Variant report

Variant	rs7977465
Chromosome Location	chr12:8634994-8634995
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10734713	0.90[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs10770775	0.85[EUR][1000 genomes]
rs10770776	0.85[EUR][1000 genomes]
rs11045643	0.85[EUR][1000 genomes]
rs11045652	0.86[EUR][1000 genomes]
rs11045708	0.85[EUR][1000 genomes]
rs11045757	0.84[EUR][1000 genomes]
rs12302854	0.85[EUR][1000 genomes]
rs12304190	0.85[EUR][1000 genomes]
rs12308954	0.85[EUR][1000 genomes]
rs12322968	0.84[EUR][1000 genomes]
rs12423976	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4242889	0.84[EUR][1000 genomes]
rs4242891	0.84[EUR][1000 genomes]
rs4242892	0.84[EUR][1000 genomes]
rs4242893	0.91[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs4242895	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4258429	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4301856	0.82[EUR][1000 genomes]
rs4303299	0.83[EUR][1000 genomes]
rs4334073	0.85[EUR][1000 genomes]
rs4427631	0.85[EUR][1000 genomes]
rs4445713	0.82[EUR][1000 genomes]
rs4447245	0.85[EUR][1000 genomes]
rs4457803	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4460883	0.85[EUR][1000 genomes]
rs4882949	0.91[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs4883154	0.84[EUR][1000 genomes]
rs4883164	0.85[EUR][1000 genomes]
rs7134303	0.85[EUR][1000 genomes]
rs7302011	0.85[EUR][1000 genomes]
rs7309596	0.85[EUR][1000 genomes]
rs7312686	0.85[EUR][1000 genomes]
rs7312713	0.84[EUR][1000 genomes]
rs7312975	0.82[EUR][1000 genomes]
rs7315590	0.85[EUR][1000 genomes]
rs7315873	0.85[EUR][1000 genomes]
rs7962791	0.85[EUR][1000 genomes]
rs7963053	0.83[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs7964875	0.85[EUR][1000 genomes]
rs7976692	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7976958	0.85[EUR][1000 genomes]
rs7978179	0.85[EUR][1000 genomes]
rs7978218	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040302	chr12:8245364-8695612	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv541397	chr12:8245364-8695612	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv1044543	chr12:8449100-8792569	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv1039504	chr12:8494944-8780137	Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv557342	chr12:8599397-8774527	Enhancers Flanking Active TSS Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv933050	chr12:8602789-8775989	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
7	nsv518772	chr12:8615809-8667579	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv518125	chr12:8615809-8671274	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv1035270	chr12:8619562-8674062	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv933555	chr12:8627165-8775989	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
11	nsv933639	chr12:8627243-8775989	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
12	nsv600	chr12:8631646-8645560	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:8628000-8638200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr12:8628400-8637400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr12:8634400-8636200	Enhancers	Fetal Thymus	thymus
4	chr12:8634400-8636600	Enhancers	Primary T cells from cord blood	blood

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