Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7089 |
| ensemblid | ENSG00000065717.16 |
| hgncid | 11838 |
| symbol | TLE2 |
| name | TLE family member 2, transcriptional corepressor |
| refseq_nuc | NM_003260.5 |
| refseq_prot | NP_003251.2 |
| ensembl_nuc | ENST00000262953.11 |
| ensembl_prot | ENSP00000262953.5 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 2997644 |
| end | 3029280 |
| strand | - |
| ver | v1.2 |
| region | chr19:2997644-3029280 |
| region5000 | chr19:2992644-3034280 |
| regionname0 | TLE2_chr19_2997644_3029280 |
| regionname5000 | TLE2_chr19_2992644_3034280 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 743 | 387 | 89 | 79 | 159 | 17 | 41 | 114 | TLE2_chr19_2992644_3034280 | TLE2 | MYPQG others(738): Show |
chr19 | 2992644 | 3034280 |
| a0002 | 0/0 | 743 | 9 | 0 | 2 | 7 | 0 | 0 | 5 | TLE2_chr19_2992644_3034280 | TLE2 | MYPQG others(738): Show |
chr19 | 2992644 | 3034280 |
| a0003 | 0/0 | 743 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | MYPQG others(738): Show |
chr19 | 2992644 | 3034280 |
| a0004 | 0/0 | 743 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | MYPQG others(738): Show |
chr19 | 2992644 | 3034280 |
| a0005 | 0/0 | 743 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | MYPQG others(738): Show |
chr19 | 2992644 | 3034280 |
| a0006 | 0/0 | 743 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | MYPQG others(738): Show |
chr19 | 2992644 | 3034280 |
| a0007 | 0/0 | 743 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | MYPQG others(738): Show |
chr19 | 2992644 | 3034280 |
| a0008 | 0/0 | 743 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | MYPQG others(738): Show |
chr19 | 2992644 | 3034280 |
| a0009 | 0/0 | 743 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | MYPQG others(738): Show |
chr19 | 2992644 | 3034280 |
| a0010 | 0/0 | 743 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | MYPQG others(738): Show |
chr19 | 2992644 | 3034280 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2229 | 266 | 60 | 52 | 107 | 16 | 30 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0001c0002 | 0/1 | 2229 | 90 | 9 | 23 | 50 | 0 | 7 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0001c0003 | 0/0 | 2229 | 9 | 4 | 3 | 0 | 1 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0001c0005 | 0/0 | 2229 | 5 | 5 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0001c0006 | 0/0 | 2229 | 3 | 3 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0001c0007 | 0/0 | 2229 | 2 | 0 | 1 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0001c0008 | 0/0 | 2229 | 2 | 2 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0001c0009 | 0/0 | 2229 | 2 | 0 | 0 | 0 | 0 | 2 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0001c0010 | 0/0 | 2229 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0001c0013 | 0/0 | 2229 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0001c0015 | 0/0 | 2229 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0001c0016 | 0/0 | 2229 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0001c0017 | 0/0 | 2229 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0001c0018 | 0/0 | 2229 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0001c0020 | 0/0 | 2229 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0001c0024 | 0/0 | 2229 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0002c0004 | 0/0 | 2229 | 8 | 0 | 1 | 7 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0002c0011 | 0/0 | 2229 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0003c0014 | 0/0 | 2229 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0004c0021 | 0/0 | 2229 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0005c0022 | 0/0 | 2229 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0006c0023 | 0/0 | 2229 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0007c0025 | 0/0 | 2229 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0008c0012 | 0/0 | 2229 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0009c0019 | 0/0 | 2229 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 | ||
| a0010c0026 | 0/0 | 2229 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | ATGTA others(2224): Show |
chr19 | 2992644 | 3034280 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2812 | 229 | 33 | 47 | 104 | 16 | 28 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0001t0002 | 0/0 | 2812 | 25 | 19 | 5 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0001t0003 | 0/0 | 2812 | 2 | 0 | 0 | 1 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0001t0004 | 0/0 | 2812 | 5 | 5 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0001t0005 | 0/0 | 2812 | 2 | 2 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0001t0008 | 0/0 | 2812 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0001t0010 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0001t0013 | 0/0 | 2812 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0002t0001 | 0/1 | 2812 | 84 | 8 | 18 | 50 | 0 | 7 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0002t0003 | 0/0 | 2812 | 5 | 0 | 5 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0002t0007 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0003t0001 | 0/0 | 2812 | 6 | 1 | 3 | 0 | 1 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0003t0002 | 0/0 | 2812 | 3 | 3 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0005t0001 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0005t0002 | 0/0 | 2812 | 3 | 3 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0005t0011 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0006t0001 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0006t0002 | 0/0 | 2812 | 2 | 2 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0007t0001 | 0/0 | 2812 | 2 | 0 | 1 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0008t0001 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0008t0002 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0009t0001 | 0/0 | 2812 | 2 | 0 | 0 | 0 | 0 | 2 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0010t0001 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0013t0001 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0015t0009 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0016t0001 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0017t0001 | 0/0 | 2812 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0018t0001 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0020t0001 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0001c0024t0001 | 0/0 | 2812 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0002c0004t0001 | 0/0 | 2812 | 8 | 0 | 1 | 7 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0002c0011t0001 | 0/0 | 2812 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0003c0014t0001 | 0/0 | 2812 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0004c0021t0001 | 0/0 | 2812 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0005c0022t0001 | 0/0 | 2812 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0006c0023t0001 | 0/0 | 2812 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0007c0025t0002 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0008c0012t0012 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0009c0019t0001 | 0/0 | 2812 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| a0010c0026t0006 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | GCCGA others(2807): Show |
chr19 | 2992644 | 3034280 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0004 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0155 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0002g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0002g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0002g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0002g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0004g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0008g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0010g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0001t0013g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0002t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0003t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0003t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0003t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0003t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0003t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0003t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0003t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0005t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0005t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0005t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0005t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0005t0011g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0006t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0006t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0006t0002g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0007t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0007t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0008t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0008t0002g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0009t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0009t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0010t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0013t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0015t0009g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0016t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0017t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0018t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0020t0001g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0001c0024t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0002c0004t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0002c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0002c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0002c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0002c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0002c0004t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0002c0004t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0002c0011t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0003c0014t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0004c0021t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0005c0022t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0006c0023t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0007c0025t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0008c0012t0012g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0009c0019t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| a0010c0026t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0014 | t0001 | g0042 | EUR | GBR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0154 | EUR | GBR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | GBR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | GBR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0334 | EUR | FIN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | FIN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | FIN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00438 | hp2 | a0002 | c0004 | t0001 | g0157 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00597 | hp1 | a0001 | c0007 | t0001 | g0280 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0366 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0359 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00733 | hp2 | a0004 | c0021 | t0001 | g0283 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00738 | hp1 | a0001 | c0002 | t0003 | g0030 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0369 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01069 | hp1 | a0001 | c0002 | t0003 | g0024 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0341 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0342 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0076 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0161 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0295 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0306 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0343 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0358 | AMR | PUR | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0340 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0166 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0167 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0365 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | IBS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | IBS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0237 | EUR | IBS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0238 | EUR | IBS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | IBS | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0367 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0363 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01928 | hp1 | a0001 | c0002 | t0003 | g0023 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0314 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0338 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01943 | hp1 | a0001 | c0002 | t0003 | g0025 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0261 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0310 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0125 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01981 | hp1 | a0001 | c0007 | t0001 | g0312 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0309 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0130 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0355 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0332 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02015 | hp2 | a0005 | c0022 | t0001 | g0068 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0318 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02129 | hp1 | a0002 | c0004 | t0001 | g0282 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02145 | hp2 | a0001 | c0020 | t0001 | g0373 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02148 | hp1 | a0002 | c0011 | t0001 | g0072 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0311 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CDX | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | CDX | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02258 | hp1 | a0001 | c0003 | t0002 | g0248 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0376 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02273 | hp2 | a0001 | c0002 | t0003 | g0026 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0285 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0375 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0364 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02615 | hp1 | a0001 | c0005 | t0001 | g0119 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0374 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02622 | hp1 | a0001 | c0005 | t0002 | g0234 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0372 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02647 | hp1 | a0001 | c0006 | t0001 | g0370 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02683 | hp1 | a0001 | c0009 | t0001 | g0060 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0061 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0357 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0126 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0345 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02717 | hp2 | a0001 | c0002 | t0007 | g0031 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0328 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0352 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02738 | hp2 | a0006 | c0023 | t0001 | g0230 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02886 | hp1 | a0001 | c0006 | t0002 | g0361 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02922 | hp1 | a0001 | c0003 | t0002 | g0249 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0082 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02965 | hp2 | a0001 | c0005 | t0002 | g0344 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02970 | hp2 | a0001 | c0005 | t0002 | g0235 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0329 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03041 | hp2 | a0001 | c0006 | t0002 | g0232 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03130 | hp2 | a0007 | c0025 | t0002 | g0294 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03195 | hp2 | a0001 | c0010 | t0001 | g0224 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03209 | hp1 | a0001 | c0016 | t0001 | g0233 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03225 | hp2 | a0001 | c0003 | t0002 | g0247 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0351 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0260 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03453 | hp2 | a0001 | c0001 | t0010 | g0377 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03486 | hp1 | a0008 | c0012 | t0012 | g0379 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03486 | hp2 | a0001 | c0013 | t0001 | g0349 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0022 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0079 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0348 | AFR | ESN | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03540 | hp2 | a0001 | c0005 | t0011 | g0378 | AFR | GWD | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0041 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | STU | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0214 | SAS | STU | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0078 | SAS | PJL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0353 | SAS | BEB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03927 | hp1 | a0001 | c0009 | t0001 | g0039 | SAS | BEB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0245 | SAS | BEB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | STU | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | STU | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0275 | SAS | STU | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | STU | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | STU | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | STU | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0300 | AFR | YRI | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | CHB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0324 | EAS | CHB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0356 | EAS | CHB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0301 | AFR | YRI | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0292 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0323 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18960 | hp1 | a0002 | c0004 | t0001 | g0011 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0320 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18967 | hp1 | a0002 | c0004 | t0001 | g0086 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18970 | hp1 | a0001 | c0001 | t0013 | g0380 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18973 | hp1 | a0002 | c0004 | t0001 | g0089 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18986 | hp1 | a0001 | c0001 | t0008 | g0321 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0322 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19010 | hp1 | a0009 | c0019 | t0001 | g0181 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19011 | hp2 | a0002 | c0004 | t0001 | g0173 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19030 | hp1 | a0001 | c0018 | t0001 | g0368 | AFR | LWK | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19030 | hp2 | a0001 | c0015 | t0009 | g0180 | AFR | LWK | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0029 | AFR | LWK | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19043 | hp2 | a0001 | c0008 | t0001 | g0362 | AFR | LWK | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19080 | hp2 | a0002 | c0004 | t0001 | g0011 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19083 | hp1 | a0001 | c0024 | t0001 | g0071 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0331 | AFR | YRI | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | YRI | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA20129 | hp1 | a0010 | c0026 | t0006 | g0020 | AFR | ASW | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | ASW | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0337 | EUR | TSI | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0304 | EUR | TSI | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0336 | EUR | TSI | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | TSI | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | GIH | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA20905 | hp2 | a0001 | c0017 | t0001 | g0303 | SAS | GIH | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01123 | hp1 | a0002 | c0004 | t0001 | g0360 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02109 | hp2 | a0001 | c0008 | t0002 | g0371 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0296 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0330 | AFR | ACB | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0346 | AFR | USA | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | USA | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | USA | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | USA | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | LWK | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | LWK | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0038 | REF | REF | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0155 | REF | REF | TLE2_chr19_2992644_3034280 | TLE2 | chr19 | 2992644 | 3034280 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:3000657 | C | T | 1 | a0008 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.2114G>A | p.Ser705Asn | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/20 | 2490/2812 | 2114/2232 | 705/743 | chr19 | 3000657 | |||
