Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55218 |
| ensemblid | ENSG00000081177.19 |
| hgncid | 20217 |
| symbol | EXD2 |
| name | exonuclease 3'-5' domain containing 2 |
| refseq_nuc | NM_001193360.2 |
| refseq_prot | NP_001180289.1 |
| ensembl_nuc | ENST00000685843.1 |
| ensembl_prot | ENSP00000510642.1 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 69191498 |
| end | 69244018 |
| strand | + |
| ver | v1.2 |
| region | chr14:69191498-69244018 |
| region5000 | chr14:69186498-69249018 |
| regionname0 | EXD2_chr14_69191498_69244018 |
| regionname5000 | EXD2_chr14_69186498_69249018 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 621 | 168 | 67 | 38 | 22 | 8 | 32 | 18 | EXD2_chr14_69186498_69249018 | EXD2 | MSRQN others(616): Show |
chr14 | 69186498 | 69249018 |
| a0002 | 1/0 | 621 | 64 | 25 | 16 | 9 | 5 | 8 | 7 | EXD2_chr14_69186498_69249018 | EXD2 | MSRQN others(616): Show |
chr14 | 69186498 | 69249018 |
| a0003 | 0/0 | 621 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | MSRQN others(616): Show |
chr14 | 69186498 | 69249018 |
| a0004 | 0/0 | 621 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | MSRQN others(616): Show |
chr14 | 69186498 | 69249018 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1863 | 101 | 53 | 21 | 5 | 5 | 17 | EXD2_chr14_69186498_69249018 | EXD2 | ATGTC others(1858): Show |
chr14 | 69186498 | 69249018 | ||
| a0001c0003 | 0/1 | 1863 | 59 | 9 | 15 | 17 | 3 | 14 | EXD2_chr14_69186498_69249018 | EXD2 | ATGTC others(1858): Show |
chr14 | 69186498 | 69249018 | ||
| a0001c0004 | 0/0 | 1863 | 5 | 3 | 2 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | ATGTC others(1858): Show |
chr14 | 69186498 | 69249018 | ||
| a0001c0007 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | ATGTC others(1858): Show |
chr14 | 69186498 | 69249018 | ||
| a0001c0008 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | ATGTC others(1858): Show |
chr14 | 69186498 | 69249018 | ||
| a0001c0009 | 0/0 | 1863 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | ATGTC others(1858): Show |
chr14 | 69186498 | 69249018 | ||
| a0002c0002 | 1/0 | 1863 | 64 | 25 | 16 | 9 | 5 | 8 | EXD2_chr14_69186498_69249018 | EXD2 | ATGTC others(1858): Show |
chr14 | 69186498 | 69249018 | ||
| a0003c0005 | 0/0 | 1863 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | ATGTC others(1858): Show |
chr14 | 69186498 | 69249018 | ||
| a0004c0006 | 0/0 | 1863 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | ATGTC others(1858): Show |
chr14 | 69186498 | 69249018 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 5009 | 48 | 15 | 16 | 1 | 2 | 14 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0001c0001t0003 | 0/0 | 5009 | 22 | 20 | 2 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0001c0001t0005 | 0/0 | 5009 | 11 | 1 | 3 | 4 | 3 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0001c0001t0006 | 0/0 | 5009 | 8 | 8 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0001c0001t0008 | 0/0 | 5009 | 3 | 3 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0001c0001t0010 | 0/0 | 5009 | 2 | 2 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0001c0001t0012 | 0/0 | 5007 | 2 | 0 | 0 | 0 | 0 | 2 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5002): Show |
chr14 | 69186498 | 69249018 |
| a0001c0001t0014 | 0/0 | 5009 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0001c0001t0015 | 0/0 | 5009 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0001c0001t0016 | 0/0 | 5009 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0001c0001t0017 | 0/0 | 5009 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0001c0001t0019 | 0/0 | 5009 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0001c0003t0001 | 0/1 | 5009 | 55 | 6 | 15 | 17 | 3 | 13 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0001c0003t0006 | 0/0 | 5009 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0001c0003t0009 | 0/0 | 5009 | 2 | 2 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0001c0003t0020 | 0/0 | 5009 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0001c0004t0007 | 0/0 | 5009 | 5 | 3 | 2 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0001c0007t0006 | 0/0 | 5009 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0001c0008t0021 | 0/0 | 5009 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0001c0009t0002 | 0/0 | 5009 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0002c0002t0001 | 1/0 | 5009 | 44 | 9 | 13 | 9 | 5 | 7 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0002c0002t0004 | 0/0 | 5009 | 16 | 12 | 3 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0002c0002t0011 | 0/0 | 5009 | 2 | 2 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0002c0002t0013 | 0/0 | 5009 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0002c0002t0018 | 0/0 | 5009 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0003c0005t0001 | 0/0 | 5009 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| a0004c0006t0002 | 0/0 | 5009 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | AGTGA others(5004): Show |
chr14 | 69186498 | 69249018 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0003g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0003g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0005g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0005g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0006g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0008g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0008g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0008g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0010g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0010g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0012g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0012g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0014g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0015g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0016g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0017g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0001t0019g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0018 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0009g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0003t0020g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0004t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0004t0007g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0004t0007g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0004t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0004t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0007t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0008t0021g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0001c0009t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0001g0209 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0004g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0011g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0011g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0013g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0002c0002t0018g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0003c0005t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| a0004c0006t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0084 | EUR | GBR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0015 | EUR | GBR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0103 | EUR | GBR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG00140 | hp2 | a0001 | c0003 | t0001 | g0022 | EUR | GBR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0196 | EUR | FIN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0039 | EUR | FIN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0082 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0023 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0197 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0067 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0157 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0049 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01069 | hp1 | a0002 | c0002 | t0004 | g0180 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0191 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0008 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0015 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0164 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0205 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01081 | hp2 | a0001 | c0004 | t0007 | g0169 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0204 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0074 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01175 | hp1 | a0002 | c0002 | t0004 | g0178 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0078 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01192 | hp2 | a0002 | c0002 | t0004 | g0186 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0137 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0003 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0021 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0052 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0158 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0059 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01496 | hp1 | a0001 | c0004 | t0007 | g0170 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0193 | AMR | CLM | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0155 | EUR | IBS | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0195 | EUR | IBS | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0156 | EUR | IBS | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0192 | EUR | IBS | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0136 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01934 | hp1 | a0001 | c0003 | t0001 | g0056 | AMR | PEL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0208 | AMR | PEL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0081 | AMR | PEL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | PEL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01981 | hp1 | a0001 | c0003 | t0001 | g0061 | AMR | PEL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0203 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | KHV | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0043 | EAS | KHV | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02135 | hp2 | a0001 | c0003 | t0001 | g0070 | EAS | KHV | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0212 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | CDX | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02155 | hp2 | a0001 | c0003 | t0001 | g0051 | EAS | CDX | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02257 | hp1 | a0001 | c0001 | t0014 | g0106 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0057 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02258 | hp1 | a0002 | c0002 | t0004 | g0013 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0130 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0200 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0199 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02451 | hp2 | a0001 | c0004 | t0007 | g0168 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02572 | hp1 | a0001 | c0001 | t0016 | g0108 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02572 | hp2 | a0001 | c0001 | t0019 | g0147 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02602 | hp1 | a0001 | c0003 | t0001 | g0041 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02615 | hp1 | a0002 | c0002 | t0004 | g0182 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02615 | hp2 | a0002 | c0002 | t0004 | g0179 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02622 | hp1 | a0001 | c0004 | t0007 | g0171 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0133 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0077 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02683 | hp1 | a0001 | c0003 | t0001 | g0083 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02717 | hp1 | a0002 | c0002 | t0004 | g0174 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0128 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0132 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02735 | hp1 | a0001 | c0003 | t0001 | g0040 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0110 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0211 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0198 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02895 | hp1 | a0001 | c0001 | t0010 | g0149 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02895 | hp2 | a0002 | c0002 | t0004 | g0175 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02896 | hp2 | a0002 | c0002 | t0011 | g0019 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02897 | hp1 | a0002 | c0002 | t0011 | g0020 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02897 | hp2 | a0001 | c0001 | t0010 | g0148 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02922 | hp1 | a0001 | c0003 | t0006 | g0145 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02965 | hp1 | a0001 | c0001 | t0008 | g0144 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0188 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0131 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0047 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03017 | hp2 | a0001 | c0009 | t0002 | g0093 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03041 | hp1 | a0002 | c0002 | t0004 | g0183 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03041 | hp2 | a0002 | c0002 | t0013 | g0201 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0162 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0071 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0213 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0206 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0165 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0214 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03225 | hp1 | a0001 | c0004 | t0007 | g0172 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03239 | hp2 | a0001 | c0001 | t0012 | g0166 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03453 | hp1 | a0001 | c0008 | t0021 | g0210 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03453 | hp2 | a0002 | c0002 | t0004 | g0176 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03486 | hp1 | a0001 | c0003 | t0009 | g0007 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0143 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0014 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03492 | hp1 | a0001 | c0003 | t0001 | g0050 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0014 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03516 | hp1 | a0002 | c0002 | t0018 | g0173 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0135 | AFR | ESN | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0129 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0054 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03669 | hp1 | a0001 | c0001 | t0015 | g0121 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0202 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0029 | SAS | STU | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03688 | hp2 | a0001 | c0003 | t0020 | g0080 | SAS | STU | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0189 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03710 | hp1 | a0001 | c0003 | t0001 | g0024 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0098 | SAS | BEB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0068 | SAS | BEB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03942 | hp1 | a0001 | c0003 | t0001 | g0053 | SAS | BEB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0190 | SAS | BEB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG04115 | hp1 | a0002 | c0002 | t0004 | g0185 | SAS | STU | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0118 | SAS | STU | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0005 | SAS | BEB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0005 | SAS | BEB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0034 | SAS | STU | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | STU | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | STU | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG04204 | hp2 | a0001 | c0003 | t0001 | g0003 | SAS | STU | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG04228 | hp1 | a0001 | c0001 | t0012 | g0167 | SAS | STU | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0006 | SAS | STU | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA18522 | hp1 | a0002 | c0002 | t0004 | g0013 | AFR | YRI | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | YRI | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA18906 | hp1 | a0002 | c0002 | t0004 | g0181 | AFR | YRI | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | YRI | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA18940 | hp1 | a0001 | c0003 | t0001 | g0075 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA18940 | hp2 | a0001 | c0001 | t0005 | g0159 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA18945 | hp1 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA18949 | hp1 | a0001 | c0003 | t0001 | g0079 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA18956 | hp1 | a0001 | c0003 | t0001 | g0044 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA18956 | hp2 | a0001 | c0003 | t0001 | g0154 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0153 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA18967 | hp2 | a0001 | c0003 | t0001 | g0060 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA18983 | hp1 | a0001 | c0001 | t0005 | g0152 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA18983 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA18989 | hp1 | a0001 | c0003 | t0001 | g0161 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA18989 | hp2 | a0003 | c0005 | t0001 | g0073 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA19002 | hp1 | a0001 | c0003 | t0001 | g0048 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA19030 | hp1 | a0001 | c0007 | t0006 | g0109 | AFR | LWK | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | LWK | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA19043 | hp1 | a0002 | c0002 | t0004 | g0177 | AFR | LWK | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0062 | AFR | LWK | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA19063 | hp2 | a0001 | c0003 | t0001 | g0069 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA19070 | hp1 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA19070 | hp2 | a0001 | c0001 | t0005 | g0160 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA19080 | hp1 | a0001 | c0003 | t0001 | g0072 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA19081 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA19090 | hp2 | a0001 | c0003 | t0001 | g0058 | EAS | JPT | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | YRI | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA19240 | hp2 | a0001 | c0001 | t0017 | g0163 | AFR | YRI | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA20129 | hp1 | a0001 | c0003 | t0009 | g0007 | AFR | ASW | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0207 | AFR | ASW | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0194 | EUR | TSI | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0055 | EUR | TSI | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0065 | EUR | TSI | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA20805 | hp2 | a0004 | c0006 | t0002 | g0094 | EUR | TSI | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0101 | SAS | GIH | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | GIH | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0037 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0134 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | ACB | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03471 | hp1 | a0002 | c0002 | t0004 | g0184 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | MSL | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0215 | AFR | USA | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| HG06807 | hp2 | a0002 | c0002 | t0004 | g0187 | AFR | USA | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0216 | AFR | USA | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | USA | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0100 | AFR | LWK | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0066 | AFR | LWK | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0018 | REF | REF | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0209 | REF | REF | EXD2_chr14_69186498_69249018 | EXD2 | chr14 | 69186498 | 69249018 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:69209744 | G | A | 1 | a0003 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.274G>A | p.Glu92Lys | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/10 | 499/5009 | 274/1866 | 92/621 | chr14 | 69209744 | |||
| chr14:69230572 | G | A | 1 | a0004 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.691G>A | p.Asp231Asn | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/10 | 916/5009 | 691/1866 | 231/621 | chr14 | 69230572 | |||
| chr14:69237836 | G | T | 3 | a0001 a0003 a0004 |
169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
missense_variant | MODERATE | c.1554G>T | p.Gln518His | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/10 | 1779/5009 | 1554/1866 | 518/621 | chr14 | 69237836 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:69228866 | C | T | 1 | a0001c0009 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.384C>T | p.Ser128Ser | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/10 | 609/5009 | 384/1866 | 128/621 | chr14 | 69228866 | |||
| chr14:69230505 | G | A | 1 | a0001c0004 | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
synonymous_variant | LOW | c.624G>A | p.Lys208Lys | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/10 | 849/5009 | 624/1866 | 208/621 | chr14 | 69230505 | |||
| chr14:69236441 | A | G | 2 | a0001c0003 a0003c0005 |
59 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(56): Show |
synonymous_variant | LOW | c.1191A>G | p.Leu397Leu | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/10 | 1416/5009 | 1191/1866 | 397/621 | chr14 | 69236441 | |||
| chr14:69237617 | C | T | 1 | a0001c0008 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1335C>T | p.Ile445Ile | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/10 | 1560/5009 | 1335/1866 | 445/621 | chr14 | 69237617 | |||
| chr14:69241046 | C | T | 1 | a0001c0007 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1812C>T | p.Asn604Asn | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 2037/5009 | 1812/1866 | 604/621 | chr14 | 69241046 | |||
| chr14:69241070 | C | T | 1 | a0001c0004 | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
synonymous_variant | LOW | c.1836C>T | p.Phe612Phe | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 2061/5009 | 1836/1866 | 612/621 | chr14 | 69241070 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:69191572 | G | A | 1 | a0001c0003t0009 | 2 | HG03486.hp1 NA20129.hp1 |
5_prime_UTR_variant | MODIFIER | c.-151G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/10 | 17899 | chr14 | 69191572 | ||||||
| chr14:69203941 | C | T | 1 | a0001c0008t0021 | 1 | HG03453.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-107C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/10 | chr14 | 69203941 | |||||||
| chr14:69203955 | C | G | 1 | a0001c0004t0007 | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-93C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/10 | 5516 | chr14 | 69203955 | ||||||
| chr14:69241346 | G | A | 1 | a0002c0002t0013 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*246G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 246 | chr14 | 69241346 | ||||||
| chr14:69241486 | CAG | C | 1 | a0001c0001t0012 | 2 | HG03239.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*387_*388delAG | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 387 | chr14 | 69241486 | ||||||
| chr14:69241524 | G | A | 7 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0014 others(4): Show |
55 | HG00140.hp1 HG00642.hp2 HG00733.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*424G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 424 | chr14 | 69241524 | ||||||
| chr14:69241526 | A | C | 1 | a0001c0001t0016 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*426A>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 426 | chr14 | 69241526 | ||||||
| chr14:69241661 | T | C | 1 | a0001c0008t0021 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*561T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 561 | chr14 | 69241661 | ||||||
| chr14:69241750 | T | C | 1 | a0001c0001t0010 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*650T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 650 | chr14 | 69241750 | ||||||
| chr14:69242047 | G | C | 1 | a0001c0001t0017 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*947G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 947 | chr14 | 69242047 | ||||||
| chr14:69242392 | T | G | 1 | a0002c0002t0018 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1292T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 1292 | chr14 | 69242392 | ||||||
| chr14:69242499 | G | A | 1 | a0001c0001t0012 | 2 | HG03239.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1399G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 1399 | chr14 | 69242499 | ||||||
| chr14:69242656 | G | A | 19 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(16): Show |
112 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*1556G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 1556 | chr14 | 69242656 | ||||||
| chr14:69242699 | C | T | 1 | a0002c0002t0004 | 16 | HG01069.hp1 HG01175.hp1 HG01192.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1599C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 1599 | chr14 | 69242699 | ||||||
| chr14:69242918 | T | G | 1 | a0001c0001t0019 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1818T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 1818 | chr14 | 69242918 | ||||||
| chr14:69243212 | C | T | 10 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0008 others(7): Show |
81 | HG00140.hp1 HG00642.hp2 HG00733.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2112C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 2112 | chr14 | 69243212 | ||||||
| chr14:69243249 | C | T | 1 | a0001c0004t0007 | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2149C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 2149 | chr14 | 69243249 | ||||||
| chr14:69243445 | G | A | 1 | a0001c0004t0007 | 5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2345G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 2345 | chr14 | 69243445 | ||||||
| chr14:69243468 | C | G | 1 | a0001c0001t0015 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2368C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 2368 | chr14 | 69243468 | ||||||
| chr14:69243470 | C | T | 1 | a0001c0001t0008 | 3 | HG02818.hp2 HG02965.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2370C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 2370 | chr14 | 69243470 | ||||||
| chr14:69243540 | C | G | 3 | a0001c0001t0005 a0001c0001t0017 a0002c0002t0011 |
14 | HG00280.hp2 HG00738.hp1 HG01074.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2440C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 2440 | chr14 | 69243540 | ||||||
| chr14:69243691 | A | G | 1 | a0001c0003t0020 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2591A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 2591 | chr14 | 69243691 | ||||||
| chr14:69243990 | G | A | 1 | a0001c0001t0014 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2890G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 10/10 | 2890 | chr14 | 69243990 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:69191678 | G | A | 1 | a0002c0002t0001g0017 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-132+87G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69191678 | |||||||
| chr14:69191810 | T | C | 2 | a0002c0002t0011g0019 a0002c0002t0011g0020 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-132+219T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69191810 | |||||||
| chr14:69191983 | C | T | 5 | a0001c0001t0006g0212 a0001c0001t0006g0213 a0001c0001t0006g0214 others(2): Show |
5 | HG02145.hp1 HG03130.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-132+392C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69191983 | |||||||
| chr14:69192016 | T | A | 162 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(159): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-132+425T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69192016 | |||||||
| chr14:69192052 | C | T | 3 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0017g0163 |
3 | HG01074.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-132+461C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69192052 | |||||||
| chr14:69192295 | A | G | 1 | a0001c0001t0006g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-132+704A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69192295 | |||||||
| chr14:69192317 | C | T | 1 | a0001c0008t0021g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-132+726C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69192317 | |||||||
| chr14:69192503 | CAG | C | 162 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(159): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-132+914_-132+915d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69192503 | ||||||
| chr14:69192509 | T | A | 4 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0023 others(1): Show |
4 | HG00140.hp2 HG00639.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-132+918T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69192509 | |||||||
| chr14:69192647 | T | G | 8 | a0001c0001t0012g0166 a0001c0001t0012g0167 a0001c0004t0007g0168 others(5): Show |
8 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-132+1056T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69192647 | |||||||
| chr14:69192834 | G | C | 1 | a0001c0001t0003g0025 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-132+1243G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69192834 | |||||||
| chr14:69192902 | G | A | 14 | a0002c0002t0001g0017 a0002c0002t0001g0026 a0002c0002t0001g0027 others(11): Show |
14 | HG01361.hp2 HG02055.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.-132+1311G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69192902 | |||||||
| chr14:69192942 | G | A | 162 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(159): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-132+1351G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69192942 | |||||||
| chr14:69193029 | G | A | 1 | a0001c0001t0005g0039 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-132+1438G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193029 | |||||||
| chr14:69193040 | A | C | 162 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(159): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-132+1449A>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193040 | |||||||
| chr14:69193050 | T | TTC | 53 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(50): Show |
59 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.-132+1469_-132+147 others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69193050 | ||||||
| chr14:69193060 | C | CT | 29 | a0001c0001t0002g0151 a0001c0001t0005g0152 a0001c0001t0005g0153 others(26): Show |
29 | HG00738.hp1 HG01074.hp2 HG01361.hp1 others(26): Show |
intron_variant | MODIFIER | c.-132+1485dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69193060 | ||||||
| chr14:69193060 | C | CTT | 5 | a0001c0001t0006g0212 a0001c0001t0006g0213 a0001c0001t0006g0214 others(2): Show |
5 | HG02145.hp1 HG03130.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-132+1484_-132+148 others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69193060 | ||||||
| chr14:69193061 | T | TC | 2 | a0001c0001t0005g0039 a0001c0003t0001g0040 |
2 | HG00280.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.-132+1470_-132+147 others(5): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193061 | |||||||
| chr14:69193118 | G | A | 1 | a0001c0008t0021g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-132+1527G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193118 | |||||||
| chr14:69193128 | A | G | 162 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(159): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-132+1537A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193128 | |||||||
| chr14:69193245 | G | C | 1 | a0001c0001t0003g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-132+1654G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193245 | |||||||
| chr14:69193259 | G | A | 2 | a0001c0001t0012g0166 a0001c0001t0012g0167 |
2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-132+1668G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193259 | |||||||
| chr14:69193275 | T | C | 1 | a0001c0003t0001g0041 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-132+1684T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193275 | |||||||
| chr14:69193279 | A | G | 162 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(159): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-132+1688A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193279 | |||||||
| chr14:69193328 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-132+1737G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193328 | |||||||
| chr14:69193339 | G | A | 1 | a0001c0001t0017g0163 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-132+1748G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193339 | |||||||
| chr14:69193825 | TA | T | 8 | a0001c0001t0012g0166 a0001c0001t0012g0167 a0001c0004t0007g0168 others(5): Show |
8 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-132+2237delA | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69193825 | ||||||
| chr14:69193863 | A | G | 1 | a0001c0008t0021g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-132+2272A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69193863 | |||||||
| chr14:69194142 | CT | C | 157 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(154): Show |
169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.-132+2565delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69194142 | ||||||
| chr14:69194345 | T | C | 170 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(167): Show |
182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.-132+2754T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69194345 | |||||||
| chr14:69194417 | T | C | 162 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(159): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-132+2826T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69194417 | |||||||
| chr14:69194496 | CT | C | 45 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(42): Show |
49 | HG00140.hp1 HG00642.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.-132+2913delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69194496 | ||||||
| chr14:69194948 | G | T | 1 | a0002c0002t0018g0173 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-132+3357G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69194948 | |||||||
| chr14:69194954 | T | C | 162 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(159): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-132+3363T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69194954 | |||||||
| chr14:69194990 | G | A | 1 | a0001c0008t0021g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-132+3399G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69194990 | |||||||
| chr14:69195092 | C | T | 162 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(159): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-132+3501C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69195092 | |||||||
| chr14:69195204 | G | A | 162 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(159): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-132+3613G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69195204 | |||||||
| chr14:69195216 | C | CA | 15 | a0002c0002t0004g0013 a0002c0002t0004g0174 a0002c0002t0004g0175 others(12): Show |
