Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8463 |
| ensemblid | ENSG00000074219.14 |
| hgncid | 11715 |
| symbol | TEAD2 |
| name | TEA domain transcription factor 2 |
| refseq_nuc | NM_001256660.2 |
| refseq_prot | NP_001243589.1 |
| ensembl_nuc | ENST00000593945.6 |
| ensembl_prot | ENSP00000469640.2 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 49340595 |
| end | 49362416 |
| strand | - |
| ver | v1.2 |
| region | chr19:49340595-49362416 |
| region5000 | chr19:49335595-49367416 |
| regionname0 | TEAD2_chr19_49340595_49362416 |
| regionname5000 | TEAD2_chr19_49335595_49367416 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 451 | 342 | 86 | 64 | 148 | 12 | 30 | 106 | TEAD2_chr19_49335595_49367416 | TEAD2 | MGEPR others(446): Show |
chr19 | 49335595 | 49367416 |
| a0002 | 0/0 | 451 | 5 | 0 | 0 | 5 | 0 | 0 | 3 | TEAD2_chr19_49335595_49367416 | TEAD2 | MGEPR others(446): Show |
chr19 | 49335595 | 49367416 |
| a0003 | 0/0 | 451 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | MGEPR others(446): Show |
chr19 | 49335595 | 49367416 |
| a0004 | 0/0 | 451 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | MGEPR others(446): Show |
chr19 | 49335595 | 49367416 |
| a0005 | 0/0 | 455 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | MGEPR others(450): Show |
chr19 | 49335595 | 49367416 |
| a0006 | 0/0 | 451 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | MGEPR others(446): Show |
chr19 | 49335595 | 49367416 |
| a0007 | 0/0 | 451 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | MGEPR others(446): Show |
chr19 | 49335595 | 49367416 |
| a0008 | 0/0 | 451 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | MGEPR others(446): Show |
chr19 | 49335595 | 49367416 |
| a0009 | 0/0 | 56 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | MEAAG others(51): Show |
chr19 | 49335595 | 49367416 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1353 | 341 | 85 | 64 | 148 | 12 | 30 | TEAD2_chr19_49335595_49367416 | TEAD2 | ATGGG others(1348): Show |
chr19 | 49335595 | 49367416 | ||
| a0001c0005 | 0/0 | 1353 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | ATGGG others(1348): Show |
chr19 | 49335595 | 49367416 | ||
| a0002c0002 | 0/0 | 1353 | 5 | 0 | 0 | 5 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | ATGGG others(1348): Show |
chr19 | 49335595 | 49367416 | ||
| a0003c0004 | 0/0 | 1353 | 2 | 2 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | ATGGG others(1348): Show |
chr19 | 49335595 | 49367416 | ||
| a0004c0003 | 0/0 | 1353 | 2 | 2 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | ATGGG others(1348): Show |
chr19 | 49335595 | 49367416 | ||
| a0005c0006 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | ATGGG others(1360): Show |
chr19 | 49335595 | 49367416 | ||
| a0006c0008 | 0/0 | 1353 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | ATGGG others(1348): Show |
chr19 | 49335595 | 49367416 | ||
| a0007c0009 | 0/0 | 1353 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | ATGGG others(1348): Show |
chr19 | 49335595 | 49367416 | ||
| a0008c0007 | 0/0 | 1353 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | ATGGG others(1348): Show |
chr19 | 49335595 | 49367416 | ||
| a0009c0010 | 0/0 | 1353 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | ATTGG others(1348): Show |
chr19 | 49335595 | 49367416 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2175 | 220 | 61 | 49 | 89 | 7 | 13 | TEAD2_chr19_49335595_49367416 | TEAD2 | GCAGC others(2170): Show |
chr19 | 49335595 | 49367416 |
| a0001c0001t0002 | 0/1 | 2176 | 112 | 24 | 15 | 50 | 5 | 17 | TEAD2_chr19_49335595_49367416 | TEAD2 | GCAGC others(2171): Show |
chr19 | 49335595 | 49367416 |
| a0001c0001t0003 | 0/0 | 2176 | 7 | 0 | 0 | 7 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | GCAGC others(2171): Show |
chr19 | 49335595 | 49367416 |
| a0001c0001t0005 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | GCAGC others(2170): Show |
chr19 | 49335595 | 49367416 |
| a0001c0001t0006 | 0/0 | 2162 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | GCAGC others(2157): Show |
chr19 | 49335595 | 49367416 |
| a0001c0005t0001 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | GCAGC others(2170): Show |
chr19 | 49335595 | 49367416 |
| a0002c0002t0001 | 0/0 | 2175 | 5 | 0 | 0 | 5 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | GCAGC others(2170): Show |
chr19 | 49335595 | 49367416 |
| a0003c0004t0001 | 0/0 | 2175 | 2 | 2 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | GCAGC others(2170): Show |
chr19 | 49335595 | 49367416 |
| a0004c0003t0004 | 0/0 | 2175 | 2 | 2 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | GCAGC others(2170): Show |
chr19 | 49335595 | 49367416 |
| a0005c0006t0001 | 0/0 | 2187 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | GCAGC others(2182): Show |
chr19 | 49335595 | 49367416 |
| a0006c0008t0002 | 0/0 | 2176 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | GCAGC others(2171): Show |
chr19 | 49335595 | 49367416 |
| a0007c0009t0001 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | GCAGC others(2170): Show |
chr19 | 49335595 | 49367416 |
| a0008c0007t0002 | 0/0 | 2176 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | GCAGC others(2171): Show |
chr19 | 49335595 | 49367416 |
| a0009c0010t0001 | 0/0 | 2175 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | GCAGC others(2170): Show |
chr19 | 49335595 | 49367416 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 30 | 1 | 11 | 16 | 0 | 2 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0002 | 0/0 | 17 | 4 | 3 | 8 | 1 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0005 | 0/0 | 10 | 9 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 2 | 3 | 2 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0008 | 1/0 | 5 | 0 | 2 | 0 | 2 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0003 | 0/0 | 13 | 2 | 0 | 8 | 1 | 2 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0004 | 0/1 | 11 | 0 | 1 | 3 | 1 | 5 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0006 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0012 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0001t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0001c0005t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0003c0004t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0003c0004t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0004c0003t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0004c0003t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0005c0006t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0006c0008t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0007c0009t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0008c0007t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| a0009c0010t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0136 | EUR | GBR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0152 | EUR | GBR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0153 | EUR | GBR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | GBR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | CHS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | CHS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | CHS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | CHS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | CLM | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | CLM | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | IBS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ACB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PEL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | KHV | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | KHV | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | KHV | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | CDX | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CDX | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CDX | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CDX | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | ACB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | ACB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02451 | hp1 | a0001 | c0005 | t0001 | g0051 | AFR | ACB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02572 | hp1 | a0003 | c0004 | t0001 | g0092 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02615 | hp1 | a0005 | c0006 | t0001 | g0046 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02647 | hp2 | a0003 | c0004 | t0001 | g0160 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02976 | hp1 | a0004 | c0003 | t0004 | g0130 | AFR | ESN | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | MSL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | STU | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | STU | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | BEB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0112 | SAS | BEB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0106 | SAS | STU | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | STU | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0171 | SAS | BEB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | STU | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG04228 | hp1 | a0006 | c0008 | t0002 | g0145 | SAS | STU | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | YRI | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18522 | hp2 | a0007 | c0009 | t0001 | g0055 | AFR | YRI | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18906 | hp1 | a0004 | c0003 | t0004 | g0173 | AFR | YRI | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | YRI | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18944 | hp1 | a0001 | c0001 | t0005 | g0073 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18982 | hp2 | a0008 | c0007 | t0002 | g0162 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | LWK | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19054 | hp2 | a0001 | c0001 | t0006 | g0076 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ASW | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ASW | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA20905 | hp1 | a0009 | c0010 | t0001 | g0202 | SAS | GIH | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | GIH | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | ACB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | USA | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | USA | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | LWK | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0004 | REF | REF | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0008 | REF | REF | TEAD2_chr19_49335595_49367416 | TEAD2 | chr19 | 49335595 | 49367416 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:49343277 | G | C | 1 | a0008 | 1 | NA18982.hp2 | missense_variant | MODERATE | c.1043C>G | p.Ser348Cys | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 11/13 | 1133/2175 | 1043/1356 | 348/451 | chr19 | 49343277 | |||
| chr19:49347218 | G | C | 1 | a0006 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.893C>G | p.Pro298Arg | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/13 | 983/2175 | 893/1356 | 298/451 | chr19 | 49347218 | |||
| chr19:49348773 | C | G | 1 | a0004 | 2 | HG02976.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.677G>C | p.Gly226Ala | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/13 | 767/2175 | 677/1356 | 226/451 | chr19 | 49348773 | |||
| chr19:49348813 | G | A | 1 | a0003 | 2 | HG02572.hp1 HG02647.hp2 |
missense_variant | MODERATE | c.637C>T | p.Pro213Ser | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/13 | 727/2175 | 637/1356 | 213/451 | chr19 | 49348813 | |||
| chr19:49355157 | T | C | 1 | a0007 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.530A>G | p.Asn177Ser | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/13 | 620/2175 | 530/1356 | 177/451 | chr19 | 49355157 | |||
| chr19:49357264 | C | A | 1 | a0002 | 5 | HG00423.hp2 HG02132.hp1 NA18943.hp1 others(2): Show |
missense_variant | MODERATE | c.348G>T | p.Gln116His | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 4/13 | 438/2175 | 348/1356 | 116/451 | chr19 | 49357264 | |||
| chr19:49359996 | G | T | 1 | a0009 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.80C>A | p.Thr27Asn | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 2/13 | 170/2175 | 80/1356 | 27/451 | chr19 | 49359996 | |||
| chr19:49360001 | C | CTCCTCAC others(5): Show |
1 | a0005 | 1 | HG02615.hp1 | disruptive_inframe_insertion | MODERATE | c.63_74dupAGGCAGTGAG others(2): Show |
p.Glu25_Gly26insGlyS others(8): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 2/13 | 164/2175 | 74/1356 | 25/451 | chr19 | 49360001 | |||
| chr19:49360018 | C | A | 1 | a0009 | 1 | NA20905.hp1 | stop_gained | HIGH | c.58G>T | p.Glu20* | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 2/13 | 148/2175 | 58/1356 | 20/451 | chr19 | 49360018 | |||
| chr19:49360019 | A | C | 1 | a0009 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.57T>G | p.Ser19Arg | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 2/13 | 147/2175 | 57/1356 | 19/451 | chr19 | 49360019 | |||
| chr19:49360020 | C | T | 1 | a0009 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.56G>A | p.Ser19Asn | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 2/13 | 146/2175 | 56/1356 | 19/451 | chr19 | 49360020 | |||
| chr19:49360036 | T | C | 1 | a0009 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.40A>G | p.Ser14Gly | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 2/13 | 130/2175 | 40/1356 | 14/451 | chr19 | 49360036 | |||
| chr19:49360073 | C | A | 1 | a0009 | 1 | NA20905.hp1 | start_lost | HIGH | c.3G>T | p.Met1? | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 2/13 | 93/2175 | 3/1356 | 1/451 | chr19 | 49360073 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:49360004 | C | T | 1 | a0001c0005 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.72G>A | p.Glu24Glu | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 2/13 | 162/2175 | 72/1356 | 24/451 | chr19 | 49360004 | |||
| chr19:49360037 | G | T | 1 | a0009c0010 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.39C>A | p.Gly13Gly | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 2/13 | 129/2175 | 39/1356 | 13/451 | chr19 | 49360037 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:49340635 | A | C | 1 | a0004c0003t0004 | 2 | HG02976.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*689T>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 13/13 | 689 | chr19 | 49340635 | ||||||
| chr19:49340700 | A | T | 1 | a0001c0001t0006 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*624T>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 13/13 | 624 | chr19 | 49340700 | ||||||
| chr19:49340780 | T | TA | 4 | a0001c0001t0002 a0001c0001t0003 a0006c0008t0002 others(1): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*543dupT | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 13/13 | 543 | chr19 | 49340780 | ||||||
| chr19:49340900 | GGGGGAGG others(6): Show |
G | 1 | a0001c0001t0006 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*411_*423delGCCACC others(7): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 13/13 | 411 | chr19 | 49340900 | ||||||
| chr19:49340906 | G | A | 1 | a0001c0001t0001 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*418C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 13/13 | 418 | chr19 | 49340906 | ||||||
| chr19:49341066 | G | A | 1 | a0001c0001t0003 | 7 | NA18955.hp1 NA18969.hp2 NA18991.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*258C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 13/13 | 258 | chr19 | 49341066 | ||||||
| chr19:49341273 | C | G | 1 | a0001c0001t0005 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*51G>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 13/13 | 51 | chr19 | 49341273 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:49341464 | T | G | 4 | a0001c0001t0002g0014 a0001c0001t0002g0041 a0001c0001t0002g0174 others(1): Show |
8 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1243-27A>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 12/12 | chr19 | 49341464 | |||||||
| chr19:49341513 | T | G | 2 | a0004c0003t0004g0130 a0004c0003t0004g0173 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1243-76A>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 12/12 | chr19 | 49341513 | |||||||
| chr19:49341686 | T | G | 4 | a0001c0001t0002g0014 a0001c0001t0002g0041 a0001c0001t0002g0174 others(1): Show |
8 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1243-249A>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 12/12 | chr19 | 49341686 | |||||||
| chr19:49341755 | G | T | 1 | a0001c0001t0001g0063 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1243-318C>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 12/12 | chr19 | 49341755 | |||||||
| chr19:49341860 | A | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0007c0009t0001g0055 |
4 | HG02965.hp2 NA18522.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1243-423T>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 12/12 | chr19 | 49341860 | |||||||
| chr19:49341875 | G | A | 4 | a0001c0001t0002g0021 a0001c0001t0002g0131 a0001c0001t0002g0137 others(1): Show |
6 | HG01109.hp2 HG01261.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1243-438C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 12/12 | chr19 | 49341875 | |||||||
| chr19:49341980 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1242+458C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 12/12 | chr19 | 49341980 | |||||||
| chr19:49341987 | A | T | 62 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(59): Show |
86 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1242+451T>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 12/12 | chr19 | 49341987 | |||||||
| chr19:49342200 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1242+238T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 12/12 | chr19 | 49342200 | |||||||
| chr19:49342227 | A | ACCACATC others(4): Show |
146 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(143): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1242+210_1242+211i others(13): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 12/12 | chr19 | 49342227 | |||||||
| chr19:49342638 | C | T | 73 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0040 others(70): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.1090-48G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 11/12 | chr19 | 49342638 | |||||||
| chr19:49342965 | G | A | 4 | a0001c0001t0002g0014 a0001c0001t0002g0041 a0001c0001t0002g0174 others(1): Show |
8 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1089+266C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 11/12 | chr19 | 49342965 | |||||||
