Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5340 |
| ensemblid | ENSG00000122194.20 |
| hgncid | 9071 |
| symbol | PLG |
| name | plasminogen |
| refseq_nuc | NM_000301.5 |
| refseq_prot | NP_000292.1 |
| ensembl_nuc | ENST00000308192.14 |
| ensembl_prot | ENSP00000308938.9 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 160702244 |
| end | 160754097 |
| strand | + |
| ver | v1.2 |
| region | chr6:160702244-160754097 |
| region5000 | chr6:160697244-160759097 |
| regionname0 | PLG_chr6_160702244_160754097 |
| regionname5000 | PLG_chr6_160697244_160759097 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 810 | 318 | 67 | 53 | 148 | 11 | 37 | 123 | PLG_chr6_160697244_160759097 | PLG | MEHKE others(805): Show |
chr6 | 160697244 | 160759097 |
| a0002 | 0/0 | 810 | 42 | 17 | 20 | 0 | 3 | 2 | 0 | PLG_chr6_160697244_160759097 | PLG | MEHKE others(805): Show |
chr6 | 160697244 | 160759097 |
| a0003 | 0/0 | 810 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | MEHKE others(805): Show |
chr6 | 160697244 | 160759097 |
| a0004 | 0/0 | 810 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | MEHKE others(805): Show |
chr6 | 160697244 | 160759097 |
| a0005 | 0/0 | 810 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | MEHKE others(805): Show |
chr6 | 160697244 | 160759097 |
| a0006 | 0/0 | 810 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | PLG_chr6_160697244_160759097 | PLG | MEHKE others(805): Show |
chr6 | 160697244 | 160759097 |
| a0007 | 0/0 | 810 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | MEHKE others(805): Show |
chr6 | 160697244 | 160759097 |
| a0008 | 0/0 | 810 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | PLG_chr6_160697244_160759097 | PLG | MEHKE others(805): Show |
chr6 | 160697244 | 160759097 |
| a0009 | 0/0 | 810 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PLG_chr6_160697244_160759097 | PLG | MEHKE others(805): Show |
chr6 | 160697244 | 160759097 |
| a0010 | 0/0 | 810 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | MEHKE others(805): Show |
chr6 | 160697244 | 160759097 |
| a0011 | 0/0 | 810 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | MEHKE others(805): Show |
chr6 | 160697244 | 160759097 |
| a0012 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | MEHKE others(805): Show |
chr6 | 160697244 | 160759097 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2430 | 119 | 11 | 15 | 71 | 6 | 15 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0001c0002 | 0/0 | 2430 | 89 | 6 | 20 | 52 | 1 | 10 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0001c0003 | 0/0 | 2430 | 37 | 3 | 7 | 21 | 1 | 5 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0001c0005 | 1/0 | 2430 | 21 | 5 | 6 | 1 | 2 | 6 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0001c0006 | 0/0 | 2430 | 19 | 19 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0001c0008 | 0/0 | 2430 | 8 | 8 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0001c0009 | 0/0 | 2430 | 7 | 2 | 4 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0001c0011 | 0/0 | 2430 | 4 | 1 | 0 | 3 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0001c0013 | 0/0 | 2430 | 4 | 4 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0001c0015 | 0/0 | 2430 | 3 | 2 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0001c0021 | 0/0 | 2430 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0001c0024 | 0/0 | 2430 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0001c0025 | 0/0 | 2430 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0001c0027 | 0/0 | 2430 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0001c0028 | 0/0 | 2430 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0001c0029 | 0/0 | 2430 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0002c0004 | 0/0 | 2430 | 29 | 8 | 16 | 0 | 3 | 2 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0002c0007 | 0/0 | 2430 | 12 | 9 | 3 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0002c0022 | 0/0 | 2430 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0003c0018 | 0/0 | 2430 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0003c0020 | 0/0 | 2430 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0004c0012 | 0/0 | 2430 | 4 | 4 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0005c0010 | 0/0 | 2430 | 4 | 4 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0006c0014 | 0/0 | 2430 | 3 | 0 | 0 | 3 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0007c0019 | 0/0 | 2430 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0008c0016 | 0/0 | 2430 | 2 | 0 | 0 | 0 | 0 | 2 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0009c0017 | 0/0 | 2430 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0010c0026 | 0/0 | 2430 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0011c0030 | 0/0 | 2430 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 | ||
| a0012c0023 | 0/0 | 2430 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | ATGGA others(2425): Show |
chr6 | 160697244 | 160759097 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3529 | 106 | 8 | 15 | 62 | 6 | 14 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0001c0001t0006 | 0/0 | 3529 | 7 | 0 | 0 | 7 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0001c0001t0007 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0001c0001t0017 | 0/0 | 3529 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0001c0001t0018 | 0/0 | 3529 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0001c0001t0019 | 0/0 | 3529 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0001c0001t0020 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0001c0001t0022 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0001c0002t0001 | 0/0 | 3529 | 87 | 5 | 20 | 51 | 1 | 10 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0001c0002t0006 | 0/0 | 3529 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0001c0002t0009 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0001c0003t0001 | 0/0 | 3529 | 37 | 3 | 7 | 21 | 1 | 5 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0001c0005t0002 | 1/0 | 3530 | 17 | 1 | 6 | 1 | 2 | 6 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0001c0005t0005 | 0/0 | 3530 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0001c0005t0010 | 0/0 | 3530 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0001c0005t0011 | 0/0 | 3530 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0001c0006t0002 | 0/0 | 3530 | 6 | 6 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0001c0006t0004 | 0/0 | 3530 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0001c0006t0005 | 0/0 | 3530 | 10 | 10 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0001c0006t0013 | 0/0 | 3530 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0001c0006t0014 | 0/0 | 3530 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0001c0008t0001 | 0/0 | 3529 | 8 | 8 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0001c0009t0002 | 0/0 | 3530 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0001c0009t0004 | 0/0 | 3530 | 3 | 2 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0001c0009t0012 | 0/0 | 3530 | 2 | 0 | 1 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0001c0011t0001 | 0/0 | 3529 | 4 | 1 | 0 | 3 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0001c0013t0001 | 0/0 | 3529 | 3 | 3 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0001c0013t0009 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0001c0015t0001 | 0/0 | 3529 | 2 | 1 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0001c0015t0009 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0001c0021t0004 | 0/0 | 3530 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0001c0024t0009 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0001c0025t0001 | 0/0 | 3529 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0001c0027t0010 | 0/0 | 3530 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0001c0028t0004 | 0/0 | 3530 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0001c0029t0015 | 0/0 | 3530 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0002c0004t0003 | 0/0 | 3530 | 21 | 1 | 15 | 0 | 3 | 2 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0002c0004t0008 | 0/0 | 3530 | 6 | 6 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0002c0004t0011 | 0/0 | 3530 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0002c0004t0016 | 0/0 | 3530 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0002c0007t0001 | 0/0 | 3529 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0002c0007t0007 | 0/0 | 3529 | 9 | 8 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0002c0007t0023 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0002c0022t0003 | 0/0 | 3530 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0003c0018t0002 | 0/0 | 3530 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0003c0020t0004 | 0/0 | 3530 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0004c0012t0001 | 0/0 | 3529 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0004c0012t0009 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0004c0012t0021 | 0/0 | 3529 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0005c0010t0004 | 0/0 | 3530 | 4 | 4 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0006c0014t0001 | 0/0 | 3529 | 3 | 0 | 0 | 3 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0007c0019t0001 | 0/0 | 3529 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0008c0016t0001 | 0/0 | 3529 | 2 | 0 | 0 | 0 | 0 | 2 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0009c0017t0006 | 0/0 | 3529 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0010c0026t0001 | 0/0 | 3529 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| a0011c0030t0003 | 0/0 | 3530 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3525): Show |
chr6 | 160697244 | 160759097 |
| a0012c0023t0001 | 0/0 | 3529 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | GTAAG others(3524): Show |
chr6 | 160697244 | 160759097 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0028 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0006g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0006g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0006g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0006g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0007g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0017g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0018g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0019g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0020g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0001t0022g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0006g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0002t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0003t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0005t0002g0005 | 1/0 | 3 | 0 | 0 | 0 | 0 | 2 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0005t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0005t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0005t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0005t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0005t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0005t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0005t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0005t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0005t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0005t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0005t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0005t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0005t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0005t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0005t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0005t0010g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0005t0010g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0005t0011g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0006t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0006t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0006t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0006t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0006t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0006t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0006t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0006t0005g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0006t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0006t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0006t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0006t0005g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0006t0005g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0006t0005g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0006t0005g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0006t0005g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0006t0013g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0006t0014g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0008t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0008t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0008t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0008t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0008t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0008t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0008t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0008t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0009t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0009t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0009t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0009t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0009t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0009t0012g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0009t0012g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0011t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0011t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0011t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0011t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0013t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0013t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0013t0009g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0015t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0015t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0015t0009g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0021t0004g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0024t0009g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0025t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0027t0010g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0028t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0001c0029t0015g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0004t0003g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0004t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0004t0003g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0004t0003g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0004t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0004t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0004t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0004t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0004t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0004t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0004t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0004t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0004t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0004t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0004t0003g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0004t0008g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0004t0008g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0004t0011g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0004t0016g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0007t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0007t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0007t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0007t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0007t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0007t0007g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0007t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0007t0007g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0007t0007g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0007t0007g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0007t0007g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0007t0023g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0002c0022t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0003c0018t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0003c0018t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0003c0020t0004g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0003c0020t0004g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0004c0012t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0004c0012t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0004c0012t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0004c0012t0021g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0005c0010t0004g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0005c0010t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0005c0010t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0006c0014t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0006c0014t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0006c0014t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0007c0019t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0007c0019t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0008c0016t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0009c0017t0006g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0010c0026t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0011c0030t0003g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| a0012c0023t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0140 | EUR | GBR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0269 | EUR | GBR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00280 | hp1 | a0001 | c0005 | t0002 | g0101 | EUR | FIN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | FIN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00323 | hp1 | a0002 | c0004 | t0003 | g0276 | EUR | FIN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00323 | hp2 | a0001 | c0005 | t0002 | g0244 | EUR | FIN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00558 | hp2 | a0001 | c0003 | t0001 | g0229 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | CHS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00639 | hp1 | a0002 | c0004 | t0003 | g0001 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0151 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00642 | hp1 | a0002 | c0004 | t0003 | g0075 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00642 | hp2 | a0001 | c0005 | t0002 | g0294 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00733 | hp2 | a0002 | c0004 | t0003 | g0021 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00735 | hp1 | a0002 | c0004 | t0003 | g0021 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00738 | hp1 | a0001 | c0005 | t0002 | g0106 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00738 | hp2 | a0002 | c0004 | t0003 | g0024 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0279 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0278 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01069 | hp2 | a0002 | c0004 | t0003 | g0076 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01070 | hp1 | a0001 | c0005 | t0002 | g0104 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01070 | hp2 | a0002 | c0004 | t0003 | g0275 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01071 | hp1 | a0002 | c0004 | t0003 | g0010 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01071 | hp2 | a0001 | c0005 | t0002 | g0102 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01074 | hp1 | a0001 | c0009 | t0002 | g0057 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0260 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01081 | hp2 | a0002 | c0004 | t0003 | g0024 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0058 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01099 | hp2 | a0010 | c0026 | t0001 | g0064 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01106 | hp1 | a0001 | c0009 | t0004 | g0063 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0107 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01109 | hp1 | a0002 | c0022 | t0003 | g0261 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01109 | hp2 | a0002 | c0004 | t0016 | g0010 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01168 | hp1 | a0002 | c0004 | t0003 | g0001 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0127 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01169 | hp1 | a0002 | c0004 | t0003 | g0001 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01243 | hp1 | a0002 | c0007 | t0007 | g0040 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0152 | AMR | PUR | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0122 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01256 | hp1 | a0003 | c0020 | t0004 | g0332 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01257 | hp2 | a0001 | c0025 | t0001 | g0284 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01258 | hp1 | a0003 | c0020 | t0004 | g0326 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01261 | hp1 | a0002 | c0004 | t0003 | g0001 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01346 | hp1 | a0001 | c0009 | t0002 | g0056 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01346 | hp2 | a0002 | c0007 | t0001 | g0274 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01358 | hp2 | a0001 | c0005 | t0002 | g0335 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01361 | hp2 | a0001 | c0005 | t0002 | g0243 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01433 | hp1 | a0002 | c0007 | t0001 | g0272 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | IBS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0069 | EUR | IBS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0125 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01884 | hp2 | a0001 | c0006 | t0005 | g0342 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0191 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01891 | hp2 | a0001 | c0006 | t0014 | g0035 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0085 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01952 | hp2 | a0003 | c0018 | t0002 | g0263 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01975 | hp1 | a0002 | c0004 | t0003 | g0001 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01978 | hp1 | a0001 | c0009 | t0012 | g0068 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0123 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02004 | hp2 | a0002 | c0004 | t0003 | g0277 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02027 | hp1 | a0001 | c0003 | t0001 | g0146 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02055 | hp2 | a0002 | c0007 | t0007 | g0091 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02080 | hp2 | a0001 | c0003 | t0001 | g0150 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02132 | hp1 | a0007 | c0019 | t0001 | g0318 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | KHV | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02145 | hp1 | a0002 | c0004 | t0008 | g0032 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0343 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02148 | hp1 | a0003 | c0018 | t0002 | g0262 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0154 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02257 | hp2 | a0004 | c0012 | t0001 | g0233 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02258 | hp1 | a0001 | c0009 | t0004 | g0026 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02258 | hp2 | a0002 | c0007 | t0007 | g0092 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02273 | hp2 | a0002 | c0004 | t0003 | g0265 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02280 | hp1 | a0002 | c0004 | t0008 | g0002 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02280 | hp2 | a0005 | c0010 | t0004 | g0019 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0121 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0201 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0149 | AMR | PEL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02451 | hp1 | a0001 | c0006 | t0002 | g0270 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02451 | hp2 | a0001 | c0001 | t0022 | g0299 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02572 | hp1 | a0001 | c0008 | t0001 | g0290 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02572 | hp2 | a0001 | c0011 | t0001 | g0230 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02602 | hp1 | a0011 | c0030 | t0003 | g0001 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0245 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02615 | hp1 | a0001 | c0001 | t0020 | g0289 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02615 | hp2 | a0002 | c0007 | t0007 | g0043 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02622 | hp1 | a0002 | c0004 | t0008 | g0002 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02622 | hp2 | a0001 | c0006 | t0005 | g0337 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02630 | hp1 | a0001 | c0008 | t0001 | g0291 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02647 | hp1 | a0001 | c0006 | t0005 | g0018 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02647 | hp2 | a0005 | c0010 | t0004 | g0019 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02683 | hp1 | a0001 | c0003 | t0001 | g0192 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02683 | hp2 | a0001 | c0001 | t0018 | g0256 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02698 | hp1 | a0002 | c0004 | t0003 | g0271 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02717 | hp1 | a0001 | c0006 | t0013 | g0237 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02717 | hp2 | a0002 | c0007 | t0007 | g0281 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0139 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02809 | hp1 | a0001 | c0008 | t0001 | g0304 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02818 | hp1 | a0001 | c0006 | t0005 | g0344 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02818 | hp2 | a0005 | c0010 | t0004 | g0235 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02886 | hp1 | a0001 | c0013 | t0001 | g0025 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02886 | hp2 | a0001 | c0008 | t0001 | g0292 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02895 | hp1 | a0001 | c0013 | t0001 | g0025 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02896 | hp1 | a0001 | c0013 | t0001 | g0341 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02896 | hp2 | a0001 | c0006 | t0005 | g0232 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02922 | hp1 | a0001 | c0006 | t0002 | g0300 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02922 | hp2 | a0001 | c0024 | t0009 | g0240 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02965 | hp1 | a0002 | c0007 | t0007 | g0038 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02965 | hp2 | a0004 | c0012 | t0001 | g0248 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02970 | hp1 | a0005 | c0010 | t0004 | g0236 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02970 | hp2 | a0001 | c0006 | t0004 | g0046 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02976 | hp1 | a0001 | c0006 | t0005 | g0094 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02976 | hp2 | a0001 | c0013 | t0009 | g0033 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03041 | hp1 | a0001 | c0006 | t0002 | g0045 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0193 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03098 | hp1 | a0001 | c0021 | t0004 | g0014 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03098 | hp2 | a0001 | c0029 | t0015 | g0031 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03130 | hp1 | a0001 | c0008 | t0001 | g0339 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03130 | hp2 | a0001 | c0006 | t0005 | g0093 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03139 | hp1 | a0001 | c0021 | t0004 | g0014 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03139 | hp2 | a0001 | c0006 | t0002 | g0041 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03195 | hp1 | a0002 | c0004 | t0008 | g0002 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03195 | hp2 | a0001 | c0006 | t0005 | g0336 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03209 | hp1 | a0002 | c0007 | t0007 | g0036 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03209 | hp2 | a0001 | c0005 | t0005 | g0234 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03225 | hp1 | a0002 | c0004 | t0011 | g0296 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03225 | hp2 | a0001 | c0005 | t0010 | g0027 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0120 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03239 | hp2 | a0001 | c0005 | t0002 | g0293 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03453 | hp2 | a0001 | c0005 | t0010 | g0298 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0119 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03486 | hp2 | a0001 | c0006 | t0005 | g0338 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03490 | hp1 | a0001 | c0015 | t0001 | g0306 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03490 | hp2 | a0008 | c0016 | t0001 | g0020 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0329 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03491 | hp2 | a0001 | c0005 | t0002 | g0005 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03492 | hp1 | a0008 | c0016 | t0001 | g0020 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03492 | hp2 | a0001 | c0005 | t0002 | g0005 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03516 | hp1 | a0001 | c0006 | t0002 | g0109 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03516 | hp2 | a0002 | c0004 | t0008 | g0002 | AFR | ESN | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03540 | hp1 | a0001 | c0006 | t0005 | g0018 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03540 | hp2 | a0001 | c0008 | t0001 | g0231 | AFR | GWD | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03669 | hp1 | a0001 | c0005 | t0002 | g0264 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0071 | SAS | STU | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03688 | hp2 | a0001 | c0005 | t0002 | g0112 | SAS | STU | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0049 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0103 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0011 | SAS | BEB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0327 | SAS | BEB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | BEB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03927 | hp2 | a0001 | c0005 | t0002 | g0246 | SAS | BEB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0160 | SAS | BEB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0132 | SAS | STU | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0328 | SAS | BEB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0147 | SAS | BEB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | STU | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0128 | SAS | STU | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0324 | SAS | STU | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0288 | AFR | YRI | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18522 | hp2 | a0002 | c0004 | t0008 | g0002 | AFR | YRI | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18612 | hp2 | a0001 | c0003 | t0001 | g0148 | EAS | CHB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18906 | hp1 | a0001 | c0027 | t0010 | g0115 | AFR | YRI | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18906 | hp2 | a0002 | c0007 | t0023 | g0048 | AFR | YRI | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18940 | hp1 | a0001 | c0011 | t0001 | g0224 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0310 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0255 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18945 | hp1 | a0001 | c0003 | t0001 | g0221 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18952 | hp1 | a0001 | c0001 | t0006 | g0319 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18953 | hp1 | a0001 | c0003 | t0001 | g0198 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18953 | hp2 | a0001 | c0001 | t0006 | g0182 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18956 | hp2 | a0001 | c0001 | t0006 | g0181 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18962 | hp1 | a0001 | c0003 | t0001 | g0311 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18962 | hp2 | a0006 | c0014 | t0001 | g0144 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18963 | hp2 | a0001 | c0011 | t0001 | g0226 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18966 | hp1 | a0012 | c0023 | t0001 | g0095 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18969 | hp2 | a0001 | c0003 | t0001 | g0312 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18971 | hp2 | a0001 | c0003 | t0001 | g0197 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18974 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18974 | hp2 | a0001 | c0001 | t0006 | g0247 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18975 | hp1 | a0001 | c0011 | t0001 | g0225 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18975 | hp2 | a0001 | c0001 | t0006 | g0184 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18978 | hp2 | a0006 | c0014 | t0001 | g0309 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18983 | hp1 | a0009 | c0017 | t0006 | g0016 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18983 | hp2 | a0001 | c0001 | t0017 | g0188 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18987 | hp1 | a0001 | c0002 | t0006 | g0051 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18988 | hp2 | a0001 | c0003 | t0001 | g0222 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18990 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19002 | hp2 | a0001 | c0001 | t0019 | g0211 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19004 | hp1 | a0001 | c0003 | t0001 | g0228 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19004 | hp2 | a0001 | c0001 | t0006 | g0183 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19009 | hp2 | a0006 | c0014 | t0001 | g0141 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19030 | hp1 | a0001 | c0008 | t0001 | g0345 | AFR | LWK | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19030 | hp2 | a0004 | c0012 | t0009 | g0034 | AFR | LWK | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19043 | hp1 | a0001 | c0002 | t0009 | g0239 | AFR | LWK | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19060 | hp2 | a0001 | c0003 | t0001 | g0199 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19063 | hp1 | a0009 | c0017 | t0006 | g0016 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19065 | hp1 | a0001 | c0003 | t0001 | g0086 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19065 | hp2 | a0001 | c0001 | t0006 | g0185 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19068 | hp1 | a0007 | c0019 | t0001 | g0307 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19068 | hp2 | a0001 | c0003 | t0001 | g0223 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19075 | hp2 | a0001 | c0003 | t0001 | g0313 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19078 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19079 | hp1 | a0001 | c0003 | t0001 | g0200 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19079 | hp2 | a0001 | c0005 | t0002 | g0105 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19088 | hp2 | a0001 | c0003 | t0001 | g0325 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA20129 | hp1 | a0001 | c0015 | t0009 | g0238 | AFR | ASW | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ASW | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA20752 | hp1 | a0002 | c0004 | t0003 | g0273 | EUR | TSI | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA20752 | hp2 | a0001 | c0009 | t0012 | g0062 | EUR | TSI | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA20805 | hp1 | a0002 | c0004 | t0003 | g0249 | EUR | TSI | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0055 | EUR | TSI | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA20905 | hp1 | a0002 | c0004 | t0003 | g0334 | SAS | GIH | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0011 | SAS | GIH | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0130 | AMR | CLM | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02109 | hp1 | a0001 | c0005 | t0011 | g0110 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02109 | hp2 | a0002 | c0007 | t0007 | g0282 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02486 | hp1 | a0002 | c0007 | t0007 | g0037 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02486 | hp2 | a0001 | c0005 | t0002 | g0295 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02559 | hp1 | a0001 | c0015 | t0001 | g0340 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG02559 | hp2 | a0001 | c0008 | t0001 | g0218 | AFR | ACB | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03471 | hp1 | a0001 | c0006 | t0002 | g0042 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG03471 | hp2 | a0002 | c0004 | t0003 | g0331 | AFR | MSL | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0157 | AFR | USA | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| HG06807 | hp2 | a0004 | c0012 | t0021 | g0305 | AFR | USA | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0047 | AFR | USA | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | USA | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA21309 | hp1 | a0001 | c0028 | t0004 | g0227 | AFR | LWK | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| NA21309 | hp2 | a0001 | c0009 | t0004 | g0044 | AFR | LWK | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0028 | REF | REF | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| homoSapiens | grch38p0 | a0001 | c0005 | t0002 | g0005 | REF | REF | PLG_chr6_160697244_160759097 | PLG | chr6 | 160697244 | 160759097 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:160706469 | A | G | 1 | a0011 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.112A>G | p.Lys38Glu | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/19 | 173/3530 | 112/2433 | 38/810 | chr6 | 160706469 | |||
| chr6:160706526 | G | A | 1 | a0005 | 4 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
missense_variant | MODERATE | c.169G>A | p.Glu57Lys | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/19 | 230/3530 | 169/2433 | 57/810 | chr6 | 160706526 | |||
| chr6:160707780 | G | A | 1 | a0008 | 2 | HG03490.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.266G>A | p.Arg89Lys | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/19 | 327/3530 | 266/2433 | 89/810 | chr6 | 160707780 | |||
| chr6:160714827 | A | T | 1 | a0007 | 2 | HG02132.hp1 NA19068.hp1 |
missense_variant | MODERATE | c.581A>T | p.Asp194Val | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/19 | 642/3530 | 581/2433 | 194/810 | chr6 | 160714827 | |||
| chr6:160714844 | A | G | 1 | a0010 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.598A>G | p.Thr200Ala | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/19 | 659/3530 | 598/2433 | 200/810 | chr6 | 160714844 | |||
| chr6:160722431 | G | T | 1 | a0009 | 2 | NA18983.hp1 NA19063.hp1 |
missense_variant | MODERATE | c.1120G>T | p.Val374Phe | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/19 | 1181/3530 | 1120/2433 | 374/810 | chr6 | 160722431 | |||
| chr6:160722533 | C | T | 1 | a0005 | 4 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
missense_variant | MODERATE | c.1222C>T | p.Arg408Trp | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/19 | 1283/3530 | 1222/2433 | 408/810 | chr6 | 160722533 | |||
| chr6:160731174 | T | A | 1 | a0004 | 4 | HG02257.hp2 HG02965.hp2 HG06807.hp2 others(1): Show |
missense_variant | MODERATE | c.1380T>A | p.Ser460Arg | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 11/19 | 1441/3530 | 1380/2433 | 460/810 | chr6 | 160731174 | |||
| chr6:160731208 | G | A | 2 | a0002 a0011 |
43 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
missense_variant | MODERATE | c.1414G>A | p.Asp472Asn | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 11/19 | 1475/3530 | 1414/2433 | 472/810 | chr6 | 160731208 | |||
| chr6:160731787 | C | T | 1 | a0003 | 4 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(1): Show |
missense_variant | MODERATE | c.1481C>T | p.Ala494Val | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/19 | 1542/3530 | 1481/2433 | 494/810 | chr6 | 160731787 | |||
| chr6:160738593 | G | A | 1 | a0006 | 3 | NA18962.hp2 NA18978.hp2 NA19009.hp2 |
missense_variant | MODERATE | c.1858G>A | p.Ala620Thr | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 15/19 | 1919/3530 | 1858/2433 | 620/810 | chr6 | 160738593 | |||
| chr6:160741375 | G | A | 1 | a0012 | 1 | NA18966.hp1 | missense_variant | MODERATE | c.2083G>A | p.Asp695Asn | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/19 | 2144/3530 | 2083/2433 | 695/810 | chr6 | 160741375 | |||
| chr6:160754097 | A | G | 2 | a0001 a0002 |
2 | HG02109.hp1 HG03225.hp1 |
splice_region_variant | LOW | c.*1036A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | chr6 | 160754097 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:160711114 | C | T | 11 | a0001c0006 a0001c0013 a0001c0015 others(8): Show |
78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
synonymous_variant | LOW | c.330C>T | p.Asn110Asn | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/19 | 391/3530 | 330/2433 | 110/810 | chr6 | 160711114 | |||
| chr6:160714828 | C | T | 1 | a0001c0027 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.582C>T | p.Asp194Asp | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/19 | 643/3530 | 582/2433 | 194/810 | chr6 | 160714828 | |||
| chr6:160716747 | T | C | 16 | a0001c0001 a0001c0006 a0001c0009 others(13): Show |
172 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(169): Show |
synonymous_variant | LOW | c.771T>C | p.Cys257Cys | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/19 | 832/3530 | 771/2433 | 257/810 | chr6 | 160716747 | |||
| chr6:160718448 | C | T | 11 | a0001c0001 a0001c0009 a0001c0011 others(8): Show |
140 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(137): Show |
synonymous_variant | LOW | c.942C>T | p.Phe314Phe | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 8/19 | 1003/3530 | 942/2433 | 314/810 | chr6 | 160718448 | |||
| chr6:160718825 | A | G | 5 | a0001c0028 a0001c0029 a0002c0004 others(2): Show |
44 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(41): Show |
synonymous_variant | LOW | c.1083A>G | p.Gln361Gln | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/19 | 1144/3530 | 1083/2433 | 361/810 | chr6 | 160718825 | |||
| chr6:160731225 | C | T | 2 | a0001c0025 a0001c0027 |
2 | HG01257.hp2 NA18906.hp1 |
synonymous_variant | LOW | c.1431C>T | p.Ser477Ser | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 11/19 | 1492/3530 | 1431/2433 | 477/810 | chr6 | 160731225 | |||
| chr6:160741374 | T | C | 2 | a0001c0003 a0001c0011 |
41 | HG00558.hp2 HG00639.hp2 HG00741.hp1 others(38): Show |
synonymous_variant | LOW | c.2082T>C | p.Ala694Ala | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/19 | 2143/3530 | 2082/2433 | 694/810 | chr6 | 160741374 | |||
| chr6:160752248 | T | C | 3 | a0001c0008 a0001c0013 a0001c0024 |
13 | HG02559.hp2 HG02572.hp1 HG02630.hp1 others(10): Show |
synonymous_variant | LOW | c.2259T>C | p.Thr753Thr | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 18/19 | 2320/3530 | 2259/2433 | 753/810 | chr6 | 160752248 | |||
| chr6:160752914 | T | G | 18 | a0001c0001 a0001c0002 a0001c0003 others(15): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(290): Show |
synonymous_variant | LOW | c.2286T>G | p.Gly762Gly | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 2347/3530 | 2286/2433 | 762/810 | chr6 | 160752914 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:160702270 | G | A | 9 | a0001c0002t0009 a0001c0006t0013 a0001c0006t0014 others(6): Show |
14 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-35G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/19 | 35 | chr6 | 160702270 | ||||||
| chr6:160753106 | A | G | 32 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(29): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(289): Show |
3_prime_UTR_variant | MODIFIER | c.*45A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 45 | chr6 | 160753106 | ||||||
| chr6:160753109 | G | A | 3 | a0001c0001t0006 a0001c0002t0006 a0009c0017t0006 |
10 | NA18952.hp1 NA18953.hp2 NA18956.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*48G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 48 | chr6 | 160753109 | ||||||
| chr6:160753345 | AT | A | 32 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(29): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(289): Show |
3_prime_UTR_variant | MODIFIER | c.*289delT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 289 | INFO_REALIGN_3_PRIME | chr6 | 160753345 | |||||
| chr6:160753415 | G | C | 1 | a0002c0004t0016 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*354G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 354 | chr6 | 160753415 | ||||||
| chr6:160753434 | G | A | 1 | a0001c0001t0017 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*373G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 373 | chr6 | 160753434 | ||||||
| chr6:160753488 | T | G | 1 | a0001c0001t0018 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*427T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 427 | chr6 | 160753488 | ||||||
| chr6:160753547 | T | C | 29 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0017 others(26): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(278): Show |
3_prime_UTR_variant | MODIFIER | c.*486T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 486 | chr6 | 160753547 | ||||||
| chr6:160753562 | A | G | 32 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(29): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(289): Show |
3_prime_UTR_variant | MODIFIER | c.*501A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 501 | chr6 | 160753562 | ||||||
| chr6:160753577 | T | C | 1 | a0001c0001t0019 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*516T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 516 | chr6 | 160753577 | ||||||
| chr6:160753598 | G | A | 1 | a0002c0004t0008 | 6 | HG02145.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*537G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 537 | chr6 | 160753598 | ||||||
| chr6:160753626 | G | A | 49 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(46): Show |
350 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(347): Show |
3_prime_UTR_variant | MODIFIER | c.*565G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 565 | chr6 | 160753626 | ||||||
| chr6:160753742 | C | T | 1 | a0001c0001t0022 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*681C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 681 | chr6 | 160753742 | ||||||
| chr6:160753775 | G | A | 1 | a0001c0001t0020 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*714G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 714 | chr6 | 160753775 | ||||||
| chr6:160753836 | G | A | 3 | a0001c0005t0005 a0001c0006t0005 a0001c0006t0013 |
12 | HG01884.hp2 HG02622.hp2 HG02647.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*775G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 775 | chr6 | 160753836 | ||||||
| chr6:160753839 | C | G | 30 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0017 others(27): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*778C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 778 | chr6 | 160753839 | ||||||
| chr6:160753842 | A | G | 1 | a0001c0006t0014 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*781A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 781 | chr6 | 160753842 | ||||||
| chr6:160753844 | G | A | 1 | a0004c0012t0021 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*783G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 783 | chr6 | 160753844 | ||||||
| chr6:160753901 | C | T | 1 | a0001c0009t0012 | 2 | HG01978.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*840C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 840 | chr6 | 160753901 | ||||||
| chr6:160753972 | C | T | 5 | a0002c0004t0003 a0002c0004t0008 a0002c0004t0016 others(2): Show |
30 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*911C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 911 | chr6 | 160753972 | ||||||
| chr6:160754047 | T | C | 2 | a0001c0005t0010 a0001c0027t0010 |
3 | HG03225.hp2 HG03453.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*986T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 19/19 | 986 | chr6 | 160754047 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:160702381 | G | T | 118 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0241 others(115): Show |
130 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.49+28G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160702381 | |||||||
| chr6:160702386 | AT | A | 4 | a0001c0002t0009g0239 a0001c0006t0013g0237 a0001c0015t0009g0238 others(1): Show |
4 | HG02717.hp1 HG02922.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+39delT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr6 | 160702386 | ||||||
| chr6:160702419 | T | C | 6 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0003t0001g0245 others(3): Show |
6 | HG00323.hp2 HG01261.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+66T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160702419 | |||||||
| chr6:160702509 | A | G | 3 | a0005c0010t0004g0019 a0005c0010t0004g0235 a0005c0010t0004g0236 |
4 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+156A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160702509 | |||||||
| chr6:160702555 | G | A | 5 | a0001c0005t0010g0027 a0001c0009t0004g0026 a0005c0010t0004g0019 others(2): Show |
6 | HG02258.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+202G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160702555 | |||||||
| chr6:160702739 | T | C | 124 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0023 others(121): Show |
138 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.49+386T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160702739 | |||||||
| chr6:160702829 | T | C | 1 | a0001c0001t0006g0247 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.49+476T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160702829 | |||||||
| chr6:160702862 | G | A | 6 | a0001c0006t0014g0035 a0001c0013t0009g0033 a0001c0029t0015g0031 others(3): Show |
10 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+509G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160702862 | |||||||
| chr6:160702879 | G | A | 11 | a0001c0001t0001g0039 a0001c0006t0002g0041 a0001c0006t0002g0042 others(8): Show |
11 | HG01243.hp1 HG02486.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.49+526G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160702879 | |||||||
| chr6:160702939 | C | CACTT | 124 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0023 others(121): Show |
138 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.49+587_49+588insCT others(2): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr6 | 160702939 | ||||||
| chr6:160702944 | G | A | 1 | a0001c0003t0001g0047 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.49+591G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160702944 | |||||||
| chr6:160703014 | T | A | 4 | a0004c0012t0001g0248 a0005c0010t0004g0019 a0005c0010t0004g0235 others(1): Show |
5 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+661T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160703014 | |||||||
| chr6:160703033 | TA | T | 15 | a0001c0002t0001g0343 a0001c0002t0009g0239 a0001c0006t0005g0336 others(12): Show |
16 | HG01884.hp2 HG02145.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.49+681delA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160703033 | |||||||
| chr6:160703093 | C | CT | 124 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0023 others(121): Show |
138 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.49+740_49+741insT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160703093 | |||||||
| chr6:160703111 | G | T | 4 | a0001c0001t0001g0008 a0001c0005t0002g0335 a0002c0004t0003g0024 others(1): Show |
7 | HG00738.hp2 HG00741.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+758G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160703111 | |||||||
| chr6:160703139 | A | C | 15 | a0001c0002t0001g0343 a0001c0002t0009g0239 a0001c0006t0005g0336 others(12): Show |
16 | HG01884.hp2 HG02145.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.49+786A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160703139 | |||||||
| chr6:160703268 | T | TA | 16 | a0001c0001t0001g0039 a0001c0001t0001g0052 a0001c0002t0001g0049 others(13): Show |
16 | HG01243.hp1 HG01256.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.49+927dupA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr6 | 160703268 | ||||||
| chr6:160703268 | T | TAA | 96 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0023 others(93): Show |
109 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.49+926_49+927dupAA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr6 | 160703268 | ||||||
| chr6:160703268 | T | TAAA | 26 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(23): Show |
