show |
9 | HG02083.hp2 NA18943.hp1 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.124-1689_124-1687d others(5): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232540 | |||||||
| chr2:70232540 | C | CAAAA | 6 | a0001c0001t0001g0014 a0001c0001t0001g0203 a0001c0001t0001g0233 others(3): Show |
7 | NA18747.hp1 NA18947.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-1690_124-1687d others(6): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232540 | |||||||
| chr2:70232540 | CA | C | 52 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(49): Show |
59 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.124-1687delT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232540 | |||||||
| chr2:70232540 | CAA | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0028 others(55): Show |
60 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.124-1688_124-1687d others(4): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232540 | |||||||
| chr2:70232540 | CAAA | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
106 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.124-1689_124-1687d others(5): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232540 | |||||||
| chr2:70232540 | CAAAA | C | 31 | a0001c0001t0001g0075 a0001c0001t0001g0113 a0001c0001t0001g0131 others(28): Show |
32 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.124-1690_124-1687d others(6): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232540 | |||||||
| chr2:70232540 | CAAAAAAA others(3): Show |
C | 7 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(4): Show |
8 | HG02109.hp1 HG02145.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.124-1696_124-1687d others(12): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232540 | |||||||
| chr2:70232540 | CAAAAAAA others(5): Show |
C | 5 | a0001c0001t0002g0309 a0001c0001t0002g0316 a0001c0001t0002g0317 others(2): Show |
5 | HG00741.hp2 HG02165.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-1698_124-1687d others(14): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232540 | |||||||
| chr2:70232540 | CAAAAAAA others(6): Show |
C | 38 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(35): Show |
39 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.124-1699_124-1687d others(15): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232540 | |||||||
| chr2:70232540 | CAAAAAAA others(7): Show |
C | 7 | a0001c0001t0002g0307 a0001c0001t0002g0328 a0001c0001t0002g0340 others(4): Show |
7 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.124-1700_124-1687d others(16): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232540 | |||||||
| chr2:70232616 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.124-1762G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232616 | |||||||
| chr2:70232654 | A | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0162 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.124-1800T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232654 | |||||||
| chr2:70232693 | A | C | 1 | a0001c0002t0007g0304 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.124-1839T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232693 | |||||||
| chr2:70232706 | T | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0155 a0001c0001t0001g0188 |
4 | NA18971.hp2 NA18981.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-1852A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232706 | |||||||
| chr2:70232721 | C | T | 1 | a0001c0001t0014g0023 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.124-1867G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232721 | |||||||
| chr2:70232813 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0082 |
2 | HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.124-1959C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232813 | |||||||
| chr2:70232847 | C | T | 2 | a0001c0001t0001g0197 a0001c0001t0001g0356 |
2 | HG02735.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.124-1993G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232847 | |||||||
| chr2:70232854 | C | T | 4 | a0001c0001t0008g0363 a0001c0001t0008g0364 a0001c0001t0008g0366 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-2000G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232854 | |||||||
| chr2:70232867 | C | CA | 7 | a0001c0001t0001g0130 a0001c0001t0001g0230 a0001c0001t0001g0233 others(4): Show |
7 | HG00741.hp1 HG03225.hp1 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.124-2014dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70232867 | |||||||
| chr2:70233144 | A | AT | 38 | a0001c0001t0001g0075 a0001c0001t0003g0004 a0001c0001t0003g0027 others(35): Show |
39 | HG00609.hp2 HG00735.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.124-2291dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233144 | |||||||
| chr2:70233174 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
168 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.124-2320A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233174 | |||||||
| chr2:70233179 | C | G | 45 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.124-2325G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233179 | |||||||
| chr2:70233264 | C | T | 58 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(55): Show |
60 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.124-2410G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233264 | |||||||
| chr2:70233279 | T | C | 8 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(5): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.124-2425A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233279 | |||||||
| chr2:70233434 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.124-2580G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233434 | |||||||
| chr2:70233456 | C | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.124-2602G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233456 | |||||||
| chr2:70233562 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.123+2517T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233562 | |||||||
| chr2:70233565 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.123+2514T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233565 | |||||||
| chr2:70233590 | A | C | 45 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.123+2489T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233590 | |||||||
| chr2:70233634 | C | T | 4 | a0001c0001t0001g0221 a0001c0001t0001g0245 a0001c0001t0001g0257 others(1): Show |
4 | HG02602.hp1 HG03239.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+2445G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233634 | |||||||
| chr2:70233764 | T | TA | 46 | a0001c0001t0001g0244 a0001c0001t0002g0019 a0001c0001t0002g0302 others(43): Show |
47 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.123+2314dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233764 | |||||||
| chr2:70233885 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0189 |
3 | HG01070.hp2 HG01071.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.123+2194T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233885 | |||||||
| chr2:70233896 | C | A | 1 | a0001c0001t0018g0303 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.123+2183G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233896 | |||||||
