Variant report

Variant	rs1588523
Chromosome Location	chr4:121766616-121766617
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10033707	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs11725662	0.86[LWK][hapmap];0.91[MKK][hapmap];0.92[YRI][hapmap]
rs13110308	0.82[AFR][1000 genomes]
rs13116962	0.83[CHB][hapmap];0.87[CHD][hapmap];0.91[LWK][hapmap];0.93[MKK][hapmap];0.88[YRI][hapmap];0.83[AFR][1000 genomes]
rs13124620	0.82[CHB][hapmap];0.92[YRI][hapmap];0.83[AFR][1000 genomes]
rs1355439	0.92[YRI][hapmap];0.88[AFR][1000 genomes]
rs1397766	0.96[YRI][hapmap];0.88[AFR][1000 genomes]
rs1511309	0.83[CHB][hapmap];0.82[JPT][hapmap]
rs1868715	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs2136998	0.83[CHD][hapmap];0.91[LWK][hapmap];0.93[MKK][hapmap];0.92[YRI][hapmap];0.86[AFR][1000 genomes]
rs2292395	0.86[AFR][1000 genomes]
rs2390053	0.85[CHD][hapmap]
rs3789140	0.83[CHB][hapmap];0.86[CHD][hapmap];0.88[LWK][hapmap];0.91[MKK][hapmap]
rs3804174	0.80[CHB][hapmap];0.81[JPT][hapmap]
rs6534215	0.81[AFR][1000 genomes]
rs6823191	0.83[AFR][1000 genomes]
rs6827372	0.92[YRI][hapmap];0.83[AFR][1000 genomes]
rs6845666	0.82[CHB][hapmap];0.92[YRI][hapmap];0.80[AFR][1000 genomes]
rs6851591	0.92[YRI][hapmap];0.83[AFR][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	nsv879852	chr4:121108734-121768496	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv998094	chr4:121504565-122374203	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1013704	chr4:121657648-121791601	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:121729600-121770400	Weak transcription	Stomach Smooth Muscle	stomach
2	chr4:121750400-121768400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr4:121755800-121774600	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr4:121756800-121779800	Weak transcription	Aorta	Aorta
5	chr4:121758200-121770400	Weak transcription	HSMM	muscle
6	chr4:121758200-121774600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr4:121759600-121775400	Weak transcription	Gastric	stomach
8	chr4:121760400-121775800	Weak transcription	Lung	lung
9	chr4:121761200-121778200	Weak transcription	Fetal Muscle Leg	muscle
10	chr4:121761200-121783600	Weak transcription	Pancreas	Pancrea
11	chr4:121761400-121774600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr4:121761400-121777600	Weak transcription	Left Ventricle	heart
13	chr4:121761600-121767400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr4:121763400-121778800	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr4:121763600-121776600	Weak transcription	Fetal Stomach	stomach
16	chr4:121763800-121769800	Weak transcription	Osteobl	bone
17	chr4:121763800-121770400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr4:121763800-121771000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr4:121763800-121776600	Weak transcription	Fetal Heart	heart
20	chr4:121764000-121770000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr4:121764200-121767800	Weak transcription	Colon Smooth Muscle	Colon
22	chr4:121764400-121769600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr4:121765800-121786600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr4:121766000-121776600	Weak transcription	Fetal Intestine Small	intestine
25	chr4:121766000-121786600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr4:121766200-121769600	Weak transcription	NHDF-Ad	bronchial
27	chr4:121766200-121790800	Weak transcription	Ovary	ovary
28	chr4:121766400-121769400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr4:121766400-121776600	Weak transcription	Fetal Intestine Large	intestine
30	chr4:121766600-121766800	Enhancers	Fetal Lung	lung

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