Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3032 |
| ensemblid | ENSG00000138029.14 |
| hgncid | 4803 |
| symbol | HADHB |
| name | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta |
| refseq_nuc | NM_000183.3 |
| refseq_prot | NP_000174.1 |
| ensembl_nuc | ENST00000317799.10 |
| ensembl_prot | ENSP00000325136.5 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 26244939 |
| end | 26290465 |
| strand | + |
| ver | v1.2 |
| region | chr2:26244939-26290465 |
| region5000 | chr2:26239939-26295465 |
| regionname0 | HADHB_chr2_26244939_26290465 |
| regionname5000 | HADHB_chr2_26239939_26295465 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 475 | 194 | 64 | 50 | 42 | 14 | 23 | 34 | HADHB_chr2_26239939_26295465 | HADHB | MTTIL others(470): Show |
chr2 | 26239939 | 26295465 |
| a0002 | 1/0 | 474 | 95 | 14 | 20 | 54 | 0 | 6 | 38 | HADHB_chr2_26239939_26295465 | HADHB | MTILT others(469): Show |
chr2 | 26239939 | 26295465 |
| a0003 | 0/0 | 474 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | MTILT others(469): Show |
chr2 | 26239939 | 26295465 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1425 | 127 | 49 | 41 | 14 | 8 | 14 | HADHB_chr2_26239939_26295465 | HADHB | ATGAC others(1420): Show |
chr2 | 26239939 | 26295465 | ||
| a0001c0003 | 0/0 | 1425 | 53 | 3 | 7 | 28 | 6 | 9 | HADHB_chr2_26239939_26295465 | HADHB | ATGAC others(1420): Show |
chr2 | 26239939 | 26295465 | ||
| a0001c0004 | 0/0 | 1425 | 8 | 8 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | ATGAC others(1420): Show |
chr2 | 26239939 | 26295465 | ||
| a0001c0005 | 0/0 | 1425 | 5 | 3 | 2 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | ATGAC others(1420): Show |
chr2 | 26239939 | 26295465 | ||
| a0001c0006 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | ATGAC others(1420): Show |
chr2 | 26239939 | 26295465 | ||
| a0002c0002 | 1/0 | 1422 | 95 | 14 | 20 | 54 | 0 | 6 | HADHB_chr2_26239939_26295465 | HADHB | ATGAC others(1417): Show |
chr2 | 26239939 | 26295465 | ||
| a0003c0007 | 0/0 | 1422 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | ATGAC others(1417): Show |
chr2 | 26239939 | 26295465 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2000 | 120 | 45 | 38 | 14 | 8 | 14 | HADHB_chr2_26239939_26295465 | HADHB | ACTTG others(1995): Show |
chr2 | 26239939 | 26295465 |
| a0001c0001t0004 | 0/0 | 2000 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | ACTTG others(1995): Show |
chr2 | 26239939 | 26295465 |
| a0001c0001t0005 | 0/0 | 2000 | 6 | 3 | 3 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | ACTTG others(1995): Show |
chr2 | 26239939 | 26295465 |
| a0001c0003t0001 | 0/0 | 2000 | 52 | 3 | 7 | 27 | 6 | 9 | HADHB_chr2_26239939_26295465 | HADHB | ACTTG others(1995): Show |
chr2 | 26239939 | 26295465 |
| a0001c0003t0006 | 0/0 | 2000 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | ACTTG others(1995): Show |
chr2 | 26239939 | 26295465 |
| a0001c0004t0003 | 0/0 | 2000 | 8 | 8 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | ACTTG others(1995): Show |
chr2 | 26239939 | 26295465 |
| a0001c0005t0004 | 0/0 | 2000 | 5 | 3 | 2 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | ACTTG others(1995): Show |
chr2 | 26239939 | 26295465 |
| a0001c0006t0001 | 0/0 | 2000 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | ACTTG others(1995): Show |
chr2 | 26239939 | 26295465 |
| a0002c0002t0001 | 0/0 | 1997 | 2 | 1 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | ACTTG others(1992): Show |
chr2 | 26239939 | 26295465 |
| a0002c0002t0002 | 1/0 | 1997 | 93 | 13 | 19 | 54 | 0 | 6 | HADHB_chr2_26239939_26295465 | HADHB | ACTTG others(1992): Show |
chr2 | 26239939 | 26295465 |
| a0003c0007t0002 | 0/0 | 1997 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | ACTTG others(1992): Show |
chr2 | 26239939 | 26295465 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0018 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0005g0005 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0005g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0001t0005g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0003t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0004t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0004t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0004t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0004t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0004t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0004t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0004t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0004t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0005t0004g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0005t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0005t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0005t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0001c0006t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0001 | 0/0 | 17 | 0 | 4 | 13 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0002 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0003 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0186 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0002c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| a0003c0007t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | GBR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | GBR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG00140 | hp2 | a0001 | c0003 | t0001 | g0029 | EUR | GBR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0046 | EUR | FIN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0039 | EUR | FIN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0211 | EAS | CHS | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | CHS | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0184 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0221 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG00733 | hp2 | a0001 | c0001 | t0005 | g0237 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0032 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0054 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0238 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0228 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0218 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01167 | hp2 | a0001 | c0005 | t0004 | g0017 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01169 | hp2 | a0001 | c0005 | t0004 | g0017 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0040 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0059 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0194 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0178 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0012 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0012 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0222 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0201 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0192 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | IBS | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | IBS | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | IBS | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0224 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0198 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01981 | hp1 | a0001 | c0003 | t0001 | g0023 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02015 | hp2 | a0001 | c0003 | t0001 | g0020 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0057 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0236 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0188 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0232 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02074 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0166 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02080 | hp1 | a0001 | c0003 | t0001 | g0049 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0225 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02129 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0179 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0206 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02135 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0213 | EAS | KHV | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0203 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02155 | hp1 | a0001 | c0003 | t0001 | g0027 | EAS | CDX | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0229 | EAS | CDX | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0190 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02300 | hp1 | a0001 | c0003 | t0001 | g0022 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0181 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02572 | hp2 | a0001 | c0004 | t0003 | g0216 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0209 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02615 | hp2 | a0001 | c0004 | t0003 | g0163 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02647 | hp1 | a0001 | c0004 | t0003 | g0183 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02717 | hp1 | a0001 | c0006 | t0001 | g0241 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02723 | hp2 | a0002 | c0002 | t0002 | g0014 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0065 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0084 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0189 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02922 | hp1 | a0001 | c0004 | t0003 | g0164 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0242 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0030 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03017 | hp2 | a0003 | c0007 | t0002 | g0082 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0067 | AFR | MSL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0182 | AFR | MSL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0235 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03195 | hp2 | a0001 | c0004 | t0003 | g0215 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03225 | hp1 | a0001 | c0004 | t0003 | g0214 | AFR | MSL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03225 | hp2 | a0001 | c0005 | t0004 | g0075 | AFR | MSL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0234 | AFR | MSL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03486 | hp2 | a0001 | c0005 | t0004 | g0083 | AFR | MSL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03490 | hp1 | a0001 | c0003 | t0001 | g0024 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03516 | hp2 | a0001 | c0004 | t0003 | g0191 | AFR | ESN | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03540 | hp2 | a0001 | c0004 | t0003 | g0185 | AFR | GWD | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03669 | hp1 | a0001 | c0003 | t0001 | g0009 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03688 | hp1 | a0001 | c0003 | t0001 | g0038 | SAS | STU | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0042 | SAS | STU | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0207 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03710 | hp1 | a0001 | c0003 | t0001 | g0041 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0219 | SAS | BEB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0197 | SAS | BEB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0177 | SAS | BEB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0043 | SAS | BEB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | STU | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | YRI | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18940 | hp1 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0227 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0212 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18947 | hp2 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18950 | hp2 | a0001 | c0003 | t0001 | g0051 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0200 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18960 | hp1 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18965 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18972 | hp1 | a0001 | c0003 | t0001 | g0031 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18979 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18982 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18988 | hp1 | a0001 | c0003 | t0001 | g0044 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0226 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18991 | hp2 | a0001 | c0003 | t0001 | g0058 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18993 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18993 | hp2 | a0001 | c0003 | t0001 | g0028 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA18994 | hp2 | a0001 | c0003 | t0001 | g0052 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19002 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19003 | hp2 | a0001 | c0003 | t0001 | g0036 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19011 | hp1 | a0001 | c0003 | t0001 | g0026 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0220 | AFR | LWK | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19055 | hp2 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19057 | hp2 | a0001 | c0003 | t0001 | g0035 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19058 | hp1 | a0001 | c0003 | t0001 | g0025 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0210 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19067 | hp1 | a0002 | c0002 | t0002 | g0193 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19067 | hp2 | a0001 | c0003 | t0001 | g0034 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0167 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19070 | hp2 | a0001 | c0003 | t0006 | g0055 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19078 | hp1 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA19090 | hp2 | a0001 | c0003 | t0001 | g0053 | EAS | JPT | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA20752 | hp1 | a0001 | c0003 | t0001 | g0021 | EUR | TSI | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0009 | EUR | TSI | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | TSI | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0048 | EUR | TSI | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0037 | AMR | CLM | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0014 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0063 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | MSL | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | USA | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| HG06807 | hp2 | a0001 | c0005 | t0004 | g0243 | AFR | USA | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | USA | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0066 | AFR | USA | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0056 | AFR | LWK | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0217 | AFR | LWK | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0018 | REF | REF | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0186 | REF | REF | HADHB_chr2_26239939_26295465 | HADHB | chr2 | 26239939 | 26295465 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:26254257 | G | GACT | 1 | a0001 | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
disruptive_inframe_insertion | MODERATE | c.5_7dupCTA | p.Thr2dup | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 2/16 | 68/1997 | 8/1425 | 3/474 | INFO_REALIGN_3_PRIME | chr2 | 26254257 | ||
| chr2:26280012 | A | G | 1 | a0001 | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
missense_variant | MODERATE | c.830A>G | p.Lys277Arg | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/16 | 890/1997 | 830/1425 | 277/474 | chr2 | 26280012 | |||