| chr19:3009574 | T | C | 1 | a0009 | 1 | NA19010.hp1 | missense_variant | MODERATE | c.1141A>G | p.Ser381Gly | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/20 | 1517/2812 | 1141/2232 | 381/743 | chr19 | 3009574 | |||
| chr19:3011088 | C | T | 1 | a0003 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.946G>A | p.Gly316Arg | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/20 | 1322/2812 | 946/2232 | 316/743 | chr19 | 3011088 | |||
| chr19:3011148 | C | T | 2 | a0002 a0008 |
10 | HG00438.hp2 HG01123.hp1 HG02129.hp1 others(7): Show |
missense_variant | MODERATE | c.886G>A | p.Ala296Thr | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/20 | 1262/2812 | 886/2232 | 296/743 | chr19 | 3011148 | |||
| chr19:3011151 | G | A | 1 | a0004 | 1 | HG00733.hp2 | missense_variant | MODERATE | c.883C>T | p.Pro295Ser | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/20 | 1259/2812 | 883/2232 | 295/743 | chr19 | 3011151 | |||
| chr19:3013697 | G | A | 1 | a0005 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.845C>T | p.Pro282Leu | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/20 | 1221/2812 | 845/2232 | 282/743 | chr19 | 3013697 | |||
| chr19:3015742 | G | A | 1 | a0006 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.589C>T | p.Pro197Ser | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/20 | 965/2812 | 589/2232 | 197/743 | chr19 | 3015742 | |||
| chr19:3019381 | G | A | 1 | a0007 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.452C>T | p.Thr151Met | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/20 | 828/2812 | 452/2232 | 151/743 | chr19 | 3019381 | |||
| chr19:3019430 | G | C | 1 | a0010 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.403C>G | p.Pro135Ala | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/20 | 779/2812 | 403/2232 | 135/743 | chr19 | 3019430 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:2997899 | G | A | 6 | a0001c0002 a0001c0010 a0001c0013 others(3): Show |
94 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
synonymous_variant | LOW | c.2181C>T | p.Ile727Ile | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 20/20 | 2557/2812 | 2181/2232 | 727/743 | chr19 | 2997899 | |||
| chr19:3000665 | G | A | 4 | a0001c0007 a0001c0015 a0002c0004 others(1): Show |
12 | HG00438.hp2 HG00597.hp1 HG01123.hp1 others(9): Show |
synonymous_variant | LOW | c.2106C>T | p.Tyr702Tyr | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/20 | 2482/2812 | 2106/2232 | 702/743 | chr19 | 3000665 | |||
| chr19:3005476 | C | T | 1 | a0001c0003 | 9 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(6): Show |
synonymous_variant | LOW | c.1857G>A | p.Arg619Arg | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/20 | 2233/2812 | 1857/2232 | 619/743 | chr19 | 3005476 | |||
| chr19:3005557 | G | A | 1 | a0001c0008 | 2 | HG02109.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.1776C>T | p.Ala592Ala | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/20 | 2152/2812 | 1776/2232 | 592/743 | chr19 | 3005557 | |||
| chr19:3005768 | G | A | 1 | a0001c0017 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.1701C>T | p.Ser567Ser | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 16/20 | 2077/2812 | 1701/2232 | 567/743 | chr19 | 3005768 | |||
| chr19:3005885 | G | A | 1 | a0001c0015 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1584C>T | p.Ser528Ser | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 16/20 | 1960/2812 | 1584/2232 | 528/743 | chr19 | 3005885 | |||
| chr19:3006450 | G | C | 1 | a0001c0018 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1470C>G | p.Ala490Ala | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 15/20 | 1846/2812 | 1470/2232 | 490/743 | chr19 | 3006450 | |||
| chr19:3006561 | C | G | 1 | a0001c0016 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.1359G>C | p.Thr453Thr | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 15/20 | 1735/2812 | 1359/2232 | 453/743 | chr19 | 3006561 | |||
| chr19:3008907 | G | A | 1 | a0001c0009 | 2 | HG02683.hp1 HG03927.hp1 |
synonymous_variant | LOW | c.1212C>T | p.Ser404Ser | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/20 | 1588/2812 | 1212/2232 | 404/743 | chr19 | 3008907 | |||
| chr19:3011032 | C | T | 2 | a0001c0005 a0001c0015 |
6 | HG02615.hp1 HG02622.hp1 HG02965.hp2 others(3): Show |
synonymous_variant | LOW | c.1002G>A | p.Thr334Thr | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/20 | 1378/2812 | 1002/2232 | 334/743 | chr19 | 3011032 | |||
| chr19:3011062 | G | A | 1 | a0001c0020 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.972C>T | p.Cys324Cys | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/20 | 1348/2812 | 972/2232 | 324/743 | chr19 | 3011062 | |||
| chr19:3011110 | C | T | 1 | a0001c0013 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.924G>A | p.Pro308Pro | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/20 | 1300/2812 | 924/2232 | 308/743 | chr19 | 3011110 | |||
| chr19:3019308 | C | A | 1 | a0001c0024 | 1 | NA19083.hp1 | synonymous_variant | LOW | c.525G>T | p.Ala175Ala | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/20 | 901/2812 | 525/2232 | 175/743 | chr19 | 3019308 | |||
| chr19:3025059 | G | A | 1 | a0001c0006 | 3 | HG02647.hp1 HG02886.hp1 HG03041.hp2 |
synonymous_variant | LOW | c.255C>T | p.Ser85Ser | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/20 | 631/2812 | 255/2232 | 85/743 | chr19 | 3025059 | |||
| chr19:3028768 | C | T | 1 | a0001c0010 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.60G>A | p.Ser20Ser | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 2/20 | 436/2812 | 60/2232 | 20/743 | chr19 | 3028768 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:2997710 | G | A | 1 | a0001c0015t0009 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*138C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 20/20 | 138 | chr19 | 2997710 | ||||||
| chr19:2997741 | G | A | 1 | a0001c0001t0008 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*107C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 20/20 | 107 | chr19 | 2997741 | ||||||
| chr19:2997792 | T | C | 10 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(7): Show |
44 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*56A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 20/20 | 56 | chr19 | 2997792 | ||||||
| chr19:3028914 | C | T | 3 | a0001c0001t0004 a0001c0002t0007 a0010c0026t0006 |
7 | HG01891.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-10G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 1/20 | 10 | chr19 | 3028914 | ||||||
| chr19:3028981 | G | A | 1 | a0001c0001t0010 | 1 | HG03453.hp2 | 5_prime_UTR_variant | MODIFIER | c.-77C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 1/20 | 77 | chr19 | 3028981 | ||||||
| chr19:3029042 | G | A | 1 | a0001c0005t0011 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-138C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 1/20 | 138 | chr19 | 3029042 | ||||||
| chr19:3029060 | C | T | 5 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(2): Show |
15 | HG00738.hp1 HG01069.hp1 HG01891.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-156G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 1/20 | 156 | chr19 | 3029060 | ||||||
| chr19:3029248 | G | A | 1 | a0008c0012t0012 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-344C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 1/20 | 344 | chr19 | 3029248 | ||||||
| chr19:3029258 | G | A | 1 | a0001c0001t0013 | 1 | NA18970.hp1 | 5_prime_UTR_variant | MODIFIER | c.-354C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 1/20 | 354 | chr19 | 3029258 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:2997972 | G | A | 1 | a0001c0002t0001g0186 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2125-17C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2997972 | |||||||
| chr19:2997972 | G | T | 1 | a0001c0008t0001g0362 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2125-17C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2997972 | |||||||
| chr19:2997978 | A | G | 36 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0052 others(33): Show |
39 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.2125-23T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2997978 | |||||||
| chr19:2998080 | C | G | 7 | a0001c0001t0002g0199 a0001c0001t0002g0301 a0001c0001t0002g0328 others(4): Show |
7 | HG01891.hp1 HG02559.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2125-125G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998080 | |||||||
| chr19:2998105 | T | C | 2 | a0001c0006t0002g0232 a0001c0006t0002g0361 |
2 | HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2125-150A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998105 | |||||||
| chr19:2998150 | A | C | 1 | a0001c0002t0001g0200 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2125-195T>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998150 | |||||||
| chr19:2998177 | T | A | 3 | a0001c0001t0001g0288 a0001c0001t0001g0293 a0009c0019t0001g0181 |
3 | HG02040.hp1 NA18979.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2125-222A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998177 | |||||||
| chr19:2998236 | AATGTGTG others(15): Show |
A | 6 | a0001c0005t0001g0119 a0001c0005t0002g0234 a0001c0005t0002g0235 others(3): Show |
6 | HG02109.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2125-303_2125-282d others(24): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998236 | |||||||
| chr19:2998237 | A | ATG | 23 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0073 others(20): Show |
23 | HG00280.hp2 HG00741.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.2125-284_2125-283d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | |||||||
| chr19:2998237 | A | ATGTG | 9 | a0001c0001t0001g0008 a0001c0001t0001g0122 a0001c0001t0001g0148 others(6): Show |
9 | HG00099.hp1 HG00323.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.2125-286_2125-283d others(6): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | |||||||
| chr19:2998237 | A | ATGTGTGT others(1): Show |
4 | a0001c0001t0002g0001 a0001c0001t0004g0002 a0001c0001t0004g0021 others(1): Show |
7 | HG01891.hp2 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2125-290_2125-283d others(10): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | |||||||
| chr19:2998237 | A | ATGTGTGT others(3): Show |
2 | a0001c0001t0002g0001 a0001c0001t0002g0331 |
3 | HG03041.hp1 HG03540.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2125-292_2125-283d others(12): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | |||||||
| chr19:2998237 | A | ATGTGTGT others(5): Show |
2 | a0001c0001t0002g0300 a0001c0001t0005g0028 |
2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2125-294_2125-283d others(14): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | |||||||
| chr19:2998237 | A | ATGTGTGT others(13): Show |
1 | a0001c0001t0004g0019 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2125-302_2125-283d others(22): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | |||||||
| chr19:2998237 | ATGTG | A | 11 | a0001c0001t0001g0267 a0001c0001t0001g0274 a0001c0001t0001g0326 others(8): Show |
11 | HG00597.hp2 HG01934.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.2125-286_2125-283d others(6): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | |||||||
| chr19:2998237 | ATGTGTG | A | 81 | a0001c0001t0001g0229 a0001c0002t0001g0010 a0001c0002t0001g0013 others(78): Show |
84 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.2125-288_2125-283d others(8): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | |||||||
| chr19:2998237 | ATGTGTGT others(1): Show |
A | 11 | a0001c0007t0001g0280 a0001c0007t0001g0312 a0001c0015t0009g0180 others(8): Show |
12 | HG00438.hp2 HG00597.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.2125-290_2125-283d others(10): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | |||||||
| chr19:2998237 | ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0002g0285 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2125-292_2125-283d others(12): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | |||||||
| chr19:2998237 | ATGTGTGT others(5): Show |
A | 5 | a0001c0001t0001g0159 a0001c0001t0001g0221 a0001c0006t0001g0370 others(2): Show |
5 | HG02145.hp1 HG02145.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2125-294_2125-283d others(14): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | |||||||
| chr19:2998237 | ATGTGTGT others(7): Show |
A | 1 | a0001c0016t0001g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2125-296_2125-283d others(16): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | |||||||
| chr19:2998237 | ATGTGTGT others(9): Show |
A | 1 | a0004c0021t0001g0283 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2125-298_2125-283d others(18): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | |||||||
| chr19:2998237 | ATGTGTGT others(11): Show |
A | 5 | a0001c0003t0001g0154 a0001c0003t0001g0214 a0001c0003t0001g0341 others(2): Show |
5 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.2125-300_2125-283d others(20): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | |||||||
| chr19:2998237 | ATGTGTGT others(15): Show |
A | 5 | a0001c0001t0001g0286 a0001c0001t0002g0231 a0001c0001t0002g0296 others(2): Show |
5 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2125-304_2125-283d others(24): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | |||||||
| chr19:2998237 | ATGTGTGT others(17): Show |
A | 1 | a0001c0003t0001g0348 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2125-306_2125-283d others(26): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998237 | |||||||
| chr19:2998243 | GTGTGT | G | 3 | a0001c0003t0002g0247 a0001c0003t0002g0248 a0001c0003t0002g0249 |
3 | HG02258.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2125-293_2125-289d others(7): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998243 | |||||||
| chr19:2998243 | GTGTGTGT | G | 13 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0083 others(10): Show |
14 | HG00738.hp2 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.2125-295_2125-289d others(9): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998243 | |||||||
| chr19:2998263 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2125-308C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998263 | |||||||
| chr19:2998264 | T | A | 1 | a0001c0001t0001g0217 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2125-309A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998264 | |||||||
| chr19:2998264 | TGTGTGTG others(4): Show |
T | 2 | a0001c0001t0001g0288 a0001c0001t0001g0293 |
2 | HG02040.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.2125-320_2125-310d others(13): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998264 | |||||||
| chr19:2998265 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2125-310C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998265 | |||||||
| chr19:2998266 | TGTGTGTG others(5): Show |
T | 1 | a0001c0001t0001g0217 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2125-323_2125-312d others(14): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998266 | |||||||
| chr19:2998268 | TGTGTGTG | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0097 a0001c0001t0001g0127 |
3 | HG00140.hp1 HG01346.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2125-320_2125-314d others(9): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998268 | |||||||
| chr19:2998270 | TGTGTG | T | 5 | a0001c0001t0001g0137 a0001c0001t0001g0273 a0001c0001t0001g0277 others(2): Show |
5 | HG01934.hp2 HG02523.hp2 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.2125-320_2125-316d others(7): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998270 | |||||||
| chr19:2998271 | G | A | 8 | a0001c0001t0001g0374 a0001c0001t0002g0034 a0001c0001t0002g0037 others(5): Show |
8 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.2125-316C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998271 | |||||||
| chr19:2998272 | TGTG | T | 127 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
137 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.2125-320_2125-318d others(5): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998272 | |||||||
| chr19:2998273 | G | A | 10 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0117 others(7): Show |
10 | HG01257.hp1 HG02129.hp2 HG03225.hp1 others(7): Show |
intron_variant | MODIFIER | c.2125-318C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998273 | |||||||
| chr19:2998274 | T | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0117 others(4): Show |
7 | HG01257.hp1 HG02129.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.2125-319A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998274 | |||||||
| chr19:2998274 | TG | T | 19 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0134 others(16): Show |
19 | HG01516.hp1 HG01516.hp2 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.2125-320delC | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998274 | |||||||
| chr19:2998275 | G | A | 147 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0070 others(144): Show |
152 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.2125-320C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998275 | |||||||
| chr19:2998275 | G | GTA | 6 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0052 others(3): Show |
8 | HG01109.hp2 HG02055.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2125-322_2125-321d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998275 | |||||||
| chr19:2998275 | G | GTGTGTGT others(3): Show |
1 | a0001c0001t0002g0330 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2125-321_2125-320i others(12): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998275 | |||||||
| chr19:2998275 | G | GTGTGTGT others(5): Show |
1 | a0007c0025t0002g0294 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2125-321_2125-320i others(14): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998275 | |||||||
| chr19:2998275 | G | GTGTGTGT others(7): Show |
2 | a0001c0001t0002g0199 a0001c0001t0002g0329 |
2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2125-321_2125-320i others(16): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998275 | |||||||
| chr19:2998275 | G | GTGTGTGT others(9): Show |
1 | a0001c0001t0002g0363 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2125-321_2125-320i others(18): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998275 | |||||||
| chr19:2998275 | G | GTGTGTGT others(11): Show |
1 | a0001c0001t0002g0328 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2125-321_2125-320i others(20): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998275 | |||||||
| chr19:2998275 | G | GTGTGTGT others(15): Show |
1 | a0001c0001t0002g0301 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2125-321_2125-320i others(24): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998275 | |||||||
| chr19:2998275 | G | T | 7 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0117 others(4): Show |
7 | HG01257.hp1 HG02129.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.2125-320C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998275 | |||||||
| chr19:2998276 | T | A | 156 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2125-321A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998276 | |||||||
| chr19:2998276 | TAA | T | 7 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0117 others(4): Show |
7 | HG01257.hp1 HG02129.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.2125-323_2125-322d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998276 | |||||||
| chr19:2998277 | A | T | 1 | a0001c0001t0001g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2125-322T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998277 | |||||||
| chr19:2998278 | A | T | 156 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2125-323T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998278 | |||||||
| chr19:2998278 | AT | A | 13 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0083 others(10): Show |
14 | HG00738.hp2 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.2125-324delA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998278 | |||||||
| chr19:2998279 | T | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0179 |
2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.2125-324A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998279 | |||||||