16 | HG01069.hp1 HG01175.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.-132+3641dupA | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69195216 | ||||||
| chr14:69195229 | AAAAG | A | 160 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(157): Show |
172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.-132+3640_-132+364 others(8): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69195229 | ||||||
| chr14:69195356 | C | T | 1 | a0001c0008t0021g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-132+3765C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69195356 | |||||||
| chr14:69195388 | A | G | 162 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(159): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-132+3797A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69195388 | |||||||
| chr14:69195400 | C | T | 162 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(159): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-132+3809C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69195400 | |||||||
| chr14:69195443 | C | T | 1 | a0001c0001t0006g0216 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-132+3852C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69195443 | |||||||
| chr14:69195491 | G | C | 1 | a0001c0008t0021g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-132+3900G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69195491 | |||||||
| chr14:69195608 | G | A | 162 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(159): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-132+4017G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69195608 | |||||||
| chr14:69195893 | A | G | 162 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(159): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-132+4302A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69195893 | |||||||
| chr14:69196250 | A | T | 1 | a0001c0003t0001g0084 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-132+4659A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69196250 | |||||||
| chr14:69196375 | C | T | 162 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(159): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-132+4784C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69196375 | |||||||
| chr14:69196584 | T | C | 2 | a0001c0001t0012g0166 a0001c0001t0012g0167 |
2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-132+4993T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69196584 | |||||||
| chr14:69196622 | CT | C | 115 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
122 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.-132+5048delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69196622 | ||||||
| chr14:69196622 | CTT | C | 51 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(48): Show |
56 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-132+5047_-132+504 others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69196622 | ||||||
| chr14:69196647 | A | G | 1 | a0001c0001t0003g0150 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-132+5056A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69196647 | |||||||
| chr14:69196689 | T | A | 3 | a0001c0001t0002g0009 a0001c0001t0002g0087 a0001c0001t0002g0088 |
4 | HG00733.hp2 HG01106.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.-132+5098T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69196689 | |||||||
| chr14:69196726 | C | T | 1 | a0001c0001t0006g0188 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-132+5135C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69196726 | |||||||
| chr14:69196762 | T | A | 1 | a0001c0001t0002g0042 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-132+5171T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69196762 | |||||||
| chr14:69196786 | C | T | 2 | a0001c0001t0010g0148 a0001c0001t0010g0149 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-132+5195C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69196786 | |||||||
| chr14:69196792 | AT | A | 105 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(102): Show |
111 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(108): Show |
intron_variant | MODIFIER | c.-132+5215delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69196792 | ||||||
| chr14:69196833 | G | A | 7 | a0001c0001t0002g0089 a0001c0001t0002g0090 a0001c0001t0002g0091 others(4): Show |
7 | HG00741.hp2 HG01255.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.-132+5242G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69196833 | |||||||
| chr14:69196883 | G | C | 1 | a0002c0002t0004g0174 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-132+5292G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69196883 | |||||||
| chr14:69197051 | C | T | 8 | a0002c0002t0004g0180 a0002c0002t0004g0181 a0002c0002t0004g0182 others(5): Show |
8 | HG01069.hp1 HG01192.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-132+5460C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69197051 | |||||||
| chr14:69197176 | G | T | 1 | a0002c0002t0001g0038 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-132+5585G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69197176 | |||||||
| chr14:69197412 | T | C | 173 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(170): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.-132+5821T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69197412 | |||||||
| chr14:69197421 | C | CT | 9 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(6): Show |
9 | HG01081.hp2 HG01496.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-132+5840dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69197421 | ||||||
| chr14:69197676 | G | A | 3 | a0001c0001t0002g0009 a0001c0001t0002g0087 a0001c0001t0002g0088 |
4 | HG00733.hp2 HG01106.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.-132+6085G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69197676 | |||||||
| chr14:69197781 | CT | C | 211 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(208): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.-131-6132delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69197781 | ||||||
| chr14:69197839 | T | A | 1 | a0002c0002t0001g0038 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-131-6078T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69197839 | |||||||
| chr14:69197913 | A | T | 55 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(52): Show |
61 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.-131-6004A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69197913 | |||||||
| chr14:69198137 | T | C | 2 | a0001c0001t0006g0188 a0001c0001t0006g0211 |
2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-131-5780T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69198137 | |||||||
| chr14:69198418 | C | T | 55 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(52): Show |
61 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.-131-5499C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69198418 | |||||||
| chr14:69198435 | C | T | 1 | a0002c0002t0004g0187 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-131-5482C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69198435 | |||||||
| chr14:69198525 | T | C | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-5392T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69198525 | |||||||
| chr14:69198529 | C | T | 1 | a0001c0003t0006g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-131-5388C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69198529 | |||||||
| chr14:69198698 | A | C | 1 | a0002c0002t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-131-5219A>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69198698 | |||||||
| chr14:69198762 | C | T | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-5155C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69198762 | |||||||
| chr14:69199115 | A | G | 159 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(156): Show |
171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-131-4802A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199115 | |||||||
| chr14:69199128 | C | T | 55 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(52): Show |
61 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.-131-4789C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199128 | |||||||
| chr14:69199163 | G | A | 1 | a0001c0003t0006g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-131-4754G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199163 | |||||||
| chr14:69199192 | C | T | 2 | a0001c0001t0006g0188 a0001c0001t0006g0211 |
2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-131-4725C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199192 | |||||||
| chr14:69199208 | C | A | 21 | a0001c0001t0005g0039 a0001c0001t0005g0152 a0001c0001t0005g0153 others(18): Show |
21 | HG00280.hp2 HG00738.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.-131-4709C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199208 | |||||||
| chr14:69199358 | T | C | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-4559T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199358 | |||||||
| chr14:69199490 | T | G | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-131-4427T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199490 | |||||||
| chr14:69199545 | G | A | 1 | a0002c0002t0004g0187 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-131-4372G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199545 | |||||||
| chr14:69199599 | A | AT | 22 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0089 others(19): Show |
25 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.-131-4305dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69199599 | ||||||
| chr14:69199599 | AT | A | 16 | a0001c0001t0005g0039 a0001c0001t0005g0152 a0001c0001t0005g0153 others(13): Show |
16 | HG00280.hp2 HG00738.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.-131-4305delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69199599 | ||||||
| chr14:69199698 | A | G | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-4219A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199698 | |||||||
| chr14:69199754 | A | G | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-4163A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199754 | |||||||
| chr14:69199775 | A | G | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-4142A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199775 | |||||||
| chr14:69199808 | G | A | 1 | a0001c0001t0002g0089 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-131-4109G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199808 | |||||||
| chr14:69199854 | A | G | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-4063A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199854 | |||||||
| chr14:69199889 | A | C | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-4028A>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199889 | |||||||
| chr14:69199955 | A | G | 156 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(153): Show |
168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.-131-3962A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69199955 | |||||||
| chr14:69200025 | G | A | 2 | a0001c0001t0012g0166 a0001c0001t0012g0167 |
2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-131-3892G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69200025 | |||||||
| chr14:69200135 | A | G | 159 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(156): Show |
171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-131-3782A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69200135 | |||||||
| chr14:69200149 | G | A | 1 | a0002c0002t0001g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-131-3768G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69200149 | |||||||
| chr14:69200157 | G | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-3760G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69200157 | |||||||
| chr14:69200385 | G | A | 1 | a0001c0001t0006g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-131-3532G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69200385 | |||||||
| chr14:69200405 | A | C | 1 | a0001c0003t0020g0080 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-131-3512A>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69200405 | |||||||
| chr14:69200493 | C | T | 1 | a0002c0002t0004g0174 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-131-3424C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69200493 | |||||||
| chr14:69200709 | CA | C | 170 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(167): Show |
183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.-131-3197delA | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69200709 | ||||||
| chr14:69200799 | C | T | 2 | a0001c0001t0006g0188 a0001c0001t0006g0211 |
2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-131-3118C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69200799 | |||||||
| chr14:69200904 | T | C | 1 | a0001c0008t0021g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-131-3013T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69200904 | |||||||
| chr14:69201132 | G | A | 55 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(52): Show |
61 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.-131-2785G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69201132 | |||||||
| chr14:69201147 | G | A | 2 | a0001c0001t0006g0188 a0001c0001t0006g0211 |
2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-131-2770G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69201147 | |||||||
| chr14:69201276 | C | T | 1 | a0001c0003t0001g0040 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-131-2641C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69201276 | |||||||
| chr14:69201344 | A | G | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-2573A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69201344 | |||||||
| chr14:69201405 | T | A | 1 | a0002c0002t0001g0189 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-131-2512T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69201405 | |||||||
| chr14:69201672 | G | GT | 11 | a0001c0001t0002g0076 a0001c0001t0002g0122 a0001c0001t0003g0141 others(8): Show |
12 | HG00741.hp1 HG01175.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-131-2217dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69201672 | ||||||
| chr14:69201672 | G | GTT | 5 | a0001c0001t0008g0110 a0001c0001t0008g0143 a0001c0001t0008g0144 others(2): Show |
5 | HG02615.hp2 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-131-2218_-131-221 others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69201672 | ||||||
| chr14:69201672 | G | GTTTTTTG others(10): Show |
3 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 |
3 | HG01081.hp2 HG01496.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-131-2239_-131-223 others(21): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69201672 | ||||||
| chr14:69201672 | G | GTTTTTTG others(11): Show |
2 | a0001c0004t0007g0171 a0001c0004t0007g0172 |
2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-131-2239_-131-223 others(22): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69201672 | ||||||
| chr14:69201672 | GT | G | 114 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(111): Show |
127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.-131-2217delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69201672 | ||||||
| chr14:69201672 | GTTTTTTT others(6): Show |
G | 2 | a0002c0002t0001g0035 a0002c0002t0001g0036 |
2 | NA19080.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-131-2229_-131-221 others(17): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69201672 | ||||||
| chr14:69201672 | GTTTTTTT others(7): Show |
G | 12 | a0002c0002t0001g0017 a0002c0002t0001g0026 a0002c0002t0001g0027 others(9): Show |
12 | HG01361.hp2 HG02055.hp2 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.-131-2230_-131-221 others(18): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69201672 | ||||||
| chr14:69201672 | GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0002g0090 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-131-2231_-131-221 others(19): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69201672 | ||||||
| chr14:69201680 | T | G | 1 | a0001c0001t0006g0215 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-131-2237T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69201680 | |||||||
| chr14:69201681 | T | G | 4 | a0001c0001t0006g0212 a0001c0001t0006g0213 a0001c0001t0006g0214 others(1): Show |
4 | HG02145.hp1 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-131-2236T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69201681 | |||||||
| chr14:69201684 | T | G | 2 | a0001c0001t0002g0127 a0001c0003t0001g0044 |
2 | HG01192.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.-131-2233T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69201684 | |||||||
| chr14:69201742 | G | C | 2 | a0001c0001t0002g0117 a0001c0001t0002g0118 |
2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-131-2175G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69201742 | |||||||
| chr14:69202043 | C | T | 1 | a0001c0008t0021g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-131-1874C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202043 | |||||||
| chr14:69202070 | C | T | 15 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0025 others(12): Show |
17 | HG01243.hp1 HG01433.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-131-1847C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202070 | |||||||
| chr14:69202071 | G | T | 1 | a0001c0001t0019g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-131-1846G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202071 | |||||||
| chr14:69202126 | A | G | 2 | a0001c0001t0012g0166 a0001c0001t0012g0167 |
2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-131-1791A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202126 | |||||||
| chr14:69202270 | G | T | 1 | a0001c0001t0002g0116 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-131-1647G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202270 | |||||||