| chr2:70233911 | T | C | 4 | a0001c0001t0008g0363 a0001c0001t0008g0364 a0001c0001t0008g0366 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+2168A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70233911 | |||||||
| chr2:70234223 | T | G | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+1856A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234223 | |||||||
| chr2:70234319 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.123+1760A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234319 | |||||||
| chr2:70234354 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.123+1725A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234354 | |||||||
| chr2:70234446 | G | T | 45 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.123+1633C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234446 | |||||||
| chr2:70234491 | C | G | 1 | a0001c0001t0001g0069 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.123+1588G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234491 | |||||||
| chr2:70234513 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.123+1566T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234513 | |||||||
| chr2:70234562 | T | C | 37 | a0001c0001t0003g0004 a0001c0001t0003g0027 a0001c0001t0003g0038 others(34): Show |
38 | HG00609.hp2 HG00735.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.123+1517A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234562 | |||||||
| chr2:70234597 | T | C | 3 | a0001c0001t0001g0069 a0001c0001t0001g0086 a0001c0001t0006g0070 |
3 | HG02055.hp2 HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.123+1482A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234597 | |||||||
| chr2:70234607 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.123+1472C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234607 | |||||||
| chr2:70234626 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.123+1453T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234626 | |||||||
| chr2:70234642 | A | T | 1 | a0001c0001t0001g0220 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.123+1437T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234642 | |||||||
| chr2:70234643 | C | A | 45 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.123+1436G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234643 | |||||||
| chr2:70234723 | G | A | 1 | a0001c0001t0018g0303 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.123+1356C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234723 | |||||||
| chr2:70234781 | C | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(87): Show |
103 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.123+1298G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234781 | |||||||
| chr2:70234782 | G | A | 1 | a0001c0001t0002g0328 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.123+1297C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234782 | |||||||
| chr2:70234844 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0241 |
2 | NA18979.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.123+1235C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234844 | |||||||
| chr2:70234881 | T | C | 1 | a0002c0004t0001g0098 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.123+1198A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70234881 | |||||||
| chr2:70235031 | GACAAACA others(5): Show |
G | 1 | a0001c0001t0001g0103 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.123+1036_123+1047d others(14): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235031 | |||||||
| chr2:70235058 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.123+1021C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235058 | |||||||
| chr2:70235107 | A | T | 3 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 |
4 | HG02109.hp1 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+972T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235107 | |||||||
| chr2:70235111 | A | T | 60 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0002g0019 others(57): Show |
62 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.123+968T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235111 | |||||||
| chr2:70235151 | C | G | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+928G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235151 | |||||||
| chr2:70235206 | G | A | 4 | a0001c0001t0001g0120 a0001c0001t0001g0180 a0001c0001t0001g0181 others(1): Show |
4 | HG00544.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+873C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235206 | |||||||
| chr2:70235303 | T | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0103 |
2 | HG02572.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.123+776A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235303 | |||||||
| chr2:70235333 | T | C | 38 | a0001c0001t0001g0075 a0001c0001t0003g0004 a0001c0001t0003g0027 others(35): Show |
39 | HG00609.hp2 HG00735.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.123+746A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235333 | |||||||
| chr2:70235346 | C | T | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+733G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235346 | |||||||
| chr2:70235415 | C | G | 46 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(43): Show |
47 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.123+664G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235415 | |||||||
| chr2:70235485 | C | T | 8 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(5): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.123+594G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235485 | |||||||
| chr2:70235541 | A | AGT | 8 | a0001c0001t0001g0160 a0001c0001t0001g0204 a0001c0001t0001g0243 others(5): Show |
8 | HG02155.hp2 HG02293.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.123+536_123+537dup others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | |||||||
| chr2:70235541 | A | AGTGT | 40 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0037 others(37): Show |
42 | HG00558.hp1 HG01109.hp1 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.123+534_123+537dup others(4): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | |||||||
| chr2:70235541 | A | AGTGTGT | 65 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(62): Show |
66 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.123+532_123+537dup others(6): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | |||||||
| chr2:70235541 | A | AGTGTGTG others(1): Show |
74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(71): Show |
85 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.123+530_123+537dup others(8): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | |||||||
| chr2:70235541 | A | AGTGTGTG others(3): Show |
49 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0025 others(46): Show |
52 | HG00423.hp1 HG00621.hp1 HG01167.hp2 others(49): Show |
intron_variant | MODIFIER | c.123+528_123+537dup others(10): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | |||||||
| chr2:70235541 | A | AGTGTGTG others(5): Show |
13 | a0001c0001t0001g0120 a0001c0001t0001g0127 a0001c0001t0001g0139 others(10): Show |
14 | HG00544.hp2 HG01074.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.123+526_123+537dup others(12): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | |||||||
| chr2:70235541 | A | AGTGTGTG others(7): Show |
