Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1738 |
| ensemblid | ENSG00000091140.15 |
| hgncid | 2898 |
| symbol | DLD |
| name | dihydrolipoamide dehydrogenase |
| refseq_nuc | NM_000108.5 |
| refseq_prot | NP_000099.2 |
| ensembl_nuc | ENST00000205402.10 |
| ensembl_prot | ENSP00000205402.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 107891183 |
| end | 107921198 |
| strand | + |
| ver | v1.2 |
| region | chr7:107891183-107921198 |
| region5000 | chr7:107886183-107926198 |
| regionname0 | DLD_chr7_107891183_107921198 |
| regionname5000 | DLD_chr7_107886183_107926198 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 509 | 398 | 94 | 75 | 175 | 16 | 36 | 140 | DLD_chr7_107886183_107926198 | DLD | MQSWS others(504): Show |
chr7 | 107886183 | 107926198 |
| a0002 | 0/0 | 509 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | MQSWS others(504): Show |
chr7 | 107886183 | 107926198 |
| a0003 | 0/0 | 509 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | MQSWS others(504): Show |
chr7 | 107886183 | 107926198 |
| a0004 | 0/0 | 509 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | MQSWS others(504): Show |
chr7 | 107886183 | 107926198 |
| a0005 | 0/0 | 509 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | MHSWS others(504): Show |
chr7 | 107886183 | 107926198 |
| a0006 | 0/0 | 509 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DLD_chr7_107886183_107926198 | DLD | MQSWS others(504): Show |
chr7 | 107886183 | 107926198 |
| a0007 | 0/0 | 509 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DLD_chr7_107886183_107926198 | DLD | MQSWS others(504): Show |
chr7 | 107886183 | 107926198 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1527 | 371 | 73 | 71 | 174 | 15 | 36 | DLD_chr7_107886183_107926198 | DLD | ATGCA others(1522): Show |
chr7 | 107886183 | 107926198 | ||
| a0001c0002 | 0/0 | 1527 | 16 | 16 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | ATGCA others(1522): Show |
chr7 | 107886183 | 107926198 | ||
| a0001c0003 | 0/0 | 1527 | 5 | 1 | 3 | 0 | 1 | 0 | DLD_chr7_107886183_107926198 | DLD | ATGCA others(1522): Show |
chr7 | 107886183 | 107926198 | ||
| a0001c0006 | 0/0 | 1527 | 2 | 2 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | ATGCA others(1522): Show |
chr7 | 107886183 | 107926198 | ||
| a0001c0007 | 0/0 | 1527 | 2 | 1 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | ATGCA others(1522): Show |
chr7 | 107886183 | 107926198 | ||
| a0001c0011 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | ATGCA others(1522): Show |
chr7 | 107886183 | 107926198 | ||
| a0001c0012 | 0/0 | 1527 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | ATGCA others(1522): Show |
chr7 | 107886183 | 107926198 | ||
| a0002c0005 | 0/0 | 1527 | 2 | 2 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | ATGCA others(1522): Show |
chr7 | 107886183 | 107926198 | ||
| a0003c0004 | 0/0 | 1527 | 2 | 2 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | ATGCA others(1522): Show |
chr7 | 107886183 | 107926198 | ||
| a0004c0009 | 0/0 | 1527 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | ATGCA others(1522): Show |
chr7 | 107886183 | 107926198 | ||
| a0005c0008 | 0/0 | 1527 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | ATGCA others(1522): Show |
chr7 | 107886183 | 107926198 | ||
| a0006c0010 | 0/0 | 1527 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | ATGCA others(1522): Show |
chr7 | 107886183 | 107926198 | ||
| a0007c0013 | 0/0 | 1527 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | ATGCA others(1522): Show |
chr7 | 107886183 | 107926198 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3537 | 111 | 7 | 25 | 70 | 2 | 6 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0001c0001t0002 | 0/0 | 3537 | 101 | 1 | 12 | 71 | 3 | 14 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0001c0001t0003 | 1/0 | 3537 | 90 | 13 | 28 | 26 | 10 | 12 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0001c0001t0004 | 0/0 | 3537 | 51 | 42 | 5 | 0 | 0 | 4 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0001c0001t0007 | 0/0 | 3537 | 3 | 3 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0001c0001t0008 | 0/0 | 3537 | 3 | 0 | 0 | 3 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0001c0001t0009 | 0/0 | 3537 | 2 | 2 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0001c0001t0010 | 0/0 | 3537 | 2 | 0 | 0 | 2 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0001c0001t0012 | 0/0 | 3537 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0001c0001t0013 | 0/0 | 3537 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0001c0001t0014 | 0/0 | 3537 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0001c0001t0015 | 0/0 | 3537 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0001c0001t0016 | 0/0 | 3537 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0001c0001t0018 | 0/0 | 3537 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0001c0001t0019 | 0/0 | 3537 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0001c0001t0020 | 0/0 | 3537 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0001c0002t0004 | 0/0 | 3537 | 10 | 10 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0001c0002t0005 | 0/0 | 3537 | 5 | 5 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0001c0002t0017 | 0/0 | 3537 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0001c0003t0001 | 0/0 | 3537 | 5 | 1 | 3 | 0 | 1 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0001c0006t0006 | 0/0 | 3536 | 2 | 2 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3531): Show |
chr7 | 107886183 | 107926198 |
| a0001c0007t0011 | 0/0 | 3537 | 2 | 1 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0001c0011t0004 | 0/0 | 3537 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0001c0012t0001 | 0/0 | 3537 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0002c0005t0006 | 0/0 | 3536 | 2 | 2 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3531): Show |
chr7 | 107886183 | 107926198 |
| a0003c0004t0004 | 0/0 | 3537 | 2 | 2 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0004c0009t0001 | 0/0 | 3537 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0005c0008t0002 | 0/0 | 3537 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0006c0010t0002 | 0/0 | 3537 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| a0007c0013t0003 | 0/0 | 3537 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | CTTGG others(3532): Show |
chr7 | 107886183 | 107926198 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 21 | 0 | 0 | 19 | 0 | 2 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0004 | 0/0 | 17 | 3 | 5 | 6 | 1 | 2 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0030 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0053 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0001 | 0/0 | 23 | 0 | 3 | 14 | 2 | 4 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0005 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0006 | 0/0 | 7 | 0 | 4 | 3 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0003 | 0/0 | 22 | 4 | 8 | 4 | 2 | 4 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0007 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0012 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0016 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0022 | 1/0 | 3 | 0 | 1 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0050 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0007g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0007g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0008g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0008g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0009g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0010g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0010g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0012g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0013g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0014g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0015g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0016g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0018g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0019g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0001t0020g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0002t0004g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0002t0004g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0002t0004g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0002t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0002t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0002t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0002t0005g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0002t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0002t0017g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0003t0001g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0003t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0006t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0006t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0007t0011g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0011t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0001c0012t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0002c0005t0006g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0003c0004t0004g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0004c0009t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0005c0008t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0006c0010t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| a0007c0013t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0203 | EUR | GBR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0148 | EUR | GBR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0112 | EUR | GBR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | GBR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0222 | EUR | FIN | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0223 | EUR | FIN | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | CHS | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | CHS | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | CHS | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | CHS | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | CHS | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | CHS | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0025 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0043 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0218 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01168 | hp2 | a0001 | c0003 | t0001 | g0096 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0120 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0204 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01243 | hp2 | a0001 | c0007 | t0011 | g0034 | AMR | PUR | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | CLM | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | CLM | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0210 | AMR | CLM | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | CLM | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | CLM | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01433 | hp1 | a0001 | c0001 | t0016 | g0067 | AMR | CLM | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01496 | hp1 | a0004 | c0009 | t0001 | g0102 | AMR | CLM | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | IBS | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0068 | EUR | IBS | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0012 | EUR | IBS | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0196 | EUR | IBS | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | ACB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0132 | AFR | ACB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01891 | hp2 | a0001 | c0001 | t0015 | g0191 | AFR | ACB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0207 | AMR | PEL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PEL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0046 | AMR | PEL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PEL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PEL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0195 | AFR | ACB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | ACB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02056 | hp2 | a0001 | c0001 | t0019 | g0010 | EAS | KHV | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | KHV | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | KHV | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02129 | hp1 | a0005 | c0008 | t0002 | g0001 | EAS | KHV | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | KHV | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | KHV | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CDX | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CDX | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | ACB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0135 | AFR | ACB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02258 | hp2 | a0001 | c0002 | t0004 | g0017 | AFR | ACB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02280 | hp1 | a0001 | c0002 | t0004 | g0023 | AFR | ACB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02280 | hp2 | a0001 | c0002 | t0005 | g0011 | AFR | ACB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0060 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0043 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02615 | hp1 | a0002 | c0005 | t0006 | g0035 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0134 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0045 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0138 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02630 | hp1 | a0001 | c0007 | t0011 | g0034 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0066 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0062 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0131 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0188 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02717 | hp2 | a0001 | c0001 | t0018 | g0124 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02723 | hp1 | a0001 | c0002 | t0005 | g0057 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0184 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02738 | hp1 | a0006 | c0010 | t0002 | g0128 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0216 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0054 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02809 | hp2 | a0001 | c0006 | t0006 | g0126 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02818 | hp2 | a0001 | c0001 | t0012 | g0088 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0230 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0059 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0221 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0052 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0194 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0052 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | ESN | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02922 | hp2 | a0001 | c0001 | t0014 | g0125 | AFR | ESN | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02965 | hp1 | a0003 | c0004 | t0004 | g0036 | AFR | ESN | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0065 | AFR | ESN | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02970 | hp1 | a0001 | c0002 | t0017 | g0056 | AFR | ESN | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0061 | AFR | ESN | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | ESN | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02976 | hp2 | a0001 | c0002 | t0004 | g0024 | AFR | ESN | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0212 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0187 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0182 | AFR | MSL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03098 | hp2 | a0001 | c0002 | t0004 | g0058 | AFR | MSL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0229 | AFR | ESN | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03130 | hp2 | a0001 | c0002 | t0005 | g0011 | AFR | ESN | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0130 | AFR | ESN | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | ESN | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | ESN | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | ESN | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03225 | hp1 | a0001 | c0002 | t0004 | g0064 | AFR | MSL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03225 | hp2 | a0003 | c0004 | t0004 | g0036 | AFR | MSL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03239 | hp2 | a0007 | c0013 | t0003 | g0047 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03453 | hp1 | a0001 | c0002 | t0004 | g0063 | AFR | MSL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | MSL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0198 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0209 | AFR | ESN | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03516 | hp2 | a0001 | c0011 | t0004 | g0123 | AFR | ESN | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0045 | AFR | GWD | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | MSL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0055 | AFR | MSL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0224 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0012 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | BEB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | STU | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0189 | SAS | STU | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0175 | SAS | BEB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | STU | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | STU | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | STU | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | STU | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0199 | SAS | STU | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18522 | hp1 | a0001 | c0002 | t0005 | g0011 | AFR | YRI | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | YRI | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | CHB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | YRI | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18906 | hp2 | a0001 | c0002 | t0004 | g0023 | AFR | YRI | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18944 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18959 | hp1 | a0001 | c0001 | t0008 | g0032 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18967 | hp1 | a0001 | c0001 | t0010 | g0176 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18991 | hp2 | a0001 | c0012 | t0001 | g0084 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA18998 | hp2 | a0001 | c0001 | t0020 | g0004 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19010 | hp1 | a0001 | c0001 | t0010 | g0177 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0140 | AFR | LWK | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | LWK | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | LWK | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19043 | hp2 | a0001 | c0002 | t0004 | g0017 | AFR | LWK | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19084 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19240 | hp1 | a0001 | c0001 | t0013 | g0087 | AFR | YRI | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0139 | AFR | YRI | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA20129 | hp1 | a0001 | c0002 | t0005 | g0011 | AFR | ASW | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA20129 | hp2 | a0001 | c0006 | t0006 | g0127 | AFR | ASW | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0208 | EUR | TSI | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0201 | EUR | TSI | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0193 | AFR | ACB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02109 | hp2 | a0002 | c0005 | t0006 | g0035 | AFR | ACB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02486 | hp1 | a0001 | c0002 | t0004 | g0017 | AFR | ACB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | ACB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | ACB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0192 | AFR | ACB | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | MSL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | MSL | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | USA | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | USA | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | USA | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA20300 | hp2 | a0001 | c0002 | t0004 | g0024 | AFR | USA | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0044 | AFR | LWK | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | LWK | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0053 | REF | REF | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0022 | REF | REF | DLD_chr7_107886183_107926198 | DLD | chr7 | 107886183 | 107926198 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:107891256 | G | C | 1 | a0005 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.6G>C | p.Gln2His | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/14 | 74/3537 | 6/1530 | 2/509 | chr7 | 107891256 | |||
| chr7:107891278 | T | C | 1 | a0004 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.28T>C | p.Ser10Pro | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/14 | 96/3537 | 28/1530 | 10/509 | chr7 | 107891278 | |||
| chr7:107891284 | G | A | 1 | a0003 | 2 | HG02965.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.34G>A | p.Ala12Thr | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/14 | 102/3537 | 34/1530 | 12/509 | chr7 | 107891284 | |||
| chr7:107901749 | G | A | 1 | a0006 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.130G>A | p.Val44Ile | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 3/14 | 198/3537 | 130/1530 | 44/509 | chr7 | 107901749 | |||
| chr7:107916829 | T | C | 1 | a0002 | 2 | HG02109.hp2 HG02615.hp1 |
missense_variant | MODERATE | c.911T>C | p.Ile304Thr | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 10/14 | 979/3537 | 911/1530 | 304/509 | chr7 | 107916829 | |||
| chr7:107918060 | C | T | 1 | a0007 | 1 | HG03239.hp2 | missense_variant&splice_region_variant | MODERATE | c.1373C>T | p.Pro458Leu | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 12/14 | 1441/3537 | 1373/1530 | 458/509 | chr7 | 107918060 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:107902375 | T | C | 2 | a0001c0006 a0002c0005 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
synonymous_variant | LOW | c.249T>C | p.Val83Val | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 4/14 | 317/3537 | 249/1530 | 83/509 | chr7 | 107902375 | |||
| chr7:107905429 | C | T | 1 | a0001c0007 | 2 | HG01243.hp2 HG02630.hp1 |
synonymous_variant | LOW | c.507C>T | p.Gly169Gly | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 7/14 | 575/3537 | 507/1530 | 169/509 | chr7 | 107905429 | |||
| chr7:107906359 | T | C | 1 | a0001c0011 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.675T>C | p.Gly225Gly | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/14 | 743/3537 | 675/1530 | 225/509 | chr7 | 107906359 | |||
| chr7:107915598 | A | G | 2 | a0001c0006 a0002c0005 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
synonymous_variant | LOW | c.777A>G | p.Lys259Lys | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 9/14 | 845/3537 | 777/1530 | 259/509 | chr7 | 107915598 | |||
| chr7:107916899 | G | A | 1 | a0001c0012 | 1 | NA18991.hp2 | synonymous_variant | LOW | c.981G>A | p.Leu327Leu | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 10/14 | 1049/3537 | 981/1530 | 327/509 | chr7 | 107916899 | |||
| chr7:107918038 | C | T | 1 | a0001c0002 | 16 | HG02258.hp2 HG02280.hp1 HG02280.hp2 others(13): Show |
synonymous_variant | LOW | c.1351C>T | p.Leu451Leu | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 12/14 | 1419/3537 | 1351/1530 | 451/509 | chr7 | 107918038 | |||
| chr7:107919057 | A | C | 1 | a0001c0003 | 5 | HG00140.hp1 HG01106.hp2 HG01168.hp2 others(2): Show |
synonymous_variant | LOW | c.1422A>C | p.Gly474Gly | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 13/14 | 1490/3537 | 1422/1530 | 474/509 | chr7 | 107919057 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:107919277 | A | T | 7 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0020 others(4): Show |
123 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*18A>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 18 | chr7 | 107919277 | ||||||
| chr7:107919287 | G | T | 5 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0019 others(2): Show |
106 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*28G>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 28 | chr7 | 107919287 | ||||||
| chr7:107919466 | G | A | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(24): Show |
312 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(309): Show |
3_prime_UTR_variant | MODIFIER | c.*207G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 207 | chr7 | 107919466 | ||||||
| chr7:107919510 | C | T | 1 | a0001c0001t0018 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*251C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 251 | chr7 | 107919510 | ||||||
| chr7:107919550 | GC | G | 2 | a0001c0006t0006 a0002c0005t0006 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*295delC | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 295 | INFO_REALIGN_3_PRIME | chr7 | 107919550 | |||||
| chr7:107919652 | G | A | 1 | a0001c0001t0009 | 2 | HG02970.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*393G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 393 | chr7 | 107919652 | ||||||