27 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.49+925_49+927dupAA others(1): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr6 | 160703268 | ||||||
| chr6:160703282 | C | T | 6 | a0001c0005t0005g0234 a0001c0006t0005g0018 a0001c0006t0005g0232 others(3): Show |
7 | HG02257.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+929C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160703282 | |||||||
| chr6:160703309 | A | G | 6 | a0001c0005t0005g0234 a0001c0006t0005g0018 a0001c0006t0005g0232 others(3): Show |
7 | HG02257.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+956A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160703309 | |||||||
| chr6:160703324 | G | A | 4 | a0001c0006t0005g0018 a0001c0006t0005g0232 a0001c0008t0001g0231 others(1): Show |
5 | HG02572.hp2 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+971G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160703324 | |||||||
| chr6:160703524 | G | A | 1 | a0001c0006t0013g0237 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.49+1171G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160703524 | |||||||
| chr6:160703842 | C | G | 4 | a0001c0002t0009g0239 a0001c0006t0013g0237 a0001c0015t0009g0238 others(1): Show |
4 | HG02717.hp1 HG02922.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+1489C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160703842 | |||||||
| chr6:160703902 | A | G | 4 | a0001c0002t0009g0239 a0001c0006t0013g0237 a0001c0015t0009g0238 others(1): Show |
4 | HG02717.hp1 HG02922.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+1549A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160703902 | |||||||
| chr6:160704168 | C | T | 3 | a0005c0010t0004g0019 a0005c0010t0004g0235 a0005c0010t0004g0236 |
4 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+1815C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704168 | |||||||
| chr6:160704198 | C | T | 1 | a0001c0003t0001g0229 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.49+1845C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704198 | |||||||
| chr6:160704251 | C | A | 1 | a0001c0005t0002g0264 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.49+1898C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704251 | |||||||
| chr6:160704328 | C | T | 1 | a0002c0004t0003g0331 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.49+1975C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704328 | |||||||
| chr6:160704387 | T | C | 85 | a0001c0001t0001g0008 a0001c0001t0001g0241 a0001c0001t0001g0242 others(82): Show |
96 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.50-2020T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704387 | |||||||
| chr6:160704422 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0029 |
3 | HG01255.hp1 HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.50-1985T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704422 | |||||||
| chr6:160704434 | C | T | 1 | a0001c0003t0001g0228 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.50-1973C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704434 | |||||||
| chr6:160704524 | T | C | 6 | a0001c0006t0014g0035 a0001c0013t0009g0033 a0001c0029t0015g0031 others(3): Show |
10 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.50-1883T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704524 | |||||||
| chr6:160704530 | G | C | 1 | a0001c0001t0001g0053 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.50-1877G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704530 | |||||||
| chr6:160704599 | T | C | 30 | a0001c0001t0001g0030 a0001c0001t0001g0054 a0001c0001t0001g0059 others(27): Show |
31 | HG00280.hp2 HG00733.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.50-1808T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704599 | |||||||
| chr6:160704748 | A | G | 1 | a0001c0028t0004g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.50-1659A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704748 | |||||||
| chr6:160704808 | A | G | 3 | a0001c0011t0001g0224 a0001c0011t0001g0225 a0001c0011t0001g0226 |
3 | NA18940.hp1 NA18963.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.50-1599A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704808 | |||||||
| chr6:160704816 | A | T | 3 | a0001c0011t0001g0224 a0001c0011t0001g0225 a0001c0011t0001g0226 |
3 | NA18940.hp1 NA18963.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.50-1591A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704816 | |||||||
| chr6:160704956 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | NA19010.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.50-1451T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160704956 | |||||||
| chr6:160705042 | C | T | 151 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0053 others(148): Show |
165 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.50-1365C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705042 | |||||||
| chr6:160705102 | G | C | 5 | a0001c0001t0001g0054 a0001c0001t0001g0074 a0001c0001t0001g0268 others(2): Show |
5 | HG01934.hp2 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-1305G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705102 | |||||||
| chr6:160705138 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG03710.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.50-1269C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705138 | |||||||
| chr6:160705178 | C | T | 1 | a0001c0006t0002g0300 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.50-1229C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705178 | |||||||
| chr6:160705213 | C | T | 4 | a0001c0003t0001g0221 a0001c0003t0001g0222 a0001c0003t0001g0223 others(1): Show |
4 | NA18945.hp1 NA18988.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-1194C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705213 | |||||||
| chr6:160705229 | A | G | 1 | a0001c0005t0002g0335 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.50-1178A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705229 | |||||||
| chr6:160705239 | T | C | 2 | a0001c0009t0004g0026 a0002c0007t0023g0048 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.50-1168T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705239 | |||||||
| chr6:160705267 | T | C | 4 | a0001c0006t0002g0300 a0001c0011t0001g0230 a0001c0015t0009g0238 others(1): Show |
4 | HG02572.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-1140T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705267 | |||||||
| chr6:160705291 | C | T | 60 | a0001c0001t0001g0052 a0001c0001t0001g0070 a0001c0001t0001g0072 others(57): Show |
61 | HG00408.hp2 HG01192.hp1 HG01256.hp1 others(58): Show |
intron_variant | MODIFIER | c.50-1116C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705291 | |||||||
| chr6:160705434 | C | T | 5 | a0001c0005t0011g0110 a0001c0006t0002g0109 a0001c0013t0001g0025 others(2): Show |
6 | HG02109.hp1 HG02559.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-973C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705434 | |||||||
| chr6:160705456 | C | T | 2 | a0001c0002t0001g0108 a0001c0002t0001g0193 |
2 | HG03041.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.50-951C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705456 | |||||||
| chr6:160705706 | G | A | 1 | a0001c0006t0002g0109 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.50-701G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705706 | |||||||
| chr6:160705709 | T | C | 1 | a0001c0015t0001g0306 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.50-698T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705709 | |||||||
| chr6:160705711 | A | T | 5 | a0001c0015t0009g0238 a0004c0012t0001g0233 a0004c0012t0001g0248 others(2): Show |
5 | HG02257.hp2 HG02965.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-696A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705711 | |||||||
| chr6:160705722 | C | T | 1 | a0001c0009t0004g0026 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.50-685C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705722 | |||||||
| chr6:160705735 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.50-672G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705735 | |||||||
| chr6:160705889 | T | A | 1 | a0001c0001t0001g0009 | 2 | HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.50-518T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705889 | |||||||
| chr6:160705950 | G | A | 1 | a0001c0006t0002g0270 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.50-457G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160705950 | |||||||
| chr6:160706093 | G | A | 23 | a0001c0006t0014g0035 a0001c0029t0015g0031 a0002c0004t0003g0001 others(20): Show |
33 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.50-314G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160706093 | |||||||
| chr6:160706135 | C | CT | 3 | a0001c0003t0001g0107 a0001c0003t0001g0191 a0001c0003t0001g0192 |
3 | HG01106.hp2 HG01891.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.50-271dupT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr6 | 160706135 | ||||||
| chr6:160706203 | T | C | 3 | a0001c0006t0005g0336 a0001c0006t0005g0337 a0001c0006t0005g0342 |
3 | HG01884.hp2 HG02622.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.50-204T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160706203 | |||||||
| chr6:160706234 | C | T | 6 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(3): Show |
6 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-173C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160706234 | |||||||
| chr6:160706268 | T | C | 1 | a0007c0019t0001g0307 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.50-139T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | chr6 | 160706268 | |||||||
| chr6:160706294 | CAG | C | 120 | a0001c0002t0001g0003 a0001c0002t0001g0006 a0001c0002t0001g0011 others(117): Show |
132 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.50-111_50-110delGA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr6 | 160706294 | ||||||
| chr6:160706546 | T | C | 8 | a0001c0002t0001g0077 a0001c0002t0001g0078 a0001c0002t0001g0079 others(5): Show |
8 | NA18954.hp2 NA18980.hp1 NA18991.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.185+4T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | chr6 | 160706546 | |||||||
| chr6:160706567 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.185+25C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | chr6 | 160706567 | |||||||
| chr6:160706643 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
7 | NA18977.hp2 NA18990.hp2 NA18999.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+101T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | chr6 | 160706643 | |||||||
| chr6:160706689 | T | C | 1 | a0001c0002t0001g0080 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.185+147T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | chr6 | 160706689 | |||||||
| chr6:160706951 | T | TA | 29 | a0001c0002t0001g0011 a0001c0002t0001g0116 a0001c0002t0001g0117 others(26): Show |
33 | HG01255.hp2 HG01256.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.185+423dupA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr6 | 160706951 | ||||||
| chr6:160706951 | T | TAA | 37 | a0001c0005t0010g0027 a0001c0005t0010g0298 a0001c0006t0002g0041 others(34): Show |
47 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.185+422_185+423dup others(2): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr6 | 160706951 | ||||||
| chr6:160706951 | T | TAAAAAA | 8 | a0002c0007t0007g0036 a0002c0007t0007g0037 a0002c0007t0007g0038 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+418_185+423dup others(6): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr6 | 160706951 | ||||||
| chr6:160707138 | C | T | 15 | a0001c0001t0001g0004 a0001c0001t0001g0087 a0001c0001t0001g0088 others(12): Show |
17 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.186-562C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | chr6 | 160707138 | |||||||
| chr6:160707209 | G | A | 6 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(3): Show |
6 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.186-491G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | chr6 | 160707209 | |||||||
| chr6:160707232 | A | T | 46 | a0001c0005t0010g0027 a0001c0005t0010g0298 a0001c0006t0014g0035 others(43): Show |
57 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.186-468A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | chr6 | 160707232 | |||||||
| chr6:160707261 | C | A | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | NA19003.hp1 NA19012.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-439C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | chr6 | 160707261 | |||||||
| chr6:160707261 | C | T | 1 | a0001c0002t0001g0206 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.186-439C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | chr6 | 160707261 | |||||||
| chr6:160707499 | G | A | 1 | a0001c0006t0004g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.186-201G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | chr6 | 160707499 | |||||||
| chr6:160707585 | G | A | 124 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0015 others(121): Show |
132 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.186-115G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 2/18 | chr6 | 160707585 | |||||||
| chr6:160707855 | A | G | 7 | a0001c0002t0001g0011 a0001c0002t0001g0071 a0001c0002t0001g0120 others(4): Show |
8 | HG01255.hp2 HG01978.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+49A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160707855 | |||||||
| chr6:160707890 | A | G | 44 | a0001c0006t0014g0035 a0001c0013t0009g0033 a0001c0015t0009g0238 others(41): Show |
55 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.292+84A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160707890 | |||||||
| chr6:160707913 | T | C | 7 | a0001c0002t0001g0011 a0001c0002t0001g0071 a0001c0002t0001g0120 others(4): Show |
8 | HG01255.hp2 HG01978.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+107T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160707913 | |||||||
| chr6:160707915 | G | A | 122 | a0001c0001t0001g0207 a0001c0002t0001g0003 a0001c0002t0001g0006 others(119): Show |
134 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.292+109G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160707915 | |||||||
| chr6:160707935 | G | A | 13 | a0001c0006t0005g0018 a0001c0006t0005g0093 a0001c0006t0005g0094 others(10): Show |
15 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.292+129G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160707935 | |||||||
| chr6:160707954 | T | C | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG00544.hp2 NA18944.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+148T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160707954 | |||||||
| chr6:160707981 | G | A | 57 | a0001c0006t0005g0018 a0001c0006t0005g0093 a0001c0006t0005g0094 others(54): Show |
70 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.292+175G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160707981 | |||||||
| chr6:160708199 | T | TA | 48 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0072 others(45): Show |
49 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.292+393_292+394ins others(1): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708199 | |||||||
| chr6:160708201 | T | G | 48 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0072 others(45): Show |
49 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.292+395T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708201 | |||||||
| chr6:160708202 | A | T | 48 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0072 others(45): Show |
49 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.292+396A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708202 | |||||||
| chr6:160708204 | A | C | 48 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0072 others(45): Show |
49 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.292+398A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708204 | |||||||
| chr6:160708362 | CT | C | 10 | a0002c0004t0011g0296 a0002c0007t0007g0036 a0002c0007t0007g0037 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.292+560delT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr6 | 160708362 | ||||||
| chr6:160708425 | A | T | 1 | a0001c0002t0001g0160 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.292+619A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708425 | |||||||
| chr6:160708593 | A | G | 10 | a0002c0004t0011g0296 a0002c0007t0007g0036 a0002c0007t0007g0037 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.292+787A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708593 | |||||||
| chr6:160708653 | G | T | 10 | a0002c0004t0011g0296 a0002c0007t0007g0036 a0002c0007t0007g0037 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.292+847G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708653 | |||||||
| chr6:160708727 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.292+921G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708727 | |||||||
| chr6:160708969 | T | TA | 32 | a0001c0013t0009g0033 a0001c0015t0009g0238 a0001c0021t0004g0014 others(29): Show |
42 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.292+1163_292+1164i others(3): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708969 | |||||||
| chr6:160708970 | T | A | 53 | a0001c0001t0001g0039 a0001c0001t0001g0054 a0001c0001t0001g0074 others(50): Show |
64 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.292+1164T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708970 | |||||||
| chr6:160708970 | T | TA | 8 | a0001c0002t0001g0124 a0001c0006t0005g0336 a0001c0006t0005g0338 others(5): Show |
8 | HG00597.hp2 HG02572.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+1176dupA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr6 | 160708970 | ||||||
| chr6:160708971 | A | T | 1 | a0001c0003t0001g0313 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.292+1165A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708971 | |||||||
| chr6:160708980 | A | C | 1 | a0001c0001t0001g0070 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.292+1174A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160708980 | |||||||
| chr6:160709135 | G | C | 1 | a0001c0002t0001g0108 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.292+1329G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160709135 | |||||||
| chr6:160709386 | C | A | 1 | a0001c0003t0001g0055 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.292+1580C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160709386 | |||||||
| chr6:160709784 | C | T | 1 | a0002c0007t0023g0048 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.293-1293C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160709784 | |||||||
| chr6:160709898 | T | C | 65 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(62): Show |
78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.293-1179T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160709898 | |||||||
| chr6:160709985 | G | A | 1 | a0002c0022t0003g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.293-1092G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160709985 | |||||||
| chr6:160710260 | C | A | 1 | a0001c0001t0001g0252 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.293-817C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710260 | |||||||
| chr6:160710343 | G | T | 3 | a0001c0021t0004g0014 a0003c0020t0004g0326 a0003c0020t0004g0332 |
4 | HG01256.hp1 HG01258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-734G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710343 | |||||||
| chr6:160710430 | G | A | 6 | a0001c0001t0001g0039 a0001c0001t0001g0054 a0001c0001t0001g0074 others(3): Show |
6 | HG01934.hp2 HG02809.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-647G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710430 | |||||||
| chr6:160710451 | G | T | 10 | a0002c0004t0011g0296 a0002c0007t0007g0036 a0002c0007t0007g0037 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.293-626G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710451 | |||||||
| chr6:160710455 | C | T | 7 | a0001c0002t0001g0050 a0001c0002t0001g0158 a0001c0002t0001g0159 others(4): Show |
7 | HG00597.hp1 HG00609.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.293-622C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710455 | |||||||
| chr6:160710480 | G | C | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | NA19012.hp2 NA19063.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.293-597G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710480 | |||||||
| chr6:160710484 | G | A | 64 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(61): Show |
77 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.293-593G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710484 | |||||||
| chr6:160710512 | G | T | 10 | a0002c0004t0011g0296 a0002c0007t0007g0036 a0002c0007t0007g0037 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.293-565G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710512 | |||||||
| chr6:160710548 | A | G | 6 | a0001c0002t0001g0119 a0001c0002t0001g0157 a0001c0002t0001g0193 others(3): Show |
6 | HG02145.hp2 HG03041.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-529A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710548 | |||||||
| chr6:160710559 | A | G | 1 | a0001c0013t0009g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.293-518A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710559 | |||||||
| chr6:160710649 | G | C | 2 | a0001c0001t0001g0169 a0012c0023t0001g0095 |
2 | NA18966.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.293-428G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710649 | |||||||
| chr6:160710786 | C | T | 65 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(62): Show |
78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.293-291C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710786 | |||||||
| chr6:160710843 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.293-234C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710843 | |||||||
| chr6:160710863 | G | A | 1 | a0001c0003t0001g0255 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.293-214G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710863 | |||||||
| chr6:160710914 | C | T | 3 | a0001c0005t0011g0110 a0001c0008t0001g0218 a0001c0008t0001g0339 |
3 | HG02109.hp1 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.293-163C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160710914 | |||||||
| chr6:160711005 | G | A | 5 | a0002c0007t0007g0036 a0002c0007t0007g0037 a0002c0007t0007g0038 others(2): Show |
5 | HG01243.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-72G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 3/18 | chr6 | 160711005 | |||||||
| chr6:160711357 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.407+166A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160711357 | |||||||
| chr6:160711385 | T | G | 65 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(62): Show |
78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.407+194T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160711385 | |||||||
| chr6:160711391 | G | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0175 a0001c0001t0001g0176 others(1): Show |
5 | HG01192.hp2 NA18969.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.407+200G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160711391 | |||||||
| chr6:160711453 | A | C | 3 | a0001c0006t0004g0046 a0001c0006t0014g0035 a0001c0015t0001g0306 |
3 | HG01891.hp2 HG02970.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.407+262A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160711453 | |||||||
| chr6:160711685 | C | T | 10 | a0002c0004t0011g0296 a0002c0007t0007g0036 a0002c0007t0007g0037 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.407+494C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160711685 | |||||||
| chr6:160711693 | T | C | 65 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(62): Show |
78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.407+502T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160711693 | |||||||
| chr6:160711772 | T | C | 65 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(62): Show |
78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.407+581T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160711772 | |||||||
| chr6:160711798 | G | A | 194 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(191): Show |
216 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.407+607G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160711798 | |||||||
| chr6:160711806 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.407+615C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160711806 | |||||||
| chr6:160712014 | C | T | 65 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(62): Show |
78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.407+823C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712014 | |||||||
| chr6:160712093 | G | C | 65 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(62): Show |
78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.408-893G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712093 | |||||||
| chr6:160712212 | G | A | 65 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(62): Show |
78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.408-774G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712212 | |||||||
| chr6:160712214 | G | C | 1 | a0001c0001t0001g0187 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.408-772G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712214 | |||||||
| chr6:160712303 | T | C | 128 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(125): Show |
137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.408-683T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712303 | |||||||
| chr6:160712311 | T | A | 5 | a0002c0007t0007g0036 a0002c0007t0007g0037 a0002c0007t0007g0038 others(2): Show |
5 | HG01243.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.408-675T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712311 | |||||||
| chr6:160712512 | A | T | 37 | a0001c0006t0005g0018 a0001c0006t0005g0093 a0001c0006t0005g0094 others(34): Show |
49 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.408-474A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712512 | |||||||
| chr6:160712527 | A | G | 28 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(25): Show |
29 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.408-459A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712527 | |||||||
| chr6:160712619 | G | A | 127 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(124): Show |
136 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.408-367G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712619 | |||||||
| chr6:160712653 | A | G | 37 | a0001c0006t0005g0018 a0001c0006t0005g0093 a0001c0006t0005g0094 others(34): Show |