| chr19:49343126 | G | A | 1 | a0001c0001t0002g0151 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1089+105C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 11/12 | chr19 | 49343126 | |||||||
| chr19:49343140 | ATGCATAC others(20): Show |
A | 2 | a0004c0003t0004g0130 a0004c0003t0004g0173 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1089+64_1089+90del others(27): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 11/12 | chr19 | 49343140 | |||||||
| chr19:49343141 | T | C | 60 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(57): Show |
84 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1089+90A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 11/12 | chr19 | 49343141 | |||||||
| chr19:49343168 | A | C | 2 | a0004c0003t0004g0130 a0004c0003t0004g0173 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1089+63T>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 11/12 | chr19 | 49343168 | |||||||
| chr19:49343207 | A | G | 1 | a0001c0001t0002g0136 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1089+24T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 11/12 | chr19 | 49343207 | |||||||
| chr19:49343538 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0189 |
3 | HG00738.hp2 HG01081.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.922-140T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49343538 | |||||||
| chr19:49343600 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.922-202C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49343600 | |||||||
| chr19:49343678 | C | A | 1 | a0001c0001t0001g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.922-280G>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49343678 | |||||||
| chr19:49343700 | T | C | 38 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0023 others(35): Show |
54 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.922-302A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49343700 | |||||||
| chr19:49343846 | C | CT | 8 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0047 others(5): Show |
18 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.922-449dupA | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49343846 | |||||||
| chr19:49343854 | T | TGG | 3 | a0001c0001t0001g0023 a0001c0001t0001g0184 a0001c0001t0001g0197 |
5 | HG02040.hp1 HG02523.hp2 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.922-457_922-456ins others(2): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49343854 | |||||||
| chr19:49343854 | T | TGGG | 12 | a0001c0001t0001g0009 a0001c0001t0001g0044 a0001c0001t0001g0084 others(9): Show |
17 | HG00597.hp1 HG00621.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.922-457_922-456ins others(3): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49343854 | |||||||
| chr19:49343854 | T | TGGGG | 15 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0045 others(12): Show |
23 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.922-457_922-456ins others(4): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49343854 | |||||||
| chr19:49343855 | T | G | 34 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0023 others(31): Show |
49 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.922-457A>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49343855 | |||||||
| chr19:49343863 | G | T | 7 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0053 others(4): Show |
9 | HG02572.hp2 HG02965.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.922-465C>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49343863 | |||||||
| chr19:49343931 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.922-533C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49343931 | |||||||
| chr19:49343939 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.922-541C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49343939 | |||||||
| chr19:49343957 | C | A | 1 | a0001c0001t0001g0181 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.922-559G>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49343957 | |||||||
| chr19:49344444 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.922-1046G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49344444 | |||||||
| chr19:49344659 | T | C | 62 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(59): Show |
86 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.922-1261A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49344659 | |||||||
| chr19:49344783 | A | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0047 others(5): Show |
18 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.922-1385T>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49344783 | |||||||
| chr19:49345023 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.922-1625C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49345023 | |||||||
| chr19:49345090 | G | T | 56 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(53): Show |
76 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.922-1692C>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49345090 | |||||||
| chr19:49345119 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.922-1721C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49345119 | |||||||
| chr19:49345292 | T | A | 1 | a0001c0001t0001g0063 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.922-1894A>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49345292 | |||||||
| chr19:49345303 | CTTCCTTC others(5): Show |
C | 1 | a0001c0001t0001g0042 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.921+1875_921+1886d others(14): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49345303 | |||||||
| chr19:49345975 | G | C | 2 | a0004c0003t0004g0130 a0004c0003t0004g0173 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.921+1215C>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49345975 | |||||||
| chr19:49346059 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0007c0009t0001g0055 |
4 | HG02965.hp2 NA18522.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.921+1131C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49346059 | |||||||
| chr19:49346165 | C | CA | 16 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0063 others(13): Show |
19 | HG00733.hp1 HG01123.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.921+1024dupT | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49346165 | |||||||
| chr19:49346165 | C | CAAA | 4 | a0001c0001t0002g0014 a0001c0001t0002g0041 a0001c0001t0002g0174 others(1): Show |
8 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.921+1022_921+1024d others(5): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49346165 | |||||||
| chr19:49346165 | CA | C | 7 | a0001c0001t0001g0049 a0001c0001t0001g0058 a0001c0001t0001g0066 others(4): Show |
7 | HG01168.hp1 HG02055.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.921+1024delT | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49346165 | |||||||
| chr19:49346165 | CAA | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0047 others(6): Show |
19 | HG01255.hp2 HG01891.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.921+1023_921+1024d others(4): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49346165 | |||||||
| chr19:49346165 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0002g0154 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.921+1014_921+1024d others(13): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49346165 | |||||||
| chr19:49346177 | A | T | 1 | a0001c0001t0001g0199 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.921+1013T>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49346177 | |||||||
| chr19:49346178 | A | T | 1 | a0001c0001t0001g0186 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.921+1012T>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49346178 | |||||||
| chr19:49346181 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.921+1009T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49346181 | |||||||
| chr19:49346181 | A | T | 34 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0023 others(31): Show |
50 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.921+1009T>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49346181 | |||||||
| chr19:49346182 | A | T | 1 | a0001c0001t0001g0182 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.921+1008T>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49346182 | |||||||
| chr19:49346185 | A | C | 2 | a0004c0003t0004g0130 a0004c0003t0004g0173 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.921+1005T>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49346185 | |||||||
| chr19:49346185 | AC | A | 36 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0023 others(33): Show |
52 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.921+1004delG | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49346185 | |||||||
| chr19:49346186 | C | A | 2 | a0001c0001t0001g0182 a0001c0001t0001g0198 |
2 | NA18969.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.921+1004G>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49346186 | |||||||
| chr19:49346599 | G | C | 1 | a0001c0001t0002g0164 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.921+591C>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49346599 | |||||||
| chr19:49346834 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.921+356C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49346834 | |||||||