| chr7:107919729 | G | T | 2 | a0001c0006t0006 a0002c0005t0006 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*470G>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 470 | chr7 | 107919729 | ||||||
| chr7:107919733 | T | C | 1 | a0001c0001t0012 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*474T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 474 | chr7 | 107919733 | ||||||
| chr7:107919746 | C | T | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(24): Show |
312 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(309): Show |
3_prime_UTR_variant | MODIFIER | c.*487C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 487 | chr7 | 107919746 | ||||||
| chr7:107919907 | G | A | 2 | a0001c0006t0006 a0002c0005t0006 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*648G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 648 | chr7 | 107919907 | ||||||
| chr7:107920014 | T | A | 1 | a0001c0001t0013 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*755T>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 755 | chr7 | 107920014 | ||||||
| chr7:107920114 | C | T | 1 | a0001c0002t0005 | 5 | HG02280.hp2 HG02723.hp1 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*855C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 855 | chr7 | 107920114 | ||||||
| chr7:107920146 | T | C | 2 | a0001c0001t0012 a0001c0001t0014 |
2 | HG02818.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*887T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 887 | chr7 | 107920146 | ||||||
| chr7:107920206 | G | T | 6 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0020 others(3): Show |
121 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*947G>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 947 | chr7 | 107920206 | ||||||
| chr7:107920237 | T | C | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(25): Show |
314 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*978T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 978 | chr7 | 107920237 | ||||||
| chr7:107920286 | T | G | 1 | a0001c0001t0019 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1027T>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 1027 | chr7 | 107920286 | ||||||
| chr7:107920314 | A | G | 1 | a0001c0002t0017 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1055A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 1055 | chr7 | 107920314 | ||||||
| chr7:107920333 | C | G | 1 | a0001c0001t0007 | 3 | HG02630.hp2 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1074C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 1074 | chr7 | 107920333 | ||||||
| chr7:107920559 | A | G | 1 | a0001c0001t0016 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1300A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 1300 | chr7 | 107920559 | ||||||
| chr7:107920710 | T | C | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(25): Show |
314 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*1451T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 1451 | chr7 | 107920710 | ||||||
| chr7:107920899 | A | G | 1 | a0001c0001t0010 | 2 | NA18967.hp1 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1640A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 1640 | chr7 | 107920899 | ||||||
| chr7:107920947 | G | A | 5 | a0001c0001t0001 a0001c0001t0008 a0001c0003t0001 others(2): Show |
120 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1688G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 1688 | chr7 | 107920947 | ||||||
| chr7:107921026 | C | T | 1 | a0001c0001t0015 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1767C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 1767 | chr7 | 107921026 | ||||||
| chr7:107921135 | G | A | 1 | a0001c0001t0008 | 3 | NA18944.hp2 NA18959.hp1 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1876G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 14/14 | 1876 | chr7 | 107921135 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:107891488 | G | A | 18 | a0001c0001t0004g0025 a0001c0001t0004g0060 a0001c0001t0004g0062 others(15): Show |
26 | HG01074.hp1 HG02258.hp2 HG02280.hp1 others(23): Show |
intron_variant | MODIFIER | c.39+199G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107891488 | |||||||
| chr7:107891498 | C | T | 2 | a0001c0001t0004g0229 a0001c0001t0004g0230 |
2 | HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.39+209C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107891498 | |||||||
| chr7:107891606 | G | C | 1 | a0001c0001t0016g0067 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.39+317G>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107891606 | |||||||
| chr7:107891627 | G | A | 4 | a0001c0001t0003g0012 a0001c0001t0003g0026 a0001c0001t0003g0068 others(1): Show |
8 | HG00642.hp1 HG00738.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.39+338G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107891627 | |||||||
| chr7:107891645 | T | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(184): Show |
314 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.39+356T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107891645 | |||||||
| chr7:107891694 | C | G | 7 | a0001c0001t0004g0015 a0001c0001t0004g0045 a0001c0001t0004g0192 others(4): Show |
11 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.39+405C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107891694 | |||||||
| chr7:107891916 | A | G | 4 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 others(1): Show |
4 | HG02132.hp1 NA18972.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+627A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107891916 | |||||||
| chr7:107891940 | C | T | 1 | a0001c0001t0004g0044 | 2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.39+651C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107891940 | |||||||
| chr7:107892020 | A | C | 1 | a0001c0001t0001g0190 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.39+731A>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107892020 | |||||||
| chr7:107892154 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.39+865G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107892154 | |||||||
| chr7:107892190 | G | T | 1 | a0001c0001t0003g0224 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.39+901G>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107892190 | |||||||
| chr7:107892212 | G | A | 1 | a0001c0001t0004g0027 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.39+923G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107892212 | |||||||
| chr7:107892273 | A | G | 6 | a0001c0001t0004g0021 a0001c0001t0004g0042 a0001c0001t0004g0043 others(3): Show |
10 | HG01109.hp2 HG01255.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-927A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107892273 | |||||||
| chr7:107892293 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0071 a0001c0001t0001g0072 others(1): Show |
6 | HG00639.hp2 HG00642.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.40-907G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107892293 | |||||||
| chr7:107892299 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.40-901A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107892299 | |||||||
| chr7:107892339 | C | T | 1 | a0001c0001t0002g0185 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.40-861C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107892339 | |||||||
| chr7:107892443 | C | T | 102 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(99): Show |
170 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.40-757C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107892443 | |||||||
| chr7:107892530 | G | A | 17 | a0001c0001t0004g0025 a0001c0001t0004g0060 a0001c0001t0004g0062 others(14): Show |
25 | HG01074.hp1 HG02258.hp2 HG02280.hp1 others(22): Show |
intron_variant | MODIFIER | c.40-670G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107892530 | |||||||
| chr7:107892530 | G | T | 1 | a0001c0001t0007g0066 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.40-670G>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107892530 | |||||||
| chr7:107892531 | C | A | 1 | a0001c0001t0007g0066 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.40-669C>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107892531 | |||||||
| chr7:107892531 | C | CTTTA | 133 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(130): Show |
241 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.40-641_40-638dupAT others(2): Show |
DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 107892531 | ||||||
| chr7:107892531 | C | CTTTATTT others(1): Show |
38 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0029 others(35): Show |
52 | HG00639.hp2 HG00741.hp1 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.40-645_40-638dupAT others(6): Show |
DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 107892531 | ||||||
| chr7:107892531 | C | CTTTATTT others(5): Show |
10 | a0001c0001t0004g0015 a0001c0001t0004g0192 a0001c0001t0004g0193 others(7): Show |
13 | HG01891.hp2 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.40-649_40-638dupAT others(10): Show |
DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 107892531 | ||||||
| chr7:107892531 | C | CTTTATTT others(9): Show |
1 | a0001c0001t0004g0045 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.40-653_40-638dupAT others(14): Show |
DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 107892531 | ||||||
| chr7:107892662 | T | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(184): Show |
314 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.40-538T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107892662 | |||||||
| chr7:107892706 | C | T | 1 | a0001c0001t0004g0184 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.40-494C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107892706 | |||||||
| chr7:107892709 | C | G | 1 | a0001c0001t0003g0223 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.40-491C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107892709 | |||||||
| chr7:107892843 | C | T | 1 | a0001c0001t0002g0183 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.40-357C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107892843 | |||||||
| chr7:107893037 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.40-163A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 1/13 | chr7 | 107893037 | |||||||
| chr7:107893469 | C | T | 1 | a0001c0001t0004g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.118+191C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107893469 | |||||||
| chr7:107893476 | G | C | 1 | a0001c0001t0014g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.118+198G>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107893476 | |||||||
| chr7:107893687 | T | C | 69 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(66): Show |
123 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.118+409T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107893687 | |||||||
| chr7:107893766 | A | C | 1 | a0001c0001t0003g0222 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.118+488A>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107893766 | |||||||
| chr7:107893777 | A | G | 2 | a0001c0006t0006g0127 a0002c0005t0006g0035 |
3 | HG02109.hp2 HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.118+499A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107893777 | |||||||
| chr7:107893793 | A | G | 57 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(54): Show |
106 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.118+515A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107893793 | |||||||
| chr7:107893968 | A | G | 1 | a0001c0001t0003g0052 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.118+690A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107893968 | |||||||
| chr7:107893998 | A | G | 1 | a0001c0001t0002g0181 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.118+720A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107893998 | |||||||
| chr7:107894148 | C | T | 1 | a0001c0001t0002g0180 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.118+870C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107894148 | |||||||
| chr7:107894393 | A | T | 1 | a0001c0001t0018g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.118+1115A>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107894393 | |||||||
| chr7:107894512 | T | C | 1 | a0001c0011t0004g0123 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.118+1234T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107894512 | |||||||
| chr7:107894785 | A | G | 1 | a0001c0001t0004g0044 | 2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.118+1507A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107894785 | |||||||
| chr7:107894791 | C | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(66): Show |
123 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.118+1513C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107894791 | |||||||