| chr14:69202275 | G | T | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-1642G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202275 | |||||||
| chr14:69202471 | C | T | 188 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(185): Show |
201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.-131-1446C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202471 | |||||||
| chr14:69202496 | G | A | 1 | a0001c0003t0006g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-131-1421G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202496 | |||||||
| chr14:69202592 | T | C | 1 | a0001c0003t0001g0045 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-131-1325T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202592 | |||||||
| chr14:69202690 | C | G | 159 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(156): Show |
171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-131-1227C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202690 | |||||||
| chr14:69202877 | T | C | 1 | a0001c0008t0021g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-131-1040T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202877 | |||||||
| chr14:69202919 | T | C | 15 | a0002c0002t0004g0013 a0002c0002t0004g0174 a0002c0002t0004g0175 others(12): Show |
16 | HG01069.hp1 HG01175.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.-131-998T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202919 | |||||||
| chr14:69202946 | T | C | 1 | a0001c0001t0002g0097 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-131-971T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69202946 | |||||||
| chr14:69203157 | C | T | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-760C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69203157 | |||||||
| chr14:69203229 | GT | G | 6 | a0001c0001t0005g0152 a0001c0001t0005g0153 a0001c0001t0005g0159 others(3): Show |
6 | NA18940.hp2 NA18956.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.-131-682delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69203229 | ||||||
| chr14:69203239 | A | AT | 57 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(54): Show |
63 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.-131-663dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69203239 | ||||||
| chr14:69203239 | AT | A | 10 | a0001c0001t0002g0111 a0001c0001t0010g0148 a0001c0001t0010g0149 others(7): Show |
10 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-131-663delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 69203239 | ||||||
| chr14:69203367 | T | C | 1 | a0001c0003t0001g0046 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-131-550T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69203367 | |||||||
| chr14:69203402 | C | G | 14 | a0002c0002t0001g0017 a0002c0002t0001g0026 a0002c0002t0001g0027 others(11): Show |
14 | HG01361.hp2 HG02055.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.-131-515C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69203402 | |||||||
| chr14:69203517 | C | A | 1 | a0001c0001t0002g0098 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-131-400C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69203517 | |||||||
| chr14:69203595 | A | G | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-322A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69203595 | |||||||
| chr14:69203652 | G | T | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131-265G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69203652 | |||||||
| chr14:69203738 | T | C | 1 | a0001c0008t0021g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-131-179T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 1/9 | chr14 | 69203738 | |||||||
| chr14:69204031 | G | A | 1 | a0001c0001t0006g0212 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-48+31G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69204031 | |||||||
| chr14:69204219 | A | G | 148 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(145): Show |
160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.-48+219A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69204219 | |||||||
| chr14:69204279 | G | A | 1 | a0002c0002t0001g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-48+279G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69204279 | |||||||
| chr14:69204312 | A | G | 1 | a0001c0004t0007g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-48+312A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69204312 | |||||||
| chr14:69204392 | T | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+392T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69204392 | |||||||
| chr14:69204509 | G | A | 1 | a0001c0001t0005g0152 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-48+509G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69204509 | |||||||
| chr14:69204547 | A | G | 8 | a0002c0002t0004g0180 a0002c0002t0004g0181 a0002c0002t0004g0182 others(5): Show |
8 | HG01069.hp1 HG01192.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48+547A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69204547 | |||||||
| chr14:69204626 | A | T | 1 | a0002c0002t0004g0187 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-48+626A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69204626 | |||||||
| chr14:69204669 | G | A | 5 | a0001c0001t0003g0141 a0001c0001t0003g0142 a0001c0001t0008g0110 others(2): Show |
5 | HG01891.hp1 HG02280.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+669G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69204669 | |||||||
| chr14:69204681 | T | TACTGACT others(8): Show |
1 | a0001c0003t0006g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-48+682_-48+683ins others(15): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69204681 | ||||||
| chr14:69204683 | A | G | 1 | a0001c0003t0006g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-48+683A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69204683 | |||||||
| chr14:69204740 | G | T | 1 | a0002c0002t0018g0173 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-48+740G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69204740 | |||||||
| chr14:69205032 | T | C | 173 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(170): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.-48+1032T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69205032 | |||||||
| chr14:69205053 | C | T | 1 | a0001c0003t0001g0041 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-48+1053C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69205053 | |||||||
| chr14:69205129 | T | G | 2 | a0001c0001t0012g0166 a0001c0001t0012g0167 |
2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-48+1129T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69205129 | |||||||
| chr14:69205215 | T | C | 4 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0017g0163 others(1): Show |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+1215T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69205215 | |||||||
| chr14:69205486 | A | T | 1 | a0004c0006t0002g0094 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-48+1486A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69205486 | |||||||
| chr14:69205629 | C | T | 14 | a0002c0002t0001g0017 a0002c0002t0001g0026 a0002c0002t0001g0027 others(11): Show |
14 | HG01361.hp2 HG02055.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.-48+1629C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69205629 | |||||||
| chr14:69205794 | A | G | 1 | a0001c0008t0021g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-48+1794A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69205794 | |||||||
| chr14:69205834 | A | T | 1 | a0001c0001t0019g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-48+1834A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69205834 | |||||||
| chr14:69205992 | C | T | 4 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0017g0163 others(1): Show |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+1992C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69205992 | |||||||
| chr14:69206110 | G | A | 1 | a0001c0001t0005g0153 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-48+2110G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206110 | |||||||
| chr14:69206151 | G | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+2151G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206151 | |||||||
| chr14:69206211 | G | T | 1 | a0001c0001t0005g0160 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-48+2211G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206211 | |||||||
| chr14:69206422 | G | C | 1 | a0001c0001t0012g0166 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-48+2422G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206422 | |||||||
| chr14:69206455 | C | CCTTTTTT others(1): Show |
6 | a0001c0001t0003g0128 a0001c0001t0003g0129 a0001c0001t0003g0141 others(3): Show |
6 | HG01891.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48+2455_-48+2456i others(10): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206455 | |||||||
| chr14:69206455 | C | CCTTTTTT others(2): Show |
7 | a0001c0001t0002g0127 a0001c0001t0003g0011 a0001c0001t0003g0012 others(4): Show |
9 | HG01192.hp1 HG01433.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48+2455_-48+2456i others(11): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206455 | |||||||
| chr14:69206455 | C | CCTTTTTT others(3): Show |
5 | a0001c0001t0003g0133 a0001c0001t0003g0134 a0001c0001t0003g0135 others(2): Show |
5 | HG02145.hp2 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+2455_-48+2456i others(12): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206455 | |||||||
| chr14:69206455 | C | CCTTTTTT others(4): Show |
8 | a0001c0001t0002g0095 a0001c0001t0002g0104 a0001c0001t0002g0151 others(5): Show |
8 | HG01243.hp1 HG01884.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48+2455_-48+2456i others(13): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206455 | |||||||
| chr14:69206455 | C | CCTTTTTT others(5): Show |
10 | a0001c0001t0002g0096 a0001c0001t0002g0098 a0001c0001t0002g0101 others(7): Show |
10 | HG00280.hp2 HG00738.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48+2455_-48+2456i others(14): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206455 | |||||||
| chr14:69206455 | C | CCTTTTTT others(6): Show |
9 | a0001c0001t0002g0086 a0001c0001t0002g0102 a0001c0001t0002g0124 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-48+2455_-48+2456i others(15): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206455 | |||||||
| chr14:69206455 | C | CCTTTTTT others(7): Show |
7 | a0001c0001t0002g0097 a0001c0001t0002g0107 a0001c0001t0003g0138 others(4): Show |
7 | HG01361.hp1 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48+2455_-48+2456i others(16): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206455 | |||||||
| chr14:69206455 | C | CCTTTTTT others(10): Show |
2 | a0001c0001t0005g0165 a0002c0002t0001g0162 |
2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-48+2455_-48+2456i others(19): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206455 | |||||||
| chr14:69206455 | C | CCTTTTTT others(11): Show |
2 | a0001c0001t0005g0164 a0001c0001t0016g0108 |
2 | HG01074.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-48+2455_-48+2456i others(20): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206455 | |||||||
| chr14:69206455 | C | CT | 11 | a0002c0002t0001g0016 a0002c0002t0001g0197 a0002c0002t0001g0198 others(8): Show |
12 | HG00642.hp1 HG00735.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-48+2486dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69206455 | ||||||
| chr14:69206455 | CTT | C | 5 | a0001c0001t0002g0089 a0001c0001t0002g0092 a0001c0001t0002g0118 others(2): Show |
5 | HG00741.hp2 HG01346.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+2485_-48+2486d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69206455 | ||||||
| chr14:69206455 | CTTT | C | 17 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0090 others(14): Show |
20 | HG00642.hp2 HG01074.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.-48+2484_-48+2486d others(5): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69206455 | ||||||
| chr14:69206455 | CTTTT | C | 9 | a0001c0001t0002g0111 a0001c0001t0006g0212 a0001c0001t0006g0213 others(6): Show |
9 | HG02145.hp1 HG02922.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.-48+2483_-48+2486d others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69206455 | ||||||
| chr14:69206455 | CTTTTTTT | C | 16 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(13): Show |
16 | HG01081.hp2 HG01361.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48+2480_-48+2486d others(9): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69206455 | ||||||
| chr14:69206455 | CTTTTTTT others(3): Show |
C | 50 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(47): Show |
56 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.-48+2477_-48+2486d others(12): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69206455 | ||||||
| chr14:69206455 | CTTTTTTT others(4): Show |
C | 2 | a0001c0003t0001g0040 a0001c0003t0001g0047 |
2 | HG02735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-48+2476_-48+2486d others(13): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69206455 | ||||||
| chr14:69206455 | CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0002g0009 a0001c0001t0002g0087 a0001c0001t0002g0088 |
4 | HG00733.hp2 HG01106.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+2474_-48+2486d others(15): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69206455 | ||||||
| chr14:69206455 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0006g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-48+2472_-48+2486d others(17): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69206455 | ||||||
| chr14:69206456 | T | C | 5 | a0001c0001t0002g0103 a0001c0001t0003g0139 a0001c0001t0010g0148 others(2): Show |
5 | HG00140.hp1 HG02559.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+2456T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206456 | |||||||
| chr14:69206458 | T | C | 5 | a0001c0001t0002g0089 a0001c0001t0002g0092 a0001c0001t0002g0118 others(2): Show |
5 | HG00741.hp2 HG01346.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+2458T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206458 | |||||||
| chr14:69206459 | T | C | 15 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0090 others(12): Show |
18 | HG00642.hp2 HG01074.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.-48+2459T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206459 | |||||||
| chr14:69206460 | T | C | 9 | a0001c0001t0002g0111 a0001c0001t0006g0212 a0001c0001t0006g0213 others(6): Show |
9 | HG02145.hp1 HG02922.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.-48+2460T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206460 | |||||||
| chr14:69206465 | T | C | 3 | a0001c0003t0001g0060 a0001c0003t0001g0061 a0001c0003t0001g0075 |
3 | HG01981.hp1 NA18940.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.-48+2465T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206465 | |||||||
| chr14:69206466 | T | C | 50 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(47): Show |
56 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.-48+2466T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206466 | |||||||
| chr14:69206467 | T | C | 2 | a0001c0003t0001g0040 a0001c0003t0001g0047 |
2 | HG02735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-48+2467T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206467 | |||||||
| chr14:69206469 | T | C | 3 | a0001c0001t0002g0009 a0001c0001t0002g0087 a0001c0001t0002g0088 |
4 | HG00733.hp2 HG01106.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+2469T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206469 | |||||||
| chr14:69206574 | G | A | 2 | a0001c0001t0012g0166 a0001c0001t0012g0167 |
2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-48+2574G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206574 | |||||||
| chr14:69206643 | G | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+2643G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206643 | |||||||
| chr14:69206790 | A | G | 1 | a0001c0001t0005g0159 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-47-2634A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206790 | |||||||
| chr14:69206964 | C | T | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-2460C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69206964 | |||||||
| chr14:69207114 | A | G | 1 | a0001c0003t0009g0007 | 2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-47-2310A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69207114 | |||||||
| chr14:69207233 | C | A | 2 | a0001c0003t0001g0048 a0001c0003t0001g0075 |
2 | NA18940.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-47-2191C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69207233 | |||||||
| chr14:69207339 | C | T | 14 | a0002c0002t0001g0017 a0002c0002t0001g0026 a0002c0002t0001g0027 others(11): Show |
14 | HG01361.hp2 HG02055.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.-47-2085C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69207339 | |||||||
| chr14:69207473 | G | A | 20 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(17): Show |
22 | HG01192.hp1 HG01243.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.-47-1951G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69207473 | |||||||
| chr14:69207615 | T | C | 1 | a0002c0002t0004g0180 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-47-1809T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69207615 | |||||||
| chr14:69207635 | G | A | 55 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(52): Show |
61 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.-47-1789G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69207635 | |||||||
| chr14:69207893 | C | CT | 34 | a0001c0001t0002g0009 a0001c0001t0002g0086 a0001c0001t0002g0087 others(31): Show |
35 | HG00140.hp1 HG00733.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.-47-1516dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69207893 | ||||||
| chr14:69207972 | G | C | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-1452G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69207972 | |||||||
