Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79694 |
| ensemblid | ENSG00000172469.17 |
| hgncid | 21072 |
| symbol | MANEA |
| name | mannosidase endo-alpha |
| refseq_nuc | NM_024641.4 |
| refseq_prot | NP_078917.2 |
| ensembl_nuc | ENST00000358812.9 |
| ensembl_prot | ENSP00000351669.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 95577535 |
| end | 95609452 |
| strand | + |
| ver | v1.2 |
| region | chr6:95577535-95609452 |
| region5000 | chr6:95572535-95614452 |
| regionname0 | MANEA_chr6_95577535_95609452 |
| regionname5000 | MANEA_chr6_95572535_95614452 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 462 | 354 | 71 | 64 | 181 | 8 | 28 | 145 | MANEA_chr6_95572535_95614452 | MANEA | MAKFR others(457): Show |
chr6 | 95572535 | 95614452 |
| a0002 | 0/0 | 462 | 25 | 0 | 8 | 15 | 1 | 1 | 11 | MANEA_chr6_95572535_95614452 | MANEA | MAKFR others(457): Show |
chr6 | 95572535 | 95614452 |
| a0003 | 0/0 | 462 | 14 | 9 | 3 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | MAKFR others(457): Show |
chr6 | 95572535 | 95614452 |
| a0004 | 0/0 | 462 | 10 | 6 | 0 | 0 | 1 | 3 | 0 | MANEA_chr6_95572535_95614452 | MANEA | MAKFR others(457): Show |
chr6 | 95572535 | 95614452 |
| a0005 | 0/0 | 462 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | MAKFR others(457): Show |
chr6 | 95572535 | 95614452 |
| a0006 | 0/0 | 462 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | MAKFR others(457): Show |
chr6 | 95572535 | 95614452 |
| a0007 | 0/0 | 462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | MAKFR others(457): Show |
chr6 | 95572535 | 95614452 |
| a0008 | 0/0 | 462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | MAKFR others(457): Show |
chr6 | 95572535 | 95614452 |
| a0009 | 0/0 | 462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | MAKFR others(457): Show |
chr6 | 95572535 | 95614452 |
| a0010 | 0/0 | 462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | MAKFR others(457): Show |
chr6 | 95572535 | 95614452 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1386 | 354 | 71 | 64 | 181 | 8 | 28 | MANEA_chr6_95572535_95614452 | MANEA | ATGGC others(1381): Show |
chr6 | 95572535 | 95614452 | ||
| a0002c0002 | 0/0 | 1386 | 24 | 0 | 8 | 15 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | ATGGC others(1381): Show |
chr6 | 95572535 | 95614452 | ||
| a0002c0011 | 0/0 | 1386 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | ATGGC others(1381): Show |
chr6 | 95572535 | 95614452 | ||
| a0003c0003 | 0/0 | 1386 | 14 | 9 | 3 | 0 | 2 | 0 | MANEA_chr6_95572535_95614452 | MANEA | ATGGC others(1381): Show |
chr6 | 95572535 | 95614452 | ||
| a0004c0004 | 0/0 | 1386 | 6 | 6 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | ATGGC others(1381): Show |
chr6 | 95572535 | 95614452 | ||
| a0004c0005 | 0/0 | 1386 | 2 | 0 | 0 | 0 | 0 | 2 | MANEA_chr6_95572535_95614452 | MANEA | ATGGC others(1381): Show |
chr6 | 95572535 | 95614452 | ||
| a0004c0007 | 0/0 | 1386 | 2 | 0 | 0 | 0 | 1 | 1 | MANEA_chr6_95572535_95614452 | MANEA | ATGGC others(1381): Show |
chr6 | 95572535 | 95614452 | ||
| a0005c0006 | 0/0 | 1386 | 2 | 0 | 0 | 0 | 2 | 0 | MANEA_chr6_95572535_95614452 | MANEA | ATGGC others(1381): Show |
chr6 | 95572535 | 95614452 | ||
| a0006c0013 | 0/0 | 1386 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | ATGGC others(1381): Show |
chr6 | 95572535 | 95614452 | ||
| a0007c0009 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | ATGGC others(1381): Show |
chr6 | 95572535 | 95614452 | ||
| a0008c0012 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | ATGGC others(1381): Show |
chr6 | 95572535 | 95614452 | ||
| a0009c0010 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | ATGGC others(1381): Show |
chr6 | 95572535 | 95614452 | ||
| a0010c0008 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | ATGGC others(1381): Show |
chr6 | 95572535 | 95614452 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4574 | 80 | 17 | 8 | 48 | 0 | 7 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4569): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0002 | 1/0 | 4578 | 69 | 3 | 30 | 28 | 2 | 5 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0003 | 0/0 | 4578 | 60 | 1 | 13 | 34 | 3 | 9 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0004 | 0/0 | 4578 | 56 | 14 | 4 | 31 | 2 | 5 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0005 | 0/1 | 4578 | 31 | 10 | 5 | 14 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0006 | 0/0 | 4578 | 7 | 6 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0008 | 0/0 | 4578 | 14 | 6 | 0 | 7 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0009 | 0/0 | 4578 | 8 | 0 | 0 | 8 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0010 | 0/0 | 4578 | 5 | 5 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0011 | 0/0 | 4574 | 3 | 3 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4569): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0012 | 0/0 | 4578 | 3 | 3 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0013 | 0/0 | 4574 | 3 | 0 | 0 | 3 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4569): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0014 | 0/0 | 4578 | 2 | 1 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0016 | 0/0 | 4578 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0017 | 0/0 | 4578 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0018 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0019 | 0/0 | 4574 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4569): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0020 | 0/0 | 4574 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4569): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0021 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0022 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0023 | 0/0 | 4578 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0025 | 0/0 | 4578 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0026 | 0/0 | 4578 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0001c0001t0027 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0002c0002t0006 | 0/0 | 4578 | 24 | 0 | 8 | 15 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0002c0011t0006 | 0/0 | 4578 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0003c0003t0007 | 0/0 | 4576 | 14 | 9 | 3 | 0 | 2 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4571): Show |
chr6 | 95572535 | 95614452 |
| a0004c0004t0005 | 0/0 | 4578 | 4 | 4 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0004c0004t0015 | 0/0 | 4578 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0004c0005t0005 | 0/0 | 4578 | 2 | 0 | 0 | 0 | 0 | 2 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0004c0007t0005 | 0/0 | 4578 | 2 | 0 | 0 | 0 | 1 | 1 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0005c0006t0005 | 0/0 | 4578 | 2 | 0 | 0 | 0 | 2 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0006c0013t0007 | 0/0 | 4576 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4571): Show |
chr6 | 95572535 | 95614452 |
| a0007c0009t0001 | 0/0 | 4574 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4569): Show |
chr6 | 95572535 | 95614452 |
| a0008c0012t0024 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0009c0010t0004 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4573): Show |
chr6 | 95572535 | 95614452 |
| a0010c0008t0001 | 0/0 | 4574 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | GAGGG others(4569): Show |
chr6 | 95572535 | 95614452 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 23 | 4 | 2 | 16 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0044 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0002 | 0/0 | 12 | 0 | 5 | 7 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0008 | 0/0 | 6 | 0 | 4 | 0 | 2 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0242 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0003 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0010 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0020 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0005g0005 | 0/1 | 7 | 0 | 1 | 5 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0005g0024 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0005g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0005g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0005g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0006g0025 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0006g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0006g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0008g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0008g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0008g0010 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0008g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0008g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0008g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0008g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0008g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0008g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0008g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0008g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0009g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0009g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0009g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0009g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0009g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0009g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0009g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0009g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0010g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0010g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0010g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0011g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0011g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0011g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0012g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0012g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0013g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0013g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0014g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0014g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0016g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0016g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0017g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0018g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0019g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0020g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0021g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0022g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0023g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0025g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0026g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0001c0001t0027g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0002c0002t0006g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0002c0002t0006g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0002c0002t0006g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0002c0002t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0002c0002t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0002c0002t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0002c0002t0006g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0002c0002t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0002c0002t0006g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0002c0002t0006g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0002c0002t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0002c0002t0006g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0002c0002t0006g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0002c0002t0006g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0002c0002t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0002c0002t0006g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0002c0002t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0002c0002t0006g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0002c0002t0006g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0002c0002t0006g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0002c0002t0006g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0002c0011t0006g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0003c0003t0007g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0003c0003t0007g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0003c0003t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0003c0003t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0003c0003t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0003c0003t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0003c0003t0007g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0003c0003t0007g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0003c0003t0007g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0003c0003t0007g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0003c0003t0007g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0003c0003t0007g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0004c0004t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0004c0004t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0004c0004t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0004c0004t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0004c0004t0015g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0004c0004t0015g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0004c0005t0005g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0004c0005t0005g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0004c0007t0005g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0004c0007t0005g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0005c0006t0005g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0005c0006t0005g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0006c0013t0007g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0007c0009t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0008c0012t0024g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0009c0010t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| a0010c0008t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0010 | EUR | GBR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0114 | EUR | GBR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0012 | EUR | GBR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00140 | hp2 | a0001 | c0001 | t0014 | g0227 | EUR | GBR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0070 | EUR | FIN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00323 | hp2 | a0002 | c0011 | t0006 | g0023 | EUR | FIN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00423 | hp1 | a0001 | c0001 | t0008 | g0018 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0204 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0201 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00597 | hp2 | a0001 | c0001 | t0022 | g0006 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00673 | hp2 | a0001 | c0001 | t0008 | g0010 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0034 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00738 | hp1 | a0002 | c0002 | t0006 | g0192 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0025 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01069 | hp1 | a0002 | c0002 | t0006 | g0179 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0116 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01070 | hp1 | a0003 | c0003 | t0007 | g0245 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0048 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0048 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01071 | hp2 | a0002 | c0002 | t0006 | g0182 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0024 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01099 | hp2 | a0003 | c0003 | t0007 | g0249 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01106 | hp1 | a0002 | c0002 | t0006 | g0178 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01109 | hp1 | a0002 | c0002 | t0006 | g0176 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01109 | hp2 | a0006 | c0013 | t0007 | g0193 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01175 | hp2 | a0003 | c0003 | t0007 | g0246 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01192 | hp1 | a0002 | c0002 | t0006 | g0183 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01243 | hp1 | a0001 | c0001 | t0025 | g0081 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0063 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0079 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0083 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0082 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01261 | hp1 | a0002 | c0002 | t0006 | g0191 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01346 | hp1 | a0001 | c0001 | t0026 | g0064 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0122 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01358 | hp2 | a0002 | c0002 | t0006 | g0190 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01361 | hp2 | a0001 | c0001 | t0023 | g0126 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0112 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01515 | hp1 | a0005 | c0006 | t0005 | g0198 | EUR | IBS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0115 | EUR | IBS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01516 | hp1 | a0003 | c0003 | t0007 | g0244 | EUR | IBS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01517 | hp2 | a0005 | c0006 | t0005 | g0202 | EUR | IBS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01884 | hp1 | a0001 | c0001 | t0012 | g0056 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0262 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01891 | hp1 | a0007 | c0009 | t0001 | g0038 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0199 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0106 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0060 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0108 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02055 | hp2 | a0003 | c0003 | t0007 | g0130 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02056 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02080 | hp2 | a0002 | c0002 | t0006 | g0046 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0030 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02132 | hp1 | a0001 | c0001 | t0009 | g0170 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02132 | hp2 | a0002 | c0002 | t0006 | g0023 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02145 | hp1 | a0001 | c0001 | t0014 | g0052 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | CDX | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02155 | hp2 | a0002 | c0002 | t0006 | g0023 | EAS | CDX | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0058 | EAS | CDX | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0104 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0254 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0010 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02258 | hp2 | a0008 | c0012 | t0024 | g0099 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0196 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0255 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02523 | hp1 | a0001 | c0001 | t0021 | g0032 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02523 | hp2 | a0002 | c0002 | t0006 | g0180 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0055 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02602 | hp2 | a0004 | c0007 | t0005 | g0235 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02615 | hp1 | a0001 | c0001 | t0010 | g0080 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02615 | hp2 | a0003 | c0003 | t0007 | g0037 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02630 | hp2 | a0003 | c0003 | t0007 | g0047 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0093 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02683 | hp2 | a0004 | c0005 | t0005 | g0237 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0020 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0260 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0251 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02818 | hp1 | a0004 | c0004 | t0005 | g0219 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02886 | hp1 | a0001 | c0001 | t0010 | g0012 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0012 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02896 | hp2 | a0001 | c0001 | t0011 | g0137 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0012 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02922 | hp2 | a0001 | c0001 | t0019 | g0135 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0261 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02965 | hp2 | a0004 | c0004 | t0005 | g0234 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02970 | hp1 | a0001 | c0001 | t0010 | g0031 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02970 | hp2 | a0003 | c0003 | t0007 | g0047 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0072 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0259 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0100 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03098 | hp1 | a0001 | c0001 | t0011 | g0141 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0208 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03130 | hp2 | a0003 | c0003 | t0007 | g0129 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03139 | hp2 | a0003 | c0003 | t0007 | g0194 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03209 | hp1 | a0004 | c0004 | t0005 | g0051 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03225 | hp2 | a0009 | c0010 | t0004 | g0121 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0097 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03453 | hp1 | a0004 | c0004 | t0015 | g0248 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0019 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03486 | hp2 | a0001 | c0001 | t0012 | g0258 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0027 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0062 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0020 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0020 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0027 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0264 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03540 | hp1 | a0001 | c0001 | t0011 | g0136 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0066 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0200 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0098 | SAS | BEB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG04115 | hp1 | a0001 | c0001 | t0008 | g0071 | SAS | STU | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | STU | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0221 | SAS | BEB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0034 | SAS | STU | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | STU | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | STU | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | STU | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0074 | AFR | YRI | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18522 | hp2 | a0004 | c0004 | t0005 | g0233 | AFR | YRI | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | CHB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18747 | hp2 | a0001 | c0001 | t0009 | g0146 | EAS | CHB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18906 | hp1 | a0010 | c0008 | t0001 | g0131 | AFR | YRI | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | YRI | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0120 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18947 | hp1 | a0001 | c0001 | t0009 | g0151 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18948 | hp2 | a0001 | c0001 | t0013 | g0004 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18951 | hp1 | a0001 | c0001 | t0005 | g0205 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18951 | hp2 | a0001 | c0001 | t0008 | g0030 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18952 | hp1 | a0002 | c0002 | t0006 | g0173 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18960 | hp2 | a0001 | c0001 | t0016 | g0086 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0049 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0124 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18966 | hp2 | a0001 | c0001 | t0009 | g0158 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18969 | hp1 | a0001 | c0001 | t0013 | g0014 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18970 | hp1 | a0002 | c0002 | t0006 | g0177 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18970 | hp2 | a0002 | c0002 | t0006 | g0045 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18971 | hp1 | a0002 | c0002 | t0006 | g0184 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18977 | hp2 | a0001 | c0001 | t0020 | g0014 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18978 | hp1 | a0001 | c0001 | t0008 | g0032 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18978 | hp2 | a0001 | c0001 | t0013 | g0004 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18980 | hp2 | a0001 | c0001 | t0009 | g0168 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18985 | hp1 | a0001 | c0001 | t0005 | g0049 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18985 | hp2 | a0001 | c0001 | t0027 | g0028 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18986 | hp1 | a0002 | c0002 | t0006 | g0174 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18987 | hp2 | a0002 | c0002 | t0006 | g0187 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18999 | hp2 | a0001 | c0001 | t0005 | g0203 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19000 | hp2 | a0002 | c0002 | t0006 | g0046 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19002 | hp1 | a0001 | c0001 | t0017 | g0029 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19003 | hp1 | a0001 | c0001 | t0005 | g0197 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19005 | hp1 | a0002 | c0002 | t0006 | g0185 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19009 | hp1 | a0001 | c0001 | t0009 | g0153 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19010 | hp1 | a0002 | c0002 | t0006 | g0186 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19011 | hp1 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0263 | AFR | LWK | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0250 | AFR | LWK | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19043 | hp1 | a0003 | c0003 | t0007 | g0128 | AFR | LWK | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19043 | hp2 | a0001 | c0001 | t0018 | g0247 | AFR | LWK | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19058 | hp1 | a0002 | c0002 | t0006 | g0045 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19058 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19064 | hp1 | a0001 | c0001 | t0008 | g0188 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19065 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19075 | hp1 | a0001 | c0001 | t0009 | g0133 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19075 | hp2 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19077 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19081 | hp1 | a0002 | c0002 | t0006 | g0175 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19085 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19090 | hp1 | a0001 | c0001 | t0016 | g0087 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19091 | hp1 | a0001 | c0001 | t0009 | g0150 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0252 | AFR | YRI | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA19240 | hp2 | a0001 | c0001 | t0012 | g0056 | AFR | YRI | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0256 | AFR | ASW | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA20129 | hp2 | a0003 | c0003 | t0007 | g0037 | AFR | ASW | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA20805 | hp1 | a0004 | c0007 | t0005 | g0051 | EUR | TSI | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA20805 | hp2 | a0003 | c0003 | t0007 | g0243 | EUR | TSI | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA20905 | hp1 | a0002 | c0002 | t0006 | g0181 | SAS | GIH | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA20905 | hp2 | a0004 | c0005 | t0005 | g0236 | SAS | GIH | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0107 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0095 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02559 | hp1 | a0003 | c0003 | t0007 | g0195 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0009 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0101 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0253 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | USA | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18955 | hp1 | a0001 | c0001 | t0017 | g0029 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0055 | AFR | USA | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| NA20300 | hp2 | a0004 | c0004 | t0015 | g0220 | AFR | USA | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0005 | REF | REF | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0242 | REF | REF | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:95586639 | T | G | 1 | a0010 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.200T>G | p.Ile67Ser | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/5 | 342/4578 | 200/1389 | 67/462 | chr6 | 95586639 | |||
| chr6:95586672 | G | C | 1 | a0007 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.233G>C | p.Ser78Thr | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/5 | 375/4578 | 233/1389 | 78/462 | chr6 | 95586672 | |||
| chr6:95586684 | C | T | 1 | a0004 | 10 | HG02602.hp2 HG02683.hp2 HG02818.hp1 others(7): Show |
missense_variant | MODERATE | c.245C>T | p.Thr82Ile | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/5 | 387/4578 | 245/1389 | 82/462 | chr6 | 95586684 | |||
| chr6:95586968 | C | T | 2 | a0003 a0006 |
15 | HG01070.hp1 HG01099.hp2 HG01109.hp2 others(12): Show |
missense_variant | MODERATE | c.529C>T | p.Arg177Cys | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/5 | 671/4578 | 529/1389 | 177/462 | chr6 | 95586968 | |||
| chr6:95586981 | T | C | 1 | a0006 | 1 | HG01109.hp2 | missense_variant&splice_region_variant | MODERATE | c.542T>C | p.Ile181Thr | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/5 | 684/4578 | 542/1389 | 181/462 | chr6 | 95586981 | |||
| chr6:95605787 | G | C | 1 | a0009 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.771G>C | p.Lys257Asn | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 913/4578 | 771/1389 | 257/462 | chr6 | 95605787 | |||
| chr6:95605879 | G | T | 1 | a0005 | 2 | HG01515.hp1 HG01517.hp2 |
missense_variant | MODERATE | c.863G>T | p.Arg288Leu | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1005/4578 | 863/1389 | 288/462 | chr6 | 95605879 | |||
| chr6:95606046 | T | A | 1 | a0002 | 25 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
missense_variant | MODERATE | c.1030T>A | p.Phe344Ile | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1172/4578 | 1030/1389 | 344/462 | chr6 | 95606046 | |||
| chr6:95606299 | G | A | 1 | a0008 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.1283G>A | p.Arg428His | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1425/4578 | 1283/1389 | 428/462 | chr6 | 95606299 | |||
| chr6:95606386 | G | A | 2 | a0003 a0006 |
15 | HG01070.hp1 HG01099.hp2 HG01109.hp2 others(12): Show |
missense_variant | MODERATE | c.1370G>A | p.Arg457His | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1512/4578 | 1370/1389 | 457/462 | chr6 | 95606386 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:95586454 | G | A | 1 | a0004c0005 | 2 | HG02683.hp2 NA20905.hp2 |
synonymous_variant | LOW | c.15G>A | p.Arg5Arg | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/5 | 157/4578 | 15/1389 | 5/462 | chr6 | 95586454 | |||
| chr6:95586736 | G | A | 2 | a0004c0005 a0004c0007 |
4 | HG02602.hp2 HG02683.hp2 NA20805.hp1 others(1): Show |
synonymous_variant | LOW | c.297G>A | p.Leu99Leu | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/5 | 439/4578 | 297/1389 | 99/462 | chr6 | 95586736 | |||
| chr6:95606378 | A | G | 1 | a0002c0011 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.1362A>G | p.Ala454Ala | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1504/4578 | 1362/1389 | 454/462 | chr6 | 95606378 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:95577570 | A | G | 14 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(11): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
5_prime_UTR_variant | MODIFIER | c.-107A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/5 | 8870 | chr6 | 95577570 | ||||||
| chr6:95577573 | T | A | 1 | a0001c0001t0011 | 3 | HG02896.hp2 HG03098.hp1 HG03540.hp1 |
5_prime_UTR_variant | MODIFIER | c.-104T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/5 | 8867 | chr6 | 95577573 | ||||||
| chr6:95577574 | C | A | 1 | a0001c0001t0011 | 3 | HG02896.hp2 HG03098.hp1 HG03540.hp1 |
5_prime_UTR_variant | MODIFIER | c.-103C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/5 | 8866 | chr6 | 95577574 | ||||||
| chr6:95577599 | T | A | 1 | a0001c0001t0021 | 1 | HG02523.hp1 | 5_prime_UTR_variant | MODIFIER | c.-78T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/5 | 8841 | chr6 | 95577599 | ||||||
| chr6:95577602 | G | A | 1 | a0001c0001t0022 | 1 | HG00597.hp2 | 5_prime_UTR_variant | MODIFIER | c.-75G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/5 | 8838 | chr6 | 95577602 | ||||||
| chr6:95606533 | A | T | 8 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0011 others(5): Show |
98 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*128A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 128 | chr6 | 95606533 | ||||||
| chr6:95606614 | A | G | 1 | a0004c0004t0015 | 2 | HG03453.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*209A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 209 | chr6 | 95606614 | ||||||
| chr6:95606664 | G | T | 7 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0017 others(4): Show |
68 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*259G>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 259 | chr6 | 95606664 | ||||||
| chr6:95606693 | C | G | 1 | a0001c0001t0012 | 3 | HG01884.hp1 HG03486.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*288C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 288 | chr6 | 95606693 | ||||||
| chr6:95606712 | C | T | 25 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(22): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*307C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 307 | chr6 | 95606712 | ||||||
| chr6:95606774 | T | C | 1 | a0001c0001t0013 | 3 | NA18948.hp2 NA18969.hp1 NA18978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*369T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 369 | chr6 | 95606774 | ||||||
| chr6:95606825 | G | A | 1 | a0001c0001t0025 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*420G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 420 | chr6 | 95606825 | ||||||
| chr6:95607059 | C | A | 25 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(22): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*654C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 654 | chr6 | 95607059 | ||||||
| chr6:95607117 | C | G | 1 | a0001c0001t0017 | 2 | NA18955.hp1 NA19002.hp1 |
3_prime_UTR_variant | MODIFIER | c.*712C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 712 | chr6 | 95607117 | ||||||
| chr6:95607140 | G | A | 6 | a0001c0001t0005 a0004c0004t0005 a0004c0004t0015 others(3): Show |
42 | HG00423.hp2 HG00558.hp1 HG01070.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*735G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 735 | chr6 | 95607140 | ||||||
| chr6:95607187 | T | A | 2 | a0001c0001t0008 a0001c0001t0010 |
19 | HG00423.hp1 HG00673.hp2 HG02055.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*782T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 782 | chr6 | 95607187 | ||||||
| chr6:95607500 | T | C | 1 | a0001c0001t0026 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1095T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1095 | chr6 | 95607500 | ||||||
| chr6:95607668 | G | A | 25 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(22): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*1263G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1263 | chr6 | 95607668 | ||||||
| chr6:95607801 | T | A | 1 | a0001c0001t0023 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1396T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1396 | chr6 | 95607801 | ||||||
| chr6:95607900 | G | A | 1 | a0001c0001t0019 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1495G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1495 | chr6 | 95607900 | ||||||
| chr6:95608039 | G | C | 25 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(22): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*1634G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1634 | chr6 | 95608039 | ||||||
| chr6:95608130 | C | T | 25 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(22): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*1725C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1725 | chr6 | 95608130 | ||||||
| chr6:95608240 | C | G | 1 | a0008c0012t0024 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1835C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1835 | chr6 | 95608240 | ||||||
| chr6:95608325 | G | A | 1 | a0001c0001t0020 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1920G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1920 | chr6 | 95608325 | ||||||
| chr6:95608436 | C | A | 1 | a0001c0001t0014 | 2 | HG00140.hp2 HG02145.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2031C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 2031 | chr6 | 95608436 | ||||||
| chr6:95608894 | GAA | G | 2 | a0003c0003t0007 a0006c0013t0007 |
15 | HG01070.hp1 HG01099.hp2 HG01109.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2496_*2497delAA | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 2496 | INFO_REALIGN_3_PRIME | chr6 | 95608894 | |||||
| chr6:95608930 | C | T | 1 | a0001c0001t0010 | 5 | HG02615.hp1 HG02886.hp1 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2525C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 2525 | chr6 | 95608930 | ||||||
| chr6:95608972 | G | A | 1 | a0001c0001t0016 | 2 | NA18960.hp2 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2567G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 2567 | chr6 | 95608972 | ||||||
| chr6:95609017 | TAGAG | T | 7 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0013 others(4): Show |
90 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*2615_*2618delAGAG | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 2615 | INFO_REALIGN_3_PRIME | chr6 | 95609017 | |||||
| chr6:95609076 | T | C | 1 | a0001c0001t0027 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2671T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 2671 | chr6 | 95609076 | ||||||
| chr6:95609130 | G | T | 35 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(32): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
3_prime_UTR_variant | MODIFIER | c.*2725G>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 2725 | chr6 | 95609130 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:95577709 | C | T | 4 | a0001c0001t0006g0025 a0001c0001t0006g0262 a0001c0001t0006g0263 others(1): Show |
6 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-39+71C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95577709 | |||||||
| chr6:95577767 | C | T | 1 | a0001c0001t0004g0261 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-39+129C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95577767 | |||||||
| chr6:95577841 | G | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(194): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-39+203G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95577841 | |||||||
| chr6:95578033 | G | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0057 |