| chr7:107894913 | A | G | 1 | a0001c0001t0003g0051 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.118+1635A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107894913 | |||||||
| chr7:107894920 | T | C | 2 | a0001c0001t0004g0130 a0001c0001t0013g0087 |
2 | HG03139.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.118+1642T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107894920 | |||||||
| chr7:107894947 | T | G | 2 | a0001c0001t0004g0229 a0001c0001t0004g0230 |
2 | HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.118+1669T>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107894947 | |||||||
| chr7:107894948 | T | C | 2 | a0001c0001t0004g0044 a0003c0004t0004g0036 |
4 | HG02055.hp2 HG02965.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+1670T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107894948 | |||||||
| chr7:107895048 | C | T | 1 | a0001c0001t0004g0025 | 2 | HG01074.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.118+1770C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107895048 | |||||||
| chr7:107895165 | A | T | 2 | a0001c0002t0005g0011 a0001c0002t0005g0057 |
5 | HG02280.hp2 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.118+1887A>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107895165 | |||||||
| chr7:107895182 | G | A | 2 | a0001c0001t0013g0087 a0001c0001t0016g0067 |
2 | HG01433.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.118+1904G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107895182 | |||||||
| chr7:107895221 | A | T | 1 | a0001c0001t0003g0221 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.118+1943A>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107895221 | |||||||
| chr7:107895331 | T | A | 1 | a0001c0001t0001g0074 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.118+2053T>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107895331 | |||||||
| chr7:107895349 | T | C | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+2071T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107895349 | |||||||
| chr7:107895482 | C | T | 1 | a0001c0001t0018g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.118+2204C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107895482 | |||||||
| chr7:107895543 | C | T | 1 | a0001c0001t0004g0184 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.118+2265C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107895543 | |||||||
| chr7:107895600 | A | G | 2 | a0001c0001t0002g0041 a0001c0001t0002g0179 |
3 | NA18962.hp2 NA18990.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.118+2322A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107895600 | |||||||
| chr7:107895853 | A | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(184): Show |
314 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.118+2575A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107895853 | |||||||
| chr7:107895972 | G | A | 43 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(40): Show |
85 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.118+2694G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107895972 | |||||||
| chr7:107895984 | G | C | 1 | a0001c0001t0004g0131 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.118+2706G>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107895984 | |||||||
| chr7:107895987 | C | T | 1 | a0001c0001t0018g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.118+2709C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107895987 | |||||||
| chr7:107896019 | T | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0090 |
2 | HG01261.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.118+2741T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107896019 | |||||||
| chr7:107896100 | G | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(76): Show |
137 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.118+2822G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107896100 | |||||||
| chr7:107896185 | A | G | 1 | a0001c0011t0004g0123 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.118+2907A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107896185 | |||||||
| chr7:107896375 | ACT | A | 4 | a0001c0001t0003g0012 a0001c0001t0003g0026 a0001c0001t0003g0068 others(1): Show |
8 | HG00642.hp1 HG00738.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.118+3102_118+3103d others(4): Show |
DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr7 | 107896375 | ||||||
| chr7:107896628 | G | A | 2 | a0001c0001t0004g0229 a0001c0001t0004g0230 |
2 | HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.118+3350G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107896628 | |||||||
| chr7:107896660 | T | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0091 |
2 | HG00544.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.118+3382T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107896660 | |||||||
| chr7:107896705 | C | G | 7 | a0001c0001t0004g0027 a0001c0001t0004g0038 a0001c0001t0004g0130 others(4): Show |
9 | HG02559.hp1 HG02622.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.118+3427C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107896705 | |||||||
| chr7:107896804 | C | T | 1 | a0001c0001t0018g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.118+3526C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107896804 | |||||||
| chr7:107896824 | C | T | 1 | a0001c0001t0004g0189 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.118+3546C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107896824 | |||||||
| chr7:107896838 | G | T | 1 | a0001c0006t0006g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.118+3560G>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107896838 | |||||||
| chr7:107896842 | G | GT | 10 | a0001c0001t0004g0025 a0001c0001t0004g0044 a0001c0002t0004g0017 others(7): Show |
19 | HG01074.hp1 HG01243.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.118+3575dupT | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr7 | 107896842 | ||||||
| chr7:107896842 | G | T | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+3564G>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107896842 | |||||||
| chr7:107896884 | T | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(73): Show |
134 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.118+3606T>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107896884 | |||||||
| chr7:107896929 | G | A | 1 | a0001c0001t0014g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.118+3651G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107896929 | |||||||
| chr7:107896939 | G | A | 1 | a0003c0004t0004g0036 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.118+3661G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107896939 | |||||||
| chr7:107897167 | G | T | 8 | a0001c0001t0004g0060 a0001c0001t0004g0062 a0001c0001t0004g0065 others(5): Show |
8 | HG02572.hp2 HG02630.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.118+3889G>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107897167 | |||||||
| chr7:107897213 | A | G | 1 | a0001c0011t0004g0123 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.118+3935A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107897213 | |||||||
| chr7:107897278 | G | T | 3 | a0001c0001t0013g0087 a0001c0001t0016g0067 a0001c0011t0004g0123 |
3 | HG01433.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.118+4000G>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107897278 | |||||||
| chr7:107897334 | A | G | 6 | a0001c0001t0002g0006 a0001c0001t0002g0164 a0001c0001t0002g0165 others(3): Show |
12 | HG01070.hp2 HG01106.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.118+4056A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107897334 | |||||||
| chr7:107897436 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.118+4158C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107897436 | |||||||
| chr7:107897482 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.118+4204T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107897482 | |||||||
| chr7:107897574 | C | CT | 8 | a0001c0001t0002g0040 a0001c0001t0002g0163 a0001c0001t0002g0178 others(5): Show |
9 | HG00423.hp1 HG03098.hp1 NA18967.hp1 others(6): Show |
intron_variant | MODIFIER | c.119-4142dupT | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr7 | 107897574 | ||||||
| chr7:107897574 | C | CTT | 4 | a0001c0002t0004g0023 a0001c0002t0004g0058 a0001c0002t0005g0011 others(1): Show |
8 | HG02280.hp1 HG02280.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.119-4143_119-4142d others(4): Show |
DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr7 | 107897574 | ||||||
| chr7:107897574 | C | CTTT | 13 | a0001c0001t0004g0025 a0001c0001t0004g0060 a0001c0001t0004g0062 others(10): Show |
17 | HG01074.hp1 HG02258.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.119-4144_119-4142d others(5): Show |
DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr7 | 107897574 | ||||||
| chr7:107897574 | CT | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(80): Show |
142 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.119-4142delT | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr7 | 107897574 | ||||||
| chr7:107897574 | CTT | C | 13 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0076 others(10): Show |
15 | HG00741.hp1 HG01168.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.119-4143_119-4142d others(4): Show |
DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr7 | 107897574 | ||||||
| chr7:107897574 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0003g0051 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.119-4151_119-4142d others(12): Show |
DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr7 | 107897574 | ||||||
| chr7:107897626 | TG | T | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-4108delG | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr7 | 107897626 | ||||||
| chr7:107897641 | C | T | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-4097C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107897641 | |||||||
| chr7:107897642 | G | A | 1 | a0001c0001t0012g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.119-4096G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107897642 | |||||||
| chr7:107897673 | G | T | 1 | a0001c0001t0003g0218 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.119-4065G>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107897673 | |||||||
| chr7:107897704 | G | C | 1 | a0001c0001t0013g0087 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.119-4034G>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107897704 | |||||||
| chr7:107897726 | G | A | 1 | a0001c0001t0004g0189 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.119-4012G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107897726 | |||||||
| chr7:107897779 | A | T | 1 | a0001c0001t0014g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.119-3959A>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107897779 | |||||||
| chr7:107897824 | C | G | 1 | a0001c0001t0004g0062 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.119-3914C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107897824 | |||||||
| chr7:107897875 | A | T | 1 | a0001c0001t0013g0087 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.119-3863A>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107897875 | |||||||
| chr7:107898058 | C | G | 184 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(181): Show |
310 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.119-3680C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107898058 | |||||||
| chr7:107898089 | C | G | 1 | a0001c0011t0004g0123 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.119-3649C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107898089 | |||||||
| chr7:107898148 | A | T | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-3590A>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107898148 | |||||||
| chr7:107898173 | T | C | 1 | a0001c0001t0014g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.119-3565T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107898173 | |||||||
| chr7:107898270 | CT | C | 116 | a0001c0001t0001g0008 a0001c0001t0001g0085 a0001c0001t0001g0086 others(113): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.119-3444delT | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr7 | 107898270 | ||||||
| chr7:107898270 | CTT | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(88): Show |
160 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.119-3445_119-3444d others(4): Show |
DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr7 | 107898270 | ||||||
| chr7:107898295 | G | A | 1 | a0001c0001t0012g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.119-3443G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107898295 | |||||||
| chr7:107898417 | G | T | 1 | a0001c0001t0003g0228 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-3321G>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107898417 | |||||||