| chr2:26285512 | A | G | 1 | a0003 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.1330A>G | p.Arg444Gly | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/16 | 1390/1997 | 1330/1425 | 444/474 | chr2 | 26285512 | |||
| chr2:26285566 | G | A | 1 | a0001 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.1384G>A | p.Gly462Arg | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/16 | 1444/1997 | 1384/1425 | 462/474 | chr2 | 26285566 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:26279284 | C | T | 1 | a0001c0005 | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
synonymous_variant | LOW | c.780C>T | p.Leu260Leu | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 9/16 | 840/1997 | 780/1425 | 260/474 | chr2 | 26279284 | |||
| chr2:26280007 | T | C | 1 | a0001c0003 | 53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
synonymous_variant | LOW | c.825T>C | p.Val275Val | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/16 | 885/1997 | 825/1425 | 275/474 | chr2 | 26280007 | |||
| chr2:26280073 | C | T | 1 | a0001c0005 | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
synonymous_variant | LOW | c.891C>T | p.Ile297Ile | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/16 | 951/1997 | 891/1425 | 297/474 | chr2 | 26280073 | |||
| chr2:26282877 | G | A | 1 | a0001c0004 | 8 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
synonymous_variant | LOW | c.966G>A | p.Ala322Ala | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 11/16 | 1026/1997 | 966/1425 | 322/474 | chr2 | 26282877 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:26290005 | A | G | 1 | a0001c0003t0006 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*52A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 16/16 | 52 | chr2 | 26290005 | ||||||
| chr2:26290089 | G | C | 9 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(6): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*136G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 16/16 | 136 | chr2 | 26290089 | ||||||
| chr2:26290149 | A | G | 2 | a0001c0001t0005 a0001c0004t0003 |
14 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*196A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 16/16 | 196 | chr2 | 26290149 | ||||||
| chr2:26290304 | C | G | 1 | a0001c0004t0003 | 8 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*351C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 16/16 | 351 | chr2 | 26290304 | ||||||
| chr2:26290439 | G | A | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0004t0003 others(1): Show |
20 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*486G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 16/16 | 486 | chr2 | 26290439 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:26245135 | A | T | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-9+145A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245135 | |||||||
| chr2:26245263 | G | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-9+273G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245263 | |||||||
| chr2:26245263 | GGTGT | G | 45 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(42): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-9+287_-9+290delTG others(2): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26245263 | ||||||
| chr2:26245265 | T | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0131 a0001c0001t0001g0132 others(2): Show |
6 | HG00099.hp2 HG01070.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+275T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245265 | |||||||
| chr2:26245265 | TGTGTGTG others(21): Show |
T | 1 | a0002c0002t0002g0220 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-9+283_-9+310delTG others(26): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26245265 | ||||||
| chr2:26245281 | G | T | 2 | a0001c0005t0004g0017 a0001c0005t0004g0243 |
3 | HG01167.hp2 HG01169.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-9+291G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245281 | |||||||
| chr2:26245283 | TGTGTGTG others(3): Show |
T | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 |
3 | NA18980.hp1 NA18989.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.-9+306_-9+315delGT others(8): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26245283 | ||||||
| chr2:26245285 | T | G | 2 | a0001c0005t0004g0017 a0001c0005t0004g0243 |
3 | HG01167.hp2 HG01169.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-9+295T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245285 | |||||||
| chr2:26245475 | G | C | 1 | a0002c0002t0002g0063 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-9+485G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245475 | |||||||
| chr2:26245497 | G | C | 45 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(42): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-9+507G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245497 | |||||||
| chr2:26245556 | A | G | 1 | a0002c0002t0002g0242 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-9+566A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245556 | |||||||
| chr2:26245563 | C | T | 2 | a0001c0001t0001g0240 a0001c0006t0001g0241 |
2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-9+573C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245563 | |||||||
| chr2:26245825 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-9+835C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245825 | |||||||
| chr2:26245850 | G | A | 3 | a0002c0002t0002g0065 a0002c0002t0002g0066 a0002c0002t0002g0067 |
3 | HG02809.hp1 HG03098.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-9+860G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245850 | |||||||
| chr2:26245910 | C | G | 45 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(42): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-9+920C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245910 | |||||||
| chr2:26245923 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-9+933C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26245923 | |||||||
| chr2:26246210 | G | A | 6 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(3): Show |
6 | HG01346.hp2 HG01358.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+1220G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26246210 | |||||||
| chr2:26246285 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-9+1295G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26246285 | |||||||
| chr2:26246347 | C | CTT | 44 | a0001c0001t0004g0234 a0001c0003t0001g0004 a0001c0003t0001g0007 others(41): Show |
50 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.-9+1370_-9+1371dup others(2): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26246347 | ||||||
| chr2:26246347 | C | CTTT | 6 | a0001c0001t0005g0005 a0001c0001t0005g0237 a0001c0001t0005g0238 others(3): Show |
9 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+1369_-9+1371dup others(3): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26246347 | ||||||
| chr2:26246347 | CT | C | 8 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0077 others(5): Show |
8 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9+1371delT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26246347 | ||||||
| chr2:26246366 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-9+1376C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26246366 | |||||||
| chr2:26246475 | G | A | 1 | a0003c0007t0002g0082 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-9+1485G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26246475 | |||||||
| chr2:26246575 | A | C | 1 | a0002c0002t0002g0232 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-9+1585A>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26246575 | |||||||
| chr2:26246589 | C | G | 51 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(48): Show |
60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.-9+1599C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26246589 | |||||||
| chr2:26246792 | TATA | T | 5 | a0001c0001t0005g0005 a0001c0001t0005g0237 a0001c0001t0005g0238 others(2): Show |
8 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+1805_-9+1807del others(3): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26246792 | ||||||
| chr2:26246920 | G | A | 45 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(42): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-9+1930G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26246920 | |||||||
| chr2:26246974 | G | A | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+1984G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26246974 | |||||||
| chr2:26247161 | C | T | 1 | a0001c0001t0005g0238 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-9+2171C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26247161 | |||||||
| chr2:26247182 | G | A | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+2192G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26247182 | |||||||
| chr2:26247276 | T | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+2286T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26247276 | |||||||
| chr2:26247349 | A | T | 2 | a0001c0005t0004g0017 a0001c0005t0004g0243 |
3 | HG01167.hp2 HG01169.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-9+2359A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26247349 | |||||||
| chr2:26247414 | T | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+2424T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26247414 | |||||||
| chr2:26247616 | T | A | 6 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(3): Show |
9 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+2626T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26247616 | |||||||
| chr2:26247700 | G | A | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+2710G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26247700 | |||||||
| chr2:26247701 | A | G | 1 | a0002c0002t0002g0242 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-9+2711A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26247701 | |||||||
| chr2:26247719 | T | G | 1 | a0002c0002t0002g0084 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-9+2729T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26247719 | |||||||
| chr2:26247888 | T | A | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+2898T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26247888 | |||||||
| chr2:26248025 | G | C | 1 | a0001c0001t0001g0085 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-9+3035G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248025 | |||||||
| chr2:26248281 | G | T | 1 | a0001c0001t0001g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-9+3291G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248281 | |||||||
| chr2:26248305 | G | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+3315G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248305 | |||||||
| chr2:26248385 | C | CTT | 4 | a0001c0001t0005g0005 a0001c0001t0005g0237 a0001c0003t0001g0235 others(1): Show |
7 | HG00733.hp2 HG01167.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+3407_-9+3408dup others(2): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26248385 | ||||||
| chr2:26248402 | A | G | 2 | a0001c0001t0001g0240 a0001c0006t0001g0241 |
2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-9+3412A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248402 | |||||||
| chr2:26248473 | T | TTTC | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+3485_-9+3486ins others(3): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26248473 | ||||||
| chr2:26248486 | A | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+3496A>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248486 | |||||||
| chr2:26248490 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-9+3500A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248490 | |||||||
| chr2:26248496 | G | C | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-9+3506G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248496 | |||||||
| chr2:26248598 | T | C | 1 | a0002c0002t0002g0087 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-9+3608T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248598 | |||||||
| chr2:26248650 | C | A | 97 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(94): Show |
101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.-9+3660C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248650 | |||||||
| chr2:26248751 | A | AAAC | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+3779_-9+3781dup others(3): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26248751 | ||||||
| chr2:26248755 | A | C | 2 | a0001c0001t0001g0240 a0001c0006t0001g0241 |
2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-9+3765A>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248755 | |||||||
| chr2:26248783 | G | A | 45 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(42): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-9+3793G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248783 | |||||||
| chr2:26248918 | G | A | 8 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0077 others(5): Show |
8 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9+3928G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248918 | |||||||
| chr2:26248972 | G | A | 1 | a0002c0002t0002g0232 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-9+3982G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26248972 | |||||||
| chr2:26249011 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-9+4021C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249011 | |||||||
| chr2:26249028 | A | G | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+4038A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249028 | |||||||
| chr2:26249081 | T | A | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+4091T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249081 | |||||||
| chr2:26249309 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-9+4319G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249309 | |||||||
| chr2:26249328 | C | T | 6 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(3): Show |
9 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+4338C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249328 | |||||||
| chr2:26249344 | C | G | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+4354C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249344 | |||||||
| chr2:26249454 | T | A | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+4464T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249454 | |||||||
| chr2:26249466 | G | A | 1 | a0002c0002t0002g0012 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-9+4476G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249466 | |||||||
| chr2:26249565 | A | G | 6 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(3): Show |
9 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+4575A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249565 | |||||||
| chr2:26249629 | T | C | 45 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(42): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-8-4618T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249629 | |||||||
| chr2:26249675 | T | G | 2 | a0001c0004t0003g0163 a0001c0004t0003g0164 |
2 | HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-8-4572T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249675 | |||||||
| chr2:26249800 | GT | G | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-4446delT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249800 | |||||||
| chr2:26249850 | T | C | 42 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(39): Show |
48 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.-8-4397T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249850 | |||||||
