Variant report

Variant	rs10206615
Chromosome Location	chr2:161049101-161049102
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:161034766..161037717-chr2:161047419..161049441,2	MCF-7	breast:
2	chr2:161047148..161049457-chr2:161049468..161051501,2	MCF-7	breast:
3	chr2:161047917..161051617-chr2:161059788..161062483,3	K562	blood:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10171644	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10184041	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10193774	1.00[ASN][1000 genomes]
rs10197183	1.00[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs10202454	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10205184	0.83[ASN][1000 genomes]
rs10205374	0.98[ASN][1000 genomes]
rs11890075	0.84[YRI][hapmap]
rs11896610	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12616323	0.80[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs13413256	1.00[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs13426637	1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs1350313	0.84[ASN][1000 genomes]
rs1457239	1.00[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs2124971	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2168672	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2290706	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs4630719	0.99[ASN][1000 genomes]
rs56011055	0.97[ASN][1000 genomes]
rs57594443	0.93[ASN][1000 genomes]
rs6432594	0.87[YRI][hapmap]
rs6432609	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6432611	0.88[ASN][1000 genomes]
rs6730023	1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs72994790	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7563802	0.90[ASN][1000 genomes]
rs7572338	0.85[ASN][1000 genomes]
rs7588696	0.89[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs7590004	0.92[ASN][1000 genomes]
rs7596372	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7603920	0.98[ASN][1000 genomes]
rs7608557	0.96[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	nsv459929	chr2:160963603-161079435	Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv583497	chr2:160963603-161079435	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1001502	chr2:160967864-161079450	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:161024000-161051000	Weak transcription	HSMMtube	muscle
2	chr2:161025600-161051000	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr2:161027200-161051400	Weak transcription	Gastric	stomach
4	chr2:161029200-161051000	Weak transcription	HSMM	muscle
5	chr2:161029400-161063200	Weak transcription	Fetal Muscle Leg	muscle
6	chr2:161038200-161051200	Weak transcription	Duodenum Mucosa	Duodenum
7	chr2:161038400-161050000	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr2:161038400-161050400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr2:161038400-161051000	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr2:161038400-161051000	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr2:161038400-161051200	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr2:161045200-161051000	Weak transcription	Fetal Intestine Large	intestine
13	chr2:161045400-161051400	Weak transcription	Fetal Intestine Small	intestine
14	chr2:161046800-161049600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr2:161047000-161049200	Strong transcription	HMEC	breast
16	chr2:161047200-161058800	Weak transcription	Psoas Muscle	Psoas
17	chr2:161047400-161050000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr2:161047400-161053200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr2:161048400-161051000	Weak transcription	Dnd41	blood
20	chr2:161048600-161061600	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr2:161049000-161050000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr2:161049000-161053600	Genic enhancers	NHEK	skin

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