Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7942 |
| ensemblid | ENSG00000112561.19 |
| hgncid | 11753 |
| symbol | TFEB |
| name | transcription factor EB |
| refseq_nuc | NM_001271944.2 |
| refseq_prot | NP_001258873.1 |
| ensembl_nuc | ENST00000373033.6 |
| ensembl_prot | ENSP00000362124.1 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 41683978 |
| end | 41735608 |
| strand | - |
| ver | v1.2 |
| region | chr6:41683978-41735608 |
| region5000 | chr6:41678978-41740608 |
| regionname0 | TFEB_chr6_41683978_41735608 |
| regionname5000 | TFEB_chr6_41678978_41740608 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 476 | 397 | 91 | 81 | 163 | 14 | 46 | 118 | TFEB_chr6_41678978_41740608 | TFEB | MASRI others(471): Show |
chr6 | 41678978 | 41740608 |
| a0002 | 0/0 | 476 | 6 | 0 | 0 | 6 | 0 | 0 | 5 | TFEB_chr6_41678978_41740608 | TFEB | MASRI others(471): Show |
chr6 | 41678978 | 41740608 |
| a0003 | 0/0 | 476 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | MASRI others(471): Show |
chr6 | 41678978 | 41740608 |
| a0004 | 0/0 | 476 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | MASRI others(471): Show |
chr6 | 41678978 | 41740608 |
| a0005 | 0/0 | 476 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | MASRI others(471): Show |
chr6 | 41678978 | 41740608 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1428 | 125 | 49 | 31 | 38 | 1 | 5 | TFEB_chr6_41678978_41740608 | TFEB | ATGGC others(1423): Show |
chr6 | 41678978 | 41740608 | ||
| a0001c0002 | 1/0 | 1428 | 96 | 7 | 16 | 58 | 4 | 10 | TFEB_chr6_41678978_41740608 | TFEB | ATGGC others(1423): Show |
chr6 | 41678978 | 41740608 | ||
| a0001c0003 | 0/0 | 1428 | 91 | 7 | 23 | 39 | 5 | 17 | TFEB_chr6_41678978_41740608 | TFEB | ATGGC others(1423): Show |
chr6 | 41678978 | 41740608 | ||
| a0001c0004 | 0/0 | 1428 | 46 | 5 | 8 | 25 | 2 | 6 | TFEB_chr6_41678978_41740608 | TFEB | ATGGC others(1423): Show |
chr6 | 41678978 | 41740608 | ||
| a0001c0005 | 0/0 | 1428 | 35 | 21 | 2 | 3 | 2 | 7 | TFEB_chr6_41678978_41740608 | TFEB | ATGGC others(1423): Show |
chr6 | 41678978 | 41740608 | ||
| a0001c0007 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | ATGGC others(1423): Show |
chr6 | 41678978 | 41740608 | ||
| a0001c0008 | 0/0 | 1428 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | ATGGC others(1423): Show |
chr6 | 41678978 | 41740608 | ||
| a0001c0010 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | ATGGC others(1423): Show |
chr6 | 41678978 | 41740608 | ||
| a0001c0012 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | ATGGC others(1423): Show |
chr6 | 41678978 | 41740608 | ||
| a0002c0006 | 0/0 | 1428 | 6 | 0 | 0 | 6 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | ATGGC others(1423): Show |
chr6 | 41678978 | 41740608 | ||
| a0003c0013 | 0/0 | 1428 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | ATGGC others(1423): Show |
chr6 | 41678978 | 41740608 | ||
| a0004c0009 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | ATGGC others(1423): Show |
chr6 | 41678978 | 41740608 | ||
| a0005c0011 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | ATGGC others(1423): Show |
chr6 | 41678978 | 41740608 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2333 | 54 | 37 | 14 | 1 | 1 | 1 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0001c0001t0002 | 0/1 | 2333 | 50 | 9 | 9 | 27 | 0 | 4 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0001c0001t0003 | 0/0 | 2333 | 19 | 2 | 7 | 10 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0001c0001t0008 | 0/0 | 2333 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0001c0001t0012 | 0/0 | 2321 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2316): Show |
chr6 | 41678978 | 41740608 |
| a0001c0002t0001 | 1/0 | 2333 | 94 | 7 | 14 | 58 | 4 | 10 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0001c0002t0007 | 0/0 | 2333 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0001c0002t0010 | 0/0 | 2333 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0001c0003t0001 | 0/0 | 2333 | 87 | 7 | 20 | 39 | 5 | 16 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0001c0003t0002 | 0/0 | 2333 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0001c0003t0004 | 0/0 | 2333 | 3 | 0 | 3 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0001c0004t0002 | 0/0 | 2333 | 43 | 5 | 8 | 23 | 2 | 5 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0001c0004t0006 | 0/0 | 2333 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | TTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0001c0004t0011 | 0/0 | 2333 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0001c0005t0001 | 0/0 | 2333 | 32 | 18 | 2 | 3 | 2 | 7 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0001c0005t0005 | 0/0 | 2333 | 2 | 2 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0001c0005t0009 | 0/0 | 2333 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0001c0007t0001 | 0/0 | 2333 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0001c0008t0002 | 0/0 | 2333 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0001c0010t0001 | 0/0 | 2333 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0001c0012t0001 | 0/0 | 2333 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0002c0006t0001 | 0/0 | 2333 | 6 | 0 | 0 | 6 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0003c0013t0001 | 0/0 | 2333 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0004c0009t0002 | 0/0 | 2333 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| a0005c0011t0001 | 0/0 | 2333 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | GTGGA others(2328): Show |
chr6 | 41678978 | 41740608 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0309 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0003g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0003g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0003g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0003g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0008g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0001t0012g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0001 | 0/0 | 10 | 0 | 1 | 9 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0002 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0007g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0002t0010g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0006 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0007 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0004g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0003t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0006g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0004t0011g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0005g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0005t0009g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0007t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0008t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0010t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0001c0012t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0002c0006t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0002c0006t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0002c0006t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0002c0006t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0002c0006t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0003c0013t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0004c0009t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| a0005c0011t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0049 | EUR | GBR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00140 | hp2 | a0001 | c0005 | t0001 | g0026 | EUR | GBR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0045 | EUR | FIN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | FIN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00323 | hp1 | a0001 | c0004 | t0002 | g0199 | EUR | FIN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0065 | EUR | FIN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00408 | hp1 | a0001 | c0004 | t0002 | g0181 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00408 | hp2 | a0001 | c0003 | t0001 | g0299 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00438 | hp1 | a0001 | c0003 | t0001 | g0080 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0349 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00544 | hp1 | a0002 | c0006 | t0001 | g0301 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00558 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00597 | hp2 | a0001 | c0003 | t0001 | g0209 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00621 | hp1 | a0001 | c0004 | t0002 | g0182 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0348 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0310 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0102 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00673 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00733 | hp2 | a0001 | c0003 | t0001 | g0160 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00735 | hp2 | a0003 | c0013 | t0001 | g0142 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0015 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00738 | hp2 | a0001 | c0004 | t0002 | g0238 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0250 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01069 | hp1 | a0001 | c0003 | t0004 | g0021 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0056 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01074 | hp2 | a0001 | c0004 | t0002 | g0237 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0143 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0087 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01099 | hp2 | a0001 | c0003 | t0004 | g0021 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01109 | hp1 | a0001 | c0003 | t0004 | g0043 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0179 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01168 | hp1 | a0001 | c0004 | t0002 | g0024 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01168 | hp2 | a0001 | c0005 | t0001 | g0118 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01169 | hp1 | a0001 | c0004 | t0002 | g0024 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0064 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0067 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0324 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01257 | hp2 | a0001 | c0003 | t0001 | g0052 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01346 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0345 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01358 | hp1 | a0001 | c0004 | t0002 | g0003 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0100 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01361 | hp1 | a0001 | c0005 | t0001 | g0269 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0013 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0061 | EUR | IBS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01515 | hp2 | a0001 | c0004 | t0002 | g0055 | EUR | IBS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0013 | EUR | IBS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0041 | EUR | IBS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0233 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01934 | hp1 | a0001 | c0008 | t0002 | g0311 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0038 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01943 | hp1 | a0001 | c0002 | t0007 | g0031 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0231 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01952 | hp1 | a0001 | c0003 | t0001 | g0232 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0230 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01975 | hp2 | a0001 | c0004 | t0002 | g0138 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01981 | hp1 | a0001 | c0001 | t0008 | g0032 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0338 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0133 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0340 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02004 | hp2 | a0001 | c0002 | t0010 | g0323 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0335 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02027 | hp1 | a0001 | c0003 | t0001 | g0169 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02040 | hp2 | a0001 | c0003 | t0001 | g0333 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02055 | hp2 | a0001 | c0005 | t0001 | g0131 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02056 | hp1 | a0001 | c0003 | t0001 | g0337 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02071 | hp1 | a0001 | c0003 | t0001 | g0312 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02071 | hp2 | a0001 | c0004 | t0002 | g0213 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02080 | hp1 | a0001 | c0003 | t0001 | g0075 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02080 | hp2 | a0001 | c0004 | t0002 | g0319 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0314 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02132 | hp1 | a0001 | c0003 | t0001 | g0211 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02132 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02145 | hp1 | a0001 | c0005 | t0001 | g0096 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02145 | hp2 | a0001 | c0005 | t0001 | g0347 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02148 | hp1 | a0001 | c0003 | t0001 | g0336 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0339 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | CDX | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | CDX | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CDX | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0342 | EAS | CDX | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02257 | hp2 | a0001 | c0005 | t0001 | g0240 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02273 | hp1 | a0001 | c0004 | t0002 | g0234 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02273 | hp2 | a0001 | c0003 | t0001 | g0101 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02280 | hp2 | a0001 | c0005 | t0001 | g0270 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0344 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02300 | hp1 | a0001 | c0004 | t0002 | g0003 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0119 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02451 | hp1 | a0001 | c0005 | t0001 | g0241 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02523 | hp1 | a0001 | c0004 | t0002 | g0215 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02523 | hp2 | a0001 | c0003 | t0001 | g0074 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0292 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02602 | hp1 | a0001 | c0003 | t0001 | g0095 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0326 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02615 | hp1 | a0001 | c0001 | t0012 | g0355 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0060 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02622 | hp2 | a0001 | c0007 | t0001 | g0262 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02647 | hp1 | a0001 | c0005 | t0005 | g0030 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02683 | hp1 | a0001 | c0003 | t0001 | g0327 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0054 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0090 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0145 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02717 | hp2 | a0001 | c0005 | t0001 | g0127 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0272 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0062 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0050 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02809 | hp1 | a0001 | c0004 | t0002 | g0350 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02818 | hp1 | a0001 | c0005 | t0001 | g0225 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0251 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02896 | hp2 | a0001 | c0005 | t0001 | g0267 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02897 | hp1 | a0001 | c0005 | t0001 | g0268 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0164 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02976 | hp1 | a0001 | c0005 | t0005 | g0030 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03017 | hp1 | a0001 | c0005 | t0001 | g0097 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03017 | hp2 | a0001 | c0004 | t0011 | g0354 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03041 | hp1 | a0001 | c0004 | t0002 | g0124 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0293 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03098 | hp2 | a0001 | c0005 | t0001 | g0257 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0258 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03209 | hp1 | a0001 | c0004 | t0002 | g0226 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03209 | hp2 | a0001 | c0010 | t0001 | g0265 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0123 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0051 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0291 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03486 | hp1 | a0001 | c0005 | t0001 | g0242 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03486 | hp2 | a0001 | c0005 | t0001 | g0277 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03490 | hp2 | a0001 | c0004 | t0002 | g0281 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03492 | hp2 | a0001 | c0004 | t0002 | g0243 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03516 | hp2 | a0001 | c0005 | t0009 | g0259 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03540 | hp1 | a0001 | c0005 | t0001 | g0221 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03540 | hp2 | a0001 | c0005 | t0001 | g0239 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0136 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0162 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03669 | hp1 | a0001 | c0004 | t0002 | g0188 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03669 | hp2 | a0001 | c0005 | t0001 | g0288 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0163 | SAS | STU | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0035 | SAS | STU | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0290 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0089 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03710 | hp1 | a0001 | c0012 | t0001 | g0121 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03710 | hp2 | a0001 | c0004 | t0002 | g0171 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0149 | SAS | BEB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | BEB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03927 | hp1 | a0001 | c0003 | t0001 | g0278 | SAS | BEB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03927 | hp2 | a0001 | c0005 | t0001 | g0161 | SAS | BEB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03942 | hp1 | a0001 | c0003 | t0001 | g0154 | SAS | BEB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0006 | SAS | BEB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0046 | SAS | STU | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0088 | SAS | STU | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG04184 | hp1 | a0001 | c0005 | t0001 | g0153 | SAS | BEB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG04184 | hp2 | a0001 | c0005 | t0001 | g0106 | SAS | BEB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG04199 | hp1 | a0001 | c0003 | t0002 | g0279 | SAS | STU | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0053 | SAS | STU | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG04204 | hp1 | a0001 | c0003 | t0001 | g0015 | SAS | STU | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG04204 | hp2 | a0001 | c0005 | t0001 | g0285 | SAS | STU | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0047 | SAS | STU | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG04228 | hp2 | a0001 | c0005 | t0001 | g0066 | SAS | STU | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0059 | AFR | YRI | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | YRI | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | CHB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18747 | hp2 | a0001 | c0003 | t0001 | g0076 | EAS | CHB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0156 | AFR | YRI | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0120 | AFR | YRI | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0329 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18939 | hp2 | a0001 | c0004 | t0002 | g0206 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18940 | hp1 | a0002 | c0006 | t0001 | g0027 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18940 | hp2 | a0001 | c0004 | t0002 | g0203 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18944 | hp1 | a0001 | c0004 | t0006 | g0003 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18946 | hp1 | a0001 | c0003 | t0001 | g0300 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0334 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18950 | hp1 | a0001 | c0005 | t0001 | g0039 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18950 | hp2 | a0002 | c0006 | t0001 | g0294 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18952 | hp1 | a0001 | c0004 | t0002 | g0341 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18952 | hp2 | a0001 | c0003 | t0001 | g0072 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0068 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18960 | hp1 | a0004 | c0009 | t0002 | g0183 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18963 | hp1 | a0001 | c0003 | t0001 | g0298 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18963 | hp2 | a0001 | c0004 | t0002 | g0205 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18966 | hp1 | a0001 | c0003 | t0001 | g0189 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18967 | hp1 | a0001 | c0003 | t0001 | g0081 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0343 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18970 | hp2 | a0001 | c0003 | t0001 | g0204 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18971 | hp2 | a0001 | c0003 | t0001 | g0283 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18973 | hp1 | a0002 | c0006 | t0001 | g0027 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18974 | hp1 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18980 | hp2 | a0001 | c0003 | t0001 | g0178 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18981 | hp1 | a0001 | c0003 | t0001 | g0082 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18982 | hp1 | a0002 | c0006 | t0001 | g0296 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18982 | hp2 | a0001 | c0004 | t0002 | g0186 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0078 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18983 | hp2 | a0001 | c0004 | t0002 | g0191 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18984 | hp2 | a0001 | c0004 | t0002 | g0190 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18988 | hp1 | a0001 | c0004 | t0002 | g0218 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18991 | hp1 | a0001 | c0004 | t0002 | g0117 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18993 | hp2 | a0001 | c0004 | t0002 | g0208 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18995 | hp2 | a0001 | c0004 | t0002 | g0192 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18999 | hp1 | a0002 | c0006 | t0001 | g0295 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19000 | hp1 | a0001 | c0004 | t0002 | g0185 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19000 | hp2 | a0001 | c0004 | t0002 | g0219 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19001 | hp2 | a0001 | c0004 | t0002 | g0184 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19004 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19009 | hp2 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19010 | hp2 | a0001 | c0005 | t0001 | g0276 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19011 | hp1 | a0001 | c0004 | t0006 | g0003 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19012 | hp1 | a0001 | c0003 | t0001 | g0071 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0036 | AFR | LWK | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | LWK | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19056 | hp2 | a0001 | c0003 | t0001 | g0037 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19059 | hp1 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19059 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19060 | hp1 | a0001 | c0004 | t0002 | g0202 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19063 | hp2 | a0001 | c0003 | t0001 | g0092 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19064 | hp2 | a0001 | c0003 | t0001 | g0084 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0318 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19067 | hp1 | a0001 | c0004 | t0002 | g0210 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19068 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19070 | hp2 | a0001 | c0003 | t0001 | g0158 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19074 | hp1 | a0001 | c0003 | t0001 | g0070 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19080 | hp2 | a0001 | c0004 | t0002 | g0198 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19087 | hp1 | a0001 | c0004 | t0002 | g0180 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19088 | hp1 | a0001 | c0003 | t0001 | g0085 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0328 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19090 | hp2 | a0001 | c0003 | t0001 | g0069 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | YRI | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA19240 | hp2 | a0001 | c0004 | t0002 | g0126 | AFR | YRI | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ASW | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA20129 | hp2 | a0005 | c0011 | t0001 | g0229 | AFR | ASW | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA20752 | hp1 | a0001 | c0005 | t0001 | g0026 | EUR | TSI | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0322 | EUR | TSI | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0098 | EUR | TSI | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0057 | EUR | TSI | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA20905 | hp1 | a0001 | c0004 | t0002 | g0034 | SAS | GIH | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | GIH | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0073 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02486 | hp2 | a0001 | c0004 | t0002 | g0125 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | USA | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| HG06807 | hp2 | a0001 | c0005 | t0001 | g0275 | AFR | USA | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18955 | hp1 | a0001 | c0005 | t0001 | g0063 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0137 | AFR | USA | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA20300 | hp2 | a0001 | c0005 | t0001 | g0282 | AFR | USA | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA21309 | hp1 | a0001 | c0005 | t0001 | g0346 | AFR | LWK | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | LWK | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0309 | REF | REF | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0159 | REF | REF | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:41684885 | G | C | 1 | a0003 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.1145C>G | p.Pro382Arg | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 9/9 | 1426/2333 | 1145/1431 | 382/476 | chr6 | 41684885 | |||
| chr6:41685059 | C | T | 1 | a0004 | 1 | NA18960.hp1 | missense_variant | MODERATE | c.971G>A | p.Arg324Gln | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 9/9 | 1252/2333 | 971/1431 | 324/476 | chr6 | 41685059 | |||
| chr6:41690743 | C | T | 1 | a0002 | 6 | HG00544.hp1 NA18940.hp1 NA18950.hp2 others(3): Show |
missense_variant | MODERATE | c.388G>A | p.Val130Met | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/9 | 669/2333 | 388/1431 | 130/476 | chr6 | 41690743 | |||
| chr6:41691062 | G | A | 1 | a0005 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.152C>T | p.Pro51Leu | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 2/9 | 433/2333 | 152/1431 | 51/476 | chr6 | 41691062 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:41684776 | C | T | 2 | a0001c0003 a0002c0006 |
97 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(94): Show |
synonymous_variant | LOW | c.1254G>A | p.Ala418Ala | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 9/9 | 1535/2333 | 1254/1431 | 418/476 | chr6 | 41684776 | |||
| chr6:41684866 | T | C | 9 | a0001c0001 a0001c0003 a0001c0004 others(6): Show |
306 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(303): Show |
synonymous_variant | LOW | c.1164A>G | p.Pro388Pro | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 9/9 | 1445/2333 | 1164/1431 | 388/476 | chr6 | 41684866 | |||
| chr6:41690786 | C | T | 1 | a0001c0012 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.345G>A | p.Pro115Pro | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/9 | 626/2333 | 345/1431 | 115/476 | chr6 | 41690786 | |||
| chr6:41690828 | C | T | 2 | a0001c0004 a0004c0009 |
47 | HG00323.hp1 HG00408.hp1 HG00621.hp1 others(44): Show |
synonymous_variant | LOW | c.303G>A | p.Gly101Gly | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/9 | 584/2333 | 303/1431 | 101/476 | chr6 | 41690828 | |||
| chr6:41691046 | G | A | 1 | a0001c0007 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.168C>T | p.Pro56Pro | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 2/9 | 449/2333 | 168/1431 | 56/476 | chr6 | 41691046 | |||
| chr6:41691061 | C | T | 1 | a0001c0008 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.153G>A | p.Pro51Pro | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 2/9 | 434/2333 | 153/1431 | 51/476 | chr6 | 41691061 | |||
| chr6:41691151 | C | T | 7 | a0001c0001 a0001c0004 a0001c0007 others(4): Show |
175 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(172): Show |
synonymous_variant | LOW | c.63G>A | p.Gln21Gln | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 2/9 | 344/2333 | 63/1431 | 21/476 | chr6 | 41691151 | |||
| chr6:41691166 | C | T | 1 | a0001c0007 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.48G>A | p.Ala16Ala | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 2/9 | 329/2333 | 48/1431 | 16/476 | chr6 | 41691166 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:41684156 | G | C | 1 | a0001c0005t0009 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*443C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 9/9 | 443 | chr6 | 41684156 | ||||||
| chr6:41684366 | G | A | 2 | a0001c0001t0003 a0001c0001t0008 |
20 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*233C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 9/9 | 233 | chr6 | 41684366 | ||||||
| chr6:41684398 | G | A | 7 | a0001c0001t0002 a0001c0003t0002 a0001c0004t0002 others(4): Show |
98 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*201C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 9/9 | 201 | chr6 | 41684398 | ||||||
| chr6:41684430 | C | A | 1 | a0001c0002t0010 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*169G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 9/9 | 169 | chr6 | 41684430 | ||||||
| chr6:41684484 | G | A | 1 | a0001c0003t0004 | 3 | HG01069.hp1 HG01099.hp2 HG01109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*115C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 9/9 | 115 | chr6 | 41684484 | ||||||
| chr6:41735397 | G | A | 1 | a0001c0004t0011 | 1 | HG03017.hp2 | 5_prime_UTR_variant | MODIFIER | c.-70C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/9 | 44184 | chr6 | 41735397 | ||||||
| chr6:41735504 | CCGCCGCC others(5): Show |
C | 1 | a0001c0001t0012 | 1 | HG02615.hp1 | 5_prime_UTR_variant | MODIFIER | c.-189_-178delCCGACG others(6): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/9 | 44292 | chr6 | 41735504 | ||||||
| chr6:41735507 | C | A | 1 | a0001c0001t0001 | 1 | HG01891.hp2 | 5_prime_UTR_variant | MODIFIER | c.-180G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/9 | 44294 | chr6 | 41735507 | ||||||
| chr6:41735571 | C | A | 1 | a0001c0005t0005 | 2 | HG02647.hp1 HG02976.hp1 |
5_prime_UTR_variant | MODIFIER | c.-244G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/9 | 44358 | chr6 | 41735571 | ||||||
| chr6:41735583 | C | T | 1 | a0001c0001t0008 | 1 | HG01981.hp1 | 5_prime_UTR_variant | MODIFIER | c.-256G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/9 | 44370 | chr6 | 41735583 | ||||||
| chr6:41735601 | C | T | 1 | a0001c0002t0007 | 1 | HG01943.hp1 | 5_prime_UTR_variant | MODIFIER | c.-274G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/9 | 44388 | chr6 | 41735601 | ||||||
| chr6:41735608 | C | A | 1 | a0001c0004t0006 | 2 | NA18944.hp1 NA19011.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-281G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/9 | chr6 | 41735608 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:41685133 | G | A | 1 | a0001c0002t0001g0140 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.952-55C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685133 | |||||||
| chr6:41685180 | G | C | 1 | a0001c0003t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.952-102C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685180 | |||||||
| chr6:41685214 | A | G | 1 | a0001c0010t0001g0265 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.952-136T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685214 | |||||||
| chr6:41685255 | A | G | 54 | a0001c0001t0001g0110 a0001c0001t0002g0083 a0001c0001t0002g0094 others(51): Show |
57 | HG00323.hp1 HG00408.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.952-177T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685255 | |||||||
| chr6:41685265 | G | A | 9 | a0001c0005t0001g0096 a0001c0005t0001g0118 a0001c0005t0001g0131 others(6): Show |
9 | HG01168.hp2 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.952-187C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685265 | |||||||
| chr6:41685300 | A | C | 1 | a0001c0005t0001g0240 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.952-222T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685300 | |||||||
| chr6:41685319 | T | A | 15 | a0001c0001t0001g0008 a0001c0001t0001g0111 a0001c0001t0001g0122 others(12): Show |
17 | HG00642.hp2 HG01081.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.952-241A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685319 | |||||||
| chr6:41685358 | A | G | 8 | a0001c0005t0001g0127 a0001c0005t0001g0239 a0001c0005t0001g0240 others(5): Show |
9 | HG02257.hp2 HG02451.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.952-280T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685358 | |||||||
| chr6:41685378 | T | C | 55 | a0001c0001t0001g0025 a0001c0001t0001g0093 a0001c0001t0001g0112 others(52): Show |
60 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.952-300A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685378 | |||||||
| chr6:41685573 | A | ACTAGAAC others(3): Show |
1 | a0001c0002t0001g0140 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.952-505_952-496dup others(10): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685573 | |||||||
| chr6:41685664 | C | T | 15 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0104 others(12): Show |
16 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.951+426G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685664 | |||||||
| chr6:41685669 | G | A | 1 | a0001c0007t0001g0262 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.951+421C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685669 | |||||||
| chr6:41685748 | G | C | 13 | a0001c0001t0001g0025 a0001c0001t0001g0112 a0001c0001t0001g0113 others(10): Show |
14 | HG01891.hp2 HG02559.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.951+342C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685748 | |||||||
| chr6:41685859 | G | A | 9 | a0001c0005t0001g0096 a0001c0005t0001g0118 a0001c0005t0001g0131 others(6): Show |
9 | HG01168.hp2 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.951+231C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685859 | |||||||
| chr6:41685984 | C | T | 5 | a0001c0001t0001g0093 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02451.hp2 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.951+106G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685984 | |||||||
| chr6:41686299 | A | G | 1 | a0001c0003t0001g0069 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.804-62T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686299 | |||||||
| chr6:41686372 | G | A | 88 | a0001c0001t0001g0110 a0001c0001t0001g0236 a0001c0001t0002g0010 others(85): Show |
99 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.804-135C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686372 | |||||||
| chr6:41686475 | C | CA | 276 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(273): Show |
309 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.804-239dupT | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686475 | |||||||
| chr6:41686495 | C | G | 1 | a0001c0002t0001g0137 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.804-258G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686495 | |||||||
| chr6:41686503 | CCTTT | C | 9 | a0001c0001t0001g0112 a0001c0001t0001g0248 a0001c0001t0001g0249 others(6): Show |
9 | HG01891.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-270_804-267del others(4): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686503 | |||||||
| chr6:41686508 | C | CT | 28 | a0001c0001t0001g0093 a0001c0001t0001g0115 a0001c0001t0001g0116 others(25): Show |
29 | HG00140.hp2 HG00408.hp2 HG01515.hp1 others(26): Show |
intron_variant | MODIFIER | c.804-272dupA | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686508 | |||||||
| chr6:41686508 | C | CTT | 78 | a0001c0002t0001g0137 a0001c0003t0001g0005 a0001c0003t0001g0006 others(75): Show |
91 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.804-273_804-272dup others(2): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686508 | |||||||
| chr6:41686508 | CT | C | 114 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0197 others(111): Show |
133 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.804-272delA | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686508 | |||||||
| chr6:41686508 | CTT | C | 10 | a0001c0001t0002g0012 a0001c0001t0002g0058 a0001c0001t0002g0083 others(7): Show |
11 | HG00558.hp1 HG00733.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.804-273_804-272del others(2): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686508 | |||||||
| chr6:41686585 | G | A | 2 | a0001c0004t0002g0124 a0001c0004t0002g0126 |
2 | HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.804-348C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686585 | |||||||
| chr6:41686604 | C | T | 13 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0104 others(10): Show |
14 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.804-367G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686604 | |||||||
| chr6:41686683 | G | T | 276 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(273): Show |
309 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.803+411C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686683 | |||||||
| chr6:41686794 | G | A | 1 | a0001c0003t0001g0144 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.803+300C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686794 | |||||||
| chr6:41686990 | A | G | 2 | a0001c0005t0001g0269 a0001c0005t0001g0270 |
2 | HG01361.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.803+104T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686990 | |||||||
| chr6:41687194 | A | G | 15 | a0001c0001t0001g0008 a0001c0001t0001g0111 a0001c0001t0001g0122 others(12): Show |
17 | HG00642.hp2 HG01081.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.728-25T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 6/8 | chr6 | 41687194 | |||||||
| chr6:41687267 | G | A | 261 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0048 others(258): Show |
293 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.728-98C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 6/8 | chr6 | 41687267 | |||||||
| chr6:41687447 | A | G | 6 | a0001c0004t0002g0180 a0001c0004t0002g0182 a0001c0004t0002g0184 others(3): Show |
6 | HG00621.hp1 NA18940.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.728-278T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 6/8 | chr6 | 41687447 | |||||||
| chr6:41687602 | C | T | 87 | a0001c0001t0001g0236 a0001c0001t0002g0010 a0001c0001t0002g0011 others(84): Show |
98 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.727+151G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 6/8 | chr6 | 41687602 | |||||||
| chr6:41687724 | G | A | 2 | a0001c0005t0001g0127 a0001c0005t0005g0030 |
3 | HG02647.hp1 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.727+29C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 6/8 | chr6 | 41687724 | |||||||
| chr6:41687739 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0132 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.727+14C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 6/8 | chr6 | 41687739 | |||||||
| chr6:41688076 | G | A | 34 | a0001c0001t0001g0236 a0001c0001t0002g0010 a0001c0001t0002g0011 others(31): Show |
42 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.550-48C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688076 | |||||||
| chr6:41688095 | C | T | 1 | a0001c0003t0002g0279 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.550-67G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688095 | |||||||
| chr6:41688154 | C | G | 15 | a0001c0001t0001g0008 a0001c0001t0001g0111 a0001c0001t0001g0122 others(12): Show |
17 | HG00642.hp2 HG01081.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.550-126G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688154 | |||||||
| chr6:41688160 | C | T | 1 | a0001c0002t0001g0140 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.550-132G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688160 | |||||||
| chr6:41688204 | A | G | 85 | a0001c0002t0001g0137 a0001c0003t0001g0005 a0001c0003t0001g0006 others(82): Show |
98 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.550-176T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688204 | |||||||
| chr6:41688237 | G | C | 20 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(17): Show |
23 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.550-209C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688237 | |||||||
| chr6:41688345 | G | T | 1 | a0001c0005t0001g0106 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.550-317C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688345 | |||||||
| chr6:41688604 | G | GGA | 150 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0048 others(147): Show |
168 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.550-578_550-577dup others(2): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688604 | |||||||
| chr6:41688753 | G | A | 1 | a0001c0004t0002g0190 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.550-725C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688753 | |||||||
| chr6:41688773 | T | C | 15 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0104 others(12): Show |