| chr2:26249985 | T | G | 1 | a0001c0001t0001g0239 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-8-4262T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26249985 | |||||||
| chr2:26250024 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-8-4223G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26250024 | |||||||
| chr2:26250033 | G | A | 1 | a0001c0001t0004g0234 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-8-4214G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26250033 | |||||||
| chr2:26250153 | T | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-4094T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26250153 | |||||||
| chr2:26250157 | A | G | 1 | a0002c0002t0002g0229 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-8-4090A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26250157 | |||||||
| chr2:26250230 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-8-4017C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26250230 | |||||||
| chr2:26250342 | A | G | 1 | a0001c0003t0001g0009 | 2 | HG03669.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-8-3905A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26250342 | |||||||
| chr2:26250377 | A | G | 3 | a0001c0001t0005g0005 a0001c0001t0005g0237 a0001c0001t0005g0238 |
6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-3870A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26250377 | |||||||
| chr2:26250789 | A | G | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-3458A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26250789 | |||||||
| chr2:26250866 | ATGT | A | 2 | a0001c0005t0004g0017 a0001c0005t0004g0243 |
3 | HG01167.hp2 HG01169.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-8-3379_-8-3377del others(3): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26250866 | ||||||
| chr2:26251036 | C | T | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-3211C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26251036 | |||||||
| chr2:26251066 | A | ACACTAAA others(323): Show |
1 | a0001c0003t0001g0020 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-8-3169_-8-3168ins others(330): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26251066 | ||||||
| chr2:26251066 | A | ACACTAAA others(324): Show |
24 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(21): Show |
30 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.-8-3169_-8-3168ins others(331): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26251066 | ||||||
| chr2:26251066 | A | ACACTAAA others(324): Show |
1 | a0001c0003t0001g0036 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-8-3169_-8-3168ins others(331): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26251066 | ||||||
| chr2:26251066 | A | ACACTAAA others(325): Show |
17 | a0001c0003t0001g0019 a0001c0003t0001g0037 a0001c0003t0001g0038 others(14): Show |
17 | HG00280.hp1 HG00280.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-8-3169_-8-3168ins others(332): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26251066 | ||||||
| chr2:26251066 | A | ACACTAAA others(325): Show |
1 | a0001c0003t0001g0052 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-8-3169_-8-3168ins others(332): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26251066 | ||||||
| chr2:26251066 | A | ACACTAAA others(326): Show |
1 | a0001c0003t0001g0053 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-8-3169_-8-3168ins others(333): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26251066 | ||||||
| chr2:26251132 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0165 |
3 | HG01069.hp2 HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.-8-3115G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26251132 | |||||||
| chr2:26251190 | T | C | 1 | a0002c0002t0002g0166 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-8-3057T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26251190 | |||||||
| chr2:26251517 | G | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-2730G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26251517 | |||||||
| chr2:26251580 | C | T | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-2667C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26251580 | |||||||
| chr2:26251661 | G | T | 1 | a0001c0001t0001g0159 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-8-2586G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26251661 | |||||||
| chr2:26251763 | T | A | 45 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(42): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-8-2484T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26251763 | |||||||
| chr2:26251951 | G | T | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-8-2296G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26251951 | |||||||
| chr2:26252035 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-8-2212C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26252035 | |||||||
| chr2:26252178 | G | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-2069G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26252178 | |||||||
| chr2:26252400 | T | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-8-1847T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26252400 | |||||||
| chr2:26252452 | CT | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-1794delT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26252452 | |||||||
| chr2:26252554 | A | G | 2 | a0001c0005t0004g0017 a0001c0005t0004g0243 |
3 | HG01167.hp2 HG01169.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-8-1693A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26252554 | |||||||
| chr2:26252608 | A | G | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-1639A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26252608 | |||||||
| chr2:26252634 | A | G | 1 | a0002c0002t0002g0242 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-8-1613A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26252634 | |||||||
| chr2:26252792 | T | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-1455T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26252792 | |||||||
| chr2:26253057 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-8-1190A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253057 | |||||||
| chr2:26253072 | C | T | 55 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(52): Show |
65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.-8-1175C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253072 | |||||||
| chr2:26253296 | G | GA | 55 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(52): Show |
65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.-8-946dupA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26253296 | ||||||
| chr2:26253361 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-8-886G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253361 | |||||||
| chr2:26253366 | T | C | 2 | a0001c0003t0001g0054 a0001c0003t0006g0055 |
2 | HG01069.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-8-881T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253366 | |||||||
| chr2:26253478 | T | C | 1 | a0001c0001t0004g0234 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-8-769T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253478 | |||||||
| chr2:26253580 | C | T | 1 | a0002c0002t0002g0228 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-8-667C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253580 | |||||||
| chr2:26253583 | T | C | 1 | a0002c0002t0002g0167 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-8-664T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253583 | |||||||
| chr2:26253683 | G | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-564G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253683 | |||||||
| chr2:26253698 | A | G | 45 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(42): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-8-549A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253698 | |||||||
| chr2:26253795 | G | A | 6 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(3): Show |
6 | HG01243.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-452G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253795 | |||||||
| chr2:26253857 | A | AAAAT | 76 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0064 others(73): Show |
78 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-8-346_-8-343dupTA others(2): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26253857 | ||||||
| chr2:26253857 | A | AAAATAAA others(1): Show |
29 | a0001c0001t0001g0006 a0001c0001t0001g0060 a0001c0001t0001g0061 others(26): Show |
31 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.-8-350_-8-343dupTA others(6): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26253857 | ||||||
| chr2:26253857 | A | AAAATAAA others(5): Show |
3 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0002c0002t0002g0227 |
3 | HG03704.hp1 NA18944.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-8-354_-8-343dupTA others(10): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26253857 | ||||||
| chr2:26253857 | AAAAT | A | 53 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(50): Show |
60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.-8-346_-8-343delTA others(2): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26253857 | ||||||
| chr2:26253857 | AAAATAAA others(1): Show |
A | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-350_-8-343delTA others(6): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 26253857 | ||||||
| chr2:26253861 | T | A | 3 | a0001c0001t0005g0005 a0001c0001t0005g0237 a0001c0003t0001g0034 |
6 | HG00733.hp2 HG01167.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-386T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253861 | |||||||
| chr2:26253865 | T | A | 39 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(36): Show |
45 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.-8-382T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253865 | |||||||
| chr2:26253869 | T | A | 12 | a0001c0003t0001g0007 a0001c0003t0001g0021 a0001c0003t0001g0022 others(9): Show |
13 | HG00280.hp2 HG01123.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8-378T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253869 | |||||||
| chr2:26253912 | G | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-335G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26253912 | |||||||
| chr2:26254109 | A | G | 168 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(165): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.-8-138A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 1/15 | chr2 | 26254109 | |||||||
| chr2:26254376 | C | T | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-54C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 2/15 | chr2 | 26254376 | |||||||
| chr2:26254682 | A | G | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+208A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26254682 | |||||||
| chr2:26254747 | T | G | 1 | a0002c0002t0002g0179 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.109+273T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26254747 | |||||||
| chr2:26254782 | G | A | 55 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(52): Show |
65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.109+308G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26254782 | |||||||
| chr2:26254845 | A | G | 2 | a0001c0003t0001g0235 a0001c0003t0001g0236 |
2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.109+371A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26254845 | |||||||
| chr2:26254923 | T | G | 1 | a0002c0002t0002g0180 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.109+449T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26254923 | |||||||
| chr2:26255185 | C | T | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+711C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255185 | |||||||
| chr2:26255193 | A | G | 1 | a0002c0002t0002g0213 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.109+719A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255193 | |||||||
| chr2:26255227 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.109+753C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255227 | |||||||
| chr2:26255228 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.109+754G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255228 | |||||||
| chr2:26255321 | G | A | 8 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0077 others(5): Show |
8 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+847G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255321 | |||||||
| chr2:26255485 | C | T | 2 | a0001c0001t0001g0240 a0001c0006t0001g0241 |
2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.109+1011C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255485 | |||||||
| chr2:26255498 | CA | C | 53 | a0001c0001t0001g0091 a0001c0001t0001g0160 a0001c0003t0001g0025 others(50): Show |
76 | HG00408.hp1 HG01070.hp1 HG01081.hp1 others(73): Show |
intron_variant | MODIFIER | c.109+1040delA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26255498 | ||||||
| chr2:26255511 | A | G | 1 | a0002c0002t0002g0067 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.109+1037A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255511 | |||||||
| chr2:26255523 | G | GA | 3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | HG02622.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.109+1055dupA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26255523 | ||||||
| chr2:26255577 | G | C | 1 | a0001c0001t0001g0230 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.109+1103G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255577 | |||||||
| chr2:26255603 | C | A | 2 | a0002c0002t0002g0181 a0002c0002t0002g0182 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.109+1129C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255603 | |||||||
| chr2:26255655 | G | A | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+1181G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255655 | |||||||
| chr2:26255818 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.109+1344G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255818 | |||||||
| chr2:26255930 | G | T | 1 | a0002c0002t0002g0014 | 2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.109+1456G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26255930 | |||||||
| chr2:26256115 | T | C | 8 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0077 others(5): Show |
8 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+1641T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26256115 | |||||||
| chr2:26256201 | G | A | 1 | a0001c0004t0003g0183 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.109+1727G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26256201 | |||||||
| chr2:26256285 | AT | A | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+1821delT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26256285 | ||||||
| chr2:26256527 | GTA | G | 163 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(160): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.109+2072_109+2073d others(4): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26256527 | ||||||
| chr2:26256527 | GTATA | G | 48 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(45): Show |
57 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.109+2070_109+2073d others(6): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26256527 | ||||||
| chr2:26256529 | A | G | 2 | a0001c0005t0004g0075 a0001c0005t0004g0083 |
2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.109+2055A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26256529 | |||||||
| chr2:26256531 | A | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0165 a0001c0005t0004g0017 others(1): Show |