| chr19:49346944 | G | A | 57 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(54): Show |
77 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.921+246C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49346944 | |||||||
| chr19:49347105 | C | G | 1 | a0001c0001t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.921+85G>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49347105 | |||||||
| chr19:49347121 | A | G | 11 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0103 others(8): Show |
13 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.921+69T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49347121 | |||||||
| chr19:49347180 | G | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0103 a0001c0001t0001g0104 others(3): Show |
8 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.921+10C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 10/12 | chr19 | 49347180 | |||||||
| chr19:49347374 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.748-11A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49347374 | |||||||
| chr19:49347425 | C | A | 1 | a0001c0001t0002g0131 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.748-62G>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49347425 | |||||||
| chr19:49347442 | C | T | 1 | a0003c0004t0001g0160 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.748-79G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49347442 | |||||||
| chr19:49347500 | T | C | 4 | a0001c0001t0002g0014 a0001c0001t0002g0041 a0001c0001t0002g0174 others(1): Show |
8 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.748-137A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49347500 | |||||||
| chr19:49347520 | C | A | 1 | a0001c0001t0002g0131 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.748-157G>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49347520 | |||||||
| chr19:49347552 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0166 |
2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.748-189G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49347552 | |||||||
| chr19:49347586 | A | C | 1 | a0001c0001t0001g0077 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.748-223T>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49347586 | |||||||
| chr19:49347593 | C | A | 1 | a0001c0001t0002g0131 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.748-230G>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49347593 | |||||||
| chr19:49347658 | G | A | 38 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0023 others(35): Show |
54 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.748-295C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49347658 | |||||||
| chr19:49347661 | T | C | 1 | a0001c0001t0002g0131 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.748-298A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49347661 | |||||||
| chr19:49347662 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.748-299G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49347662 | |||||||
| chr19:49347672 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.748-309A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49347672 | |||||||
| chr19:49347729 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.748-366C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49347729 | |||||||
| chr19:49347796 | T | C | 52 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0023 others(49): Show |
81 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.748-433A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49347796 | |||||||
| chr19:49347897 | T | C | 2 | a0004c0003t0004g0130 a0004c0003t0004g0173 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.748-534A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49347897 | |||||||
| chr19:49347925 | G | A | 2 | a0001c0001t0002g0152 a0001c0001t0002g0158 |
2 | HG00099.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.748-562C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49347925 | |||||||
| chr19:49347949 | G | A | 1 | a0001c0001t0002g0022 | 3 | NA18952.hp2 NA19081.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.748-586C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49347949 | |||||||
| chr19:49347967 | A | G | 1 | a0001c0001t0001g0032 | 2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.748-604T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49347967 | |||||||
| chr19:49348134 | G | A | 4 | a0001c0001t0002g0014 a0001c0001t0002g0041 a0001c0001t0002g0174 others(1): Show |
8 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.747+569C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49348134 | |||||||
| chr19:49348171 | CT | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(27): Show |
71 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.747+531delA | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49348171 | |||||||
| chr19:49348383 | A | G | 6 | a0001c0001t0002g0014 a0001c0001t0002g0041 a0001c0001t0002g0174 others(3): Show |
10 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.747+320T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49348383 | |||||||
| chr19:49348489 | CCAGCTGC others(2): Show |
C | 70 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0040 others(67): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.747+205_747+213del others(9): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49348489 | |||||||
| chr19:49348502 | C | T | 1 | a0002c0002t0001g0099 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.747+201G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49348502 | |||||||
| chr19:49348679 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.747+24G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49348679 | |||||||
| chr19:49348684 | G | A | 62 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(59): Show |
86 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.747+19C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 9/12 | chr19 | 49348684 | |||||||
| chr19:49348931 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.605-86T>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49348931 | |||||||
| chr19:49348990 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.605-145A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49348990 | |||||||
| chr19:49349450 | G | T | 1 | a0001c0001t0001g0196 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.605-605C>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49349450 | |||||||
| chr19:49349567 | C | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0093 |
2 | NA18943.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.605-722G>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49349567 | |||||||
| chr19:49349731 | G | C | 1 | a0001c0001t0001g0182 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.605-886C>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49349731 | |||||||
| chr19:49349748 | C | G | 2 | a0004c0003t0004g0130 a0004c0003t0004g0173 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.605-903G>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49349748 | |||||||
| chr19:49349900 | A | T | 7 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0053 others(4): Show |
9 | HG02572.hp2 HG02965.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.605-1055T>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49349900 | |||||||
| chr19:49349938 | C | G | 2 | a0004c0003t0004g0130 a0004c0003t0004g0173 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.605-1093G>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49349938 | |||||||
| chr19:49350223 | T | C | 1 | a0001c0001t0001g0026 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.604+1078A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49350223 | |||||||
| chr19:49350229 | C | T | 6 | a0001c0001t0003g0036 a0001c0001t0003g0121 a0001c0001t0003g0122 others(3): Show |
7 | NA18955.hp1 NA18969.hp2 NA18991.hp2 others(4): Show |
intron_variant | MODIFIER | c.604+1072G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49350229 | |||||||
| chr19:49350305 | T | G | 5 | a0001c0001t0001g0019 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
7 | HG00733.hp1 HG01243.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.604+996A>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49350305 | |||||||
| chr19:49350365 | T | C | 9 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0103 others(6): Show |
11 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.604+936A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49350365 | |||||||
| chr19:49350389 | G | A | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0056 |
3 | HG02572.hp2 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.604+912C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49350389 | |||||||
| chr19:49350518 | G | T | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.604+783C>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49350518 | |||||||
| chr19:49350519 | G | T | 1 | a0003c0004t0001g0160 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.604+782C>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49350519 | |||||||
| chr19:49350624 | C | T | 62 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(59): Show |
86 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.604+677G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49350624 | |||||||