3 | HG00639.hp1 HG00642.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.-39+395G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95578033 | |||||||
| chr6:95578121 | C | T | 2 | a0001c0001t0005g0259 a0001c0001t0005g0260 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-39+483C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95578121 | |||||||
| chr6:95578136 | A | T | 2 | a0001c0001t0012g0056 a0001c0001t0012g0258 |
3 | HG01884.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-39+498A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95578136 | |||||||
| chr6:95578268 | TTTG | T | 4 | a0003c0003t0007g0047 a0003c0003t0007g0194 a0003c0003t0007g0195 others(1): Show |
5 | HG01109.hp2 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-39+636_-39+638del others(3): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95578268 | ||||||
| chr6:95578383 | AAAC | A | 3 | a0002c0002t0006g0190 a0002c0002t0006g0191 a0002c0002t0006g0192 |
3 | HG00738.hp1 HG01261.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-39+754_-39+756del others(3): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95578383 | ||||||
| chr6:95578396 | G | T | 1 | a0001c0001t0003g0189 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-39+758G>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95578396 | |||||||
| chr6:95578468 | T | C | 3 | a0001c0001t0003g0059 a0001c0001t0004g0058 a0001c0001t0004g0060 |
3 | HG02015.hp1 HG02083.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.-39+830T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95578468 | |||||||
| chr6:95578510 | A | G | 1 | a0001c0001t0008g0188 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-39+872A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95578510 | |||||||
| chr6:95578512 | A | C | 22 | a0002c0002t0006g0023 a0002c0002t0006g0045 a0002c0002t0006g0046 others(19): Show |
25 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.-39+874A>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95578512 | |||||||
| chr6:95578518 | G | A | 109 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0010 others(106): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.-39+880G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95578518 | |||||||
| chr6:95578549 | T | G | 1 | a0002c0002t0006g0173 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-39+911T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95578549 | |||||||
| chr6:95578579 | A | T | 1 | a0001c0001t0002g0257 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-39+941A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95578579 | |||||||
| chr6:95579096 | C | T | 4 | a0001c0001t0005g0055 a0001c0001t0005g0254 a0001c0001t0005g0255 others(1): Show |
5 | HG02257.hp2 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-39+1458C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95579096 | |||||||
| chr6:95579098 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-39+1460C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95579098 | |||||||
| chr6:95579298 | G | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(56): Show |
98 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-39+1660G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95579298 | |||||||
| chr6:95579369 | C | G | 2 | a0001c0001t0005g0055 a0001c0001t0005g0256 |
3 | HG02572.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-39+1731C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95579369 | |||||||
| chr6:95579890 | A | G | 1 | a0001c0001t0003g0127 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-39+2252A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95579890 | |||||||
| chr6:95580048 | A | G | 1 | a0001c0001t0023g0126 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-39+2410A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580048 | |||||||
| chr6:95580105 | A | G | 2 | a0001c0001t0005g0251 a0001c0001t0005g0252 |
2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-39+2467A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580105 | |||||||
| chr6:95580117 | A | G | 1 | a0001c0001t0002g0250 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-39+2479A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580117 | |||||||
| chr6:95580174 | G | A | 15 | a0001c0001t0005g0005 a0001c0001t0005g0024 a0001c0001t0005g0048 others(12): Show |
24 | HG00423.hp2 HG00558.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-39+2536G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580174 | |||||||
| chr6:95580183 | G | C | 1 | a0001c0001t0003g0061 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-39+2545G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580183 | |||||||
| chr6:95580231 | T | C | 1 | a0010c0008t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-39+2593T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580231 | |||||||
| chr6:95580455 | G | A | 4 | a0001c0001t0003g0062 a0001c0001t0003g0063 a0001c0001t0003g0065 others(1): Show |
4 | HG01243.hp2 HG01346.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39+2817G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580455 | |||||||
| chr6:95580497 | G | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-39+2859G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580497 | |||||||
| chr6:95580542 | G | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-39+2904G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580542 | |||||||
| chr6:95580586 | G | A | 1 | a0001c0001t0003g0066 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-39+2948G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580586 | |||||||
| chr6:95580686 | C | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-39+3048C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580686 | |||||||
| chr6:95580716 | C | T | 1 | a0001c0001t0005g0205 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-39+3078C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580716 | |||||||
| chr6:95580724 | C | CA | 21 | a0001c0001t0001g0132 a0001c0001t0002g0007 a0001c0001t0002g0206 others(18): Show |
29 | HG01952.hp1 HG01978.hp2 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.-39+3104dupA | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95580724 | ||||||
| chr6:95580724 | CA | C | 27 | a0001c0001t0001g0172 a0001c0001t0003g0061 a0001c0001t0018g0247 others(24): Show |
30 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.-39+3104delA | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95580724 | ||||||
| chr6:95580786 | A | T | 9 | a0003c0003t0007g0037 a0003c0003t0007g0128 a0003c0003t0007g0129 others(6): Show |
10 | HG01070.hp1 HG01099.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.-39+3148A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580786 | |||||||
| chr6:95580903 | T | C | 282 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(279): Show |
407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.-39+3265T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580903 | |||||||
| chr6:95581078 | T | C | 4 | a0002c0002t0006g0045 a0002c0002t0006g0046 a0002c0002t0006g0174 others(1): Show |
6 | HG02080.hp2 NA18970.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39+3440T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95581078 | |||||||
| chr6:95581122 | G | C | 5 | a0003c0003t0007g0243 a0003c0003t0007g0244 a0003c0003t0007g0245 others(2): Show |
5 | HG01070.hp1 HG01099.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.-39+3484G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95581122 | |||||||
| chr6:95581268 | G | C | 12 | a0001c0001t0001g0038 a0001c0001t0001g0134 a0001c0001t0001g0138 others(9): Show |
12 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-39+3630G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95581268 | |||||||
| chr6:95581299 | T | C | 3 | a0001c0001t0001g0039 a0001c0001t0001g0144 a0001c0001t0001g0145 |
4 | HG02622.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39+3661T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95581299 | |||||||
| chr6:95581318 | C | G | 4 | a0003c0003t0007g0037 a0003c0003t0007g0128 a0003c0003t0007g0129 others(1): Show |
5 | HG02055.hp2 HG02615.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-39+3680C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95581318 | |||||||
| chr6:95581354 | T | G | 1 | a0001c0001t0002g0206 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-39+3716T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95581354 | |||||||
| chr6:95581510 | CTTTTCAT others(4): Show |
C | 15 | a0001c0001t0005g0005 a0001c0001t0005g0024 a0001c0001t0005g0048 others(12): Show |
24 | HG00423.hp2 HG00558.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-39+3875_-39+3885d others(13): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95581510 | ||||||
| chr6:95581683 | T | C | 5 | a0001c0001t0002g0015 a0001c0001t0002g0207 a0001c0001t0002g0213 others(2): Show |
8 | HG00738.hp2 HG01081.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-39+4045T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95581683 | |||||||
| chr6:95581770 | C | T | 26 | a0001c0001t0003g0059 a0001c0001t0004g0006 a0001c0001t0004g0013 others(23): Show |
42 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.-39+4132C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95581770 | |||||||
| chr6:95581795 | T | A | 1 | a0001c0001t0002g0215 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-39+4157T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95581795 | |||||||
| chr6:95581950 | A | G | 1 | a0001c0001t0004g0112 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-39+4312A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95581950 | |||||||
| chr6:95582076 | C | T | 1 | a0001c0001t0003g0111 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-38-4326C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95582076 | |||||||
| chr6:95582106 | GTGATGTC others(2): Show |
G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-4291_-38-4283d others(11): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95582106 | ||||||
| chr6:95582122 | G | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-4280G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95582122 | |||||||
| chr6:95582173 | C | CT | 50 | a0001c0001t0001g0044 a0001c0001t0001g0142 a0001c0001t0001g0143 others(47): Show |
55 | HG00423.hp2 HG01123.hp2 HG01255.hp2 others(52): Show |
intron_variant | MODIFIER | c.-38-4201dupT | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95582173 | ||||||
| chr6:95582173 | CT | C | 37 | a0001c0001t0001g0022 a0001c0001t0001g0147 a0001c0001t0002g0209 others(34): Show |
44 | HG00323.hp1 HG00323.hp2 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.-38-4201delT | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95582173 | ||||||
| chr6:95582173 | CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0003g0069 a0001c0001t0003g0189 |
2 | HG02015.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.-38-4214_-38-4201d others(16): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95582173 | ||||||
| chr6:95582180 | T | G | 3 | a0001c0001t0005g0208 a0001c0001t0005g0251 a0001c0001t0005g0252 |
3 | HG02809.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38-4222T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95582180 | |||||||
| chr6:95582223 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-38-4179G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95582223 | |||||||
| chr6:95582711 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-3691T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95582711 | |||||||
| chr6:95582958 | C | T | 1 | a0001c0001t0004g0261 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-38-3444C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95582958 | |||||||
| chr6:95583045 | T | G | 22 | a0002c0002t0006g0023 a0002c0002t0006g0045 a0002c0002t0006g0046 others(19): Show |
25 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.-38-3357T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583045 | |||||||
| chr6:95583107 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-3295T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583107 | |||||||
| chr6:95583112 | A | G | 4 | a0001c0001t0002g0007 a0001c0001t0002g0209 a0001c0001t0002g0211 others(1): Show |
9 | NA18950.hp1 NA18952.hp2 NA18989.hp2 others(6): Show |
intron_variant | MODIFIER | c.-38-3290A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583112 | |||||||
| chr6:95583113 | T | C | 1 | a0001c0001t0018g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38-3289T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583113 | |||||||
| chr6:95583233 | T | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(240): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.-38-3169T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583233 | |||||||
| chr6:95583235 | A | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-3167A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583235 | |||||||
| chr6:95583268 | A | G | 1 | a0001c0001t0003g0103 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-38-3134A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583268 | |||||||
| chr6:95583413 | A | T | 34 | a0001c0001t0003g0059 a0001c0001t0004g0006 a0001c0001t0004g0013 others(31): Show |
50 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.-38-2989A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583413 | |||||||
| chr6:95583447 | G | A | 33 | a0001c0001t0005g0005 a0001c0001t0005g0024 a0001c0001t0005g0048 others(30): Show |