16 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.550-745A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688773 | |||||||
| chr6:41688859 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.550-831G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688859 | |||||||
| chr6:41688902 | G | A | 2 | a0001c0002t0001g0123 a0001c0002t0001g0163 |
2 | HG03239.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.549+829C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688902 | |||||||
| chr6:41688990 | C | T | 275 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(272): Show |
308 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.549+741G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688990 | |||||||
| chr6:41688994 | C | T | 1 | a0001c0004t0002g0215 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.549+737G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688994 | |||||||
| chr6:41689149 | A | G | 5 | a0001c0001t0001g0093 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02451.hp2 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.549+582T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41689149 | |||||||
| chr6:41689197 | C | A | 1 | a0001c0001t0001g0317 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.549+534G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41689197 | |||||||
| chr6:41689358 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.549+373G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41689358 | |||||||
| chr6:41689590 | A | G | 274 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(271): Show |
307 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.549+141T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41689590 | |||||||
| chr6:41689621 | C | T | 17 | a0001c0001t0001g0025 a0001c0001t0001g0112 a0001c0001t0001g0113 others(14): Show |
18 | HG01891.hp2 HG02559.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.549+110G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41689621 | |||||||
| chr6:41689935 | G | A | 15 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0104 others(12): Show |
16 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.469-124C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41689935 | |||||||
| chr6:41689964 | T | A | 17 | a0001c0001t0003g0004 a0001c0001t0003g0077 a0001c0001t0003g0079 others(14): Show |
20 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.469-153A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41689964 | |||||||
| chr6:41690072 | G | A | 14 | a0001c0001t0003g0004 a0001c0001t0003g0077 a0001c0001t0003g0079 others(11): Show |
17 | HG00597.hp1 HG00609.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.469-261C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41690072 | |||||||
| chr6:41690135 | C | T | 1 | a0001c0001t0002g0302 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.469-324G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41690135 | |||||||
| chr6:41690135 | CT | C | 34 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0048 others(31): Show |
37 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.469-325delA | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41690135 | |||||||
| chr6:41690136 | T | C | 1 | a0001c0001t0002g0302 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.469-325A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41690136 | |||||||
| chr6:41690169 | C | T | 101 | a0001c0002t0001g0137 a0001c0003t0001g0005 a0001c0003t0001g0006 others(98): Show |
115 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.469-358G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41690169 | |||||||
| chr6:41690240 | C | G | 2 | a0001c0005t0001g0127 a0001c0005t0005g0030 |
3 | HG02647.hp1 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.468+423G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41690240 | |||||||
| chr6:41690287 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.468+376G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41690287 | |||||||
| chr6:41690344 | G | C | 1 | a0001c0001t0001g0220 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.468+319C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41690344 | |||||||
| chr6:41690374 | G | C | 144 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0048 others(141): Show |
161 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.468+289C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41690374 | |||||||
| chr6:41690516 | G | T | 2 | a0001c0001t0001g0252 a0001c0001t0012g0355 |
2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.468+147C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41690516 | |||||||
| chr6:41690655 | T | A | 6 | a0001c0004t0002g0180 a0001c0004t0002g0182 a0001c0004t0002g0184 others(3): Show |
6 | HG00621.hp1 NA18940.hp2 NA18960.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.468+8A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41690655 | |||||||
| chr6:41691325 | C | T | 1 | a0001c0002t0001g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-22-90G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41691325 | |||||||
| chr6:41691566 | C | T | 140 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(137): Show |
155 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.-22-331G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41691566 | |||||||
| chr6:41691589 | G | A | 55 | a0001c0001t0001g0110 a0001c0001t0001g0112 a0001c0001t0002g0083 others(52): Show |
58 | HG00323.hp1 HG00408.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-22-354C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41691589 | |||||||
| chr6:41691622 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-22-387G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41691622 | |||||||
| chr6:41691759 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-22-524G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41691759 | |||||||
| chr6:41691895 | C | T | 1 | a0001c0001t0002g0332 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-22-660G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41691895 | |||||||
| chr6:41691994 | C | A | 16 | a0001c0001t0003g0004 a0001c0001t0003g0077 a0001c0001t0003g0079 others(13): Show |
19 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.-22-759G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41691994 | |||||||
| chr6:41692016 | C | T | 15 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0104 others(12): Show |
16 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.-22-781G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41692016 | |||||||
| chr6:41692128 | A | T | 1 | a0001c0004t0002g0184 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-22-893T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41692128 | |||||||
| chr6:41692129 | T | A | 1 | a0001c0004t0002g0184 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-22-894A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41692129 | |||||||
| chr6:41692359 | C | T | 15 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0104 others(12): Show |
16 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.-22-1124G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41692359 | |||||||
| chr6:41692363 | T | TGCAGTTC others(4): Show |
1 | a0001c0001t0002g0302 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-22-1139_-22-1129d others(13): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41692363 | |||||||
| chr6:41692446 | C | T | 1 | a0002c0006t0001g0295 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-22-1211G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41692446 | |||||||
| chr6:41692459 | C | G | 2 | a0001c0001t0001g0122 a0001c0001t0001g0132 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-22-1224G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41692459 | |||||||
| chr6:41692791 | T | G | 4 | a0001c0002t0001g0133 a0001c0002t0001g0143 a0001c0002t0007g0031 others(1): Show |
4 | HG00735.hp2 HG01081.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-1556A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41692791 | |||||||
| chr6:41692852 | T | C | 15 | a0001c0001t0001g0008 a0001c0001t0001g0111 a0001c0001t0001g0122 others(12): Show |
17 | HG00642.hp2 HG01081.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22-1617A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41692852 | |||||||
| chr6:41693017 | T | G | 15 | a0001c0001t0001g0008 a0001c0001t0001g0111 a0001c0001t0001g0122 others(12): Show |
17 | HG00642.hp2 HG01081.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22-1782A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41693017 | |||||||
| chr6:41693280 | A | G | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-22-2045T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41693280 | |||||||
| chr6:41693487 | C | G | 1 | a0001c0001t0002g0302 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-22-2252G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41693487 | |||||||
| chr6:41693517 | A | T | 1 | a0001c0001t0003g0335 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-22-2282T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41693517 | |||||||
| chr6:41693604 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0012g0355 |
2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-22-2369G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41693604 | |||||||
| chr6:41693785 | C | T | 1 | a0001c0001t0002g0302 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-22-2550G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41693785 | |||||||
| chr6:41693841 | C | T | 1 | a0001c0005t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-22-2606G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41693841 | |||||||
| chr6:41693922 | C | T | 1 | a0001c0001t0002g0289 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-22-2687G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41693922 | |||||||
| chr6:41694057 | C | A | 6 | a0001c0005t0001g0239 a0001c0005t0001g0240 a0001c0005t0001g0241 others(3): Show |
6 | HG02257.hp2 HG02451.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-2822G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694057 | |||||||
| chr6:41694281 | A | G | 38 | a0001c0001t0001g0025 a0001c0001t0001g0093 a0001c0001t0001g0113 others(35): Show |
42 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.-22-3046T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694281 | |||||||
| chr6:41694395 | A | C | 2 | a0001c0005t0001g0127 a0001c0005t0005g0030 |
3 | HG02647.hp1 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-22-3160T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694395 | |||||||
| chr6:41694485 | G | A | 2 | a0001c0005t0001g0127 a0001c0005t0005g0030 |
3 | HG02647.hp1 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-22-3250C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694485 | |||||||
| chr6:41694515 | T | C | 1 | a0001c0005t0001g0282 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-22-3280A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694515 | |||||||
| chr6:41694545 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0132 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-22-3310C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694545 | |||||||
| chr6:41694561 | G | A | 89 | a0001c0001t0001g0110 a0001c0001t0001g0112 a0001c0001t0001g0236 others(86): Show |
100 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.-22-3326C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694561 | |||||||
| chr6:41694739 | C | G | 16 | a0001c0001t0003g0004 a0001c0001t0003g0077 a0001c0001t0003g0079 others(13): Show |
19 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.-22-3504G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694739 | |||||||
| chr6:41694750 | C | T | 1 | a0001c0001t0002g0316 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-22-3515G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694750 | |||||||
| chr6:41694838 | C | T | 273 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(270): Show |
306 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.-22-3603G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694838 | |||||||
| chr6:41694839 | T | C | 3 | a0001c0001t0002g0083 a0001c0001t0002g0289 a0001c0001t0002g0290 |
3 | HG02015.hp2 HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-22-3604A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694839 | |||||||
| chr6:41694852 | C | T | 1 | a0001c0004t0002g0191 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-22-3617G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694852 | |||||||
| chr6:41694860 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-22-3625G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694860 | |||||||
| chr6:41694903 | G | T | 1 | a0005c0011t0001g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-22-3668C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694903 | |||||||
| chr6:41694910 | C | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0111 a0001c0001t0001g0122 others(20): Show |
26 | HG00642.hp2 HG01081.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.-22-3675G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694910 | |||||||
| chr6:41694958 | C | A | 18 | a0001c0001t0001g0025 a0001c0001t0001g0093 a0001c0001t0001g0113 others(15): Show |
19 | HG01891.hp2 HG02451.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.-22-3723G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694958 | |||||||
| chr6:41694964 | G | T | 1 | a0001c0001t0002g0302 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-22-3729C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694964 | |||||||
| chr6:41695019 | C | T | 1 | a0001c0001t0002g0310 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-22-3784G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41695019 | |||||||
| chr6:41695045 | T | C | 23 | a0001c0001t0001g0008 a0001c0001t0001g0111 a0001c0001t0001g0122 others(20): Show |
26 | HG00642.hp2 HG01081.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.-22-3810A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41695045 | |||||||
| chr6:41695105 | G | C | 173 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(170): Show |
192 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.-22-3870C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41695105 | |||||||
| chr6:41695151 | T | G | 9 | a0001c0005t0001g0096 a0001c0005t0001g0118 a0001c0005t0001g0131 others(6): Show |
9 | HG01168.hp2 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22-3916A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41695151 | |||||||
| chr6:41695152 | C | G | 177 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(174): Show |
196 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.-22-3917G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41695152 | |||||||
| chr6:41695198 | T | C | 3 | a0001c0001t0001g0274 a0001c0003t0001g0333 a0001c0010t0001g0265 |
3 | HG02040.hp2 HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-22-3963A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41695198 | |||||||
| chr6:41695554 | C | G | 3 | a0001c0001t0002g0297 a0001c0001t0002g0304 a0001c0001t0002g0315 |
3 | HG00423.hp1 HG00609.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.-22-4319G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41695554 | |||||||
| chr6:41695673 | T | G | 2 | a0001c0003t0001g0068 a0001c0003t0001g0071 |
2 | NA18954.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-22-4438A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41695673 | |||||||
| chr6:41695712 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-22-4477C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41695712 | |||||||
| chr6:41696003 | G | A | 4 | a0001c0002t0001g0017 a0001c0002t0001g0120 a0001c0002t0001g0258 others(1): Show |
5 | HG01255.hp2 HG03130.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-4768C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696003 | |||||||
| chr6:41696258 | C | A | 14 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0104 others(11): Show |
15 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.-22-5023G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696258 | |||||||
| chr6:41696294 | C | A | 160 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0048 others(157): Show |
178 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.-22-5059G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696294 | |||||||
| chr6:41696343 | C | T | 18 | a0001c0002t0001g0045 a0001c0005t0001g0096 a0001c0005t0001g0118 others(15): Show |
19 | HG00280.hp1 HG01168.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-22-5108G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696343 | |||||||
| chr6:41696383 | C | T | 272 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(269): Show |
305 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.-22-5148G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696383 | |||||||
| chr6:41696385 | A | T | 1 | a0001c0001t0002g0302 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-22-5150T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696385 | |||||||
| chr6:41696490 | C | T | 134 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0048 others(131): Show |
149 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.-22-5255G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696490 | |||||||
| chr6:41696619 | G | A | 2 | a0001c0004t0002g0180 a0001c0004t0002g0185 |
2 | NA19000.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-22-5384C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696619 | |||||||
| chr6:41696763 | G | T | 89 | a0001c0001t0001g0110 a0001c0001t0001g0112 a0001c0001t0001g0236 others(86): Show |
100 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.-22-5528C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696763 | |||||||
| chr6:41696823 | G | A | 3 | a0001c0003t0001g0013 a0001c0003t0001g0067 a0001c0003t0001g0073 |
4 | HG01123.hp1 HG01192.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-5588C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696823 | |||||||
| chr6:41696950 | C | A | 1 | a0001c0002t0001g0324 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-22-5715G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696950 | |||||||
| chr6:41696989 | T | C | 267 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0048 others(264): Show |
299 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.-22-5754A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696989 | |||||||
| chr6:41696999 | T | C | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-22-5764A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696999 | |||||||
| chr6:41697045 | C | A | 2 | a0001c0002t0001g0147 a0001c0002t0001g0152 |
2 | NA18967.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.-22-5810G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697045 | |||||||
| chr6:41697135 | T | C | 266 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0048 others(263): Show |
298 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.-22-5900A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697135 | |||||||
| chr6:41697213 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-22-5978C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697213 | |||||||
| chr6:41697318 | G | C | 8 | a0001c0005t0001g0127 a0001c0005t0001g0239 a0001c0005t0001g0240 others(5): Show |
9 | HG02257.hp2 HG02451.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22-6083C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697318 | |||||||
| chr6:41697354 | A | G | 268 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0048 others(265): Show |
300 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.-22-6119T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697354 | |||||||
| chr6:41697408 | C | CAA | 5 | a0002c0006t0001g0027 a0002c0006t0001g0294 a0002c0006t0001g0295 others(2): Show |
6 | HG00544.hp1 NA18940.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-6175_-22-6174d others(4): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | |||||||
| chr6:41697408 | C | CAAAAA | 9 | a0001c0001t0003g0004 a0001c0001t0003g0164 a0001c0001t0003g0166 others(6): Show |
12 | HG00597.hp1 HG01346.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.-22-6178_-22-6174d others(7): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | |||||||
| chr6:41697408 | C | CAAAAAAA others(2): Show |
11 | a0001c0001t0001g0008 a0001c0001t0001g0111 a0001c0001t0001g0130 others(8): Show |
13 | HG02257.hp1 HG02895.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.-22-6182_-22-6174d others(11): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | |||||||
| chr6:41697408 | C | CAAAAAAA others(3): Show |
15 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0104 others(12): Show |
17 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22-6183_-22-6174d others(12): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | |||||||
| chr6:41697408 | C | CAAAAAAA others(4): Show |
38 | a0001c0001t0001g0105 a0001c0001t0001g0196 a0001c0001t0001g0197 others(35): Show |
41 | HG00323.hp1 HG00408.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-22-6184_-22-6174d others(13): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | |||||||
| chr6:41697408 | C | CAAAAAAA others(5): Show |
26 | a0001c0001t0002g0223 a0001c0002t0001g0286 a0001c0002t0001g0287 others(23): Show |
27 | HG00140.hp2 HG00323.hp2 HG01943.hp2 others(24): Show |
intron_variant | MODIFIER | c.-22-6185_-22-6174d others(14): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | |||||||
| chr6:41697408 | C | CAAAAAAA others(6): Show |
55 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0002t0001g0137 others(52): Show |
62 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.-22-6186_-22-6174d others(15): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | |||||||
| chr6:41697408 | C | CAAAAAAA others(7): Show |