1 | a0001c0001t0008g0363 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.123+524_123+537dup others(14): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | |||||||
| chr2:70235541 | A | AGTGTGTG others(17): Show |
1 | a0001c0002t0007g0301 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.123+514_123+537dup others(24): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | |||||||
| chr2:70235541 | A | AGTGTGTG others(21): Show |
1 | a0001c0002t0007g0349 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.123+510_123+537dup others(28): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | |||||||
| chr2:70235541 | A | AGTGTGTG others(29): Show |
1 | a0001c0002t0007g0305 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123+537_123+538ins others(36): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | |||||||
| chr2:70235541 | A | AGTGTGTG others(31): Show |
1 | a0001c0002t0007g0304 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.123+537_123+538ins others(38): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | |||||||
| chr2:70235541 | AGT | A | 10 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0069 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.123+536_123+537del others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235541 | |||||||
| chr2:70235572 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.123+507T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235572 | |||||||
| chr2:70235575 | T | C | 45 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.123+504A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235575 | |||||||
| chr2:70235588 | T | C | 45 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.123+491A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235588 | |||||||
| chr2:70235603 | A | G | 4 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(1): Show |
5 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+476T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235603 | |||||||
| chr2:70235765 | T | C | 1 | a0001c0001t0004g0020 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.123+314A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235765 | |||||||
| chr2:70235796 | CAT | C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0208 |
3 | HG03017.hp1 HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.123+281_123+282del others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235796 | |||||||
| chr2:70235852 | A | G | 1 | a0001c0002t0007g0301 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.123+227T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235852 | |||||||
| chr2:70235917 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.123+162A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235917 | |||||||
| chr2:70235985 | A | G | 1 | a0002c0004t0001g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.123+94T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70235985 | |||||||
| chr2:70236036 | T | TA | 11 | a0001c0001t0001g0289 a0001c0001t0002g0317 a0001c0001t0004g0020 others(8): Show |
12 | HG01192.hp1 HG01433.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.123+42dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | 70236036 | |||||||
| chr2:70236202 | C | CT | 15 | a0001c0001t0001g0087 a0001c0001t0001g0095 a0001c0001t0001g0138 others(12): Show |
15 | HG01099.hp2 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.27-28dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70236202 | |||||||
| chr2:70236219 | A | G | 4 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(1): Show |
5 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.27-44T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70236219 | |||||||
| chr2:70236233 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.27-58A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70236233 | |||||||
| chr2:70236460 | A | T | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-285T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70236460 | |||||||
| chr2:70236507 | T | C | 2 | a0001c0001t0003g0038 a0001c0001t0003g0040 |
2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.27-332A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70236507 | |||||||
| chr2:70236669 | C | T | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-494G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70236669 | |||||||
| chr2:70236688 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0082 |
2 | HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.27-513C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70236688 | |||||||
| chr2:70236712 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.27-537G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70236712 | |||||||
| chr2:70236901 | A | C | 29 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0030 others(26): Show |
30 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.27-726T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70236901 | |||||||
| chr2:70237126 | G | A | 17 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0090 others(14): Show |
17 | HG01243.hp1 HG01884.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.27-951C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70237126 | |||||||
| chr2:70237379 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.27-1204G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70237379 | |||||||
| chr2:70237619 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.27-1444G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70237619 | |||||||
| chr2:70237721 | G | A | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-1546C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70237721 | |||||||
| chr2:70237870 | G | A | 1 | a0001c0001t0003g0043 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.27-1695C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70237870 | |||||||
| chr2:70237870 | G | GA | 6 | a0001c0001t0001g0289 a0001c0001t0001g0357 a0001c0001t0001g0358 others(3): Show |
6 | HG01433.hp1 HG02257.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.27-1696dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70237870 | |||||||
| chr2:70237940 | T | C | 1 | a0001c0001t0002g0337 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.27-1765A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70237940 | |||||||
| chr2:70238164 | T | TA | 37 | a0001c0001t0003g0004 a0001c0001t0003g0027 a0001c0001t0003g0038 others(34): Show |
38 | HG00609.hp2 HG00735.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.27-1990dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238164 | |||||||
| chr2:70238165 | A | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.27-1990T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238165 | |||||||
| chr2:70238245 | T | C | 47 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0002g0019 others(44): Show |
48 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.27-2070A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238245 | |||||||
| chr2:70238249 | C | T | 1 | a0001c0001t0018g0303 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.27-2074G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238249 | |||||||
| chr2:70238249 | CGTTCCCC others(32): Show |
C | 1 | a0001c0001t0002g0343 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.27-2113_27-2075del others(39): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238249 | |||||||