49 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.408-333A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712653 | |||||||
| chr6:160712677 | G | C | 10 | a0002c0004t0011g0296 a0002c0007t0007g0036 a0002c0007t0007g0037 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.408-309G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712677 | |||||||
| chr6:160712906 | G | A | 10 | a0002c0004t0011g0296 a0002c0007t0007g0036 a0002c0007t0007g0037 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.408-80G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 4/18 | chr6 | 160712906 | |||||||
| chr6:160713241 | C | G | 22 | a0001c0029t0015g0031 a0002c0004t0003g0001 a0002c0004t0003g0010 others(19): Show |
32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.547+116C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713241 | |||||||
| chr6:160713255 | AC | A | 13 | a0001c0006t0005g0018 a0001c0006t0005g0093 a0001c0006t0005g0094 others(10): Show |
15 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.547+134delC | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 160713255 | ||||||
| chr6:160713272 | A | ATT | 4 | a0001c0006t0004g0046 a0001c0006t0014g0035 a0001c0013t0009g0033 others(1): Show |
4 | HG01891.hp2 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.547+147_547+148ins others(2): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713272 | |||||||
| chr6:160713273 | A | AT | 22 | a0001c0029t0015g0031 a0002c0004t0003g0001 a0002c0004t0003g0010 others(19): Show |
32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.547+160dupT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 160713273 | ||||||
| chr6:160713273 | A | ATT | 23 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(20): Show |
25 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.547+159_547+160dup others(2): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 160713273 | ||||||
| chr6:160713273 | A | ATTTT | 11 | a0001c0021t0004g0014 a0002c0004t0011g0296 a0002c0007t0007g0036 others(8): Show |
12 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.547+157_547+160dup others(4): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 160713273 | ||||||
| chr6:160713273 | A | T | 4 | a0001c0006t0004g0046 a0001c0006t0014g0035 a0001c0013t0009g0033 others(1): Show |
4 | HG01891.hp2 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.547+148A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713273 | |||||||
| chr6:160713342 | C | T | 1 | a0002c0004t0003g0277 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.547+217C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713342 | |||||||
| chr6:160713389 | C | A | 1 | a0001c0028t0004g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.547+264C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713389 | |||||||
| chr6:160713492 | C | A | 1 | a0001c0006t0004g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.547+367C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713492 | |||||||
| chr6:160713505 | G | A | 1 | a0001c0005t0011g0110 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.547+380G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713505 | |||||||
| chr6:160713535 | C | T | 10 | a0002c0004t0011g0296 a0002c0007t0007g0036 a0002c0007t0007g0037 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.547+410C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713535 | |||||||
| chr6:160713540 | A | C | 4 | a0002c0007t0007g0091 a0002c0007t0007g0092 a0002c0007t0007g0281 others(1): Show |
4 | HG02055.hp2 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.547+415A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713540 | |||||||
| chr6:160713698 | A | G | 1 | a0001c0002t0001g0133 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.547+573A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713698 | |||||||
| chr6:160713700 | A | G | 65 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(62): Show |
78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.547+575A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713700 | |||||||
| chr6:160713773 | T | C | 22 | a0001c0029t0015g0031 a0002c0004t0003g0001 a0002c0004t0003g0010 others(19): Show |
32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.547+648T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713773 | |||||||
| chr6:160713788 | G | T | 1 | a0001c0009t0012g0068 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.547+663G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713788 | |||||||
| chr6:160713879 | A | T | 11 | a0001c0006t0004g0046 a0002c0004t0011g0296 a0002c0007t0007g0036 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.547+754A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713879 | |||||||
| chr6:160713907 | C | T | 1 | a0001c0002t0001g0156 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.547+782C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713907 | |||||||
| chr6:160713908 | G | A | 65 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(62): Show |
78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.547+783G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160713908 | |||||||
| chr6:160714079 | C | T | 128 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(125): Show |
137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.548-715C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714079 | |||||||
| chr6:160714113 | G | A | 1 | a0001c0011t0001g0230 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.548-681G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714113 | |||||||
| chr6:160714170 | C | T | 13 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(10): Show |
13 | HG01099.hp2 HG01106.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.548-624C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714170 | |||||||
| chr6:160714258 | C | T | 2 | a0001c0002t0001g0280 a0001c0002t0001g0301 |
2 | NA18979.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.548-536C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714258 | |||||||
| chr6:160714281 | G | A | 30 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(27): Show |
32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.548-513G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714281 | |||||||
| chr6:160714445 | C | T | 6 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(3): Show |
6 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.548-349C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714445 | |||||||
| chr6:160714474 | G | GA | 33 | a0001c0029t0015g0031 a0002c0004t0003g0001 a0002c0004t0003g0010 others(30): Show |
43 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.548-320_548-319ins others(1): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714474 | |||||||
| chr6:160714535 | G | C | 1 | a0001c0028t0004g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.548-259G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714535 | |||||||
| chr6:160714635 | CTTATTGC others(5): Show |
C | 22 | a0001c0029t0015g0031 a0002c0004t0003g0001 a0002c0004t0003g0010 others(19): Show |
32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.548-148_548-137del others(12): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 160714635 | ||||||
| chr6:160714659 | T | A | 1 | a0001c0021t0004g0014 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.548-135T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714659 | |||||||
| chr6:160714660 | G | A | 1 | a0001c0021t0004g0014 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.548-134G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714660 | |||||||
| chr6:160714676 | A | G | 10 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(7): Show |
10 | HG01891.hp2 HG02451.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.548-118A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714676 | |||||||
| chr6:160714722 | T | C | 2 | a0001c0006t0014g0035 a0001c0013t0009g0033 |
2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.548-72T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 5/18 | chr6 | 160714722 | |||||||
| chr6:160715026 | T | A | 129 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(126): Show |
138 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.668+112T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160715026 | |||||||
| chr6:160715262 | G | A | 161 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(158): Show |
180 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.668+348G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160715262 | |||||||
| chr6:160715453 | G | A | 162 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(159): Show |
181 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.668+539G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160715453 | |||||||
| chr6:160715485 | G | A | 1 | a0001c0002t0001g0120 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.668+571G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160715485 | |||||||
| chr6:160715549 | G | A | 6 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(3): Show |
6 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.668+635G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160715549 | |||||||
| chr6:160715731 | A | C | 2 | a0003c0020t0004g0326 a0003c0020t0004g0332 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.668+817A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160715731 | |||||||
| chr6:160715746 | C | T | 1 | a0001c0002t0001g0155 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.668+832C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160715746 | |||||||
| chr6:160715821 | G | A | 1 | a0002c0004t0011g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.669-824G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160715821 | |||||||
| chr6:160715864 | G | A | 1 | a0001c0003t0001g0255 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.669-781G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160715864 | |||||||
| chr6:160716123 | T | C | 1 | a0002c0004t0003g0331 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.669-522T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160716123 | |||||||
| chr6:160716131 | C | G | 1 | a0001c0002t0001g0154 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.669-514C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160716131 | |||||||
| chr6:160716226 | A | G | 30 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(27): Show |
32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.669-419A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160716226 | |||||||
| chr6:160716341 | T | C | 1 | a0001c0028t0004g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.669-304T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160716341 | |||||||
| chr6:160716481 | C | T | 1 | a0001c0001t0001g0009 | 2 | HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.669-164C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160716481 | |||||||
| chr6:160716486 | T | C | 22 | a0001c0029t0015g0031 a0002c0004t0003g0001 a0002c0004t0003g0010 others(19): Show |
32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.669-159T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160716486 | |||||||
| chr6:160716491 | T | A | 194 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(191): Show |
215 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.669-154T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160716491 | |||||||
| chr6:160716631 | T | G | 33 | a0001c0029t0015g0031 a0002c0004t0003g0001 a0002c0004t0003g0010 others(30): Show |
43 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.669-14T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 6/18 | chr6 | 160716631 | |||||||
| chr6:160716958 | G | A | 139 | a0001c0002t0001g0003 a0001c0002t0001g0006 a0001c0002t0001g0011 others(136): Show |
161 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.787+195G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160716958 | |||||||
| chr6:160716990 | T | G | 1 | a0001c0001t0001g0169 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.787+227T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160716990 | |||||||
| chr6:160717149 | G | C | 127 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(124): Show |
136 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.787+386G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160717149 | |||||||
| chr6:160717321 | G | T | 1 | a0001c0021t0004g0014 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.787+558G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160717321 | |||||||
| chr6:160717438 | C | T | 1 | a0002c0007t0023g0048 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.787+675C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160717438 | |||||||
| chr6:160717462 | CT | C | 158 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(155): Show |
169 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.787+708delT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr6 | 160717462 | ||||||
| chr6:160717570 | T | A | 1 | a0001c0002t0009g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.788-724T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160717570 | |||||||
| chr6:160717724 | A | G | 1 | a0001c0005t0002g0106 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.788-570A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160717724 | |||||||
| chr6:160717816 | C | G | 117 | a0001c0002t0001g0003 a0001c0002t0001g0006 a0001c0002t0001g0011 others(114): Show |
129 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.788-478C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160717816 | |||||||
| chr6:160717885 | A | G | 196 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(193): Show |
217 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.788-409A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160717885 | |||||||
| chr6:160717963 | A | G | 1 | a0002c0007t0023g0048 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.788-331A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160717963 | |||||||
| chr6:160717989 | C | T | 4 | a0001c0002t0001g0117 a0001c0002t0001g0118 a0001c0002t0001g0201 others(1): Show |
4 | HG02040.hp1 HG02300.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.788-305C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160717989 | |||||||
| chr6:160718026 | C | T | 161 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(158): Show |
172 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.788-268C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160718026 | |||||||
| chr6:160718055 | A | G | 1 | a0001c0002t0001g0153 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.788-239A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160718055 | |||||||
| chr6:160718089 | A | C | 1 | a0001c0002t0009g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.788-205A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160718089 | |||||||
| chr6:160718118 | G | A | 1 | a0001c0015t0001g0306 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.788-176G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160718118 | |||||||
| chr6:160718246 | G | A | 10 | a0002c0004t0011g0296 a0002c0007t0007g0036 a0002c0007t0007g0037 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.788-48G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | chr6 | 160718246 | |||||||
| chr6:160718255 | A | AAT | 5 | a0001c0015t0009g0238 a0004c0012t0001g0233 a0004c0012t0001g0248 others(2): Show |
5 | HG02257.hp2 HG02965.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.788-30_788-29dupAT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr6 | 160718255 | ||||||
| chr6:160718470 | G | A | 131 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(128): Show |
140 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.950+14G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 8/18 | chr6 | 160718470 | |||||||
| chr6:160719104 | G | A | 1 | a0001c0021t0004g0014 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1096+266G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160719104 | |||||||
| chr6:160719136 | C | G | 6 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(3): Show |
6 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1096+298C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160719136 | |||||||
| chr6:160719265 | T | C | 1 | a0001c0015t0001g0306 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1096+427T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160719265 | |||||||
| chr6:160719866 | AT | A | 5 | a0001c0015t0009g0238 a0004c0012t0001g0233 a0004c0012t0001g0248 others(2): Show |
5 | HG02257.hp2 HG02965.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1096+1033delT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 160719866 | ||||||
| chr6:160719873 | C | G | 5 | a0001c0015t0009g0238 a0004c0012t0001g0233 a0004c0012t0001g0248 others(2): Show |
5 | HG02257.hp2 HG02965.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1096+1035C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160719873 | |||||||
| chr6:160720126 | T | C | 136 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(133): Show |
145 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1096+1288T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160720126 | |||||||
| chr6:160720152 | C | T | 200 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(197): Show |
222 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.1096+1314C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160720152 | |||||||
| chr6:160720292 | C | T | 3 | a0001c0013t0001g0025 a0001c0013t0001g0341 a0001c0015t0001g0340 |
4 | HG02559.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+1454C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160720292 | |||||||
| chr6:160720298 | G | A | 1 | a0001c0002t0001g0126 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1096+1460G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160720298 | |||||||
| chr6:160720395 | TTTTTC | T | 4 | a0001c0015t0009g0238 a0004c0012t0001g0233 a0004c0012t0001g0248 others(1): Show |
4 | HG02257.hp2 HG02965.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096+1572_1096+157 others(9): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 160720395 | ||||||
| chr6:160720410 | C | CT | 115 | a0001c0002t0001g0003 a0001c0002t0001g0006 a0001c0002t0001g0012 others(112): Show |
126 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.1096+1599dupT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 160720410 | ||||||
| chr6:160720410 | C | CTT | 49 | a0001c0002t0001g0011 a0001c0002t0001g0071 a0001c0002t0001g0120 others(46): Show |
59 | HG00323.hp1 HG00597.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1096+1598_1096+159 others(6): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 160720410 | ||||||
| chr6:160720410 | C | CTTT | 11 | a0001c0002t0001g0082 a0001c0006t0005g0336 a0001c0006t0005g0338 others(8): Show |
12 | HG01109.hp2 HG01169.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1096+1597_1096+159 others(7): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 160720410 | ||||||
| chr6:160720410 | CTTTTTT | C | 56 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0053 others(53): Show |
58 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.1096+1594_1096+159 others(10): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 160720410 | ||||||
| chr6:160720410 | CTTTTTTT | C | 75 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
81 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1096+1593_1096+159 others(11): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 160720410 | ||||||
| chr6:160720488 | C | T | 1 | a0001c0028t0004g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1096+1650C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160720488 | |||||||
| chr6:160720568 | T | C | 3 | a0001c0013t0001g0025 a0001c0013t0001g0341 a0001c0015t0001g0340 |
4 | HG02559.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+1730T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160720568 | |||||||
| chr6:160720649 | A | G | 1 | a0001c0028t0004g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1097-1759A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160720649 | |||||||
| chr6:160720779 | T | C | 1 | a0001c0002t0001g0127 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1097-1629T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160720779 | |||||||
| chr6:160720970 | A | G | 13 | a0001c0006t0005g0018 a0001c0006t0005g0093 a0001c0006t0005g0094 others(10): Show |
15 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.1097-1438A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160720970 | |||||||
| chr6:160721094 | A | C | 13 | a0001c0006t0005g0018 a0001c0006t0005g0093 a0001c0006t0005g0094 others(10): Show |
15 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.1097-1314A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160721094 | |||||||
| chr6:160721792 | C | A | 1 | a0001c0006t0014g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1097-616C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160721792 | |||||||
| chr6:160721803 | T | A | 1 | a0001c0003t0001g0128 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1097-605T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160721803 | |||||||
| chr6:160721957 | C | G | 1 | a0001c0027t0010g0115 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1097-451C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160721957 | |||||||
| chr6:160721996 | T | C | 1 | a0001c0006t0014g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1097-412T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160721996 | |||||||
| chr6:160722112 | G | A | 1 | a0001c0005t0002g0264 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1097-296G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160722112 | |||||||
| chr6:160722158 | T | C | 65 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(62): Show |
77 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1097-250T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160722158 | |||||||
| chr6:160722167 | A | G | 2 | a0002c0004t0008g0002 a0002c0004t0008g0032 |
6 | HG02145.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1097-241A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160722167 | |||||||
| chr6:160722201 | A | C | 30 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(27): Show |
32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1097-207A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160722201 | |||||||
| chr6:160722326 | C | T | 1 | a0001c0005t0002g0105 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1097-82C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160722326 | |||||||
| chr6:160722344 | A | G | 22 | a0002c0004t0003g0001 a0002c0004t0003g0010 a0002c0004t0003g0021 others(19): Show |
32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1097-64A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 9/18 | chr6 | 160722344 | |||||||
| chr6:160722576 | T | C | 33 | a0002c0004t0003g0001 a0002c0004t0003g0010 a0002c0004t0003g0021 others(30): Show |
43 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1256+9T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160722576 | |||||||
| chr6:160722602 | A | G | 30 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(27): Show |
32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1256+35A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160722602 | |||||||
| chr6:160722808 | G | T | 1 | a0001c0006t0004g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1256+241G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160722808 | |||||||
| chr6:160722919 | T | G | 1 | a0001c0002t0001g0081 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1256+352T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160722919 | |||||||
| chr6:160722998 | T | A | 1 | a0001c0001t0001g0314 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1256+431T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160722998 | |||||||
| chr6:160723090 | A | AGTGTGTA others(19): Show |
7 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(4): Show |
7 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1256+560_1256+585d others(28): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 160723090 | ||||||
| chr6:160723090 | A | AGTGTGTA others(45): Show |
4 | a0004c0012t0001g0233 a0004c0012t0001g0248 a0004c0012t0009g0034 others(1): Show |
4 | HG02257.hp2 HG02965.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1256+534_1256+585d others(54): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 160723090 | ||||||
| chr6:160723097 | A | ATATATAT others(45): Show |
1 | a0001c0006t0014g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1256+581_1256+582i others(54): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 160723097 | ||||||
| chr6:160723143 | G | A | 1 | a0001c0001t0001g0314 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1256+576G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723143 | |||||||
| chr6:160723176 | G | GTA | 18 | a0001c0006t0005g0018 a0001c0006t0005g0093 a0001c0006t0005g0094 others(15): Show |
20 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.1256+621_1256+622d others(4): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 160723176 | ||||||
| chr6:160723242 | T | A | 1 | a0001c0001t0001g0008 | 3 | HG00741.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1256+675T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723242 | |||||||
| chr6:160723304 | A | G | 30 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(27): Show |
32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1256+737A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723304 | |||||||
| chr6:160723329 | A | T | 7 | a0001c0002t0001g0050 a0001c0002t0001g0158 a0001c0002t0001g0159 others(4): Show |
7 | HG00597.hp1 HG00609.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.1256+762A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723329 | |||||||
| chr6:160723519 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1256+952C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723519 | |||||||
| chr6:160723538 | A | C | 1 | a0001c0008t0001g0304 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1256+971A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723538 | |||||||
| chr6:160723697 | G | A | 30 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(27): Show |
32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1256+1130G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723697 | |||||||
| chr6:160723747 | T | C | 30 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(27): Show |
32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1256+1180T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723747 | |||||||
| chr6:160723768 | A | G | 22 | a0002c0004t0003g0001 a0002c0004t0003g0010 a0002c0004t0003g0021 others(19): Show |
32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1256+1201A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723768 | |||||||
| chr6:160723835 | C | T | 1 | a0002c0004t0011g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1256+1268C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723835 | |||||||