6 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+2057A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26256531 | |||||||
| chr2:26256583 | C | G | 5 | a0001c0001t0005g0005 a0001c0001t0005g0237 a0001c0001t0005g0238 others(2): Show |
8 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.109+2109C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26256583 | |||||||
| chr2:26256867 | C | A | 3 | a0001c0003t0001g0041 a0001c0003t0001g0042 a0001c0003t0001g0043 |
3 | HG03688.hp2 HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.109+2393C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26256867 | |||||||
| chr2:26257043 | A | G | 8 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0077 others(5): Show |
8 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+2569A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257043 | |||||||
| chr2:26257078 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.109+2604A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257078 | |||||||
| chr2:26257084 | C | T | 6 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(3): Show |
6 | HG01243.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+2610C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257084 | |||||||
| chr2:26257160 | G | A | 45 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(42): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.109+2686G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257160 | |||||||
| chr2:26257269 | C | T | 1 | a0001c0004t0003g0183 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.109+2795C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257269 | |||||||
| chr2:26257375 | C | T | 45 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(42): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.109+2901C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257375 | |||||||
| chr2:26257560 | C | T | 42 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0012 others(39): Show |
64 | HG00408.hp1 HG01081.hp1 HG01192.hp2 others(61): Show |
intron_variant | MODIFIER | c.109+3086C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257560 | |||||||
| chr2:26257752 | G | T | 1 | a0001c0001t0001g0074 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.109+3278G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257752 | |||||||
| chr2:26257774 | C | G | 1 | a0002c0002t0002g0177 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.109+3300C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257774 | |||||||
| chr2:26257836 | A | G | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+3362A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257836 | |||||||
| chr2:26257892 | G | A | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+3418G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257892 | |||||||
| chr2:26257906 | C | G | 2 | a0001c0005t0004g0075 a0001c0005t0004g0083 |
2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.109+3432C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257906 | |||||||
| chr2:26257930 | C | A | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+3456C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257930 | |||||||
| chr2:26257989 | A | G | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+3515A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26257989 | |||||||
| chr2:26258116 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.109+3642G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26258116 | |||||||
| chr2:26258173 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.109+3699A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26258173 | |||||||
| chr2:26258176 | C | G | 1 | a0001c0003t0001g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.109+3702C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26258176 | |||||||
| chr2:26258190 | T | C | 6 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(3): Show |
9 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.109+3716T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26258190 | |||||||
| chr2:26258419 | C | T | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+3945C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26258419 | |||||||
| chr2:26258433 | A | G | 1 | a0001c0003t0001g0050 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.109+3959A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26258433 | |||||||
| chr2:26258578 | A | G | 229 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(226): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.109+4104A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26258578 | |||||||
| chr2:26258591 | G | A | 45 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0060 others(42): Show |
48 | HG00099.hp1 HG00140.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.109+4117G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26258591 | |||||||
| chr2:26258917 | C | T | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+4443C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26258917 | |||||||
| chr2:26258938 | T | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-4442T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26258938 | |||||||
| chr2:26259091 | C | G | 45 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(42): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.110-4289C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26259091 | |||||||
| chr2:26259117 | T | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-4263T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26259117 | |||||||
| chr2:26259261 | A | G | 13 | a0001c0001t0001g0011 a0001c0001t0001g0089 a0001c0001t0001g0102 others(10): Show |
14 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.110-4119A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26259261 | |||||||
| chr2:26259492 | C | T | 1 | a0001c0003t0001g0049 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.110-3888C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26259492 | |||||||
| chr2:26259493 | C | G | 45 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(42): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.110-3887C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26259493 | |||||||
| chr2:26259544 | A | T | 1 | a0001c0001t0001g0230 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.110-3836A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26259544 | |||||||
| chr2:26259558 | A | G | 6 | a0002c0002t0002g0014 a0002c0002t0002g0063 a0002c0002t0002g0181 others(3): Show |
7 | HG02257.hp2 HG02486.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.110-3822A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26259558 | |||||||
| chr2:26259826 | C | T | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-3554C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26259826 | |||||||
| chr2:26259946 | C | T | 1 | a0001c0003t0001g0024 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.110-3434C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26259946 | |||||||
| chr2:26259964 | G | A | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 |
3 | NA18980.hp1 NA18989.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.110-3416G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26259964 | |||||||
| chr2:26260013 | T | C | 2 | a0001c0001t0001g0240 a0001c0006t0001g0241 |
2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.110-3367T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260013 | |||||||
| chr2:26260081 | G | GGTT | 2 | a0001c0005t0004g0017 a0001c0005t0004g0243 |
3 | HG01167.hp2 HG01169.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.110-3299_110-3298i others(5): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260081 | |||||||
| chr2:26260081 | G | GT | 50 | a0001c0001t0001g0101 a0001c0001t0001g0116 a0001c0001t0001g0117 others(47): Show |
56 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.110-3281dupT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26260081 | ||||||
| chr2:26260081 | G | GTT | 10 | a0001c0001t0004g0234 a0001c0003t0001g0009 a0001c0003t0001g0023 others(7): Show |
11 | HG00738.hp1 HG01981.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.110-3282_110-3281d others(4): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26260081 | ||||||
| chr2:26260081 | G | GTTT | 3 | a0001c0001t0005g0005 a0001c0001t0005g0237 a0001c0001t0005g0238 |
6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.110-3283_110-3281d others(5): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26260081 | ||||||
| chr2:26260176 | T | G | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-3204T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260176 | |||||||
| chr2:26260203 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.110-3177T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260203 | |||||||
| chr2:26260222 | T | C | 5 | a0002c0002t0002g0063 a0002c0002t0002g0181 a0002c0002t0002g0182 others(2): Show |
5 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-3158T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260222 | |||||||
| chr2:26260240 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0246 others(1): Show |
4 | HG01934.hp1 HG02257.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-3140C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260240 | |||||||
| chr2:26260359 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.110-3021G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260359 | |||||||
| chr2:26260491 | G | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0165 |
3 | HG01069.hp2 HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.110-2889G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260491 | |||||||
| chr2:26260510 | T | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-2870T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260510 | |||||||
| chr2:26260594 | C | G | 8 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0077 others(5): Show |
8 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.110-2786C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260594 | |||||||
| chr2:26260596 | C | T | 1 | a0002c0002t0002g0207 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.110-2784C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260596 | |||||||
| chr2:26260602 | A | C | 1 | a0001c0001t0004g0234 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.110-2778A>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260602 | |||||||
| chr2:26260696 | C | G | 1 | a0002c0002t0002g0232 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.110-2684C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260696 | |||||||
| chr2:26260832 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.110-2548C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260832 | |||||||
| chr2:26260833 | A | G | 2 | a0002c0002t0002g0206 a0002c0002t0002g0209 |
2 | HG02132.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.110-2547A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26260833 | |||||||
| chr2:26261190 | AAAC | A | 3 | a0001c0001t0005g0005 a0001c0001t0005g0237 a0001c0001t0005g0238 |
6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.110-2179_110-2177d others(5): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26261190 | ||||||
| chr2:26261212 | A | AC | 18 | a0001c0001t0001g0011 a0001c0001t0001g0068 a0001c0001t0001g0069 others(15): Show |
19 | HG00735.hp2 HG01109.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.110-2158dupC | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26261212 | ||||||
| chr2:26261212 | A | ACC | 65 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0060 others(62): Show |
68 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(65): Show |
intron_variant | MODIFIER | c.110-2159_110-2158d others(4): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26261212 | ||||||
| chr2:26261212 | A | ACCC | 16 | a0001c0001t0001g0073 a0001c0001t0001g0090 a0001c0001t0001g0114 others(13): Show |
16 | HG00741.hp2 HG01175.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.110-2160_110-2158d others(5): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26261212 | ||||||
| chr2:26261212 | AC | A | 14 | a0001c0003t0001g0235 a0001c0003t0001g0236 a0001c0004t0003g0163 others(11): Show |
15 | HG01167.hp2 HG01169.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.110-2158delC | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26261212 | ||||||
| chr2:26261257 | A | G | 8 | a0001c0004t0003g0163 a0001c0004t0003g0164 a0001c0004t0003g0183 others(5): Show |
8 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.110-2123A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26261257 | |||||||
| chr2:26261321 | A | T | 2 | a0001c0005t0004g0075 a0001c0005t0004g0083 |
2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.110-2059A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26261321 | |||||||
| chr2:26261481 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.110-1899G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26261481 | |||||||
| chr2:26261500 | C | T | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-1880C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26261500 | |||||||
| chr2:26261512 | T | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-1868T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26261512 | |||||||
| chr2:26261535 | G | A | 1 | a0001c0003t0001g0059 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.110-1845G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26261535 | |||||||
| chr2:26261642 | T | G | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-1738T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26261642 | |||||||
| chr2:26261770 | A | G | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-1610A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26261770 | |||||||
| chr2:26261990 | A | G | 6 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(3): Show |
6 | HG01243.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.110-1390A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26261990 | |||||||
| chr2:26262167 | C | T | 1 | a0001c0001t0004g0234 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.110-1213C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26262167 | |||||||
| chr2:26262337 | G | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-1043G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26262337 | |||||||
| chr2:26262455 | A | T | 1 | a0002c0002t0001g0218 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.110-925A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26262455 | |||||||
| chr2:26262471 | C | T | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-909C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26262471 | |||||||
| chr2:26262718 | A | G | 45 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(42): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.110-662A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26262718 | |||||||
| chr2:26262722 | C | T | 2 | a0001c0003t0001g0021 a0001c0003t0001g0040 |
2 | HG01175.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.110-658C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26262722 | |||||||
| chr2:26262892 | A | C | 1 | a0001c0003t0001g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.110-488A>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26262892 | |||||||
| chr2:26263144 | C | G | 1 | a0002c0002t0002g0177 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.110-236C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | chr2 | 26263144 | |||||||
| chr2:26263298 | TA | T | 14 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(11): Show |
14 | HG01168.hp1 HG01346.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.110-65delA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 26263298 | ||||||