| chr2:70238260 | G | GT | 101 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(98): Show |
106 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.27-2086dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238260 | |||||||
| chr2:70238260 | G | GTT | 9 | a0001c0001t0001g0281 a0001c0001t0001g0290 a0001c0001t0001g0291 others(6): Show |
9 | HG00544.hp1 HG02071.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.27-2087_27-2086dup others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238260 | |||||||
| chr2:70238260 | G | GTTTT | 17 | a0001c0001t0002g0309 a0001c0001t0002g0311 a0001c0001t0002g0318 others(14): Show |
17 | HG00621.hp1 HG01943.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.27-2089_27-2086dup others(4): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238260 | |||||||
| chr2:70238260 | G | GTTTTT | 17 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0307 others(14): Show |
18 | HG00673.hp1 HG00741.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.27-2090_27-2086dup others(5): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238260 | |||||||
| chr2:70238260 | G | GTTTTTT | 6 | a0001c0001t0002g0306 a0001c0001t0002g0310 a0001c0001t0002g0314 others(3): Show |
6 | HG01934.hp2 HG02071.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-2091_27-2086dup others(6): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238260 | |||||||
| chr2:70238260 | G | GTTTTTTT others(18): Show |
1 | a0001c0001t0001g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-2110_27-2086dup others(25): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238260 | |||||||
| chr2:70238260 | G | GTTTTTTT others(45): Show |
1 | a0001c0001t0001g0116 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.27-2086_27-2085ins others(52): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238260 | |||||||
| chr2:70238260 | GT | G | 25 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0031 others(22): Show |
26 | HG01109.hp1 HG01167.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.27-2086delA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238260 | |||||||
| chr2:70238260 | GTTTTTTT others(5): Show |
G | 3 | a0001c0001t0001g0120 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG02976.hp2 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.27-2097_27-2086del others(12): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238260 | |||||||
| chr2:70238260 | GTTTTTTT others(11): Show |
G | 1 | a0001c0002t0007g0349 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.27-2103_27-2086del others(18): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238260 | |||||||
| chr2:70238263 | T | TG | 3 | a0001c0001t0005g0361 a0001c0001t0005g0362 a0001c0001t0005g0365 |
3 | HG02109.hp1 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.27-2089_27-2088ins others(1): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238263 | |||||||
| chr2:70238264 | T | G | 1 | a0001c0001t0005g0022 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.27-2089A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238264 | |||||||
| chr2:70238428 | G | A | 5 | a0001c0001t0001g0111 a0001c0001t0008g0363 a0001c0001t0008g0364 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.27-2253C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238428 | |||||||
| chr2:70238472 | C | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG02976.hp2 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.27-2297G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238472 | |||||||
| chr2:70238497 | A | T | 1 | a0001c0001t0002g0343 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.27-2322T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238497 | |||||||
| chr2:70238574 | A | C | 3 | a0001c0001t0001g0069 a0001c0001t0001g0086 a0001c0001t0006g0070 |
3 | HG02055.hp2 HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.27-2399T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238574 | |||||||
| chr2:70238625 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.27-2450G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238625 | |||||||
| chr2:70238698 | T | A | 60 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0002g0019 others(57): Show |
62 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.27-2523A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238698 | |||||||
| chr2:70238842 | G | T | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-2667C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238842 | |||||||
| chr2:70238918 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.27-2743G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238918 | |||||||
| chr2:70238921 | A | G | 6 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.27-2746T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238921 | |||||||
| chr2:70238939 | C | T | 8 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(5): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-2764G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70238939 | |||||||
| chr2:70239155 | T | C | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-2980A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239155 | |||||||
| chr2:70239156 | G | A | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-2981C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239156 | |||||||
| chr2:70239157 | A | G | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-2982T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239157 | |||||||
| chr2:70239178 | C | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(188): Show |
207 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.27-3003G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239178 | |||||||
| chr2:70239206 | C | A | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-3031G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239206 | |||||||
| chr2:70239251 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.27-3076G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239251 | |||||||
| chr2:70239360 | T | C | 58 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(55): Show |
60 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.27-3185A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239360 | |||||||
| chr2:70239388 | G | A | 8 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(5): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-3213C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239388 | |||||||
| chr2:70239417 | T | C | 1 | a0001c0001t0019g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.27-3242A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239417 | |||||||
| chr2:70239495 | C | A | 1 | a0001c0001t0002g0338 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.27-3320G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239495 | |||||||
| chr2:70239694 | G | A | 5 | a0001c0001t0001g0209 a0001c0001t0001g0218 a0001c0001t0001g0267 others(2): Show |
5 | NA18953.hp2 NA18967.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.27-3519C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239694 | |||||||
| chr2:70239863 | A | T | 1 | a0001c0001t0001g0166 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.27-3688T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239863 | |||||||
| chr2:70239904 | C | A | 1 | a0001c0001t0001g0258 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.27-3729G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70239904 | |||||||