| chr6:160723906 | A | G | 1 | a0001c0006t0014g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1256+1339A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723906 | |||||||
| chr6:160723916 | C | T | 30 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(27): Show |
32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1256+1349C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160723916 | |||||||
| chr6:160724055 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1256+1488C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160724055 | |||||||
| chr6:160724118 | C | G | 1 | a0001c0009t0004g0026 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1256+1551C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160724118 | |||||||
| chr6:160724144 | A | T | 63 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(60): Show |
75 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1256+1577A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160724144 | |||||||
| chr6:160724202 | T | C | 55 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0072 others(52): Show |
56 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.1256+1635T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160724202 | |||||||
| chr6:160724214 | A | C | 28 | a0001c0001t0001g0015 a0001c0001t0001g0098 a0001c0001t0001g0175 others(25): Show |
30 | HG00558.hp1 HG01192.hp2 HG02132.hp1 others(27): Show |
intron_variant | MODIFIER | c.1256+1647A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160724214 | |||||||
| chr6:160724265 | A | G | 30 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(27): Show |
32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1256+1698A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160724265 | |||||||
| chr6:160724341 | C | T | 1 | a0001c0028t0004g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1256+1774C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160724341 | |||||||
| chr6:160724361 | A | G | 1 | a0001c0002t0001g0201 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1256+1794A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160724361 | |||||||
| chr6:160724471 | T | C | 2 | a0003c0020t0004g0326 a0003c0020t0004g0332 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1256+1904T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160724471 | |||||||
| chr6:160725009 | G | A | 1 | a0001c0009t0012g0068 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1256+2442G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160725009 | |||||||
| chr6:160725186 | A | G | 201 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(198): Show |
223 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1256+2619A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160725186 | |||||||
| chr6:160725602 | A | G | 30 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(27): Show |
32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1256+3035A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160725602 | |||||||
| chr6:160725672 | A | G | 63 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(60): Show |
75 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1256+3105A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160725672 | |||||||
| chr6:160725739 | A | G | 1 | a0001c0001t0022g0299 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1256+3172A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160725739 | |||||||
| chr6:160725743 | A | G | 1 | a0003c0018t0002g0263 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1256+3176A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160725743 | |||||||
| chr6:160725771 | A | G | 30 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(27): Show |
32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1256+3204A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160725771 | |||||||
| chr6:160725852 | GA | G | 15 | a0001c0006t0005g0018 a0001c0006t0005g0093 a0001c0006t0005g0094 others(12): Show |
17 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.1256+3290delA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 160725852 | ||||||
| chr6:160726023 | G | A | 1 | a0001c0002t0001g0129 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1256+3456G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726023 | |||||||
| chr6:160726070 | A | C | 15 | a0001c0006t0005g0018 a0001c0006t0005g0093 a0001c0006t0005g0094 others(12): Show |
17 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.1256+3503A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726070 | |||||||
| chr6:160726336 | A | T | 22 | a0002c0004t0003g0001 a0002c0004t0003g0010 a0002c0004t0003g0021 others(19): Show |
32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1256+3769A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726336 | |||||||
| chr6:160726348 | T | C | 1 | a0001c0001t0001g0316 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1256+3781T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726348 | |||||||
| chr6:160726364 | G | A | 1 | a0001c0001t0001g0302 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1256+3797G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726364 | |||||||
| chr6:160726378 | T | G | 1 | a0001c0001t0001g0170 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1256+3811T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726378 | |||||||
| chr6:160726408 | G | C | 30 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(27): Show |
32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1256+3841G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726408 | |||||||
| chr6:160726413 | T | C | 1 | a0001c0006t0014g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1256+3846T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726413 | |||||||
| chr6:160726587 | T | TA | 28 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(25): Show |
30 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.1256+4020_1256+402 others(5): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726587 | |||||||
| chr6:160726588 | T | A | 31 | a0001c0003t0001g0125 a0001c0006t0002g0041 a0001c0006t0002g0042 others(28): Show |
33 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.1256+4021T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726588 | |||||||
| chr6:160726588 | T | TA | 142 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(139): Show |
151 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.1256+4031dupA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 160726588 | ||||||
| chr6:160726589 | A | T | 1 | a0002c0004t0011g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1256+4022A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726589 | |||||||
| chr6:160726687 | C | G | 1 | a0001c0002t0001g0297 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1256+4120C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726687 | |||||||
| chr6:160726861 | T | C | 1 | a0001c0001t0001g0171 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1257-4190T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726861 | |||||||
| chr6:160726939 | A | G | 7 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(4): Show |
7 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1257-4112A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160726939 | |||||||
| chr6:160727064 | C | T | 4 | a0004c0012t0001g0233 a0004c0012t0001g0248 a0004c0012t0009g0034 others(1): Show |
4 | HG02257.hp2 HG02965.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1257-3987C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727064 | |||||||
| chr6:160727065 | G | A | 1 | a0002c0004t0011g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1257-3986G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727065 | |||||||
| chr6:160727115 | T | C | 30 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(27): Show |
32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1257-3936T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727115 | |||||||
| chr6:160727156 | G | A | 4 | a0001c0006t0014g0035 a0005c0010t0004g0019 a0005c0010t0004g0235 others(1): Show |
5 | HG01891.hp2 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1257-3895G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727156 | |||||||
| chr6:160727189 | T | A | 1 | a0001c0005t0002g0246 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1257-3862T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727189 | |||||||
| chr6:160727333 | G | A | 1 | a0001c0002t0001g0130 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1257-3718G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727333 | |||||||
| chr6:160727367 | G | T | 198 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(195): Show |
220 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1257-3684G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727367 | |||||||
| chr6:160727376 | T | TA | 30 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(27): Show |
32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1257-3667dupA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 160727376 | ||||||
| chr6:160727464 | A | C | 35 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(32): Show |
37 | HG01243.hp1 HG01256.hp1 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.1257-3587A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727464 | |||||||
| chr6:160727692 | C | T | 1 | a0001c0027t0010g0115 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1257-3359C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727692 | |||||||
| chr6:160727730 | T | C | 30 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(27): Show |
32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1257-3321T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727730 | |||||||
| chr6:160727905 | T | G | 2 | a0002c0004t0003g0331 a0002c0022t0003g0261 |
2 | HG01109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1257-3146T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160727905 | |||||||
| chr6:160728103 | A | T | 1 | a0001c0002t0001g0297 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1257-2948A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160728103 | |||||||
| chr6:160728290 | G | T | 5 | a0001c0005t0002g0243 a0001c0005t0002g0244 a0001c0005t0002g0294 others(2): Show |
5 | HG00323.hp2 HG00642.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1257-2761G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160728290 | |||||||
| chr6:160728292 | A | G | 34 | a0001c0003t0001g0007 a0001c0003t0001g0047 a0001c0003t0001g0055 others(31): Show |
36 | HG00558.hp2 HG00639.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.1257-2759A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160728292 | |||||||
| chr6:160728328 | T | C | 1 | a0001c0001t0001g0252 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1257-2723T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160728328 | |||||||
| chr6:160728335 | T | TAAGAGTC others(103): Show |
15 | a0001c0006t0005g0018 a0001c0006t0005g0093 a0001c0006t0005g0094 others(12): Show |
17 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.1257-2662_1257-266 others(114): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 160728335 | ||||||
| chr6:160728335 | T | TAAGAGTC others(103): Show |
298 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(295): Show |
331 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(328): Show |
intron_variant | MODIFIER | c.1257-2662_1257-266 others(114): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 160728335 | ||||||
| chr6:160728560 | C | T | 7 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(4): Show |
7 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1257-2491C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160728560 | |||||||
| chr6:160728657 | T | C | 1 | a0001c0009t0004g0026 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1257-2394T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160728657 | |||||||
| chr6:160728683 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1257-2368G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160728683 | |||||||
| chr6:160728886 | A | G | 30 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(27): Show |
32 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1257-2165A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160728886 | |||||||
| chr6:160729038 | G | T | 1 | a0001c0001t0001g0061 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1257-2013G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160729038 | |||||||
| chr6:160729145 | G | GA | 22 | a0002c0004t0003g0001 a0002c0004t0003g0010 a0002c0004t0003g0021 others(19): Show |
32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1257-1900dupA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 160729145 | ||||||
| chr6:160729219 | G | T | 33 | a0002c0004t0003g0001 a0002c0004t0003g0010 a0002c0004t0003g0021 others(30): Show |
43 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1257-1832G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160729219 | |||||||
| chr6:160729291 | G | A | 5 | a0002c0007t0007g0036 a0002c0007t0007g0037 a0002c0007t0007g0038 others(2): Show |
5 | HG01243.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1257-1760G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160729291 | |||||||
| chr6:160729296 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1257-1755C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160729296 | |||||||
| chr6:160729500 | T | C | 9 | a0002c0007t0007g0036 a0002c0007t0007g0037 a0002c0007t0007g0038 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1257-1551T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160729500 | |||||||
| chr6:160729518 | T | C | 1 | a0001c0006t0005g0093 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1257-1533T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160729518 | |||||||
| chr6:160729958 | A | G | 1 | a0001c0028t0004g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1257-1093A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160729958 | |||||||
| chr6:160730116 | A | G | 1 | a0001c0021t0004g0014 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1257-935A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160730116 | |||||||
| chr6:160730133 | G | T | 1 | a0001c0002t0001g0157 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1257-918G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160730133 | |||||||
| chr6:160730168 | G | A | 1 | a0001c0002t0001g0082 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1257-883G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160730168 | |||||||
| chr6:160730188 | T | C | 1 | a0005c0010t0004g0235 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1257-863T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160730188 | |||||||
| chr6:160730216 | G | A | 1 | a0001c0003t0001g0260 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1257-835G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160730216 | |||||||
| chr6:160730424 | C | T | 15 | a0001c0006t0005g0018 a0001c0006t0005g0093 a0001c0006t0005g0094 others(12): Show |
17 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.1257-627C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160730424 | |||||||
| chr6:160730679 | C | A | 1 | a0001c0009t0004g0044 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1257-372C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160730679 | |||||||
| chr6:160730936 | T | C | 6 | a0001c0006t0004g0046 a0001c0015t0001g0306 a0004c0012t0001g0233 others(3): Show |
6 | HG02257.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1257-115T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160730936 | |||||||
| chr6:160730989 | G | T | 4 | a0002c0007t0007g0091 a0002c0007t0007g0092 a0002c0007t0007g0281 others(1): Show |
4 | HG02055.hp2 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1257-62G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 10/18 | chr6 | 160730989 | |||||||
| chr6:160731262 | A | G | 23 | a0002c0004t0003g0001 a0002c0004t0003g0010 a0002c0004t0003g0021 others(20): Show |
33 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1438+30A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 11/18 | chr6 | 160731262 | |||||||
| chr6:160731325 | C | T | 1 | a0001c0003t0001g0047 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1438+93C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 11/18 | chr6 | 160731325 | |||||||
| chr6:160731360 | G | A | 1 | a0001c0021t0004g0014 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1438+128G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 11/18 | chr6 | 160731360 | |||||||
| chr6:160731416 | C | T | 4 | a0004c0012t0001g0233 a0004c0012t0001g0248 a0004c0012t0009g0034 others(1): Show |
4 | HG02257.hp2 HG02965.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1438+184C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 11/18 | chr6 | 160731416 | |||||||
| chr6:160731417 | G | A | 289 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(286): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.1438+185G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 11/18 | chr6 | 160731417 | |||||||
| chr6:160731491 | A | G | 1 | a0002c0004t0011g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1439-254A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 11/18 | chr6 | 160731491 | |||||||
| chr6:160732048 | A | C | 23 | a0002c0004t0003g0001 a0002c0004t0003g0010 a0002c0004t0003g0021 others(20): Show |
33 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1587+155A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160732048 | |||||||
| chr6:160732151 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1587+258C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160732151 | |||||||
| chr6:160732168 | T | C | 1 | a0002c0007t0023g0048 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1587+275T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160732168 | |||||||
| chr6:160732256 | GA | G | 15 | a0001c0006t0005g0018 a0001c0006t0005g0093 a0001c0006t0005g0094 others(12): Show |
17 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.1587+369delA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 160732256 | ||||||
| chr6:160732325 | T | G | 3 | a0005c0010t0004g0019 a0005c0010t0004g0235 a0005c0010t0004g0236 |
4 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1587+432T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160732325 | |||||||
| chr6:160732495 | T | C | 23 | a0002c0004t0003g0001 a0002c0004t0003g0010 a0002c0004t0003g0021 others(20): Show |
33 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1587+602T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160732495 | |||||||
| chr6:160732529 | T | C | 23 | a0002c0004t0003g0001 a0002c0004t0003g0010 a0002c0004t0003g0021 others(20): Show |
33 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1587+636T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160732529 | |||||||
| chr6:160732626 | G | A | 1 | a0002c0007t0023g0048 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1587+733G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160732626 | |||||||
| chr6:160732663 | G | C | 17 | a0001c0006t0005g0018 a0001c0006t0005g0093 a0001c0006t0005g0094 others(14): Show |
19 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1587+770G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160732663 | |||||||
| chr6:160732690 | C | A | 6 | a0001c0008t0001g0231 a0001c0008t0001g0290 a0001c0008t0001g0291 others(3): Show |
6 | HG02572.hp1 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1587+797C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160732690 | |||||||
| chr6:160732958 | G | A | 108 | a0001c0002t0001g0003 a0001c0002t0001g0006 a0001c0002t0001g0011 others(105): Show |
120 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.1588-1037G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160732958 | |||||||
| chr6:160733075 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1588-920G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733075 | |||||||
| chr6:160733200 | G | T | 22 | a0002c0004t0003g0001 a0002c0004t0003g0010 a0002c0004t0003g0021 others(19): Show |
32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1588-795G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733200 | |||||||
| chr6:160733205 | G | A | 1 | a0001c0021t0004g0014 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1588-790G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733205 | |||||||
| chr6:160733385 | G | C | 1 | a0001c0003t0001g0055 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1588-610G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733385 | |||||||
| chr6:160733401 | G | C | 1 | a0002c0007t0007g0036 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1588-594G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733401 | |||||||
| chr6:160733418 | G | A | 1 | a0001c0003t0001g0125 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1588-577G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733418 | |||||||
| chr6:160733492 | C | T | 11 | a0001c0028t0004g0227 a0002c0004t0011g0296 a0002c0007t0007g0036 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1588-503C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733492 | |||||||
| chr6:160733493 | G | A | 1 | a0001c0005t0011g0110 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1588-502G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733493 | |||||||
| chr6:160733543 | T | TAGAA | 70 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(67): Show |
84 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.1588-449_1588-446d others(6): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 160733543 | ||||||
| chr6:160733684 | AG | A | 3 | a0001c0009t0004g0044 a0003c0020t0004g0326 a0003c0020t0004g0332 |
3 | HG01256.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1588-310delG | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733684 | |||||||
| chr6:160733685 | G | C | 65 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(62): Show |
78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.1588-310G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733685 | |||||||
| chr6:160733686 | A | C | 3 | a0001c0009t0004g0044 a0003c0020t0004g0326 a0003c0020t0004g0332 |
3 | HG01256.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1588-309A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733686 | |||||||
| chr6:160733705 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1588-290G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733705 | |||||||
| chr6:160733708 | G | C | 1 | a0001c0011t0001g0230 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1588-287G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733708 | |||||||
| chr6:160733831 | C | G | 1 | a0002c0004t0011g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1588-164C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733831 | |||||||
| chr6:160733844 | C | CAA | 4 | a0002c0004t0003g0076 a0002c0004t0003g0275 a0002c0004t0003g0276 others(1): Show |
4 | HG00323.hp1 HG01069.hp2 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1588-150_1588-149i others(4): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 160733844 | ||||||
| chr6:160733844 | C | CAAA | 17 | a0002c0004t0003g0001 a0002c0004t0003g0010 a0002c0004t0003g0021 others(14): Show |
27 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.1588-150_1588-149i others(5): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 160733844 | ||||||
| chr6:160733844 | C | CAAAA | 3 | a0002c0004t0003g0271 a0002c0004t0008g0032 a0002c0004t0011g0296 |
3 | HG02145.hp1 HG02698.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1588-150_1588-149i others(6): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 160733844 | ||||||
| chr6:160733846 | G | A | 24 | a0002c0004t0003g0001 a0002c0004t0003g0010 a0002c0004t0003g0021 others(21): Show |
34 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1588-149G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733846 | |||||||
| chr6:160733846 | G | GA | 8 | a0001c0002t0001g0071 a0001c0002t0001g0343 a0001c0002t0009g0239 others(5): Show |
8 | HG02027.hp1 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1588-127dupA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 160733846 | ||||||
| chr6:160733846 | GA | G | 10 | a0001c0008t0001g0231 a0001c0008t0001g0290 a0001c0008t0001g0291 others(7): Show |
10 | HG01074.hp1 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1588-127delA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 160733846 | ||||||
| chr6:160733846 | GAAA | G | 26 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(23): Show |
28 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1588-129_1588-127d others(5): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 160733846 | ||||||
| chr6:160733846 | GAAAA | G | 11 | a0001c0006t0005g0232 a0001c0006t0005g0336 a0001c0006t0005g0338 others(8): Show |
13 | HG01891.hp2 HG02280.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.1588-130_1588-127d others(6): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 160733846 | ||||||
| chr6:160733846 | GAAAAAA | G | 127 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(124): Show |
136 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1588-132_1588-127d others(8): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr6 | 160733846 | ||||||
| chr6:160733869 | G | A | 9 | a0002c0007t0007g0036 a0002c0007t0007g0037 a0002c0007t0007g0038 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1588-126G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733869 | |||||||
| chr6:160733923 | C | T | 38 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(35): Show |
42 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.1588-72C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733923 | |||||||
| chr6:160733992 | C | T | 1 | a0001c0001t0001g0323 | 1 | NA18977.hp1 | splice_region_variant&intron_variant | LOW | c.1588-3C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 12/18 | chr6 | 160733992 | |||||||
| chr6:160734143 | A | C | 1 | a0001c0006t0014g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1681+55A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734143 | |||||||
| chr6:160734216 | T | A | 1 | a0001c0001t0001g0208 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1681+128T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734216 | |||||||
| chr6:160734232 | T | C | 1 | a0008c0016t0001g0020 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1681+144T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734232 | |||||||
| chr6:160734242 | C | G | 1 | a0001c0003t0001g0313 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1681+154C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734242 | |||||||
| chr6:160734455 | G | A | 1 | a0001c0002t0001g0131 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1681+367G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734455 | |||||||
| chr6:160734496 | G | A | 1 | a0001c0003t0001g0311 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1681+408G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734496 | |||||||
