Variant report

Variant	rs17802011
Chromosome Location	chr8:104361854-104361855
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:104357721..104360271-chr8:104361773..104363841,2	MCF-7	breast:
2	chr8:104361257..104363033-chr8:104364036..104366163,2	MCF-7	breast:
3	chr8:104361320..104364178-chr8:104414745..104417725,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000164933	Chromatin interaction

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs12156164	1.00[AFR][1000 genomes]
rs12680121	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs1389689	1.00[AFR][1000 genomes]
rs1494279	1.00[AFR][1000 genomes]
rs1608184	1.00[AFR][1000 genomes]
rs1610204	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs16870276	1.00[AFR][1000 genomes]
rs16870349	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17207827	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17228576	1.00[CEU][hapmap]
rs17801975	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17802089	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.80[AMR][1000 genomes]
rs17803441	1.00[GIH][hapmap]
rs2687347	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2687355	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2687356	0.83[AMR][1000 genomes]
rs2687367	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2917546	1.00[CEU][hapmap]
rs2917547	1.00[CEU][hapmap]
rs2917548	1.00[CEU][hapmap];1.00[CHD][hapmap]
rs2934725	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3098226	1.00[CEU][hapmap]
rs3134257	1.00[CEU][hapmap]
rs3134260	1.00[CEU][hapmap]
rs3134269	1.00[CEU][hapmap]
rs62525463	1.00[AFR][1000 genomes]
rs62525466	1.00[AFR][1000 genomes]
rs62525469	1.00[AFR][1000 genomes]
rs62525470	1.00[AFR][1000 genomes]
rs62527608	1.00[AFR][1000 genomes]
rs62527612	1.00[AFR][1000 genomes]
rs62527613	1.00[AFR][1000 genomes]
rs62528473	1.00[AFR][1000 genomes]
rs62528474	1.00[AFR][1000 genomes]
rs62528478	1.00[AFR][1000 genomes]
rs6468868	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.92[TSI][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7005750	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs703808	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs703809	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7815503	1.00[AFR][1000 genomes]
rs827525	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs827527	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs827529	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs827531	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs827532	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs827542	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs827543	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs827544	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs827545	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs827548	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs827549	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs827551	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs827553	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs827589	1.00[CEU][hapmap];1.00[GIH][hapmap];0.94[AMR][1000 genomes]
rs827591	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs827594	0.88[AMR][1000 genomes]
rs827600	0.88[AMR][1000 genomes]
rs860410	0.87[EUR][1000 genomes]
rs861169	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429931	chr8:104097396-104878014	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
2	esv1848810	chr8:104128496-104369288	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
3	esv1844303	chr8:104128696-104369090	Genic enhancers Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
4	nsv1023181	chr8:104298542-104366365	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv1020476	chr8:104312212-104924482	Genic enhancers Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
6	nsv539704	chr8:104312212-104924482	Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
7	nsv1016395	chr8:104327541-104473005	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
8	nsv1023048	chr8:104355188-104872701	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
9	nsv539705	chr8:104355188-104872701	ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
10	nsv1021345	chr8:104361854-104879684	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104355000-104363200	Enhancers	NHLF	lung
2	chr8:104355600-104362000	Enhancers	Osteobl	bone
3	chr8:104355600-104362600	Enhancers	NHDF-Ad	bronchial
4	chr8:104355800-104363800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr8:104357800-104383400	Weak transcription	Aorta	Aorta
6	chr8:104359000-104363800	Enhancers	Fetal Heart	heart
7	chr8:104359200-104362800	Enhancers	Fetal Stomach	stomach
8	chr8:104359600-104362000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr8:104359800-104362000	Enhancers	HUVEC	blood vessel
10	chr8:104360200-104365800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr8:104360400-104364200	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr8:104360800-104363600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr8:104361000-104362000	Enhancers	Thymus	Thymus
14	chr8:104361000-104362000	Flanking Active TSS	HSMM	muscle
15	chr8:104361000-104363000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr8:104361000-104363000	Enhancers	Fetal Thymus	thymus
17	chr8:104361000-104363600	Enhancers	Placenta Amnion	Placenta Amnion
18	chr8:104361200-104362000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr8:104361200-104362000	Enhancers	Pancreas	Pancrea
20	chr8:104361200-104362200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr8:104361200-104363200	Enhancers	Placenta	Placenta
22	chr8:104361200-104364000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr8:104361400-104362600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr8:104361400-104363000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr8:104361400-104363800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr8:104361400-104365400	Weak transcription	Dnd41	blood
27	chr8:104361600-104362000	Enhancers	HSMMtube	muscle
28	chr8:104361600-104362400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr8:104361600-104362800	Enhancers	Muscle Satellite Cultured Cells	--
30	chr8:104361600-104363200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr8:104361600-104365200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr8:104361600-104365400	Weak transcription	Gastric	stomach
33	chr8:104361800-104362200	Enhancers	NH-A	brain

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