Variant report

Variant	rs10911693
Chromosome Location	chr1:185214512-185214513
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

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

rs_ID	r²[population]
rs10174	0.83[CHB][hapmap];0.94[JPT][hapmap]
rs10218496	0.96[EUR][1000 genomes]
rs10453829	0.92[CEU][hapmap];0.81[EUR][1000 genomes]
rs10489579	0.92[CEU][hapmap];0.81[EUR][1000 genomes]
rs10489580	0.92[CEU][hapmap]
rs10798000	0.92[CEU][hapmap]
rs10798002	0.80[ASN][1000 genomes]
rs10911702	0.83[CHB][hapmap];0.95[JPT][hapmap]
rs10911704	0.95[JPT][hapmap]
rs12024023	0.92[CEU][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12026391	0.83[CHB][hapmap];0.95[JPT][hapmap]
rs12041704	0.95[JPT][hapmap];0.80[ASN][1000 genomes]
rs12045671	0.80[EUR][1000 genomes]
rs12096987	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs12118722	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12119471	0.96[EUR][1000 genomes]
rs12120377	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12127840	0.96[EUR][1000 genomes]
rs12135172	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs12404187	0.92[CEU][hapmap]
rs1336752	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1415072	0.92[CEU][hapmap];0.81[EUR][1000 genomes]
rs1591585	0.92[CEU][hapmap];0.85[EUR][1000 genomes]
rs1969750	0.81[EUR][1000 genomes]
rs2025227	0.80[EUR][1000 genomes]
rs2050566	0.92[CEU][hapmap];0.81[EUR][1000 genomes]
rs2146328	0.92[CEU][hapmap];0.81[EUR][1000 genomes]
rs2378909	0.80[ASN][1000 genomes]
rs2378910	0.83[CHB][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs2383269	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs3766717	0.86[EUR][1000 genomes]
rs57731138	0.85[EUR][1000 genomes]
rs6424972	0.92[CEU][hapmap]
rs6424974	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6660169	0.92[CEU][hapmap];0.82[EUR][1000 genomes]
rs6666742	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs6670117	0.80[EUR][1000 genomes]
rs6673303	0.92[CEU][hapmap];0.84[EUR][1000 genomes]
rs6685627	0.81[ASN][1000 genomes]
rs6698109	0.92[CEU][hapmap];0.82[EUR][1000 genomes]
rs6698122	0.92[CEU][hapmap];0.81[EUR][1000 genomes]
rs7123	0.83[CHB][hapmap];0.95[JPT][hapmap]
rs726567	0.95[JPT][hapmap]
rs7512245	0.94[EUR][1000 genomes]
rs7512290	0.92[CEU][hapmap]
rs7522617	0.81[EUR][1000 genomes]
rs7533198	0.92[CEU][hapmap];0.81[EUR][1000 genomes]
rs7535064	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7535261	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7539658	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs7543962	0.92[CEU][hapmap];0.82[EUR][1000 genomes]
rs7550586	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7550599	0.95[EUR][1000 genomes]
rs7552662	0.83[EUR][1000 genomes]
rs7553819	0.87[EUR][1000 genomes]
rs7556183	0.81[EUR][1000 genomes]
rs883753	0.83[CHB][hapmap];0.95[JPT][hapmap];0.81[YRI][hapmap];0.82[ASN][1000 genomes]
rs951428	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.98[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	nsv1001323	chr1:184525419-185315876	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
2	nsv535222	chr1:184525419-185315876	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
3	nsv548398	chr1:185136458-186003094	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 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	chr1:185127600-185218200	Weak transcription	Right Ventricle	heart
2	chr1:185170800-185218200	Weak transcription	Pancreas	Pancrea
3	chr1:185175600-185217000	Weak transcription	Fetal Stomach	stomach
4	chr1:185192600-185218600	Weak transcription	Aorta	Aorta
5	chr1:185192600-185221000	Weak transcription	Fetal Intestine Small	intestine
6	chr1:185193600-185214600	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr1:185193600-185219200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr1:185193600-185219400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr1:185193800-185220400	Weak transcription	Brain Hippocampus Middle	brain
10	chr1:185193800-185263600	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr1:185194000-185218600	Weak transcription	Lung	lung
12	chr1:185197200-185218200	Weak transcription	Left Ventricle	heart
13	chr1:185197600-185220400	Weak transcription	Ovary	ovary
14	chr1:185202400-185218800	Weak transcription	Brain Anterior Caudate	brain
15	chr1:185206400-185218200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr1:185209000-185218800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr1:185210400-185218400	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr1:185210600-185250400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr1:185211000-185215800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr1:185212000-185218200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr1:185213200-185214600	Enhancers	NHEK	skin
22	chr1:185213200-185214800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr1:185213200-185214800	Enhancers	K562	blood
24	chr1:185213200-185215000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr1:185213400-185214600	Enhancers	NHDF-Ad	bronchial
26	chr1:185213400-185214600	Enhancers	Osteobl	bone
27	chr1:185214000-185215200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr1:185214200-185214800	Weak transcription	Muscle Satellite Cultured Cells	--

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