| chr14:69208193 | TGGCCA | T | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-1225_-47-1221d others(7): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69208193 | ||||||
| chr14:69208210 | A | AT | 162 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(159): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-47-1196dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69208210 | ||||||
| chr14:69208210 | A | ATT | 10 | a0001c0001t0002g0102 a0001c0001t0002g0122 a0001c0003t0001g0048 others(7): Show |
10 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-47-1197_-47-1196d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 69208210 | ||||||
| chr14:69208233 | C | T | 4 | a0001c0001t0003g0138 a0001c0001t0003g0139 a0001c0001t0003g0150 others(1): Show |
4 | HG01884.hp1 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-1191C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208233 | |||||||
| chr14:69208296 | C | T | 4 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0023 others(1): Show |
4 | HG00140.hp2 HG00639.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-1128C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208296 | |||||||
| chr14:69208356 | G | A | 11 | a0001c0001t0005g0039 a0001c0001t0005g0152 a0001c0001t0005g0153 others(8): Show |
11 | HG00280.hp2 HG00738.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47-1068G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208356 | |||||||
| chr14:69208450 | T | A | 2 | a0002c0002t0001g0190 a0002c0002t0001g0197 |
2 | HG00735.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-47-974T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208450 | |||||||
| chr14:69208463 | G | A | 1 | a0001c0003t0001g0062 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-47-961G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208463 | |||||||
| chr14:69208517 | C | G | 1 | a0002c0002t0001g0037 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-47-907C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208517 | |||||||
| chr14:69208559 | C | G | 2 | a0001c0001t0002g0010 a0001c0001t0002g0115 |
3 | HG02486.hp1 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-47-865C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208559 | |||||||
| chr14:69208651 | A | G | 10 | a0001c0001t0003g0141 a0001c0001t0003g0142 a0001c0001t0008g0110 others(7): Show |
10 | HG01081.hp2 HG01496.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47-773A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208651 | |||||||
| chr14:69208696 | C | T | 1 | a0001c0003t0001g0083 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-47-728C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208696 | |||||||
| chr14:69208800 | C | G | 1 | a0001c0001t0006g0212 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-47-624C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208800 | |||||||
| chr14:69208805 | G | C | 173 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(170): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.-47-619G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208805 | |||||||
| chr14:69208891 | C | T | 4 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0017g0163 others(1): Show |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-533C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69208891 | |||||||
| chr14:69209366 | T | G | 11 | a0001c0001t0005g0039 a0001c0001t0005g0152 a0001c0001t0005g0153 others(8): Show |
11 | HG00280.hp2 HG00738.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.-47-58T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 2/9 | chr14 | 69209366 | |||||||
| chr14:69209824 | TA | T | 41 | a0001c0001t0002g0127 a0001c0001t0003g0011 a0001c0001t0003g0012 others(38): Show |
43 | HG01081.hp2 HG01192.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.333+39delA | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69209824 | ||||||
| chr14:69209874 | C | T | 1 | a0002c0002t0001g0016 | 2 | HG00642.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.333+71C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69209874 | |||||||
| chr14:69209893 | G | A | 1 | a0002c0002t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.333+90G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69209893 | |||||||
| chr14:69210246 | C | G | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+443C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69210246 | |||||||
| chr14:69210263 | C | T | 14 | a0002c0002t0001g0017 a0002c0002t0001g0026 a0002c0002t0001g0027 others(11): Show |
14 | HG01361.hp2 HG02055.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+460C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69210263 | |||||||
| chr14:69210535 | C | T | 2 | a0001c0003t0001g0074 a0001c0003t0001g0082 |
2 | HG00639.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.333+732C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69210535 | |||||||
| chr14:69211794 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.333+1991C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69211794 | |||||||
| chr14:69211815 | G | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+2012G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69211815 | |||||||
| chr14:69211880 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.333+2077G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69211880 | |||||||
| chr14:69211927 | A | G | 1 | a0001c0008t0021g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.333+2124A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69211927 | |||||||
| chr14:69211949 | A | C | 1 | a0001c0008t0021g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.333+2146A>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69211949 | |||||||
| chr14:69212268 | T | C | 1 | a0002c0002t0018g0173 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.333+2465T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212268 | |||||||
| chr14:69212293 | C | G | 1 | a0002c0002t0001g0037 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.333+2490C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212293 | |||||||
| chr14:69212295 | T | G | 1 | a0002c0002t0001g0037 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.333+2492T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212295 | |||||||
| chr14:69212329 | A | T | 1 | a0001c0001t0012g0166 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.333+2526A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212329 | |||||||
| chr14:69212333 | C | T | 1 | a0001c0001t0014g0106 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.333+2530C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212333 | |||||||
| chr14:69212678 | A | C | 1 | a0002c0002t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.333+2875A>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212678 | |||||||
| chr14:69212687 | C | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+2884C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212687 | |||||||
| chr14:69212689 | A | G | 1 | a0001c0001t0005g0039 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.333+2886A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212689 | |||||||
| chr14:69212699 | AT | A | 61 | a0001c0001t0002g0097 a0001c0001t0002g0113 a0001c0001t0002g0115 others(58): Show |
64 | HG01069.hp1 HG01175.hp2 HG01192.hp1 others(61): Show |
intron_variant | MODIFIER | c.333+2922delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69212699 | ||||||
| chr14:69212699 | ATT | A | 115 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(112): Show |
125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.333+2921_333+2922d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69212699 | ||||||
| chr14:69212699 | ATTTT | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+2919_333+2922d others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69212699 | ||||||
| chr14:69212739 | A | T | 12 | a0002c0002t0001g0017 a0002c0002t0001g0026 a0002c0002t0001g0027 others(9): Show |
12 | HG01361.hp2 HG02056.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.333+2936A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212739 | |||||||
| chr14:69212750 | C | A | 2 | a0001c0003t0001g0005 a0001c0003t0001g0049 |
3 | HG00738.hp2 HG04184.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.333+2947C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212750 | |||||||
| chr14:69212910 | G | A | 56 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(53): Show |
62 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.333+3107G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212910 | |||||||
| chr14:69212920 | G | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+3117G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212920 | |||||||
| chr14:69212958 | G | A | 10 | a0001c0001t0002g0001 a0001c0001t0002g0091 a0001c0001t0002g0099 others(7): Show |
12 | HG00642.hp2 HG01074.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.333+3155G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69212958 | |||||||
| chr14:69213054 | G | A | 16 | a0001c0001t0002g0127 a0001c0001t0003g0011 a0001c0001t0003g0012 others(13): Show |
18 | HG01192.hp1 HG01243.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.333+3251G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69213054 | |||||||
| chr14:69213070 | A | G | 1 | a0001c0001t0006g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.333+3267A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69213070 | |||||||
| chr14:69213084 | C | CT | 64 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(61): Show |
70 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.333+3297dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213084 | ||||||
| chr14:69213312 | C | T | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+3509C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69213312 | |||||||
| chr14:69213373 | CT | C | 19 | a0002c0002t0001g0191 a0002c0002t0001g0198 a0002c0002t0001g0199 others(16): Show |
20 | HG01069.hp1 HG01069.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.333+3595delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213373 | ||||||
| chr14:69213373 | CTTTT | C | 6 | a0001c0001t0003g0142 a0001c0001t0005g0159 a0001c0003t0001g0005 others(3): Show |
7 | HG01891.hp1 HG02257.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.333+3592_333+3595d others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213373 | ||||||
| chr14:69213373 | CTTTTT | C | 131 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(128): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.333+3591_333+3595d others(7): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213373 | ||||||
| chr14:69213373 | CTTTTTT | C | 32 | a0001c0001t0002g0095 a0001c0001t0002g0111 a0001c0001t0003g0011 others(29): Show |
34 | HG01243.hp1 HG01361.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.333+3590_333+3595d others(8): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213373 | ||||||
| chr14:69213379 | T | C | 5 | a0001c0001t0006g0212 a0001c0001t0006g0213 a0001c0001t0006g0214 others(2): Show |
5 | HG02145.hp1 HG03130.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.333+3576T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69213379 | |||||||
| chr14:69213537 | A | AT | 13 | a0002c0002t0004g0013 a0002c0002t0004g0174 a0002c0002t0004g0175 others(10): Show |
14 | HG01069.hp1 HG01192.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+3754dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213537 | ||||||
| chr14:69213537 | A | ATTTT | 24 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0089 others(21): Show |
27 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.333+3751_333+3754d others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213537 | ||||||
| chr14:69213537 | A | ATTTTT | 48 | a0001c0001t0002g0091 a0001c0001t0002g0095 a0001c0001t0002g0096 others(45): Show |
49 | HG00280.hp2 HG01074.hp2 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.333+3750_333+3754d others(7): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213537 | ||||||
| chr14:69213537 | A | ATTTTTT | 32 | a0001c0001t0002g0086 a0001c0001t0002g0101 a0001c0001t0002g0103 others(29): Show |
33 | HG00140.hp1 HG00738.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.333+3749_333+3754d others(8): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213537 | ||||||
| chr14:69213537 | A | ATTTTTTT | 57 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(54): Show |
61 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.333+3748_333+3754d others(9): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213537 | ||||||
| chr14:69213537 | A | ATTTTTTT others(1): Show |
8 | a0001c0003t0001g0004 a0001c0003t0001g0005 a0001c0003t0001g0046 others(5): Show |
10 | HG01981.hp1 HG02135.hp2 HG04184.hp1 others(7): Show |
intron_variant | MODIFIER | c.333+3747_333+3754d others(10): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213537 | ||||||
| chr14:69213537 | ATT | A | 5 | a0001c0001t0002g0009 a0001c0001t0002g0087 a0001c0001t0002g0088 others(2): Show |
6 | HG00733.hp2 HG01106.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.333+3753_333+3754d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69213537 | ||||||
| chr14:69213724 | T | C | 188 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(185): Show |
201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.333+3921T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69213724 | |||||||
| chr14:69213808 | T | C | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+4005T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69213808 | |||||||
| chr14:69214037 | ATT | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+4237_333+4238d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69214037 | ||||||
| chr14:69214781 | T | G | 5 | a0001c0001t0003g0138 a0001c0001t0003g0139 a0001c0001t0003g0150 others(2): Show |
5 | HG01884.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+4978T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69214781 | |||||||
| chr14:69214986 | T | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+5183T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69214986 | |||||||
| chr14:69215001 | T | G | 195 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(192): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.333+5198T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215001 | |||||||
| chr14:69215134 | A | G | 2 | a0001c0001t0006g0188 a0001c0001t0006g0211 |
2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.333+5331A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215134 | |||||||
| chr14:69215142 | G | T | 1 | a0001c0001t0002g0146 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.333+5339G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215142 | |||||||
| chr14:69215162 | C | T | 2 | a0001c0001t0006g0188 a0001c0001t0006g0211 |
2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.333+5359C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215162 | |||||||
| chr14:69215243 | G | A | 56 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(53): Show |
62 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.333+5440G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215243 | |||||||
| chr14:69215279 | G | T | 1 | a0001c0001t0002g0096 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.333+5476G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215279 | |||||||
| chr14:69215285 | A | G | 2 | a0001c0003t0001g0055 a0001c0003t0001g0056 |
2 | HG01934.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.333+5482A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215285 | |||||||
| chr14:69215294 | ATATATGT others(3): Show |
A | 4 | a0001c0003t0001g0053 a0001c0003t0001g0054 a0001c0003t0006g0145 others(1): Show |
4 | HG02922.hp1 HG03654.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.333+5493_333+5502d others(12): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215294 | ||||||
| chr14:69215294 | ATATATGT others(5): Show |
A | 52 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(49): Show |
58 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.333+5493_333+5504d others(14): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215294 | ||||||
| chr14:69215298 | A | ATG | 51 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(48): Show |
55 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.333+5529_333+5530d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215298 | ||||||
| chr14:69215298 | A | ATGTG | 13 | a0001c0001t0002g0086 a0001c0001t0002g0101 a0001c0001t0002g0102 others(10): Show |
13 | HG00140.hp1 HG02109.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.333+5527_333+5530d others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215298 | ||||||
| chr14:69215298 | A | ATGTGTG | 20 | a0001c0001t0002g0098 a0001c0001t0002g0127 a0001c0001t0003g0012 others(17): Show |
20 | HG01074.hp2 HG01192.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.333+5525_333+5530d others(8): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215298 | ||||||
| chr14:69215298 | A | ATGTGTGT others(1): Show |
19 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0128 others(16): Show |
20 | HG01361.hp2 HG01891.hp1 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.333+5523_333+5530d others(10): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215298 | ||||||
| chr14:69215298 | A | ATGTGTGT others(3): Show |
10 | a0001c0001t0003g0130 a0001c0001t0003g0138 a0001c0001t0003g0150 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.333+5521_333+5530d others(12): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215298 | ||||||
| chr14:69215298 | A | ATGTGTGT others(5): Show |
1 | a0001c0008t0021g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.333+5519_333+5530d others(14): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215298 | ||||||
| chr14:69215298 | A | G | 1 | a0001c0001t0006g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.333+5495A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215298 | |||||||
| chr14:69215298 | ATG | A | 2 | a0002c0002t0001g0038 a0002c0002t0001g0194 |
2 | HG02055.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.333+5529_333+5530d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215298 | ||||||