43 | HG00423.hp2 HG00558.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.-38-2955G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583447 | |||||||
| chr6:95583548 | ATTTAC | A | 4 | a0001c0001t0005g0055 a0001c0001t0005g0254 a0001c0001t0005g0255 others(1): Show |
5 | HG02257.hp2 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38-2851_-38-2847d others(7): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95583548 | ||||||
| chr6:95583595 | A | G | 9 | a0003c0003t0007g0037 a0003c0003t0007g0128 a0003c0003t0007g0129 others(6): Show |
10 | HG01070.hp1 HG01099.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38-2807A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583595 | |||||||
| chr6:95583731 | T | C | 1 | a0004c0004t0005g0233 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-38-2671T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583731 | |||||||
| chr6:95583759 | GT | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-2640delT | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95583759 | ||||||
| chr6:95583766 | T | C | 1 | a0001c0001t0023g0126 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-38-2636T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583766 | |||||||
| chr6:95583834 | T | G | 1 | a0001c0001t0001g0132 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-38-2568T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583834 | |||||||
| chr6:95583879 | A | G | 1 | a0001c0001t0005g0208 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-38-2523A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583879 | |||||||
| chr6:95584057 | T | C | 1 | a0001c0001t0004g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-38-2345T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584057 | |||||||
| chr6:95584084 | C | T | 10 | a0004c0004t0005g0051 a0004c0004t0005g0219 a0004c0004t0005g0233 others(7): Show |
10 | HG02602.hp2 HG02683.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.-38-2318C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584084 | |||||||
| chr6:95584144 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-38-2258G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584144 | |||||||
| chr6:95584227 | G | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-2175G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584227 | |||||||
| chr6:95584323 | G | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-2079G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584323 | |||||||
| chr6:95584480 | C | T | 3 | a0001c0001t0003g0059 a0001c0001t0004g0058 a0001c0001t0004g0060 |
3 | HG02015.hp1 HG02083.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.-38-1922C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584480 | |||||||
| chr6:95584800 | C | G | 17 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0016 others(14): Show |
38 | HG01074.hp2 HG01167.hp2 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.-38-1602C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584800 | |||||||
| chr6:95584819 | G | T | 1 | a0001c0001t0003g0097 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-38-1583G>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584819 | |||||||
| chr6:95584828 | C | G | 33 | a0001c0001t0005g0005 a0001c0001t0005g0024 a0001c0001t0005g0048 others(30): Show |
43 | HG00423.hp2 HG00558.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.-38-1574C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584828 | |||||||
| chr6:95584874 | C | T | 5 | a0001c0001t0006g0025 a0001c0001t0006g0253 a0001c0001t0006g0262 others(2): Show |
7 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38-1528C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584874 | |||||||
| chr6:95584904 | C | A | 1 | a0004c0004t0005g0234 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-38-1498C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584904 | |||||||
| chr6:95584905 | G | A | 1 | a0001c0001t0003g0073 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-38-1497G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584905 | |||||||
| chr6:95584975 | T | C | 3 | a0001c0001t0005g0208 a0001c0001t0005g0251 a0001c0001t0005g0252 |
3 | HG02809.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38-1427T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584975 | |||||||
| chr6:95585002 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-1400C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585002 | |||||||
| chr6:95585003 | G | A | 13 | a0003c0003t0007g0037 a0003c0003t0007g0047 a0003c0003t0007g0128 others(10): Show |
15 | HG01070.hp1 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-38-1399G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585003 | |||||||
| chr6:95585135 | C | CAT | 16 | a0001c0001t0005g0005 a0001c0001t0005g0024 a0001c0001t0005g0048 others(13): Show |
25 | HG00423.hp2 HG00558.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-38-1251_-38-1250d others(4): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95585135 | ||||||
| chr6:95585135 | C | CATAT | 6 | a0001c0001t0005g0055 a0001c0001t0005g0254 a0001c0001t0005g0255 others(3): Show |
7 | HG01515.hp1 HG01517.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38-1253_-38-1250d others(6): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95585135 | ||||||
| chr6:95585135 | CAT | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-1251_-38-1250d others(4): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95585135 | ||||||
| chr6:95585248 | A | G | 5 | a0001c0001t0006g0025 a0001c0001t0006g0253 a0001c0001t0006g0262 others(2): Show |
7 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38-1154A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585248 | |||||||
| chr6:95585342 | C | T | 1 | a0001c0001t0003g0096 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-38-1060C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585342 | |||||||
| chr6:95585377 | A | G | 15 | a0001c0001t0005g0005 a0001c0001t0005g0024 a0001c0001t0005g0048 others(12): Show |
24 | HG00423.hp2 HG00558.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-38-1025A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585377 | |||||||
| chr6:95585379 | G | A | 1 | a0001c0001t0006g0253 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-38-1023G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585379 | |||||||
| chr6:95585414 | A | G | 1 | a0004c0004t0005g0234 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-38-988A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585414 | |||||||
| chr6:95585514 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-38-888G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585514 | |||||||
| chr6:95585557 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-845T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585557 | |||||||
| chr6:95585647 | T | TA | 3 | a0001c0001t0003g0059 a0001c0001t0004g0058 a0001c0001t0004g0060 |
3 | HG02015.hp1 HG02083.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.-38-754dupA | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95585647 | ||||||
| chr6:95585767 | A | T | 2 | a0001c0001t0005g0251 a0001c0001t0005g0252 |
2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38-635A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585767 | |||||||
| chr6:95585886 | T | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-516T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585886 | |||||||
| chr6:95585908 | A | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(56): Show |
98 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-38-494A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585908 | |||||||
| chr6:95585917 | A | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(56): Show |
98 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-38-485A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585917 | |||||||
| chr6:95586027 | G | T | 1 | a0001c0001t0004g0095 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-38-375G>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95586027 | |||||||
| chr6:95586103 | A | G | 1 | a0001c0001t0005g0201 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-38-299A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95586103 | |||||||
| chr6:95586103 | A | T | 1 | a0004c0005t0005g0237 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-38-299A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95586103 | |||||||
| chr6:95586104 | T | G | 1 | a0004c0005t0005g0237 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-38-298T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95586104 | |||||||
| chr6:95586174 | T | C | 22 | a0002c0002t0006g0023 a0002c0002t0006g0045 a0002c0002t0006g0046 others(19): Show |
25 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.-38-228T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95586174 | |||||||
| chr6:95586213 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-38-189C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95586213 | |||||||
| chr6:95586252 | G | A | 1 | a0001c0001t0002g0241 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-38-150G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95586252 | |||||||
| chr6:95586293 | TATTA | T | 27 | a0001c0001t0006g0025 a0001c0001t0006g0253 a0001c0001t0006g0262 others(24): Show |
32 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.-38-104_-38-101del others(4): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95586293 | ||||||
| chr6:95586336 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-38-66G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95586336 | |||||||
| chr6:95586993 | G | GTATA | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(55): Show |
97 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.544+20_544+23dupAT others(2): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 95586993 | ||||||
| chr6:95587005 | A | ATATATG | 22 | a0001c0001t0004g0020 a0001c0001t0004g0034 a0001c0001t0004g0114 others(19): Show |
28 | HG00099.hp2 HG00323.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.544+23_544+24insAT others(4): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 95587005 | ||||||
| chr6:95587005 | A | ATATATGT others(1): Show |
3 | a0002c0002t0006g0190 a0002c0002t0006g0191 a0002c0002t0006g0192 |
3 | HG00738.hp1 HG01261.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.544+23_544+24insAT others(6): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 95587005 | ||||||
| chr6:95587005 | A | ATATG | 109 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0010 others(106): Show |
146 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.544+23_544+24insAT others(2): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 95587005 | ||||||
| chr6:95587013 | T | G | 1 | a0009c0010t0004g0121 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.544+30T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95587013 | |||||||
| chr6:95587019 | C | G | 1 | a0009c0010t0004g0121 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.544+36C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95587019 | |||||||
| chr6:95587021 | G | C | 1 | a0009c0010t0004g0121 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.544+38G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95587021 | |||||||
| chr6:95587299 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(205): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.544+316T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95587299 | |||||||
| chr6:95587426 | G | A | 1 | a0001c0001t0018g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.544+443G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95587426 | |||||||
| chr6:95587442 | A | T | 1 | a0001c0001t0001g0166 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.544+459A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95587442 | |||||||
| chr6:95587451 | GGATCTGA others(9): Show |
G | 2 | a0001c0001t0004g0074 a0002c0002t0006g0176 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.544+485_544+500del others(16): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 95587451 | ||||||
| chr6:95587534 | A | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(56): Show |
98 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.544+551A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95587534 | |||||||
| chr6:95587722 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.544+739A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95587722 | |||||||
| chr6:95587851 | C | T | 2 | a0001c0001t0005g0251 a0001c0001t0005g0252 |
2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.544+868C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95587851 | |||||||
| chr6:95587979 | C | T | 1 | a0001c0001t0002g0050 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.544+996C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95587979 | |||||||
| chr6:95588040 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.544+1057C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95588040 | |||||||
| chr6:95588119 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.544+1136T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95588119 | |||||||
| chr6:95588347 | A | G | 1 | a0001c0001t0003g0093 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.544+1364A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95588347 | |||||||
| chr6:95588398 | T | G | 108 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0010 others(105): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.544+1415T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95588398 | |||||||