| chr19:49350816 | C | A | 2 | a0004c0003t0004g0130 a0004c0003t0004g0173 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.604+485G>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49350816 | |||||||
| chr19:49350820 | A | G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0056 others(2): Show |
6 | HG02572.hp2 HG02965.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.604+481T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49350820 | |||||||
| chr19:49350829 | C | T | 1 | a0001c0001t0002g0140 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.604+472G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49350829 | |||||||
| chr19:49350903 | G | A | 2 | a0004c0003t0004g0130 a0004c0003t0004g0173 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.604+398C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49350903 | |||||||
| chr19:49350947 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0189 a0001c0001t0001g0190 |
4 | HG00738.hp2 HG01081.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.604+354C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49350947 | |||||||
| chr19:49350965 | T | C | 62 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(59): Show |
86 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.604+336A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49350965 | |||||||
| chr19:49351048 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG00621.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.604+253C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49351048 | |||||||
| chr19:49351097 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.604+204A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49351097 | |||||||
| chr19:49351288 | C | T | 7 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0053 others(4): Show |
9 | HG02572.hp2 HG02965.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.604+13G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 8/12 | chr19 | 49351288 | |||||||
| chr19:49351444 | A | G | 2 | a0004c0003t0004g0130 a0004c0003t0004g0173 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.540-79T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49351444 | |||||||
| chr19:49351459 | G | T | 2 | a0001c0001t0002g0174 a0001c0001t0002g0175 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.540-94C>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49351459 | |||||||
| chr19:49351481 | C | T | 6 | a0001c0001t0002g0014 a0001c0001t0002g0041 a0001c0001t0002g0174 others(3): Show |
10 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.540-116G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49351481 | |||||||
| chr19:49351669 | A | G | 1 | a0001c0001t0002g0035 | 2 | HG00642.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.540-304T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49351669 | |||||||
| chr19:49351711 | C | T | 1 | a0001c0001t0002g0012 | 4 | HG02148.hp1 NA18939.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.540-346G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49351711 | |||||||
| chr19:49351756 | C | T | 6 | a0001c0001t0002g0020 a0001c0001t0002g0161 a0001c0001t0002g0163 others(3): Show |
8 | HG00558.hp1 HG02056.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.540-391G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49351756 | |||||||
| chr19:49351801 | C | A | 38 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0023 others(35): Show |
54 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.540-436G>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49351801 | |||||||
| chr19:49351857 | G | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | HG00438.hp2 HG02074.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.540-492C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49351857 | |||||||
| chr19:49351859 | G | A | 1 | a0001c0001t0001g0040 | 2 | HG01070.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.540-494C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49351859 | |||||||
| chr19:49351870 | G | C | 57 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0023 others(54): Show |
79 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.540-505C>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49351870 | |||||||
| chr19:49352114 | C | G | 59 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(56): Show |
83 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.540-749G>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49352114 | |||||||
| chr19:49352170 | G | A | 4 | a0001c0001t0002g0014 a0001c0001t0002g0041 a0001c0001t0002g0174 others(1): Show |
8 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.540-805C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49352170 | |||||||
| chr19:49352185 | G | A | 7 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0053 others(4): Show |
9 | HG02572.hp2 HG02965.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.540-820C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49352185 | |||||||
| chr19:49352225 | G | A | 1 | a0001c0001t0002g0171 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.540-860C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49352225 | |||||||
| chr19:49352440 | C | T | 4 | a0001c0001t0002g0014 a0001c0001t0002g0041 a0001c0001t0002g0174 others(1): Show |
8 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.540-1075G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49352440 | |||||||
| chr19:49352446 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.540-1081G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49352446 | |||||||
| chr19:49352585 | G | T | 1 | a0001c0001t0006g0076 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.540-1220C>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49352585 | |||||||
| chr19:49352648 | T | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0007c0009t0001g0055 |
4 | HG02965.hp2 NA18522.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.540-1283A>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49352648 | |||||||
| chr19:49352792 | G | A | 3 | a0001c0001t0001g0087 a0004c0003t0004g0130 a0004c0003t0004g0173 |
3 | HG00639.hp2 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.540-1427C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49352792 | |||||||
| chr19:49353373 | A | G | 3 | a0001c0001t0001g0181 a0001c0001t0001g0196 a0001c0001t0001g0198 |
3 | HG02622.hp1 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.539+1775T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49353373 | |||||||
| chr19:49353528 | C | T | 2 | a0004c0003t0004g0130 a0004c0003t0004g0173 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.539+1620G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49353528 | |||||||
| chr19:49353718 | A | G | 1 | a0001c0001t0002g0139 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.539+1430T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49353718 | |||||||
| chr19:49353784 | CT | C | 11 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0088 others(8): Show |
12 | HG01167.hp2 HG01884.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.539+1363delA | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49353784 | |||||||
| chr19:49353813 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.539+1335G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49353813 | |||||||
| chr19:49353817 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.539+1331T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49353817 | |||||||
| chr19:49353857 | T | C | 2 | a0004c0003t0004g0130 a0004c0003t0004g0173 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.539+1291A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49353857 | |||||||
| chr19:49353950 | G | GTT | 2 | a0001c0001t0002g0014 a0001c0001t0002g0174 |
5 | HG02109.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.539+1196_539+1197d others(4): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49353950 | |||||||
| chr19:49353952 | T | TTTA | 43 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(40): Show |
61 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.539+1195_539+1196i others(5): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49353952 | |||||||
| chr19:49353956 | T | A | 10 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0103 others(7): Show |
12 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.539+1192A>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49353956 | |||||||
| chr19:49353957 | G | A | 36 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0023 others(33): Show |
52 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.539+1191C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49353957 | |||||||
| chr19:49353957 | G | GT | 6 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0091 others(3): Show |
6 | HG01175.hp2 HG01243.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.539+1190dupA | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49353957 | |||||||
| chr19:49353957 | G | T | 23 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0026 others(20): Show |
31 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.539+1191C>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49353957 | |||||||
| chr19:49353957 | GT | G | 77 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0024 others(74): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.539+1190delA | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49353957 | |||||||