| chr2:26263538 | T | C | 1 | a0001c0001t0005g0238 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.209+59T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26263538 | |||||||
| chr2:26263687 | C | T | 1 | a0001c0003t0001g0031 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.209+208C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26263687 | |||||||
| chr2:26264035 | G | A | 1 | a0002c0002t0002g0222 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.209+556G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26264035 | |||||||
| chr2:26264457 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.209+978G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26264457 | |||||||
| chr2:26264498 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.209+1019C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26264498 | |||||||
| chr2:26264546 | T | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.209+1067T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26264546 | |||||||
| chr2:26264553 | C | CA | 94 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(91): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.209+1094dupA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26264553 | ||||||
| chr2:26264553 | C | CAA | 10 | a0001c0001t0001g0060 a0001c0001t0001g0073 a0001c0001t0001g0090 others(7): Show |
10 | HG00738.hp2 HG01952.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.209+1093_209+1094d others(4): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26264553 | ||||||
| chr2:26264553 | CA | C | 10 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(7): Show |
13 | HG00733.hp2 HG01069.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.209+1094delA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26264553 | ||||||
| chr2:26264573 | A | G | 41 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0012 others(38): Show |
63 | HG00408.hp1 HG01081.hp1 HG01192.hp2 others(60): Show |
intron_variant | MODIFIER | c.209+1094A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26264573 | |||||||
| chr2:26264625 | A | ATG | 45 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(42): Show |
52 | HG00140.hp2 HG00280.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.209+1156_209+1157d others(4): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26264625 | ||||||
| chr2:26264625 | A | G | 1 | a0001c0003t0001g0046 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.209+1146A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26264625 | |||||||
| chr2:26264625 | ATG | A | 3 | a0001c0001t0005g0005 a0001c0001t0005g0237 a0001c0001t0005g0238 |
6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.209+1156_209+1157d others(4): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26264625 | ||||||
| chr2:26264749 | C | T | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.209+1270C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26264749 | |||||||
| chr2:26264838 | A | T | 1 | a0002c0002t0002g0187 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.209+1359A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26264838 | |||||||
| chr2:26264864 | C | T | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.209+1385C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26264864 | |||||||
| chr2:26265002 | AAAG | A | 3 | a0001c0001t0005g0005 a0001c0001t0005g0237 a0001c0001t0005g0238 |
6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.209+1533_209+1535d others(5): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26265002 | ||||||
| chr2:26265041 | G | A | 2 | a0001c0003t0001g0235 a0001c0003t0001g0236 |
2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.209+1562G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26265041 | |||||||
| chr2:26265338 | G | A | 1 | a0002c0002t0001g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.209+1859G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26265338 | |||||||
| chr2:26265347 | A | G | 1 | a0001c0001t0004g0234 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.209+1868A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26265347 | |||||||
| chr2:26265352 | T | G | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0239 others(2): Show |
5 | HG01934.hp1 HG02257.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.209+1873T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26265352 | |||||||
| chr2:26265358 | G | A | 6 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0078 others(3): Show |
6 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.209+1879G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26265358 | |||||||
| chr2:26265497 | G | C | 1 | a0002c0002t0002g0177 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.209+2018G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26265497 | |||||||
| chr2:26265585 | A | G | 55 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(52): Show |
65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.209+2106A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26265585 | |||||||
| chr2:26265595 | C | G | 1 | a0001c0003t0001g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.209+2116C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26265595 | |||||||
| chr2:26265597 | A | AAAC | 9 | a0001c0001t0001g0102 a0001c0001t0001g0151 a0001c0001t0001g0240 others(6): Show |
12 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.209+2142_209+2144d others(5): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26265597 | ||||||
| chr2:26265597 | A | AAACAACA others(2): Show |
42 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(39): Show |
48 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.209+2136_209+2144d others(11): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26265597 | ||||||
| chr2:26265597 | A | AAACAACA others(8): Show |
2 | a0001c0003t0001g0039 a0001c0003t0001g0046 |
2 | HG00280.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.209+2130_209+2144d others(17): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26265597 | ||||||
| chr2:26265597 | AAAC | A | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.209+2142_209+2144d others(5): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26265597 | ||||||
| chr2:26265953 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.209+2474C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26265953 | |||||||
| chr2:26266172 | G | A | 10 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(7): Show |
14 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.209+2693G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266172 | |||||||
| chr2:26266220 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.209+2741C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266220 | |||||||
| chr2:26266570 | T | A | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.209+3091T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266570 | |||||||
| chr2:26266655 | G | A | 1 | a0002c0002t0002g0242 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.209+3176G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266655 | |||||||
| chr2:26266708 | T | C | 55 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(52): Show |
65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.209+3229T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266708 | |||||||
| chr2:26266709 | A | G | 1 | a0002c0002t0002g0180 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.209+3230A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266709 | |||||||
| chr2:26266748 | C | T | 1 | a0001c0003t0001g0033 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.210-3205C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266748 | |||||||
| chr2:26266752 | C | T | 1 | a0001c0003t0001g0059 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.210-3201C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266752 | |||||||
| chr2:26266753 | A | G | 55 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(52): Show |
65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.210-3200A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266753 | |||||||
| chr2:26266862 | A | T | 55 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(52): Show |
65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.210-3091A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266862 | |||||||
| chr2:26266871 | C | CA | 11 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(8): Show |
14 | HG00733.hp2 HG01069.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.210-3059dupA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | ||||||
| chr2:26266871 | C | CAAAAAAA others(3): Show |
50 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(47): Show |
54 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.210-3068_210-3059d others(12): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | ||||||
| chr2:26266871 | C | CAAAAAAA others(4): Show |
18 | a0001c0001t0001g0060 a0001c0001t0001g0089 a0001c0001t0001g0092 others(15): Show |
18 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.210-3069_210-3059d others(13): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | ||||||
| chr2:26266871 | C | CAAAAAAA others(5): Show |
10 | a0001c0001t0001g0085 a0001c0001t0001g0095 a0001c0001t0001g0104 others(7): Show |
10 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.210-3070_210-3059d others(14): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | ||||||
| chr2:26266871 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0239 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.210-3071_210-3059d others(15): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | ||||||
| chr2:26266871 | C | CAAAAAAA others(7): Show |
6 | a0001c0001t0001g0080 a0001c0001t0001g0119 a0001c0001t0001g0151 others(3): Show |
6 | HG01934.hp1 HG02257.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.210-3072_210-3059d others(16): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | ||||||
| chr2:26266871 | C | CAAAAAAA others(8): Show |
5 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG01884.hp1 HG02559.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-3073_210-3059d others(17): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | ||||||
| chr2:26266871 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0074 a0001c0001t0001g0077 |
2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.210-3074_210-3059d others(18): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | ||||||
| chr2:26266871 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0118 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.210-3078_210-3059d others(22): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | ||||||
| chr2:26266871 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0123 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.210-3079_210-3059d others(23): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | ||||||
| chr2:26266871 | C | CAAAAAAA others(23): Show |
1 | a0001c0001t0001g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.210-3059_210-3058i others(32): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | ||||||
| chr2:26266871 | C | CAAAAAAA others(24): Show |
2 | a0001c0001t0001g0072 a0001c0001t0001g0244 |
2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.210-3059_210-3058i others(33): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | ||||||
| chr2:26266871 | C | CAAAAAAA others(25): Show |
1 | a0001c0001t0001g0064 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.210-3059_210-3058i others(34): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | ||||||
| chr2:26266871 | CA | C | 8 | a0001c0004t0003g0163 a0001c0004t0003g0164 a0001c0004t0003g0183 others(5): Show |
8 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.210-3059delA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26266871 | ||||||
| chr2:26266930 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.210-3023T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266930 | |||||||
| chr2:26266998 | A | G | 1 | a0002c0002t0002g0203 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.210-2955A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26266998 | |||||||
| chr2:26267029 | C | T | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-2924C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26267029 | |||||||
| chr2:26267063 | T | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-2890T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26267063 | |||||||
| chr2:26267119 | A | C | 5 | a0001c0001t0005g0005 a0001c0001t0005g0237 a0001c0001t0005g0238 others(2): Show |
8 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.210-2834A>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26267119 | |||||||
| chr2:26267142 | TTAAAAA | T | 6 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(3): Show |
6 | HG01243.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.210-2806_210-2801d others(8): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26267142 | ||||||
| chr2:26267189 | T | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-2764T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26267189 | |||||||
| chr2:26267229 | G | T | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-2724G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26267229 | |||||||
| chr2:26267527 | A | T | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-2426A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26267527 | |||||||
| chr2:26267608 | C | T | 1 | a0001c0001t0004g0234 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.210-2345C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26267608 | |||||||
| chr2:26267631 | A | G | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-2322A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26267631 | |||||||
| chr2:26267743 | G | T | 45 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(42): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.210-2210G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26267743 | |||||||
| chr2:26267771 | C | CA | 51 | a0001c0001t0001g0085 a0001c0001t0001g0090 a0001c0001t0001g0091 others(48): Show |
73 | HG00408.hp1 HG01081.hp1 HG01123.hp1 others(70): Show |
intron_variant | MODIFIER | c.210-2164dupA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26267771 | ||||||
| chr2:26267850 | T | C | 1 | a0001c0003t0001g0020 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.210-2103T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26267850 | |||||||
| chr2:26268003 | G | A | 3 | a0001c0001t0005g0005 a0001c0001t0005g0237 a0001c0001t0005g0238 |
6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.210-1950G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26268003 | |||||||
| chr2:26268052 | A | G | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-1901A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26268052 | |||||||
| chr2:26268067 | A | G | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-1886A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26268067 | |||||||
| chr2:26268154 | T | TAAATA | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-1796_210-1792d others(7): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26268154 | ||||||
| chr2:26268254 | A | G | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-1699A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26268254 | |||||||
| chr2:26268297 | T | C | 47 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(44): Show |
53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.210-1656T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26268297 | |||||||
| chr2:26268312 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.210-1641A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26268312 | |||||||
| chr2:26268481 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0165 |
3 | HG01069.hp2 HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.210-1472C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26268481 | |||||||
