Variant report
Variant | rs1102568 |
---|---|
Chromosome Location | chr6:27176374-27176375 |
allele | A/C |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000265565 | Chromatin interaction |
ENSG00000184825 | Chromatin interaction |
ENSG00000197903 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10484392 | 1.00[AMR][1000 genomes] |
rs10484394 | 1.00[AMR][1000 genomes] |
rs1102566 | 1.00[AMR][1000 genomes] |
rs11753245 | 1.00[AMR][1000 genomes] |
rs11753248 | 1.00[ASN][1000 genomes] |
rs11753378 | 1.00[AMR][1000 genomes] |
rs11753483 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs11753580 | 1.00[AMR][1000 genomes] |
rs11755519 | 1.00[AMR][1000 genomes] |
rs11755651 | 1.00[AMR][1000 genomes] |
rs11755813 | 1.00[AMR][1000 genomes] |
rs11756304 | 1.00[AMR][1000 genomes] |
rs11757216 | 1.00[ASN][1000 genomes] |
rs11757963 | 1.00[AMR][1000 genomes] |
rs11759167 | 1.00[AMR][1000 genomes] |
rs11759771 | 1.00[AMR][1000 genomes] |
rs11965377 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs11965529 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11966985 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs11967073 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs11969536 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs11970261 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs16894241 | 1.00[AMR][1000 genomes] |
rs16894520 | 1.00[AMR][1000 genomes] |
rs16895602 | 1.00[AMR][1000 genomes] |
rs16897417 | 1.00[AMR][1000 genomes] |
rs2021277 | 0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2021278 | 1.00[AMR][1000 genomes] |
rs2022271 | 1.00[AMR][1000 genomes] |
rs2092113 | 1.00[AMR][1000 genomes] |
rs2893912 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs34979454 | 1.00[ASN][1000 genomes] |
rs3800316 | 1.00[CHB][hapmap] |
rs55656206 | 1.00[AMR][1000 genomes] |
rs55867104 | 1.00[AMR][1000 genomes] |
rs55925824 | 1.00[AMR][1000 genomes] |
rs56141916 | 1.00[AMR][1000 genomes] |
rs56156722 | 1.00[AMR][1000 genomes] |
rs57603020 | 1.00[AMR][1000 genomes] |
rs58130043 | 1.00[AMR][1000 genomes] |
rs58265076 | 1.00[AMR][1000 genomes] |
rs58900251 | 1.00[AMR][1000 genomes] |
rs58977511 | 1.00[AMR][1000 genomes] |
rs59757260 | 1.00[AMR][1000 genomes] |
rs60259667 | 1.00[AMR][1000 genomes] |
rs61185098 | 1.00[AMR][1000 genomes] |
rs61392315 | 1.00[AMR][1000 genomes] |
rs73737997 | 1.00[AMR][1000 genomes] |
rs73737999 | 1.00[AMR][1000 genomes] |
rs73738226 | 1.00[AMR][1000 genomes] |
rs73738236 | 1.00[AMR][1000 genomes] |
rs73738237 | 1.00[AMR][1000 genomes] |
rs73738707 | 1.00[AMR][1000 genomes] |
rs73738713 | 1.00[AMR][1000 genomes] |
rs73738717 | 1.00[AMR][1000 genomes] |
rs73738718 | 1.00[AMR][1000 genomes] |
rs73738731 | 1.00[AMR][1000 genomes] |
rs73738732 | 1.00[AMR][1000 genomes] |
rs73738733 | 1.00[AMR][1000 genomes] |
rs73738734 | 1.00[AMR][1000 genomes] |
rs73738738 | 1.00[AMR][1000 genomes] |
rs73738739 | 1.00[AMR][1000 genomes] |
rs73738741 | 1.00[AMR][1000 genomes] |
rs73738749 | 1.00[AMR][1000 genomes] |
rs73738797 | 1.00[ASN][1000 genomes] |
rs73739510 | 1.00[AMR][1000 genomes] |
rs73739515 | 1.00[AMR][1000 genomes] |
rs73739517 | 1.00[AMR][1000 genomes] |
rs73739519 | 1.00[AMR][1000 genomes] |
rs73739521 | 1.00[AMR][1000 genomes] |
rs73739522 | 1.00[AMR][1000 genomes] |
rs73739531 | 1.00[AMR][1000 genomes] |
rs73739534 | 1.00[AMR][1000 genomes] |
rs73739545 | 1.00[AMR][1000 genomes] |
rs73739557 | 1.00[AMR][1000 genomes] |
rs73739578 | 1.00[AMR][1000 genomes] |
rs73739581 | 1.00[AMR][1000 genomes] |
rs73739582 | 1.00[AMR][1000 genomes] |
rs73739586 | 1.00[AMR][1000 genomes] |
rs73739587 | 1.00[AMR][1000 genomes] |
rs73739589 | 1.00[AMR][1000 genomes] |
rs73739591 | 1.00[AMR][1000 genomes] |
rs73739594 | 1.00[AMR][1000 genomes] |
rs73739595 | 1.00[AMR][1000 genomes] |
rs73739598 | 1.00[AMR][1000 genomes] |
rs73739600 | 1.00[AMR][1000 genomes] |
rs73740278 | 1.00[AMR][1000 genomes] |
rs73740404 | 1.00[AMR][1000 genomes] |
rs73740405 | 1.00[AMR][1000 genomes] |
rs73740406 | 1.00[AMR][1000 genomes] |
rs73740408 | 1.00[ASN][1000 genomes] |
rs73740409 | 1.00[AMR][1000 genomes] |
rs73740414 | 1.00[AMR][1000 genomes] |
rs73740432 | 1.00[AMR][1000 genomes] |
rs7449898 | 1.00[AMR][1000 genomes] |
rs7755679 | 1.00[AMR][1000 genomes] |
rs7759741 | 1.00[CHB][hapmap] |
rs858966 | 1.00[AMR][1000 genomes] |
rs858971 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
rs858978 | 0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs858979 | 0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs858983 | 1.00[CEU][hapmap];1.00[EUR][1000 genomes] |
rs9366681 | 1.00[AMR][1000 genomes] |
rs9467990 | 1.00[CEU][hapmap] |
rs996246 | 1.00[AMR][1000 genomes] |
rs9969094 | 1.00[CEU][hapmap];1.00[CHB][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv948921 | chr6:26556890-27443957 | Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 472 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:27174000-27179600 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
2 | chr6:27174400-27179000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
3 | chr6:27174400-27181400 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
4 | chr6:27174800-27177000 | Weak transcription | K562 | blood |
5 | chr6:27175000-27177000 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |
6 | chr6:27175800-27176400 | Enhancers | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
7 | chr6:27176000-27176600 | Enhancers | H9 Cell Line | embryonic stem cell |
8 | chr6:27176200-27176400 | Flanking Bivalent TSS/Enh | ES-I3 Cell Line | embryonic stem cell |
9 | chr6:27176200-27177000 | Active TSS | iPS-15b Cell Line | embryonic stem cell |
10 | chr6:27176200-27177200 | Active TSS | ES-WA7 Cell Line | embryonic stem cell |
11 | chr6:27176200-27177200 | Active TSS | H1 Cell Line | embryonic stem cell |
12 | chr6:27176200-27177200 | Active TSS | HUES6 Cell Line | embryonic stem cell |