Variant report

Variant	rs10805974
Chromosome Location	chr6:74440514-74440515
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:74405938..74408265-chr6:74438560..74441116,2	MCF-7	breast:

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10498895	0.84[CEU][hapmap]
rs12203043	0.89[GIH][hapmap]
rs12662725	0.84[CEU][hapmap]
rs1392913	0.96[CEU][hapmap];0.85[CHB][hapmap];0.96[GIH][hapmap];0.88[TSI][hapmap];0.89[EUR][1000 genomes]
rs17760906	0.84[CEU][hapmap];0.80[CHB][hapmap]
rs2033736	0.84[CEU][hapmap]
rs2164755	0.84[CEU][hapmap]
rs2351528	0.84[CEU][hapmap]
rs4342388	0.92[CEU][hapmap];0.85[CHB][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4708077	0.89[GIH][hapmap];0.92[MEX][hapmap]
rs4708082	0.84[CEU][hapmap]
rs4708088	0.81[CEU][hapmap]
rs5023688	0.84[CEU][hapmap]
rs6453700	0.84[CEU][hapmap]
rs6901628	0.82[GIH][hapmap]
rs6918612	0.84[CEU][hapmap]
rs6921996	0.84[CEU][hapmap]
rs6923034	0.86[GIH][hapmap];0.83[MEX][hapmap]
rs6932012	0.92[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.88[TSI][hapmap];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7771585	0.84[CEU][hapmap]
rs7774119	0.82[GIH][hapmap]
rs9293937	0.87[MEX][hapmap]
rs9293941	0.84[CEU][hapmap]
rs9442954	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9442955	0.91[CEU][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9442956	0.89[GIH][hapmap]
rs9442960	0.84[CEU][hapmap]
rs9442961	0.84[CEU][hapmap]
rs9447017	0.83[CEU][hapmap];0.80[CHB][hapmap];0.80[JPT][hapmap]
rs9447019	0.84[CEU][hapmap]
rs9447029	0.87[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1027968	chr6:74155378-74521923	Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
2	nsv538305	chr6:74155378-74521923	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
3	nsv1023250	chr6:74189642-74605976	Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	172 gene(s)	inside rSNPs	diseases
4	nsv538306	chr6:74189642-74605976	Strong transcription Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	172 gene(s)	inside rSNPs	diseases
5	nsv463154	chr6:74412048-74775904	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	nsv603695	chr6:74412048-74775904	Flanking Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74408000-74446800	Weak transcription	Dnd41	blood
2	chr6:74414800-74474600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr6:74423600-74441000	Weak transcription	Stomach Smooth Muscle	stomach
4	chr6:74424200-74443200	Weak transcription	Right Atrium	heart
5	chr6:74425000-74443600	Weak transcription	Lung	lung
6	chr6:74425200-74475800	Weak transcription	Hela-S3	cervix
7	chr6:74425400-74483200	Weak transcription	A549	lung
8	chr6:74430600-74455400	Weak transcription	Right Ventricle	heart
9	chr6:74432400-74440800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr6:74432400-74442600	Weak transcription	Left Ventricle	heart
11	chr6:74432400-74444200	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr6:74432800-74442600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr6:74433000-74442200	Weak transcription	Colon Smooth Muscle	Colon
14	chr6:74433000-74448000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr6:74433000-74456400	Weak transcription	Primary T helper cells PMA-I stimulated	--
16	chr6:74433000-74456400	Weak transcription	HSMM	muscle
17	chr6:74433400-74448600	Weak transcription	NH-A	brain
18	chr6:74433400-74456400	Weak transcription	NHLF	lung
19	chr6:74433600-74455000	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr6:74434600-74448400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr6:74435200-74443800	Weak transcription	Thymus	Thymus
22	chr6:74435400-74448200	Weak transcription	Adipose Nuclei	Adipose
23	chr6:74435600-74442600	Strong transcription	NHDF-Ad	bronchial
24	chr6:74435600-74443000	Weak transcription	Fetal Thymus	thymus
25	chr6:74435600-74445200	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr6:74435600-74454600	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr6:74435800-74442600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr6:74435800-74475400	Weak transcription	Primary T cells from cord blood	blood
29	chr6:74437200-74442200	Weak transcription	NHEK	skin
30	chr6:74438400-74527200	Weak transcription	Esophagus	oesophagus
31	chr6:74438800-74441000	Weak transcription	Aorta	Aorta
32	chr6:74439000-74441200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr6:74439000-74441200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr6:74439000-74442200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr6:74439000-74443200	Weak transcription	Fetal Stomach	stomach
36	chr6:74439200-74443000	Weak transcription	GM12878-XiMat	blood
37	chr6:74439600-74441200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr6:74439600-74442400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr6:74439600-74446200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr6:74439600-74451200	Strong transcription	HMEC	breast
41	chr6:74439800-74441600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr6:74439800-74442200	Strong transcription	Placenta Amnion	Placenta Amnion
43	chr6:74439800-74444400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr6:74440000-74440600	Strong transcription	Osteobl	bone
45	chr6:74440000-74442200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr6:74440000-74444200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr6:74440200-74441400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr6:74440200-74441400	Strong transcription	HUVEC	blood vessel
49	chr6:74440200-74442400	Strong transcription	Fetal Muscle Trunk	muscle
50	chr6:74440200-74442600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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