| chr2:70240039 | T | G | 58 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(55): Show |
60 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.27-3864A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70240039 | |||||||
| chr2:70240136 | A | C | 4 | a0001c0001t0001g0289 a0001c0001t0004g0286 a0001c0001t0004g0287 others(1): Show |
4 | HG01433.hp1 HG02257.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-3961T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70240136 | |||||||
| chr2:70240271 | T | C | 1 | a0001c0001t0003g0041 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.27-4096A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70240271 | |||||||
| chr2:70240489 | C | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0232 a0001c0001t0001g0233 others(5): Show |
9 | HG02083.hp2 NA18747.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-4314G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70240489 | |||||||
| chr2:70240881 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.27-4706G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70240881 | |||||||
| chr2:70240886 | CA | C | 8 | a0001c0001t0001g0078 a0001c0001t0001g0107 a0001c0001t0001g0108 others(5): Show |
8 | HG01891.hp1 HG02486.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.27-4712delT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70240886 | |||||||
| chr2:70240920 | A | C | 1 | a0001c0001t0002g0313 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.27-4745T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70240920 | |||||||
| chr2:70241265 | C | A | 1 | a0001c0001t0006g0125 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.27-5090G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241265 | |||||||
| chr2:70241281 | A | G | 8 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(5): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-5106T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241281 | |||||||
| chr2:70241305 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.27-5130C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241305 | |||||||
| chr2:70241390 | C | T | 8 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(5): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-5215G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241390 | |||||||
| chr2:70241393 | G | C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG02040.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.27-5218C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241393 | |||||||
| chr2:70241435 | T | A | 1 | a0001c0001t0001g0031 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.27-5260A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241435 | |||||||
| chr2:70241453 | A | AAAAAAGT others(52): Show |
1 | a0001c0001t0002g0343 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.27-5337_27-5279dup others(59): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241453 | |||||||
| chr2:70241558 | C | A | 1 | a0001c0001t0001g0165 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.27-5383G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241558 | |||||||
| chr2:70241561 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0119 |
2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.27-5386C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241561 | |||||||
| chr2:70241566 | G | A | 8 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(5): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-5391C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241566 | |||||||
| chr2:70241590 | G | GT | 10 | a0001c0001t0001g0289 a0001c0001t0004g0020 a0001c0001t0004g0286 others(7): Show |
11 | HG01192.hp1 HG01433.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.27-5416dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241590 | |||||||
| chr2:70241658 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.27-5483C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241658 | |||||||
| chr2:70241697 | T | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.27-5522A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241697 | |||||||
| chr2:70241835 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.27-5660A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241835 | |||||||
| chr2:70241850 | G | C | 37 | a0001c0001t0003g0004 a0001c0001t0003g0027 a0001c0001t0003g0038 others(34): Show |
38 | HG00609.hp2 HG00735.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.27-5675C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241850 | |||||||
| chr2:70241897 | C | T | 23 | a0001c0001t0002g0019 a0001c0001t0002g0306 a0001c0001t0002g0307 others(20): Show |
24 | HG00544.hp2 HG00621.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.27-5722G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70241897 | |||||||
| chr2:70242025 | A | G | 6 | a0001c0001t0004g0020 a0001c0001t0004g0350 a0001c0001t0004g0351 others(3): Show |
7 | HG01192.hp1 HG01884.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.27-5850T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242025 | |||||||
| chr2:70242054 | A | G | 1 | a0001c0001t0002g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.27-5879T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242054 | |||||||
| chr2:70242087 | C | T | 3 | a0001c0001t0001g0069 a0001c0001t0001g0086 a0001c0001t0006g0070 |
3 | HG02055.hp2 HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.27-5912G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242087 | |||||||
| chr2:70242256 | G | A | 8 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(5): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-6081C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242256 | |||||||
| chr2:70242310 | T | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0231 |
2 | HG00099.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.26+6095A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242310 | |||||||
| chr2:70242423 | C | T | 45 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.26+5982G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242423 | |||||||
| chr2:70242485 | A | G | 1 | a0001c0001t0002g0323 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.26+5920T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242485 | |||||||
| chr2:70242494 | C | CA | 154 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0014 others(151): Show |
160 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.26+5910dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242494 | |||||||
| chr2:70242494 | C | CAA | 35 | a0001c0001t0001g0018 a0001c0001t0001g0034 a0001c0001t0001g0035 others(32): Show |
37 | HG00544.hp2 HG00741.hp2 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.26+5909_26+5910dup others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242494 | |||||||
| chr2:70242494 | C | CAAA | 24 | a0001c0001t0002g0340 a0001c0001t0002g0341 a0001c0001t0003g0004 others(21): Show |
27 | HG00621.hp1 HG00642.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.26+5908_26+5910dup others(3): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242494 | |||||||
| chr2:70242494 | C | CAAAA | 18 | a0001c0001t0001g0086 a0001c0001t0001g0289 a0001c0001t0003g0045 others(15): Show |
18 | HG00609.hp2 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.26+5907_26+5910dup others(4): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242494 | |||||||
