Variant report

Variant	rs17154817
Chromosome Location	chr7:80790848-80790849
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:80786547..80788746-chr7:80790222..80791891,2	MCF-7	breast:
2	chr7:80545430..80553146-chr7:80785929..80793151,13	MCF-7	breast:
3	chr7:80565444..80567748-chr7:80788627..80790911,2	MCF-7	breast:
4	chr7:80562846..80565574-chr7:80788453..80790857,2	MCF-7	breast:
5	chr7:80570676..80574921-chr7:80787209..80790875,5	MCF-7	breast:
6	chr7:80788038..80791953-chr7:80793633..80797401,3	MCF-7	breast:
7	chr7:80546824..80550725-chr7:80786794..80792719,12	MCF-7	breast:

Variant related genes	Relation type
ENSG00000075223	Chromatin interaction

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10278323	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10954499	1.00[CEU][hapmap];0.82[CHB][hapmap];0.90[JPT][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11976988	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12707235	0.99[ASN][1000 genomes]
rs12707236	0.91[ASN][1000 genomes]
rs13231640	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs179172	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28640159	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs327663	0.86[ASN][1000 genomes]
rs327667	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs327669	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs327670	0.86[ASN][1000 genomes]
rs327671	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs327672	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs327673	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs327675	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs327676	0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs327677	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs327678	1.00[CEU][hapmap];0.90[JPT][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs327683	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs327724	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs327726	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs327727	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs327728	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs327729	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs327730	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs327731	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs327732	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs471729	1.00[CEU][hapmap];0.90[JPT][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs479878	1.00[CEU][hapmap];0.90[JPT][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs483587	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs491746	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs496019	1.00[CEU][hapmap];0.90[JPT][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs496185	1.00[CEU][hapmap];0.90[JPT][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs499628	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs505919	1.00[CEU][hapmap]
rs515646	1.00[CEU][hapmap];0.90[JPT][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs522649	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs523448	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs526305	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs527292	1.00[CEU][hapmap]
rs531769	1.00[CEU][hapmap];0.90[JPT][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs532663	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs542368	1.00[CEU][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs547784	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs550114	1.00[CEU][hapmap];0.90[JPT][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs560921	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs561061	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs561914	1.00[CEU][hapmap];0.89[JPT][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs565429	1.00[CEU][hapmap];0.90[JPT][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs566471	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs567313	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs567339	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs571662	1.00[CEU][hapmap];0.90[JPT][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs573578	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs581142	1.00[CEU][hapmap];0.90[JPT][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6952239	0.85[ASN][1000 genomes]
rs7778447	0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034690	chr7:80520004-80987682	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	nsv888556	chr7:80695828-80797794	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv831044	chr7:80721773-80918591	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80780600-80791000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:80785200-80796400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr7:80787600-80792600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr7:80788600-80791200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr7:80789000-80791000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:80789600-80791200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:80789600-80792800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr7:80790000-80792400	Enhancers	HSMM	muscle
9	chr7:80790000-80792600	Enhancers	HSMMtube	muscle
10	chr7:80790000-80793000	Enhancers	Muscle Satellite Cultured Cells	--
11	chr7:80790200-80791400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr7:80790400-80793400	Enhancers	A549	lung
13	chr7:80790600-80791000	Enhancers	HepG2	liver
14	chr7:80790600-80791200	Enhancers	NH-A	brain
15	chr7:80790600-80791400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr7:80790600-80791400	Enhancers	Hela-S3	cervix
17	chr7:80790600-80791400	Enhancers	NHLF	lung
18	chr7:80790600-80791400	Enhancers	Osteobl	bone
19	chr7:80790600-80791600	Enhancers	HMEC	breast
20	chr7:80790600-80792600	Enhancers	K562	blood
21	chr7:80790600-80792800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr7:80790600-80793000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr7:80790800-80791200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr7:80790800-80791400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr7:80790800-80791400	Enhancers	Fetal Lung	lung
26	chr7:80790800-80791400	Enhancers	Left Ventricle	heart
27	chr7:80790800-80792000	Enhancers	Fetal Heart	heart
28	chr7:80790800-80792000	Enhancers	NHDF-Ad	bronchial

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