23 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0014 others(20): Show |
29 | HG00438.hp1 HG00642.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.-22-6187_-22-6174d others(16): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | |||||||
| chr6:41697408 | C | CAAAAAAA others(8): Show |
13 | a0001c0001t0001g0113 a0001c0003t0001g0060 a0001c0003t0001g0069 others(10): Show |
13 | HG02071.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-22-6188_-22-6174d others(17): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | |||||||
| chr6:41697408 | C | CAAAAAAA others(10): Show |
4 | a0001c0001t0001g0093 a0001c0001t0001g0115 a0001c0001t0001g0129 others(1): Show |
4 | HG02451.hp2 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-6190_-22-6174d others(19): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | |||||||
| chr6:41697408 | C | CAAAAAAA others(11): Show |
5 | a0001c0005t0001g0118 a0001c0005t0001g0225 a0001c0005t0001g0257 others(2): Show |
5 | HG01168.hp2 HG02818.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22-6191_-22-6174d others(20): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | |||||||
| chr6:41697408 | C | CAAAAAAA others(12): Show |
3 | a0001c0001t0001g0116 a0001c0002t0001g0258 a0001c0005t0001g0346 |
3 | HG02647.hp2 HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-22-6192_-22-6174d others(21): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | |||||||
| chr6:41697408 | C | CAAAAAAA others(13): Show |
3 | a0001c0001t0001g0114 a0001c0005t0001g0131 a0001c0005t0001g0347 |
3 | HG02055.hp2 HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-22-6174_-22-6173i others(22): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | |||||||
| chr6:41697408 | C | CAAAAAAA others(14): Show |
5 | a0001c0001t0001g0248 a0001c0001t0001g0263 a0001c0001t0001g0264 others(2): Show |
5 | HG02145.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22-6174_-22-6173i others(23): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | |||||||
| chr6:41697408 | C | CAAAAAAA others(15): Show |
3 | a0001c0001t0001g0249 a0001c0001t0001g0252 a0001c0001t0012g0355 |
3 | HG02615.hp1 HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-22-6174_-22-6173i others(24): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | |||||||
| chr6:41697408 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0001g0273 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-22-6174_-22-6173i others(26): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | |||||||
| chr6:41697408 | CAAAAAAA | C | 59 | a0001c0001t0001g0048 a0001c0001t0001g0110 a0001c0001t0001g0274 others(56): Show |
67 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.-22-6180_-22-6174d others(9): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | |||||||
| chr6:41697427 | A | AAAAAAAA others(9): Show |
1 | a0001c0002t0001g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-22-6193_-22-6192i others(18): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697427 | |||||||
| chr6:41697487 | A | G | 3 | a0001c0001t0001g0245 a0001c0001t0001g0252 a0001c0001t0012g0355 |
3 | HG02615.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-22-6252T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697487 | |||||||
| chr6:41697503 | A | AC | 232 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0048 others(229): Show |
263 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.-22-6269dupG | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697503 | |||||||
| chr6:41697503 | A | C | 1 | a0001c0001t0001g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-22-6268T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697503 | |||||||
| chr6:41697503 | AC | A | 15 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0105 others(12): Show |
16 | HG00280.hp2 HG00323.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.-22-6269delG | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697503 | |||||||
| chr6:41697511 | C | G | 1 | a0001c0002t0001g0195 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-22-6276G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697511 | |||||||
| chr6:41697524 | T | A | 4 | a0001c0001t0001g0110 a0001c0001t0002g0107 a0001c0001t0002g0108 others(1): Show |
4 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-6289A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697524 | |||||||
| chr6:41697619 | A | G | 6 | a0001c0005t0001g0239 a0001c0005t0001g0240 a0001c0005t0001g0241 others(3): Show |
6 | HG02257.hp2 HG02451.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-6384T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697619 | |||||||
| chr6:41697624 | T | A | 1 | a0001c0001t0002g0325 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-22-6389A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697624 | |||||||
| chr6:41697649 | C | T | 2 | a0001c0001t0002g0016 a0001c0001t0002g0091 |
3 | HG01243.hp1 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-22-6414G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697649 | |||||||
| chr6:41697688 | G | C | 1 | a0001c0001t0002g0029 | 2 | HG00544.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.-22-6453C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697688 | |||||||
| chr6:41697745 | C | T | 54 | a0001c0001t0001g0187 a0001c0001t0001g0194 a0001c0001t0001g0196 others(51): Show |
57 | HG00323.hp1 HG00408.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.-22-6510G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697745 | |||||||
| chr6:41697768 | T | G | 55 | a0001c0001t0001g0187 a0001c0001t0001g0194 a0001c0001t0001g0196 others(52): Show |
58 | HG00323.hp1 HG00408.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-22-6533A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697768 | |||||||
| chr6:41697912 | G | C | 19 | a0001c0001t0001g0317 a0001c0001t0002g0011 a0001c0001t0002g0028 others(16): Show |
22 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.-22-6677C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697912 | |||||||
| chr6:41697947 | G | C | 1 | a0001c0001t0012g0355 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-22-6712C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697947 | |||||||
| chr6:41698038 | G | GA | 36 | a0001c0001t0001g0093 a0001c0001t0001g0115 a0001c0001t0001g0116 others(33): Show |
39 | HG00597.hp1 HG00741.hp2 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.-22-6804dupT | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41698038 | |||||||
| chr6:41698153 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-22-6918C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41698153 | |||||||
| chr6:41698169 | C | T | 67 | a0001c0001t0001g0187 a0001c0001t0001g0194 a0001c0001t0001g0196 others(64): Show |
70 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-22-6934G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41698169 | |||||||
| chr6:41698327 | G | A | 19 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0220 others(16): Show |
22 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.-22-7092C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41698327 | |||||||
| chr6:41698554 | A | C | 21 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0105 others(18): Show |
24 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.-22-7319T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41698554 | |||||||
| chr6:41698620 | G | A | 3 | a0001c0001t0001g0105 a0001c0003t0001g0035 a0001c0005t0001g0106 |
3 | HG02738.hp2 HG03688.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-22-7385C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41698620 | |||||||
| chr6:41698628 | T | G | 1 | a0001c0001t0001g0260 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-22-7393A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41698628 | |||||||
| chr6:41698840 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-22-7605G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41698840 | |||||||
| chr6:41698901 | T | A | 1 | a0001c0005t0001g0346 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-22-7666A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41698901 | |||||||
| chr6:41699295 | A | C | 20 | a0001c0001t0001g0114 a0001c0001t0001g0245 a0001c0001t0001g0274 others(17): Show |
23 | HG00597.hp1 HG00741.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.-22-8060T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699295 | |||||||
| chr6:41699299 | C | T | 54 | a0001c0001t0001g0048 a0001c0001t0001g0110 a0001c0001t0001g0317 others(51): Show |
60 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.-22-8064G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699299 | |||||||
| chr6:41699354 | C | T | 1 | a0001c0001t0002g0308 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-22-8119G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699354 | |||||||
| chr6:41699377 | T | C | 1 | a0001c0005t0001g0275 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-22-8142A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699377 | |||||||
| chr6:41699454 | G | A | 1 | a0001c0001t0002g0289 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-22-8219C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699454 | |||||||
| chr6:41699460 | G | A | 1 | a0001c0002t0001g0328 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-22-8225C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699460 | |||||||
| chr6:41699560 | A | C | 1 | a0001c0002t0001g0172 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-22-8325T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699560 | |||||||
| chr6:41699575 | G | A | 1 | a0001c0004t0002g0243 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-22-8340C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699575 | |||||||
| chr6:41699640 | C | T | 2 | a0001c0001t0001g0122 a0001c0001t0001g0132 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-22-8405G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699640 | |||||||
| chr6:41699768 | A | C | 38 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0105 others(35): Show |
44 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.-22-8533T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699768 | |||||||
| chr6:41699802 | G | A | 1 | a0001c0002t0001g0176 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-22-8567C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699802 | |||||||
| chr6:41699840 | G | C | 1 | a0001c0005t0001g0275 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-22-8605C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699840 | |||||||
| chr6:41699896 | A | T | 2 | a0001c0001t0001g0048 a0001c0001t0002g0058 |
2 | HG00733.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-22-8661T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699896 | |||||||
| chr6:41700025 | C | T | 2 | a0001c0001t0002g0289 a0001c0001t0002g0290 |
2 | HG02015.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-22-8790G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700025 | |||||||
| chr6:41700188 | T | C | 69 | a0001c0001t0001g0110 a0001c0001t0001g0187 a0001c0001t0001g0196 others(66): Show |
73 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-22-8953A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700188 | |||||||
| chr6:41700205 | G | A | 1 | a0001c0008t0002g0311 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-22-8970C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700205 | |||||||
| chr6:41700213 | TC | T | 18 | a0001c0001t0001g0025 a0001c0001t0001g0224 a0001c0001t0001g0246 others(15): Show |
19 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-22-8979delG | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700213 | |||||||
| chr6:41700232 | T | C | 1 | a0001c0008t0002g0311 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-22-8997A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700232 | |||||||
| chr6:41700238 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-22-9003C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700238 | |||||||
| chr6:41700334 | C | T | 1 | a0001c0002t0001g0136 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-22-9099G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700334 | |||||||
| chr6:41700383 | G | A | 1 | a0001c0003t0001g0035 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-22-9148C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700383 | |||||||
| chr6:41700390 | C | T | 1 | a0002c0006t0001g0301 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-22-9155G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700390 | |||||||
| chr6:41700402 | C | G | 1 | a0002c0006t0001g0301 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-22-9167G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700402 | |||||||
| chr6:41700407 | A | G | 1 | a0002c0006t0001g0301 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-22-9172T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700407 | |||||||
| chr6:41700458 | T | A | 118 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0105 others(115): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.-22-9223A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700458 | |||||||
| chr6:41700465 | C | CA | 13 | a0001c0001t0001g0113 a0001c0002t0001g0148 a0001c0002t0001g0271 others(10): Show |
13 | HG00438.hp1 HG01981.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.-22-9231dupT | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700465 | |||||||
| chr6:41700465 | CA | C | 92 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0132 others(89): Show |
99 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.-22-9231delT | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700465 | |||||||
| chr6:41700465 | CAA | C | 56 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(53): Show |
62 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.-22-9232_-22-9231d others(4): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700465 | |||||||
| chr6:41700550 | C | T | 2 | a0001c0005t0001g0347 a0001c0005t0009g0259 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-22-9315G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700550 | |||||||
| chr6:41700797 | G | C | 1 | a0001c0003t0001g0072 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-22-9562C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700797 | |||||||
| chr6:41700842 | C | A | 15 | a0001c0001t0003g0004 a0001c0001t0003g0119 a0001c0001t0003g0164 others(12): Show |
18 | HG00597.hp1 HG00741.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.-22-9607G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700842 | |||||||
| chr6:41700880 | G | C | 2 | a0001c0005t0001g0269 a0001c0005t0001g0270 |
2 | HG01361.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-22-9645C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700880 | |||||||
| chr6:41700916 | G | T | 1 | a0001c0004t0002g0181 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-22-9681C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700916 | |||||||
| chr6:41700926 | C | T | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-22-9691G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700926 | |||||||
| chr6:41701155 | A | C | 12 | a0001c0001t0003g0004 a0001c0001t0003g0119 a0001c0001t0003g0166 others(9): Show |
15 | HG00597.hp1 HG01346.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.-22-9920T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701155 | |||||||
| chr6:41701182 | C | T | 1 | a0001c0001t0002g0022 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-22-9947G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701182 | |||||||
| chr6:41701272 | C | A | 1 | a0001c0001t0002g0302 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-22-10037G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701272 | |||||||
| chr6:41701273 | A | C | 1 | a0001c0001t0002g0302 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-22-10038T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701273 | |||||||
| chr6:41701274 | C | A | 1 | a0001c0001t0002g0302 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-22-10039G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701274 | |||||||
| chr6:41701498 | G | T | 1 | a0001c0001t0001g0352 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-22-10263C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701498 | |||||||
| chr6:41701638 | A | C | 3 | a0001c0002t0001g0086 a0001c0002t0001g0134 a0001c0003t0001g0204 |
3 | NA18970.hp2 NA19082.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-22-10403T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701638 | |||||||
| chr6:41701722 | A | T | 1 | a0001c0002t0001g0200 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-22-10487T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701722 | |||||||
| chr6:41701829 | C | G | 4 | a0001c0002t0001g0322 a0001c0002t0001g0324 a0001c0002t0010g0323 others(1): Show |
4 | HG01255.hp1 HG02004.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-10594G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701829 | |||||||
| chr6:41701939 | C | T | 7 | a0001c0002t0001g0258 a0001c0005t0001g0096 a0001c0005t0001g0118 others(4): Show |
7 | HG01168.hp2 HG02145.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-22-10704G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701939 | |||||||
| chr6:41701940 | G | A | 4 | a0001c0005t0001g0239 a0001c0005t0001g0240 a0001c0005t0001g0241 others(1): Show |
4 | HG02257.hp2 HG02451.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-10705C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701940 | |||||||
| chr6:41701944 | C | CAAA | 39 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0113 others(36): Show |
42 | HG00642.hp2 HG01070.hp1 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.-22-10712_-22-1071 others(7): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701944 | |||||||
| chr6:41701944 | C | CAAAA | 76 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0105 others(73): Show |
82 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.-22-10713_-22-1071 others(8): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701944 | |||||||
| chr6:41701944 | C | CAAAAA | 12 | a0001c0001t0003g0201 a0001c0002t0001g0167 a0001c0002t0001g0168 others(9): Show |
12 | HG00438.hp2 HG01952.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.-22-10714_-22-1071 others(9): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701944 | |||||||
| chr6:41701944 | CA | C | 6 | a0001c0001t0001g0093 a0001c0001t0001g0122 a0001c0001t0002g0083 others(3): Show |
6 | HG00639.hp1 HG01993.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-10710delT | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701944 | |||||||
| chr6:41701991 | C | T | 4 | a0001c0002t0001g0167 a0001c0004t0002g0117 a0001c0004t0002g0218 others(1): Show |
4 | NA18988.hp1 NA18991.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-10756G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701991 | |||||||
| chr6:41702320 | T | C | 138 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(135): Show |
148 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.-22-11085A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41702320 | |||||||
| chr6:41702445 | G | T | 1 | a0001c0003t0001g0189 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-22-11210C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41702445 | |||||||
| chr6:41702474 | A | G | 1 | a0001c0005t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-22-11239T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41702474 | |||||||
| chr6:41702615 | TCAGCCTA others(7): Show |
T | 22 | a0001c0002t0001g0280 a0001c0002t0001g0286 a0001c0003t0001g0009 others(19): Show |
26 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.-22-11394_-22-1138 others(18): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41702615 | |||||||
| chr6:41702865 | C | G | 3 | a0001c0001t0001g0274 a0001c0005t0001g0257 a0001c0010t0001g0265 |
3 | HG02630.hp1 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-22-11630G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41702865 | |||||||
| chr6:41702870 | C | T | 60 | a0001c0001t0003g0077 a0001c0001t0003g0079 a0001c0003t0001g0006 others(57): Show |
68 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.-22-11635G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41702870 | |||||||
| chr6:41702895 | C | T | 68 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0187 others(65): Show |
71 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.-22-11660G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41702895 | |||||||
| chr6:41702988 | C | T | 22 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0105 others(19): Show |
25 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.-22-11753G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41702988 | |||||||
| chr6:41702993 | G | A | 2 | a0001c0001t0002g0016 a0001c0001t0002g0091 |
3 | HG01243.hp1 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-22-11758C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41702993 | |||||||
| chr6:41703031 | C | T | 123 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(120): Show |
132 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.-22-11796G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41703031 | |||||||
| chr6:41703170 | G | T | 2 | a0001c0002t0001g0020 a0001c0002t0001g0176 |
3 | NA18944.hp2 NA18999.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-22-11935C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41703170 | |||||||
| chr6:41703349 | C | A | 1 | a0001c0002t0001g0307 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-22-12114G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41703349 | |||||||
| chr6:41703480 | T | TCAGCCTC others(2): Show |
126 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(123): Show |
135 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.-22-12254_-22-1224 others(13): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41703480 | |||||||