| chr2:26268493 | T | G | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-1460T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26268493 | |||||||
| chr2:26268524 | A | G | 86 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(83): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.210-1429A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26268524 | |||||||
| chr2:26268630 | A | G | 5 | a0001c0004t0003g0163 a0001c0004t0003g0164 a0001c0004t0003g0214 others(2): Show |
5 | HG02572.hp2 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.210-1323A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26268630 | |||||||
| chr2:26268763 | A | C | 1 | a0001c0005t0004g0243 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.210-1190A>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26268763 | |||||||
| chr2:26269042 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0137 |
2 | HG01168.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.210-911G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26269042 | |||||||
| chr2:26269201 | C | T | 6 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(3): Show |
6 | HG01243.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.210-752C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26269201 | |||||||
| chr2:26269249 | T | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-704T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26269249 | |||||||
| chr2:26269352 | G | A | 1 | a0002c0002t0002g0084 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.210-601G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26269352 | |||||||
| chr2:26269443 | A | G | 6 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(3): Show |
9 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.210-510A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26269443 | |||||||
| chr2:26269496 | T | C | 219 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(216): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.210-457T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26269496 | |||||||
| chr2:26269499 | C | T | 7 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0108 others(4): Show |
7 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.210-454C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | chr2 | 26269499 | |||||||
| chr2:26269813 | TGATGGAC others(7): Show |
T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0244 |
2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.210-136_210-123del others(14): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 26269813 | ||||||
| chr2:26270235 | A | T | 1 | a0002c0002t0002g0177 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.254+238A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26270235 | |||||||
| chr2:26270308 | G | A | 3 | a0002c0002t0002g0192 a0002c0002t0002g0219 a0002c0002t0002g0221 |
3 | HG00642.hp2 HG01433.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.254+311G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26270308 | |||||||
| chr2:26270579 | A | G | 1 | a0002c0002t0001g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.254+582A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26270579 | |||||||
| chr2:26270640 | C | T | 8 | a0001c0004t0003g0163 a0001c0004t0003g0164 a0001c0004t0003g0183 others(5): Show |
8 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.254+643C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26270640 | |||||||
| chr2:26270729 | C | A | 161 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(158): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.254+732C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26270729 | |||||||
| chr2:26270749 | A | G | 1 | a0001c0003t0001g0024 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.254+752A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26270749 | |||||||
| chr2:26270878 | C | CT | 10 | a0001c0001t0001g0079 a0001c0001t0001g0118 a0001c0001t0001g0123 others(7): Show |
10 | HG00642.hp2 HG01433.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.254+899dupT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 26270878 | ||||||
| chr2:26270878 | CT | C | 48 | a0001c0001t0001g0072 a0001c0001t0001g0244 a0001c0003t0001g0004 others(45): Show |
54 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.254+899delT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 26270878 | ||||||
| chr2:26270885 | T | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.254+888T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26270885 | |||||||
| chr2:26270910 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.254+913G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26270910 | |||||||
| chr2:26270934 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.254+937A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26270934 | |||||||
| chr2:26271004 | G | A | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.254+1007G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26271004 | |||||||
| chr2:26271056 | C | CT | 47 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(44): Show |
53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.254+1071dupT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 26271056 | ||||||
| chr2:26271067 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.254+1070T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26271067 | |||||||
| chr2:26271451 | G | C | 8 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0077 others(5): Show |
8 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.254+1454G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26271451 | |||||||
| chr2:26271483 | G | A | 4 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(1): Show |
7 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.254+1486G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26271483 | |||||||
| chr2:26271502 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.254+1505C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26271502 | |||||||
| chr2:26271560 | T | A | 3 | a0001c0001t0005g0005 a0001c0001t0005g0237 a0001c0001t0005g0238 |
6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.254+1563T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26271560 | |||||||
| chr2:26271761 | A | G | 1 | a0002c0002t0002g0188 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.254+1764A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26271761 | |||||||
| chr2:26271827 | G | C | 47 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(44): Show |
53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.255-1824G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26271827 | |||||||
| chr2:26271887 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.255-1764A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26271887 | |||||||
| chr2:26271909 | A | T | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.255-1742A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26271909 | |||||||
| chr2:26271918 | A | T | 22 | a0001c0001t0001g0006 a0001c0001t0001g0060 a0001c0001t0001g0061 others(19): Show |
24 | HG00639.hp1 HG01074.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.255-1733A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26271918 | |||||||
| chr2:26272227 | G | A | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.255-1424G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26272227 | |||||||
| chr2:26272241 | T | C | 1 | a0001c0003t0001g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.255-1410T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26272241 | |||||||
| chr2:26272346 | C | CT | 7 | a0001c0001t0001g0144 a0001c0001t0004g0234 a0001c0001t0005g0005 others(4): Show |
10 | HG00733.hp2 HG00735.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.255-1289dupT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 26272346 | ||||||
| chr2:26272346 | CT | C | 44 | a0001c0005t0004g0017 a0001c0005t0004g0243 a0002c0002t0002g0001 others(41): Show |
67 | HG00408.hp1 HG01081.hp1 HG01167.hp2 others(64): Show |
intron_variant | MODIFIER | c.255-1289delT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 26272346 | ||||||
| chr2:26272424 | C | T | 2 | a0001c0001t0001g0240 a0001c0006t0001g0241 |
2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.255-1227C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26272424 | |||||||
| chr2:26272674 | G | A | 1 | a0002c0002t0002g0184 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.255-977G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26272674 | |||||||
| chr2:26272695 | A | G | 6 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(3): Show |
6 | HG01243.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.255-956A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26272695 | |||||||
| chr2:26272808 | G | T | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.255-843G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26272808 | |||||||
| chr2:26272810 | A | G | 2 | a0001c0001t0001g0240 a0001c0006t0001g0241 |
2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.255-841A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26272810 | |||||||
| chr2:26272901 | T | C | 5 | a0001c0001t0005g0005 a0001c0001t0005g0237 a0001c0001t0005g0238 others(2): Show |
8 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.255-750T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26272901 | |||||||
| chr2:26272956 | G | A | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.255-695G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26272956 | |||||||
| chr2:26273084 | T | C | 2 | a0001c0003t0001g0235 a0001c0003t0001g0236 |
2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.255-567T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26273084 | |||||||
| chr2:26273244 | C | CAAACTAA others(15): Show |
2 | a0001c0001t0001g0240 a0001c0006t0001g0241 |
2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.255-406_255-405ins others(22): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 26273244 | ||||||
| chr2:26273246 | G | A | 2 | a0001c0001t0001g0240 a0001c0006t0001g0241 |
2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.255-405G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26273246 | |||||||
| chr2:26273247 | G | A | 2 | a0001c0001t0001g0240 a0001c0006t0001g0241 |
2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.255-404G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26273247 | |||||||
| chr2:26273261 | T | A | 91 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(88): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.255-390T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26273261 | |||||||
| chr2:26273263 | A | AT | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.255-380dupT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 26273263 | ||||||
| chr2:26273318 | G | C | 45 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(42): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.255-333G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26273318 | |||||||
| chr2:26273431 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.255-220A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26273431 | |||||||
| chr2:26273441 | C | G | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.255-210C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26273441 | |||||||
| chr2:26273556 | C | T | 7 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(4): Show |
7 | HG00639.hp1 HG00642.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.255-95C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 5/15 | chr2 | 26273556 | |||||||
| chr2:26273850 | G | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+100G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26273850 | |||||||
| chr2:26274075 | T | C | 1 | a0002c0002t0002g0195 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.354+325T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274075 | |||||||
| chr2:26274157 | C | A | 3 | a0001c0001t0005g0005 a0001c0001t0005g0237 a0001c0001t0005g0238 |
6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.354+407C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274157 | |||||||
| chr2:26274158 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.354+408T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274158 | |||||||
| chr2:26274313 | G | A | 1 | a0001c0001t0001g0011 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.354+563G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274313 | |||||||
| chr2:26274360 | C | G | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+610C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274360 | |||||||
| chr2:26274406 | T | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0105 |
2 | HG01257.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.354+656T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274406 | |||||||
| chr2:26274414 | G | C | 1 | a0002c0002t0002g0177 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.354+664G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274414 | |||||||
| chr2:26274445 | A | G | 1 | a0002c0002t0002g0184 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.354+695A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274445 | |||||||
| chr2:26274584 | A | G | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+834A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274584 | |||||||
| chr2:26274585 | C | A | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+835C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274585 | |||||||
| chr2:26274659 | G | A | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+909G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274659 | |||||||
| chr2:26274673 | C | T | 45 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(42): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.354+923C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274673 | |||||||
| chr2:26274785 | C | G | 2 | a0001c0003t0001g0030 a0001c0003t0001g0057 |
2 | HG02040.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.354+1035C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26274785 | |||||||
| chr2:26275005 | C | T | 2 | a0001c0005t0004g0075 a0001c0005t0004g0083 |
2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.354+1255C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26275005 | |||||||
| chr2:26275190 | ATTTCTTA others(77): Show |
A | 3 | a0002c0002t0002g0015 a0002c0002t0002g0187 a0002c0002t0002g0188 |
4 | HG00408.hp2 HG02056.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.354+1488_354+1571d others(86): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 26275190 | ||||||
| chr2:26275263 | T | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+1513T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26275263 | |||||||
| chr2:26275354 | G | A | 42 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0012 others(39): Show |
64 | HG00408.hp1 HG01081.hp1 HG01192.hp2 others(61): Show |
intron_variant | MODIFIER | c.354+1604G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26275354 | |||||||
| chr2:26275591 | G | GC | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.355-1479dupC | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 26275591 | ||||||
| chr2:26275946 | A | C | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.355-1127A>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26275946 | |||||||
| chr2:26276357 | G | A | 2 | a0001c0003t0001g0019 a0001c0003t0001g0049 |
2 | HG02080.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.355-716G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26276357 | |||||||
| chr2:26276485 | C | T | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.355-588C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26276485 | |||||||