| chr14:69215298 | ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0006g0188 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.333+5521_333+5530d others(12): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215298 | ||||||
| chr14:69215332 | G | A | 1 | a0001c0003t0006g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.333+5529G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215332 | |||||||
| chr14:69215334 | A | G | 1 | a0002c0002t0001g0034 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.333+5531A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215334 | |||||||
| chr14:69215340 | C | CAAT | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+5539_333+5541d others(5): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215340 | ||||||
| chr14:69215360 | G | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+5557G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215360 | |||||||
| chr14:69215366 | C | T | 14 | a0002c0002t0001g0017 a0002c0002t0001g0026 a0002c0002t0001g0027 others(11): Show |
14 | HG01361.hp2 HG02055.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+5563C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215366 | |||||||
| chr14:69215409 | G | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+5606G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215409 | |||||||
| chr14:69215411 | G | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+5608G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215411 | |||||||
| chr14:69215443 | G | T | 3 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0017g0163 |
3 | HG01074.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.333+5640G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215443 | |||||||
| chr14:69215505 | A | G | 15 | a0002c0002t0004g0013 a0002c0002t0004g0174 a0002c0002t0004g0175 others(12): Show |
16 | HG01069.hp1 HG01175.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.333+5702A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215505 | |||||||
| chr14:69215761 | A | T | 195 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(192): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.333+5958A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215761 | |||||||
| chr14:69215787 | G | A | 1 | a0001c0001t0002g0063 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.333+5984G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215787 | |||||||
| chr14:69215819 | C | CT | 25 | a0001c0001t0002g0127 a0001c0001t0003g0011 a0001c0001t0003g0012 others(22): Show |
27 | HG00140.hp2 HG00639.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.333+6028dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215819 | ||||||
| chr14:69215819 | C | CTT | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+6027_333+6028d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69215819 | ||||||
| chr14:69215865 | T | A | 1 | a0001c0001t0006g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.333+6062T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215865 | |||||||
| chr14:69215895 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.333+6092G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69215895 | |||||||
| chr14:69216070 | T | C | 24 | a0001c0001t0002g0009 a0001c0001t0002g0086 a0001c0001t0002g0087 others(21): Show |
25 | HG00140.hp1 HG00733.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.333+6267T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69216070 | |||||||
| chr14:69216073 | C | T | 2 | a0001c0001t0006g0213 a0001c0001t0006g0214 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.333+6270C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69216073 | |||||||
| chr14:69216251 | C | T | 5 | a0001c0001t0003g0141 a0001c0001t0003g0142 a0001c0001t0008g0110 others(2): Show |
5 | HG01891.hp1 HG02280.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+6448C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69216251 | |||||||
| chr14:69216305 | T | C | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+6502T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69216305 | |||||||
| chr14:69216359 | T | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+6556T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69216359 | |||||||
| chr14:69216607 | C | T | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0104 others(4): Show |
7 | HG01891.hp2 HG02109.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.333+6804C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69216607 | |||||||
| chr14:69216739 | A | G | 173 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(170): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.333+6936A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69216739 | |||||||
| chr14:69216946 | A | G | 14 | a0002c0002t0001g0017 a0002c0002t0001g0026 a0002c0002t0001g0027 others(11): Show |
14 | HG01361.hp2 HG02055.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+7143A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69216946 | |||||||
| chr14:69217315 | G | C | 56 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(53): Show |
62 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.333+7512G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69217315 | |||||||
| chr14:69217411 | G | A | 1 | a0001c0001t0002g0103 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.333+7608G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69217411 | |||||||
| chr14:69217542 | C | CT | 5 | a0001c0001t0003g0129 a0001c0001t0005g0164 a0001c0001t0005g0165 others(2): Show |
5 | HG01074.hp2 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+7749dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69217542 | ||||||
| chr14:69217552 | T | A | 5 | a0001c0003t0001g0008 a0001c0003t0001g0074 a0001c0003t0001g0081 others(2): Show |
6 | HG00639.hp1 HG01071.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.333+7749T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69217552 | |||||||
| chr14:69217645 | T | C | 1 | a0002c0002t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.333+7842T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69217645 | |||||||
| chr14:69217714 | A | G | 2 | a0002c0002t0004g0185 a0002c0002t0004g0186 |
2 | HG01192.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.333+7911A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69217714 | |||||||
| chr14:69218220 | C | T | 1 | a0002c0002t0001g0207 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.333+8417C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69218220 | |||||||
| chr14:69218221 | G | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+8418G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69218221 | |||||||
| chr14:69218305 | A | G | 4 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0017g0163 others(1): Show |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.333+8502A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69218305 | |||||||
| chr14:69218378 | A | G | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+8575A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69218378 | |||||||
| chr14:69218536 | G | A | 2 | a0001c0001t0003g0138 a0001c0001t0003g0139 |
2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.333+8733G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69218536 | |||||||
| chr14:69218556 | T | A | 1 | a0001c0001t0002g0091 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.333+8753T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69218556 | |||||||
| chr14:69218593 | G | T | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+8790G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69218593 | |||||||
| chr14:69218774 | C | A | 2 | a0001c0004t0007g0169 a0001c0004t0007g0170 |
2 | HG01081.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.333+8971C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69218774 | |||||||
| chr14:69219270 | A | G | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+9467A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69219270 | |||||||
| chr14:69219399 | G | A | 1 | a0001c0001t0002g0102 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.334-9417G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69219399 | |||||||
| chr14:69219417 | T | C | 1 | a0001c0001t0006g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.334-9399T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69219417 | |||||||
| chr14:69219459 | G | A | 2 | a0001c0001t0012g0166 a0001c0001t0012g0167 |
2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.334-9357G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69219459 | |||||||
| chr14:69219551 | T | C | 2 | a0001c0001t0006g0188 a0001c0001t0006g0211 |
2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.334-9265T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69219551 | |||||||
| chr14:69219802 | G | A | 2 | a0001c0001t0012g0166 a0001c0001t0012g0167 |
2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.334-9014G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69219802 | |||||||
| chr14:69219845 | G | A | 1 | a0002c0002t0004g0174 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.334-8971G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69219845 | |||||||
| chr14:69219878 | G | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-8938G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69219878 | |||||||
| chr14:69220030 | T | A | 2 | a0001c0001t0002g0091 a0001c0001t0002g0114 |
2 | HG01255.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.334-8786T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220030 | |||||||
| chr14:69220244 | T | C | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-8572T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220244 | |||||||
| chr14:69220253 | G | GT | 14 | a0001c0001t0002g0091 a0002c0002t0001g0002 a0002c0002t0001g0015 others(11): Show |
15 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.334-8528dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | ||||||
| chr14:69220253 | G | GTT | 11 | a0001c0001t0002g0010 a0001c0001t0002g0099 a0001c0001t0002g0111 others(8): Show |
11 | HG00642.hp2 HG00735.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.334-8529_334-8528d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | ||||||
| chr14:69220253 | G | GTTT | 15 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0087 others(12): Show |
18 | HG00733.hp2 HG01074.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.334-8530_334-8528d others(5): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | ||||||
| chr14:69220253 | G | GTTTT | 11 | a0001c0001t0002g0010 a0001c0001t0002g0092 a0001c0001t0002g0097 others(8): Show |
11 | HG00140.hp1 HG01074.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.334-8531_334-8528d others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | ||||||
| chr14:69220253 | G | GTTTTT | 11 | a0001c0001t0002g0086 a0001c0001t0002g0090 a0001c0001t0002g0098 others(8): Show |
11 | HG01891.hp2 HG02257.hp1 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.334-8532_334-8528d others(7): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | ||||||
| chr14:69220253 | G | GTTTTTT | 5 | a0001c0001t0002g0089 a0001c0001t0002g0107 a0001c0001t0002g0126 others(2): Show |
5 | HG00741.hp2 HG01346.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.334-8533_334-8528d others(8): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | ||||||
| chr14:69220253 | G | GTTTTTTG others(4): Show |
1 | a0001c0001t0005g0157 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.334-8557_334-8556i others(13): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | ||||||
| chr14:69220253 | G | GTTTTTTG others(5): Show |
3 | a0001c0001t0005g0155 a0001c0001t0005g0156 a0001c0001t0005g0158 |
3 | HG01361.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.334-8557_334-8556i others(14): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | ||||||
| chr14:69220253 | G | GTTTTTTG others(6): Show |
4 | a0001c0001t0005g0039 a0001c0001t0005g0159 a0001c0001t0005g0160 others(1): Show |
4 | HG00280.hp2 NA18940.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-8557_334-8556i others(15): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | ||||||
| chr14:69220253 | G | GTTTTTTG others(7): Show |
1 | a0001c0003t0001g0161 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.334-8557_334-8556i others(16): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | ||||||
| chr14:69220253 | G | GTTTTTTG others(11): Show |
2 | a0001c0001t0005g0152 a0001c0001t0005g0153 |
2 | NA18967.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.334-8557_334-8556i others(20): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | ||||||
| chr14:69220253 | G | GTTTTTTT others(15): Show |
1 | a0001c0001t0003g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.334-8549_334-8528d others(24): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | ||||||
| chr14:69220253 | G | GTTTTTTT others(16): Show |
1 | a0002c0002t0018g0173 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.334-8550_334-8528d others(25): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | ||||||
| chr14:69220253 | GTTTT | G | 10 | a0001c0001t0003g0012 a0001c0001t0003g0025 a0001c0001t0003g0085 others(7): Show |
10 | HG01243.hp1 HG01433.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.334-8531_334-8528d others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | ||||||
| chr14:69220253 | GTTTTT | G | 9 | a0001c0001t0003g0012 a0001c0001t0003g0132 a0001c0001t0003g0134 others(6): Show |
9 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.334-8532_334-8528d others(7): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | ||||||
| chr14:69220253 | GTTTTTT | G | 21 | a0001c0001t0002g0076 a0001c0001t0003g0141 a0001c0001t0003g0150 others(18): Show |
22 | HG00735.hp2 HG00738.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.334-8533_334-8528d others(8): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | ||||||
| chr14:69220253 | GTTTTTTT | G | 39 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(36): Show |
43 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.334-8534_334-8528d others(9): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | ||||||
| chr14:69220253 | GTTTTTTT others(2): Show |
G | 6 | a0002c0002t0001g0017 a0002c0002t0001g0028 a0002c0002t0001g0029 others(3): Show |
6 | HG01361.hp2 HG02055.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-8536_334-8528d others(11): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | ||||||
| chr14:69220253 | GTTTTTTT others(3): Show |
G | 8 | a0002c0002t0001g0026 a0002c0002t0001g0027 a0002c0002t0001g0031 others(5): Show |
8 | HG02056.hp1 HG02155.hp1 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.334-8537_334-8528d others(12): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | ||||||
| chr14:69220253 | GTTTTTTT others(6): Show |
G | 3 | a0001c0001t0006g0188 a0002c0002t0001g0203 a0002c0002t0001g0204 |
3 | HG01106.hp2 HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.334-8540_334-8528d others(15): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | ||||||
| chr14:69220253 | GTTTTTTT others(7): Show |
G | 3 | a0001c0001t0003g0129 a0001c0001t0006g0211 a0001c0001t0016g0108 |
3 | HG02572.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.334-8541_334-8528d others(16): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | ||||||
| chr14:69220253 | GTTTTTTT others(8): Show |
G | 2 | a0002c0002t0001g0206 a0002c0002t0004g0187 |
2 | HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.334-8542_334-8528d others(17): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220253 | ||||||
| chr14:69220258 | T | C | 1 | a0001c0004t0007g0171 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.334-8558T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220258 | |||||||
| chr14:69220259 | T | C | 4 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(1): Show |
4 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-8557T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220259 | |||||||
| chr14:69220302 | G | A | 1 | a0002c0002t0001g0202 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.334-8514G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220302 | |||||||
| chr14:69220357 | A | G | 173 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(170): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.334-8459A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220357 | |||||||
| chr14:69220363 | C | T | 1 | a0001c0001t0002g0123 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.334-8453C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220363 | |||||||
| chr14:69220419 | C | T | 1 | a0001c0003t0020g0080 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.334-8397C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220419 | |||||||
| chr14:69220431 | C | T | 1 | a0002c0002t0004g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.334-8385C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220431 | |||||||
| chr14:69220557 | A | AT | 14 | a0001c0001t0002g0089 a0001c0001t0002g0090 a0001c0001t0002g0092 others(11): Show |
14 | HG00741.hp2 HG01346.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.334-8243dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220557 | ||||||
| chr14:69220557 | AT | A | 6 | a0001c0001t0003g0130 a0001c0001t0010g0148 a0001c0003t0001g0062 others(3): Show |
6 | HG01943.hp1 HG02258.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-8243delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69220557 | ||||||
| chr14:69220574 | A | T | 1 | a0001c0001t0006g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.334-8242A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220574 | |||||||
| chr14:69220652 | T | C | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-8164T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220652 | |||||||
| chr14:69220714 | C | G | 1 | a0002c0002t0001g0196 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.334-8102C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220714 | |||||||
| chr14:69220783 | C | T | 1 | a0001c0008t0021g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.334-8033C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69220783 | |||||||