| chr6:41703611 | A | G | 8 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0351 others(5): Show |
9 | HG02647.hp1 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22-12376T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41703611 | |||||||
| chr6:41703639 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-22-12404A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41703639 | |||||||
| chr6:41703644 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-22-12409C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41703644 | |||||||
| chr6:41703837 | A | T | 8 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0351 others(5): Show |
9 | HG02647.hp1 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22-12602T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41703837 | |||||||
| chr6:41703840 | C | A | 21 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0105 others(18): Show |
24 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.-22-12605G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41703840 | |||||||
| chr6:41703924 | T | C | 1 | a0001c0003t0001g0338 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-22-12689A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41703924 | |||||||
| chr6:41703939 | A | G | 171 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(168): Show |
188 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.-22-12704T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41703939 | |||||||
| chr6:41704140 | T | C | 1 | a0001c0002t0001g0162 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-22-12905A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41704140 | |||||||
| chr6:41704214 | G | A | 68 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0187 others(65): Show |
71 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.-22-12979C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41704214 | |||||||
| chr6:41704272 | G | A | 3 | a0001c0001t0001g0105 a0001c0003t0001g0035 a0001c0005t0001g0106 |
3 | HG02738.hp2 HG03688.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-22-13037C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41704272 | |||||||
| chr6:41704273 | C | A | 3 | a0001c0001t0001g0105 a0001c0003t0001g0035 a0001c0005t0001g0106 |
3 | HG02738.hp2 HG03688.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-22-13038G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41704273 | |||||||
| chr6:41704303 | C | G | 91 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0105 others(88): Show |
97 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.-22-13068G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41704303 | |||||||
| chr6:41704581 | G | A | 35 | a0001c0001t0003g0004 a0001c0001t0003g0119 a0001c0001t0003g0164 others(32): Show |
42 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.-22-13346C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41704581 | |||||||
| chr6:41704731 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0002g0058 |
2 | HG00733.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-22-13496G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41704731 | |||||||
| chr6:41704750 | GGGAAGCA others(12): Show |
G | 2 | a0001c0003t0001g0047 a0001c0003t0001g0052 |
2 | HG01257.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-22-13534_-22-1351 others(23): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41704750 | |||||||
| chr6:41704901 | A | G | 134 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(131): Show |
143 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.-22-13666T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41704901 | |||||||
| chr6:41705031 | T | C | 79 | a0001c0001t0001g0110 a0001c0001t0001g0317 a0001c0001t0002g0012 others(76): Show |
89 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.-22-13796A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41705031 | |||||||
| chr6:41705118 | C | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0227 a0001c0001t0001g0228 others(1): Show |
5 | HG01257.hp1 HG01258.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-13883G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41705118 | |||||||
| chr6:41705320 | C | T | 1 | a0001c0002t0001g0322 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-22-14085G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41705320 | |||||||
| chr6:41705329 | T | C | 21 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0105 others(18): Show |
24 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.-22-14094A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41705329 | |||||||
| chr6:41705560 | C | T | 2 | a0001c0001t0001g0105 a0001c0005t0001g0106 |
2 | HG02738.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-22-14325G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41705560 | |||||||
| chr6:41705842 | G | A | 70 | a0001c0001t0001g0187 a0001c0001t0001g0194 a0001c0001t0001g0196 others(67): Show |
74 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-22-14607C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41705842 | |||||||
| chr6:41705908 | G | A | 46 | a0001c0001t0002g0012 a0001c0001t0002g0058 a0001c0001t0002g0297 others(43): Show |
53 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.-22-14673C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41705908 | |||||||
| chr6:41705989 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-22-14754C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41705989 | |||||||
| chr6:41706073 | T | C | 1 | a0001c0005t0001g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-22-14838A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706073 | |||||||
| chr6:41706362 | G | T | 18 | a0001c0001t0002g0297 a0001c0003t0001g0009 a0001c0003t0001g0160 others(15): Show |
22 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(19): Show |
intron_variant | MODIFIER | c.-22-15127C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706362 | |||||||
| chr6:41706366 | T | C | 1 | a0001c0004t0002g0341 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-22-15131A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706366 | |||||||
| chr6:41706491 | C | A | 1 | a0001c0004t0002g0055 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-22-15256G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706491 | |||||||
| chr6:41706508 | C | T | 114 | a0001c0001t0001g0187 a0001c0001t0001g0194 a0001c0001t0001g0196 others(111): Show |
126 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.-22-15273G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706508 | |||||||
| chr6:41706566 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-22-15331T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706566 | |||||||
| chr6:41706567 | C | T | 1 | a0001c0003t0001g0088 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-22-15332G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706567 | |||||||
| chr6:41706606 | G | C | 9 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0224 others(6): Show |
9 | HG01168.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22-15371C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706606 | |||||||
| chr6:41706667 | T | C | 4 | a0001c0005t0001g0239 a0001c0005t0001g0240 a0001c0005t0001g0241 others(1): Show |
4 | HG02257.hp2 HG02451.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-15432A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706667 | |||||||
| chr6:41706686 | G | A | 23 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0105 others(20): Show |
26 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.-22-15451C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706686 | |||||||
| chr6:41706739 | A | G | 1 | a0001c0002t0001g0120 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-22-15504T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706739 | |||||||
| chr6:41706772 | A | G | 1 | a0001c0004t0002g0171 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-22-15537T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706772 | |||||||
| chr6:41706777 | C | G | 22 | a0001c0001t0001g0352 a0001c0001t0002g0290 a0001c0001t0002g0297 others(19): Show |
26 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.-22-15542G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706777 | |||||||
| chr6:41706818 | T | C | 2 | a0001c0003t0001g0073 a0001c0004t0002g0024 |
3 | HG01123.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-22-15583A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706818 | |||||||
| chr6:41706824 | C | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-22-15589G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706824 | |||||||
| chr6:41706905 | A | T | 1 | a0001c0003t0001g0064 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-22-15670T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706905 | |||||||
| chr6:41706937 | C | T | 3 | a0001c0001t0003g0164 a0001c0001t0003g0165 a0001c0001t0003g0250 |
3 | HG00741.hp2 HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-22-15702G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706937 | |||||||
| chr6:41707367 | C | T | 1 | a0001c0004t0002g0213 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-22-16132G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41707367 | |||||||
| chr6:41707487 | G | A | 1 | a0001c0001t0002g0103 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-22-16252C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41707487 | |||||||
| chr6:41707582 | G | A | 1 | a0001c0002t0001g0214 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-22-16347C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41707582 | |||||||
| chr6:41707629 | G | A | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-22-16394C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41707629 | |||||||
| chr6:41707653 | G | A | 1 | a0001c0002t0001g0149 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-22-16418C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41707653 | |||||||
| chr6:41707930 | A | C | 1 | a0001c0003t0001g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-22-16695T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41707930 | |||||||
| chr6:41707975 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-22-16740C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41707975 | |||||||
| chr6:41707982 | G | A | 70 | a0001c0001t0001g0093 a0001c0001t0001g0187 a0001c0001t0001g0194 others(67): Show |
75 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-22-16747C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41707982 | |||||||
| chr6:41708002 | T | C | 286 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(283): Show |
329 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(326): Show |
intron_variant | MODIFIER | c.-22-16767A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708002 | |||||||
| chr6:41708009 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-22-16774C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708009 | |||||||
| chr6:41708029 | G | C | 4 | a0001c0005t0001g0267 a0001c0005t0001g0268 a0001c0005t0001g0269 others(1): Show |
4 | HG01361.hp1 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-16794C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708029 | |||||||
| chr6:41708083 | G | A | 1 | a0001c0005t0001g0275 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-22-16848C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708083 | |||||||
| chr6:41708108 | C | A | 1 | a0001c0001t0001g0273 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-22-16873G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708108 | |||||||
| chr6:41708240 | G | A | 2 | a0001c0001t0001g0253 a0001c0004t0002g0208 |
2 | HG01081.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-22-17005C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708240 | |||||||
| chr6:41708254 | C | G | 4 | a0001c0005t0001g0267 a0001c0005t0001g0268 a0001c0005t0001g0269 others(1): Show |
4 | HG01361.hp1 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-17019G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708254 | |||||||
| chr6:41708264 | A | C | 18 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
19 | HG01168.hp2 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-22-17029T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708264 | |||||||
| chr6:41708351 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-22-17116C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708351 | |||||||
| chr6:41708383 | T | C | 2 | a0001c0002t0001g0173 a0001c0002t0001g0244 |
2 | NA18747.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-22-17148A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708383 | |||||||
| chr6:41708531 | G | A | 23 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0220 others(20): Show |
26 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.-22-17296C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708531 | |||||||
| chr6:41708569 | C | T | 4 | a0001c0005t0001g0267 a0001c0005t0001g0268 a0001c0005t0001g0269 others(1): Show |
4 | HG01361.hp1 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-17334G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708569 | |||||||
| chr6:41708644 | C | T | 2 | a0001c0001t0002g0016 a0001c0001t0002g0091 |
3 | HG01243.hp1 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-22-17409G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708644 | |||||||
| chr6:41708696 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-22-17461T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708696 | |||||||
| chr6:41708714 | G | A | 26 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0105 others(23): Show |
29 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.-22-17479C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708714 | |||||||
| chr6:41708761 | G | A | 23 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0220 others(20): Show |
26 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.-22-17526C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708761 | |||||||
| chr6:41708772 | G | A | 1 | a0001c0004t0002g0202 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-22-17537C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708772 | |||||||
| chr6:41708789 | C | G | 1 | a0001c0003t0001g0326 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-22-17554G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708789 | |||||||
| chr6:41709144 | T | A | 3 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0010t0001g0265 |
3 | HG01891.hp2 HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-22-17909A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709144 | |||||||
| chr6:41709144 | T | C | 238 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(235): Show |
273 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.-22-17909A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709144 | |||||||
| chr6:41709293 | TTCA | T | 25 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0220 others(22): Show |
28 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.-22-18061_-22-1805 others(7): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709293 | |||||||
| chr6:41709411 | C | A | 69 | a0001c0001t0001g0093 a0001c0001t0001g0187 a0001c0001t0001g0194 others(66): Show |
74 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-22-18176G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709411 | |||||||
| chr6:41709461 | T | C | 1 | a0001c0001t0002g0022 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-22-18226A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709461 | |||||||
| chr6:41709529 | G | GTGGA | 8 | a0001c0001t0001g0187 a0001c0001t0002g0029 a0001c0001t0002g0303 others(5): Show |
9 | HG00544.hp2 HG00673.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22-18298_-22-1829 others(8): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709529 | |||||||
| chr6:41709529 | G | GTGGATGG others(1): Show |
85 | a0001c0001t0001g0093 a0001c0001t0001g0194 a0001c0001t0001g0196 others(82): Show |
94 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.-22-18302_-22-1829 others(12): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709529 | |||||||
| chr6:41709529 | G | GTGGATGG others(5): Show |
19 | a0001c0001t0002g0290 a0001c0001t0003g0004 a0001c0001t0003g0119 others(16): Show |
22 | HG00597.hp1 HG00741.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.-22-18306_-22-1829 others(16): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709529 | |||||||
| chr6:41709529 | G | GTGGATGG others(9): Show |
2 | a0001c0001t0003g0335 a0001c0001t0003g0342 |
2 | HG02015.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.-22-18310_-22-1829 others(20): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709529 | |||||||
| chr6:41709529 | GTGGA | G | 11 | a0001c0001t0001g0008 a0001c0001t0001g0245 a0001c0001t0001g0252 others(8): Show |
13 | HG00642.hp2 HG01081.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.-22-18298_-22-1829 others(8): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709529 | |||||||
| chr6:41709529 | GTGGATGG others(1): Show |
G | 81 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0105 others(78): Show |
100 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.-22-18302_-22-1829 others(12): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709529 | |||||||
| chr6:41709529 | GTGGATGG others(5): Show |
G | 23 | a0001c0001t0001g0025 a0001c0001t0001g0113 a0001c0001t0001g0114 others(20): Show |
24 | HG01168.hp2 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.-22-18306_-22-1829 others(16): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709529 | |||||||
| chr6:41709595 | C | T | 4 | a0001c0005t0001g0267 a0001c0005t0001g0268 a0001c0005t0001g0269 others(1): Show |
4 | HG01361.hp1 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-18360G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709595 | |||||||
| chr6:41709768 | T | C | 1 | a0001c0002t0001g0054 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-22-18533A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709768 | |||||||
| chr6:41709918 | T | C | 4 | a0001c0005t0001g0267 a0001c0005t0001g0268 a0001c0005t0001g0269 others(1): Show |
4 | HG01361.hp1 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-18683A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709918 | |||||||
| chr6:41709987 | T | C | 72 | a0001c0001t0001g0093 a0001c0001t0001g0187 a0001c0001t0001g0194 others(69): Show |
77 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-22-18752A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709987 | |||||||
| chr6:41710026 | C | T | 5 | a0001c0005t0001g0239 a0001c0005t0001g0240 a0001c0005t0001g0241 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-18791G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41710026 | |||||||
| chr6:41710080 | C | T | 2 | a0001c0003t0001g0291 a0001c0003t0001g0292 |
2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-22-18845G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41710080 | |||||||
| chr6:41710283 | A | T | 79 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0001c0001t0001g0187 others(76): Show |
84 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-22-19048T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41710283 | |||||||
| chr6:41710321 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-22-19086T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41710321 | |||||||
| chr6:41710410 | C | A | 73 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0001c0001t0001g0187 others(70): Show |
78 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.-22-19175G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41710410 | |||||||
| chr6:41710440 | C | G | 1 | a0001c0005t0001g0269 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-22-19205G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41710440 | |||||||
| chr6:41710989 | T | C | 197 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0093 others(194): Show |
229 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.-22-19754A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41710989 | |||||||
| chr6:41711117 | T | G | 1 | a0001c0001t0001g0263 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-22-19882A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41711117 | |||||||
| chr6:41711207 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-22-19972G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41711207 | |||||||
| chr6:41711490 | G | A | 1 | a0001c0005t0009g0259 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-22-20255C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41711490 | |||||||
| chr6:41711953 | C | T | 23 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0220 others(20): Show |
26 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.-22-20718G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41711953 | |||||||
| chr6:41712125 | G | A | 4 | a0001c0005t0001g0267 a0001c0005t0001g0268 a0001c0005t0001g0269 others(1): Show |
4 | HG01361.hp1 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-20890C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41712125 | |||||||
| chr6:41712237 | A | G | 1 | a0001c0002t0001g0020 | 2 | NA18999.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-22-21002T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41712237 | |||||||
| chr6:41712376 | T | C | 1 | a0001c0001t0002g0325 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-22-21141A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41712376 | |||||||
| chr6:41712509 | A | G | 187 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0093 others(184): Show |
216 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-22-21274T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41712509 | |||||||
| chr6:41712772 | G | A | 49 | a0001c0001t0001g0112 a0001c0001t0001g0122 a0001c0001t0001g0129 others(46): Show |
