Variant report

Variant	rs7634195
Chromosome Location	chr3:105516856-105516857
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs11919893	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11926659	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12486371	0.83[CEU][hapmap]
rs12496588	0.84[CEU][hapmap]
rs12497428	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12632980	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13090949	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13326550	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13433776	1.00[CEU][hapmap];0.83[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1503923	0.81[ASN][1000 genomes]
rs16851596	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16851705	0.86[ASN][1000 genomes]
rs16851706	0.83[ASN][1000 genomes]
rs2120103	0.90[CHB][hapmap];0.89[JPT][hapmap];0.93[ASN][1000 genomes]
rs2120104	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2399056	0.92[CEU][hapmap]
rs3772512	0.80[CEU][hapmap]
rs6437616	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6766168	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6776593	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6778745	0.83[CEU][hapmap]
rs6780432	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6791765	0.83[CEU][hapmap]
rs7638504	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7639888	0.83[CEU][hapmap]
rs894541	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9811776	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9814582	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9837243	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9838755	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9846445	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9849559	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9872895	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9876110	0.83[CEU][hapmap]
rs9880744	0.84[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877309	chr3:105373836-105542435	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv2755185	chr3:105378310-105597310	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:105482800-105517400	Weak transcription	Fetal Intestine Large	intestine
2	chr3:105483200-105555200	Weak transcription	Placenta	Placenta
3	chr3:105486800-105519000	Weak transcription	Esophagus	oesophagus
4	chr3:105489600-105525400	Weak transcription	Fetal Intestine Small	intestine
5	chr3:105495400-105517200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr3:105505000-105527800	Weak transcription	Pancreas	Pancrea
7	chr3:105505000-105548200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr3:105505600-105517400	Weak transcription	Brain Substantia Nigra	brain
9	chr3:105506600-105518200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr3:105509800-105527800	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr3:105510000-105517400	Weak transcription	Stomach Mucosa	stomach
12	chr3:105510600-105521200	Weak transcription	Fetal Brain Male	brain
13	chr3:105511400-105566400	Weak transcription	Aorta	Aorta
14	chr3:105511800-105520400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr3:105512000-105520600	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr3:105512200-105517200	Weak transcription	Fetal Lung	lung
17	chr3:105512200-105517400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr3:105512200-105517400	Weak transcription	Fetal Heart	heart
19	chr3:105512200-105517400	Weak transcription	Ovary	ovary
20	chr3:105512200-105517400	Weak transcription	Small Intestine	intestine
21	chr3:105512200-105519000	Weak transcription	Psoas Muscle	Psoas
22	chr3:105512200-105519000	Weak transcription	Right Atrium	heart
23	chr3:105512200-105519200	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr3:105512200-105520200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr3:105512200-105520400	Weak transcription	Brain Cingulate Gyrus	brain
26	chr3:105512200-105527200	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr3:105512200-105534200	Weak transcription	Left Ventricle	heart
28	chr3:105512400-105524400	Weak transcription	NHLF	lung
29	chr3:105512600-105518200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr3:105512600-105520400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
31	chr3:105512600-105524000	Weak transcription	HSMMtube	muscle
32	chr3:105512600-105524600	Weak transcription	Colon Smooth Muscle	Colon
33	chr3:105512600-105525200	Weak transcription	HSMM	muscle
34	chr3:105512800-105517400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr3:105512800-105517400	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr3:105512800-105517400	Weak transcription	A549	lung
37	chr3:105513400-105517200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr3:105513400-105517200	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr3:105513400-105517800	Weak transcription	Osteobl	bone
40	chr3:105513800-105517200	Weak transcription	NHDF-Ad	bronchial
41	chr3:105514000-105517600	Weak transcription	Right Ventricle	heart
42	chr3:105514400-105521600	Enhancers	Primary B cells from peripheral blood	blood
43	chr3:105515000-105517000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr3:105515200-105518800	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr3:105515400-105528200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr3:105515400-105539000	Weak transcription	Fetal Muscle Trunk	muscle
47	chr3:105515600-105517400	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr3:105515800-105517200	Enhancers	Primary B cells from cord blood	blood
49	chr3:105515800-105521600	Enhancers	Primary T killer memory cells from peripheral blood	blood
50	chr3:105516000-105517000	ZNF genes & repeats	GM12878-XiMat	blood

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