| chr19:49353960 | T | G | 1 | a0001c0001t0002g0149 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.539+1188A>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49353960 | |||||||
| chr19:49353962 | T | A | 1 | a0001c0001t0001g0192 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.539+1186A>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49353962 | |||||||
| chr19:49353970 | T | G | 2 | a0001c0001t0001g0193 a0001c0001t0001g0199 |
2 | HG03942.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.539+1178A>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49353970 | |||||||
| chr19:49353971 | G | T | 32 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0023 others(29): Show |
48 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.539+1177C>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49353971 | |||||||
| chr19:49353998 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.539+1150G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49353998 | |||||||
| chr19:49354036 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0090 a0001c0001t0001g0094 |
5 | HG00735.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.539+1112C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49354036 | |||||||
| chr19:49354043 | C | T | 3 | a0001c0001t0002g0013 a0001c0001t0002g0154 a0001c0001t0002g0155 |
6 | HG02257.hp2 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.539+1105G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49354043 | |||||||
| chr19:49354221 | T | C | 2 | a0003c0004t0001g0092 a0003c0004t0001g0160 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.539+927A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49354221 | |||||||
| chr19:49354314 | G | A | 2 | a0004c0003t0004g0130 a0004c0003t0004g0173 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.539+834C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49354314 | |||||||
| chr19:49354334 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.539+814C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49354334 | |||||||
| chr19:49354451 | C | T | 1 | a0001c0001t0002g0132 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.539+697G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49354451 | |||||||
| chr19:49354510 | G | GA | 8 | a0001c0001t0001g0018 a0001c0001t0001g0062 a0001c0001t0001g0095 others(5): Show |
10 | HG01070.hp1 HG01071.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.539+637dupT | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49354510 | |||||||
| chr19:49354544 | G | A | 2 | a0001c0001t0002g0152 a0001c0001t0002g0158 |
2 | HG00099.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.539+604C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49354544 | |||||||
| chr19:49354582 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.539+566G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49354582 | |||||||
| chr19:49354735 | C | T | 2 | a0004c0003t0004g0130 a0004c0003t0004g0173 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.539+413G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49354735 | |||||||
| chr19:49354823 | A | C | 59 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(56): Show |
83 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.539+325T>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49354823 | |||||||
| chr19:49354897 | C | T | 1 | a0001c0001t0002g0136 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.539+251G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49354897 | |||||||
| chr19:49354953 | G | C | 1 | a0001c0001t0001g0181 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.539+195C>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49354953 | |||||||
| chr19:49354960 | T | C | 3 | a0001c0001t0001g0050 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | HG02109.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.539+188A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49354960 | |||||||
| chr19:49354985 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.539+163C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49354985 | |||||||
| chr19:49355003 | A | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(57): Show |
125 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.539+145T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49355003 | |||||||
| chr19:49355021 | G | GCATA | 23 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0050 others(20): Show |
30 | HG00408.hp1 HG00408.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.539+123_539+126dup others(4): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49355021 | |||||||
| chr19:49355021 | G | GCATACAT others(1): Show |
3 | a0001c0001t0001g0178 a0001c0001t0001g0183 a0001c0001t0001g0184 |
3 | HG00741.hp1 HG02165.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.539+119_539+126dup others(8): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49355021 | |||||||
| chr19:49355021 | G | GCATACAT others(5): Show |
30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0023 others(27): Show |
47 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.539+115_539+126dup others(12): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49355021 | |||||||
| chr19:49355021 | G | GCATACAT others(9): Show |
4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | NA19056.hp2 NA19091.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.539+111_539+126dup others(16): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 7/12 | chr19 | 49355021 | |||||||
| chr19:49355505 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.373-86C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 5/12 | chr19 | 49355505 | |||||||
| chr19:49355589 | G | A | 4 | a0001c0001t0002g0014 a0001c0001t0002g0041 a0001c0001t0002g0174 others(1): Show |
8 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.373-170C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 5/12 | chr19 | 49355589 | |||||||
| chr19:49355598 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.373-179C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 5/12 | chr19 | 49355598 | |||||||
| chr19:49355601 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0135 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.373-182G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 5/12 | chr19 | 49355601 | |||||||
| chr19:49355792 | A | AT | 12 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0053 others(9): Show |
18 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.372+166dupA | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 5/12 | chr19 | 49355792 | |||||||
| chr19:49355878 | C | A | 4 | a0001c0001t0002g0014 a0001c0001t0002g0041 a0001c0001t0002g0174 others(1): Show |
8 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.372+81G>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 5/12 | chr19 | 49355878 | |||||||
| chr19:49356017 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.361-47C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 4/12 | chr19 | 49356017 | |||||||
| chr19:49356067 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0047 others(4): Show |
17 | HG01255.hp2 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.361-97C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 4/12 | chr19 | 49356067 | |||||||
| chr19:49356269 | A | G | 5 | a0001c0001t0002g0039 a0001c0001t0002g0108 a0001c0001t0002g0132 others(2): Show |
6 | HG01346.hp2 NA18950.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.361-299T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 4/12 | chr19 | 49356269 | |||||||
| chr19:49356378 | C | CA | 87 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(84): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.361-409dupT | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 4/12 | chr19 | 49356378 | |||||||
| chr19:49356378 | C | CAA | 15 | a0001c0001t0001g0037 a0001c0001t0001g0056 a0001c0001t0001g0096 others(12): Show |
17 | HG01175.hp1 HG01243.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.361-410_361-409dup others(2): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 4/12 | chr19 | 49356378 | |||||||
| chr19:49356378 | CA | C | 14 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0042 others(11): Show |
29 | HG01074.hp1 HG01255.hp2 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.361-409delT | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 4/12 | chr19 | 49356378 | |||||||
| chr19:49356401 | C | A | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.361-431G>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 4/12 | chr19 | 49356401 | |||||||
| chr19:49356403 | A | G | 4 | a0001c0001t0002g0014 a0001c0001t0002g0041 a0001c0001t0002g0174 others(1): Show |
8 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.361-433T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 4/12 | chr19 | 49356403 | |||||||
| chr19:49356594 | C | G | 1 | a0004c0003t0004g0130 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.361-624G>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 4/12 | chr19 | 49356594 | |||||||
| chr19:49356596 | G | C | 1 | a0001c0001t0002g0113 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.361-626C>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 4/12 | chr19 | 49356596 | |||||||
| chr19:49356650 | G | C | 7 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0053 others(4): Show |