65 | HG00423.hp2 HG00735.hp2 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.-22-21537C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41712772 | |||||||
| chr6:41712928 | T | C | 226 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(223): Show |
258 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.-22-21693A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41712928 | |||||||
| chr6:41712976 | C | G | 1 | a0001c0005t0001g0063 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-22-21741G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41712976 | |||||||
| chr6:41713086 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0224 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-22-21851C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713086 | |||||||
| chr6:41713273 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0252 a0001c0001t0001g0253 others(3): Show |
8 | HG00642.hp2 HG01081.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-22-22038G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713273 | |||||||
| chr6:41713298 | G | A | 27 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0220 others(24): Show |
30 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.-23+22052C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713298 | |||||||
| chr6:41713303 | G | A | 1 | a0001c0004t0002g0243 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-23+22047C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713303 | |||||||
| chr6:41713306 | G | A | 9 | a0001c0001t0002g0331 a0001c0002t0001g0305 a0001c0002t0001g0306 others(6): Show |
9 | HG02602.hp2 HG02683.hp1 HG04199.hp1 others(6): Show |
intron_variant | MODIFIER | c.-23+22044C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713306 | |||||||
| chr6:41713445 | G | A | 28 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0220 others(25): Show |
31 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.-23+21905C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713445 | |||||||
| chr6:41713488 | C | T | 2 | a0001c0002t0001g0017 a0001c0002t0001g0120 |
3 | HG01255.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-23+21862G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713488 | |||||||
| chr6:41713490 | C | T | 3 | a0001c0001t0001g0105 a0001c0003t0001g0035 a0001c0005t0001g0106 |
3 | HG02738.hp2 HG03688.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-23+21860G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713490 | |||||||
| chr6:41713494 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-23+21856G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713494 | |||||||
| chr6:41713498 | T | A | 1 | a0001c0003t0001g0061 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-23+21852A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713498 | |||||||
| chr6:41713592 | G | A | 184 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0093 others(181): Show |
213 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.-23+21758C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713592 | |||||||
| chr6:41713602 | G | A | 184 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0093 others(181): Show |
213 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.-23+21748C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713602 | |||||||
| chr6:41713835 | G | A | 2 | a0001c0003t0001g0059 a0001c0003t0001g0060 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-23+21515C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713835 | |||||||
| chr6:41713884 | T | A | 225 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(222): Show |
257 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.-23+21466A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713884 | |||||||
| chr6:41713946 | C | T | 1 | a0001c0002t0001g0155 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-23+21404G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713946 | |||||||
| chr6:41713953 | G | A | 2 | a0001c0005t0001g0267 a0001c0005t0001g0268 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-23+21397C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713953 | |||||||
| chr6:41713954 | C | T | 3 | a0001c0002t0001g0046 a0001c0004t0002g0034 a0001c0004t0002g0186 |
3 | HG04115.hp1 NA18982.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-23+21396G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713954 | |||||||
| chr6:41714016 | C | T | 1 | a0001c0001t0012g0355 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-23+21334G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714016 | |||||||
| chr6:41714025 | C | T | 9 | a0001c0002t0001g0251 a0001c0002t0001g0258 a0001c0003t0001g0272 others(6): Show |
9 | HG01168.hp2 HG02145.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-23+21325G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714025 | |||||||
| chr6:41714049 | G | A | 186 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0093 others(183): Show |
215 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-23+21301C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714049 | |||||||
| chr6:41714097 | G | A | 25 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0220 others(22): Show |
26 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-23+21253C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714097 | |||||||
| chr6:41714110 | C | CGT | 28 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0220 others(25): Show |
31 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.-23+21238_-23+2123 others(6): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714110 | |||||||
| chr6:41714110 | C | T | 1 | a0001c0004t0002g0180 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-23+21240G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714110 | |||||||
| chr6:41714111 | G | A | 87 | a0001c0001t0001g0105 a0001c0001t0001g0122 a0001c0001t0001g0129 others(84): Show |
108 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.-23+21239C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714111 | |||||||
| chr6:41714133 | A | G | 6 | a0001c0004t0002g0180 a0001c0004t0002g0181 a0001c0004t0002g0182 others(3): Show |
6 | HG00408.hp1 HG00621.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+21217T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714133 | |||||||
| chr6:41714140 | C | T | 24 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0220 others(21): Show |
27 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.-23+21210G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714140 | |||||||
| chr6:41714140 | CGT | C | 169 | a0001c0001t0001g0025 a0001c0001t0001g0093 a0001c0001t0001g0105 others(166): Show |
196 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.-23+21208_-23+2120 others(6): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714140 | |||||||
| chr6:41714142 | T | TGTGTGCA others(9): Show |
15 | a0001c0001t0001g0008 a0001c0001t0001g0252 a0001c0001t0001g0253 others(12): Show |
17 | HG00642.hp2 HG01081.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.-23+21207_-23+2120 others(20): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714142 | |||||||
| chr6:41714142 | T | TGTGTGCA others(17): Show |
2 | a0001c0001t0001g0260 a0001c0001t0001g0264 |
2 | HG02572.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-23+21207_-23+2120 others(28): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714142 | |||||||
| chr6:41714167 | ATG | A | 49 | a0001c0001t0001g0112 a0001c0001t0001g0122 a0001c0001t0001g0129 others(46): Show |
65 | HG00423.hp2 HG00735.hp2 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.-23+21181_-23+2118 others(6): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714167 | |||||||
| chr6:41714174 | CGT | C | 92 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0093 others(89): Show |
100 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.-23+21174_-23+2117 others(6): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714174 | |||||||
| chr6:41714179 | G | A | 1 | a0001c0005t0001g0285 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-23+21171C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714179 | |||||||
| chr6:41714200 | C | T | 91 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0093 others(88): Show |
99 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.-23+21150G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714200 | |||||||
| chr6:41714230 | C | T | 24 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0220 others(21): Show |
27 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.-23+21120G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714230 | |||||||
| chr6:41714309 | C | G | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-23+21041G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714309 | |||||||
| chr6:41714316 | C | G | 1 | a0001c0001t0002g0332 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-23+21034G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714316 | |||||||
| chr6:41714484 | C | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0224 |
3 | HG02622.hp1 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-23+20866G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714484 | |||||||
| chr6:41714685 | C | A | 88 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(85): Show |
109 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.-23+20665G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714685 | |||||||
| chr6:41714718 | C | A | 1 | a0001c0002t0001g0286 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-23+20632G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714718 | |||||||
| chr6:41714719 | G | A | 2 | a0001c0001t0003g0164 a0001c0001t0003g0250 |
2 | HG00741.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-23+20631C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714719 | |||||||
| chr6:41714743 | C | T | 1 | a0001c0003t0001g0037 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-23+20607G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714743 | |||||||
| chr6:41714748 | C | T | 33 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0220 others(30): Show |
35 | HG00280.hp1 HG00642.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.-23+20602G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714748 | |||||||
| chr6:41714856 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-23+20494A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714856 | |||||||
| chr6:41714876 | C | T | 1 | a0001c0002t0001g0162 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-23+20474G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714876 | |||||||
| chr6:41715024 | C | T | 1 | a0001c0002t0001g0044 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-23+20326G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715024 | |||||||
| chr6:41715121 | C | T | 2 | a0001c0003t0001g0160 a0001c0005t0001g0161 |
2 | HG00733.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-23+20229G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715121 | |||||||
| chr6:41715161 | C | T | 1 | a0001c0001t0003g0164 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-23+20189G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715161 | |||||||
| chr6:41715223 | A | G | 1 | a0001c0001t0003g0335 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-23+20127T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715223 | |||||||
| chr6:41715331 | C | T | 1 | a0001c0008t0002g0311 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-23+20019G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715331 | |||||||
| chr6:41715539 | G | A | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-23+19811C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715539 | |||||||
| chr6:41715585 | G | A | 4 | a0001c0003t0001g0231 a0001c0003t0001g0232 a0001c0003t0001g0233 others(1): Show |
4 | HG01928.hp1 HG01943.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+19765C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715585 | |||||||
| chr6:41715626 | C | T | 1 | a0001c0003t0001g0084 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-23+19724G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715626 | |||||||
| chr6:41715657 | G | A | 23 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0105 others(20): Show |
24 | HG00280.hp2 HG00642.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.-23+19693C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715657 | |||||||
| chr6:41715676 | GA | G | 37 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0104 others(34): Show |
41 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.-23+19673delT | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715676 | |||||||
| chr6:41715682 | A | G | 9 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(6): Show |
9 | HG01884.hp1 HG02486.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-23+19668T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715682 | |||||||
| chr6:41715714 | C | T | 5 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(2): Show |
5 | HG01884.hp1 HG02886.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+19636G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715714 | |||||||
| chr6:41715803 | C | T | 1 | a0001c0001t0012g0355 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-23+19547G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715803 | |||||||
| chr6:41715804 | G | A | 1 | a0001c0003t0001g0169 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-23+19546C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715804 | |||||||
| chr6:41715949 | C | T | 12 | a0001c0001t0002g0175 a0001c0002t0001g0020 a0001c0002t0001g0172 others(9): Show |
14 | HG00438.hp2 HG01069.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.-23+19401G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715949 | |||||||
| chr6:41715967 | C | T | 4 | a0001c0005t0001g0239 a0001c0005t0001g0240 a0001c0005t0001g0241 others(1): Show |
4 | HG02257.hp2 HG02451.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+19383G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715967 | |||||||
| chr6:41715974 | C | T | 13 | a0001c0001t0001g0025 a0001c0001t0001g0114 a0001c0001t0001g0260 others(10): Show |
14 | HG01361.hp1 HG02280.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-23+19376G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715974 | |||||||
| chr6:41716063 | G | A | 1 | a0001c0001t0002g0151 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-23+19287C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716063 | |||||||
| chr6:41716066 | A | G | 3 | a0001c0002t0001g0305 a0001c0002t0001g0306 a0001c0002t0001g0307 |
3 | NA18941.hp1 NA19077.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-23+19284T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716066 | |||||||
| chr6:41716268 | C | G | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG01884.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+19082G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716268 | |||||||
| chr6:41716282 | C | G | 7 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(4): Show |
7 | HG01884.hp1 HG02145.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23+19068G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716282 | |||||||
| chr6:41716419 | A | AG | 19 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(16): Show |
20 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.-23+18930_-23+1893 others(5): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716419 | |||||||
| chr6:41716448 | C | A | 1 | a0001c0002t0001g0287 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-23+18902G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716448 | |||||||
| chr6:41716536 | G | C | 1 | a0001c0004t0002g0171 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-23+18814C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716536 | |||||||
| chr6:41716564 | A | T | 1 | a0001c0001t0002g0083 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-23+18786T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716564 | |||||||
| chr6:41716652 | A | G | 44 | a0001c0001t0002g0012 a0001c0001t0003g0077 a0001c0001t0003g0079 others(41): Show |
52 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.-23+18698T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716652 | |||||||
| chr6:41716653 | A | G | 1 | a0001c0003t0001g0061 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-23+18697T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716653 | |||||||
| chr6:41716907 | A | C | 42 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0104 others(39): Show |
44 | HG00280.hp2 HG00642.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.-23+18443T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716907 | |||||||
| chr6:41716946 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-23+18404C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716946 | |||||||
| chr6:41717278 | C | T | 2 | a0001c0003t0001g0014 a0001c0003t0001g0080 |
3 | HG00438.hp1 NA18974.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.-23+18072G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41717278 | |||||||
| chr6:41717416 | A | G | 1 | a0001c0005t0001g0275 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-23+17934T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41717416 | |||||||
| chr6:41717640 | C | G | 1 | a0001c0001t0002g0330 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-23+17710G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41717640 | |||||||
| chr6:41717658 | C | A | 1 | a0001c0004t0002g0213 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-23+17692G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41717658 | |||||||
| chr6:41717676 | A | C | 19 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(16): Show |
20 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.-23+17674T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41717676 | |||||||
| chr6:41717701 | A | C | 3 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0244 |
3 | NA18747.hp1 NA19077.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-23+17649T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41717701 | |||||||
| chr6:41717788 | G | A | 6 | a0001c0002t0001g0207 a0001c0003t0001g0169 a0001c0003t0001g0209 others(3): Show |
6 | HG00597.hp2 HG02027.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23+17562C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41717788 | |||||||
| chr6:41717807 | G | C | 1 | a0001c0001t0003g0079 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-23+17543C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41717807 | |||||||
| chr6:41717911 | G | C | 12 | a0001c0001t0001g0025 a0001c0001t0001g0260 a0001c0001t0001g0261 others(9): Show |
13 | HG01361.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-23+17439C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41717911 | |||||||
| chr6:41718054 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-23+17296A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718054 | |||||||
| chr6:41718071 | G | T | 1 | a0001c0005t0001g0277 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-23+17279C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718071 | |||||||
| chr6:41718161 | T | C | 23 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0105 others(20): Show |
24 | HG00280.hp2 HG00642.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.-23+17189A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718161 | |||||||
| chr6:41718185 | G | GT | 72 | a0001c0001t0001g0008 a0001c0001t0001g0187 a0001c0001t0001g0194 others(69): Show |
79 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-23+17164dupA | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718185 | |||||||
| chr6:41718185 | GT | G | 7 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(4): Show |
7 | HG01884.hp1 HG02145.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23+17164delA | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718185 | |||||||
| chr6:41718188 | T | C | 2 | a0001c0005t0001g0240 a0001c0005t0001g0241 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-23+17162A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718188 | |||||||
| chr6:41718280 | C | T | 1 | a0001c0003t0001g0298 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-23+17070G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718280 | |||||||
| chr6:41718285 | T | C | 1 | a0001c0002t0001g0019 | 2 | NA18993.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-23+17065A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718285 | |||||||
| chr6:41718346 | C | G | 1 | a0001c0001t0001g0273 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-23+17004G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718346 | |||||||
| chr6:41718383 | A | AT | 7 | a0001c0002t0001g0042 a0001c0003t0001g0005 a0001c0003t0001g0041 others(4): Show |
9 | HG01074.hp1 HG01099.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.-23+16966dupA | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718383 | |||||||
| chr6:41718391 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-23+16959C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718391 | |||||||
| chr6:41718401 | A | G | 5 | a0001c0003t0001g0014 a0001c0003t0001g0033 a0001c0003t0001g0080 others(2): Show |
6 | HG00438.hp1 NA18967.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+16949T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718401 | |||||||
| chr6:41718675 | C | CT | 22 | a0001c0001t0001g0025 a0001c0001t0001g0105 a0001c0001t0001g0246 others(19): Show |
23 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.-23+16674dupA | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718675 | |||||||
| chr6:41718724 | T | C | 1 | a0001c0003t0001g0272 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-23+16626A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718724 | |||||||