| chr19:2998288 | T | G | 3 | a0001c0003t0002g0247 a0001c0003t0002g0248 a0001c0003t0002g0249 |
3 | HG02258.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2125-333A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998288 | |||||||
| chr19:2998290 | T | G | 17 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0083 others(14): Show |
18 | HG00738.hp2 HG02258.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.2125-335A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998290 | |||||||
| chr19:2998292 | T | G | 18 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0083 others(15): Show |
19 | HG00738.hp2 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.2125-337A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998292 | |||||||
| chr19:2998293 | T | G | 1 | a0001c0001t0002g0199 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2125-338A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998293 | |||||||
| chr19:2998307 | T | G | 1 | a0001c0001t0001g0216 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2125-352A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998307 | |||||||
| chr19:2998406 | C | A | 141 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0083 others(138): Show |
146 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.2125-451G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998406 | |||||||
| chr19:2998483 | GGC | G | 130 | a0001c0001t0001g0203 a0001c0001t0001g0209 a0001c0001t0001g0221 others(127): Show |
134 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.2125-530_2125-529d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998483 | |||||||
| chr19:2998556 | G | A | 1 | a0001c0006t0001g0370 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2125-601C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998556 | |||||||
| chr19:2998651 | C | T | 14 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0083 others(11): Show |
15 | HG00738.hp2 HG02559.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2125-696G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998651 | |||||||
| chr19:2998709 | G | A | 1 | a0001c0002t0001g0295 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2125-754C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2998709 | |||||||
| chr19:2999034 | C | T | 7 | a0001c0001t0002g0199 a0001c0001t0002g0301 a0001c0001t0002g0328 others(4): Show |
7 | HG02559.hp2 HG02723.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.2125-1079G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999034 | |||||||
| chr19:2999040 | C | G | 160 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0083 others(157): Show |
165 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(162): Show |
intron_variant | MODIFIER | c.2125-1085G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999040 | |||||||
| chr19:2999047 | C | T | 3 | a0001c0001t0001g0203 a0001c0001t0001g0209 a0001c0001t0010g0377 |
3 | HG03225.hp1 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2125-1092G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999047 | |||||||
| chr19:2999054 | G | A | 1 | a0001c0006t0002g0232 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2125-1099C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999054 | |||||||
| chr19:2999109 | C | G | 160 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(157): Show |
170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.2125-1154G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999109 | |||||||
| chr19:2999261 | G | A | 14 | a0001c0001t0001g0203 a0001c0001t0001g0209 a0001c0001t0010g0377 others(11): Show |
15 | HG00438.hp2 HG00597.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.2125-1306C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999261 | |||||||
| chr19:2999277 | G | A | 21 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0014 others(18): Show |
25 | HG00738.hp2 HG01109.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.2125-1322C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999277 | |||||||
| chr19:2999482 | C | T | 1 | a0001c0001t0008g0321 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2124+1165G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999482 | |||||||
| chr19:2999494 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2124+1153T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999494 | |||||||
| chr19:2999499 | G | A | 2 | a0001c0002t0001g0367 a0001c0006t0001g0370 |
2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2124+1148C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999499 | |||||||
| chr19:2999554 | C | T | 1 | a0001c0002t0001g0095 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2124+1093G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999554 | |||||||
| chr19:2999555 | G | A | 102 | a0001c0001t0001g0209 a0001c0001t0001g0221 a0001c0001t0001g0229 others(99): Show |
105 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.2124+1092C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999555 | |||||||
| chr19:2999595 | C | T | 14 | a0001c0001t0002g0199 a0001c0001t0002g0301 a0001c0001t0002g0328 others(11): Show |
14 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.2124+1052G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999595 | |||||||
| chr19:2999626 | C | A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0096 others(1): Show |
4 | NA18747.hp1 NA18975.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.2124+1021G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999626 | |||||||
| chr19:2999671 | A | G | 14 | a0001c0001t0001g0053 a0001c0001t0001g0137 a0001c0001t0001g0163 others(11): Show |
14 | HG00408.hp1 HG00642.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.2124+976T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999671 | |||||||
| chr19:2999687 | G | A | 1 | a0001c0003t0001g0214 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2124+960C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999687 | |||||||
| chr19:2999726 | C | CA | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
194 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.2124+920dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999726 | |||||||
| chr19:2999737 | AAAG | A | 138 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0083 others(135): Show |
143 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.2124+907_2124+909d others(5): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999737 | |||||||
| chr19:2999759 | G | A | 11 | a0001c0001t0001g0229 a0001c0002t0001g0076 a0001c0002t0001g0161 others(8): Show |
11 | HG00639.hp2 HG01099.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.2124+888C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999759 | |||||||
| chr19:2999761 | A | G | 146 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0083 others(143): Show |
151 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.2124+886T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999761 | |||||||
| chr19:2999806 | G | C | 160 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(157): Show |
170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.2124+841C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999806 | |||||||
| chr19:2999868 | A | G | 1 | a0001c0006t0002g0361 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2124+779T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999868 | |||||||
| chr19:2999987 | C | T | 7 | a0001c0001t0002g0199 a0001c0001t0002g0301 a0001c0001t0002g0328 others(4): Show |
7 | HG02559.hp2 HG02723.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.2124+660G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 2999987 | |||||||
| chr19:3000012 | G | C | 146 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0056 others(143): Show |
151 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.2124+635C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000012 | |||||||
| chr19:3000164 | T | C | 155 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0032 others(152): Show |
162 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.2124+483A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000164 | |||||||
| chr19:3000217 | G | A | 18 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0083 others(15): Show |
19 | HG00738.hp2 HG01891.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.2124+430C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000217 | |||||||
| chr19:3000218 | C | T | 1 | a0001c0016t0001g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2124+429G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000218 | |||||||
| chr19:3000276 | C | T | 1 | a0001c0020t0001g0373 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2124+371G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000276 | |||||||
| chr19:3000289 | G | A | 154 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0056 others(151): Show |
159 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.2124+358C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000289 | |||||||
| chr19:3000366 | T | G | 1 | a0001c0002t0001g0366 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2124+281A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000366 | |||||||
| chr19:3000374 | T | C | 147 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0056 others(144): Show |
152 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.2124+273A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000374 | |||||||
| chr19:3000434 | C | G | 1 | a0001c0006t0002g0361 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2124+213G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000434 | |||||||
| chr19:3000493 | G | C | 9 | a0001c0001t0001g0242 a0001c0001t0001g0374 a0001c0001t0002g0034 others(6): Show |
9 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.2124+154C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000493 | |||||||
| chr19:3000502 | C | T | 1 | a0001c0008t0002g0371 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2124+145G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000502 | |||||||
| chr19:3000601 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0010g0377 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2124+46G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 19/19 | chr19 | 3000601 | |||||||
| chr19:3000767 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2048-44C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3000767 | |||||||
| chr19:3000785 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2048-62C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3000785 | |||||||
| chr19:3000824 | C | CT | 220 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(217): Show |
238 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.2048-102dupA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3000824 | |||||||
| chr19:3000824 | C | CTT | 98 | a0001c0001t0001g0056 a0001c0001t0001g0081 a0001c0001t0001g0101 others(95): Show |
102 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.2048-103_2048-102d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3000824 | |||||||
| chr19:3000841 | T | TTC | 6 | a0001c0001t0002g0199 a0001c0001t0002g0301 a0001c0001t0002g0328 others(3): Show |
6 | HG02559.hp2 HG02723.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2048-119_2048-118i others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3000841 | |||||||
| chr19:3000969 | C | T | 11 | a0001c0001t0001g0229 a0001c0002t0001g0076 a0001c0002t0001g0161 others(8): Show |
11 | HG00639.hp2 HG01099.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.2048-246G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3000969 | |||||||
| chr19:3000970 | G | C | 1 | a0001c0016t0001g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2048-247C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3000970 | |||||||
| chr19:3001130 | G | A | 1 | a0007c0025t0002g0294 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2048-407C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001130 | |||||||
| chr19:3001230 | G | A | 1 | a0001c0008t0002g0371 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2048-507C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001230 | |||||||
| chr19:3001272 | CA | C | 321 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(318): Show |
342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.2048-550delT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001272 | |||||||
| chr19:3001272 | CAA | C | 9 | a0001c0001t0001g0139 a0001c0001t0001g0244 a0001c0001t0002g0062 others(6): Show |
9 | HG01169.hp1 HG02615.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2048-551_2048-550d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001272 | |||||||
| chr19:3001286 | A | T | 1 | a0001c0002t0007g0031 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2048-563T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001286 | |||||||
| chr19:3001352 | C | T | 3 | a0001c0002t0001g0175 a0001c0002t0001g0183 a0001c0002t0001g0271 |
3 | HG00558.hp2 HG00609.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2048-629G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001352 | |||||||
| chr19:3001364 | C | T | 1 | a0004c0021t0001g0283 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2048-641G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001364 | |||||||
| chr19:3001365 | G | A | 1 | a0001c0015t0009g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2048-642C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001365 | |||||||
| chr19:3001392 | G | C | 83 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(80): Show |
90 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.2048-669C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001392 | |||||||
| chr19:3001419 | T | TTTTG | 11 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0052 others(8): Show |
14 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2048-700_2048-697d others(6): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001419 | |||||||
| chr19:3001419 | TTTTG | T | 10 | a0001c0001t0001g0203 a0001c0001t0001g0251 a0001c0001t0001g0252 others(7): Show |
10 | HG02572.hp2 HG02647.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.2048-700_2048-697d others(6): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001419 | |||||||
| chr19:3001498 | T | A | 5 | a0001c0001t0001g0093 a0001c0001t0001g0120 a0001c0002t0001g0175 others(2): Show |
5 | HG00733.hp1 HG02109.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.2048-775A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001498 | |||||||
| chr19:3001499 | A | T | 3 | a0001c0002t0001g0177 a0001c0002t0001g0178 a0001c0002t0001g0262 |
3 | NA18967.hp2 NA19083.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.2048-776T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001499 | |||||||
| chr19:3001613 | G | A | 5 | a0001c0001t0002g0121 a0001c0002t0001g0013 a0001c0002t0001g0082 others(2): Show |
6 | HG02257.hp2 HG02717.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2047+740C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001613 | |||||||
| chr19:3001649 | A | C | 22 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0052 others(19): Show |
25 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.2047+704T>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001649 | |||||||
| chr19:3001704 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2047+649C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001704 | |||||||
| chr19:3001791 | C | CT | 16 | a0001c0001t0001g0032 a0001c0001t0001g0143 a0001c0001t0001g0246 others(13): Show |
16 | HG00099.hp2 HG00621.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.2047+561dupA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001791 | |||||||
| chr19:3001791 | C | CTT | 18 | a0001c0001t0001g0014 a0001c0001t0001g0083 a0001c0001t0001g0250 others(15): Show |
19 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.2047+560_2047+561d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001791 | |||||||
| chr19:3001791 | CT | C | 44 | a0001c0001t0001g0144 a0001c0001t0001g0193 a0001c0001t0001g0203 others(41): Show |
50 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.2047+561delA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001791 | |||||||
| chr19:3001791 | CTT | C | 160 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.2047+560_2047+561d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001791 | |||||||
| chr19:3001791 | CTTT | C | 15 | a0001c0001t0001g0046 a0001c0001t0001g0054 a0001c0001t0001g0075 others(12): Show |
15 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.2047+559_2047+561d others(5): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001791 | |||||||
| chr19:3001797 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2047+556A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001797 | |||||||
| chr19:3001876 | C | T | 16 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0083 others(13): Show |
17 | HG00738.hp2 HG01891.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.2047+477G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001876 | |||||||
| chr19:3001877 | G | A | 3 | a0001c0003t0002g0247 a0001c0003t0002g0248 a0001c0003t0002g0249 |
3 | HG02258.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2047+476C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001877 | |||||||
| chr19:3001957 | C | A | 6 | a0001c0001t0002g0231 a0001c0001t0002g0296 a0001c0001t0002g0375 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2047+396G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3001957 | |||||||
| chr19:3002000 | G | A | 1 | a0001c0016t0001g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2047+353C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3002000 | |||||||
| chr19:3002013 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2047+340C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3002013 | |||||||
| chr19:3002082 | G | C | 1 | a0001c0001t0001g0153 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2047+271C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3002082 | |||||||
| chr19:3002115 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2047+238T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3002115 | |||||||
| chr19:3002150 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2047+203G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3002150 | |||||||
| chr19:3002288 | T | C | 1 | a0001c0016t0001g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2047+65A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 18/19 | chr19 | 3002288 | |||||||
| chr19:3002655 | C | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0319 |
2 | NA18945.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1897-152G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3002655 | |||||||
| chr19:3002690 | C | T | 4 | a0001c0001t0001g0115 a0001c0001t0001g0147 a0001c0001t0001g0158 others(1): Show |
4 | HG02027.hp2 NA18953.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1897-187G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3002690 | |||||||
| chr19:3002703 | C | CTT | 17 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0052 others(14): Show |
20 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1897-202_1897-201d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3002703 | |||||||
| chr19:3002899 | G | A | 32 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0052 others(29): Show |
35 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1897-396C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3002899 | |||||||
| chr19:3002946 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1897-443C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3002946 | |||||||
| chr19:3003000 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0273 |
2 | NA19084.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1897-497G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003000 | |||||||
| chr19:3003025 | G | A | 1 | a0001c0002t0001g0364 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1897-522C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003025 | |||||||
| chr19:3003072 | C | G | 1 | a0001c0016t0001g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1897-569G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003072 | |||||||
| chr19:3003079 | A | AC | 8 | a0001c0001t0002g0001 a0001c0001t0002g0300 a0001c0001t0002g0331 others(5): Show |
13 | HG01891.hp2 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1897-577dupG | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003079 | |||||||
| chr19:3003080 | C | A | 1 | a0001c0016t0001g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1897-577G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003080 | |||||||
| chr19:3003142 | C | T | 91 | a0001c0001t0001g0056 a0001c0001t0001g0229 a0001c0002t0001g0010 others(88): Show |
94 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1897-639G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003142 | |||||||
| chr19:3003168 | A | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0134 |
2 | HG01928.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1897-665T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003168 | |||||||
| chr19:3003178 | C | G | 1 | a0001c0002t0001g0079 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1897-675G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003178 | |||||||
