Variant report

Variant	rs4633915
Chromosome Location	chr2:63141282-63141283
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10166922	1.00[CHD][hapmap]
rs11683932	1.00[LWK][hapmap]
rs11686081	1.00[LWK][hapmap]
rs13397638	1.00[LWK][hapmap]
rs13417661	1.00[LWK][hapmap]
rs17473979	1.00[LWK][hapmap]
rs34310142	1.00[CHD][hapmap]
rs6729573	1.00[LWK][hapmap]
rs9973608	1.00[CHD][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	nsv535767	chr2:62461582-63413596	Bivalent Enhancer Strong transcription Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	esv3417336	chr2:62957866-63749654	Strong transcription Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv428041	chr2:63027947-63206574	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1006848	chr2:63061816-63631407	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
5	esv2756598	chr2:63085848-63491438	Strong transcription Bivalent/Poised TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	esv3340700	chr2:63127412-63534998	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:63102400-63146200	Weak transcription	Aorta	Aorta
2	chr2:63102600-63149800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr2:63102800-63150200	Weak transcription	Esophagus	oesophagus
4	chr2:63104000-63147800	Weak transcription	Fetal Stomach	stomach
5	chr2:63106000-63149600	Weak transcription	Stomach Smooth Muscle	stomach
6	chr2:63106200-63149400	Weak transcription	Ovary	ovary
7	chr2:63107000-63150200	Weak transcription	HSMM	muscle
8	chr2:63107200-63141600	Weak transcription	Primary B cells from cord blood	blood
9	chr2:63107200-63146000	Weak transcription	Primary hematopoietic stem cells	blood
10	chr2:63107200-63146000	Weak transcription	Left Ventricle	heart
11	chr2:63108200-63149200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr2:63108200-63149600	Weak transcription	Fetal Lung	lung
13	chr2:63122800-63166600	Weak transcription	HMEC	breast
14	chr2:63123000-63149400	Weak transcription	NHLF	lung
15	chr2:63123600-63144200	Weak transcription	A549	lung
16	chr2:63123600-63146200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr2:63123600-63148800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr2:63123800-63149800	Weak transcription	NHEK	skin
19	chr2:63126200-63146000	Weak transcription	Primary T cells from cord blood	blood
20	chr2:63129400-63148800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr2:63131200-63148600	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr2:63131400-63149800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr2:63131600-63149400	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr2:63131800-63147000	Weak transcription	Liver	Liver
25	chr2:63133600-63149200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr2:63134800-63144200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr2:63134800-63147200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr2:63135000-63147000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr2:63135400-63148600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr2:63137400-63147000	Weak transcription	HepG2	liver
31	chr2:63139200-63149800	Weak transcription	Rectal Smooth Muscle	rectum
32	chr2:63140000-63141400	Enhancers	Dnd41	blood
33	chr2:63140400-63144400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr2:63140400-63148400	Weak transcription	Adipose Nuclei	Adipose
35	chr2:63140600-63141400	Enhancers	Brain Germinal Matrix	brain
36	chr2:63140600-63149600	Weak transcription	NHDF-Ad	bronchial
37	chr2:63141000-63147200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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