| chr6:41718768 | T | G | 1 | a0001c0003t0001g0211 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-23+16582A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718768 | |||||||
| chr6:41718811 | A | C | 4 | a0001c0005t0001g0239 a0001c0005t0001g0240 a0001c0005t0001g0241 others(1): Show |
4 | HG02257.hp2 HG02451.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+16539T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718811 | |||||||
| chr6:41718842 | C | T | 1 | a0001c0003t0001g0272 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-23+16508G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718842 | |||||||
| chr6:41718855 | G | A | 63 | a0001c0001t0001g0187 a0001c0001t0001g0194 a0001c0001t0001g0196 others(60): Show |
68 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-23+16495C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718855 | |||||||
| chr6:41718895 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-23+16455C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718895 | |||||||
| chr6:41718953 | C | T | 63 | a0001c0001t0001g0187 a0001c0001t0001g0194 a0001c0001t0001g0196 others(60): Show |
68 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-23+16397G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718953 | |||||||
| chr6:41719108 | T | C | 18 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+16242A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719108 | |||||||
| chr6:41719142 | G | A | 12 | a0001c0001t0001g0025 a0001c0001t0001g0260 a0001c0001t0001g0261 others(9): Show |
13 | HG01361.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-23+16208C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719142 | |||||||
| chr6:41719213 | C | T | 6 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(3): Show |
6 | HG01884.hp1 HG02145.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+16137G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719213 | |||||||
| chr6:41719225 | C | T | 12 | a0001c0001t0001g0025 a0001c0001t0001g0260 a0001c0001t0001g0261 others(9): Show |
13 | HG01361.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-23+16125G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719225 | |||||||
| chr6:41719226 | G | A | 2 | a0001c0001t0002g0016 a0001c0001t0002g0091 |
3 | HG01243.hp1 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-23+16124C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719226 | |||||||
| chr6:41719250 | A | G | 6 | a0001c0001t0002g0297 a0002c0006t0001g0027 a0002c0006t0001g0294 others(3): Show |
7 | HG00423.hp1 HG00544.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23+16100T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719250 | |||||||
| chr6:41719253 | G | A | 5 | a0001c0003t0001g0014 a0001c0003t0001g0033 a0001c0003t0001g0080 others(2): Show |
6 | HG00438.hp1 NA18967.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+16097C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719253 | |||||||
| chr6:41719305 | T | C | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG01081.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-23+16045A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719305 | |||||||
| chr6:41719514 | G | C | 41 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0104 others(38): Show |
43 | HG00280.hp2 HG00642.hp1 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.-23+15836C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719514 | |||||||
| chr6:41719519 | G | A | 2 | a0001c0001t0002g0330 a0001c0001t0002g0332 |
2 | HG00558.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-23+15831C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719519 | |||||||
| chr6:41719603 | G | A | 1 | a0001c0001t0001g0352 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-23+15747C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719603 | |||||||
| chr6:41719628 | T | C | 178 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(175): Show |
195 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.-23+15722A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719628 | |||||||
| chr6:41719699 | C | T | 1 | a0001c0004t0002g0034 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-23+15651G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719699 | |||||||
| chr6:41719904 | TCCTGAGG others(14): Show |
T | 6 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(3): Show |
6 | HG01884.hp1 HG02145.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+15425_-23+1544 others(25): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719904 | |||||||
| chr6:41719960 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-23+15390C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719960 | |||||||
| chr6:41720001 | A | G | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-23+15349T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720001 | |||||||
| chr6:41720045 | A | G | 1 | a0001c0004t0002g0171 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-23+15305T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720045 | |||||||
| chr6:41720177 | C | CA | 65 | a0001c0001t0001g0187 a0001c0001t0001g0194 a0001c0001t0001g0196 others(62): Show |
70 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-23+15172dupT | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720177 | |||||||
| chr6:41720182 | C | T | 18 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+15168G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720182 | |||||||
| chr6:41720362 | C | A | 49 | a0001c0001t0001g0112 a0001c0001t0001g0122 a0001c0001t0001g0129 others(46): Show |
65 | HG00423.hp2 HG00735.hp2 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.-23+14988G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720362 | |||||||
| chr6:41720450 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-23+14900C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720450 | |||||||
| chr6:41720479 | T | C | 5 | a0001c0001t0002g0212 a0001c0004t0002g0117 a0001c0004t0002g0213 others(2): Show |
5 | HG02071.hp2 HG02155.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+14871A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720479 | |||||||
| chr6:41720493 | G | A | 18 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+14857C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720493 | |||||||
| chr6:41720664 | A | T | 47 | a0001c0001t0001g0112 a0001c0001t0001g0122 a0001c0001t0001g0129 others(44): Show |
63 | HG00423.hp2 HG00735.hp2 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.-23+14686T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720664 | |||||||
| chr6:41720706 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-23+14644G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720706 | |||||||
| chr6:41720928 | C | T | 4 | a0001c0005t0001g0239 a0001c0005t0001g0240 a0001c0005t0001g0241 others(1): Show |
4 | HG02257.hp2 HG02451.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+14422G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720928 | |||||||
| chr6:41720954 | G | A | 1 | a0001c0001t0003g0235 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-23+14396C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720954 | |||||||
| chr6:41721022 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-23+14328G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721022 | |||||||
| chr6:41721025 | G | C | 1 | a0001c0004t0002g0055 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-23+14325C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721025 | |||||||
| chr6:41721252 | T | C | 53 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0274 others(50): Show |
61 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.-23+14098A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721252 | |||||||
| chr6:41721261 | T | C | 29 | a0001c0001t0001g0025 a0001c0001t0001g0224 a0001c0001t0001g0246 others(26): Show |
31 | HG01168.hp2 HG01361.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.-23+14089A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721261 | |||||||
| chr6:41721313 | A | G | 18 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+14037T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721313 | |||||||
| chr6:41721368 | C | T | 2 | a0001c0005t0001g0267 a0001c0005t0001g0268 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-23+13982G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721368 | |||||||
| chr6:41721372 | T | TAC | 45 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0104 others(42): Show |
48 | HG00280.hp2 HG00558.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.-23+13976_-23+1397 others(6): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721372 | |||||||
| chr6:41721372 | T | TACAC | 42 | a0001c0001t0001g0344 a0001c0001t0002g0284 a0001c0001t0002g0290 others(39): Show |
50 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.-23+13974_-23+1397 others(8): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721372 | |||||||
| chr6:41721372 | T | TACACAC | 9 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0351 others(6): Show |
9 | HG00544.hp1 HG01346.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-23+13972_-23+1397 others(10): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721372 | |||||||
| chr6:41721372 | TAC | T | 8 | a0001c0001t0002g0016 a0001c0001t0002g0091 a0001c0002t0001g0120 others(5): Show |
9 | HG01243.hp1 HG02717.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-23+13976_-23+1397 others(6): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721372 | |||||||
| chr6:41721372 | TACAC | T | 50 | a0001c0001t0001g0112 a0001c0001t0001g0122 a0001c0001t0001g0129 others(47): Show |
65 | HG00423.hp2 HG00735.hp2 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.-23+13974_-23+1397 others(8): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721372 | |||||||
| chr6:41721372 | TACACACA others(1): Show |
T | 15 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(12): Show |
16 | HG01884.hp1 HG02145.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.-23+13970_-23+1397 others(12): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721372 | |||||||
| chr6:41721372 | TACACACA others(7): Show |
T | 1 | a0001c0004t0002g0171 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-23+13964_-23+1397 others(18): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721372 | |||||||
| chr6:41721376 | C | T | 2 | a0001c0005t0001g0269 a0001c0005t0001g0270 |
2 | HG01361.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-23+13974G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721376 | |||||||
| chr6:41721568 | C | T | 1 | a0001c0001t0002g0170 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-23+13782G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721568 | |||||||
| chr6:41721616 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-23+13734G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721616 | |||||||
| chr6:41721643 | G | T | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-23+13707C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721643 | |||||||
| chr6:41721850 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-23+13500T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721850 | |||||||
| chr6:41721977 | A | ATAT | 5 | a0001c0002t0001g0123 a0001c0005t0001g0239 a0001c0005t0001g0240 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+13370_-23+1337 others(7): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721977 | |||||||
| chr6:41722015 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0002g0094 |
2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-23+13335C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722015 | |||||||
| chr6:41722092 | G | C | 1 | a0001c0004t0002g0215 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-23+13258C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722092 | |||||||
| chr6:41722231 | C | G | 2 | a0001c0003t0001g0059 a0001c0003t0001g0060 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-23+13119G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722231 | |||||||
| chr6:41722286 | G | C | 18 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+13064C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722286 | |||||||
| chr6:41722314 | T | C | 2 | a0001c0003t0001g0056 a0001c0003t0001g0057 |
2 | HG01074.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-23+13036A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722314 | |||||||
| chr6:41722353 | A | T | 1 | a0001c0005t0001g0276 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-23+12997T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722353 | |||||||
| chr6:41722564 | C | T | 18 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+12786G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722564 | |||||||
| chr6:41722592 | A | G | 4 | a0001c0001t0001g0351 a0001c0001t0001g0352 a0001c0001t0001g0353 others(1): Show |
4 | HG02809.hp1 HG06807.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+12758T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722592 | |||||||
| chr6:41722634 | G | T | 18 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+12716C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722634 | |||||||
| chr6:41722756 | G | A | 18 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+12594C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722756 | |||||||
| chr6:41722904 | G | A | 1 | a0001c0003t0001g0272 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-23+12446C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722904 | |||||||
| chr6:41722986 | C | T | 3 | a0001c0001t0001g0105 a0001c0003t0001g0035 a0001c0005t0001g0106 |
3 | HG02738.hp2 HG03688.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-23+12364G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722986 | |||||||
| chr6:41723042 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-23+12308C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723042 | |||||||
| chr6:41723085 | C | A | 217 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(214): Show |
247 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.-23+12265G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723085 | |||||||
| chr6:41723285 | C | T | 18 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+12065G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723285 | |||||||
| chr6:41723314 | C | A | 14 | a0001c0001t0001g0344 a0001c0001t0003g0004 a0001c0001t0003g0166 others(11): Show |
17 | HG00597.hp1 HG01346.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.-23+12036G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723314 | |||||||
| chr6:41723388 | C | A | 18 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+11962G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723388 | |||||||
| chr6:41723400 | TTCACACA others(5): Show |
T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-23+11938_-23+1194 others(16): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723400 | |||||||
| chr6:41723429 | ACT | A | 5 | a0001c0001t0001g0224 a0001c0001t0002g0222 a0001c0001t0002g0223 others(2): Show |
5 | HG01168.hp2 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+11919_-23+1192 others(6): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723429 | |||||||
| chr6:41723444 | CGCGTGT | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0252 a0001c0001t0001g0253 others(7): Show |
12 | HG00642.hp2 HG01081.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+11900_-23+1190 others(10): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723444 | |||||||
| chr6:41723558 | A | G | 53 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0274 others(50): Show |
61 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.-23+11792T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723558 | |||||||
| chr6:41723563 | C | CCTCATTT others(9): Show |
1 | a0001c0001t0001g0122 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-23+11771_-23+1178 others(20): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723563 | |||||||
| chr6:41723614 | T | C | 18 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+11736A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723614 | |||||||
| chr6:41723638 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-23+11712A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723638 | |||||||
| chr6:41723750 | C | A | 18 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+11600G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723750 | |||||||
| chr6:41723756 | C | T | 18 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+11594G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723756 | |||||||
| chr6:41723762 | G | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0252 a0001c0001t0001g0253 others(7): Show |
12 | HG00642.hp2 HG01081.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+11588C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723762 | |||||||
| chr6:41723770 | C | T | 3 | a0001c0003t0001g0336 a0001c0003t0001g0337 a0001c0003t0001g0338 |
3 | HG01981.hp2 HG02056.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-23+11580G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723770 | |||||||
| chr6:41723861 | C | A | 17 | a0001c0001t0001g0344 a0001c0001t0003g0004 a0001c0001t0003g0164 others(14): Show |
20 | HG00597.hp1 HG00741.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.-23+11489G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723861 | |||||||
| chr6:41723928 | C | G | 18 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+11422G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723928 | |||||||
| chr6:41723965 | C | A | 6 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(3): Show |
6 | HG01884.hp1 HG02145.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+11385G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723965 | |||||||
| chr6:41724018 | C | A | 1 | a0001c0004t0002g0226 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-23+11332G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724018 | |||||||
| chr6:41724044 | G | A | 18 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+11306C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724044 | |||||||
| chr6:41724194 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-23+11156G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724194 | |||||||
| chr6:41724277 | C | T | 1 | a0001c0002t0001g0040 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-23+11073G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724277 | |||||||
| chr6:41724355 | T | C | 18 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+10995A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724355 | |||||||
| chr6:41724391 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0252 a0001c0001t0001g0253 others(3): Show |
8 | HG00642.hp2 HG01081.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-23+10959G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724391 | |||||||
| chr6:41724486 | G | C | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-23+10864C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724486 | |||||||
| chr6:41724586 | T | C | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-23+10764A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724586 | |||||||
| chr6:41724634 | G | A | 18 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+10716C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724634 | |||||||
| chr6:41724664 | C | T | 64 | a0001c0001t0001g0187 a0001c0001t0001g0194 a0001c0001t0001g0196 others(61): Show |
69 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.-23+10686G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724664 | |||||||
| chr6:41724749 | C | T | 9 | a0001c0001t0001g0224 a0001c0001t0002g0022 a0001c0001t0002g0222 others(6): Show |
10 | HG01168.hp2 HG02615.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.-23+10601G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724749 | |||||||
| chr6:41724758 | C | T | 18 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+10592G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724758 | |||||||
| chr6:41724815 | G | A | 15 | a0001c0001t0001g0344 a0001c0001t0002g0290 a0001c0001t0003g0004 others(12): Show |
18 | HG00597.hp1 HG01346.hp2 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.-23+10535C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724815 | |||||||
| chr6:41724815 | G | T | 64 | a0001c0001t0001g0187 a0001c0001t0001g0194 a0001c0001t0001g0196 others(61): Show |
69 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.-23+10535C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724815 | |||||||
| chr6:41724819 | G | A | 1 | a0001c0012t0001g0121 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-23+10531C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724819 | |||||||
| chr6:41724957 | G | A | 54 | a0001c0001t0001g0112 a0001c0001t0001g0122 a0001c0001t0001g0129 others(51): Show |
70 | HG00423.hp2 HG00735.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.-23+10393C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724957 | |||||||
| chr6:41724994 | C | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-23+10356G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724994 | |||||||
| chr6:41725063 | G | A | 1 | a0001c0003t0001g0158 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-23+10287C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41725063 | |||||||
| chr6:41725074 | G | A | 291 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(288): Show |
334 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.-23+10276C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41725074 | |||||||
| chr6:41725404 | G | T | 1 | a0001c0005t0001g0039 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-23+9946C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41725404 | |||||||
| chr6:41725570 | A | G | 1 | a0001c0001t0002g0304 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-23+9780T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41725570 | |||||||