| chr14:69221048 | T | C | 1 | a0001c0001t0005g0152 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.334-7768T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221048 | |||||||
| chr14:69221135 | C | T | 1 | a0001c0003t0001g0069 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.334-7681C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221135 | |||||||
| chr14:69221169 | G | A | 1 | a0001c0003t0001g0055 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.334-7647G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221169 | |||||||
| chr14:69221204 | T | C | 1 | a0001c0001t0002g0098 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.334-7612T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221204 | |||||||
| chr14:69221230 | C | T | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-7586C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221230 | |||||||
| chr14:69221329 | C | T | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-7487C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221329 | |||||||
| chr14:69221425 | A | T | 1 | a0001c0001t0012g0167 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.334-7391A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221425 | |||||||
| chr14:69221490 | T | C | 173 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(170): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.334-7326T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221490 | |||||||
| chr14:69221521 | A | G | 1 | a0001c0001t0002g0120 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.334-7295A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221521 | |||||||
| chr14:69221539 | A | T | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-7277A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221539 | |||||||
| chr14:69221658 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.334-7158C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221658 | |||||||
| chr14:69221709 | A | G | 1 | a0001c0001t0006g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.334-7107A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221709 | |||||||
| chr14:69221724 | T | A | 2 | a0001c0001t0012g0166 a0001c0001t0012g0167 |
2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.334-7092T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221724 | |||||||
| chr14:69221754 | C | T | 1 | a0002c0002t0018g0173 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.334-7062C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221754 | |||||||
| chr14:69221760 | C | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-7056C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221760 | |||||||
| chr14:69221909 | T | TA | 43 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0003g0012 others(40): Show |
45 | HG00738.hp1 HG00738.hp2 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.334-6878dupA | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69221909 | ||||||
| chr14:69221909 | T | TAA | 54 | a0001c0001t0002g0009 a0001c0001t0002g0086 a0001c0001t0002g0087 others(51): Show |
60 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.334-6879_334-6878d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69221909 | ||||||
| chr14:69221909 | T | TAAA | 18 | a0001c0001t0002g0065 a0001c0001t0002g0088 a0001c0001t0002g0091 others(15): Show |
18 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.334-6880_334-6878d others(5): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69221909 | ||||||
| chr14:69221909 | T | TAAAA | 11 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0042 others(8): Show |
14 | HG00741.hp1 HG01074.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.334-6881_334-6878d others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69221909 | ||||||
| chr14:69221909 | TA | T | 28 | a0001c0001t0006g0211 a0002c0002t0001g0014 a0002c0002t0001g0015 others(25): Show |
31 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.334-6878delA | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69221909 | ||||||
| chr14:69221909 | TAAAA | T | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-6881_334-6878d others(6): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69221909 | ||||||
| chr14:69221909 | TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0002g0101 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.334-6890_334-6878d others(15): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69221909 | ||||||
| chr14:69221959 | G | T | 1 | a0001c0008t0021g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.334-6857G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221959 | |||||||
| chr14:69221960 | C | T | 2 | a0002c0002t0001g0195 a0002c0002t0001g0205 |
2 | HG01081.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.334-6856C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69221960 | |||||||
| chr14:69222086 | CA | C | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-6715delA | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69222086 | ||||||
| chr14:69222207 | T | G | 21 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0089 others(18): Show |
24 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.334-6609T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69222207 | |||||||
| chr14:69222325 | G | T | 173 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(170): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.334-6491G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69222325 | |||||||
| chr14:69222630 | A | G | 15 | a0002c0002t0004g0013 a0002c0002t0004g0174 a0002c0002t0004g0175 others(12): Show |
16 | HG01069.hp1 HG01175.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.334-6186A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69222630 | |||||||
| chr14:69222702 | C | CT | 56 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(53): Show |
62 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.334-6106dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69222702 | ||||||
| chr14:69222708 | T | G | 1 | a0001c0001t0002g0116 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.334-6108T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69222708 | |||||||
| chr14:69222760 | G | T | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-6056G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69222760 | |||||||
| chr14:69223295 | C | CT | 4 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0017g0163 others(1): Show |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-5520dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69223295 | ||||||
| chr14:69223771 | AT | A | 12 | a0002c0002t0001g0017 a0002c0002t0001g0026 a0002c0002t0001g0027 others(9): Show |
12 | HG01361.hp2 HG02056.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.334-5043delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69223771 | ||||||
| chr14:69223850 | C | T | 1 | a0002c0002t0001g0194 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.334-4966C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69223850 | |||||||
| chr14:69224512 | G | C | 1 | a0001c0001t0002g0127 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.334-4304G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69224512 | |||||||
| chr14:69224623 | AT | A | 4 | a0002c0002t0001g0014 a0002c0002t0001g0193 a0002c0002t0001g0195 others(1): Show |
5 | HG01081.hp1 HG01496.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-4185delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69224623 | ||||||
| chr14:69224632 | A | T | 1 | a0001c0001t0002g0064 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.334-4184A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69224632 | |||||||
| chr14:69224848 | G | A | 2 | a0001c0001t0006g0188 a0001c0001t0006g0211 |
2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.334-3968G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69224848 | |||||||
| chr14:69224944 | A | C | 1 | a0001c0001t0002g0127 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.334-3872A>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69224944 | |||||||
| chr14:69224969 | G | A | 1 | a0001c0003t0001g0072 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.334-3847G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69224969 | |||||||
| chr14:69224973 | C | T | 1 | a0001c0001t0005g0164 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.334-3843C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69224973 | |||||||
| chr14:69225002 | C | T | 1 | a0001c0008t0021g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.334-3814C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69225002 | |||||||
| chr14:69225478 | A | G | 1 | a0001c0001t0006g0188 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.334-3338A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69225478 | |||||||
| chr14:69225484 | C | T | 1 | a0001c0008t0021g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.334-3332C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69225484 | |||||||
| chr14:69225513 | T | A | 1 | a0002c0002t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.334-3303T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69225513 | |||||||
| chr14:69225582 | A | G | 56 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(53): Show |
62 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.334-3234A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69225582 | |||||||
| chr14:69225837 | A | G | 1 | a0001c0001t0006g0188 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.334-2979A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69225837 | |||||||
| chr14:69225848 | A | G | 6 | a0001c0001t0003g0138 a0001c0001t0003g0139 a0001c0001t0003g0150 others(3): Show |
6 | HG01884.hp1 HG02559.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-2968A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69225848 | |||||||
| chr14:69225977 | A | C | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-2839A>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69225977 | |||||||
| chr14:69226101 | A | G | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-2715A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69226101 | |||||||
| chr14:69226237 | C | G | 3 | a0001c0001t0006g0100 a0001c0001t0006g0188 a0001c0001t0006g0211 |
3 | HG02886.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.334-2579C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69226237 | |||||||
| chr14:69226238 | C | T | 1 | a0002c0002t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.334-2578C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69226238 | |||||||
| chr14:69226386 | T | C | 1 | a0001c0003t0001g0060 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.334-2430T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69226386 | |||||||
| chr14:69226402 | G | A | 56 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(53): Show |
62 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.334-2414G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69226402 | |||||||
| chr14:69226750 | A | T | 1 | a0001c0008t0021g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.334-2066A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69226750 | |||||||
| chr14:69226773 | GT | G | 159 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0064 others(156): Show |
170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.334-2024delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69226773 | ||||||
| chr14:69226880 | G | A | 1 | a0002c0002t0001g0037 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.334-1936G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69226880 | |||||||
| chr14:69226923 | T | C | 1 | a0001c0009t0002g0093 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.334-1893T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69226923 | |||||||
| chr14:69227002 | T | C | 1 | a0001c0001t0006g0188 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.334-1814T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69227002 | |||||||
| chr14:69227108 | C | T | 1 | a0002c0002t0001g0037 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.334-1708C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69227108 | |||||||
| chr14:69227145 | C | T | 5 | a0001c0001t0003g0138 a0001c0001t0003g0139 a0001c0001t0003g0150 others(2): Show |
5 | HG01884.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-1671C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69227145 | |||||||
| chr14:69227602 | C | T | 2 | a0001c0001t0012g0166 a0001c0001t0012g0167 |
2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.334-1214C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69227602 | |||||||
| chr14:69227646 | G | A | 4 | a0001c0003t0001g0062 a0001c0003t0001g0066 a0001c0003t0001g0071 others(1): Show |
4 | HG02630.hp1 HG03098.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-1170G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69227646 | |||||||
| chr14:69227656 | T | C | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-1160T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69227656 | |||||||
| chr14:69227829 | A | G | 168 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(165): Show |
180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.334-987A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69227829 | |||||||
| chr14:69227927 | A | AT | 93 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(90): Show |
99 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.334-880dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69227927 | ||||||
| chr14:69227979 | C | G | 14 | a0002c0002t0001g0017 a0002c0002t0001g0026 a0002c0002t0001g0027 others(11): Show |
14 | HG01361.hp2 HG02055.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.334-837C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69227979 | |||||||
| chr14:69228185 | CT | C | 95 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(92): Show |
102 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.334-608delT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69228185 | ||||||
| chr14:69228185 | CTT | C | 49 | a0001c0001t0002g0088 a0001c0001t0002g0096 a0001c0001t0002g0102 others(46): Show |
51 | HG00140.hp1 HG00280.hp2 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.334-609_334-608del others(2): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69228185 | ||||||
| chr14:69228185 | CTTT | C | 38 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(35): Show |
42 | HG00642.hp2 HG00733.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.334-610_334-608del others(3): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 69228185 | ||||||
| chr14:69228230 | C | T | 1 | a0001c0008t0021g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.334-586C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69228230 | |||||||
| chr14:69228290 | C | T | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-526C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69228290 | |||||||
| chr14:69228440 | C | G | 2 | a0001c0003t0001g0048 a0001c0003t0001g0075 |
2 | NA18940.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.334-376C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69228440 | |||||||
| chr14:69228488 | A | G | 175 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(172): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.334-328A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69228488 | |||||||
| chr14:69228551 | C | T | 14 | a0002c0002t0001g0017 a0002c0002t0001g0026 a0002c0002t0001g0027 others(11): Show |
14 | HG01361.hp2 HG02055.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.334-265C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69228551 | |||||||
| chr14:69228593 | C | A | 1 | a0001c0001t0006g0212 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.334-223C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69228593 | |||||||
| chr14:69228630 | T | C | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-186T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69228630 | |||||||
| chr14:69228674 | C | T | 1 | a0002c0002t0001g0200 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.334-142C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 3/9 | chr14 | 69228674 | |||||||
| chr14:69229075 | G | A | 151 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(148): Show |
163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
splice_region_variant&intron_variant | LOW | c.590+3G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/9 | chr14 | 69229075 | |||||||
| chr14:69229109 | C | T | 1 | a0001c0003t0001g0047 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.590+37C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/9 | chr14 | 69229109 | |||||||
| chr14:69229228 | C | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.590+156C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/9 | chr14 | 69229228 | |||||||
| chr14:69229455 | T | C | 55 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(52): Show |
61 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.590+383T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/9 | chr14 | 69229455 | |||||||
| chr14:69229552 | C | A | 15 | a0002c0002t0004g0013 a0002c0002t0004g0174 a0002c0002t0004g0175 others(12): Show |
16 | HG01069.hp1 HG01175.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.590+480C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/9 | chr14 | 69229552 | |||||||
| chr14:69229619 | C | G | 56 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(53): Show |
62 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.590+547C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/9 | chr14 | 69229619 | |||||||
| chr14:69230212 | C | T | 3 | a0001c0001t0008g0110 a0001c0001t0008g0143 a0001c0001t0008g0144 |
3 | HG02818.hp2 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.591-260C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/9 | chr14 | 69230212 | |||||||
| chr14:69230353 | G | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.591-119G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/9 | chr14 | 69230353 | |||||||
| chr14:69230437 | C | T | 1 | a0001c0001t0019g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.591-35C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/9 | chr14 | 69230437 | |||||||