| chr7:107898429 | T | C | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-3309T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107898429 | |||||||
| chr7:107898533 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.119-3205G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107898533 | |||||||
| chr7:107898578 | G | A | 1 | a0001c0001t0007g0054 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.119-3160G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107898578 | |||||||
| chr7:107898635 | G | A | 1 | a0001c0001t0004g0229 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.119-3103G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107898635 | |||||||
| chr7:107898651 | C | G | 7 | a0001c0001t0004g0015 a0001c0001t0004g0045 a0001c0001t0004g0192 others(4): Show |
11 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.119-3087C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107898651 | |||||||
| chr7:107898652 | G | A | 1 | a0001c0001t0012g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.119-3086G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107898652 | |||||||
| chr7:107898684 | G | A | 78 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
136 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.119-3054G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107898684 | |||||||
| chr7:107898853 | G | A | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-2885G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107898853 | |||||||
| chr7:107898886 | A | C | 1 | a0001c0001t0012g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.119-2852A>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107898886 | |||||||
| chr7:107898996 | G | T | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-2742G>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107898996 | |||||||
| chr7:107899236 | T | G | 1 | a0001c0001t0004g0131 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.119-2502T>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107899236 | |||||||
| chr7:107899239 | T | C | 6 | a0001c0001t0003g0047 a0001c0001t0003g0225 a0001c0001t0003g0226 others(3): Show |
6 | HG02129.hp2 HG02132.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-2499T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107899239 | |||||||
| chr7:107899302 | G | C | 1 | a0001c0001t0003g0048 | 2 | HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.119-2436G>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107899302 | |||||||
| chr7:107899390 | A | T | 1 | a0001c0001t0003g0215 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.119-2348A>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107899390 | |||||||
| chr7:107899459 | C | T | 1 | a0001c0011t0004g0123 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.119-2279C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107899459 | |||||||
| chr7:107899460 | C | T | 1 | a0001c0001t0018g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.119-2278C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107899460 | |||||||
| chr7:107899574 | T | C | 1 | a0001c0001t0014g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.119-2164T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107899574 | |||||||
| chr7:107899629 | A | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(66): Show |
123 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.119-2109A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107899629 | |||||||
| chr7:107899665 | G | C | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-2073G>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107899665 | |||||||
| chr7:107899717 | T | C | 18 | a0001c0001t0004g0025 a0001c0001t0004g0060 a0001c0001t0004g0062 others(15): Show |
26 | HG01074.hp1 HG02258.hp2 HG02280.hp1 others(23): Show |
intron_variant | MODIFIER | c.119-2021T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107899717 | |||||||
| chr7:107899781 | A | G | 6 | a0001c0001t0004g0025 a0001c0002t0004g0017 a0001c0002t0004g0024 others(3): Show |
10 | HG01074.hp1 HG02258.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-1957A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107899781 | |||||||
| chr7:107899799 | T | C | 69 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(66): Show |
123 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.119-1939T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107899799 | |||||||
| chr7:107899960 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(184): Show |
314 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.119-1778G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107899960 | |||||||
| chr7:107900055 | C | T | 1 | a0001c0001t0001g0018 | 3 | HG00642.hp2 HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.119-1683C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107900055 | |||||||
| chr7:107900131 | A | G | 1 | a0001c0001t0004g0184 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.119-1607A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107900131 | |||||||
| chr7:107900346 | C | A | 1 | a0001c0001t0010g0176 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.119-1392C>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107900346 | |||||||
| chr7:107900412 | A | G | 1 | a0001c0001t0002g0160 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.119-1326A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107900412 | |||||||
| chr7:107900445 | C | T | 6 | a0001c0001t0004g0021 a0001c0001t0004g0042 a0001c0001t0004g0043 others(3): Show |
10 | HG01109.hp2 HG01255.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.119-1293C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107900445 | |||||||
| chr7:107900548 | A | T | 2 | a0001c0001t0004g0182 a0001c0001t0004g0184 |
2 | HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.119-1190A>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107900548 | |||||||
| chr7:107900635 | C | T | 1 | a0001c0001t0012g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.119-1103C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107900635 | |||||||
| chr7:107900739 | G | A | 1 | a0001c0001t0003g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.119-999G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107900739 | |||||||
| chr7:107900767 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.119-971C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107900767 | |||||||
| chr7:107901112 | A | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(184): Show |
314 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.119-626A>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107901112 | |||||||
| chr7:107901337 | C | T | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-401C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107901337 | |||||||
| chr7:107901430 | G | C | 4 | a0001c0001t0004g0015 a0001c0001t0004g0192 a0001c0001t0004g0195 others(1): Show |
7 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.119-308G>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107901430 | |||||||
| chr7:107901540 | T | C | 1 | a0001c0001t0002g0039 | 2 | HG02132.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.119-198T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107901540 | |||||||
| chr7:107901628 | T | G | 1 | a0001c0001t0018g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.119-110T>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107901628 | |||||||
| chr7:107901631 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.119-107T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107901631 | |||||||
| chr7:107901653 | G | A | 2 | a0001c0001t0004g0044 a0003c0004t0004g0036 |
4 | HG02055.hp2 HG02965.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-85G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107901653 | |||||||
| chr7:107901659 | T | G | 1 | a0001c0001t0004g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.119-79T>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 2/13 | chr7 | 107901659 | |||||||
| chr7:107901916 | T | A | 1 | a0001c0001t0002g0170 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.198+99T>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 3/13 | chr7 | 107901916 | |||||||
| chr7:107901921 | A | AACTCTAT others(127): Show |
1 | a0001c0006t0006g0127 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.198+108_198+241dup others(134): Show |
DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 107901921 | ||||||
| chr7:107902070 | A | G | 2 | a0001c0001t0013g0087 a0001c0001t0016g0067 |
2 | HG01433.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.198+253A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 3/13 | chr7 | 107902070 | |||||||
| chr7:107902115 | A | T | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-210A>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 3/13 | chr7 | 107902115 | |||||||
| chr7:107902126 | A | G | 3 | a0001c0001t0001g0075 a0001c0001t0001g0083 a0001c0001t0001g0091 |
3 | HG00544.hp1 HG02083.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.199-199A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 3/13 | chr7 | 107902126 | |||||||
| chr7:107902197 | TATTTTAG | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(66): Show |
123 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.199-127_199-121del others(7): Show |
DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 3/13 | chr7 | 107902197 | |||||||
| chr7:107902217 | T | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(184): Show |
314 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.199-108T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 3/13 | chr7 | 107902217 | |||||||
| chr7:107902439 | A | G | 1 | a0001c0001t0004g0229 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.267+46A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 4/13 | chr7 | 107902439 | |||||||
| chr7:107902510 | C | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0073 |
2 | HG00639.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.267+117C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 4/13 | chr7 | 107902510 | |||||||
| chr7:107902628 | C | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0071 a0001c0001t0001g0072 others(3): Show |
8 | HG00639.hp2 HG00642.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.267+235C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 4/13 | chr7 | 107902628 | |||||||
| chr7:107902863 | T | C | 1 | a0001c0001t0002g0170 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.267+470T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 4/13 | chr7 | 107902863 | |||||||
| chr7:107902908 | A | G | 79 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(76): Show |
138 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.267+515A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 4/13 | chr7 | 107902908 | |||||||
| chr7:107902979 | A | G | 1 | a0001c0001t0013g0087 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.268-499A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 4/13 | chr7 | 107902979 | |||||||
| chr7:107902988 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.268-490T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 4/13 | chr7 | 107902988 | |||||||
| chr7:107903028 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.268-450A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 4/13 | chr7 | 107903028 | |||||||
| chr7:107903100 | A | G | 3 | a0001c0003t0001g0096 a0001c0003t0001g0112 a0001c0003t0001g0120 |
3 | HG00140.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.268-378A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 4/13 | chr7 | 107903100 | |||||||
| chr7:107903136 | C | T | 1 | a0001c0001t0003g0201 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.268-342C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 4/13 | chr7 | 107903136 | |||||||
| chr7:107903139 | CTG | C | 4 | a0001c0001t0002g0009 a0001c0001t0002g0169 a0001c0001t0002g0171 others(1): Show |
8 | HG02083.hp2 HG02135.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.268-337_268-336del others(2): Show |
DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 107903139 | ||||||
| chr7:107903152 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.268-326A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 4/13 | chr7 | 107903152 | |||||||
| chr7:107903187 | C | T | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-291C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 4/13 | chr7 | 107903187 | |||||||
| chr7:107903303 | G | A | 1 | a0001c0001t0018g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.268-175G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 4/13 | chr7 | 107903303 | |||||||
| chr7:107903309 | C | G | 1 | a0001c0001t0003g0214 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.268-169C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 4/13 | chr7 | 107903309 | |||||||
| chr7:107903319 | G | A | 2 | a0001c0001t0002g0147 a0001c0002t0004g0063 |
