Variant report

Variant	rs10183049
Chromosome Location	chr2:113589571-113589572
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

rs_ID	r²[population]
rs10176689	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10181385	1.00[EUR][1000 genomes]
rs10190942	1.00[AMR][1000 genomes]
rs10206303	1.00[AMR][1000 genomes]
rs1143626	1.00[EUR][1000 genomes]
rs1143641	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13424846	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2063918	1.00[EUR][1000 genomes]
rs4849116	1.00[EUR][1000 genomes]
rs60696592	1.00[EUR][1000 genomes]
rs61134068	1.00[EUR][1000 genomes]
rs61677777	1.00[EUR][1000 genomes]
rs72950372	1.00[EUR][1000 genomes]
rs72954024	1.00[EUR][1000 genomes]
rs72954033	1.00[EUR][1000 genomes]
rs72954034	1.00[EUR][1000 genomes]
rs72954038	1.00[EUR][1000 genomes]
rs7591401	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113582400-113592000	Weak transcription	NH-A	brain
2	chr2:113583000-113592200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr2:113583600-113591200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr2:113583600-113592000	Weak transcription	Osteobl	bone
5	chr2:113587000-113589600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr2:113587200-113590400	Weak transcription	Fetal Intestine Small	intestine
7	chr2:113587400-113590200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr2:113587600-113593800	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr2:113588000-113591200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr2:113588000-113593600	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr2:113588400-113590000	Enhancers	HUVEC	blood vessel
12	chr2:113588800-113589600	Enhancers	Spleen	Spleen
13	chr2:113588800-113589800	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
14	chr2:113588800-113590200	Enhancers	Primary B cells from peripheral blood	blood
15	chr2:113588800-113590600	Enhancers	Fetal Thymus	thymus
16	chr2:113588800-113590600	Enhancers	GM12878-XiMat	blood
17	chr2:113588800-113591000	Enhancers	Lung	lung
18	chr2:113588800-113591800	Genic enhancers	Primary monocytes fromperipheralblood	blood
19	chr2:113589000-113589800	Enhancers	Adipose Nuclei	Adipose
20	chr2:113589000-113590000	Genic enhancers	NHEK	skin
21	chr2:113589000-113593600	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
22	chr2:113589000-113594000	Transcr. at gene 5' and 3'	Primary neutrophils fromperipheralblood	blood
23	chr2:113589200-113589600	Enhancers	Esophagus	oesophagus
24	chr2:113589200-113589600	Enhancers	Stomach Mucosa	stomach
25	chr2:113589200-113590000	Enhancers	Fetal Muscle Leg	muscle
26	chr2:113589200-113590200	Flanking Active TSS	Primary B cells from cord blood	blood
27	chr2:113589400-113589600	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr2:113589400-113589800	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr2:113589400-113590400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr2:113589400-113590400	Flanking Active TSS	Primary hematopoietic stem cells	blood
31	chr2:113589400-113590600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr2:113589400-113591000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr2:113589400-113591200	Weak transcription	Small Intestine	intestine
34	chr2:113589400-113591600	Genic enhancers	HMEC	breast
35	chr2:113589400-113592200	Weak transcription	Pancreas	Pancrea

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