| chr2:70242494 | C | CAAAAA | 8 | a0001c0001t0001g0100 a0001c0001t0003g0049 a0001c0001t0003g0051 others(5): Show |
8 | HG01934.hp1 HG01993.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.26+5906_26+5910dup others(5): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242494 | |||||||
| chr2:70242494 | C | CAAAAAAA others(3): Show |
8 | a0001c0001t0001g0078 a0001c0001t0001g0107 a0001c0001t0001g0108 others(5): Show |
8 | HG01891.hp1 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.26+5901_26+5910dup others(10): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242494 | |||||||
| chr2:70242494 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0113 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.26+5900_26+5910dup others(11): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242494 | |||||||
| chr2:70242562 | G | A | 4 | a0001c0001t0001g0214 a0001c0001t0001g0266 a0001c0001t0001g0281 others(1): Show |
4 | NA18963.hp2 NA19055.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.26+5843C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242562 | |||||||
| chr2:70242659 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.26+5746G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242659 | |||||||
| chr2:70242681 | C | T | 1 | a0001c0001t0018g0303 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.26+5724G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242681 | |||||||
| chr2:70242818 | T | C | 3 | a0001c0001t0001g0069 a0001c0001t0001g0086 a0001c0001t0006g0070 |
3 | HG02055.hp2 HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.26+5587A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242818 | |||||||
| chr2:70242968 | T | C | 29 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0030 others(26): Show |
30 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.26+5437A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70242968 | |||||||
| chr2:70243187 | AGG | A | 2 | a0001c0001t0004g0020 a0001c0001t0004g0354 |
3 | HG02922.hp1 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.26+5216_26+5217del others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243187 | |||||||
| chr2:70243194 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.26+5211C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243194 | |||||||
| chr2:70243221 | T | G | 1 | a0001c0001t0001g0267 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.26+5184A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243221 | |||||||
| chr2:70243226 | G | A | 58 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(55): Show |
60 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.26+5179C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243226 | |||||||
| chr2:70243305 | T | C | 50 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(47): Show |
51 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.26+5100A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243305 | |||||||
| chr2:70243331 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.26+5074C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243331 | |||||||
| chr2:70243542 | A | C | 4 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(1): Show |
5 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.26+4863T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243542 | |||||||
| chr2:70243671 | T | C | 1 | a0001c0001t0001g0268 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.26+4734A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243671 | |||||||
| chr2:70243748 | T | C | 1 | a0001c0002t0007g0304 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.26+4657A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243748 | |||||||
| chr2:70243877 | T | G | 1 | a0001c0001t0003g0071 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.26+4528A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243877 | |||||||
| chr2:70243891 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.26+4514G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243891 | |||||||
| chr2:70243897 | T | C | 5 | a0001c0001t0001g0036 a0001c0001t0001g0114 a0001c0001t0001g0115 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.26+4508A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70243897 | |||||||
| chr2:70244122 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.26+4283T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244122 | |||||||
| chr2:70244363 | C | T | 8 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(5): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.26+4042G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244363 | |||||||
| chr2:70244503 | T | C | 1 | a0001c0002t0007g0349 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.26+3902A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244503 | |||||||
| chr2:70244569 | T | C | 1 | a0001c0001t0018g0303 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.26+3836A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244569 | |||||||
| chr2:70244608 | G | A | 1 | a0001c0001t0018g0303 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.26+3797C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244608 | |||||||
| chr2:70244611 | G | A | 1 | a0001c0001t0003g0072 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.26+3794C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244611 | |||||||
| chr2:70244625 | GGAGATC | G | 3 | a0001c0001t0001g0120 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG02976.hp2 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.26+3774_26+3779del others(6): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244625 | |||||||
| chr2:70244701 | G | C | 3 | a0001c0001t0001g0120 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG02976.hp2 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.26+3704C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244701 | |||||||
| chr2:70244704 | G | A | 8 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(5): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.26+3701C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244704 | |||||||
| chr2:70244767 | A | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
277 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.26+3638T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244767 | |||||||
| chr2:70244782 | C | G | 45 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.26+3623G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244782 | |||||||
| chr2:70244829 | T | C | 60 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0002g0019 others(57): Show |
62 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.26+3576A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244829 | |||||||
| chr2:70244834 | C | CA | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(112): Show |
128 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.26+3570dupT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244834 | |||||||
| chr2:70244834 | C | CAA | 24 | a0001c0001t0001g0097 a0001c0001t0001g0182 a0001c0001t0001g0183 others(21): Show |
25 | HG00558.hp1 HG01109.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.26+3569_26+3570dup others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244834 | |||||||
| chr2:70244834 | CA | C | 36 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0030 others(33): Show |