9 | HG02572.hp2 HG02965.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.360+602C>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 4/12 | chr19 | 49356650 | |||||||
| chr19:49356703 | G | A | 2 | a0001c0001t0002g0112 a0001c0001t0002g0159 |
2 | HG03017.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.360+549C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 4/12 | chr19 | 49356703 | |||||||
| chr19:49357149 | T | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG01106.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.360+103A>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 4/12 | chr19 | 49357149 | |||||||
| chr19:49357234 | GT | G | 1 | a0001c0001t0001g0017 | 3 | HG02056.hp1 HG02071.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.360+17delA | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 4/12 | chr19 | 49357234 | |||||||
| chr19:49357414 | A | G | 2 | a0001c0001t0001g0052 a0001c0005t0001g0051 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.298-100T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 3/12 | chr19 | 49357414 | |||||||
| chr19:49357598 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.298-284G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 3/12 | chr19 | 49357598 | |||||||
| chr19:49357866 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.298-552C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 3/12 | chr19 | 49357866 | |||||||
| chr19:49357995 | G | A | 75 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0040 others(72): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.298-681C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 3/12 | chr19 | 49357995 | |||||||
| chr19:49358054 | G | A | 1 | a0004c0003t0004g0173 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.298-740C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 3/12 | chr19 | 49358054 | |||||||
| chr19:49358133 | C | T | 75 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0040 others(72): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.298-819G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 3/12 | chr19 | 49358133 | |||||||
| chr19:49358377 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.297+1058A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 3/12 | chr19 | 49358377 | |||||||
| chr19:49358394 | GAC | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0047 others(5): Show |
18 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.297+1039_297+1040d others(4): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 3/12 | chr19 | 49358394 | |||||||
| chr19:49358548 | G | T | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.297+887C>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 3/12 | chr19 | 49358548 | |||||||
| chr19:49358570 | G | A | 5 | a0001c0001t0002g0161 a0001c0001t0002g0163 a0001c0001t0002g0164 others(2): Show |
5 | HG02135.hp2 NA18946.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+865C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 3/12 | chr19 | 49358570 | |||||||
| chr19:49358640 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.297+795A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 3/12 | chr19 | 49358640 | |||||||
| chr19:49358656 | T | C | 5 | a0001c0001t0002g0014 a0001c0001t0002g0041 a0001c0001t0002g0174 others(2): Show |
9 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+779A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 3/12 | chr19 | 49358656 | |||||||
| chr19:49358696 | G | GATCTTGG others(9): Show |
1 | a0009c0010t0001g0202 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.297+723_297+738dup others(16): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 3/12 | chr19 | 49358696 | |||||||
| chr19:49358874 | G | A | 7 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0053 others(4): Show |
9 | HG02572.hp2 HG02965.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.297+561C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 3/12 | chr19 | 49358874 | |||||||
| chr19:49358895 | A | C | 143 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(140): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.297+540T>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 3/12 | chr19 | 49358895 | |||||||
| chr19:49359036 | C | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02165.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.297+399G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 3/12 | chr19 | 49359036 | |||||||
| chr19:49359037 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.297+398C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 3/12 | chr19 | 49359037 | |||||||
| chr19:49359208 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0047 others(6): Show |
19 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.297+227C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 3/12 | chr19 | 49359208 | |||||||
| chr19:49359271 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.297+164G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 3/12 | chr19 | 49359271 | |||||||
| chr19:49359283 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.297+152A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 3/12 | chr19 | 49359283 | |||||||
| chr19:49359322 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.297+113G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 3/12 | chr19 | 49359322 | |||||||
| chr19:49359374 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.297+61C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 3/12 | chr19 | 49359374 | |||||||
| chr19:49359668 | C | T | 16 | a0001c0001t0001g0037 a0001c0001t0001g0123 a0001c0001t0002g0006 others(13): Show |
29 | HG00544.hp2 HG00597.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.233-169G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 2/12 | chr19 | 49359668 | |||||||
| chr19:49359673 | TCACGCAC others(3): Show |
T | 1 | a0001c0001t0003g0121 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.232+161_232+170del others(10): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 2/12 | chr19 | 49359673 | |||||||
| chr19:49359784 | C | G | 67 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(64): Show |
101 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.232+60G>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 2/12 | chr19 | 49359784 | |||||||
| chr19:49359821 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.232+23C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 2/12 | chr19 | 49359821 | |||||||
| chr19:49360174 | GAGGGAGG others(7): Show |
G | 1 | a0009c0010t0001g0202 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-6-107_-6-94delAGC others(11): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49360174 | |||||||
| chr19:49360211 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-6-130C>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49360211 | |||||||
| chr19:49360232 | T | G | 55 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(52): Show |
87 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.-6-151A>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49360232 | |||||||
| chr19:49360348 | G | A | 2 | a0001c0001t0001g0052 a0001c0005t0001g0051 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-6-267C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49360348 | |||||||
| chr19:49360359 | G | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0047 others(6): Show |
19 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-6-278C>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49360359 | |||||||
| chr19:49360452 | T | C | 133 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0018 others(130): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-6-371A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49360452 | |||||||
| chr19:49360452 | T | G | 9 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0047 others(6): Show |
19 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-6-371A>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49360452 | |||||||
| chr19:49360666 | A | G | 55 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(52): Show |
87 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.-6-585T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49360666 | |||||||
| chr19:49360729 | AGAGGGGG others(17): Show |
A | 46 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0023 others(43): Show |
68 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.-6-672_-6-649delCC others(22): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49360729 | |||||||
| chr19:49360753 | G | A | 1 | a0001c0001t0002g0003 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-6-672C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49360753 | |||||||
| chr19:49360794 | C | T | 46 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0023 others(43): Show |
68 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.-6-713G>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49360794 | |||||||
| chr19:49360799 | A | AG | 84 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0019 others(81): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.-6-719dupC | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49360799 | |||||||
| chr19:49360799 | AG | A | 55 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(52): Show |
87 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.-6-719delC | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49360799 | |||||||