| chr19:3003340 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1897-837A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003340 | |||||||
| chr19:3003353 | C | T | 1 | a0001c0002t0001g0082 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1897-850G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003353 | |||||||
| chr19:3003444 | C | A | 1 | a0001c0015t0009g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1897-941G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003444 | |||||||
| chr19:3003650 | C | CA | 14 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0083 others(11): Show |
15 | HG00738.hp2 HG01891.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1897-1148dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003650 | |||||||
| chr19:3003693 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1897-1190T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003693 | |||||||
| chr19:3003729 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1897-1226C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003729 | |||||||
| chr19:3003758 | G | A | 1 | a0001c0016t0001g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1897-1255C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003758 | |||||||
| chr19:3003958 | C | T | 1 | a0001c0002t0001g0345 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1897-1455G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003958 | |||||||
| chr19:3003975 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1896+1462C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003975 | |||||||
| chr19:3003987 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0052 others(14): Show |
20 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1896+1450C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003987 | |||||||
| chr19:3003995 | C | T | 9 | a0001c0003t0001g0154 a0001c0003t0001g0214 a0001c0003t0001g0341 others(6): Show |
9 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1896+1442G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3003995 | |||||||
| chr19:3004032 | G | A | 1 | a0001c0016t0001g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1896+1405C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004032 | |||||||
| chr19:3004041 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1896+1396G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004041 | |||||||
| chr19:3004255 | G | C | 4 | a0001c0003t0001g0154 a0001c0003t0001g0341 a0001c0003t0001g0342 others(1): Show |
4 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1896+1182C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004255 | |||||||
| chr19:3004336 | GTTGGACA others(102): Show |
G | 1 | a0001c0016t0001g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1896+992_1896+1100 others(3): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004336 | |||||||
| chr19:3004366 | G | A | 1 | a0001c0015t0009g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1896+1071C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004366 | |||||||
| chr19:3004501 | T | C | 12 | a0001c0001t0001g0221 a0001c0001t0001g0347 a0001c0001t0002g0231 others(9): Show |
12 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1896+936A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004501 | |||||||
| chr19:3004509 | C | T | 4 | a0001c0002t0001g0087 a0001c0002t0001g0088 a0001c0002t0001g0092 others(1): Show |
4 | NA18944.hp2 NA18964.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.1896+928G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004509 | |||||||
| chr19:3004614 | C | CA | 27 | a0001c0001t0001g0135 a0001c0001t0001g0149 a0001c0001t0001g0221 others(24): Show |
27 | HG01167.hp2 HG01169.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1896+822dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004614 | |||||||
| chr19:3004614 | CA | C | 51 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0046 others(48): Show |
58 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1896+822delT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004614 | |||||||
| chr19:3004643 | C | G | 42 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0052 others(39): Show |
50 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.1896+794G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004643 | |||||||
| chr19:3004794 | G | A | 57 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0014 others(54): Show |
66 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.1896+643C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004794 | |||||||
| chr19:3004798 | T | G | 1 | a0001c0002t0001g0268 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1896+639A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004798 | |||||||
| chr19:3004843 | G | C | 60 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0014 others(57): Show |
69 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.1896+594C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004843 | |||||||
| chr19:3004894 | C | T | 2 | a0001c0002t0001g0345 a0001c0002t0001g0364 |
2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1896+543G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3004894 | |||||||
| chr19:3005062 | T | C | 1 | a0001c0003t0001g0214 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1896+375A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3005062 | |||||||
| chr19:3005110 | C | G | 35 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0014 others(32): Show |
39 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.1896+327G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3005110 | |||||||
| chr19:3005147 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1896+290C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3005147 | |||||||
| chr19:3005198 | G | T | 1 | a0001c0009t0001g0060 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1896+239C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3005198 | |||||||
| chr19:3005233 | G | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0052 others(17): Show |
23 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1896+204C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3005233 | |||||||
| chr19:3005278 | G | A | 159 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(156): Show |
169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.1896+159C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3005278 | |||||||
| chr19:3005290 | A | G | 9 | a0001c0003t0001g0154 a0001c0003t0001g0214 a0001c0003t0001g0341 others(6): Show |
9 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1896+147T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3005290 | |||||||
| chr19:3005349 | G | A | 1 | a0001c0002t0001g0346 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1896+88C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3005349 | |||||||
| chr19:3005413 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1896+24G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3005413 | |||||||
| chr19:3005427 | C | T | 4 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0276 others(1): Show |
4 | HG00673.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1896+10G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 17/19 | chr19 | 3005427 | |||||||
| chr19:3005691 | G | C | 1 | a0001c0001t0001g0240 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1748+30C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 16/19 | chr19 | 3005691 | |||||||
| chr19:3006134 | C | T | 1 | a0001c0002t0001g0015 | 2 | NA18947.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1501-166G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 15/19 | chr19 | 3006134 | |||||||
| chr19:3006149 | A | G | 1 | a0001c0002t0001g0345 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1501-181T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 15/19 | chr19 | 3006149 | |||||||
| chr19:3006179 | C | A | 1 | a0004c0021t0001g0283 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1501-211G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 15/19 | chr19 | 3006179 | |||||||
| chr19:3006229 | A | T | 70 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0014 others(67): Show |
79 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.1500+191T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 15/19 | chr19 | 3006229 | |||||||
| chr19:3006238 | A | AAT | 242 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(239): Show |
262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1500+181_1500+182i others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 15/19 | chr19 | 3006238 | |||||||
| chr19:3006276 | C | T | 337 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(334): Show |
360 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(357): Show |
intron_variant | MODIFIER | c.1500+144G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 15/19 | chr19 | 3006276 | |||||||
| chr19:3006302 | T | C | 1 | a0001c0015t0009g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1500+118A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 15/19 | chr19 | 3006302 | |||||||
| chr19:3006710 | C | A | 1 | a0001c0015t0009g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1251-41G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3006710 | |||||||
| chr19:3006773 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1251-104C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3006773 | |||||||
| chr19:3006773 | G | GTGTTTTT others(12): Show |
3 | a0001c0003t0001g0154 a0001c0003t0001g0341 a0001c0003t0001g0342 |
3 | HG00099.hp2 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1251-123_1251-105d others(21): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3006773 | |||||||
| chr19:3006946 | C | A | 6 | a0001c0001t0002g0199 a0001c0001t0002g0301 a0001c0001t0002g0328 others(3): Show |
6 | HG02559.hp2 HG02723.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1251-277G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3006946 | |||||||
| chr19:3007054 | G | C | 5 | a0001c0001t0002g0034 a0001c0001t0002g0037 a0001c0001t0002g0062 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1251-385C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007054 | |||||||
| chr19:3007119 | G | A | 3 | a0001c0003t0002g0247 a0001c0003t0002g0248 a0001c0003t0002g0249 |
3 | HG02258.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1251-450C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007119 | |||||||
| chr19:3007321 | T | C | 245 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(242): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1251-652A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007321 | |||||||
| chr19:3007338 | C | T | 2 | a0001c0005t0001g0119 a0001c0005t0002g0344 |
2 | HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1251-669G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007338 | |||||||
| chr19:3007359 | G | C | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0064 others(1): Show |
4 | HG01993.hp2 HG02080.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251-690C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007359 | |||||||
| chr19:3007370 | A | G | 341 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(338): Show |
364 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.1251-701T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007370 | |||||||
| chr19:3007429 | T | C | 1 | a0001c0002t0001g0162 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1251-760A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007429 | |||||||
| chr19:3007646 | C | T | 6 | a0001c0001t0001g0110 a0001c0001t0001g0193 a0001c0001t0001g0297 others(3): Show |
6 | NA18944.hp1 NA18952.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.1251-977G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007646 | |||||||
| chr19:3007677 | G | A | 1 | a0001c0002t0001g0320 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1251-1008C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007677 | |||||||
| chr19:3007700 | A | C | 245 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(242): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1251-1031T>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007700 | |||||||
| chr19:3007807 | C | A | 9 | a0001c0001t0002g0001 a0001c0001t0002g0300 a0001c0001t0002g0331 others(6): Show |
14 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1250+1062G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007807 | |||||||
| chr19:3007942 | G | A | 7 | a0001c0001t0002g0034 a0001c0001t0002g0037 a0001c0001t0002g0062 others(4): Show |
7 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1250+927C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3007942 | |||||||
| chr19:3008069 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1250+800C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008069 | |||||||
| chr19:3008083 | GAAAAC | G | 96 | a0001c0001t0001g0056 a0001c0001t0001g0229 a0001c0001t0001g0351 others(93): Show |
99 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.1250+781_1250+785d others(7): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008083 | |||||||
| chr19:3008151 | A | G | 1 | a0001c0006t0002g0361 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1250+718T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008151 | |||||||
| chr19:3008153 | G | A | 7 | a0001c0001t0002g0034 a0001c0001t0002g0037 a0001c0001t0002g0062 others(4): Show |
7 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1250+716C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008153 | |||||||
| chr19:3008197 | A | G | 1 | a0001c0016t0001g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1250+672T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008197 | |||||||
| chr19:3008321 | G | A | 2 | a0001c0008t0001g0362 a0001c0008t0002g0371 |
2 | HG02109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1250+548C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008321 | |||||||
| chr19:3008352 | G | T | 1 | a0001c0001t0001g0269 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1250+517C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008352 | |||||||
| chr19:3008455 | C | CT | 31 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0083 others(28): Show |
32 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1250+413dupA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008455 | |||||||
| chr19:3008455 | C | CTT | 85 | a0001c0001t0001g0056 a0001c0001t0001g0229 a0001c0001t0001g0374 others(82): Show |
88 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.1250+412_1250+413d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008455 | |||||||
| chr19:3008462 | T | C | 1 | a0001c0001t0001g0196 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1250+407A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008462 | |||||||
| chr19:3008490 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1250+379C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008490 | |||||||
| chr19:3008500 | G | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(159): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.1250+369C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008500 | |||||||
| chr19:3008507 | A | G | 1 | a0001c0015t0009g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1250+362T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008507 | |||||||
| chr19:3008598 | C | G | 88 | a0001c0001t0001g0056 a0001c0001t0001g0229 a0001c0001t0001g0374 others(85): Show |
91 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.1250+271G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008598 | |||||||
| chr19:3008599 | C | T | 162 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(159): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.1250+270G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008599 | |||||||
| chr19:3008604 | C | A | 1 | a0001c0001t0002g0363 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1250+265G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008604 | |||||||
| chr19:3008695 | C | A | 95 | a0001c0001t0001g0056 a0001c0001t0001g0229 a0001c0001t0001g0374 others(92): Show |
98 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.1250+174G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008695 | |||||||
| chr19:3008854 | C | CA | 3 | a0001c0001t0001g0176 a0001c0001t0001g0336 a0001c0001t0001g0369 |
3 | HG00741.hp1 HG04228.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1250+14dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 14/19 | chr19 | 3008854 | |||||||
| chr19:3008991 | C | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0052 others(10): Show |
16 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1174-46G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/19 | chr19 | 3008991 | |||||||
| chr19:3008992 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1174-47G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/19 | chr19 | 3008992 | |||||||
| chr19:3009010 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1174-65G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/19 | chr19 | 3009010 | |||||||
| chr19:3009011 | G | A | 16 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0083 others(13): Show |
17 | HG00738.hp2 HG01884.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1174-66C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/19 | chr19 | 3009011 | |||||||
| chr19:3009083 | A | C | 1 | a0001c0006t0001g0370 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1174-138T>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/19 | chr19 | 3009083 | |||||||
| chr19:3009163 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1174-218G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/19 | chr19 | 3009163 | |||||||
| chr19:3009222 | T | G | 94 | a0001c0001t0001g0056 a0001c0001t0001g0229 a0001c0001t0001g0374 others(91): Show |
97 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.1174-277A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/19 | chr19 | 3009222 | |||||||
| chr19:3009287 | C | T | 1 | a0001c0002t0001g0111 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1173+255G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/19 | chr19 | 3009287 | |||||||
| chr19:3009336 | G | A | 8 | a0001c0003t0001g0154 a0001c0003t0001g0214 a0001c0003t0001g0341 others(5): Show |
8 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1173+206C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/19 | chr19 | 3009336 | |||||||
| chr19:3009340 | T | C | 4 | a0001c0001t0001g0221 a0001c0001t0001g0347 a0001c0001t0002g0285 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173+202A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/19 | chr19 | 3009340 | |||||||
| chr19:3009517 | C | G | 1 | a0001c0006t0002g0361 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1173+25G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 13/19 | chr19 | 3009517 | |||||||
| chr19:3009707 | G | A | 1 | a0001c0003t0001g0348 | 1 | HG03516.hp2 | splice_region_variant&intron_variant | LOW | c.1013-5C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009707 | |||||||
| chr19:3009734 | C | T | 1 | a0001c0006t0002g0361 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1013-32G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009734 | |||||||
| chr19:3009735 | G | A | 9 | a0001c0003t0001g0154 a0001c0003t0001g0214 a0001c0003t0001g0341 others(6): Show |
9 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1013-33C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009735 | |||||||
| chr19:3009755 | C | T | 5 | a0001c0001t0002g0301 a0001c0001t0002g0328 a0001c0001t0002g0329 others(2): Show |
5 | HG02559.hp2 HG02723.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1013-53G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009755 | |||||||
| chr19:3009772 | G | A | 9 | a0001c0006t0001g0370 a0002c0004t0001g0011 a0002c0004t0001g0086 others(6): Show |
10 | HG00438.hp2 HG01123.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.1013-70C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009772 | |||||||
| chr19:3009776 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1013-74G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009776 | |||||||
| chr19:3009790 | T | C | 325 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(322): Show |
348 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.1013-88A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009790 | |||||||
| chr19:3009836 | C | G | 95 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0203 others(92): Show |
98 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1013-134G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009836 | |||||||
| chr19:3009872 | C | T | 95 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0203 others(92): Show |
98 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1013-170G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009872 | |||||||
| chr19:3009885 | C | CT | 241 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1013-184dupA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009885 | |||||||
| chr19:3009887 | C | CTCTTTTT | 7 | a0001c0001t0002g0034 a0001c0001t0002g0037 a0001c0001t0002g0062 others(4): Show |
7 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1013-186_1013-185i others(9): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009887 | |||||||