2 | HG03453.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.268-159G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 4/13 | chr7 | 107903319 | |||||||
| chr7:107903335 | G | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0076 |
3 | NA18939.hp1 NA18960.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.268-143G>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 4/13 | chr7 | 107903335 | |||||||
| chr7:107903374 | G | A | 1 | a0001c0001t0004g0042 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.268-104G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 4/13 | chr7 | 107903374 | |||||||
| chr7:107903407 | A | G | 2 | a0001c0001t0003g0200 a0001c0001t0003g0213 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.268-71A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 4/13 | chr7 | 107903407 | |||||||
| chr7:107903602 | CTGTCTAA others(11): Show |
C | 1 | a0001c0001t0004g0065 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.337+63_337+80delAG others(16): Show |
DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr7 | 107903602 | ||||||
| chr7:107903652 | A | G | 2 | a0001c0001t0003g0050 a0001c0001t0003g0215 |
3 | HG00738.hp2 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.337+105A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 5/13 | chr7 | 107903652 | |||||||
| chr7:107903701 | A | C | 2 | a0001c0002t0004g0023 a0001c0002t0004g0058 |
3 | HG02280.hp1 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.337+154A>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 5/13 | chr7 | 107903701 | |||||||
| chr7:107903763 | C | G | 184 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(181): Show |
310 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.337+216C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 5/13 | chr7 | 107903763 | |||||||
| chr7:107903872 | A | G | 79 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(76): Show |
138 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.337+325A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 5/13 | chr7 | 107903872 | |||||||
| chr7:107903875 | A | G | 1 | a0001c0001t0002g0167 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.337+328A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 5/13 | chr7 | 107903875 | |||||||
| chr7:107904011 | G | C | 1 | a0001c0001t0003g0203 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.337+464G>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 5/13 | chr7 | 107904011 | |||||||
| chr7:107904086 | G | A | 69 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(66): Show |
123 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.337+539G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 5/13 | chr7 | 107904086 | |||||||
| chr7:107904220 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.337+673G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 5/13 | chr7 | 107904220 | |||||||
| chr7:107904297 | T | C | 69 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(66): Show |
123 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.338-661T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 5/13 | chr7 | 107904297 | |||||||
| chr7:107904321 | A | G | 1 | a0001c0002t0004g0024 | 2 | HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.338-637A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 5/13 | chr7 | 107904321 | |||||||
| chr7:107904348 | A | G | 1 | a0001c0001t0004g0135 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.338-610A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 5/13 | chr7 | 107904348 | |||||||
| chr7:107904582 | T | A | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.338-376T>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 5/13 | chr7 | 107904582 | |||||||
| chr7:107904633 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.338-325C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 5/13 | chr7 | 107904633 | |||||||
| chr7:107904659 | C | T | 1 | a0001c0001t0002g0173 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.338-299C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 5/13 | chr7 | 107904659 | |||||||
| chr7:107904676 | G | A | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.338-282G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 5/13 | chr7 | 107904676 | |||||||
| chr7:107904877 | T | A | 6 | a0001c0001t0003g0051 a0001c0001t0003g0198 a0001c0001t0003g0201 others(3): Show |
7 | HG00280.hp2 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.338-81T>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 5/13 | chr7 | 107904877 | |||||||
| chr7:107905101 | A | C | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.438+43A>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 6/13 | chr7 | 107905101 | |||||||
| chr7:107905101 | A | G | 1 | a0001c0001t0003g0217 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.438+43A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 6/13 | chr7 | 107905101 | |||||||
| chr7:107905141 | G | A | 69 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(66): Show |
123 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.438+83G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 6/13 | chr7 | 107905141 | |||||||
| chr7:107905284 | G | T | 1 | a0001c0002t0005g0057 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.439-77G>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 6/13 | chr7 | 107905284 | |||||||
| chr7:107905354 | T | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(184): Show |
314 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(311): Show |
splice_region_variant&intron_variant | LOW | c.439-7T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 6/13 | chr7 | 107905354 | |||||||
| chr7:107905771 | G | T | 3 | a0001c0001t0013g0087 a0001c0001t0016g0067 a0001c0011t0004g0123 |
3 | HG01433.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.582+267G>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 7/13 | chr7 | 107905771 | |||||||
| chr7:107905833 | A | C | 2 | a0001c0001t0004g0229 a0001c0001t0004g0230 |
2 | HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.582+329A>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 7/13 | chr7 | 107905833 | |||||||
| chr7:107906139 | A | G | 1 | a0001c0001t0004g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.583-128A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 7/13 | chr7 | 107906139 | |||||||
| chr7:107906188 | T | C | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.583-79T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 7/13 | chr7 | 107906188 | |||||||
| chr7:107906196 | A | G | 7 | a0001c0001t0004g0015 a0001c0001t0004g0045 a0001c0001t0004g0192 others(4): Show |
11 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.583-71A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 7/13 | chr7 | 107906196 | |||||||
| chr7:107906375 | G | A | 17 | a0001c0001t0004g0060 a0001c0001t0004g0062 a0001c0001t0004g0065 others(14): Show |
24 | HG02258.hp2 HG02280.hp1 HG02280.hp2 others(21): Show |
splice_region_variant&intron_variant | LOW | c.684+7G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107906375 | |||||||
| chr7:107906473 | G | C | 2 | a0001c0001t0004g0229 a0001c0001t0004g0230 |
2 | HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.684+105G>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107906473 | |||||||
| chr7:107906492 | A | G | 112 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(109): Show |
184 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.684+124A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107906492 | |||||||
| chr7:107906557 | G | C | 112 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(109): Show |
184 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.684+189G>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107906557 | |||||||
| chr7:107906602 | A | T | 1 | a0001c0001t0002g0165 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.684+234A>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107906602 | |||||||
| chr7:107906722 | T | C | 1 | a0001c0001t0018g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.684+354T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107906722 | |||||||
| chr7:107906939 | C | T | 1 | a0001c0001t0012g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.684+571C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107906939 | |||||||
| chr7:107907050 | A | G | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.684+682A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107907050 | |||||||
| chr7:107907063 | T | G | 1 | a0001c0001t0004g0184 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.684+695T>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107907063 | |||||||
| chr7:107907147 | G | A | 2 | a0001c0002t0005g0011 a0001c0002t0005g0057 |
5 | HG02280.hp2 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.684+779G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107907147 | |||||||
| chr7:107907196 | T | C | 2 | a0001c0002t0004g0023 a0001c0002t0004g0058 |
3 | HG02280.hp1 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.684+828T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107907196 | |||||||
| chr7:107907204 | G | A | 3 | a0001c0001t0003g0049 a0001c0001t0003g0205 a0001c0001t0003g0206 |
4 | HG00673.hp1 HG02080.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.684+836G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107907204 | |||||||
| chr7:107907402 | A | G | 1 | a0001c0001t0004g0065 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.684+1034A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107907402 | |||||||
| chr7:107907527 | C | G | 1 | a0001c0001t0003g0212 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.684+1159C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107907527 | |||||||
| chr7:107907782 | G | A | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.684+1414G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107907782 | |||||||
| chr7:107907854 | C | T | 1 | a0001c0001t0003g0224 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.684+1486C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107907854 | |||||||
| chr7:107907858 | A | G | 1 | a0001c0001t0003g0211 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.684+1490A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107907858 | |||||||
| chr7:107907870 | A | G | 1 | a0001c0001t0002g0158 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.684+1502A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107907870 | |||||||
| chr7:107907872 | G | C | 1 | a0001c0001t0010g0176 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.684+1504G>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107907872 | |||||||
| chr7:107907977 | A | G | 1 | a0001c0001t0004g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.684+1609A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107907977 | |||||||
| chr7:107908034 | C | T | 1 | a0001c0001t0012g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.684+1666C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107908034 | |||||||
| chr7:107908153 | C | CT | 67 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(64): Show |
121 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.684+1800dupT | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 107908153 | ||||||
| chr7:107908153 | C | T | 2 | a0001c0001t0004g0132 a0001c0001t0004g0134 |
2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.684+1785C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107908153 | |||||||
| chr7:107908185 | G | C | 18 | a0001c0001t0004g0025 a0001c0001t0004g0060 a0001c0001t0004g0062 others(15): Show |
26 | HG01074.hp1 HG02258.hp2 HG02280.hp1 others(23): Show |
intron_variant | MODIFIER | c.684+1817G>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107908185 | |||||||
| chr7:107908225 | A | G | 1 | a0001c0001t0004g0065 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.684+1857A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107908225 | |||||||
| chr7:107908284 | G | A | 1 | a0001c0001t0003g0199 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.684+1916G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107908284 | |||||||
| chr7:107908285 | A | G | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.684+1917A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107908285 | |||||||
| chr7:107908307 | C | T | 5 | a0001c0001t0002g0005 a0001c0001t0002g0144 a0001c0001t0002g0145 others(2): Show |
11 | HG00423.hp1 HG00438.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.684+1939C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107908307 | |||||||
| chr7:107908311 | C | T | 1 | a0001c0001t0012g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.684+1943C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107908311 | |||||||
| chr7:107908312 | G | A | 1 | a0001c0001t0002g0173 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.684+1944G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107908312 | |||||||