| chr14:69230457 | C | G | 1 | a0001c0007t0006g0109 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.591-15C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/9 | chr14 | 69230457 | |||||||
| chr14:69230468 | T | C | 1 | a0001c0003t0001g0078 | 1 | HG01175.hp2 | splice_region_variant&intron_variant | LOW | c.591-4T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 4/9 | chr14 | 69230468 | |||||||
| chr14:69230736 | C | G | 93 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(90): Show |
99 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.717+138C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69230736 | |||||||
| chr14:69230847 | G | A | 173 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(170): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.717+249G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69230847 | |||||||
| chr14:69230883 | A | G | 3 | a0001c0001t0002g0089 a0001c0009t0002g0093 a0004c0006t0002g0094 |
3 | HG00741.hp2 HG03017.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.717+285A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69230883 | |||||||
| chr14:69231023 | G | C | 1 | a0001c0004t0007g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.717+425G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231023 | |||||||
| chr14:69231124 | A | AT | 22 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0025 others(19): Show |
24 | HG01243.hp1 HG01433.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.717+534dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 69231124 | ||||||
| chr14:69231134 | T | C | 2 | a0001c0001t0012g0166 a0001c0001t0012g0167 |
2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.717+536T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231134 | |||||||
| chr14:69231160 | A | T | 1 | a0001c0001t0002g0087 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.717+562A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231160 | |||||||
| chr14:69231164 | T | C | 56 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(53): Show |
62 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.717+566T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231164 | |||||||
| chr14:69231236 | C | T | 1 | a0001c0003t0001g0047 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.717+638C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231236 | |||||||
| chr14:69231260 | C | A | 1 | a0001c0003t0006g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.717+662C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231260 | |||||||
| chr14:69231372 | G | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+774G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231372 | |||||||
| chr14:69231414 | G | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+816G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231414 | |||||||
| chr14:69231501 | C | G | 2 | a0002c0002t0001g0029 a0002c0002t0001g0034 |
2 | HG03688.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.717+903C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231501 | |||||||
| chr14:69231510 | A | G | 4 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0017g0163 others(1): Show |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.717+912A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231510 | |||||||
| chr14:69231619 | G | C | 1 | a0001c0001t0006g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.717+1021G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231619 | |||||||
| chr14:69231721 | G | C | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+1123G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231721 | |||||||
| chr14:69231820 | CCT | C | 56 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0064 others(53): Show |
62 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.717+1225_717+1226d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 69231820 | ||||||
| chr14:69231909 | T | TA | 34 | a0001c0001t0005g0152 a0001c0001t0005g0153 a0001c0001t0005g0155 others(31): Show |
34 | HG00735.hp2 HG00738.hp1 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.717+1338dupA | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 69231909 | ||||||
| chr14:69231909 | T | TAA | 7 | a0001c0001t0005g0039 a0001c0001t0005g0158 a0001c0001t0005g0159 others(4): Show |
7 | HG00280.hp2 HG01361.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+1337_717+1338d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 69231909 | ||||||
| chr14:69231909 | TA | T | 71 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(68): Show |
77 | HG00733.hp2 HG00735.hp1 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.717+1338delA | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 69231909 | ||||||
| chr14:69231909 | TAA | T | 6 | a0001c0001t0003g0138 a0001c0001t0003g0139 a0001c0001t0003g0150 others(3): Show |
6 | HG01074.hp2 HG01884.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.717+1337_717+1338d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 69231909 | ||||||
| chr14:69231909 | TAAAAAA | T | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+1333_717+1338d others(8): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 69231909 | ||||||
| chr14:69231975 | C | T | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+1377C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69231975 | |||||||
| chr14:69232293 | T | A | 1 | a0002c0002t0018g0173 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.717+1695T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69232293 | |||||||
| chr14:69232429 | T | C | 1 | a0002c0002t0018g0173 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.717+1831T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69232429 | |||||||
| chr14:69232456 | C | T | 3 | a0001c0004t0007g0168 a0001c0004t0007g0171 a0001c0004t0007g0172 |
3 | HG02451.hp2 HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.717+1858C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69232456 | |||||||
| chr14:69232511 | A | C | 1 | a0002c0002t0001g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.717+1913A>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69232511 | |||||||
| chr14:69232806 | A | G | 2 | a0001c0001t0006g0100 a0001c0001t0006g0211 |
2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.718-1894A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69232806 | |||||||
| chr14:69232842 | T | C | 51 | a0001c0003t0001g0003 a0001c0003t0001g0004 a0001c0003t0001g0005 others(48): Show |
57 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.718-1858T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69232842 | |||||||
| chr14:69233062 | T | C | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.718-1638T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233062 | |||||||
| chr14:69233063 | G | C | 1 | a0001c0001t0019g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.718-1637G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233063 | |||||||
| chr14:69233153 | G | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.718-1547G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233153 | |||||||
| chr14:69233392 | A | T | 1 | a0001c0001t0002g0146 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.718-1308A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233392 | |||||||
| chr14:69233412 | A | T | 3 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0017g0163 |
3 | HG01074.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.718-1288A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233412 | |||||||
| chr14:69233431 | T | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.718-1269T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233431 | |||||||
| chr14:69233513 | G | A | 1 | a0001c0001t0003g0150 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.718-1187G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233513 | |||||||
| chr14:69233564 | C | T | 3 | a0001c0001t0006g0100 a0001c0001t0006g0188 a0001c0001t0006g0211 |
3 | HG02886.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.718-1136C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233564 | |||||||
| chr14:69233688 | G | C | 1 | a0001c0003t0001g0072 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.718-1012G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233688 | |||||||
| chr14:69233857 | C | T | 51 | a0001c0003t0001g0003 a0001c0003t0001g0004 a0001c0003t0001g0005 others(48): Show |
57 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.718-843C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233857 | |||||||
| chr14:69233912 | G | A | 2 | a0002c0002t0001g0029 a0002c0002t0001g0034 |
2 | HG03688.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.718-788G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233912 | |||||||
| chr14:69233963 | C | T | 1 | a0001c0001t0015g0121 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.718-737C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69233963 | |||||||
| chr14:69234052 | C | G | 1 | a0002c0002t0004g0183 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.718-648C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69234052 | |||||||
| chr14:69234082 | T | A | 5 | a0001c0001t0002g0001 a0001c0001t0002g0111 a0001c0001t0002g0116 others(2): Show |
7 | HG00642.hp2 HG01074.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.718-618T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69234082 | |||||||
| chr14:69234204 | T | C | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.718-496T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 5/9 | chr14 | 69234204 | |||||||
| chr14:69235097 | T | C | 1 | a0001c0008t0021g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1049+66T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 6/9 | chr14 | 69235097 | |||||||
| chr14:69235146 | C | A | 158 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(155): Show |
170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1049+115C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 6/9 | chr14 | 69235146 | |||||||
| chr14:69235233 | T | G | 1 | a0001c0001t0002g0127 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1049+202T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 6/9 | chr14 | 69235233 | |||||||
| chr14:69235380 | G | T | 11 | a0001c0001t0005g0039 a0001c0001t0005g0152 a0001c0001t0005g0153 others(8): Show |
11 | HG00280.hp2 HG00738.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1049+349G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 6/9 | chr14 | 69235380 | |||||||
| chr14:69235611 | T | C | 52 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(49): Show |
56 | HG00140.hp1 HG00642.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.1050-435T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 6/9 | chr14 | 69235611 | |||||||
| chr14:69235623 | T | C | 1 | a0001c0001t0014g0106 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1050-423T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 6/9 | chr14 | 69235623 | |||||||
| chr14:69235777 | G | T | 3 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0017g0163 |
3 | HG01074.hp2 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1050-269G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 6/9 | chr14 | 69235777 | |||||||
| chr14:69235875 | G | A | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1050-171G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 6/9 | chr14 | 69235875 | |||||||
| chr14:69236700 | C | T | 1 | a0002c0002t0001g0017 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1292+158C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/9 | chr14 | 69236700 | |||||||
| chr14:69236871 | G | C | 165 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(162): Show |
178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1292+329G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/9 | chr14 | 69236871 | |||||||
| chr14:69236961 | C | T | 1 | a0002c0002t0001g0016 | 2 | HG00642.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1292+419C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/9 | chr14 | 69236961 | |||||||
| chr14:69237024 | T | C | 2 | a0001c0001t0012g0166 a0001c0001t0012g0167 |
2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1292+482T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/9 | chr14 | 69237024 | |||||||
| chr14:69237039 | C | A | 1 | a0003c0005t0001g0073 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1292+497C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/9 | chr14 | 69237039 | |||||||
| chr14:69237042 | T | C | 1 | a0001c0003t0001g0078 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1292+500T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/9 | chr14 | 69237042 | |||||||
| chr14:69237232 | G | A | 1 | a0001c0003t0001g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1293-343G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/9 | chr14 | 69237232 | |||||||
| chr14:69237294 | C | G | 1 | a0002c0002t0001g0038 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1293-281C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/9 | chr14 | 69237294 | |||||||
| chr14:69237314 | A | T | 1 | a0001c0003t0006g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1293-261A>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/9 | chr14 | 69237314 | |||||||
| chr14:69237335 | A | G | 195 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(192): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.1293-240A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/9 | chr14 | 69237335 | |||||||
| chr14:69237442 | T | C | 1 | a0002c0002t0001g0193 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1293-133T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 8/9 | chr14 | 69237442 | |||||||
| chr14:69237945 | G | A | 11 | a0001c0001t0005g0039 a0001c0001t0005g0152 a0001c0001t0005g0153 others(8): Show |
11 | HG00280.hp2 HG00738.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1649+14G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69237945 | |||||||
| chr14:69237950 | G | T | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1649+19G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69237950 | |||||||
| chr14:69238305 | C | T | 2 | a0002c0002t0001g0037 a0002c0002t0001g0038 |
2 | HG02055.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1649+374C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69238305 | |||||||
| chr14:69238424 | A | G | 1 | a0001c0001t0006g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1649+493A>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69238424 | |||||||
| chr14:69238599 | G | GT | 33 | a0001c0001t0002g0090 a0001c0001t0005g0153 a0001c0001t0005g0159 others(30): Show |
34 | HG01069.hp1 HG01175.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.1649+685dupT | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 69238599 | ||||||
| chr14:69238599 | GTT | G | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1649+684_1649+685d others(4): Show |
EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 69238599 | ||||||
| chr14:69238688 | G | A | 1 | a0001c0003t0001g0048 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1649+757G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69238688 | |||||||
| chr14:69238757 | C | G | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1649+826C>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69238757 | |||||||
| chr14:69239232 | G | C | 2 | a0001c0001t0006g0100 a0001c0001t0006g0211 |
2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1649+1301G>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69239232 | |||||||
| chr14:69239242 | G | A | 5 | a0001c0001t0003g0138 a0001c0001t0003g0139 a0001c0001t0003g0150 others(2): Show |
5 | HG01884.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1649+1311G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69239242 | |||||||
| chr14:69239254 | G | T | 2 | a0001c0001t0006g0100 a0001c0001t0006g0211 |
2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1649+1323G>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69239254 | |||||||
| chr14:69239401 | T | A | 1 | a0001c0003t0001g0043 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1649+1470T>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69239401 | |||||||
| chr14:69239459 | C | T | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1650-1425C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69239459 | |||||||
| chr14:69239679 | T | G | 1 | a0001c0001t0002g0127 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1650-1205T>G | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69239679 | |||||||
| chr14:69239686 | C | A | 5 | a0001c0001t0002g0001 a0001c0001t0002g0111 a0001c0001t0002g0116 others(2): Show |
7 | HG00642.hp2 HG01074.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.1650-1198C>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69239686 | |||||||
| chr14:69239808 | G | A | 2 | a0001c0001t0012g0166 a0001c0001t0012g0167 |
2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1650-1076G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69239808 | |||||||
| chr14:69239858 | T | C | 5 | a0001c0004t0007g0168 a0001c0004t0007g0169 a0001c0004t0007g0170 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1650-1026T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69239858 | |||||||
| chr14:69240047 | G | A | 2 | a0001c0001t0012g0166 a0001c0001t0012g0167 |
2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1650-837G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69240047 | |||||||
| chr14:69240355 | C | T | 1 | a0001c0003t0001g0083 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1650-529C>T | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69240355 | |||||||
| chr14:69240638 | G | A | 15 | a0002c0002t0001g0017 a0002c0002t0001g0026 a0002c0002t0001g0027 others(12): Show |
15 | HG01361.hp2 HG02055.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.1650-246G>A | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69240638 | |||||||
| chr14:69240870 | T | C | 2 | a0002c0002t0001g0030 a0002c0002t0001g0031 |
2 | NA19002.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1650-14T>C | EXD2 | ENSG00000081177.19 | transcript | ENST00000685843.1 | protein_coding | 9/9 | chr14 | 69240870 |