Variant report
Variant | rs17100100 |
---|---|
Chromosome Location | chr1:77731277-77731278 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr1:77725962..77727892-chr1:77729929..77731695,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1010061 | 1.00[ASN][1000 genomes] |
rs10443176 | 1.00[ASN][1000 genomes] |
rs10518445 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11162275 | 1.00[ASN][1000 genomes] |
rs11162284 | 1.00[ASN][1000 genomes] |
rs11162287 | 1.00[ASN][1000 genomes] |
rs11576574 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12077763 | 1.00[ASN][1000 genomes] |
rs12090495 | 1.00[ASN][1000 genomes] |
rs12119019 | 1.00[ASN][1000 genomes] |
rs12120921 | 1.00[ASN][1000 genomes] |
rs12123535 | 1.00[ASN][1000 genomes] |
rs12126662 | 1.00[ASN][1000 genomes] |
rs12143529 | 1.00[ASN][1000 genomes] |
rs1305486 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1502525 | 1.00[ASN][1000 genomes] |
rs17100141 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17100143 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17100304 | 1.00[ASN][1000 genomes] |
rs17368950 | 1.00[ASN][1000 genomes] |
rs1827448 | 1.00[ASN][1000 genomes] |
rs1993266 | 1.00[ASN][1000 genomes] |
rs2004962 | 0.93[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs41292260 | 1.00[ASN][1000 genomes] |
rs41292264 | 1.00[ASN][1000 genomes] |
rs4949772 | 1.00[ASN][1000 genomes] |
rs4949773 | 1.00[ASN][1000 genomes] |
rs4949778 | 1.00[ASN][1000 genomes] |
rs56666939 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs57267651 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs57389685 | 1.00[ASN][1000 genomes] |
rs60792794 | 1.00[ASN][1000 genomes] |
rs61782906 | 1.00[ASN][1000 genomes] |
rs6603937 | 1.00[ASN][1000 genomes] |
rs6696605 | 1.00[ASN][1000 genomes] |
rs72683932 | 1.00[ASN][1000 genomes] |
rs72944757 | 1.00[ASN][1000 genomes] |
rs73002568 | 1.00[ASN][1000 genomes] |
rs73004429 | 1.00[ASN][1000 genomes] |
rs73004430 | 1.00[ASN][1000 genomes] |
rs73004434 | 1.00[ASN][1000 genomes] |
rs7519485 | 1.00[ASN][1000 genomes] |
rs7544099 | 1.00[ASN][1000 genomes] |
rs7550325 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv432398 | chr1:77707391-77740836 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
2 | nsv1005183 | chr1:77728990-77949309 | Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
3 | nsv535010 | chr1:77728990-77949309 | Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
4 | nsv932557 | chr1:77730247-77958687 | Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:77730600-77731400 | Bivalent Enhancer | iPS-15b Cell Line | embryonic stem cell |
2 | chr1:77730800-77731400 | Bivalent Enhancer | H1 Cell Line | embryonic stem cell |
3 | chr1:77730800-77731400 | Enhancers | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
4 | chr1:77730800-77731400 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |
5 | chr1:77730800-77731400 | Bivalent Enhancer | ES-UCSF4 Cell Line | embryonic stem cell |