| chr6:95588619 | T | G | 1 | a0009c0010t0004g0121 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.544+1636T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95588619 | |||||||
| chr6:95588858 | T | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.544+1875T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95588858 | |||||||
| chr6:95588867 | A | G | 10 | a0001c0001t0003g0011 a0001c0001t0003g0069 a0001c0001t0003g0088 others(7): Show |
14 | HG00438.hp2 HG00558.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.544+1884A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95588867 | |||||||
| chr6:95588952 | A | T | 9 | a0003c0003t0007g0037 a0003c0003t0007g0128 a0003c0003t0007g0129 others(6): Show |
10 | HG01070.hp1 HG01099.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.544+1969A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95588952 | |||||||
| chr6:95589076 | C | A | 33 | a0001c0001t0005g0005 a0001c0001t0005g0024 a0001c0001t0005g0048 others(30): Show |
43 | HG00423.hp2 HG00558.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.544+2093C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95589076 | |||||||
| chr6:95589094 | A | T | 109 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0010 others(106): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.544+2111A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95589094 | |||||||
| chr6:95589133 | TAAAG | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.544+2154_544+2157d others(6): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 95589133 | ||||||
| chr6:95589242 | G | T | 5 | a0001c0001t0006g0025 a0001c0001t0006g0253 a0001c0001t0006g0262 others(2): Show |
7 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.544+2259G>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95589242 | |||||||
| chr6:95589423 | T | C | 1 | a0001c0001t0003g0011 | 5 | NA18964.hp1 NA18971.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.544+2440T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95589423 | |||||||
| chr6:95589525 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.544+2542A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95589525 | |||||||
| chr6:95589625 | T | C | 7 | a0001c0001t0001g0152 a0001c0001t0009g0133 a0001c0001t0009g0146 others(4): Show |
7 | NA18747.hp2 NA18947.hp1 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.544+2642T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95589625 | |||||||
| chr6:95589641 | G | A | 22 | a0002c0002t0006g0023 a0002c0002t0006g0045 a0002c0002t0006g0046 others(19): Show |
25 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.544+2658G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95589641 | |||||||
| chr6:95589701 | G | A | 13 | a0003c0003t0007g0037 a0003c0003t0007g0047 a0003c0003t0007g0128 others(10): Show |
15 | HG01070.hp1 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.544+2718G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95589701 | |||||||
| chr6:95589870 | G | C | 1 | a0001c0001t0003g0088 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.544+2887G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95589870 | |||||||
| chr6:95589966 | C | T | 109 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0010 others(106): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.544+2983C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95589966 | |||||||
| chr6:95590022 | C | T | 1 | a0009c0010t0004g0121 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.544+3039C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95590022 | |||||||
| chr6:95590023 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.544+3040A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95590023 | |||||||
| chr6:95590323 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.544+3340T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95590323 | |||||||
| chr6:95590629 | A | G | 1 | a0009c0010t0004g0121 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.544+3646A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95590629 | |||||||
| chr6:95590771 | T | C | 15 | a0001c0001t0005g0005 a0001c0001t0005g0024 a0001c0001t0005g0048 others(12): Show |
24 | HG00423.hp2 HG00558.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.544+3788T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95590771 | |||||||
| chr6:95590849 | G | A | 2 | a0001c0001t0012g0056 a0001c0001t0012g0258 |
3 | HG01884.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.544+3866G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95590849 | |||||||
| chr6:95591027 | T | C | 1 | a0001c0001t0004g0261 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.544+4044T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591027 | |||||||
| chr6:95591080 | T | A | 2 | a0001c0001t0012g0056 a0001c0001t0012g0258 |
3 | HG01884.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.544+4097T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591080 | |||||||
| chr6:95591088 | T | C | 109 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0010 others(106): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.544+4105T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591088 | |||||||
| chr6:95591125 | A | G | 22 | a0002c0002t0006g0023 a0002c0002t0006g0045 a0002c0002t0006g0046 others(19): Show |
25 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.544+4142A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591125 | |||||||
| chr6:95591390 | C | G | 1 | a0001c0001t0002g0239 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.544+4407C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591390 | |||||||
| chr6:95591488 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.544+4505A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591488 | |||||||
| chr6:95591675 | T | C | 1 | a0001c0001t0004g0122 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.544+4692T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591675 | |||||||
| chr6:95591690 | C | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.544+4707C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591690 | |||||||
| chr6:95591737 | G | A | 1 | a0001c0001t0002g0222 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.544+4754G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591737 | |||||||
| chr6:95591747 | G | T | 1 | a0001c0001t0004g0020 | 3 | HG02735.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.544+4764G>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591747 | |||||||
| chr6:95591779 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.544+4796C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591779 | |||||||
| chr6:95591862 | C | T | 2 | a0002c0002t0006g0185 a0002c0002t0006g0187 |
2 | NA18987.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.545-4875C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591862 | |||||||
| chr6:95591923 | C | T | 1 | a0001c0001t0005g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.545-4814C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591923 | |||||||
| chr6:95591982 | G | A | 1 | a0001c0001t0003g0075 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.545-4755G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591982 | |||||||
| chr6:95591999 | G | C | 1 | a0001c0001t0004g0095 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.545-4738G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591999 | |||||||
| chr6:95592092 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.545-4645A>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95592092 | |||||||
| chr6:95592367 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.545-4370T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95592367 | |||||||
| chr6:95592391 | G | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.545-4346G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95592391 | |||||||
| chr6:95592528 | C | T | 1 | a0001c0001t0009g0153 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.545-4209C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95592528 | |||||||
| chr6:95592611 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.545-4126T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95592611 | |||||||
| chr6:95592937 | A | G | 1 | a0001c0001t0005g0200 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.545-3800A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95592937 | |||||||
| chr6:95592948 | A | G | 1 | a0001c0001t0002g0228 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.545-3789A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95592948 | |||||||
| chr6:95593023 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.545-3714T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95593023 | |||||||
| chr6:95593209 | C | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.545-3528C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95593209 | |||||||
| chr6:95593210 | G | A | 33 | a0001c0001t0005g0005 a0001c0001t0005g0024 a0001c0001t0005g0048 others(30): Show |
43 | HG00423.hp2 HG00558.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.545-3527G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95593210 | |||||||
| chr6:95593239 | T | C | 3 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0238 |
3 | HG02293.hp1 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.545-3498T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95593239 | |||||||
| chr6:95593370 | T | G | 1 | a0001c0001t0001g0155 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.545-3367T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95593370 | |||||||
| chr6:95593601 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.545-3136C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95593601 | |||||||
| chr6:95593672 | T | C | 1 | a0001c0001t0003g0076 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.545-3065T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95593672 | |||||||
| chr6:95593986 | T | G | 1 | a0001c0001t0003g0077 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.545-2751T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95593986 | |||||||
| chr6:95594018 | T | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(239): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.545-2719T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95594018 | |||||||
| chr6:95594032 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.545-2705A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95594032 | |||||||
| chr6:95594060 | CA | C | 6 | a0001c0001t0006g0025 a0001c0001t0006g0253 a0001c0001t0006g0262 others(3): Show |
8 | HG00741.hp1 HG01517.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.545-2666delA | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 95594060 | ||||||
| chr6:95594181 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.545-2556A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95594181 | |||||||
| chr6:95594374 | A | G | 2 | a0001c0001t0016g0086 a0001c0001t0016g0087 |
2 | NA18960.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.545-2363A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95594374 | |||||||
| chr6:95594448 | T | C | 1 | a0001c0001t0004g0115 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.545-2289T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95594448 | |||||||
| chr6:95594462 | A | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(240): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.545-2275A>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95594462 | |||||||
| chr6:95594642 | G | C | 1 | a0001c0001t0001g0156 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.545-2095G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95594642 | |||||||
| chr6:95594804 | T | G | 12 | a0001c0001t0005g0208 a0001c0001t0005g0251 a0001c0001t0005g0252 others(9): Show |
12 | HG02602.hp2 HG02683.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.545-1933T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95594804 | |||||||
| chr6:95594817 | T | C | 2 | a0001c0001t0002g0216 a0001c0001t0002g0225 |
2 | HG01496.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.545-1920T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95594817 | |||||||
| chr6:95594958 | G | A | 1 | a0001c0001t0002g0215 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.545-1779G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95594958 | |||||||
| chr6:95595030 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.545-1707G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95595030 | |||||||
| chr6:95595191 | C | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.545-1546C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95595191 | |||||||
| chr6:95595213 | C | G | 1 | a0001c0001t0004g0122 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.545-1524C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95595213 | |||||||
| chr6:95595419 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.545-1318C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95595419 | |||||||
| chr6:95595598 | A | T | 1 | a0001c0001t0006g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.545-1139A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95595598 | |||||||
| chr6:95595659 | A | C | 1 | a0002c0002t0006g0184 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.545-1078A>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95595659 | |||||||