| chr2:26277004 | T | A | 1 | a0001c0001t0001g0161 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.355-69T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26277004 | |||||||
| chr2:26277047 | C | A | 1 | a0001c0003t0001g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.355-26C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 6/15 | chr2 | 26277047 | |||||||
| chr2:26277182 | C | T | 1 | a0002c0002t0002g0063 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.442+22C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26277182 | |||||||
| chr2:26277233 | C | CT | 17 | a0001c0001t0001g0006 a0001c0001t0001g0060 a0001c0001t0001g0061 others(14): Show |
19 | HG00639.hp1 HG00642.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.442+95dupT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 26277233 | ||||||
| chr2:26277233 | CT | C | 36 | a0001c0001t0001g0013 a0001c0001t0001g0074 a0001c0001t0001g0076 others(33): Show |
40 | HG00639.hp2 HG00733.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.442+95delT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 26277233 | ||||||
| chr2:26277233 | CTT | C | 40 | a0001c0001t0001g0162 a0001c0003t0001g0004 a0001c0003t0001g0007 others(37): Show |
45 | HG00280.hp1 HG00280.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.442+94_442+95delTT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 26277233 | ||||||
| chr2:26277284 | C | G | 2 | a0001c0003t0001g0235 a0001c0003t0001g0236 |
2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.442+124C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26277284 | |||||||
| chr2:26277683 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0165 |
3 | HG01069.hp2 HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.442+523C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26277683 | |||||||
| chr2:26277763 | G | A | 1 | a0001c0005t0004g0243 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.442+603G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26277763 | |||||||
| chr2:26277935 | T | G | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.443-679T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26277935 | |||||||
| chr2:26277936 | C | T | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.443-678C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26277936 | |||||||
| chr2:26277937 | A | G | 1 | a0002c0002t0001g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.443-677A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26277937 | |||||||
| chr2:26278131 | G | T | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.443-483G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26278131 | |||||||
| chr2:26278135 | G | A | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.443-479G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26278135 | |||||||
| chr2:26278219 | T | TA | 6 | a0001c0001t0001g0064 a0001c0001t0001g0072 a0001c0001t0001g0118 others(3): Show |
6 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.443-394dupA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 26278219 | ||||||
| chr2:26278222 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.443-392G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26278222 | |||||||
| chr2:26278231 | G | A | 6 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(3): Show |
9 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.443-383G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26278231 | |||||||
| chr2:26278376 | T | G | 3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | HG02622.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.443-238T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26278376 | |||||||
| chr2:26278521 | C | T | 7 | a0001c0003t0001g0007 a0001c0003t0001g0021 a0001c0003t0001g0024 others(4): Show |
8 | HG00280.hp2 HG01123.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.443-93C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 7/15 | chr2 | 26278521 | |||||||
| chr2:26279085 | C | A | 55 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(52): Show |
65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.631-50C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 8/15 | chr2 | 26279085 | |||||||
| chr2:26279878 | T | G | 1 | a0001c0001t0001g0127 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.812-116T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 9/15 | chr2 | 26279878 | |||||||
| chr2:26279900 | C | T | 47 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(44): Show |
53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.812-94C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 9/15 | chr2 | 26279900 | |||||||
| chr2:26279989 | A | T | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.812-5A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 9/15 | chr2 | 26279989 | |||||||
| chr2:26280278 | C | T | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.933+163C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280278 | |||||||
| chr2:26280291 | C | G | 3 | a0001c0003t0001g0056 a0001c0003t0001g0235 a0001c0003t0001g0236 |
3 | HG02055.hp2 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.933+176C>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280291 | |||||||
| chr2:26280570 | A | G | 178 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(175): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.933+455A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280570 | |||||||
| chr2:26280571 | G | A | 42 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0012 others(39): Show |
64 | HG00408.hp1 HG01081.hp1 HG01192.hp2 others(61): Show |
intron_variant | MODIFIER | c.933+456G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280571 | |||||||
| chr2:26280578 | T | C | 16 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(13): Show |
20 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.933+463T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280578 | |||||||
| chr2:26280606 | A | G | 42 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0012 others(39): Show |
64 | HG00408.hp1 HG01081.hp1 HG01192.hp2 others(61): Show |
intron_variant | MODIFIER | c.933+491A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280606 | |||||||
| chr2:26280648 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.933+533T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280648 | |||||||
| chr2:26280682 | G | A | 25 | a0001c0001t0001g0011 a0001c0001t0001g0085 a0001c0001t0001g0086 others(22): Show |
26 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.933+567G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280682 | |||||||
| chr2:26280695 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.933+580A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280695 | |||||||
| chr2:26280775 | C | T | 3 | a0001c0001t0001g0101 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02109.hp2 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.933+660C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280775 | |||||||
| chr2:26280786 | T | C | 63 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(60): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.933+671T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280786 | |||||||
| chr2:26280853 | C | CA | 6 | a0001c0001t0001g0089 a0001c0001t0001g0096 a0001c0001t0001g0098 others(3): Show |
6 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.933+766dupA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 26280853 | ||||||
| chr2:26280853 | CA | C | 85 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0060 others(82): Show |
99 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.933+766delA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 26280853 | ||||||
| chr2:26280853 | CAA | C | 67 | a0001c0001t0001g0013 a0001c0001t0001g0074 a0001c0001t0001g0076 others(64): Show |
85 | HG00408.hp1 HG00639.hp2 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.933+765_933+766del others(2): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 26280853 | ||||||
| chr2:26280853 | CAAA | C | 44 | a0001c0001t0005g0005 a0001c0001t0005g0238 a0001c0003t0001g0004 others(41): Show |
53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.933+764_933+766del others(3): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 26280853 | ||||||
| chr2:26280853 | CAAAAAAA others(3): Show |
C | 2 | a0001c0003t0001g0025 a0001c0003t0001g0056 |
2 | NA19058.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.933+757_933+766del others(10): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 26280853 | ||||||
| chr2:26280926 | A | G | 2 | a0001c0003t0001g0019 a0001c0003t0001g0049 |
2 | HG02080.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.933+811A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26280926 | |||||||
| chr2:26281151 | T | TGTA | 47 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(44): Show |
53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.933+1038_933+1040d others(5): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 26281151 | ||||||
| chr2:26281301 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0165 |
3 | HG01069.hp2 HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.933+1186A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26281301 | |||||||
| chr2:26281314 | A | T | 1 | a0001c0001t0001g0127 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.933+1199A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26281314 | |||||||
| chr2:26281542 | A | G | 2 | a0001c0003t0001g0008 a0001c0003t0001g0045 |
3 | HG02074.hp1 NA18954.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.934-1303A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26281542 | |||||||
| chr2:26281568 | G | A | 1 | a0001c0003t0001g0024 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.934-1277G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26281568 | |||||||
| chr2:26281611 | C | T | 1 | a0001c0003t0001g0033 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.934-1234C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26281611 | |||||||
| chr2:26281663 | G | T | 1 | a0002c0002t0002g0177 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.934-1182G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26281663 | |||||||
| chr2:26281787 | GC | G | 3 | a0001c0001t0005g0005 a0001c0001t0005g0237 a0001c0001t0005g0238 |
6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.934-1057delC | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26281787 | |||||||
| chr2:26282248 | T | G | 1 | a0001c0003t0001g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.934-597T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26282248 | |||||||
| chr2:26282251 | C | CTT | 11 | a0001c0004t0003g0163 a0001c0004t0003g0164 a0001c0004t0003g0183 others(8): Show |
12 | HG01167.hp2 HG01169.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.934-574_934-573dup others(2): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 26282251 | ||||||
| chr2:26282251 | CT | C | 54 | a0001c0001t0001g0073 a0001c0001t0001g0102 a0001c0001t0001g0111 others(51): Show |
63 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.934-573delT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 26282251 | ||||||
| chr2:26282255 | T | C | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.934-590T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26282255 | |||||||
| chr2:26282461 | C | T | 1 | a0001c0003t0001g0059 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.934-384C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26282461 | |||||||
| chr2:26282469 | C | T | 8 | a0001c0004t0003g0163 a0001c0004t0003g0164 a0001c0004t0003g0183 others(5): Show |
8 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.934-376C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26282469 | |||||||
| chr2:26282505 | C | T | 3 | a0002c0002t0002g0192 a0002c0002t0002g0219 a0002c0002t0002g0221 |
3 | HG00642.hp2 HG01433.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.934-340C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26282505 | |||||||
| chr2:26282576 | T | G | 3 | a0001c0001t0005g0005 a0001c0001t0005g0237 a0001c0001t0005g0238 |
6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.934-269T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26282576 | |||||||
| chr2:26282578 | T | C | 2 | a0001c0005t0004g0017 a0001c0005t0004g0243 |
3 | HG01167.hp2 HG01169.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.934-267T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26282578 | |||||||
| chr2:26282620 | G | T | 1 | a0002c0002t0002g0229 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.934-225G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 10/15 | chr2 | 26282620 | |||||||
| chr2:26282990 | A | G | 47 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(44): Show |
53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.1014-14A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 11/15 | chr2 | 26282990 | |||||||
| chr2:26283231 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1061+180T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 12/15 | chr2 | 26283231 | |||||||
| chr2:26283449 | G | A | 12 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(9): Show |
15 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1061+398G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 12/15 | chr2 | 26283449 | |||||||
| chr2:26283531 | T | A | 4 | a0002c0002t0002g0001 a0002c0002t0002g0210 a0002c0002t0002g0211 others(1): Show |
4 | HG00408.hp1 NA18612.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.1061+480T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 12/15 | chr2 | 26283531 | |||||||
| chr2:26284208 | A | T | 45 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0012 others(42): Show |
67 | HG00408.hp1 HG01081.hp1 HG01192.hp2 others(64): Show |
splice_region_variant&intron_variant | LOW | c.1149+4A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 13/15 | chr2 | 26284208 | |||||||
| chr2:26284238 | A | G | 2 | a0001c0001t0001g0240 a0001c0006t0001g0241 |
2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1149+34A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 13/15 | chr2 | 26284238 | |||||||
| chr2:26284322 | A | G | 3 | a0001c0001t0005g0005 a0001c0001t0005g0237 a0001c0001t0005g0238 |
6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1149+118A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 13/15 | chr2 | 26284322 | |||||||
| chr2:26284350 | A | T | 1 | a0001c0001t0004g0234 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1149+146A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 13/15 | chr2 | 26284350 | |||||||
| chr2:26284548 | C | T | 9 | a0001c0001t0001g0064 a0001c0001t0001g0072 a0001c0001t0001g0118 others(6): Show |
9 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1150-335C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 13/15 | chr2 | 26284548 | |||||||
| chr2:26284556 | A | T | 1 | a0001c0003t0001g0034 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1150-327A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 13/15 | chr2 | 26284556 | |||||||
| chr2:26284619 | A | G | 8 | a0001c0004t0003g0163 a0001c0004t0003g0164 a0001c0004t0003g0183 others(5): Show |
8 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1150-264A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 13/15 | chr2 | 26284619 | |||||||
| chr2:26284856 | T | C | 47 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(44): Show |
53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.1150-27T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 13/15 | chr2 | 26284856 | |||||||
| chr2:26285013 | T | A | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1224+56T>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 14/15 | chr2 | 26285013 | |||||||
| chr2:26285048 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0134 |