| chr19:3009887 | C | CTCTTTTT others(1): Show |
86 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0203 others(83): Show |
89 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.1013-186_1013-185i others(10): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009887 | |||||||
| chr19:3009887 | C | T | 247 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(244): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.1013-185G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009887 | |||||||
| chr19:3009900 | G | T | 95 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0203 others(92): Show |
98 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1013-198C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009900 | |||||||
| chr19:3009904 | G | T | 95 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0203 others(92): Show |
98 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1013-202C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009904 | |||||||
| chr19:3009954 | G | A | 93 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0203 others(90): Show |
96 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.1013-252C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009954 | |||||||
| chr19:3009970 | T | C | 93 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0203 others(90): Show |
96 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.1013-268A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3009970 | |||||||
| chr19:3010061 | C | T | 4 | a0001c0003t0001g0348 a0001c0003t0002g0247 a0001c0003t0002g0248 others(1): Show |
4 | HG02258.hp1 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1013-359G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010061 | |||||||
| chr19:3010087 | A | T | 1 | a0001c0001t0001g0187 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1013-385T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010087 | |||||||
| chr19:3010101 | C | T | 3 | a0001c0001t0001g0347 a0001c0001t0002g0285 a0001c0002t0001g0364 |
3 | HG02280.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1013-399G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010101 | |||||||
| chr19:3010117 | A | C | 1 | a0001c0001t0001g0096 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1013-415T>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010117 | |||||||
| chr19:3010220 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1013-518A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010220 | |||||||
| chr19:3010235 | A | C | 6 | a0001c0001t0001g0110 a0001c0001t0001g0193 a0001c0001t0001g0297 others(3): Show |
6 | NA18944.hp1 NA18952.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.1013-533T>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010235 | |||||||
| chr19:3010294 | C | T | 4 | a0001c0001t0001g0077 a0001c0001t0001g0093 a0001c0001t0001g0304 others(1): Show |
4 | HG00639.hp2 HG00733.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.1013-592G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010294 | |||||||
| chr19:3010295 | G | A | 12 | a0001c0001t0001g0014 a0001c0001t0001g0083 a0001c0001t0001g0246 others(9): Show |
13 | HG00738.hp2 HG01891.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1013-593C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010295 | |||||||
| chr19:3010325 | T | C | 1 | a0001c0001t0005g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1013-623A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010325 | |||||||
| chr19:3010368 | A | G | 89 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0203 others(86): Show |
92 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1012+654T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010368 | |||||||
| chr19:3010369 | A | G | 1 | a0001c0002t0001g0309 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1012+653T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010369 | |||||||
| chr19:3010370 | A | T | 1 | a0001c0008t0001g0362 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1012+652T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010370 | |||||||
| chr19:3010372 | AAG | A | 88 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0203 others(85): Show |
91 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.1012+648_1012+649d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010372 | |||||||
| chr19:3010375 | G | GA | 14 | a0001c0001t0001g0094 a0001c0001t0001g0135 a0001c0001t0001g0192 others(11): Show |
14 | HG01123.hp2 HG01884.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.1012+646dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010375 | |||||||
| chr19:3010376 | A | G | 89 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0203 others(86): Show |
92 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1012+646T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010376 | |||||||
| chr19:3010399 | C | G | 1 | a0001c0001t0001g0374 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1012+623G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010399 | |||||||
| chr19:3010500 | A | T | 4 | a0001c0003t0001g0348 a0001c0003t0002g0247 a0001c0003t0002g0248 others(1): Show |
4 | HG02258.hp1 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012+522T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010500 | |||||||
| chr19:3010650 | T | C | 98 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0203 others(95): Show |
101 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1012+372A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010650 | |||||||
| chr19:3010805 | C | T | 89 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0203 others(86): Show |
92 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1012+217G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010805 | |||||||
| chr19:3010842 | G | A | 5 | a0001c0001t0002g0001 a0001c0001t0002g0300 a0001c0001t0004g0019 others(2): Show |
8 | HG02280.hp1 HG02486.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1012+180C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 12/19 | chr19 | 3010842 | |||||||
| chr19:3011174 | G | T | 1 | a0001c0016t0001g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.874-14C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011174 | |||||||
| chr19:3011247 | G | A | 1 | a0001c0001t0001g0374 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.874-87C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011247 | |||||||
| chr19:3011282 | C | G | 5 | a0001c0001t0002g0001 a0001c0001t0002g0300 a0001c0001t0004g0019 others(2): Show |
8 | HG02280.hp1 HG02486.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.874-122G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011282 | |||||||
| chr19:3011319 | G | C | 1 | a0001c0006t0002g0361 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.874-159C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011319 | |||||||
| chr19:3011353 | C | T | 5 | a0001c0001t0001g0221 a0001c0001t0001g0347 a0001c0001t0002g0285 others(2): Show |
5 | HG02145.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.874-193G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011353 | |||||||
| chr19:3011389 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.874-229C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011389 | |||||||
| chr19:3011414 | C | T | 91 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0203 others(88): Show |
94 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.874-254G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011414 | |||||||
| chr19:3011519 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.874-359C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011519 | |||||||
| chr19:3011529 | C | CA | 17 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0032 others(14): Show |
20 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.874-370dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011529 | |||||||
| chr19:3011529 | CA | C | 102 | a0001c0001t0001g0056 a0001c0001t0001g0083 a0001c0001t0001g0100 others(99): Show |
105 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.874-370delT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011529 | |||||||
| chr19:3011567 | A | G | 92 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0203 others(89): Show |
95 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.874-407T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011567 | |||||||
| chr19:3011599 | C | A | 1 | a0004c0021t0001g0283 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.874-439G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011599 | |||||||
| chr19:3011606 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.874-446A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011606 | |||||||
| chr19:3011621 | C | T | 2 | a0001c0005t0001g0119 a0001c0005t0002g0344 |
2 | HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.874-461G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011621 | |||||||
| chr19:3011662 | G | A | 92 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0203 others(89): Show |
95 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.874-502C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011662 | |||||||
| chr19:3011749 | C | A | 6 | a0001c0005t0001g0119 a0001c0005t0002g0234 a0001c0005t0002g0235 others(3): Show |
6 | HG02615.hp1 HG02622.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.874-589G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011749 | |||||||
| chr19:3011777 | G | C | 1 | a0001c0001t0001g0110 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.874-617C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011777 | |||||||
| chr19:3011811 | T | C | 1 | a0001c0001t0001g0316 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.874-651A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011811 | |||||||
| chr19:3011952 | C | G | 2 | a0001c0001t0002g0062 a0001c0001t0002g0165 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.874-792G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3011952 | |||||||
| chr19:3012107 | G | A | 97 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0203 others(94): Show |
100 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.874-947C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012107 | |||||||
| chr19:3012240 | G | A | 21 | a0001c0001t0001g0014 a0001c0001t0001g0083 a0001c0001t0001g0246 others(18): Show |
26 | HG00438.hp2 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.874-1080C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012240 | |||||||
| chr19:3012261 | A | AAAAC | 97 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0203 others(94): Show |
100 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.874-1105_874-1102d others(6): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012261 | |||||||
| chr19:3012314 | C | T | 2 | a0001c0002t0001g0340 a0001c0005t0001g0119 |
2 | HG01255.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.874-1154G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012314 | |||||||
| chr19:3012328 | G | A | 4 | a0001c0001t0001g0221 a0001c0001t0001g0347 a0001c0001t0002g0285 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.874-1168C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012328 | |||||||
| chr19:3012365 | G | A | 1 | a0001c0016t0001g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.874-1205C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012365 | |||||||
| chr19:3012450 | C | T | 1 | a0001c0001t0002g0199 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.873+1219G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012450 | |||||||
| chr19:3012515 | C | A | 1 | a0001c0002t0001g0078 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.873+1154G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012515 | |||||||
| chr19:3012528 | T | C | 101 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0203 others(98): Show |
106 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.873+1141A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012528 | |||||||
| chr19:3012559 | A | G | 16 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0032 others(13): Show |
19 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.873+1110T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012559 | |||||||
| chr19:3012649 | A | C | 1 | a0001c0001t0001g0209 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.873+1020T>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012649 | |||||||
| chr19:3012668 | C | A | 1 | a0001c0001t0001g0374 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.873+1001G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012668 | |||||||
| chr19:3012748 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.873+921C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012748 | |||||||
| chr19:3012760 | C | T | 7 | a0001c0001t0001g0374 a0001c0001t0004g0002 a0001c0001t0004g0021 others(4): Show |
9 | HG01891.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.873+909G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012760 | |||||||
| chr19:3012885 | G | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0032 others(12): Show |
18 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.873+784C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012885 | |||||||
| chr19:3012892 | C | T | 13 | a0001c0001t0001g0353 a0001c0001t0001g0374 a0001c0001t0002g0034 others(10): Show |
15 | HG01074.hp2 HG01255.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.873+777G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012892 | |||||||
| chr19:3012916 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.873+753G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012916 | |||||||
| chr19:3012940 | A | G | 3 | a0001c0003t0001g0348 a0001c0003t0002g0247 a0001c0003t0002g0248 |
3 | HG02258.hp1 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.873+729T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012940 | |||||||
| chr19:3012971 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.873+698C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3012971 | |||||||
| chr19:3013020 | G | A | 7 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
7 | HG02572.hp2 HG02647.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.873+649C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013020 | |||||||
| chr19:3013060 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.873+609G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013060 | |||||||
| chr19:3013112 | G | C | 1 | a0001c0020t0001g0373 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.873+557C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013112 | |||||||
| chr19:3013173 | G | A | 1 | a0001c0003t0002g0249 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.873+496C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013173 | |||||||
| chr19:3013220 | G | T | 6 | a0001c0001t0001g0353 a0001c0001t0002g0034 a0001c0001t0002g0037 others(3): Show |
6 | HG01074.hp2 HG01255.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.873+449C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013220 | |||||||
| chr19:3013229 | A | G | 155 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0014 others(152): Show |
168 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.873+440T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013229 | |||||||
| chr19:3013288 | G | A | 1 | a0004c0021t0001g0283 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.873+381C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013288 | |||||||
| chr19:3013289 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.873+380C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013289 | |||||||
| chr19:3013376 | A | G | 104 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(101): Show |
110 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.873+293T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013376 | |||||||
| chr19:3013523 | T | TA | 5 | a0001c0001t0001g0050 a0001c0001t0001g0065 a0001c0001t0001g0281 others(2): Show |
7 | HG01891.hp2 HG02818.hp2 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.873+145dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013523 | |||||||
| chr19:3013538 | A | C | 4 | a0001c0001t0001g0115 a0001c0001t0001g0147 a0001c0001t0001g0158 others(1): Show |
4 | HG02027.hp2 NA18953.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.873+131T>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013538 | |||||||
| chr19:3013551 | A | G | 1 | a0001c0006t0002g0361 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.873+118T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013551 | |||||||
| chr19:3013618 | G | A | 172 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(169): Show |
187 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(184): Show |
intron_variant | MODIFIER | c.873+51C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013618 | |||||||
| chr19:3013625 | C | T | 2 | a0001c0001t0001g0374 a0001c0003t0001g0348 |
2 | HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.873+44G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013625 | |||||||
| chr19:3013626 | G | A | 17 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0080 others(14): Show |
19 | HG00609.hp2 HG02109.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.873+43C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 11/19 | chr19 | 3013626 | |||||||
| chr19:3013948 | G | A | 3 | a0001c0001t0001g0347 a0001c0001t0002g0285 a0001c0002t0001g0364 |
3 | HG02280.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.724-130C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 10/19 | chr19 | 3013948 | |||||||
| chr19:3013973 | T | A | 125 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0032 others(122): Show |
132 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.724-155A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 10/19 | chr19 | 3013973 | |||||||
| chr19:3013988 | A | AT | 16 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0032 others(13): Show |
19 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.724-171dupA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 10/19 | chr19 | 3013988 | |||||||
| chr19:3013988 | AT | A | 200 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(197): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.724-171delA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 10/19 | chr19 | 3013988 | |||||||
| chr19:3014015 | G | A | 2 | a0001c0001t0005g0029 a0001c0002t0001g0078 |
2 | HG03710.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.724-197C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 10/19 | chr19 | 3014015 | |||||||
| chr19:3014275 | T | C | 6 | a0001c0001t0001g0353 a0001c0001t0002g0034 a0001c0001t0002g0037 others(3): Show |
6 | HG01074.hp2 HG01255.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.723+295A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 10/19 | chr19 | 3014275 | |||||||
| chr19:3014428 | C | T | 2 | a0001c0001t0002g0375 a0001c0001t0002g0376 |
2 | HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.723+142G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 10/19 | chr19 | 3014428 | |||||||
| chr19:3014433 | C | T | 1 | a0001c0008t0002g0371 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.723+137G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 10/19 | chr19 | 3014433 | |||||||
| chr19:3014557 | C | T | 1 | a0001c0009t0001g0039 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.723+13G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 10/19 | chr19 | 3014557 | |||||||
| chr19:3014641 | A | G | 138 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0032 others(135): Show |
150 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.679-27T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3014641 | |||||||
| chr19:3014649 | C | A | 168 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.679-35G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3014649 | |||||||
| chr19:3014666 | A | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0202 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.679-52T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3014666 | |||||||
| chr19:3014677 | G | A | 5 | a0001c0001t0001g0168 a0001c0001t0001g0333 a0001c0001t0001g0337 others(2): Show |
5 | HG01168.hp2 HG01361.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.679-63C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3014677 | |||||||
| chr19:3014868 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.679-254A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3014868 | |||||||
| chr19:3014875 | C | G | 1 | a0001c0001t0001g0035 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.679-261G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3014875 | |||||||
| chr19:3015022 | T | TAATA | 4 | a0001c0003t0002g0247 a0001c0003t0002g0248 a0001c0003t0002g0249 others(1): Show |
4 | HG02258.hp1 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.679-412_679-409dup others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015022 | |||||||
| chr19:3015058 | C | CA | 79 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0040 others(76): Show |
85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.679-445dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015058 | |||||||