| chr6:160734540 | G | A | 1 | a0001c0006t0014g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1681+452G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734540 | |||||||
| chr6:160734717 | T | C | 1 | a0001c0001t0001g0286 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1681+629T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734717 | |||||||
| chr6:160734745 | GA | G | 36 | a0001c0001t0001g0065 a0001c0001t0001g0164 a0001c0001t0001g0179 others(33): Show |
43 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1681+676delA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 160734745 | ||||||
| chr6:160734745 | GAA | G | 32 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(29): Show |
39 | HG01069.hp2 HG01256.hp1 HG01258.hp1 others(36): Show |
intron_variant | MODIFIER | c.1681+675_1681+676d others(4): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 160734745 | ||||||
| chr6:160734745 | GAAAAAAA | G | 13 | a0001c0001t0001g0015 a0001c0001t0001g0066 a0001c0001t0001g0070 others(10): Show |
14 | HG00558.hp1 HG01192.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.1681+670_1681+676d others(9): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 160734745 | ||||||
| chr6:160734759 | A | G | 112 | a0001c0002t0001g0003 a0001c0002t0001g0006 a0001c0002t0001g0011 others(109): Show |
124 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.1681+671A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734759 | |||||||
| chr6:160734761 | A | G | 5 | a0001c0001t0001g0052 a0001c0001t0001g0097 a0001c0001t0001g0215 others(2): Show |
5 | HG02015.hp2 NA18955.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1681+673A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734761 | |||||||
| chr6:160734790 | C | T | 6 | a0001c0001t0007g0288 a0002c0007t0007g0036 a0002c0007t0007g0037 others(3): Show |
6 | HG01243.hp1 HG02486.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1681+702C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734790 | |||||||
| chr6:160734994 | T | A | 1 | a0001c0028t0004g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1681+906T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160734994 | |||||||
| chr6:160735008 | C | CTGCCCAG others(8): Show |
18 | a0001c0006t0005g0018 a0001c0006t0005g0093 a0001c0006t0005g0094 others(15): Show |
20 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1681+922_1681+936d others(17): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 160735008 | ||||||
| chr6:160735199 | G | A | 7 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(4): Show |
7 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1681+1111G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160735199 | |||||||
| chr6:160735264 | C | T | 22 | a0002c0004t0003g0001 a0002c0004t0003g0010 a0002c0004t0003g0021 others(19): Show |
32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1681+1176C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160735264 | |||||||
| chr6:160735435 | G | C | 3 | a0001c0009t0004g0044 a0003c0020t0004g0326 a0003c0020t0004g0332 |
3 | HG01256.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1681+1347G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160735435 | |||||||
| chr6:160735635 | G | A | 23 | a0001c0001t0001g0097 a0002c0004t0003g0001 a0002c0004t0003g0010 others(20): Show |
33 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1682-1252G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160735635 | |||||||
| chr6:160735784 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1682-1103T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160735784 | |||||||
| chr6:160735897 | T | A | 202 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(199): Show |
225 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.1682-990T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160735897 | |||||||
| chr6:160736114 | G | A | 1 | a0001c0002t0001g0155 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1682-773G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160736114 | |||||||
| chr6:160736138 | C | T | 3 | a0005c0010t0004g0019 a0005c0010t0004g0235 a0005c0010t0004g0236 |
4 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1682-749C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160736138 | |||||||
| chr6:160736386 | TAC | T | 10 | a0001c0001t0007g0288 a0002c0007t0007g0036 a0002c0007t0007g0037 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1682-486_1682-485d others(4): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 160736386 | ||||||
| chr6:160736775 | T | C | 5 | a0001c0001t0001g0052 a0001c0001t0001g0097 a0001c0001t0001g0215 others(2): Show |
5 | HG02015.hp2 NA18955.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1682-112T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 13/18 | chr6 | 160736775 | |||||||
| chr6:160737047 | C | T | 1 | a0001c0005t0010g0298 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1802+40C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737047 | |||||||
| chr6:160737105 | C | T | 1 | a0001c0021t0004g0014 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1802+98C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737105 | |||||||
| chr6:160737169 | T | C | 4 | a0001c0008t0001g0231 a0001c0008t0001g0290 a0001c0008t0001g0292 others(1): Show |
4 | HG02572.hp1 HG02886.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1802+162T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737169 | |||||||
| chr6:160737173 | TA | T | 7 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(4): Show |
7 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1802+167delA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737173 | |||||||
| chr6:160737243 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1802+236C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737243 | |||||||
| chr6:160737413 | T | C | 4 | a0001c0001t0001g0172 a0001c0001t0001g0174 a0001c0001t0001g0209 others(1): Show |
4 | HG00408.hp1 HG03654.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1802+406T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737413 | |||||||
| chr6:160737465 | T | C | 16 | a0001c0005t0005g0234 a0001c0006t0005g0018 a0001c0006t0005g0093 others(13): Show |
18 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.1802+458T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737465 | |||||||
| chr6:160737630 | T | C | 1 | a0002c0004t0011g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1802+623T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737630 | |||||||
| chr6:160737697 | G | A | 5 | a0001c0009t0004g0026 a0004c0012t0001g0233 a0004c0012t0001g0248 others(2): Show |
5 | HG02257.hp2 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1802+690G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737697 | |||||||
| chr6:160737702 | T | C | 208 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(205): Show |
231 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.1802+695T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737702 | |||||||
| chr6:160737948 | C | T | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | NA19003.hp1 NA19012.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.1803-590C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737948 | |||||||
| chr6:160737966 | C | CA | 33 | a0001c0001t0007g0288 a0002c0004t0003g0001 a0002c0004t0003g0010 others(30): Show |
43 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1803-572_1803-571i others(3): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737966 | |||||||
| chr6:160737967 | T | A | 39 | a0001c0005t0005g0234 a0001c0006t0002g0041 a0001c0006t0002g0042 others(36): Show |
43 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.1803-571T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737967 | |||||||
| chr6:160737969 | T | A | 33 | a0001c0001t0007g0288 a0002c0004t0003g0001 a0002c0004t0003g0010 others(30): Show |
43 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1803-569T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737969 | |||||||
| chr6:160737970 | A | AC | 39 | a0001c0005t0005g0234 a0001c0006t0002g0041 a0001c0006t0002g0042 others(36): Show |
43 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.1803-568_1803-567i others(3): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737970 | |||||||
| chr6:160737974 | T | C | 72 | a0001c0001t0007g0288 a0001c0005t0005g0234 a0001c0006t0002g0041 others(69): Show |
86 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.1803-564T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737974 | |||||||
| chr6:160737984 | A | G | 72 | a0001c0001t0007g0288 a0001c0005t0005g0234 a0001c0006t0002g0041 others(69): Show |
86 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.1803-554A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160737984 | |||||||
| chr6:160738190 | G | A | 1 | a0002c0007t0023g0048 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1803-348G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160738190 | |||||||
| chr6:160738324 | A | G | 1 | a0001c0005t0011g0110 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1803-214A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160738324 | |||||||
| chr6:160738334 | T | G | 39 | a0001c0005t0005g0234 a0001c0006t0002g0041 a0001c0006t0002g0042 others(36): Show |
43 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.1803-204T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160738334 | |||||||
| chr6:160738366 | C | T | 1 | a0001c0005t0011g0110 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1803-172C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 14/18 | chr6 | 160738366 | |||||||
| chr6:160738627 | C | A | 2 | a0001c0021t0004g0014 a0001c0028t0004g0227 |
3 | HG03098.hp1 HG03139.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1877+15C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 15/18 | chr6 | 160738627 | |||||||
| chr6:160739051 | G | A | 202 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(199): Show |
225 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.1878-17G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 15/18 | chr6 | 160739051 | |||||||
| chr6:160739062 | T | C | 1 | a0001c0005t0002g0294 | 1 | HG00642.hp2 | splice_region_variant&intron_variant | LOW | c.1878-6T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 15/18 | chr6 | 160739062 | |||||||
| chr6:160739293 | G | A | 1 | a0001c0002t0001g0132 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2018+85G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160739293 | |||||||
| chr6:160739309 | T | C | 4 | a0001c0001t0001g0253 a0001c0001t0001g0257 a0001c0001t0001g0258 others(1): Show |
4 | HG00408.hp2 HG00609.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.2018+101T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160739309 | |||||||
| chr6:160739473 | T | C | 33 | a0001c0005t0005g0234 a0001c0006t0002g0041 a0001c0006t0002g0042 others(30): Show |
35 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.2018+265T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160739473 | |||||||
| chr6:160739508 | C | T | 3 | a0001c0009t0004g0026 a0001c0021t0004g0014 a0001c0028t0004g0227 |
4 | HG02258.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2018+300C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160739508 | |||||||
| chr6:160739509 | G | A | 16 | a0001c0005t0005g0234 a0001c0006t0005g0018 a0001c0006t0005g0093 others(13): Show |
18 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.2018+301G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160739509 | |||||||
| chr6:160739608 | G | C | 2 | a0001c0021t0004g0014 a0001c0028t0004g0227 |
3 | HG03098.hp1 HG03139.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2018+400G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160739608 | |||||||
| chr6:160739612 | G | A | 34 | a0001c0003t0001g0007 a0001c0003t0001g0047 a0001c0003t0001g0055 others(31): Show |
36 | HG00558.hp2 HG00639.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.2018+404G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160739612 | |||||||
| chr6:160739727 | TTC | T | 129 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(126): Show |
138 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.2018+520_2018+521d others(4): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160739727 | |||||||
| chr6:160739760 | C | CA | 24 | a0001c0002t0001g0132 a0001c0003t0001g0146 a0001c0003t0001g0147 others(21): Show |
25 | HG01256.hp1 HG01258.hp1 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.2018+563dupA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr6 | 160739760 | ||||||
| chr6:160739760 | C | CAA | 16 | a0001c0005t0005g0234 a0001c0006t0005g0018 a0001c0006t0005g0093 others(13): Show |
18 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.2018+562_2018+563d others(4): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr6 | 160739760 | ||||||
| chr6:160739794 | CA | C | 35 | a0001c0005t0005g0234 a0001c0006t0002g0041 a0001c0006t0002g0042 others(32): Show |
38 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.2018+596delA | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr6 | 160739794 | ||||||
| chr6:160740051 | G | A | 1 | a0001c0006t0014g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2018+843G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740051 | |||||||
| chr6:160740186 | G | A | 1 | a0001c0021t0004g0014 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2018+978G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740186 | |||||||
| chr6:160740270 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2019-1041C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740270 | |||||||
| chr6:160740323 | T | C | 7 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(4): Show |
7 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2019-988T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740323 | |||||||
| chr6:160740463 | C | T | 7 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(4): Show |
7 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2019-848C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740463 | |||||||
| chr6:160740476 | C | A | 1 | a0001c0027t0010g0115 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2019-835C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740476 | |||||||
| chr6:160740527 | C | A | 27 | a0001c0006t0014g0035 a0002c0004t0003g0001 a0002c0004t0003g0010 others(24): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.2019-784C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740527 | |||||||
| chr6:160740599 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0170 |
2 | NA18971.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2019-712G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740599 | |||||||
| chr6:160740640 | A | G | 5 | a0001c0001t0006g0183 a0001c0001t0006g0184 a0001c0001t0006g0185 others(2): Show |
5 | NA18952.hp1 NA18975.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.2019-671A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740640 | |||||||
| chr6:160740726 | A | G | 1 | a0001c0006t0005g0094 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2019-585A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740726 | |||||||
| chr6:160740834 | G | A | 1 | a0001c0002t0001g0130 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2019-477G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740834 | |||||||
| chr6:160740872 | G | C | 10 | a0002c0004t0003g0024 a0002c0004t0003g0075 a0002c0004t0003g0249 others(7): Show |
11 | HG00642.hp1 HG00738.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.2019-439G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160740872 | |||||||
| chr6:160740945 | TTCCATGC others(5): Show |
T | 7 | a0001c0006t0002g0041 a0001c0006t0002g0042 a0001c0006t0002g0045 others(4): Show |
7 | HG02451.hp1 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2019-363_2019-352d others(14): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr6 | 160740945 | ||||||
| chr6:160741038 | G | A | 1 | a0001c0021t0004g0014 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2019-273G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160741038 | |||||||
| chr6:160741179 | T | C | 4 | a0001c0006t0014g0035 a0005c0010t0004g0019 a0005c0010t0004g0235 others(1): Show |
5 | HG01891.hp2 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2019-132T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160741179 | |||||||
| chr6:160741258 | A | G | 2 | a0001c0009t0002g0056 a0001c0009t0002g0057 |
2 | HG01074.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.2019-53A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160741258 | |||||||
| chr6:160741295 | G | A | 1 | a0002c0004t0011g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2019-16G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 16/18 | chr6 | 160741295 | |||||||
| chr6:160741446 | G | A | 6 | a0001c0008t0001g0218 a0001c0008t0001g0339 a0001c0013t0001g0025 others(3): Show |
7 | HG02559.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2125+29G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160741446 | |||||||
| chr6:160741465 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2125+48G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160741465 | |||||||
| chr6:160741587 | A | T | 1 | a0001c0028t0004g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2125+170A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160741587 | |||||||
| chr6:160741739 | G | A | 1 | a0001c0021t0004g0014 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2125+322G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160741739 | |||||||
| chr6:160741851 | T | A | 3 | a0001c0002t0001g0121 a0001c0002t0001g0122 a0001c0002t0001g0123 |
3 | HG01255.hp2 HG01978.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.2125+434T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160741851 | |||||||
| chr6:160742022 | A | G | 1 | a0001c0028t0004g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2125+605A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742022 | |||||||
| chr6:160742042 | A | T | 272 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(269): Show |
304 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.2125+625A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742042 | |||||||
| chr6:160742069 | T | G | 2 | a0001c0021t0004g0014 a0001c0028t0004g0227 |
3 | HG03098.hp1 HG03139.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2125+652T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742069 | |||||||
| chr6:160742217 | G | T | 7 | a0001c0002t0001g0011 a0001c0002t0001g0071 a0001c0002t0001g0120 others(4): Show |
8 | HG01255.hp2 HG01978.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.2125+800G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742217 | |||||||
| chr6:160742244 | C | G | 3 | a0005c0010t0004g0019 a0005c0010t0004g0235 a0005c0010t0004g0236 |
4 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2125+827C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742244 | |||||||
| chr6:160742372 | T | C | 3 | a0001c0009t0004g0044 a0003c0020t0004g0326 a0003c0020t0004g0332 |
3 | HG01256.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2125+955T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742372 | |||||||
| chr6:160742463 | G | T | 1 | a0001c0003t0001g0047 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2125+1046G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742463 | |||||||
| chr6:160742497 | G | T | 1 | a0001c0001t0001g0178 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2125+1080G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742497 | |||||||
| chr6:160742497 | GT | G | 55 | a0001c0001t0001g0269 a0001c0002t0001g0011 a0001c0002t0001g0017 others(52): Show |
58 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.2125+1090delT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160742497 | ||||||
| chr6:160742498 | T | G | 10 | a0001c0001t0007g0288 a0002c0007t0007g0036 a0002c0007t0007g0037 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2125+1081T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742498 | |||||||
| chr6:160742566 | T | C | 1 | a0001c0002t0001g0297 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2125+1149T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742566 | |||||||
| chr6:160742742 | G | A | 12 | a0001c0008t0001g0218 a0001c0008t0001g0231 a0001c0008t0001g0290 others(9): Show |
13 | HG02559.hp2 HG02572.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2125+1325G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742742 | |||||||
| chr6:160742745 | A | G | 229 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(226): Show |
249 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.2125+1328A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742745 | |||||||
| chr6:160742924 | T | C | 4 | a0001c0001t0001g0253 a0001c0001t0001g0257 a0001c0001t0001g0258 others(1): Show |
4 | HG00408.hp2 HG00609.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.2125+1507T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742924 | |||||||
| chr6:160742957 | T | C | 1 | a0001c0005t0010g0027 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2125+1540T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742957 | |||||||
| chr6:160742979 | G | A | 1 | a0002c0004t0011g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2125+1562G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160742979 | |||||||
| chr6:160743011 | CT | C | 60 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0003t0001g0007 others(57): Show |
65 | HG00558.hp2 HG00639.hp2 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.2125+1613delT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160743011 | ||||||
| chr6:160743011 | CTT | C | 26 | a0001c0002t0001g0156 a0001c0002t0001g0310 a0001c0005t0011g0110 others(23): Show |
36 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.2125+1612_2125+161 others(6): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160743011 | ||||||
| chr6:160743011 | CTTT | C | 62 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0169 others(59): Show |
67 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.2125+1611_2125+161 others(7): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160743011 | ||||||
| chr6:160743011 | CTTTT | C | 165 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0015 others(162): Show |
180 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.2125+1610_2125+161 others(8): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160743011 | ||||||
| chr6:160743068 | G | C | 1 | a0001c0005t0010g0298 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2125+1651G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743068 | |||||||
| chr6:160743155 | A | C | 12 | a0001c0001t0007g0288 a0001c0021t0004g0014 a0001c0028t0004g0227 others(9): Show |
13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2125+1738A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743155 | |||||||
| chr6:160743158 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2125+1741T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743158 | |||||||
| chr6:160743258 | C | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0029 |
3 | HG01255.hp1 HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.2125+1841C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743258 | |||||||
| chr6:160743317 | G | A | 1 | a0001c0021t0004g0014 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2125+1900G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743317 | |||||||
| chr6:160743587 | G | C | 1 | a0001c0006t0014g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2125+2170G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743587 | |||||||
| chr6:160743637 | T | C | 2 | a0001c0005t0011g0110 a0002c0004t0011g0296 |
2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2125+2220T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743637 | |||||||
| chr6:160743643 | C | T | 1 | a0001c0001t0018g0256 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2125+2226C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743643 | |||||||
| chr6:160743655 | T | G | 1 | a0001c0002t0001g0133 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2125+2238T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743655 | |||||||
| chr6:160743692 | C | T | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0069 others(1): Show |
4 | HG01123.hp1 HG01192.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2125+2275C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743692 | |||||||
| chr6:160743768 | C | G | 6 | a0001c0001t0001g0173 a0001c0001t0001g0207 a0001c0001t0001g0208 others(3): Show |
6 | HG01167.hp2 HG02040.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.2125+2351C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743768 | |||||||
| chr6:160743780 | G | A | 1 | a0001c0005t0011g0110 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2125+2363G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743780 | |||||||
| chr6:160743792 | G | A | 1 | a0001c0021t0004g0014 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2125+2375G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743792 | |||||||
| chr6:160743945 | AT | A | 3 | a0005c0010t0004g0019 a0005c0010t0004g0235 a0005c0010t0004g0236 |
4 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2125+2529delT | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160743945 | |||||||
| chr6:160744029 | G | A | 11 | a0001c0001t0007g0288 a0001c0028t0004g0227 a0002c0007t0007g0036 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2125+2612G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160744029 | |||||||
| chr6:160744120 | T | C | 1 | a0001c0011t0001g0230 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2125+2703T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160744120 | |||||||
| chr6:160744267 | C | A | 1 | a0002c0007t0023g0048 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2125+2850C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160744267 | |||||||
| chr6:160744293 | C | T | 10 | a0001c0001t0007g0288 a0002c0007t0007g0036 a0002c0007t0007g0037 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2125+2876C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160744293 | |||||||
| chr6:160744399 | T | C | 10 | a0001c0001t0007g0288 a0002c0007t0007g0036 a0002c0007t0007g0037 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2125+2982T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160744399 | |||||||
| chr6:160744517 | A | G | 4 | a0001c0006t0014g0035 a0005c0010t0004g0019 a0005c0010t0004g0235 others(1): Show |
5 | HG01891.hp2 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2125+3100A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160744517 | |||||||
| chr6:160744612 | A | C | 12 | a0001c0001t0007g0288 a0001c0021t0004g0014 a0001c0028t0004g0227 others(9): Show |
13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2125+3195A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160744612 | |||||||
| chr6:160745136 | GGAAA | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0175 a0001c0001t0001g0176 others(1): Show |