| chr6:41725630 | G | A | 1 | a0001c0003t0001g0272 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-23+9720C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41725630 | |||||||
| chr6:41725739 | T | G | 21 | a0001c0001t0001g0025 a0001c0001t0001g0105 a0001c0001t0001g0246 others(18): Show |
22 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.-23+9611A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41725739 | |||||||
| chr6:41725775 | T | A | 1 | a0001c0001t0002g0022 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-23+9575A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41725775 | |||||||
| chr6:41725852 | C | G | 64 | a0001c0001t0001g0187 a0001c0001t0001g0194 a0001c0001t0001g0196 others(61): Show |
69 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.-23+9498G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41725852 | |||||||
| chr6:41725878 | C | T | 1 | a0002c0006t0001g0294 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-23+9472G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41725878 | |||||||
| chr6:41726357 | C | T | 3 | a0001c0003t0001g0291 a0001c0003t0001g0292 a0001c0003t0001g0293 |
3 | HG02572.hp1 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-23+8993G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41726357 | |||||||
| chr6:41726413 | T | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0252 a0001c0001t0001g0253 others(7): Show |
12 | HG00642.hp2 HG01081.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+8937A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41726413 | |||||||
| chr6:41726472 | C | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0252 a0001c0001t0001g0253 others(7): Show |
12 | HG00642.hp2 HG01081.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+8878G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41726472 | |||||||
| chr6:41726482 | C | T | 1 | a0001c0003t0001g0169 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-23+8868G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41726482 | |||||||
| chr6:41726483 | A | G | 82 | a0001c0001t0001g0025 a0001c0001t0001g0187 a0001c0001t0001g0194 others(79): Show |
88 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.-23+8867T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41726483 | |||||||
| chr6:41726507 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-23+8843C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41726507 | |||||||
| chr6:41726604 | A | C | 18 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+8746T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41726604 | |||||||
| chr6:41726629 | T | C | 18 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+8721A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41726629 | |||||||
| chr6:41726698 | C | T | 1 | a0001c0002t0001g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-23+8652G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41726698 | |||||||
| chr6:41726885 | C | T | 82 | a0001c0001t0001g0025 a0001c0001t0001g0187 a0001c0001t0001g0194 others(79): Show |
88 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.-23+8465G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41726885 | |||||||
| chr6:41726906 | C | T | 2 | a0001c0002t0001g0167 a0001c0002t0001g0168 |
2 | NA18974.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.-23+8444G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41726906 | |||||||
| chr6:41727034 | C | T | 53 | a0001c0001t0001g0112 a0001c0001t0001g0122 a0001c0001t0001g0129 others(50): Show |
69 | HG00423.hp2 HG00735.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.-23+8316G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41727034 | |||||||
| chr6:41727035 | G | A | 23 | a0001c0001t0001g0023 a0001c0001t0001g0104 a0001c0001t0001g0105 others(20): Show |
24 | HG00280.hp2 HG00642.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.-23+8315C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41727035 | |||||||
| chr6:41727058 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-23+8292C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41727058 | |||||||
| chr6:41727198 | G | T | 1 | a0001c0003t0001g0037 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-23+8152C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41727198 | |||||||
| chr6:41727332 | T | C | 1 | a0001c0003t0001g0087 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-23+8018A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41727332 | |||||||
| chr6:41727375 | G | C | 1 | a0001c0005t0001g0347 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-23+7975C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41727375 | |||||||
| chr6:41727464 | C | G | 40 | a0001c0001t0001g0274 a0001c0001t0001g0344 a0001c0001t0001g0351 others(37): Show |
45 | HG00140.hp2 HG00597.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.-23+7886G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41727464 | |||||||
| chr6:41727787 | C | A | 3 | a0001c0004t0002g0117 a0001c0004t0002g0218 a0001c0004t0002g0219 |
3 | NA18988.hp1 NA18991.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-23+7563G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41727787 | |||||||
| chr6:41727816 | C | A | 2 | a0001c0001t0001g0352 a0001c0001t0001g0353 |
2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-23+7534G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41727816 | |||||||
| chr6:41727935 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-23+7415C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41727935 | |||||||
| chr6:41728296 | T | G | 1 | a0001c0002t0001g0334 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-23+7054A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41728296 | |||||||
| chr6:41728369 | C | T | 1 | a0001c0001t0003g0335 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-23+6981G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41728369 | |||||||
| chr6:41728561 | C | T | 79 | a0001c0001t0001g0187 a0001c0001t0001g0194 a0001c0001t0001g0196 others(76): Show |
85 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.-23+6789G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41728561 | |||||||
| chr6:41728676 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0002g0094 |
2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-23+6674A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41728676 | |||||||
| chr6:41728723 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-23+6627C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41728723 | |||||||
| chr6:41729074 | C | A | 1 | a0001c0003t0001g0272 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-23+6276G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41729074 | |||||||
| chr6:41729093 | G | A | 1 | a0001c0001t0001g0353 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-23+6257C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41729093 | |||||||
| chr6:41729104 | G | A | 4 | a0001c0003t0001g0007 a0001c0003t0001g0015 a0001c0003t0001g0088 others(1): Show |
7 | HG00738.hp1 HG03654.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.-23+6246C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41729104 | |||||||
| chr6:41729151 | C | T | 18 | a0001c0001t0001g0274 a0001c0001t0001g0344 a0001c0001t0003g0004 others(15): Show |
21 | HG00597.hp1 HG00741.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.-23+6199G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41729151 | |||||||
| chr6:41729581 | C | T | 1 | a0001c0003t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-23+5769G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41729581 | |||||||
| chr6:41729775 | A | G | 9 | a0001c0001t0001g0224 a0001c0001t0002g0022 a0001c0001t0002g0222 others(6): Show |
10 | HG01168.hp2 HG02615.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.-23+5575T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41729775 | |||||||
| chr6:41729821 | G | C | 1 | a0001c0003t0001g0035 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-23+5529C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41729821 | |||||||
| chr6:41729910 | G | A | 1 | a0001c0002t0001g0162 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-23+5440C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41729910 | |||||||
| chr6:41729915 | C | T | 1 | a0001c0005t0001g0097 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-23+5435G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41729915 | |||||||
| chr6:41730017 | G | A | 1 | a0001c0003t0001g0272 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-23+5333C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730017 | |||||||
| chr6:41730122 | G | GA | 60 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0274 others(57): Show |
68 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.-23+5227dupT | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730122 | |||||||
| chr6:41730122 | GA | G | 112 | a0001c0001t0001g0048 a0001c0001t0001g0093 a0001c0001t0001g0115 others(109): Show |
128 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.-23+5227delT | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730122 | |||||||
| chr6:41730174 | A | C | 1 | a0001c0001t0001g0273 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-23+5176T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730174 | |||||||
| chr6:41730254 | C | G | 1 | a0001c0002t0001g0018 | 2 | NA18991.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.-23+5096G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730254 | |||||||
| chr6:41730393 | C | A | 2 | a0001c0001t0002g0016 a0001c0001t0002g0091 |
3 | HG01243.hp1 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-23+4957G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730393 | |||||||
| chr6:41730396 | A | G | 66 | a0001c0001t0001g0187 a0001c0001t0001g0194 a0001c0001t0001g0196 others(63): Show |
71 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.-23+4954T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730396 | |||||||
| chr6:41730439 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-23+4911C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730439 | |||||||
| chr6:41730715 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-23+4635T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730715 | |||||||
| chr6:41730764 | G | C | 14 | a0001c0001t0001g0025 a0001c0001t0001g0245 a0001c0001t0001g0260 others(11): Show |
15 | HG01361.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-23+4586C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730764 | |||||||
| chr6:41730804 | G | A | 1 | a0001c0002t0001g0163 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-23+4546C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730804 | |||||||
| chr6:41730895 | C | A | 2 | a0001c0001t0001g0105 a0001c0005t0001g0106 |
2 | HG02738.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-23+4455G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730895 | |||||||
| chr6:41731049 | A | G | 3 | a0001c0001t0003g0164 a0001c0001t0003g0165 a0001c0001t0003g0250 |
3 | HG00741.hp2 HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-23+4301T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731049 | |||||||
| chr6:41731241 | A | G | 1 | a0001c0012t0001g0121 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-23+4109T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731241 | |||||||
| chr6:41731312 | G | A | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG01884.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+4038C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731312 | |||||||
| chr6:41731357 | T | C | 1 | a0001c0002t0001g0348 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-23+3993A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731357 | |||||||
| chr6:41731498 | T | A | 4 | a0001c0001t0001g0236 a0001c0004t0002g0024 a0001c0004t0002g0237 others(1): Show |
5 | HG00735.hp1 HG00738.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23+3852A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731498 | |||||||
| chr6:41731514 | C | G | 1 | a0001c0004t0011g0354 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-23+3836G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731514 | |||||||
| chr6:41731515 | C | T | 1 | a0001c0003t0001g0035 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-23+3835G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731515 | |||||||
| chr6:41731555 | G | A | 5 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0002g0107 others(2): Show |
5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23+3795C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731555 | |||||||
| chr6:41731644 | C | A | 3 | a0001c0001t0001g0351 a0001c0001t0001g0352 a0001c0001t0001g0353 |
3 | HG06807.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-23+3706G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731644 | |||||||
| chr6:41731774 | C | T | 1 | a0001c0002t0001g0020 | 2 | NA18999.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-23+3576G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731774 | |||||||
| chr6:41731813 | C | G | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0003t0001g0272 |
3 | HG02630.hp2 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-23+3537G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731813 | |||||||
| chr6:41731821 | C | T | 12 | a0001c0001t0001g0025 a0001c0001t0001g0260 a0001c0001t0001g0261 others(9): Show |
13 | HG01361.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-23+3529G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731821 | |||||||
| chr6:41731842 | C | G | 2 | a0001c0002t0001g0017 a0001c0002t0001g0120 |
3 | HG01255.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-23+3508G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731842 | |||||||
| chr6:41731983 | C | T | 8 | a0001c0001t0001g0025 a0001c0001t0001g0260 a0001c0001t0001g0261 others(5): Show |
9 | HG02559.hp2 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-23+3367G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731983 | |||||||
| chr6:41732083 | G | A | 1 | a0001c0003t0001g0092 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-23+3267C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41732083 | |||||||
| chr6:41732105 | C | T | 2 | a0001c0001t0002g0302 a0001c0001t0002g0303 |
2 | NA18945.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.-23+3245G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41732105 | |||||||
| chr6:41732123 | T | C | 299 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0025 others(296): Show |
333 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.-23+3227A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41732123 | |||||||
| chr6:41732247 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-23+3103C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41732247 | |||||||
| chr6:41732406 | C | T | 1 | a0001c0004t0002g0034 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-23+2944G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41732406 | |||||||
| chr6:41732451 | T | A | 1 | a0001c0001t0001g0273 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-23+2899A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41732451 | |||||||
| chr6:41732698 | T | G | 4 | a0001c0005t0001g0239 a0001c0005t0001g0240 a0001c0005t0001g0241 others(1): Show |
4 | HG02257.hp2 HG02451.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+2652A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41732698 | |||||||
| chr6:41732856 | C | A | 5 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0002g0107 others(2): Show |
5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23+2494G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41732856 | |||||||
| chr6:41733118 | G | A | 1 | a0001c0004t0002g0243 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-23+2232C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41733118 | |||||||
| chr6:41733120 | T | C | 10 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0002g0099 others(7): Show |
10 | HG00280.hp2 HG00642.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-23+2230A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41733120 | |||||||
| chr6:41733291 | A | G | 1 | a0001c0001t0003g0119 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-23+2059T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41733291 | |||||||
| chr6:41733292 | T | C | 1 | a0001c0002t0001g0244 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-23+2058A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41733292 | |||||||
| chr6:41733312 | T | G | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-23+2038A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41733312 | |||||||
| chr6:41733469 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0002g0094 |
2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-23+1881A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41733469 | |||||||
| chr6:41733574 | C | A | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG01884.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+1776G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41733574 | |||||||
| chr6:41733586 | G | A | 1 | a0001c0001t0003g0250 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-23+1764C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41733586 | |||||||
| chr6:41733699 | AC | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0252 a0001c0001t0001g0253 others(7): Show |
12 | HG00642.hp2 HG01081.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+1650delG | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41733699 | |||||||
| chr6:41733903 | G | A | 12 | a0001c0001t0001g0025 a0001c0001t0001g0260 a0001c0001t0001g0261 others(9): Show |
13 | HG01361.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-23+1447C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41733903 | |||||||
| chr6:41733991 | C | G | 1 | a0001c0005t0001g0118 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-23+1359G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41733991 | |||||||
| chr6:41734314 | C | G | 1 | a0001c0004t0002g0117 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-23+1036G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734314 | |||||||
| chr6:41734318 | G | C | 1 | a0001c0002t0001g0271 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-23+1032C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734318 | |||||||
| chr6:41734489 | G | C | 10 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0002g0099 others(7): Show |
10 | HG00280.hp2 HG00642.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-23+861C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734489 | |||||||
| chr6:41734494 | G | A | 1 | a0001c0003t0001g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-23+856C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734494 | |||||||
| chr6:41734619 | A | T | 30 | a0001c0001t0002g0284 a0001c0001t0002g0289 a0001c0001t0002g0290 others(27): Show |
35 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.-23+731T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734619 | |||||||
| chr6:41734824 | G | C | 1 | a0001c0005t0001g0096 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-23+526C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734824 | |||||||
| chr6:41734844 | C | T | 165 | a0001c0001t0001g0048 a0001c0001t0001g0093 a0001c0001t0001g0113 others(162): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.-23+506G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734844 | |||||||
| chr6:41734881 | C | A | 10 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0002g0099 others(7): Show |
10 | HG00280.hp2 HG00642.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-23+469G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734881 | |||||||
| chr6:41734925 | G | A | 1 | a0001c0003t0001g0272 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-23+425C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734925 | |||||||
| chr6:41734951 | G | T | 2 | a0001c0001t0001g0274 a0001c0005t0001g0275 |
2 | HG02630.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-23+399C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734951 | |||||||
| chr6:41734960 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-23+390G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734960 | |||||||
| chr6:41734970 | G | A | 4 | a0001c0001t0001g0351 a0001c0001t0001g0352 a0001c0001t0001g0353 others(1): Show |
4 | HG02809.hp1 HG06807.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+380C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734970 | |||||||
| chr6:41734989 | C | G | 5 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0002g0107 others(2): Show |
5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23+361G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734989 | |||||||
| chr6:41735031 | C | T | 1 | a0001c0003t0001g0033 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-23+319G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41735031 | |||||||
| chr6:41735142 | C | T | 10 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0002g0099 others(7): Show |
10 | HG00280.hp2 HG00642.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-23+208G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41735142 | |||||||
| chr6:41735241 | C | T | 73 | a0001c0001t0001g0048 a0001c0001t0001g0093 a0001c0001t0002g0011 others(70): Show |
85 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.-23+109G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41735241 | |||||||
| chr6:41735293 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-23+57C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41735293 | |||||||
| chr6:41735303 | G | A | 89 | a0001c0001t0001g0274 a0001c0001t0001g0317 a0001c0001t0001g0344 others(86): Show |
101 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-23+47C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41735303 |