2 | HG01515.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1224+91G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 14/15 | chr2 | 26285048 | |||||||
| chr2:26285208 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1225-199C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 14/15 | chr2 | 26285208 | |||||||
| chr2:26285319 | A | G | 48 | a0001c0001t0001g0230 a0001c0003t0001g0004 a0001c0003t0001g0007 others(45): Show |
54 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.1225-88A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 14/15 | chr2 | 26285319 | |||||||
| chr2:26285333 | G | A | 1 | a0002c0002t0002g0222 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1225-74G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 14/15 | chr2 | 26285333 | |||||||
| chr2:26285345 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1225-62G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 14/15 | chr2 | 26285345 | |||||||
| chr2:26285628 | G | A | 8 | a0001c0004t0003g0163 a0001c0004t0003g0164 a0001c0004t0003g0183 others(5): Show |
8 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1389+57G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26285628 | |||||||
| chr2:26285739 | G | GT | 6 | a0001c0001t0001g0157 a0002c0002t0002g0166 a0002c0002t0002g0182 others(3): Show |
6 | HG02056.hp1 HG02074.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1389+186dupT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | ||||||
| chr2:26285739 | G | GTTTTTTT others(1): Show |
32 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(29): Show |
38 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1389+179_1389+186d others(10): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | ||||||
| chr2:26285739 | G | GTTTTTTT others(2): Show |
12 | a0001c0003t0001g0028 a0001c0003t0001g0030 a0001c0003t0001g0034 others(9): Show |
12 | HG00280.hp2 HG01175.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1389+178_1389+186d others(11): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | ||||||
| chr2:26285739 | G | GTTTTTTT others(3): Show |
7 | a0001c0001t0001g0151 a0001c0001t0005g0005 a0001c0001t0005g0237 others(4): Show |
10 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1389+177_1389+186d others(12): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | ||||||
| chr2:26285739 | G | GTTTTTTT others(4): Show |
2 | a0001c0001t0001g0077 a0001c0001t0004g0234 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1389+176_1389+186d others(13): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | ||||||
| chr2:26285739 | G | GTTTTTTT others(5): Show |
6 | a0001c0001t0001g0013 a0001c0001t0001g0074 a0001c0001t0001g0078 others(3): Show |
7 | HG01069.hp2 HG01071.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1389+175_1389+186d others(14): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | ||||||
| chr2:26285739 | G | GTTTTTTT others(6): Show |
5 | a0001c0001t0001g0076 a0001c0001t0001g0162 a0001c0001t0001g0165 others(2): Show |
5 | HG01106.hp2 HG03225.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1389+174_1389+186d others(15): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | ||||||
| chr2:26285739 | G | GTTTTTTT others(11): Show |
1 | a0001c0001t0001g0109 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1389+182_1389+183i others(20): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | ||||||
| chr2:26285739 | G | GTTTTTTT others(8): Show |
1 | a0001c0001t0001g0230 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1389+172_1389+186d others(17): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | ||||||
| chr2:26285739 | G | GTTTTTTT others(10): Show |
2 | a0001c0001t0001g0086 a0001c0001t0001g0089 |
2 | HG00741.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1389+170_1389+186d others(19): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | ||||||
| chr2:26285739 | G | GTTTTTTT others(11): Show |
30 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0088 others(27): Show |
33 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.1389+169_1389+186d others(20): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | ||||||
| chr2:26285739 | G | GTTTTTTT others(12): Show |
32 | a0001c0001t0001g0061 a0001c0001t0001g0073 a0001c0001t0001g0085 others(29): Show |
32 | HG00099.hp2 HG00642.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1389+186_1389+187i others(21): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | ||||||
| chr2:26285739 | G | GTTTTTTT others(13): Show |
18 | a0001c0001t0001g0010 a0001c0001t0001g0060 a0001c0001t0001g0062 others(15): Show |
19 | HG00735.hp1 HG01261.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.1389+186_1389+187i others(22): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | ||||||
| chr2:26285739 | G | GTTTTTTT others(14): Show |
10 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0091 others(7): Show |
10 | HG01255.hp2 HG01981.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1389+186_1389+187i others(23): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | ||||||
| chr2:26285739 | G | GTTTTTTT others(15): Show |
3 | a0001c0001t0001g0069 a0001c0001t0001g0123 a0001c0001t0001g0158 |
3 | HG02280.hp1 HG03130.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1389+186_1389+187i others(24): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | ||||||
| chr2:26285739 | G | GTTTTTTT others(16): Show |
3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0128 |
3 | HG01346.hp2 HG01358.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1389+186_1389+187i others(25): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | ||||||
| chr2:26285739 | G | GTTTTTTT others(17): Show |
1 | a0001c0001t0001g0104 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1389+186_1389+187i others(26): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | ||||||
| chr2:26285739 | G | GTTTTTTT others(20): Show |
1 | a0001c0001t0001g0245 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1389+186_1389+187i others(29): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26285739 | ||||||
| chr2:26285847 | C | T | 4 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(1): Show |
7 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1389+276C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26285847 | |||||||
| chr2:26285913 | T | C | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1389+342T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26285913 | |||||||
| chr2:26285984 | C | T | 6 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(3): Show |
6 | HG01243.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1389+413C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26285984 | |||||||
| chr2:26286273 | A | G | 1 | a0001c0004t0003g0185 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1389+702A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26286273 | |||||||
| chr2:26286594 | G | C | 16 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(13): Show |
20 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.1389+1023G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26286594 | |||||||
| chr2:26286612 | C | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG00738.hp2 HG02145.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1389+1041C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26286612 | |||||||
| chr2:26286726 | G | A | 1 | a0001c0003t0001g0050 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1389+1155G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26286726 | |||||||
| chr2:26286749 | G | A | 47 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(44): Show |
53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.1389+1178G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26286749 | |||||||
| chr2:26286782 | A | G | 42 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0012 others(39): Show |
64 | HG00408.hp1 HG01081.hp1 HG01192.hp2 others(61): Show |
intron_variant | MODIFIER | c.1389+1211A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26286782 | |||||||
| chr2:26286811 | TTG | T | 12 | a0001c0004t0003g0163 a0001c0004t0003g0164 a0001c0004t0003g0183 others(9): Show |
13 | HG01167.hp2 HG01169.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1389+1242_1389+124 others(6): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26286811 | ||||||
| chr2:26286812 | TG | T | 2 | a0001c0001t0005g0005 a0001c0001t0005g0238 |
5 | HG01074.hp1 HG01167.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1389+1242delG | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26286812 | |||||||
| chr2:26286813 | G | GT | 16 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0072 others(13): Show |
16 | HG01261.hp2 HG01517.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1389+1260dupT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26286813 | ||||||
| chr2:26286813 | G | T | 10 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(7): Show |
10 | HG00639.hp2 HG00733.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.1389+1242G>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26286813 | |||||||
| chr2:26286813 | GT | G | 45 | a0001c0001t0001g0112 a0002c0002t0002g0001 a0002c0002t0002g0003 others(42): Show |
67 | HG00408.hp1 HG01070.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.1389+1260delT | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26286813 | ||||||
| chr2:26286819 | T | G | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1389+1248T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26286819 | |||||||
| chr2:26286823 | T | G | 1 | a0002c0002t0001g0218 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1389+1252T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26286823 | |||||||
| chr2:26286850 | T | C | 7 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0077 others(4): Show |
7 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1389+1279T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26286850 | |||||||
| chr2:26287161 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1389+1590G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26287161 | |||||||
| chr2:26287227 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1389+1656C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26287227 | |||||||
| chr2:26287281 | A | T | 1 | a0001c0001t0001g0142 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1389+1710A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26287281 | |||||||
| chr2:26287414 | G | A | 8 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(5): Show |
12 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1389+1843G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26287414 | |||||||
| chr2:26287787 | T | G | 25 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0077 others(22): Show |
29 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1390-2131T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26287787 | |||||||
| chr2:26287995 | G | A | 1 | a0001c0001t0004g0234 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1390-1923G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26287995 | |||||||
| chr2:26288015 | G | C | 4 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(1): Show |
7 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1390-1903G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26288015 | |||||||
| chr2:26288065 | G | A | 3 | a0001c0001t0005g0005 a0001c0001t0005g0237 a0001c0001t0005g0238 |
6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1390-1853G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26288065 | |||||||
| chr2:26288070 | T | C | 16 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(13): Show |
20 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.1390-1848T>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26288070 | |||||||
| chr2:26288104 | C | T | 8 | a0001c0001t0004g0234 a0001c0001t0005g0005 a0001c0001t0005g0237 others(5): Show |
12 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1390-1814C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26288104 | |||||||
| chr2:26288190 | G | A | 8 | a0001c0004t0003g0163 a0001c0004t0003g0164 a0001c0004t0003g0183 others(5): Show |
8 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1390-1728G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26288190 | |||||||
| chr2:26288339 | A | G | 1 | a0001c0003t0001g0044 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1390-1579A>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26288339 | |||||||
| chr2:26288633 | C | T | 4 | a0001c0005t0004g0017 a0001c0005t0004g0075 a0001c0005t0004g0083 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1390-1285C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26288633 | |||||||
| chr2:26288708 | C | CA | 13 | a0001c0001t0005g0005 a0001c0001t0005g0237 a0001c0001t0005g0238 others(10): Show |
16 | HG00733.hp2 HG01074.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1390-1202dupA | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26288708 | ||||||
| chr2:26288708 | C | CAA | 5 | a0001c0001t0004g0234 a0001c0005t0004g0017 a0001c0005t0004g0075 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1390-1203_1390-120 others(6): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26288708 | ||||||
| chr2:26288973 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1390-945C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26288973 | |||||||
| chr2:26289016 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0112 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1390-902C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26289016 | |||||||
| chr2:26289017 | G | A | 1 | a0002c0002t0002g0210 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1390-901G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26289017 | |||||||
| chr2:26289066 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1390-852C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26289066 | |||||||
| chr2:26289106 | C | T | 1 | a0001c0001t0005g0238 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1390-812C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26289106 | |||||||
| chr2:26289125 | C | A | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1390-793C>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26289125 | |||||||
| chr2:26289241 | C | T | 1 | a0002c0002t0002g0198 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1390-677C>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26289241 | |||||||
| chr2:26289242 | G | A | 2 | a0002c0002t0001g0217 a0002c0002t0001g0218 |
2 | HG01109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1390-676G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26289242 | |||||||
| chr2:26289432 | T | TCACTTAA others(11): Show |
8 | a0001c0004t0003g0163 a0001c0004t0003g0164 a0001c0004t0003g0183 others(5): Show |
8 | HG02572.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1390-484_1390-467d others(20): Show |
HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 26289432 | ||||||
| chr2:26289671 | A | T | 1 | a0001c0003t0001g0046 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1390-247A>T | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26289671 | |||||||
| chr2:26289733 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1390-185G>A | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26289733 | |||||||
| chr2:26289733 | G | C | 1 | a0002c0002t0002g0197 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1390-185G>C | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26289733 | |||||||
| chr2:26289865 | T | G | 49 | a0001c0003t0001g0004 a0001c0003t0001g0007 a0001c0003t0001g0008 others(46): Show |
55 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.1390-53T>G | HADHB | ENSG00000138029.14 | transcript | ENST00000317799.10 | protein_coding | 15/15 | chr2 | 26289865 |