| chr19:3015058 | C | CAA | 95 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0122 others(92): Show |
98 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.679-446_679-445dup others(2): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015058 | |||||||
| chr19:3015058 | CAA | C | 168 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.679-446_679-445del others(2): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015058 | |||||||
| chr19:3015058 | CAAA | C | 10 | a0001c0001t0001g0014 a0001c0001t0001g0083 a0001c0001t0001g0084 others(7): Show |
11 | HG00738.hp2 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.679-447_679-445del others(3): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015058 | |||||||
| chr19:3015152 | C | T | 1 | a0001c0002t0001g0340 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.678+501G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015152 | |||||||
| chr19:3015285 | T | C | 1 | a0001c0001t0002g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.678+368A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015285 | |||||||
| chr19:3015453 | C | T | 1 | a0002c0011t0001g0072 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.678+200G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015453 | |||||||
| chr19:3015483 | C | A | 6 | a0001c0001t0001g0353 a0001c0001t0002g0034 a0001c0001t0002g0037 others(3): Show |
6 | HG01074.hp2 HG01255.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.678+170G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015483 | |||||||
| chr19:3015517 | C | T | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.678+136G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015517 | |||||||
| chr19:3015547 | C | T | 6 | a0001c0001t0001g0353 a0001c0001t0002g0034 a0001c0001t0002g0037 others(3): Show |
6 | HG01074.hp2 HG01255.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.678+106G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015547 | |||||||
| chr19:3015548 | G | A | 1 | a0001c0016t0001g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.678+105C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 9/19 | chr19 | 3015548 | |||||||
| chr19:3015870 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0319 |
2 | NA18945.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.571-110G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3015870 | |||||||
| chr19:3015905 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0093 |
2 | HG00733.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.571-145G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3015905 | |||||||
| chr19:3015939 | CTGTTT | C | 6 | a0001c0001t0001g0353 a0001c0001t0002g0034 a0001c0001t0002g0037 others(3): Show |
6 | HG01074.hp2 HG01255.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-184_571-180del others(5): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3015939 | |||||||
| chr19:3016054 | A | G | 5 | a0001c0005t0001g0119 a0001c0005t0002g0234 a0001c0005t0002g0344 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-294T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016054 | |||||||
| chr19:3016208 | T | C | 1 | a0001c0003t0001g0348 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.571-448A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016208 | |||||||
| chr19:3016419 | C | CA | 94 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0056 others(91): Show |
97 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.571-660dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016419 | |||||||
| chr19:3016419 | C | CAA | 144 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(141): Show |
155 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.571-661_571-660dup others(2): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016419 | |||||||
| chr19:3016419 | C | CAAA | 30 | a0001c0001t0001g0046 a0001c0001t0001g0050 a0001c0001t0001g0054 others(27): Show |
30 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.571-662_571-660dup others(3): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016419 | |||||||
| chr19:3016419 | CA | C | 18 | a0001c0001t0001g0265 a0001c0001t0001g0353 a0001c0001t0002g0034 others(15): Show |
19 | HG00738.hp1 HG01069.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.571-660delT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016419 | |||||||
| chr19:3016419 | CAA | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0032 others(17): Show |
23 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.571-661_571-660del others(2): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016419 | |||||||
| chr19:3016504 | C | T | 1 | a0001c0001t0002g0328 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.571-744G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016504 | |||||||
| chr19:3016589 | CA | C | 310 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(307): Show |
327 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.571-830delT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016589 | |||||||
| chr19:3016589 | CAA | C | 45 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0032 others(42): Show |
49 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.571-831_571-830del others(2): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016589 | |||||||
| chr19:3016589 | CAAA | C | 8 | a0001c0001t0001g0014 a0001c0001t0001g0051 a0001c0001t0001g0074 others(5): Show |
9 | HG00639.hp1 HG00738.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.571-832_571-830del others(3): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016589 | |||||||
| chr19:3016707 | G | A | 6 | a0001c0005t0001g0119 a0001c0005t0002g0234 a0001c0005t0002g0235 others(3): Show |
6 | HG02615.hp1 HG02622.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-947C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016707 | |||||||
| chr19:3016715 | G | T | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 |
3 | HG00741.hp2 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.571-955C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016715 | |||||||
| chr19:3016725 | A | G | 139 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0032 others(136): Show |
149 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.571-965T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016725 | |||||||
| chr19:3016793 | T | C | 2 | a0001c0005t0001g0119 a0001c0005t0002g0235 |
2 | HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.571-1033A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016793 | |||||||
| chr19:3016879 | C | T | 7 | a0001c0001t0001g0353 a0001c0001t0002g0034 a0001c0001t0002g0037 others(4): Show |
7 | HG01074.hp2 HG01255.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.570+961G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016879 | |||||||
| chr19:3016900 | T | A | 7 | a0001c0001t0001g0353 a0001c0001t0002g0034 a0001c0001t0002g0037 others(4): Show |
7 | HG01074.hp2 HG01255.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.570+940A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016900 | |||||||
| chr19:3016923 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.570+917G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016923 | |||||||
| chr19:3016935 | C | A | 1 | a0001c0018t0001g0368 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.570+905G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016935 | |||||||
| chr19:3016954 | T | G | 77 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0203 others(74): Show |
80 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.570+886A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3016954 | |||||||
| chr19:3017010 | T | C | 1 | a0001c0002t0001g0200 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.570+830A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017010 | |||||||
| chr19:3017049 | G | GTTATAGG others(32): Show |
41 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0032 others(38): Show |
47 | HG00323.hp2 HG00735.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.570+790_570+791ins others(39): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017049 | |||||||
| chr19:3017079 | C | G | 1 | a0001c0002t0001g0174 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.570+761G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017079 | |||||||
| chr19:3017143 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.570+697A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017143 | |||||||
| chr19:3017160 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.570+680G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017160 | |||||||
| chr19:3017195 | T | TGGTGCAA others(9): Show |
2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG00642.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.570+629_570+644dup others(16): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017195 | |||||||
| chr19:3017232 | GGTC | G | 3 | a0001c0001t0001g0374 a0001c0008t0001g0362 a0001c0008t0002g0371 |
3 | HG02109.hp2 HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.570+605_570+607del others(3): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017232 | |||||||
| chr19:3017241 | G | A | 1 | a0001c0002t0001g0047 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.570+599C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017241 | |||||||
| chr19:3017241 | G | GA | 160 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0032 others(157): Show |
172 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(169): Show |
intron_variant | MODIFIER | c.570+598dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017241 | |||||||
| chr19:3017297 | T | C | 3 | a0001c0001t0002g0331 a0001c0001t0004g0002 a0001c0001t0004g0021 |
5 | HG01891.hp2 HG02818.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+543A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017297 | |||||||
| chr19:3017317 | T | C | 28 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0032 others(25): Show |
31 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.570+523A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017317 | |||||||
| chr19:3017432 | G | GT | 21 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0070 others(18): Show |
21 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.570+407dupA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017432 | |||||||
| chr19:3017439 | T | C | 1 | a0001c0002t0001g0126 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.570+401A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017439 | |||||||
| chr19:3017444 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.570+396G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017444 | |||||||
| chr19:3017452 | C | CT | 50 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0035 others(47): Show |
56 | HG00140.hp1 HG00323.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.570+387dupA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017452 | |||||||
| chr19:3017452 | C | CTT | 37 | a0001c0001t0001g0044 a0001c0001t0001g0056 a0001c0001t0001g0066 others(34): Show |
39 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.570+386_570+387dup others(2): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017452 | |||||||
| chr19:3017452 | C | CTTT | 74 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0016 others(71): Show |
79 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.570+385_570+387dup others(3): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017452 | |||||||
| chr19:3017452 | CT | C | 6 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0001t0001g0228 others(3): Show |
6 | HG01099.hp2 HG01256.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+387delA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017452 | |||||||
| chr19:3017483 | C | G | 2 | a0001c0001t0001g0195 a0001c0001t0001g0242 |
2 | HG03017.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.570+357G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017483 | |||||||
| chr19:3017514 | G | A | 1 | a0001c0001t0002g0199 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.570+326C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017514 | |||||||
| chr19:3017522 | C | T | 1 | a0001c0016t0001g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.570+318G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017522 | |||||||
| chr19:3017607 | C | T | 5 | a0001c0001t0001g0054 a0001c0001t0001g0096 a0001c0001t0001g0137 others(2): Show |
5 | NA18747.hp1 NA18747.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+233G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017607 | |||||||
| chr19:3017615 | C | T | 165 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0014 others(162): Show |
178 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.570+225G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017615 | |||||||
| chr19:3017624 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0372 |
2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.570+216C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017624 | |||||||
| chr19:3017818 | T | C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG00642.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.570+22A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017818 | |||||||
| chr19:3017822 | A | G | 10 | a0001c0001t0001g0209 a0001c0001t0001g0307 a0001c0002t0001g0013 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.570+18T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017822 | |||||||
| chr19:3017826 | T | C | 2 | a0001c0002t0001g0364 a0001c0003t0001g0348 |
2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.570+14A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 8/19 | chr19 | 3017826 | |||||||
| chr19:3017890 | G | C | 3 | a0001c0001t0001g0284 a0001c0001t0002g0062 a0001c0001t0002g0165 |
3 | HG01167.hp2 HG01169.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.551-31C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3017890 | |||||||
| chr19:3017920 | C | T | 1 | a0001c0001t0001g0354 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.551-61G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3017920 | |||||||
| chr19:3017931 | G | A | 22 | a0001c0001t0001g0014 a0001c0001t0001g0203 a0001c0001t0001g0251 others(19): Show |
23 | HG00738.hp2 HG02145.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.551-72C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3017931 | |||||||
| chr19:3017955 | CCCCCCGC others(8): Show |
C | 1 | a0001c0024t0001g0071 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.551-111_551-97delT others(14): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3017955 | |||||||
| chr19:3017958 | C | T | 2 | a0001c0001t0001g0066 a0001c0002t0001g0078 |
2 | HG03704.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.551-99G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3017958 | |||||||
| chr19:3017960 | C | T | 26 | a0001c0001t0001g0014 a0001c0001t0001g0203 a0001c0001t0001g0221 others(23): Show |
27 | HG00738.hp2 HG02145.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.551-101G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3017960 | |||||||
| chr19:3017961 | G | A | 24 | a0001c0001t0001g0032 a0001c0001t0001g0052 a0001c0001t0001g0080 others(21): Show |
27 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.551-102C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3017961 | |||||||
| chr19:3017965 | C | T | 11 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0070 others(8): Show |
12 | HG00280.hp2 HG00323.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.551-106G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3017965 | |||||||
| chr19:3017978 | CAG | C | 19 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0074 others(16): Show |
19 | HG00639.hp1 HG00639.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.551-121_551-120del others(2): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3017978 | |||||||
| chr19:3018085 | C | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0052 others(4): Show |
10 | HG01109.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.551-226G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018085 | |||||||
| chr19:3018164 | C | A | 7 | a0001c0001t0001g0016 a0001c0001t0001g0242 a0001c0001t0002g0034 others(4): Show |
8 | HG01257.hp1 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.551-305G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018164 | |||||||
| chr19:3018233 | G | C | 126 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(123): Show |
137 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.551-374C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018233 | |||||||
| chr19:3018257 | G | A | 1 | a0001c0006t0001g0370 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.551-398C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018257 | |||||||
| chr19:3018295 | C | CATTT | 13 | a0001c0001t0001g0096 a0001c0001t0001g0120 a0001c0001t0001g0122 others(10): Show |
13 | HG00280.hp1 HG01168.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.551-440_551-437dup others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018295 | |||||||
| chr19:3018371 | C | G | 1 | a0001c0001t0001g0077 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.551-512G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018371 | |||||||
| chr19:3018485 | G | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0052 others(11): Show |
17 | HG01109.hp2 HG01891.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.551-626C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018485 | |||||||
| chr19:3018524 | C | G | 1 | a0001c0005t0001g0119 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.551-665G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018524 | |||||||
| chr19:3018653 | C | T | 1 | a0001c0005t0001g0119 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.550+630G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018653 | |||||||
| chr19:3018727 | G | A | 1 | a0001c0002t0001g0346 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.550+556C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018727 | |||||||
| chr19:3018742 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.550+541C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018742 | |||||||
| chr19:3018763 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.550+520G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018763 | |||||||
| chr19:3018837 | C | G | 1 | a0001c0001t0001g0335 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.550+446G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018837 | |||||||
| chr19:3018838 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.550+445C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018838 | |||||||
| chr19:3018899 | T | A | 1 | a0009c0019t0001g0181 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.550+384A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3018899 | |||||||
| chr19:3019087 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.550+196C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3019087 | |||||||
| chr19:3019095 | G | A | 1 | a0001c0001t0001g0374 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.550+188C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3019095 | |||||||
| chr19:3019125 | T | G | 6 | a0001c0001t0001g0372 a0001c0001t0004g0002 a0001c0001t0004g0019 others(3): Show |
8 | HG01891.hp2 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.550+158A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3019125 | |||||||
| chr19:3019135 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.550+148G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3019135 | |||||||
| chr19:3019268 | G | A | 1 | a0001c0001t0001g0359 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.550+15C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 7/19 | chr19 | 3019268 | |||||||
| chr19:3019490 | G | A | 1 | a0001c0010t0001g0224 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.370-27C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 6/19 | chr19 | 3019490 | |||||||
| chr19:3019499 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.370-36C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 6/19 | chr19 | 3019499 | |||||||
| chr19:3019539 | A | G | 1 | a0001c0013t0001g0349 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.370-76T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 6/19 | chr19 | 3019539 | |||||||
| chr19:3019662 | G | A | 31 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0033 others(28): Show |
34 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.369+37C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 6/19 | chr19 | 3019662 | |||||||
| chr19:3019857 | G | A | 1 | a0001c0002t0001g0295 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.295-84C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3019857 | |||||||
| chr19:3019901 | T | C | 8 | a0001c0001t0001g0220 a0001c0001t0001g0333 a0001c0001t0001g0334 others(5): Show |
8 | HG00280.hp1 HG01168.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.295-128A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3019901 | |||||||
| chr19:3019988 | T | G | 96 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(93): Show |
103 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.295-215A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3019988 | |||||||
