Variant report

Variant	rs10185707
Chromosome Location	chr2:100635533-100635534
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:100633994..100635890-chr2:100636752..100639350,2	MCF-7	breast:

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10198062	1.00[EUR][1000 genomes]
rs10211423	1.00[EUR][1000 genomes]
rs13385193	0.82[EUR][1000 genomes]
rs13392222	0.88[EUR][1000 genomes]
rs17023362	0.82[EUR][1000 genomes]
rs17023378	0.82[EUR][1000 genomes]
rs17023391	0.84[EUR][1000 genomes]
rs17023393	0.84[EUR][1000 genomes]
rs17023453	0.89[EUR][1000 genomes]
rs17023459	0.89[EUR][1000 genomes]
rs17352514	0.92[EUR][1000 genomes]
rs17352745	0.91[EUR][1000 genomes]
rs17352801	0.91[EUR][1000 genomes]
rs17352808	0.91[EUR][1000 genomes]
rs17436983	0.90[EUR][1000 genomes]
rs17437101	0.94[EUR][1000 genomes]
rs17437248	0.88[EUR][1000 genomes]
rs17437282	0.91[EUR][1000 genomes]
rs17437338	0.91[EUR][1000 genomes]
rs2001722	0.81[EUR][1000 genomes]
rs2309775	0.82[EUR][1000 genomes]
rs2309776	0.84[EUR][1000 genomes]
rs4485586	0.94[EUR][1000 genomes]
rs55649403	0.85[EUR][1000 genomes]
rs55681051	0.85[EUR][1000 genomes]
rs62149303	0.89[EUR][1000 genomes]
rs62149304	0.92[EUR][1000 genomes]
rs62149305	0.94[EUR][1000 genomes]
rs62149307	0.94[EUR][1000 genomes]
rs62149310	0.94[EUR][1000 genomes]
rs62149311	0.93[EUR][1000 genomes]
rs62149314	0.94[EUR][1000 genomes]
rs62149316	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62149319	0.89[EUR][1000 genomes]
rs62149320	0.91[EUR][1000 genomes]
rs62149321	0.91[EUR][1000 genomes]
rs62149341	0.91[EUR][1000 genomes]
rs62149343	0.87[EUR][1000 genomes]
rs62149348	0.82[EUR][1000 genomes]
rs6719214	0.92[EUR][1000 genomes]
rs6736239	0.85[EUR][1000 genomes]
rs6750214	0.90[EUR][1000 genomes]
rs72819165	0.85[EUR][1000 genomes]
rs72819167	0.91[EUR][1000 genomes]
rs9308832	0.84[EUR][1000 genomes]

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	nsv1003343	chr2:100241560-100848900	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv535843	chr2:100241560-100848900	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:100615600-100638400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:100624800-100657800	Weak transcription	Brain Germinal Matrix	brain
3	chr2:100626600-100637800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr2:100626800-100637600	Weak transcription	Primary hematopoietic stem cells	blood
5	chr2:100627000-100637800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr2:100627200-100635800	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr2:100627800-100637800	Strong transcription	Primary B cells from cord blood	blood
8	chr2:100629400-100649600	Weak transcription	Fetal Brain Female	brain
9	chr2:100631800-100637400	Strong transcription	Primary B cells from peripheral blood	blood
10	chr2:100633400-100635800	Enhancers	NHDF-Ad	bronchial
11	chr2:100633400-100645800	Weak transcription	Gastric	stomach
12	chr2:100633600-100635800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr2:100633600-100638800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr2:100633600-100639600	Weak transcription	Thymus	Thymus
15	chr2:100633600-100652400	Weak transcription	Ovary	ovary
16	chr2:100633600-100653000	Weak transcription	Fetal Lung	lung
17	chr2:100633600-100660600	Weak transcription	Lung	lung
18	chr2:100633800-100635600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr2:100633800-100635600	Weak transcription	Dnd41	blood
20	chr2:100633800-100636000	Enhancers	Osteobl	bone
21	chr2:100634000-100635800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr2:100634000-100636000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr2:100634000-100637600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr2:100634200-100635600	Enhancers	NHLF	lung
25	chr2:100634400-100638200	Weak transcription	Primary T cells from cord blood	blood
26	chr2:100634600-100635800	Enhancers	Colon Smooth Muscle	Colon
27	chr2:100634600-100636000	Enhancers	NH-A	brain
28	chr2:100634800-100637400	Enhancers	Fetal Brain Male	brain
29	chr2:100635200-100635600	Enhancers	Stomach Smooth Muscle	stomach
30	chr2:100635200-100636600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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