5 | HG01192.hp2 NA18969.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.2125+3722_2125+372 others(8): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160745136 | ||||||
| chr6:160745162 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2125+3745C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745162 | |||||||
| chr6:160745222 | C | T | 1 | a0001c0001t0006g0185 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2125+3805C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745222 | |||||||
| chr6:160745281 | C | T | 1 | a0001c0003t0001g0055 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2125+3864C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745281 | |||||||
| chr6:160745382 | A | ACCCTTTA others(1): Show |
21 | a0002c0004t0003g0001 a0002c0004t0003g0010 a0002c0004t0003g0021 others(18): Show |
31 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.2125+3967_2125+397 others(12): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160745382 | ||||||
| chr6:160745392 | A | G | 21 | a0002c0004t0003g0001 a0002c0004t0003g0010 a0002c0004t0003g0021 others(18): Show |
31 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.2125+3975A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745392 | |||||||
| chr6:160745427 | T | C | 1 | a0001c0005t0002g0335 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2125+4010T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745427 | |||||||
| chr6:160745468 | C | T | 3 | a0001c0009t0004g0044 a0003c0020t0004g0326 a0003c0020t0004g0332 |
3 | HG01256.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2125+4051C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745468 | |||||||
| chr6:160745470 | C | T | 147 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(144): Show |
162 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.2125+4053C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745470 | |||||||
| chr6:160745523 | A | G | 10 | a0001c0001t0007g0288 a0002c0007t0007g0036 a0002c0007t0007g0037 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2125+4106A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745523 | |||||||
| chr6:160745534 | A | G | 1 | a0002c0007t0023g0048 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2125+4117A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745534 | |||||||
| chr6:160745578 | C | A | 7 | a0001c0001t0001g0180 a0001c0002t0001g0050 a0001c0002t0001g0158 others(4): Show |
7 | HG00597.hp1 HG00609.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.2125+4161C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745578 | |||||||
| chr6:160745761 | G | T | 3 | a0005c0010t0004g0019 a0005c0010t0004g0235 a0005c0010t0004g0236 |
4 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2125+4344G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745761 | |||||||
| chr6:160745983 | G | T | 1 | a0001c0021t0004g0014 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2125+4566G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160745983 | |||||||
| chr6:160746108 | G | C | 1 | a0001c0002t0001g0082 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2125+4691G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160746108 | |||||||
| chr6:160746112 | G | A | 1 | a0002c0007t0023g0048 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2125+4695G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160746112 | |||||||
| chr6:160746184 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2125+4767T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160746184 | |||||||
| chr6:160746198 | A | T | 1 | a0001c0028t0004g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2125+4781A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160746198 | |||||||
| chr6:160746387 | T | C | 1 | a0002c0004t0003g0265 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2125+4970T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160746387 | |||||||
| chr6:160746420 | A | G | 152 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(149): Show |
167 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.2125+5003A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160746420 | |||||||
| chr6:160746624 | C | G | 11 | a0001c0001t0007g0288 a0001c0028t0004g0227 a0002c0007t0007g0036 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2125+5207C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160746624 | |||||||
| chr6:160746963 | T | C | 1 | a0001c0003t0001g0128 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2126-5152T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160746963 | |||||||
| chr6:160746983 | G | A | 10 | a0001c0001t0007g0288 a0002c0007t0007g0036 a0002c0007t0007g0037 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2126-5132G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160746983 | |||||||
| chr6:160747278 | C | T | 11 | a0001c0001t0007g0288 a0001c0028t0004g0227 a0002c0007t0007g0036 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2126-4837C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747278 | |||||||
| chr6:160747365 | A | T | 42 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0003t0001g0007 others(39): Show |
45 | HG00558.hp2 HG00639.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.2126-4750A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747365 | |||||||
| chr6:160747420 | G | C | 11 | a0001c0001t0007g0288 a0001c0028t0004g0227 a0002c0007t0007g0036 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2126-4695G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747420 | |||||||
| chr6:160747441 | G | A | 1 | a0001c0001t0020g0289 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2126-4674G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747441 | |||||||
| chr6:160747446 | C | A | 1 | a0001c0009t0004g0063 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2126-4669C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747446 | |||||||
| chr6:160747485 | G | A | 11 | a0001c0001t0007g0288 a0001c0028t0004g0227 a0002c0007t0007g0036 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2126-4630G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747485 | |||||||
| chr6:160747516 | G | A | 259 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(256): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.2126-4599G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747516 | |||||||
| chr6:160747571 | A | C | 2 | a0001c0006t0005g0337 a0001c0006t0005g0342 |
2 | HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2126-4544A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747571 | |||||||
| chr6:160747621 | G | GTTTT | 313 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(310): Show |
348 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(345): Show |
intron_variant | MODIFIER | c.2126-4491_2126-449 others(8): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160747621 | ||||||
| chr6:160747662 | G | A | 1 | a0005c0010t0004g0236 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2126-4453G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747662 | |||||||
| chr6:160747675 | G | GATTTCAA others(32): Show |
1 | a0001c0002t0001g0196 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2126-4435_2126-439 others(43): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160747675 | ||||||
| chr6:160747727 | T | C | 313 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(310): Show |
348 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(345): Show |
intron_variant | MODIFIER | c.2126-4388T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747727 | |||||||
| chr6:160747778 | T | C | 2 | a0001c0006t0005g0337 a0001c0006t0005g0342 |
2 | HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2126-4337T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747778 | |||||||
| chr6:160747894 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2126-4221A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747894 | |||||||
| chr6:160747917 | G | T | 22 | a0001c0028t0004g0227 a0002c0004t0003g0001 a0002c0004t0003g0010 others(19): Show |
32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.2126-4198G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747917 | |||||||
| chr6:160747929 | G | T | 259 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(256): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.2126-4186G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747929 | |||||||
| chr6:160747938 | A | G | 12 | a0001c0008t0001g0218 a0001c0008t0001g0231 a0001c0008t0001g0290 others(9): Show |
13 | HG02559.hp2 HG02572.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2126-4177A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160747938 | |||||||
| chr6:160748064 | T | A | 12 | a0001c0001t0007g0288 a0001c0021t0004g0014 a0001c0028t0004g0227 others(9): Show |
13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2126-4051T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748064 | |||||||
| chr6:160748076 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2126-4039G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748076 | |||||||
| chr6:160748108 | G | C | 12 | a0001c0001t0007g0288 a0001c0021t0004g0014 a0001c0028t0004g0227 others(9): Show |
13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2126-4007G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748108 | |||||||
| chr6:160748162 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2126-3953G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748162 | |||||||
| chr6:160748237 | G | A | 2 | a0001c0005t0010g0027 a0001c0005t0010g0298 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2126-3878G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748237 | |||||||
| chr6:160748313 | AGAAAGAA others(1): Show |
A | 11 | a0001c0001t0007g0288 a0001c0021t0004g0014 a0001c0028t0004g0227 others(8): Show |
13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2126-3782_2126-377 others(12): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748313 | ||||||
| chr6:160748332 | A | AG | 3 | a0002c0007t0007g0038 a0002c0007t0007g0043 a0005c0010t0004g0236 |
3 | HG02615.hp2 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2126-3783_2126-378 others(5): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748332 | |||||||
| chr6:160748334 | G | A | 3 | a0002c0007t0007g0038 a0002c0007t0007g0043 a0005c0010t0004g0236 |
3 | HG02615.hp2 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2126-3781G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748334 | |||||||
| chr6:160748338 | G | A | 3 | a0002c0007t0007g0038 a0002c0007t0007g0043 a0005c0010t0004g0236 |
3 | HG02615.hp2 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2126-3777G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748338 | |||||||
| chr6:160748348 | A | AAGAGAAA others(35): Show |
1 | a0001c0002t0001g0329 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2126-3734_2126-373 others(46): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748348 | ||||||
| chr6:160748348 | A | AAGAGAAA others(37): Show |
1 | a0001c0002t0001g0108 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2126-3734_2126-373 others(48): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748348 | ||||||
| chr6:160748348 | A | AAGAGAAA others(25): Show |
1 | a0001c0001t0001g0212 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(36): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748348 | ||||||
| chr6:160748348 | A | AAGAGAAA others(29): Show |
24 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0023 others(21): Show |
30 | HG00423.hp1 HG00609.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(40): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748348 | ||||||
| chr6:160748348 | A | AAGAGAAA others(31): Show |
1 | a0001c0002t0001g0259 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(42): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748348 | ||||||
| chr6:160748348 | A | AAGAGAAA others(33): Show |
11 | a0001c0001t0001g0266 a0001c0002t0001g0058 a0001c0002t0001g0081 others(8): Show |
14 | HG01081.hp1 HG01099.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(44): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748348 | ||||||
| chr6:160748348 | A | AAGAGAAA others(35): Show |
1 | a0001c0003t0001g0327 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(46): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748348 | ||||||
| chr6:160748348 | A | AAGAGAAA others(30): Show |
1 | a0001c0002t0001g0193 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2126-3741_2126-374 others(41): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748348 | ||||||
| chr6:160748348 | A | AAGAGAAA others(25): Show |
1 | a0001c0002t0001g0124 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2126-3742_2126-374 others(36): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748348 | ||||||
| chr6:160748348 | A | AAGAGAAA others(29): Show |
2 | a0001c0001t0001g0069 a0001c0011t0001g0226 |
2 | HG01517.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.2126-3742_2126-374 others(40): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748348 | ||||||
| chr6:160748348 | A | AAGAGAAA others(27): Show |
2 | a0001c0008t0001g0290 a0001c0008t0001g0304 |
2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2126-3746_2126-374 others(38): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748348 | ||||||
| chr6:160748348 | A | G | 1 | a0002c0007t0007g0037 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2126-3767A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748348 | |||||||
| chr6:160748350 | G | A | 1 | a0002c0007t0007g0037 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2126-3765G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748350 | |||||||
| chr6:160748350 | G | GAA | 3 | a0002c0007t0007g0038 a0002c0007t0007g0043 a0005c0010t0004g0236 |
3 | HG02615.hp2 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2126-3764_2126-376 others(6): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAA | 13 | a0001c0005t0002g0243 a0001c0005t0002g0295 a0001c0005t0005g0234 others(10): Show |
14 | HG00323.hp1 HG01361.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.2126-3718_2126-371 others(8): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(1): Show |
7 | a0001c0005t0002g0294 a0001c0006t0002g0041 a0001c0006t0004g0046 others(4): Show |
7 | HG00642.hp2 HG02148.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2126-3722_2126-371 others(12): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(5): Show |
2 | a0001c0005t0002g0101 a0001c0005t0002g0264 |
2 | HG00280.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.2126-3726_2126-371 others(16): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(9): Show |
3 | a0001c0005t0010g0298 a0001c0009t0002g0056 a0001c0009t0012g0068 |
3 | HG01346.hp1 HG01978.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2126-3730_2126-371 others(20): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(45): Show |
1 | a0001c0001t0001g0070 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2126-3730_2126-372 others(56): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(37): Show |
1 | a0001c0001t0001g0060 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2126-3734_2126-373 others(48): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(41): Show |
1 | a0001c0001t0001g0059 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2126-3734_2126-373 others(52): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(47): Show |
1 | a0001c0002t0001g0134 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2126-3734_2126-373 others(58): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(45): Show |
1 | a0001c0002t0001g0135 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2126-3734_2126-373 others(56): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(45): Show |
1 | a0001c0002t0001g0078 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2126-3734_2126-373 others(56): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(33): Show |
1 | a0001c0001t0020g0289 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(44): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(33): Show |
38 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0039 others(35): Show |
42 | HG00408.hp1 HG00558.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(44): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(37): Show |
17 | a0001c0001t0001g0004 a0001c0001t0001g0161 a0001c0001t0001g0175 others(14): Show |
20 | HG00140.hp2 HG00597.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(48): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(41): Show |
3 | a0001c0001t0001g0207 a0001c0001t0006g0319 a0001c0002t0001g0130 |
3 | HG01123.hp2 NA18612.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(52): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(45): Show |
4 | a0001c0001t0001g0209 a0001c0001t0006g0183 a0001c0002t0001g0154 others(1): Show |
4 | HG02148.hp2 NA19000.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(56): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(45): Show |
1 | a0001c0001t0001g0254 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(56): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(40): Show |
1 | a0004c0012t0021g0305 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(51): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(44): Show |
1 | a0001c0001t0001g0173 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(55): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(48): Show |
1 | a0004c0012t0009g0034 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(59): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(35): Show |
2 | a0001c0002t0001g0122 a0001c0002t0001g0126 |
2 | HG01255.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(46): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(39): Show |
3 | a0001c0002t0001g0121 a0001c0002t0001g0136 a0001c0002t0001g0251 |
3 | HG02293.hp1 NA18944.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(50): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(47): Show |
1 | a0001c0002t0001g0117 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(58): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(38): Show |
1 | a0001c0001t0001g0330 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(49): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(36): Show |
1 | a0001c0003t0001g0192 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(47): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(37): Show |
10 | a0001c0002t0001g0017 a0001c0002t0001g0085 a0001c0002t0001g0132 others(7): Show |
11 | HG01952.hp1 HG02080.hp2 HG04115.hp2 others(8): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(48): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(41): Show |
10 | a0001c0002t0001g0082 a0001c0002t0001g0084 a0001c0002t0001g0116 others(7): Show |
10 | HG01069.hp1 HG01891.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(52): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(45): Show |
9 | a0001c0002t0001g0022 a0001c0002t0001g0083 a0001c0002t0001g0118 others(6): Show |
10 | HG00558.hp2 HG02040.hp1 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(56): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(49): Show |
5 | a0001c0002t0001g0049 a0001c0002t0001g0111 a0001c0003t0001g0086 others(2): Show |
5 | HG02300.hp2 HG03704.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(60): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(53): Show |
2 | a0001c0002t0001g0156 a0001c0003t0001g0148 |
2 | NA18612.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(64): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(38): Show |
1 | a0001c0002t0001g0310 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(49): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(43): Show |
1 | a0001c0002t0001g0080 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(54): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(47): Show |
1 | a0001c0002t0001g0131 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(58): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(41): Show |
1 | a0001c0002t0001g0142 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(52): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(45): Show |
1 | a0001c0003t0001g0200 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(56): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(38): Show |
2 | a0001c0001t0001g0177 a0002c0007t0001g0274 |
2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.2126-3741_2126-374 others(49): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(40): Show |
1 | a0001c0002t0001g0123 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2126-3741_2126-374 others(51): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(39): Show |
1 | a0001c0002t0001g0301 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2126-3741_2126-374 others(50): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(33): Show |
1 | a0001c0001t0001g0090 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2126-3742_2126-374 others(44): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(37): Show |
1 | a0001c0002t0001g0159 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2126-3742_2126-374 others(48): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(35): Show |
1 | a0001c0003t0001g0125 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2126-3742_2126-374 others(46): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(33): Show |
3 | a0001c0008t0001g0218 a0001c0011t0001g0224 a0001c0011t0001g0225 |
3 | HG02559.hp2 NA18940.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.2126-3742_2126-374 others(44): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(37): Show |
2 | a0001c0002t0001g0195 a0001c0008t0001g0339 |
2 | HG03130.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2126-3742_2126-374 others(48): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(41): Show |
2 | a0001c0002t0001g0077 a0001c0002t0001g0194 |
2 | NA18991.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2126-3742_2126-374 others(52): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(36): Show |
1 | a0001c0003t0001g0311 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2126-3742_2126-374 others(47): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(41): Show |
1 | a0006c0014t0001g0309 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2126-3742_2126-374 others(52): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(31): Show |
1 | a0001c0024t0009g0240 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2126-3746_2126-374 others(42): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(28): Show |
1 | a0001c0008t0001g0292 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2126-3746_2126-374 others(39): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(29): Show |
1 | a0001c0013t0001g0025 | 2 | HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2126-3746_2126-374 others(40): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(33): Show |
1 | a0001c0013t0001g0341 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2126-3746_2126-374 others(44): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(39): Show |
1 | a0001c0008t0001g0291 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2126-3746_2126-374 others(50): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(33): Show |
1 | a0002c0007t0023g0048 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2126-3746_2126-374 others(44): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(30): Show |
1 | a0001c0008t0001g0345 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2126-3749_2126-374 others(41): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748350 | G | GAGAAAGA others(32): Show |
1 | a0001c0008t0001g0231 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2126-3749_2126-374 others(43): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748350 | ||||||
| chr6:160748354 | A | AAGAAAGA others(31): Show |
1 | a0001c0002t0001g0071 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2126-3734_2126-373 others(42): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748354 | ||||||
| chr6:160748354 | A | AAGAAAGA others(23): Show |
1 | a0001c0001t0001g0098 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(34): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748354 | ||||||
| chr6:160748354 | A | AAGAAAGA others(25): Show |
22 | a0001c0001t0001g0030 a0001c0001t0001g0052 a0001c0001t0001g0053 others(19): Show |
22 | HG00733.hp1 HG02071.hp1 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(36): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748354 | ||||||
| chr6:160748354 | A | AAGAAAGA others(27): Show |
1 | a0001c0002t0001g0011 | 2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(38): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748354 | ||||||
| chr6:160748354 | A | AAGAAAGA others(29): Show |
7 | a0001c0001t0001g0241 a0001c0001t0001g0267 a0001c0002t0001g0133 others(4): Show |
7 | HG00544.hp1 HG00639.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(40): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748354 | ||||||
| chr6:160748354 | A | AAGAAAGA others(33): Show |
1 | a0001c0002t0001g0143 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(44): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748354 | ||||||
| chr6:160748354 | A | AAGAAAGA others(26): Show |
1 | a0007c0019t0001g0307 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2126-3741_2126-374 others(37): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748354 | ||||||
| chr6:160748354 | A | AAGAAAGA others(21): Show |
1 | a0001c0001t0001g0252 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2126-3742_2126-374 others(32): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748354 | ||||||
| chr6:160748354 | A | AAGAAAGA others(23): Show |
1 | a0001c0013t0009g0033 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2126-3742_2126-374 others(34): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748354 | ||||||
| chr6:160748357 | A | AAAGAAAG others(26): Show |
1 | a0001c0002t0009g0239 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(37): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748357 | ||||||
| chr6:160748358 | A | AAGAAAGA others(17): Show |
1 | a0001c0001t0001g0213 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(28): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748358 | ||||||
| chr6:160748358 | A | AAGAAAGA others(21): Show |
8 | a0001c0001t0001g0054 a0001c0001t0001g0066 a0001c0001t0001g0258 others(5): Show |
8 | HG00408.hp2 HG02451.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(32): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748358 | ||||||
| chr6:160748358 | A | AAGAAAGA others(23): Show |
1 | a0001c0001t0017g0188 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(34): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748358 | ||||||
| chr6:160748358 | A | AAGAAAGA others(25): Show |
3 | a0001c0002t0001g0079 a0001c0003t0001g0152 a0001c0003t0001g0199 |
3 | HG01243.hp2 NA18954.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(36): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748358 | ||||||
