Variant report

Variant	rs186479680
Chromosome Location	chr2:36925227-36925228
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010985	chr2:36707157-36942066	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	nsv535642	chr2:36707157-36942066	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv1007757	chr2:36838387-37011384	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv535643	chr2:36838387-37011384	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1004483	chr2:36875235-37356812	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv535644	chr2:36875235-37356812	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv873878	chr2:36908661-36942266	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	esv1794298	chr2:36924040-36929933	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:36922800-36925400	Flanking Active TSS	Osteobl	bone
2	chr2:36922800-36925800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr2:36922800-36925800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr2:36923200-36925600	Active TSS	NHDF-Ad	bronchial
5	chr2:36923400-36925400	Flanking Active TSS	HUVEC	blood vessel
6	chr2:36923400-36925600	Active TSS	Right Atrium	heart
7	chr2:36923400-36925800	Active TSS	Ovary	ovary
8	chr2:36923800-36925400	Active TSS	Breast Myoepithelial Primary Cells	Breast
9	chr2:36924000-36925400	Active TSS	Adipose Nuclei	Adipose
10	chr2:36924400-36925600	Active TSS	Skeletal Muscle Male	skeletal muscle
11	chr2:36924400-36925800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:36924400-36925800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr2:36924600-36925600	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr2:36924600-36927200	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr2:36924600-36927200	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr2:36924600-36927200	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr2:36924800-36928400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr2:36924800-36928800	Weak transcription	NHLF	lung
19	chr2:36925000-36928000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr2:36925000-36928400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr2:36925000-36928400	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr2:36925000-36928400	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr2:36925200-36925400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr2:36925200-36925600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr2:36925200-36925600	Enhancers	Muscle Satellite Cultured Cells	--
26	chr2:36925200-36925600	Enhancers	NHEK	skin
27	chr2:36925200-36925800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr2:36925200-36926800	Enhancers	Hela-S3	cervix
29	chr2:36925200-36927600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr2:36925200-36927600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr2:36925200-36927800	Weak transcription	HMEC	breast
32	chr2:36925200-36928200	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr2:36925200-36928400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr2:36925200-36928400	Weak transcription	Fetal Lung	lung
35	chr2:36925200-36928400	Weak transcription	NH-A	brain
36	chr2:36925200-36930600	Weak transcription	A549	lung
37	chr2:36925200-36931400	Weak transcription	HSMMtube	muscle

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