| chr7:107908391 | C | T | 2 | a0001c0001t0018g0124 a0001c0011t0004g0123 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.684+2023C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107908391 | |||||||
| chr7:107908462 | G | A | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.684+2094G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107908462 | |||||||
| chr7:107908571 | G | C | 1 | a0001c0001t0004g0025 | 2 | HG01074.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.684+2203G>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107908571 | |||||||
| chr7:107908627 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.684+2259A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107908627 | |||||||
| chr7:107908666 | C | CA | 8 | a0001c0001t0001g0031 a0001c0001t0001g0114 a0001c0001t0001g0122 others(5): Show |
9 | HG01081.hp1 HG01928.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.684+2313dupA | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 107908666 | ||||||
| chr7:107908666 | CA | C | 71 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(68): Show |
126 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.684+2313delA | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 107908666 | ||||||
| chr7:107908677 | A | AC | 3 | a0001c0001t0004g0015 a0001c0001t0004g0195 a0001c0001t0015g0191 |
6 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.684+2309_684+2310i others(3): Show |
DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107908677 | |||||||
| chr7:107908677 | A | C | 4 | a0001c0001t0004g0045 a0001c0001t0004g0192 a0001c0001t0004g0193 others(1): Show |
5 | HG02109.hp1 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.684+2309A>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107908677 | |||||||
| chr7:107908681 | AC | A | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.684+2317delC | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 107908681 | ||||||
| chr7:107908741 | A | G | 9 | a0001c0001t0004g0027 a0001c0001t0004g0038 a0001c0001t0004g0130 others(6): Show |
11 | HG01891.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.684+2373A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107908741 | |||||||
| chr7:107908787 | C | T | 3 | a0001c0001t0013g0087 a0001c0001t0016g0067 a0001c0011t0004g0123 |
3 | HG01433.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.684+2419C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107908787 | |||||||
| chr7:107908863 | C | G | 6 | a0001c0001t0004g0025 a0001c0002t0004g0017 a0001c0002t0004g0024 others(3): Show |
10 | HG01074.hp1 HG02258.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.684+2495C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107908863 | |||||||
| chr7:107908874 | G | A | 1 | a0004c0009t0001g0102 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.684+2506G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107908874 | |||||||
| chr7:107909067 | T | C | 5 | a0001c0001t0003g0012 a0001c0001t0003g0026 a0001c0001t0003g0068 others(2): Show |
9 | HG00642.hp1 HG00738.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.684+2699T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107909067 | |||||||
| chr7:107909104 | T | C | 1 | a0001c0001t0004g0065 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.684+2736T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107909104 | |||||||
| chr7:107909105 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0109 |
3 | HG01081.hp1 HG04204.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.684+2737A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107909105 | |||||||
| chr7:107909130 | C | T | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.684+2762C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107909130 | |||||||
| chr7:107909244 | A | G | 1 | a0001c0001t0003g0210 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.684+2876A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107909244 | |||||||
| chr7:107909501 | T | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(184): Show |
314 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.684+3133T>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107909501 | |||||||
| chr7:107909535 | T | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0115 |
2 | NA18953.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.684+3167T>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107909535 | |||||||
| chr7:107909573 | T | C | 2 | a0001c0001t0002g0166 a0001c0001t0002g0167 |
2 | NA18944.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.684+3205T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107909573 | |||||||
| chr7:107909753 | G | A | 1 | a0001c0001t0004g0065 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.684+3385G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107909753 | |||||||
| chr7:107909839 | C | CT | 7 | a0001c0001t0003g0016 a0001c0001t0003g0207 a0001c0001t0003g0210 others(4): Show |
10 | HG00741.hp2 HG01261.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.684+3496dupT | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 107909839 | ||||||
| chr7:107909839 | CT | C | 76 | a0001c0001t0001g0033 a0001c0001t0001g0090 a0001c0001t0001g0095 others(73): Show |
135 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.684+3496delT | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 107909839 | ||||||
| chr7:107909839 | CTT | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(85): Show |
152 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.684+3495_684+3496d others(4): Show |
DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 107909839 | ||||||
| chr7:107909839 | CTTT | C | 10 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0075 others(7): Show |
13 | HG01975.hp2 NA18959.hp1 NA18967.hp2 others(10): Show |
intron_variant | MODIFIER | c.684+3494_684+3496d others(5): Show |
DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 107909839 | ||||||
| chr7:107909868 | A | G | 1 | a0001c0001t0004g0044 | 2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.684+3500A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107909868 | |||||||
| chr7:107909915 | C | T | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.684+3547C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107909915 | |||||||
| chr7:107910031 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.684+3663A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107910031 | |||||||
| chr7:107910329 | A | T | 1 | a0001c0001t0002g0154 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.684+3961A>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107910329 | |||||||
| chr7:107910563 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(184): Show |
314 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.684+4195G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107910563 | |||||||
| chr7:107910738 | C | G | 1 | a0001c0001t0002g0153 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.684+4370C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107910738 | |||||||
| chr7:107910940 | C | G | 1 | a0001c0001t0013g0087 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.685-4566C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107910940 | |||||||
| chr7:107910977 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.685-4529G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107910977 | |||||||
| chr7:107911085 | T | C | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-4421T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107911085 | |||||||
| chr7:107911166 | C | T | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-4340C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107911166 | |||||||
| chr7:107911314 | C | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(76): Show |
137 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.685-4192C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107911314 | |||||||
| chr7:107911503 | G | A | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-4003G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107911503 | |||||||
| chr7:107911575 | A | G | 2 | a0001c0001t0004g0229 a0001c0001t0004g0230 |
2 | HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.685-3931A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107911575 | |||||||
| chr7:107911642 | T | A | 3 | a0001c0001t0001g0077 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | HG00741.hp1 HG02148.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.685-3864T>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107911642 | |||||||
| chr7:107911643 | T | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(86): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.685-3863T>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107911643 | |||||||
| chr7:107911691 | G | GT | 3 | a0001c0001t0001g0118 a0001c0002t0005g0011 a0001c0002t0005g0057 |
6 | HG02004.hp1 HG02280.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.685-3806dupT | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 107911691 | ||||||
| chr7:107911691 | G | T | 1 | a0001c0001t0002g0178 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.685-3815G>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107911691 | |||||||
| chr7:107911759 | T | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0094 others(9): Show |
33 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.685-3747T>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107911759 | |||||||
| chr7:107911825 | A | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(184): Show |
314 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.685-3681A>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107911825 | |||||||
| chr7:107911908 | C | T | 1 | a0001c0011t0004g0123 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.685-3598C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107911908 | |||||||
| chr7:107911944 | G | C | 3 | a0001c0001t0007g0054 a0001c0001t0007g0059 a0001c0001t0007g0066 |
3 | HG02630.hp2 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.685-3562G>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107911944 | |||||||
| chr7:107912050 | T | G | 2 | a0001c0001t0004g0045 a0001c0001t0012g0088 |
3 | HG02622.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.685-3456T>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107912050 | |||||||
| chr7:107912240 | C | G | 184 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(181): Show |
310 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.685-3266C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107912240 | |||||||
| chr7:107912295 | C | T | 1 | a0001c0001t0012g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.685-3211C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107912295 | |||||||
| chr7:107912296 | G | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(76): Show |
137 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.685-3210G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107912296 | |||||||
| chr7:107912780 | T | C | 3 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0105 |
3 | HG00741.hp1 HG01256.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.685-2726T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107912780 | |||||||
| chr7:107912872 | C | T | 1 | a0001c0001t0014g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.685-2634C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107912872 | |||||||
| chr7:107912928 | T | A | 1 | a0001c0001t0002g0181 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.685-2578T>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107912928 | |||||||
| chr7:107912964 | T | C | 1 | a0001c0001t0002g0150 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.685-2542T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107912964 | |||||||
| chr7:107913013 | A | G | 1 | a0001c0001t0002g0152 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.685-2493A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107913013 | |||||||
| chr7:107913139 | T | G | 1 | a0001c0001t0002g0166 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.685-2367T>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107913139 | |||||||
| chr7:107913274 | T | TGAA | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-2231_685-2229d others(5): Show |
DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 107913274 | ||||||
| chr7:107913380 | A | G | 2 | a0001c0002t0005g0011 a0001c0002t0005g0057 |
5 | HG02280.hp2 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.685-2126A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107913380 | |||||||
| chr7:107913436 | A | G | 2 | a0001c0001t0002g0166 a0001c0001t0002g0167 |
2 | NA18944.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.685-2070A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107913436 | |||||||
| chr7:107913438 | A | C | 1 | a0001c0001t0012g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.685-2068A>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107913438 | |||||||
