Variant report

Variant	rs695217
Chromosome Location	chr10:96977553-96977554
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10128123	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.81[EUR][1000 genomes]
rs10218877	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10509683	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs10882566	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10882568	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.81[EUR][1000 genomes]
rs10882569	0.81[EUR][1000 genomes]
rs11188223	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11188225	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11188227	0.81[EUR][1000 genomes]
rs11188228	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.81[EUR][1000 genomes]
rs11188229	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs11188230	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs11572093	0.82[CHB][hapmap]
rs11596737	0.81[CEU][hapmap]
rs11598953	1.00[JPT][hapmap]
rs11599884	0.81[EUR][1000 genomes]
rs11872	1.00[JPT][hapmap]
rs12245722	0.86[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs12262878	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs12413028	0.92[CEU][hapmap]
rs12415795	0.92[CEU][hapmap]
rs12764831	1.00[JPT][hapmap]
rs12769820	0.83[EUR][1000 genomes]
rs1341164	0.82[CHB][hapmap]
rs16872	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17524438	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1934955	0.82[CHB][hapmap]
rs1934957	0.82[CHB][hapmap]
rs1934982	0.82[CHB][hapmap]
rs1934983	0.82[CHB][hapmap]
rs2071426	0.85[CHB][hapmap]
rs2185571	0.82[CHB][hapmap]
rs2449809	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2478477	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs2478478	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2478479	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs35999600	0.81[EUR][1000 genomes]
rs489807	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs509736	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs513661	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs589801	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs591157	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs591171	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs592055	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs594448	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs610046	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs611343	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs612490	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs613340	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs614682	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs626415	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs627173	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs628102	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs633345	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs637465	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs637939	1.00[CHB][hapmap]
rs648695	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6583967	0.82[CHB][hapmap]
rs659949	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs664093	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs672860	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs685607	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs688706	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs689207	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7089303	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs7909072	1.00[CEU][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv497859	chr10:96058024-97027747	Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers 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	41 gene(s)	inside rSNPs	diseases
2	nsv529726	chr10:96632494-97106315	Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	esv21432	chr10:96856006-96996043	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	esv1834151	chr10:96925446-96992955	Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv15160	chr10:96942869-97074756	Bivalent Enhancer Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96944200-96990400	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr10:96949800-96980600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr10:96956200-96979000	Weak transcription	Pancreas	Pancrea
4	chr10:96956200-96990400	Weak transcription	Aorta	Aorta
5	chr10:96960200-96988800	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr10:96961800-96989400	Weak transcription	Primary T cells from cord blood	blood
7	chr10:96962000-96990000	Weak transcription	Fetal Intestine Small	intestine
8	chr10:96965000-96988000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr10:96965400-96983000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr10:96965400-96989400	Weak transcription	Fetal Intestine Large	intestine
11	chr10:96969200-96979400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr10:96969200-96979600	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr10:96969200-96990200	Weak transcription	Left Ventricle	heart
14	chr10:96969400-96980200	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr10:96969400-96980200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr10:96969400-96980400	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr10:96969400-96981600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr10:96969400-96984800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr10:96969400-96990400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr10:96970200-96992400	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr10:96971800-96989400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr10:96972200-96988000	Weak transcription	Adipose Nuclei	Adipose
23	chr10:96972400-96987400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr10:96972400-96987800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr10:96972600-96989600	Weak transcription	Fetal Thymus	thymus
26	chr10:96973600-96981000	Weak transcription	Gastric	stomach
27	chr10:96974800-96981000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr10:96975400-96980600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr10:96975400-96990200	Weak transcription	Primary hematopoietic stem cells	blood
30	chr10:96975600-96979000	Strong transcription	ES-I3 Cell Line	embryonic stem cell
31	chr10:96975600-96990000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr10:96975800-96981000	Weak transcription	Duodenum Mucosa	Duodenum
33	chr10:96976000-96990000	Weak transcription	Primary B cells from cord blood	blood
34	chr10:96976200-96981200	Weak transcription	Primary B cells from peripheral blood	blood
35	chr10:96976400-96978400	Enhancers	Muscle Satellite Cultured Cells	--
36	chr10:96976400-96978600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr10:96976400-96989600	Weak transcription	GM12878-XiMat	blood
38	chr10:96976600-96981000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr10:96976800-96979600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr10:96976800-96980200	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr10:96976800-96987400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr10:96977000-96978600	Enhancers	HMEC	breast
43	chr10:96977200-96977600	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr10:96977200-96978200	Enhancers	HSMM	muscle
45	chr10:96977200-96978600	Enhancers	Osteobl	bone
46	chr10:96977400-96977600	Enhancers	H9 Cell Line	embryonic stem cell
47	chr10:96977400-96978000	Enhancers	NHEK	skin
48	chr10:96977400-96978200	Enhancers	NHLF	lung
49	chr10:96977400-96978400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr10:96977400-96978400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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