| chr19:3019994 | C | T | 1 | a0001c0001t0001g0374 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.295-221G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3019994 | |||||||
| chr19:3020008 | C | T | 8 | a0001c0001t0001g0220 a0001c0001t0001g0333 a0001c0001t0001g0334 others(5): Show |
8 | HG00280.hp1 HG01168.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.295-235G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020008 | |||||||
| chr19:3020116 | A | T | 48 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0203 others(45): Show |
50 | HG00280.hp1 HG00738.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.295-343T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020116 | |||||||
| chr19:3020191 | G | A | 1 | a0001c0010t0001g0224 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.295-418C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020191 | |||||||
| chr19:3020230 | T | C | 198 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(195): Show |
215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.295-457A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020230 | |||||||
| chr19:3020354 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.295-581G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020354 | |||||||
| chr19:3020377 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.295-604G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020377 | |||||||
| chr19:3020401 | A | G | 1 | a0001c0024t0001g0071 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.295-628T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020401 | |||||||
| chr19:3020543 | C | A | 1 | a0001c0002t0001g0260 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.295-770G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020543 | |||||||
| chr19:3020592 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.295-819A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020592 | |||||||
| chr19:3020616 | C | T | 7 | a0001c0001t0001g0236 a0001c0001t0003g0022 a0001c0002t0003g0023 others(4): Show |
7 | HG00738.hp1 HG01069.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.295-843G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020616 | |||||||
| chr19:3020617 | G | A | 2 | a0001c0001t0001g0096 a0001c0002t0001g0183 |
2 | HG00558.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.295-844C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020617 | |||||||
| chr19:3020644 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.295-871A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020644 | |||||||
| chr19:3020649 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0184 a0001c0001t0001g0196 |
3 | NA18939.hp1 NA18986.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.295-876C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020649 | |||||||
| chr19:3020680 | A | T | 50 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0203 others(47): Show |
52 | HG00280.hp1 HG00738.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.295-907T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020680 | |||||||
| chr19:3020693 | A | G | 198 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(195): Show |
215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.295-920T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020693 | |||||||
| chr19:3020784 | G | A | 1 | a0001c0001t0002g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.295-1011C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020784 | |||||||
| chr19:3020881 | T | C | 3 | a0001c0005t0002g0234 a0001c0005t0002g0235 a0001c0005t0011g0378 |
3 | HG02622.hp1 HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.295-1108A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3020881 | |||||||
| chr19:3021088 | C | CA | 26 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(23): Show |
26 | HG00621.hp2 HG01243.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.295-1316dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021088 | |||||||
| chr19:3021088 | CA | C | 39 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(36): Show |
41 | HG01255.hp2 HG02055.hp2 HG02273.hp1 others(38): Show |
intron_variant | MODIFIER | c.295-1316delT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021088 | |||||||
| chr19:3021088 | CAA | C | 10 | a0001c0001t0001g0033 a0001c0001t0001g0250 a0001c0001t0001g0372 others(7): Show |
12 | HG00140.hp2 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.295-1317_295-1316d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021088 | |||||||
| chr19:3021090 | A | AAC | 12 | a0001c0001t0001g0014 a0001c0001t0001g0217 a0001c0001t0001g0223 others(9): Show |
13 | HG00738.hp2 HG01943.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.295-1318_295-1317i others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021090 | |||||||
| chr19:3021111 | AAAAG | A | 84 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(81): Show |
92 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.295-1342_295-1339d others(6): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021111 | |||||||
| chr19:3021112 | AAAG | A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0221 a0001c0001t0001g0279 others(9): Show |
12 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.295-1342_295-1340d others(5): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021112 | |||||||
| chr19:3021113 | AAG | A | 6 | a0001c0001t0001g0265 a0001c0001t0002g0329 a0001c0001t0002g0375 others(3): Show |
6 | HG02258.hp2 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-1342_295-1341d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021113 | |||||||
| chr19:3021114 | A | AAAAAAAA others(5): Show |
1 | a0001c0002t0003g0026 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.295-1342_295-1341i others(14): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021114 | |||||||
| chr19:3021114 | A | AAAAAAAA others(6): Show |
2 | a0001c0001t0001g0236 a0001c0002t0003g0023 |
2 | HG01928.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.295-1342_295-1341i others(15): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021114 | |||||||
| chr19:3021114 | A | AAAAAAAA others(4): Show |
3 | a0001c0002t0003g0024 a0001c0002t0003g0025 a0001c0002t0003g0030 |
3 | HG00738.hp1 HG01069.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.295-1342_295-1341i others(13): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021114 | |||||||
| chr19:3021114 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0003g0027 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.295-1342_295-1341i others(14): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021114 | |||||||
| chr19:3021114 | A | AG | 22 | a0001c0001t0001g0012 a0001c0001t0001g0132 a0001c0001t0001g0135 others(19): Show |
23 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.295-1342dupC | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021114 | |||||||
| chr19:3021114 | A | G | 18 | a0001c0001t0001g0058 a0001c0001t0001g0116 a0001c0001t0001g0149 others(15): Show |
18 | HG00544.hp2 HG00609.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.295-1341T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021114 | |||||||
| chr19:3021114 | AG | A | 32 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(29): Show |
33 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.295-1342delC | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021114 | |||||||
| chr19:3021115 | G | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0074 others(8): Show |
11 | HG01109.hp1 HG01109.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.295-1342C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021115 | |||||||
| chr19:3021116 | G | C | 1 | a0001c0002t0001g0197 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.295-1343C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021116 | |||||||
| chr19:3021118 | G | T | 86 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(83): Show |
93 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.295-1345C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021118 | |||||||
| chr19:3021122 | G | C | 2 | a0001c0003t0001g0348 a0001c0013t0001g0349 |
2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.295-1349C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021122 | |||||||
| chr19:3021122 | G | GT | 17 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0217 others(14): Show |
18 | HG00738.hp2 HG00741.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.295-1350_295-1349i others(3): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021122 | |||||||
| chr19:3021123 | G | T | 5 | a0001c0001t0001g0032 a0001c0001t0002g0363 a0001c0002t0001g0346 others(2): Show |
5 | HG01891.hp1 HG02109.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.295-1350C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021123 | |||||||
| chr19:3021128 | T | C | 48 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0203 others(45): Show |
50 | HG00280.hp1 HG00738.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.295-1355A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021128 | |||||||
| chr19:3021144 | C | G | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.295-1371G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021144 | |||||||
| chr19:3021235 | T | C | 1 | a0001c0001t0001g0213 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.295-1462A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021235 | |||||||
| chr19:3021338 | G | C | 17 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0217 others(14): Show |
18 | HG00738.hp2 HG00741.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.295-1565C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021338 | |||||||
| chr19:3021359 | C | T | 1 | a0001c0002t0001g0346 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.295-1586G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021359 | |||||||
| chr19:3021360 | G | A | 86 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(83): Show |
93 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.295-1587C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021360 | |||||||
| chr19:3021436 | T | A | 1 | a0001c0001t0001g0244 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.295-1663A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021436 | |||||||
| chr19:3021534 | A | G | 1 | a0001c0016t0001g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.295-1761T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021534 | |||||||
| chr19:3021548 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.295-1775G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021548 | |||||||
| chr19:3021571 | T | C | 1 | a0001c0001t0001g0307 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.295-1798A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021571 | |||||||
| chr19:3021606 | G | A | 3 | a0001c0001t0001g0067 a0001c0002t0001g0198 a0001c0024t0001g0071 |
3 | NA18961.hp1 NA19074.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.295-1833C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021606 | |||||||
| chr19:3021652 | G | A | 2 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
2 | NA18944.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.295-1879C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021652 | |||||||
| chr19:3021771 | C | T | 9 | a0001c0001t0001g0236 a0001c0001t0003g0022 a0001c0001t0003g0027 others(6): Show |
9 | HG00738.hp1 HG01069.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.295-1998G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021771 | |||||||
| chr19:3021798 | G | C | 43 | a0001c0001t0001g0014 a0001c0001t0001g0217 a0001c0001t0001g0220 others(40): Show |
45 | HG00280.hp1 HG00738.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.295-2025C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021798 | |||||||
| chr19:3021835 | A | T | 2 | a0001c0001t0002g0375 a0001c0001t0002g0376 |
2 | HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.295-2062T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021835 | |||||||
| chr19:3021926 | T | C | 10 | a0001c0001t0001g0350 a0001c0001t0001g0351 a0001c0001t0001g0352 others(7): Show |
11 | HG01123.hp1 HG01243.hp2 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.295-2153A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021926 | |||||||
| chr19:3021931 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.295-2158G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021931 | |||||||
| chr19:3021968 | T | C | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.295-2195A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021968 | |||||||
| chr19:3021988 | G | A | 1 | a0001c0001t0002g0363 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.295-2215C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3021988 | |||||||
| chr19:3022053 | A | G | 46 | a0001c0001t0001g0014 a0001c0001t0001g0217 a0001c0001t0001g0220 others(43): Show |
48 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.295-2280T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022053 | |||||||
| chr19:3022067 | A | G | 61 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0051 others(58): Show |
64 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.295-2294T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022067 | |||||||
| chr19:3022109 | C | T | 15 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0052 others(12): Show |
20 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.295-2336G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022109 | |||||||
| chr19:3022176 | G | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0033 others(13): Show |
19 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.295-2403C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022176 | |||||||
| chr19:3022288 | G | A | 1 | a0001c0016t0001g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.295-2515C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022288 | |||||||
| chr19:3022349 | A | AC | 11 | a0001c0001t0001g0046 a0001c0001t0001g0094 a0001c0001t0001g0096 others(8): Show |
11 | HG00621.hp2 HG00741.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.295-2577dupG | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022349 | |||||||
| chr19:3022356 | C | A | 98 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
108 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.295-2583G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022356 | |||||||
| chr19:3022434 | T | C | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(107): Show |
120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.294+2586A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022434 | |||||||
| chr19:3022477 | T | C | 126 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0017 others(123): Show |
135 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.294+2543A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022477 | |||||||
| chr19:3022542 | A | T | 21 | a0001c0001t0001g0093 a0001c0001t0001g0221 a0001c0001t0001g0269 others(18): Show |
22 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.294+2478T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022542 | |||||||
| chr19:3022738 | G | A | 1 | a0001c0002t0001g0346 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.294+2282C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022738 | |||||||
| chr19:3022987 | G | C | 8 | a0001c0001t0001g0299 a0001c0001t0001g0327 a0001c0001t0002g0300 others(5): Show |
8 | HG02055.hp1 HG02559.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.294+2033C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3022987 | |||||||
| chr19:3023054 | A | ATCT | 30 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0014 others(27): Show |
34 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.294+1963_294+1965d others(5): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023054 | |||||||
| chr19:3023057 | T | TTC | 39 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0223 others(36): Show |
41 | HG00639.hp2 HG00738.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.294+1962_294+1963i others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023057 | |||||||
| chr19:3023059 | T | C | 121 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(118): Show |
132 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.294+1961A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023059 | |||||||
| chr19:3023099 | G | A | 3 | a0001c0006t0001g0370 a0001c0006t0002g0232 a0001c0006t0002g0361 |
3 | HG02647.hp1 HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.294+1921C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023099 | |||||||
| chr19:3023120 | A | T | 130 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(127): Show |
138 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.294+1900T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023120 | |||||||
| chr19:3023145 | C | T | 7 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.294+1875G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023145 | |||||||
| chr19:3023146 | C | A | 1 | a0001c0002t0001g0356 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.294+1874G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023146 | |||||||
| chr19:3023147 | C | G | 17 | a0001c0001t0001g0220 a0001c0001t0001g0333 a0001c0001t0001g0334 others(14): Show |
17 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.294+1873G>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023147 | |||||||
| chr19:3023273 | T | C | 1 | a0001c0001t0001g0263 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.294+1747A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023273 | |||||||
| chr19:3023276 | C | A | 5 | a0001c0001t0004g0002 a0001c0001t0004g0019 a0001c0001t0004g0021 others(2): Show |
7 | HG01891.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.294+1744G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023276 | |||||||
| chr19:3023276 | C | T | 155 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.294+1744G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023276 | |||||||
| chr19:3023370 | G | A | 1 | a0001c0006t0002g0232 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.294+1650C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023370 | |||||||
| chr19:3023537 | T | C | 1 | a0001c0002t0001g0364 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.294+1483A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023537 | |||||||
| chr19:3023552 | A | G | 133 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(130): Show |
143 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.294+1468T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023552 | |||||||
| chr19:3023566 | C | T | 17 | a0001c0001t0001g0220 a0001c0001t0001g0333 a0001c0001t0001g0334 others(14): Show |
17 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.294+1454G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023566 | |||||||
| chr19:3023672 | T | C | 117 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(114): Show |
125 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.294+1348A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023672 | |||||||
| chr19:3023683 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0202 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.294+1337C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023683 | |||||||
| chr19:3023690 | C | T | 8 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0002t0001g0085 others(5): Show |
8 | HG02293.hp2 NA18944.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.294+1330G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023690 | |||||||
| chr19:3023753 | G | A | 131 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(128): Show |
139 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.294+1267C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023753 | |||||||
| chr19:3023812 | C | A | 131 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(128): Show |
139 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.294+1208G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023812 | |||||||
| chr19:3023863 | G | A | 114 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(111): Show |
122 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.294+1157C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023863 | |||||||
| chr19:3023873 | CAG | C | 16 | a0001c0001t0001g0236 a0001c0001t0003g0022 a0001c0001t0003g0027 others(13): Show |
18 | HG00738.hp1 HG01069.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.294+1145_294+1146d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023873 | |||||||
| chr19:3023888 | T | TCA | 59 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0032 others(56): Show |
62 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.294+1130_294+1131d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023888 | |||||||
| chr19:3023888 | T | TCACA | 2 | a0001c0001t0001g0014 a0001c0013t0001g0349 |
3 | HG00738.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.294+1128_294+1131d others(6): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023888 | |||||||
| chr19:3023897 | C | T | 1 | a0001c0002t0001g0346 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.294+1123G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023897 | |||||||
| chr19:3023907 | CAAAAGAA others(4): Show |