| chr6:95595797 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.545-940C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95595797 | |||||||
| chr6:95595948 | C | T | 5 | a0001c0001t0001g0038 a0001c0001t0001g0139 a0001c0001t0001g0142 others(2): Show |
5 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.545-789C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95595948 | |||||||
| chr6:95596063 | A | G | 1 | a0001c0001t0018g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.545-674A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95596063 | |||||||
| chr6:95596218 | G | C | 1 | a0001c0001t0001g0156 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.545-519G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95596218 | |||||||
| chr6:95596885 | CT | C | 2 | a0001c0001t0003g0011 a0001c0001t0008g0188 |
6 | NA18964.hp1 NA18971.hp2 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+43delT | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95596885 | ||||||
| chr6:95596895 | A | G | 1 | a0001c0001t0002g0232 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.654+49A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95596895 | |||||||
| chr6:95597236 | A | G | 4 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0238 others(1): Show |
4 | HG02293.hp1 HG03139.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.654+390A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95597236 | |||||||
| chr6:95597344 | A | C | 3 | a0004c0005t0005g0236 a0004c0005t0005g0237 a0004c0007t0005g0235 |
3 | HG02602.hp2 HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.654+498A>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95597344 | |||||||
| chr6:95597487 | C | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0057 a0001c0001t0001g0157 |
4 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(1): Show |
intron_variant | MODIFIER | c.654+641C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95597487 | |||||||
| chr6:95597853 | C | T | 1 | a0001c0001t0002g0050 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.654+1007C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95597853 | |||||||
| chr6:95598046 | A | AT | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(165): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.654+1208dupT | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95598046 | ||||||
| chr6:95598218 | T | C | 1 | a0001c0001t0004g0095 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.654+1372T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95598218 | |||||||
| chr6:95598324 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.654+1478T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95598324 | |||||||
| chr6:95598427 | G | A | 1 | a0002c0002t0006g0177 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.654+1581G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95598427 | |||||||
| chr6:95598487 | A | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | NA19007.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.654+1641A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95598487 | |||||||
| chr6:95598998 | A | G | 5 | a0003c0003t0007g0243 a0003c0003t0007g0244 a0003c0003t0007g0245 others(2): Show |
5 | HG01070.hp1 HG01099.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.654+2152A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95598998 | |||||||
| chr6:95599093 | A | G | 1 | a0001c0001t0014g0227 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.654+2247A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95599093 | |||||||
| chr6:95599137 | G | T | 5 | a0003c0003t0007g0243 a0003c0003t0007g0244 a0003c0003t0007g0245 others(2): Show |
5 | HG01070.hp1 HG01099.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.654+2291G>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95599137 | |||||||
| chr6:95599157 | G | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.654+2311G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95599157 | |||||||
| chr6:95599288 | C | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.654+2442C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95599288 | |||||||
| chr6:95599330 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.654+2484T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95599330 | |||||||
| chr6:95599408 | G | A | 21 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0026 others(18): Show |
30 | HG00408.hp2 HG00438.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.654+2562G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95599408 | |||||||
| chr6:95599412 | A | G | 1 | a0001c0001t0002g0231 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.654+2566A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95599412 | |||||||
| chr6:95599416 | CA | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(189): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.654+2586delA | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95599416 | ||||||
| chr6:95599435 | G | A | 1 | a0004c0004t0005g0233 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.654+2589G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95599435 | |||||||
| chr6:95599436 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.654+2590A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95599436 | |||||||
| chr6:95599660 | T | C | 108 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0010 others(105): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.654+2814T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95599660 | |||||||
| chr6:95600085 | T | C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0167 |
2 | HG00673.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.654+3239T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95600085 | |||||||
| chr6:95600411 | T | A | 1 | a0001c0001t0003g0189 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.654+3565T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95600411 | |||||||
| chr6:95600507 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.654+3661C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95600507 | |||||||
| chr6:95600593 | A | ATGAATAT others(7): Show |
1 | a0001c0001t0002g0250 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.654+3747_654+3748i others(16): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95600593 | |||||||
| chr6:95600835 | T | C | 1 | a0001c0001t0012g0258 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.654+3989T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95600835 | |||||||
| chr6:95600859 | A | C | 27 | a0001c0001t0006g0025 a0001c0001t0006g0253 a0001c0001t0006g0262 others(24): Show |
32 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.655-3968A>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95600859 | |||||||
| chr6:95601175 | T | G | 5 | a0001c0001t0006g0025 a0001c0001t0006g0253 a0001c0001t0006g0262 others(2): Show |
7 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.655-3652T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95601175 | |||||||
| chr6:95601263 | C | T | 1 | a0001c0001t0005g0256 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.655-3564C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95601263 | |||||||
| chr6:95601334 | G | T | 1 | a0001c0001t0001g0152 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.655-3493G>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95601334 | |||||||
| chr6:95601380 | T | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.655-3447T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95601380 | |||||||
| chr6:95601433 | G | C | 4 | a0001c0001t0004g0020 a0001c0001t0004g0034 a0001c0001t0004g0114 others(1): Show |
7 | HG00099.hp2 HG00735.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.655-3394G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95601433 | |||||||
| chr6:95601556 | A | G | 10 | a0004c0004t0005g0051 a0004c0004t0005g0219 a0004c0004t0005g0233 others(7): Show |
10 | HG02602.hp2 HG02683.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.655-3271A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95601556 | |||||||
| chr6:95601652 | C | T | 1 | a0001c0001t0005g0259 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.655-3175C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95601652 | |||||||
| chr6:95601689 | G | A | 2 | a0001c0001t0004g0115 a0001c0001t0004g0116 |
2 | HG01069.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.655-3138G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95601689 | |||||||
| chr6:95601716 | A | ATTT | 5 | a0001c0001t0005g0252 a0003c0003t0007g0037 a0003c0003t0007g0128 others(2): Show |
6 | HG02055.hp2 HG02615.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-3085_655-3083d others(5): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | ||||||
| chr6:95601716 | A | ATTTTTTT others(4): Show |
5 | a0003c0003t0007g0243 a0003c0003t0007g0244 a0003c0003t0007g0245 others(2): Show |
5 | HG01070.hp1 HG01099.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.655-3093_655-3083d others(13): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | ||||||
| chr6:95601716 | A | ATTTTTTT others(5): Show |
4 | a0003c0003t0007g0047 a0003c0003t0007g0195 a0003c0003t0007g0246 others(1): Show |
5 | HG01175.hp2 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.655-3094_655-3083d others(14): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | ||||||
| chr6:95601716 | A | ATTTTTTT others(6): Show |
1 | a0003c0003t0007g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.655-3095_655-3083d others(15): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | ||||||
| chr6:95601716 | A | ATTTTTTT others(14): Show |
2 | a0004c0005t0005g0236 a0004c0005t0005g0237 |
2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.655-3103_655-3083d others(23): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | ||||||
| chr6:95601716 | A | ATTTTTTT others(15): Show |
1 | a0004c0004t0005g0233 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.655-3104_655-3083d others(24): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | ||||||
| chr6:95601716 | A | ATTTTTTT others(17): Show |
1 | a0001c0001t0018g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.655-3106_655-3083d others(26): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | ||||||
| chr6:95601716 | A | ATTTTTTT others(20): Show |
1 | a0004c0007t0005g0235 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.655-3087_655-3086i others(29): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | ||||||
| chr6:95601716 | AT | A | 5 | a0001c0001t0001g0163 a0001c0001t0003g0067 a0001c0001t0003g0109 others(2): Show |
6 | HG00735.hp1 HG02818.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.655-3083delT | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | ||||||
| chr6:95601716 | ATT | A | 52 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(49): Show |
64 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.655-3084_655-3083d others(4): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | ||||||
| chr6:95601716 | ATTT | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(165): Show |
272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.655-3085_655-3083d others(5): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | ||||||
| chr6:95601716 | ATTTT | A | 18 | a0001c0001t0002g0232 a0001c0001t0004g0117 a0001c0001t0009g0158 others(15): Show |
20 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.655-3086_655-3083d others(6): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | ||||||
| chr6:95601716 | ATTTTT | A | 5 | a0001c0001t0006g0025 a0001c0001t0006g0253 a0001c0001t0006g0262 others(2): Show |
7 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.655-3087_655-3083d others(7): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | ||||||
| chr6:95601716 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0165 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.655-3092_655-3083d others(12): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | ||||||
| chr6:95601716 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0004g0261 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.655-3094_655-3083d others(14): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | ||||||
| chr6:95601816 | T | G | 1 | a0002c0002t0006g0190 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.655-3011T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95601816 | |||||||
| chr6:95601946 | A | G | 1 | a0001c0001t0002g0222 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.655-2881A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95601946 | |||||||
| chr6:95602218 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0038 others(36): Show |
69 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.655-2609G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95602218 | |||||||
| chr6:95602298 | C | A | 1 | a0001c0001t0004g0113 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.655-2529C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95602298 | |||||||
| chr6:95602525 | G | A | 2 | a0001c0001t0012g0056 a0001c0001t0012g0258 |
3 | HG01884.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.655-2302G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95602525 | |||||||
| chr6:95602585 | T | G | 1 | a0001c0001t0018g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.655-2242T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95602585 | |||||||
| chr6:95602674 | A | G | 2 | a0001c0001t0004g0115 a0001c0001t0004g0116 |
2 | HG01069.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.655-2153A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95602674 | |||||||