| chr6:160748358 | A | AAGAAAGA others(22): Show |
1 | a0001c0001t0001g0174 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2126-3741_2126-374 others(33): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748358 | ||||||
| chr6:160748358 | A | AAGAAAGA others(25): Show |
1 | a0006c0014t0001g0144 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2126-3742_2126-374 others(36): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748358 | ||||||
| chr6:160748361 | A | AAAGAAAG others(23): Show |
1 | a0001c0003t0001g0128 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2126-3741_2126-374 others(34): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748361 | ||||||
| chr6:160748362 | A | AAGAAAGA others(15): Show |
1 | a0001c0001t0001g0283 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(26): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748362 | ||||||
| chr6:160748362 | A | AAGAAAGA others(17): Show |
2 | a0001c0001t0001g0302 a0012c0023t0001g0095 |
2 | NA18966.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(28): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748362 | ||||||
| chr6:160748362 | A | AAGAAAGA others(21): Show |
1 | a0001c0002t0001g0140 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(32): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748362 | ||||||
| chr6:160748365 | A | AAAGAAAG others(20): Show |
1 | a0006c0014t0001g0141 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(31): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748365 | ||||||
| chr6:160748366 | A | AAGAAAGA others(13): Show |
3 | a0001c0001t0001g0166 a0001c0001t0001g0168 a0001c0001t0001g0208 |
3 | HG00544.hp2 HG02293.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(24): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748366 | ||||||
| chr6:160748366 | A | AAGAAAGA others(17): Show |
2 | a0001c0002t0001g0129 a0001c0011t0001g0230 |
2 | HG02015.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(28): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748366 | ||||||
| chr6:160748370 | A | AAGAAAGA others(9): Show |
1 | a0001c0001t0001g0167 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2126-3738_2126-373 others(20): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748370 | ||||||
| chr6:160748370 | A | AAGAAAGA others(35): Show |
1 | a0001c0002t0001g0006 | 3 | HG00735.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2126-3738_2126-373 others(46): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748370 | ||||||
| chr6:160748374 | A | AAGAAAGA others(13): Show |
1 | a0001c0002t0001g0196 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2126-3734_2126-373 others(24): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748374 | ||||||
| chr6:160748378 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2126-3737A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748378 | |||||||
| chr6:160748381 | AAAGAAAG others(13): Show |
A | 1 | a0001c0009t0004g0063 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2126-3718_2126-369 others(24): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748381 | ||||||
| chr6:160748382 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2126-3733A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748382 | |||||||
| chr6:160748385 | AAAGAAAG others(9): Show |
A | 3 | a0001c0005t0002g0105 a0001c0006t0005g0338 a0001c0029t0015g0031 |
3 | HG03098.hp2 HG03486.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.2126-3713_2126-369 others(20): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748385 | ||||||
| chr6:160748389 | AAAGAAAG others(5): Show |
A | 6 | a0002c0004t0003g0001 a0002c0004t0003g0021 a0002c0004t0003g0024 others(3): Show |
8 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.2126-3714_2126-370 others(16): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748389 | ||||||
| chr6:160748393 | AAAGAAAG others(1): Show |
A | 13 | a0001c0005t0002g0244 a0001c0005t0002g0335 a0001c0006t0002g0109 others(10): Show |
13 | HG00323.hp2 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.2126-3714_2126-370 others(12): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748393 | ||||||
| chr6:160748397 | AAAGG | A | 14 | a0001c0005t0002g0246 a0001c0006t0002g0042 a0001c0006t0005g0336 others(11): Show |
15 | HG01070.hp2 HG01074.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2126-3714_2126-371 others(8): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748397 | ||||||
| chr6:160748401 | G | A | 309 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(306): Show |
335 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(332): Show |
intron_variant | MODIFIER | c.2126-3714G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748401 | |||||||
| chr6:160748401 | GAAGAAAG others(3): Show |
G | 1 | a0002c0007t0007g0091 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2126-3713_2126-370 others(14): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748401 | |||||||
| chr6:160748403 | AGAAAGAA others(6): Show |
A | 1 | a0001c0021t0004g0014 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2126-3710_2126-369 others(17): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748403 | ||||||
| chr6:160748404 | G | GAA | 9 | a0001c0001t0018g0256 a0001c0002t0001g0130 a0001c0003t0001g0313 others(6): Show |
9 | HG01123.hp2 HG01346.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2126-3709_2126-370 others(6): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748404 | ||||||
| chr6:160748409 | A | G | 1 | a0002c0004t0003g0001 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2126-3706A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748409 | |||||||
| chr6:160748411 | A | G | 2 | a0002c0007t0007g0036 a0002c0007t0007g0281 |
2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2126-3704A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748411 | |||||||
| chr6:160748413 | A | G | 2 | a0001c0001t0007g0288 a0002c0007t0007g0040 |
2 | HG01243.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2126-3702A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748413 | |||||||
| chr6:160748414 | A | G | 3 | a0001c0001t0007g0288 a0002c0007t0007g0040 a0006c0014t0001g0309 |
3 | HG01243.hp1 NA18522.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.2126-3701A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748414 | |||||||
| chr6:160748415 | AGG | A | 5 | a0002c0004t0003g0001 a0002c0007t0007g0036 a0002c0007t0007g0091 others(2): Show |
5 | HG01169.hp1 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2126-3698_2126-369 others(6): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748415 | ||||||
| chr6:160748416 | G | A | 139 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(136): Show |
154 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.2126-3699G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748416 | |||||||
| chr6:160748416 | G | GAA | 3 | a0001c0002t0001g0129 a0006c0014t0001g0141 a0006c0014t0001g0144 |
3 | HG02015.hp1 NA18962.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2126-3699_2126-369 others(6): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748416 | |||||||
| chr6:160748417 | G | A | 143 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(140): Show |
159 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.2126-3698G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748417 | |||||||
| chr6:160748417 | G | GGAAA | 121 | a0001c0001t0001g0165 a0001c0001t0001g0266 a0001c0001t0001g0267 others(118): Show |
128 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.2126-3691_2126-368 others(8): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748417 | ||||||
| chr6:160748427 | A | G | 137 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(134): Show |
152 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.2126-3688A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748427 | |||||||
| chr6:160748428 | G | A | 2 | a0001c0002t0001g0130 a0001c0002t0001g0308 |
2 | HG01123.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.2126-3687G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748428 | |||||||
| chr6:160748430 | A | G | 2 | a0001c0002t0001g0130 a0001c0002t0001g0308 |
2 | HG01123.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.2126-3685A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748430 | |||||||
| chr6:160748431 | C | A | 142 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(139): Show |
157 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2126-3684C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748431 | |||||||
| chr6:160748435 | A | C | 2 | a0001c0002t0001g0130 a0001c0002t0001g0308 |
2 | HG01123.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.2126-3680A>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748435 | |||||||
| chr6:160748439 | A | AGAGAAC | 139 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(136): Show |
154 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.2126-3674_2126-367 others(10): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748439 | ||||||
| chr6:160748441 | A | AAGGG | 19 | a0001c0009t0004g0026 a0002c0004t0003g0001 a0002c0004t0003g0010 others(16): Show |
28 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.2126-3642_2126-363 others(8): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748441 | ||||||
| chr6:160748441 | AAGGG | A | 12 | a0001c0005t0002g0106 a0001c0006t0005g0018 a0001c0006t0005g0093 others(9): Show |
13 | HG00738.hp1 HG01106.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.2126-3642_2126-363 others(8): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748441 | ||||||
| chr6:160748441 | AAGGGAGG others(1): Show |
A | 118 | a0001c0001t0001g0165 a0001c0001t0001g0266 a0001c0001t0001g0267 others(115): Show |
125 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.2126-3646_2126-363 others(12): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748441 | ||||||
| chr6:160748441 | AAGGGAGG others(5): Show |
A | 16 | a0001c0001t0007g0288 a0001c0005t0011g0110 a0001c0021t0004g0014 others(13): Show |
18 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2126-3650_2126-363 others(16): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748441 | ||||||
| chr6:160748441 | AAGGGAGG others(9): Show |
A | 1 | a0001c0005t0002g0105 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2126-3654_2126-363 others(20): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160748441 | ||||||
| chr6:160748443 | G | A | 141 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(138): Show |
156 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.2126-3672G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748443 | |||||||
| chr6:160748443 | G | C | 1 | a0002c0007t0007g0282 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2126-3672G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748443 | |||||||
| chr6:160748445 | G | A | 142 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(139): Show |
157 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2126-3670G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748445 | |||||||
| chr6:160748447 | G | A | 140 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
155 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.2126-3668G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748447 | |||||||
| chr6:160748449 | G | A | 140 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
155 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.2126-3666G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748449 | |||||||
| chr6:160748451 | G | A | 2 | a0002c0007t0007g0282 a0002c0007t0023g0048 |
2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2126-3664G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748451 | |||||||
| chr6:160748453 | G | A | 2 | a0002c0007t0007g0282 a0002c0007t0023g0048 |
2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2126-3662G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748453 | |||||||
| chr6:160748707 | C | T | 271 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(268): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.2126-3408C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748707 | |||||||
| chr6:160748783 | C | T | 271 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(268): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.2126-3332C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748783 | |||||||
| chr6:160748795 | T | C | 12 | a0001c0001t0007g0288 a0001c0021t0004g0014 a0001c0028t0004g0227 others(9): Show |
13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2126-3320T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748795 | |||||||
| chr6:160748803 | C | T | 1 | a0001c0021t0004g0014 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2126-3312C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748803 | |||||||
| chr6:160748891 | C | T | 1 | a0001c0021t0004g0014 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2126-3224C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160748891 | |||||||
| chr6:160749093 | C | T | 3 | a0005c0010t0004g0019 a0005c0010t0004g0235 a0005c0010t0004g0236 |
4 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2126-3022C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749093 | |||||||
| chr6:160749205 | C | T | 3 | a0001c0009t0004g0044 a0003c0020t0004g0326 a0003c0020t0004g0332 |
3 | HG01256.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2126-2910C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749205 | |||||||
| chr6:160749238 | A | G | 1 | a0001c0002t0001g0157 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2126-2877A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749238 | |||||||
| chr6:160749357 | C | CCAT | 12 | a0001c0001t0007g0288 a0001c0021t0004g0014 a0001c0028t0004g0227 others(9): Show |
13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2126-2756_2126-275 others(7): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160749357 | ||||||
| chr6:160749369 | C | A | 12 | a0001c0001t0007g0288 a0001c0021t0004g0014 a0001c0028t0004g0227 others(9): Show |
13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2126-2746C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749369 | |||||||
| chr6:160749396 | C | T | 12 | a0001c0001t0007g0288 a0001c0021t0004g0014 a0001c0028t0004g0227 others(9): Show |
13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2126-2719C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749396 | |||||||
| chr6:160749482 | TCAC | T | 272 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(269): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.2126-2613_2126-261 others(7): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160749482 | ||||||
| chr6:160749538 | A | T | 2 | a0001c0005t0011g0110 a0002c0004t0011g0296 |
2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2126-2577A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749538 | |||||||
| chr6:160749553 | A | G | 1 | a0001c0002t0001g0058 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2126-2562A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749553 | |||||||
| chr6:160749571 | C | T | 10 | a0001c0001t0007g0288 a0002c0007t0007g0036 a0002c0007t0007g0037 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2126-2544C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749571 | |||||||
| chr6:160749588 | C | T | 1 | a0001c0003t0001g0128 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2126-2527C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749588 | |||||||
| chr6:160749609 | T | C | 12 | a0001c0001t0007g0288 a0001c0021t0004g0014 a0001c0028t0004g0227 others(9): Show |
13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2126-2506T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749609 | |||||||
| chr6:160749626 | C | T | 2 | a0001c0006t0005g0337 a0001c0006t0005g0342 |
2 | HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2126-2489C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749626 | |||||||
| chr6:160749633 | CACCACCA others(5): Show |
C | 1 | a0001c0003t0001g0260 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2126-2471_2126-246 others(16): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160749633 | ||||||
| chr6:160749656 | TCAC | T | 11 | a0001c0005t0005g0234 a0001c0006t0005g0018 a0001c0006t0005g0093 others(8): Show |
12 | HG01884.hp2 HG02622.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.2126-2453_2126-245 others(7): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160749656 | ||||||
| chr6:160749660 | CACCATCA others(8): Show |
C | 10 | a0001c0001t0007g0288 a0002c0007t0007g0036 a0002c0007t0007g0037 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2126-2441_2126-242 others(19): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160749660 | ||||||
| chr6:160749719 | C | T | 1 | a0001c0002t0001g0050 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2126-2396C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749719 | |||||||
| chr6:160749776 | C | A | 2 | a0001c0005t0010g0027 a0001c0005t0010g0298 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2126-2339C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749776 | |||||||
| chr6:160749803 | A | G | 99 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0002t0001g0011 others(96): Show |
105 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.2126-2312A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749803 | |||||||
| chr6:160749823 | A | G | 74 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0053 others(71): Show |
76 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.2126-2292A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749823 | |||||||
| chr6:160749903 | G | GCCACCAC others(8): Show |
272 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(269): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.2126-2203_2126-220 others(19): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160749903 | ||||||
| chr6:160749968 | C | A | 1 | a0001c0028t0004g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2126-2147C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160749968 | |||||||
| chr6:160750059 | T | G | 1 | a0001c0001t0020g0289 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2126-2056T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750059 | |||||||
| chr6:160750081 | T | C | 12 | a0001c0001t0007g0288 a0001c0021t0004g0014 a0001c0028t0004g0227 others(9): Show |
13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2126-2034T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750081 | |||||||
| chr6:160750238 | C | T | 1 | a0001c0009t0004g0026 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2126-1877C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750238 | |||||||
| chr6:160750268 | C | A | 1 | a0001c0001t0001g0098 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2126-1847C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750268 | |||||||
| chr6:160750282 | C | G | 1 | a0001c0015t0001g0340 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2126-1833C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750282 | |||||||
| chr6:160750331 | T | C | 12 | a0001c0001t0007g0288 a0001c0021t0004g0014 a0001c0028t0004g0227 others(9): Show |
13 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2126-1784T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750331 | |||||||
| chr6:160750497 | A | G | 1 | a0001c0002t0001g0071 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2126-1618A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750497 | |||||||
| chr6:160750534 | A | G | 1 | a0001c0006t0014g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2126-1581A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750534 | |||||||
| chr6:160750632 | C | G | 298 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(295): Show |
332 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(329): Show |
intron_variant | MODIFIER | c.2126-1483C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750632 | |||||||
| chr6:160750650 | T | A | 22 | a0001c0005t0011g0110 a0002c0004t0003g0001 a0002c0004t0003g0010 others(19): Show |
32 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.2126-1465T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750650 | |||||||
| chr6:160750660 | T | C | 1 | a0001c0028t0004g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2126-1455T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750660 | |||||||
| chr6:160750754 | G | A | 10 | a0001c0001t0007g0288 a0002c0007t0007g0036 a0002c0007t0007g0037 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2126-1361G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750754 | |||||||
| chr6:160750825 | T | C | 13 | a0001c0005t0002g0102 a0001c0005t0002g0104 a0001c0005t0002g0105 others(10): Show |
13 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.2126-1290T>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750825 | |||||||
| chr6:160750887 | C | T | 260 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(257): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.2126-1228C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750887 | |||||||
| chr6:160750982 | TCA | T | 15 | a0001c0005t0005g0234 a0001c0006t0005g0018 a0001c0006t0005g0093 others(12): Show |
16 | HG01106.hp1 HG01256.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2126-1131_2126-113 others(6): Show |
PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr6 | 160750982 | ||||||
| chr6:160750985 | C | G | 15 | a0001c0005t0005g0234 a0001c0006t0005g0018 a0001c0006t0005g0093 others(12): Show |
16 | HG01106.hp1 HG01256.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2126-1130C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750985 | |||||||
| chr6:160750987 | C | A | 15 | a0001c0005t0005g0234 a0001c0006t0005g0018 a0001c0006t0005g0093 others(12): Show |
16 | HG01106.hp1 HG01256.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2126-1128C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750987 | |||||||
| chr6:160750989 | C | T | 15 | a0001c0005t0005g0234 a0001c0006t0005g0018 a0001c0006t0005g0093 others(12): Show |
16 | HG01106.hp1 HG01256.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2126-1126C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160750989 | |||||||
| chr6:160751111 | G | C | 1 | a0001c0028t0004g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2126-1004G>C | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751111 | |||||||
| chr6:160751239 | C | A | 3 | a0001c0009t0004g0044 a0003c0020t0004g0326 a0003c0020t0004g0332 |
3 | HG01256.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2126-876C>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751239 | |||||||
| chr6:160751240 | A | G | 3 | a0001c0009t0004g0044 a0003c0020t0004g0326 a0003c0020t0004g0332 |
3 | HG01256.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2126-875A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751240 | |||||||
| chr6:160751241 | A | T | 3 | a0001c0009t0004g0044 a0003c0020t0004g0326 a0003c0020t0004g0332 |
3 | HG01256.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2126-874A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751241 | |||||||
| chr6:160751242 | A | T | 3 | a0001c0009t0004g0044 a0003c0020t0004g0326 a0003c0020t0004g0332 |
3 | HG01256.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2126-873A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751242 | |||||||
| chr6:160751243 | G | T | 3 | a0001c0009t0004g0044 a0003c0020t0004g0326 a0003c0020t0004g0332 |
3 | HG01256.hp1 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2126-872G>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751243 | |||||||
| chr6:160751265 | A | G | 2 | a0001c0002t0001g0049 a0001c0002t0001g0139 |
2 | HG02735.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2126-850A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751265 | |||||||
| chr6:160751278 | C | G | 5 | a0001c0001t0001g0039 a0001c0001t0001g0054 a0001c0001t0001g0074 others(2): Show |
5 | HG01934.hp2 HG02559.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2126-837C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751278 | |||||||
| chr6:160751279 | G | A | 1 | a0002c0022t0003g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2126-836G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751279 | |||||||
| chr6:160751342 | C | T | 3 | a0001c0001t0001g0065 a0001c0001t0001g0186 a0001c0002t0001g0160 |
3 | HG03942.hp1 NA18954.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.2126-773C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751342 | |||||||
| chr6:160751385 | A | G | 1 | a0001c0006t0014g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2126-730A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751385 | |||||||
| chr6:160751403 | G | A | 1 | a0001c0001t0001g0320 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2126-712G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751403 | |||||||
| chr6:160751526 | A | T | 3 | a0005c0010t0004g0019 a0005c0010t0004g0235 a0005c0010t0004g0236 |
4 | HG02280.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2126-589A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751526 | |||||||
| chr6:160751773 | T | G | 1 | a0002c0022t0003g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2126-342T>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751773 | |||||||
| chr6:160751910 | C | G | 270 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(267): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.2126-205C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751910 | |||||||
| chr6:160751961 | A | T | 1 | a0001c0001t0001g0258 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2126-154A>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160751961 | |||||||
| chr6:160752040 | G | A | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG00544.hp2 NA18944.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2126-75G>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160752040 | |||||||
| chr6:160752060 | C | G | 12 | a0001c0008t0001g0218 a0001c0008t0001g0231 a0001c0008t0001g0290 others(9): Show |
13 | HG02559.hp2 HG02572.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2126-55C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160752060 | |||||||
| chr6:160752069 | T | A | 1 | a0001c0001t0001g0219 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2126-46T>A | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 17/18 | chr6 | 160752069 | |||||||
| chr6:160752317 | C | T | 1 | a0001c0002t0001g0011 | 2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2271+57C>T | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 18/18 | chr6 | 160752317 | |||||||
| chr6:160752578 | A | G | 270 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(267): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.2271+318A>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 18/18 | chr6 | 160752578 | |||||||
| chr6:160752696 | C | G | 4 | a0001c0005t0002g0243 a0001c0005t0002g0294 a0001c0005t0002g0295 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.2272-204C>G | PLG | ENSG00000122194.20 | transcript | ENST00000308192.14 | protein_coding | 18/18 | chr6 | 160752696 |