C | 99 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(96): Show |
106 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.294+1102_294+1112d others(13): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023907 | |||||||
| chr19:3023908 | AAAAGAAA others(2): Show |
A | 15 | a0001c0001t0001g0221 a0001c0001t0001g0350 a0001c0001t0001g0351 others(12): Show |
16 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.294+1103_294+1111d others(11): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023908 | |||||||
| chr19:3023918 | A | C | 15 | a0001c0001t0001g0221 a0001c0001t0001g0350 a0001c0001t0001g0351 others(12): Show |
16 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.294+1102T>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023918 | |||||||
| chr19:3023994 | C | CT | 44 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(41): Show |
51 | HG00323.hp1 HG00639.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.294+1025dupA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023994 | |||||||
| chr19:3023994 | CT | C | 97 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(94): Show |
104 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.294+1025delA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023994 | |||||||
| chr19:3023994 | CTT | C | 7 | a0001c0001t0001g0226 a0001c0001t0001g0255 a0001c0001t0001g0302 others(4): Show |
7 | HG01358.hp1 HG01975.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+1024_294+1025d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3023994 | |||||||
| chr19:3024020 | G | C | 2 | a0001c0003t0001g0348 a0001c0013t0001g0349 |
2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.294+1000C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024020 | |||||||
| chr19:3024052 | G | C | 2 | a0001c0003t0001g0348 a0001c0013t0001g0349 |
2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.294+968C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024052 | |||||||
| chr19:3024053 | C | T | 131 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(128): Show |
139 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.294+967G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024053 | |||||||
| chr19:3024079 | C | T | 100 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(97): Show |
107 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.294+941G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024079 | |||||||
| chr19:3024167 | A | AT | 24 | a0001c0001t0001g0236 a0001c0001t0003g0022 a0001c0001t0003g0027 others(21): Show |
26 | HG00738.hp1 HG01069.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.294+852dupA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024167 | |||||||
| chr19:3024315 | T | C | 182 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.294+705A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024315 | |||||||
| chr19:3024382 | C | A | 2 | a0001c0001t0001g0209 a0001c0002t0001g0013 |
3 | HG02257.hp2 HG03453.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.294+638G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024382 | |||||||
| chr19:3024437 | A | G | 176 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(173): Show |
190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.294+583T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024437 | |||||||
| chr19:3024456 | C | T | 6 | a0001c0001t0001g0343 a0001c0002t0001g0367 a0001c0005t0002g0344 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+564G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024456 | |||||||
| chr19:3024546 | T | C | 5 | a0001c0002t0001g0261 a0001c0002t0001g0309 a0001c0002t0001g0310 others(2): Show |
5 | HG01975.hp1 HG01978.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.294+474A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024546 | |||||||
| chr19:3024599 | G | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0014 others(15): Show |
22 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.294+421C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024599 | |||||||
| chr19:3024626 | G | A | 90 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(87): Show |
97 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.294+394C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024626 | |||||||
| chr19:3024665 | C | CA | 3 | a0001c0006t0001g0370 a0001c0006t0002g0232 a0001c0006t0002g0361 |
3 | HG02647.hp1 HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.294+354_294+355ins others(1): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024665 | |||||||
| chr19:3024751 | G | A | 1 | a0001c0016t0001g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.294+269C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024751 | |||||||
| chr19:3024876 | G | C | 18 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0014 others(15): Show |
22 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.294+144C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024876 | |||||||
| chr19:3024905 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG01358.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.294+115G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024905 | |||||||
| chr19:3024954 | G | A | 1 | a0001c0006t0002g0361 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.294+66C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024954 | |||||||
| chr19:3024979 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.294+41C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 5/19 | chr19 | 3024979 | |||||||
| chr19:3025191 | A | G | 9 | a0001c0001t0001g0343 a0001c0002t0001g0345 a0001c0002t0001g0367 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.232-109T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025191 | |||||||
| chr19:3025269 | T | A | 2 | a0001c0001t0001g0218 a0001c0002t0001g0210 |
2 | NA19012.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.232-187A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025269 | |||||||
| chr19:3025369 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.232-287C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025369 | |||||||
| chr19:3025382 | GGCAGACG others(20): Show |
G | 2 | a0001c0001t0002g0363 a0001c0008t0001g0362 |
2 | HG01891.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.232-327_232-301del others(27): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025382 | |||||||
| chr19:3025434 | C | T | 1 | a0001c0002t0001g0346 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.232-352G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025434 | |||||||
| chr19:3025481 | G | T | 11 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(8): Show |
11 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.232-399C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025481 | |||||||
| chr19:3025659 | C | T | 19 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0014 others(16): Show |
23 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.232-577G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025659 | |||||||
| chr19:3025705 | G | C | 16 | a0001c0001t0001g0018 a0001c0001t0001g0263 a0001c0001t0001g0313 others(13): Show |
17 | HG00558.hp1 HG01934.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.232-623C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025705 | |||||||
| chr19:3025707 | A | G | 49 | a0001c0001t0001g0032 a0001c0001t0001g0221 a0001c0001t0001g0236 others(46): Show |
52 | HG00642.hp2 HG00738.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.232-625T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025707 | |||||||
| chr19:3025806 | G | A | 2 | a0001c0003t0001g0348 a0001c0013t0001g0349 |
2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.232-724C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025806 | |||||||
| chr19:3025817 | A | AG | 49 | a0001c0001t0001g0032 a0001c0001t0001g0221 a0001c0001t0001g0236 others(46): Show |
52 | HG00642.hp2 HG00738.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.232-736dupC | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025817 | |||||||
| chr19:3025823 | G | T | 1 | a0001c0016t0001g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.232-741C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025823 | |||||||
| chr19:3025902 | C | A | 7 | a0001c0001t0001g0343 a0001c0002t0001g0345 a0001c0002t0001g0367 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.232-820G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025902 | |||||||
| chr19:3025920 | G | T | 1 | a0001c0002t0001g0239 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.232-838C>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025920 | |||||||
| chr19:3025997 | C | A | 1 | a0001c0001t0001g0212 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.232-915G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025997 | |||||||
| chr19:3025998 | A | C | 1 | a0001c0001t0001g0212 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.232-916T>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3025998 | |||||||
| chr19:3026010 | T | C | 12 | a0001c0001t0001g0220 a0001c0001t0001g0333 a0001c0001t0001g0334 others(9): Show |
12 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.232-928A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026010 | |||||||
| chr19:3026065 | T | G | 1 | a0001c0001t0001g0016 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.232-983A>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026065 | |||||||
| chr19:3026104 | C | T | 7 | a0001c0001t0001g0343 a0001c0002t0001g0345 a0001c0002t0001g0367 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.232-1022G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026104 | |||||||
| chr19:3026228 | C | A | 13 | a0001c0001t0001g0221 a0001c0001t0001g0350 a0001c0001t0001g0351 others(10): Show |
14 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.232-1146G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026228 | |||||||
| chr19:3026281 | T | C | 10 | a0001c0001t0001g0032 a0001c0001t0001g0372 a0001c0001t0001g0374 others(7): Show |
10 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.232-1199A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026281 | |||||||
| chr19:3026363 | G | A | 1 | a0001c0002t0001g0210 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.232-1281C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026363 | |||||||
| chr19:3026401 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.232-1319A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026401 | |||||||
| chr19:3026403 | A | G | 52 | a0001c0001t0001g0032 a0001c0001t0001g0221 a0001c0001t0001g0236 others(49): Show |
55 | HG00642.hp2 HG00738.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.232-1321T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026403 | |||||||
| chr19:3026452 | AT | A | 9 | a0001c0001t0001g0336 a0001c0001t0001g0337 a0001c0001t0001g0338 others(6): Show |
9 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.232-1371delA | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026452 | |||||||
| chr19:3026454 | T | TAA | 5 | a0001c0001t0001g0032 a0001c0001t0001g0372 a0001c0001t0002g0363 others(2): Show |
5 | HG01891.hp1 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.232-1373_232-1372i others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026454 | |||||||
| chr19:3026454 | TTA | T | 3 | a0001c0001t0001g0220 a0001c0001t0001g0333 a0001c0001t0001g0334 |
3 | HG00280.hp1 HG01168.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.231+1373_232-1373d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026454 | |||||||
| chr19:3026455 | T | A | 11 | a0001c0001t0001g0032 a0001c0001t0001g0246 a0001c0001t0001g0372 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.232-1373A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026455 | |||||||
| chr19:3026455 | T | TA | 12 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0215 others(9): Show |
12 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.231+1373dupT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026455 | |||||||
| chr19:3026455 | TA | T | 54 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0050 others(51): Show |
58 | HG00099.hp1 HG00609.hp1 HG01074.hp1 others(55): Show |
intron_variant | MODIFIER | c.231+1373delT | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026455 | |||||||
| chr19:3026455 | TAA | T | 80 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(77): Show |
89 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.231+1372_231+1373d others(4): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026455 | |||||||
| chr19:3026455 | TAAA | T | 15 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(12): Show |
15 | HG00544.hp1 HG01975.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.231+1371_231+1373d others(5): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026455 | |||||||
| chr19:3026456 | A | T | 1 | a0001c0002t0001g0174 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.231+1373T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026456 | |||||||
| chr19:3026481 | C | T | 1 | a0001c0016t0001g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.231+1348G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026481 | |||||||
| chr19:3026570 | G | GCAGAACC others(13): Show |
5 | a0001c0001t0001g0343 a0001c0002t0001g0345 a0001c0002t0001g0367 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+1239_231+1258d others(22): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026570 | |||||||
| chr19:3026586 | T | TATCTCAG others(33): Show |
9 | a0001c0001t0001g0032 a0001c0001t0001g0374 a0001c0001t0002g0375 others(6): Show |
9 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.231+1242_231+1243i others(42): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026586 | |||||||
| chr19:3026586 | T | TATCTCAG others(53): Show |
4 | a0001c0001t0001g0372 a0001c0001t0002g0363 a0001c0008t0001g0362 others(1): Show |
4 | HG01891.hp1 HG02109.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+1242_231+1243i others(62): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026586 | |||||||
| chr19:3026592 | T | A | 13 | a0001c0001t0001g0032 a0001c0001t0001g0372 a0001c0001t0001g0374 others(10): Show |
13 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.231+1237A>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026592 | |||||||
| chr19:3026592 | TGAACCCT others(13): Show |
T | 109 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(106): Show |
116 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.231+1217_231+1236d others(22): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026592 | |||||||
| chr19:3026596 | C | T | 1 | a0001c0005t0002g0344 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.231+1233G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026596 | |||||||
| chr19:3026606 | A | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0372 a0001c0001t0002g0363 others(2): Show |
5 | HG01891.hp1 HG02109.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+1223T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026606 | |||||||
| chr19:3026650 | G | A | 10 | a0001c0001t0001g0032 a0001c0001t0001g0372 a0001c0001t0001g0374 others(7): Show |
10 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.231+1179C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026650 | |||||||
| chr19:3026812 | G | A | 13 | a0001c0001t0001g0032 a0001c0001t0001g0372 a0001c0001t0001g0374 others(10): Show |
13 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.231+1017C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026812 | |||||||
| chr19:3026868 | C | T | 3 | a0001c0003t0002g0247 a0001c0003t0002g0248 a0001c0003t0002g0249 |
3 | HG02258.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.231+961G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026868 | |||||||
| chr19:3026869 | T | C | 180 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(177): Show |
194 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.231+960A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026869 | |||||||
| chr19:3026921 | C | T | 1 | a0001c0002t0001g0015 | 2 | NA18947.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.231+908G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026921 | |||||||
| chr19:3026926 | GACCTTGA others(93): Show |
G | 6 | a0001c0001t0001g0007 a0001c0001t0001g0045 a0001c0001t0001g0046 others(3): Show |
7 | HG01256.hp2 HG01361.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.231+803_231+902del others(100): Show |
TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026926 | |||||||
| chr19:3026987 | A | G | 34 | a0001c0001t0001g0221 a0001c0001t0001g0236 a0001c0001t0001g0350 others(31): Show |
37 | HG00642.hp2 HG00738.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.231+842T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3026987 | |||||||
| chr19:3027034 | G | A | 1 | a0001c0001t0002g0222 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.231+795C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3027034 | |||||||
| chr19:3027124 | T | C | 14 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0014 others(11): Show |
18 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.231+705A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3027124 | |||||||
| chr19:3027190 | T | C | 1 | a0001c0001t0001g0374 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.231+639A>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3027190 | |||||||
| chr19:3027234 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02080.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.231+595T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3027234 | |||||||
| chr19:3027345 | A | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0033 others(8): Show |
14 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.231+484T>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3027345 | |||||||
| chr19:3027560 | C | T | 19 | a0001c0001t0001g0236 a0001c0001t0003g0022 a0001c0001t0003g0027 others(16): Show |
21 | HG00738.hp1 HG01069.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.231+269G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3027560 | |||||||
| chr19:3027760 | C | A | 1 | a0001c0003t0001g0365 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.231+69G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 4/19 | chr19 | 3027760 | |||||||
| chr19:3028011 | G | A | 1 | a0001c0002t0001g0366 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.187-138C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 3/19 | chr19 | 3028011 | |||||||
| chr19:3028109 | G | A | 2 | a0001c0002t0001g0367 a0001c0018t0001g0368 |
2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.186+210C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 3/19 | chr19 | 3028109 | |||||||
| chr19:3028199 | G | C | 1 | a0001c0001t0001g0223 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.186+120C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 3/19 | chr19 | 3028199 | |||||||
| chr19:3028213 | C | T | 9 | a0001c0001t0001g0372 a0001c0001t0001g0374 a0001c0001t0002g0375 others(6): Show |
9 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.186+106G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 3/19 | chr19 | 3028213 | |||||||
| chr19:3028225 | G | A | 1 | a0001c0001t0001g0369 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.186+94C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 3/19 | chr19 | 3028225 | |||||||
| chr19:3028254 | G | A | 1 | a0001c0006t0001g0370 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.186+65C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 3/19 | chr19 | 3028254 | |||||||
| chr19:3028403 | A | G | 1 | a0001c0001t0002g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.123-21T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 2/19 | chr19 | 3028403 | |||||||
| chr19:3028465 | C | A | 2 | a0001c0001t0001g0372 a0001c0008t0002g0371 |
2 | HG02109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.123-83G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 2/19 | chr19 | 3028465 | |||||||
| chr19:3028574 | C | T | 6 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(3): Show |
6 | HG01358.hp1 HG02602.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+132G>A | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 2/19 | chr19 | 3028574 | |||||||
| chr19:3028604 | C | A | 3 | a0001c0001t0001g0374 a0001c0010t0001g0224 a0001c0020t0001g0373 |
3 | HG02145.hp2 HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.122+102G>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 2/19 | chr19 | 3028604 | |||||||
| chr19:3028821 | G | A | 2 | a0001c0001t0002g0375 a0001c0001t0002g0376 |
2 | HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.25-18C>T | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 1/19 | chr19 | 3028821 | |||||||
| chr19:3028873 | G | C | 162 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(159): Show |
171 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(168): Show |
splice_region_variant&intron_variant | LOW | c.24+8C>G | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 1/19 | chr19 | 3028873 | |||||||
| chr19:3028875 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG02896.hp1 | splice_region_variant&intron_variant | LOW | c.24+6T>C | TLE2 | ENSG00000065717.16 | transcript | ENST00000262953.11 | protein_coding | 1/19 | chr19 | 3028875 |