| chr6:95602743 | G | A | 1 | a0001c0001t0019g0135 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.655-2084G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95602743 | |||||||
| chr6:95602877 | G | A | 1 | a0001c0001t0005g0201 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.655-1950G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95602877 | |||||||
| chr6:95602933 | T | A | 1 | a0001c0001t0003g0027 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.655-1894T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95602933 | |||||||
| chr6:95602962 | G | A | 1 | a0001c0001t0003g0078 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.655-1865G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95602962 | |||||||
| chr6:95603026 | C | CA | 22 | a0001c0001t0002g0052 a0001c0001t0002g0054 a0001c0001t0002g0207 others(19): Show |
25 | HG00741.hp1 HG01109.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.655-1775dupA | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95603026 | ||||||
| chr6:95603026 | CA | C | 106 | a0001c0001t0002g0215 a0001c0001t0002g0226 a0001c0001t0002g0230 others(103): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.655-1775delA | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95603026 | ||||||
| chr6:95603052 | A | AAAAAAC | 7 | a0001c0001t0001g0152 a0001c0001t0009g0133 a0001c0001t0009g0146 others(4): Show |
7 | HG02132.hp1 NA18747.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.655-1775_655-1774i others(8): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603052 | |||||||
| chr6:95603052 | A | AC | 14 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0040 others(11): Show |
24 | HG00438.hp1 HG00597.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.655-1775_655-1774i others(3): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603052 | |||||||
| chr6:95603052 | A | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0038 others(30): Show |
61 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.655-1775A>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603052 | |||||||
| chr6:95603102 | A | C | 1 | a0001c0001t0002g0250 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655-1725A>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603102 | |||||||
| chr6:95603182 | T | C | 1 | a0009c0010t0004g0121 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.655-1645T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603182 | |||||||
| chr6:95603300 | A | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.655-1527A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603300 | |||||||
| chr6:95603388 | A | C | 27 | a0001c0001t0006g0025 a0001c0001t0006g0253 a0001c0001t0006g0262 others(24): Show |
32 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.655-1439A>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603388 | |||||||
| chr6:95603397 | C | T | 1 | a0001c0001t0001g0039 | 2 | HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.655-1430C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603397 | |||||||
| chr6:95603507 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.655-1320A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603507 | |||||||
| chr6:95603545 | A | AT | 4 | a0001c0001t0005g0055 a0001c0001t0005g0254 a0001c0001t0005g0255 others(1): Show |
5 | HG02257.hp2 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.655-1274dupT | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95603545 | ||||||
| chr6:95603553 | T | A | 109 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0010 others(106): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.655-1274T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603553 | |||||||
| chr6:95603636 | A | G | 1 | a0001c0001t0004g0100 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.655-1191A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603636 | |||||||
| chr6:95603769 | G | C | 1 | a0001c0001t0017g0029 | 2 | NA18955.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.655-1058G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603769 | |||||||
| chr6:95603945 | C | A | 3 | a0001c0001t0003g0079 a0001c0001t0003g0082 a0001c0001t0025g0081 |
3 | HG01243.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.655-882C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603945 | |||||||
| chr6:95603992 | T | A | 2 | a0001c0001t0012g0056 a0001c0001t0012g0258 |
3 | HG01884.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.655-835T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603992 | |||||||
| chr6:95604016 | C | CAT | 5 | a0001c0001t0004g0122 a0003c0003t0007g0037 a0003c0003t0007g0128 others(2): Show |
6 | HG01346.hp2 HG02055.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-799_655-798dup others(2): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604016 | ||||||
| chr6:95604042 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.655-785G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95604042 | |||||||
| chr6:95604045 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.655-782C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95604045 | |||||||
| chr6:95604056 | A | AGGTGTGT others(5): Show |
4 | a0001c0001t0004g0072 a0001c0001t0004g0100 a0001c0001t0004g0101 others(1): Show |
4 | HG02258.hp2 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.655-771_655-770ins others(12): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95604056 | |||||||
| chr6:95604060 | A | G | 5 | a0001c0001t0004g0072 a0001c0001t0004g0100 a0001c0001t0004g0101 others(2): Show |
5 | HG01433.hp2 HG02258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.655-767A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95604060 | |||||||
| chr6:95604061 | G | GGGGTGT | 4 | a0003c0003t0007g0047 a0003c0003t0007g0194 a0003c0003t0007g0195 others(1): Show |
5 | HG01109.hp2 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.655-765_655-764ins others(6): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | ||||||
| chr6:95604061 | G | GGGGTGTG others(5): Show |
2 | a0003c0003t0007g0128 a0003c0003t0007g0243 |
2 | NA19043.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.655-765_655-764ins others(12): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | ||||||
| chr6:95604061 | G | GGGGTGTG others(7): Show |
4 | a0003c0003t0007g0244 a0003c0003t0007g0245 a0003c0003t0007g0246 others(1): Show |
4 | HG01070.hp1 HG01099.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.655-765_655-764ins others(14): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | ||||||
| chr6:95604061 | G | GGGGTGTG others(9): Show |
1 | a0003c0003t0007g0129 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.655-765_655-764ins others(16): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | ||||||
| chr6:95604061 | G | GGGGTGTG others(11): Show |
2 | a0003c0003t0007g0037 a0003c0003t0007g0130 |
3 | HG02055.hp2 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.655-765_655-764ins others(18): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | ||||||
| chr6:95604061 | G | GGT | 33 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0160 others(30): Show |
40 | HG00558.hp1 HG00673.hp1 HG01123.hp1 others(37): Show |
intron_variant | MODIFIER | c.655-733_655-732dup others(2): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | ||||||
| chr6:95604061 | G | GGTGT | 37 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0038 others(34): Show |
69 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.655-735_655-732dup others(4): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | ||||||
| chr6:95604061 | G | GGTGTGT | 6 | a0001c0001t0001g0041 a0001c0001t0001g0147 a0001c0001t0001g0156 others(3): Show |
8 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.655-737_655-732dup others(6): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | ||||||
| chr6:95604061 | G | GGTGTGTG others(1): Show |
27 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0026 others(24): Show |
38 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.655-739_655-732dup others(8): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | ||||||
| chr6:95604061 | G | GGTGTGTG others(3): Show |
18 | a0001c0001t0001g0057 a0001c0001t0001g0159 a0001c0001t0003g0012 others(15): Show |
23 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-741_655-732dup others(10): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | ||||||
| chr6:95604061 | G | GGTGTGTG others(5): Show |
25 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0033 others(22): Show |
36 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.655-743_655-732dup others(12): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | ||||||
| chr6:95604061 | G | GGTGTGTG others(7): Show |
25 | a0001c0001t0003g0009 a0001c0001t0003g0011 a0001c0001t0003g0062 others(22): Show |
33 | HG00099.hp2 HG01243.hp1 HG01358.hp2 others(30): Show |
intron_variant | MODIFIER | c.655-745_655-732dup others(14): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | ||||||
| chr6:95604061 | G | GGTGTGTG others(9): Show |
29 | a0001c0001t0003g0019 a0001c0001t0003g0027 a0001c0001t0003g0028 others(26): Show |
34 | HG00438.hp2 HG00642.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.655-747_655-732dup others(16): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | ||||||
| chr6:95604061 | G | GGTGTGTG others(11): Show |
8 | a0001c0001t0003g0065 a0001c0001t0004g0013 a0001c0001t0004g0017 others(5): Show |
14 | HG00621.hp2 HG01346.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.655-749_655-732dup others(18): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | ||||||
| chr6:95604061 | G | GGTGTGTG others(13): Show |
13 | a0001c0001t0003g0059 a0001c0001t0003g0066 a0001c0001t0004g0006 others(10): Show |
19 | HG00597.hp2 HG01069.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.655-751_655-732dup others(20): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | ||||||
| chr6:95604061 | G | GGTGTGTG others(15): Show |
2 | a0001c0001t0003g0083 a0001c0001t0004g0117 |
2 | HG01257.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.655-753_655-732dup others(22): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | ||||||
| chr6:95604061 | G | GGTGTGTG others(17): Show |
1 | a0001c0001t0004g0124 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.655-755_655-732dup others(24): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | ||||||
| chr6:95604061 | G | GGTGTGTG others(19): Show |
2 | a0001c0001t0003g0084 a0001c0001t0004g0060 |
2 | HG01175.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.655-757_655-732dup others(26): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | ||||||
| chr6:95604061 | G | T | 5 | a0001c0001t0004g0072 a0001c0001t0004g0100 a0001c0001t0004g0101 others(2): Show |
5 | HG01433.hp2 HG02258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.655-766G>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95604061 | |||||||
| chr6:95604273 | G | C | 4 | a0003c0003t0007g0047 a0003c0003t0007g0194 a0003c0003t0007g0195 others(1): Show |
5 | HG01109.hp2 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.655-554G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95604273 | |||||||
| chr6:95604466 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.655-361C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95604466 | |||||||
| chr6:95604611 | T | C | 1 | a0001c0001t0023g0126 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.655-216T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95604611 | |||||||
| chr6:95604718 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.655-109T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95604718 | |||||||
| chr6:95604937 | A | G | 5 | a0001c0001t0004g0072 a0001c0001t0004g0100 a0001c0001t0004g0101 others(2): Show |
5 | HG01433.hp2 HG02258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.731+34A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 4/4 | chr6 | 95604937 | |||||||
| chr6:95605111 | T | C | 3 | a0002c0002t0006g0176 a0002c0002t0006g0178 a0002c0002t0006g0181 |
3 | HG01106.hp1 HG01109.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.731+208T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 4/4 | chr6 | 95605111 | |||||||
| chr6:95605193 | A | T | 2 | a0005c0006t0005g0198 a0005c0006t0005g0202 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.731+290A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 4/4 | chr6 | 95605193 | |||||||
| chr6:95605303 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.731+400C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 4/4 | chr6 | 95605303 | |||||||
| chr6:95605454 | T | C | 118 | a0001c0001t0001g0152 a0001c0001t0003g0003 a0001c0001t0003g0009 others(115): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.732-294T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 4/4 | chr6 | 95605454 | |||||||
| chr6:95605474 | G | A | 12 | a0001c0001t0001g0038 a0001c0001t0001g0134 a0001c0001t0001g0138 others(9): Show |
12 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.732-274G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 4/4 | chr6 | 95605474 | |||||||
| chr6:95605565 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.732-183C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 4/4 | chr6 | 95605565 | |||||||
| chr6:95605602 | T | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(192): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.732-146T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 4/4 | chr6 | 95605602 |