37 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.26+3570delT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244834 | |||||||
| chr2:70244834 | CAA | C | 39 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(36): Show |
40 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.26+3569_26+3570del others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244834 | |||||||
| chr2:70244865 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.26+3540G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70244865 | |||||||
| chr2:70245031 | G | C | 1 | a0001c0001t0002g0345 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.26+3374C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245031 | |||||||
| chr2:70245246 | C | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0028 |
3 | HG00735.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.26+3159G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245246 | |||||||
| chr2:70245247 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.26+3158T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245247 | |||||||
| chr2:70245350 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(86): Show |
102 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.26+3055C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245350 | |||||||
| chr2:70245353 | C | T | 4 | a0001c0002t0007g0301 a0001c0002t0007g0304 a0001c0002t0007g0305 others(1): Show |
4 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+3052G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245353 | |||||||
| chr2:70245391 | C | G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0030 others(27): Show |
31 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.26+3014G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245391 | |||||||
| chr2:70245453 | T | A | 1 | a0001c0001t0004g0020 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.26+2952A>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245453 | |||||||
| chr2:70245803 | A | G | 1 | a0001c0001t0025g0321 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.26+2602T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245803 | |||||||
| chr2:70245816 | C | T | 1 | a0001c0001t0002g0320 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.26+2589G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245816 | |||||||
| chr2:70245860 | A | G | 1 | a0001c0001t0020g0219 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.26+2545T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245860 | |||||||
| chr2:70245898 | C | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0028 |
3 | HG00735.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.26+2507G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245898 | |||||||
| chr2:70245914 | A | AT | 27 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0075 others(24): Show |
29 | HG00544.hp1 HG01358.hp2 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.26+2490dupA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245914 | |||||||
| chr2:70245914 | A | ATT | 14 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(11): Show |
15 | HG01192.hp1 HG01433.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.26+2489_26+2490dup others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245914 | |||||||
| chr2:70245914 | A | ATTT | 28 | a0001c0001t0001g0069 a0001c0001t0003g0004 a0001c0001t0003g0027 others(25): Show |
29 | HG00735.hp2 HG01175.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.26+2488_26+2490dup others(3): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245914 | |||||||
| chr2:70245914 | A | ATTTT | 12 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(9): Show |
12 | HG00609.hp2 HG01099.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.26+2487_26+2490dup others(4): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245914 | |||||||
| chr2:70245914 | AT | A | 47 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0093 others(44): Show |
48 | HG00621.hp1 HG00673.hp1 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.26+2490delA | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245914 | |||||||
| chr2:70245914 | ATT | A | 10 | a0001c0001t0005g0022 a0001c0001t0005g0365 a0001c0001t0008g0366 others(7): Show |
11 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.26+2489_26+2490del others(2): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245914 | |||||||
| chr2:70245914 | ATTTTTTT others(2): Show |
A | 28 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0030 others(25): Show |
29 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.26+2482_26+2490del others(9): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245914 | |||||||
| chr2:70245914 | ATTTTTTT others(7): Show |
A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(86): Show |
102 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.26+2477_26+2490del others(14): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245914 | |||||||
| chr2:70245954 | C | T | 1 | a0001c0002t0007g0304 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.26+2451G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245954 | |||||||
| chr2:70245985 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.26+2420C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70245985 | |||||||
| chr2:70246048 | C | T | 5 | a0001c0001t0001g0037 a0001c0002t0007g0301 a0001c0002t0007g0304 others(2): Show |
5 | HG02723.hp2 HG03453.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.26+2357G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246048 | |||||||
| chr2:70246058 | G | C | 2 | a0001c0001t0011g0346 a0001c0001t0011g0347 |
2 | NA18948.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.26+2347C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246058 | |||||||
| chr2:70246178 | C | G | 8 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(5): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.26+2227G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246178 | |||||||
| chr2:70246284 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.26+2121A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246284 | |||||||
| chr2:70246321 | C | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
269 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.26+2084G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246321 | |||||||
| chr2:70246435 | GTCAAGGT others(10): Show |
G | 1 | a0001c0001t0002g0348 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1953_26+1969del others(17): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246435 | |||||||
| chr2:70246454 | G | C | 1 | a0001c0001t0002g0348 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1951C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246454 | |||||||
| chr2:70246488 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.26+1917G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246488 | |||||||
| chr2:70246511 | A | T | 1 | a0001c0001t0002g0348 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1894T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246511 | |||||||
| chr2:70246522 | G | T | 1 | a0001c0001t0002g0348 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1883C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246522 | |||||||
| chr2:70246527 | G | T | 1 | a0001c0001t0002g0348 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1878C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246527 | |||||||