| chr7:107913486 | T | C | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-2020T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107913486 | |||||||
| chr7:107913504 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.685-2002G>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107913504 | |||||||
| chr7:107913648 | T | A | 1 | a0001c0002t0005g0057 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.685-1858T>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107913648 | |||||||
| chr7:107913763 | C | T | 1 | a0001c0001t0018g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.685-1743C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107913763 | |||||||
| chr7:107913985 | G | A | 1 | a0001c0001t0004g0025 | 2 | HG01074.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.685-1521G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107913985 | |||||||
| chr7:107914012 | G | A | 1 | a0001c0001t0004g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.685-1494G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107914012 | |||||||
| chr7:107914064 | G | T | 1 | a0001c0001t0001g0117 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.685-1442G>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107914064 | |||||||
| chr7:107914115 | C | G | 1 | a0001c0001t0014g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.685-1391C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107914115 | |||||||
| chr7:107914145 | C | G | 1 | a0001c0001t0001g0080 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.685-1361C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107914145 | |||||||
| chr7:107914196 | A | G | 1 | a0001c0001t0002g0142 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.685-1310A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107914196 | |||||||
| chr7:107914245 | T | C | 2 | a0001c0001t0003g0026 a0001c0001t0003g0069 |
3 | HG00738.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.685-1261T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107914245 | |||||||
| chr7:107914248 | A | C | 7 | a0001c0001t0004g0015 a0001c0001t0004g0045 a0001c0001t0004g0192 others(4): Show |
11 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.685-1258A>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107914248 | |||||||
| chr7:107914318 | C | G | 1 | a0001c0001t0007g0066 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.685-1188C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107914318 | |||||||
| chr7:107914420 | T | G | 8 | a0001c0001t0004g0025 a0001c0002t0004g0017 a0001c0002t0004g0023 others(5): Show |
13 | HG01074.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.685-1086T>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107914420 | |||||||
| chr7:107914429 | A | G | 1 | a0001c0001t0004g0184 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.685-1077A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107914429 | |||||||
| chr7:107914662 | A | G | 1 | a0001c0001t0014g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.685-844A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107914662 | |||||||
| chr7:107914694 | G | T | 1 | a0001c0001t0014g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.685-812G>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107914694 | |||||||
| chr7:107914734 | G | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(66): Show |
123 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.685-772G>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107914734 | |||||||
| chr7:107914809 | G | A | 1 | a0001c0001t0004g0188 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.685-697G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107914809 | |||||||
| chr7:107914919 | T | A | 2 | a0001c0001t0004g0229 a0001c0001t0004g0230 |
2 | HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.685-587T>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107914919 | |||||||
| chr7:107915120 | G | C | 1 | a0001c0001t0018g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.685-386G>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107915120 | |||||||
| chr7:107915283 | T | C | 1 | a0001c0001t0018g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.685-223T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107915283 | |||||||
| chr7:107915353 | A | G | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-153A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107915353 | |||||||
| chr7:107915363 | G | A | 2 | a0001c0001t0001g0079 a0001c0012t0001g0084 |
2 | NA18991.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.685-143G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107915363 | |||||||
| chr7:107915492 | T | A | 4 | a0001c0001t0016g0067 a0001c0001t0018g0124 a0001c0002t0004g0023 others(1): Show |
5 | HG01433.hp1 HG02280.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.685-14T>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 8/13 | chr7 | 107915492 | |||||||
| chr7:107915820 | A | G | 4 | a0001c0001t0004g0019 a0001c0001t0004g0133 a0001c0001t0004g0135 others(1): Show |
6 | HG02258.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.875+124A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 9/13 | chr7 | 107915820 | |||||||
| chr7:107915855 | C | A | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.875+159C>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 9/13 | chr7 | 107915855 | |||||||
| chr7:107915915 | C | T | 2 | a0001c0001t0009g0055 a0001c0001t0009g0061 |
2 | HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.875+219C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 9/13 | chr7 | 107915915 | |||||||
| chr7:107915922 | T | G | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.875+226T>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 9/13 | chr7 | 107915922 | |||||||
| chr7:107915977 | T | C | 11 | a0001c0001t0004g0015 a0001c0001t0004g0045 a0001c0001t0004g0182 others(8): Show |
15 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.875+281T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 9/13 | chr7 | 107915977 | |||||||
| chr7:107916053 | T | C | 1 | a0001c0002t0004g0023 | 2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.875+357T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 9/13 | chr7 | 107916053 | |||||||
| chr7:107916098 | A | G | 57 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(54): Show |
106 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.875+402A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 9/13 | chr7 | 107916098 | |||||||
| chr7:107916178 | C | T | 79 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(76): Show |
138 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.875+482C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 9/13 | chr7 | 107916178 | |||||||
| chr7:107916229 | C | G | 1 | a0001c0001t0016g0067 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.875+533C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 9/13 | chr7 | 107916229 | |||||||
| chr7:107916239 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.875+543A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 9/13 | chr7 | 107916239 | |||||||
| chr7:107916294 | A | G | 79 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0006 others(76): Show |
138 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.876-500A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 9/13 | chr7 | 107916294 | |||||||
| chr7:107916387 | A | G | 1 | a0001c0011t0004g0123 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.876-407A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 9/13 | chr7 | 107916387 | |||||||
| chr7:107916419 | A | T | 1 | a0001c0001t0018g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.876-375A>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 9/13 | chr7 | 107916419 | |||||||
| chr7:107916541 | G | A | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.876-253G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 9/13 | chr7 | 107916541 | |||||||
| chr7:107916544 | T | C | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.876-250T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 9/13 | chr7 | 107916544 | |||||||
| chr7:107916620 | C | T | 1 | a0001c0001t0012g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.876-174C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 9/13 | chr7 | 107916620 | |||||||
| chr7:107916621 | G | A | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.876-173G>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 9/13 | chr7 | 107916621 | |||||||
| chr7:107916740 | C | G | 1 | a0001c0001t0016g0067 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.876-54C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 9/13 | chr7 | 107916740 | |||||||
| chr7:107917022 | T | G | 1 | a0001c0001t0003g0216 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1046+58T>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 10/13 | chr7 | 107917022 | |||||||
| chr7:107917182 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1047-91T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 10/13 | chr7 | 107917182 | |||||||
| chr7:107917475 | A | G | 1 | a0001c0001t0003g0215 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1236+13A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 11/13 | chr7 | 107917475 | |||||||
| chr7:107917666 | A | G | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1236+204A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 11/13 | chr7 | 107917666 | |||||||
| chr7:107917763 | A | G | 1 | a0001c0001t0018g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1237-161A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 11/13 | chr7 | 107917763 | |||||||
| chr7:107917793 | C | A | 1 | a0001c0001t0003g0211 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1237-131C>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 11/13 | chr7 | 107917793 | |||||||
| chr7:107917797 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1237-127C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 11/13 | chr7 | 107917797 | |||||||
| chr7:107917822 | C | G | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237-102C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 11/13 | chr7 | 107917822 | |||||||
| chr7:107918168 | A | G | 1 | a0001c0001t0004g0188 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1374+107A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 12/13 | chr7 | 107918168 | |||||||
| chr7:107918177 | A | G | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1374+116A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 12/13 | chr7 | 107918177 | |||||||
| chr7:107918189 | G | C | 1 | a0001c0001t0003g0209 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1374+128G>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 12/13 | chr7 | 107918189 | |||||||
| chr7:107918223 | T | C | 1 | a0001c0001t0002g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1374+162T>C | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 12/13 | chr7 | 107918223 | |||||||
| chr7:107918598 | C | G | 1 | a0006c0010t0002g0128 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1375-412C>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 12/13 | chr7 | 107918598 | |||||||
| chr7:107918606 | A | G | 1 | a0001c0011t0004g0123 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1375-404A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 12/13 | chr7 | 107918606 | |||||||
| chr7:107918692 | A | G | 56 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(53): Show |
107 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1375-318A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 12/13 | chr7 | 107918692 | |||||||
| chr7:107918695 | C | T | 1 | a0001c0001t0014g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1375-315C>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 12/13 | chr7 | 107918695 | |||||||
| chr7:107918778 | A | G | 2 | a0001c0001t0004g0229 a0001c0001t0004g0230 |
2 | HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1375-232A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 12/13 | chr7 | 107918778 | |||||||
| chr7:107918808 | T | A | 1 | a0001c0001t0004g0044 | 2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1375-202T>A | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 12/13 | chr7 | 107918808 | |||||||
| chr7:107918893 | TAAAG | T | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1375-113_1375-110d others(6): Show |
DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 107918893 | ||||||
| chr7:107918944 | A | G | 1 | a0001c0001t0003g0206 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1375-66A>G | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 12/13 | chr7 | 107918944 | |||||||
| chr7:107919164 | G | T | 3 | a0001c0006t0006g0126 a0001c0006t0006g0127 a0002c0005t0006g0035 |
4 | HG02109.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1465-30G>T | DLD | ENSG00000091140.15 | transcript | ENST00000205402.10 | protein_coding | 13/13 | chr7 | 107919164 |