| chr19:49360828 | A | G | 9 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0047 others(6): Show |
19 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-6-747T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49360828 | |||||||
| chr19:49360834 | C | A | 6 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
7 | HG02572.hp2 HG02965.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6-753G>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49360834 | |||||||
| chr19:49360884 | C | A | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-6-803G>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49360884 | |||||||
| chr19:49360919 | A | G | 9 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0047 others(6): Show |
19 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-6-838T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49360919 | |||||||
| chr19:49360962 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0047 others(6): Show |
19 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-6-881C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49360962 | |||||||
| chr19:49360964 | AGGGGACA others(17): Show |
A | 1 | a0004c0003t0004g0173 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-6-907_-6-884delCT others(22): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49360964 | |||||||
| chr19:49360973 | A | G | 1 | a0001c0001t0002g0003 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-6-892T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49360973 | |||||||
| chr19:49361032 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0047 others(6): Show |
19 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-6-951C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361032 | |||||||
| chr19:49361033 | GGGGGGAC others(12): Show |
G | 9 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0047 others(6): Show |
19 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-6-971_-6-953delTC others(17): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361033 | |||||||
| chr19:49361038 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-6-957C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361038 | |||||||
| chr19:49361089 | A | G | 55 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(52): Show |
87 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.-6-1008T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361089 | |||||||
| chr19:49361155 | C | CA | 55 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(52): Show |
87 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.-6-1075_-6-1074ins others(1): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361155 | |||||||
| chr19:49361155 | C | CG | 26 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0018 others(23): Show |
35 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.-6-1075dupC | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361155 | |||||||
| chr19:49361159 | G | A | 55 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(52): Show |
87 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.-6-1078C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361159 | |||||||
| chr19:49361160 | G | C | 1 | a0001c0001t0001g0102 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-6-1079C>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361160 | |||||||
| chr19:49361166 | G | A | 46 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0023 others(43): Show |
68 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.-6-1085C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361166 | |||||||
| chr19:49361197 | C | CAGAG | 9 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0047 others(6): Show |
19 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-6-1120_-6-1117dup others(4): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361197 | |||||||
| chr19:49361207 | G | GACAGAGA others(17): Show |
127 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0018 others(124): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-7+1125_-7+1126ins others(24): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361207 | |||||||
| chr19:49361230 | T | G | 15 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(12): Show |
26 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-7+1103A>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361230 | |||||||
| chr19:49361231 | G | A | 15 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(12): Show |
26 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-7+1102C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361231 | |||||||
| chr19:49361241 | C | CAG | 15 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(12): Show |
26 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-7+1090_-7+1091dup others(2): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361241 | |||||||
| chr19:49361252 | G | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(12): Show |
26 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-7+1081C>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361252 | |||||||
| chr19:49361262 | C | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0047 others(6): Show |
19 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-7+1071G>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361262 | |||||||
| chr19:49361272 | A | G | 16 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(13): Show |
28 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.-7+1061T>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361272 | |||||||
| chr19:49361297 | GGA | G | 16 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(13): Show |
28 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.-7+1034_-7+1035del others(2): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361297 | |||||||
| chr19:49361300 | C | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(13): Show |
28 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.-7+1033G>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361300 | |||||||
| chr19:49361317 | G | GA | 16 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(13): Show |
28 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.-7+1015_-7+1016ins others(1): Show |
TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361317 | |||||||
| chr19:49361322 | A | AC | 16 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(13): Show |
28 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.-7+1010dupG | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361322 | |||||||
| chr19:49361325 | C | G | 16 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(13): Show |
28 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.-7+1008G>C | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361325 | |||||||
| chr19:49361330 | T | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(13): Show |
28 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.-7+1003A>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361330 | |||||||
| chr19:49361379 | G | A | 46 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0023 others(43): Show |
68 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.-7+954C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361379 | |||||||
| chr19:49361398 | A | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0047 others(6): Show |
19 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-7+935T>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361398 | |||||||
| chr19:49361482 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0047 others(6): Show |
19 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-7+851C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361482 | |||||||
| chr19:49361718 | G | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG00544.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.-7+615C>A | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361718 | |||||||
| chr19:49361808 | A | AG | 55 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(52): Show |
87 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.-7+524dupC | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361808 | |||||||
| chr19:49361861 | G | A | 1 | a0001c0001t0001g0040 | 2 | HG01070.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-7+472C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49361861 | |||||||
| chr19:49362057 | A | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0047 others(6): Show |
19 | HG01255.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-7+276T>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49362057 | |||||||
| chr19:49362125 | C | A | 1 | a0004c0003t0004g0173 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7+208G>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49362125 | |||||||
| chr19:49362221 | G | A | 39 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0023 others(36): Show |
59 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-7+112C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49362221 | |||||||
| chr19:49362271 | G | C | 35 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0023 others(32): Show |
51 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-7+62C>G | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49362271 | |||||||
| chr19:49362274 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-7+59C>T | TEAD2 | ENSG00000074219.14 | transcript | ENST00000593945.6 | protein_coding | 1/12 | chr19 | 49362274 |