| chr2:70246534 | G | T | 1 | a0001c0001t0002g0348 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1871C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246534 | |||||||
| chr2:70246545 | A | AAAGCTTA others(3): Show |
1 | a0001c0001t0002g0348 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1859_26+1860ins others(10): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246545 | |||||||
| chr2:70246546 | T | G | 1 | a0001c0001t0002g0348 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1859A>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246546 | |||||||
| chr2:70246552 | A | T | 1 | a0001c0001t0002g0348 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1853T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246552 | |||||||
| chr2:70246554 | G | A | 1 | a0001c0001t0002g0348 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1851C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246554 | |||||||
| chr2:70246565 | A | T | 1 | a0001c0001t0002g0348 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1840T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246565 | |||||||
| chr2:70246581 | G | A | 1 | a0001c0001t0002g0348 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1824C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246581 | |||||||
| chr2:70246582 | T | C | 1 | a0001c0001t0002g0348 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1823A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246582 | |||||||
| chr2:70246584 | A | T | 1 | a0001c0001t0002g0348 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1821T>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246584 | |||||||
| chr2:70246592 | A | G | 1 | a0001c0001t0002g0348 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1813T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246592 | |||||||
| chr2:70246594 | G | A | 1 | a0001c0001t0002g0348 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1811C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246594 | |||||||
| chr2:70246599 | G | T | 1 | a0001c0001t0002g0348 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1806C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246599 | |||||||
| chr2:70246611 | C | A | 1 | a0001c0001t0002g0348 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.26+1794G>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246611 | |||||||
| chr2:70246641 | T | C | 45 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.26+1764A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246641 | |||||||
| chr2:70246805 | A | G | 60 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0002g0019 others(57): Show |
62 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.26+1600T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246805 | |||||||
| chr2:70246834 | C | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(2): Show |
5 | HG02735.hp1 HG02738.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.26+1571G>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246834 | |||||||
| chr2:70246926 | G | A | 4 | a0001c0001t0001g0289 a0001c0001t0004g0286 a0001c0001t0004g0287 others(1): Show |
4 | HG01433.hp1 HG02257.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+1479C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246926 | |||||||
| chr2:70246950 | C | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0028 |
3 | HG00735.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.26+1455G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70246950 | |||||||
| chr2:70247127 | T | C | 46 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(43): Show |
47 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.26+1278A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247127 | |||||||
| chr2:70247245 | C | G | 46 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(43): Show |
47 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.26+1160G>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247245 | |||||||
| chr2:70247295 | G | A | 11 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 others(8): Show |
11 | HG00544.hp1 HG02040.hp2 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.26+1110C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247295 | |||||||
| chr2:70247365 | T | C | 45 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.26+1040A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247365 | |||||||
| chr2:70247397 | G | T | 1 | a0001c0001t0002g0302 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.26+1008C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247397 | |||||||
| chr2:70247528 | A | C | 1 | a0001c0002t0007g0301 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.26+877T>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247528 | |||||||
| chr2:70247611 | G | T | 1 | a0001c0001t0003g0027 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.26+794C>A | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247611 | |||||||
| chr2:70247650 | AAT | A | 8 | a0001c0001t0005g0022 a0001c0001t0005g0361 a0001c0001t0005g0362 others(5): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.26+753_26+754delAT | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247650 | |||||||
| chr2:70247697 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.26+708T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247697 | |||||||
| chr2:70247799 | G | C | 1 | a0001c0002t0007g0349 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.26+606C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247799 | |||||||
| chr2:70247850 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.26+555T>C | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247850 | |||||||
| chr2:70247877 | T | C | 50 | a0001c0001t0002g0019 a0001c0001t0002g0302 a0001c0001t0002g0306 others(47): Show |
51 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.26+528A>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247877 | |||||||
| chr2:70247953 | G | A | 6 | a0001c0001t0004g0020 a0001c0001t0004g0350 a0001c0001t0004g0351 others(3): Show |
7 | HG01192.hp1 HG01884.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.26+452C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70247953 | |||||||
| chr2:70248018 | TAAG | T | 9 | a0001c0001t0001g0024 a0001c0001t0005g0022 a0001c0001t0005g0361 others(6): Show |
10 | HG00642.hp2 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.26+384_26+386delCT others(1): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70248018 | |||||||
| chr2:70248021 | G | C | 17 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0090 others(14): Show |
17 | HG01243.hp1 HG01884.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.26+384C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70248021 | |||||||
| chr2:70248137 | G | C | 1 | a0001c0001t0001g0355 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.26+268C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70248137 | |||||||
| chr2:70248248 | G | C | 1 | a0001c0001t0001g0356 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.26+157C>G | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70248248 | |||||||
| chr2:70248283 | G | A | 2 | a0001c0001t0001g0357 a0001c0001t0001g0358 |
2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.26+122C>T | TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | 70248283 |