Variant report

Variant	rs185724757
Chromosome Location	chr10:49790280-49790281
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:49776352..49778788-chr10:49787790..49790511,2	K562	blood:

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895371	chr10:49492075-50232180	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv895372	chr10:49576878-49933488	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv550815	chr10:49774633-49794481	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv550816	chr10:49782417-49794481	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1046588	chr10:49790254-49806169	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49786200-49792800	Enhancers	Brain Substantia Nigra	brain
2	chr10:49787000-49791800	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr10:49787600-49790600	Enhancers	Brain Hippocampus Middle	brain
4	chr10:49787800-49791200	Weak transcription	Spleen	Spleen
5	chr10:49787800-49791400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr10:49787800-49792400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr10:49787800-49793200	Weak transcription	Gastric	stomach
8	chr10:49787800-49796800	Weak transcription	Right Atrium	heart
9	chr10:49788000-49792600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr10:49788000-49792800	Strong transcription	HUVEC	blood vessel
11	chr10:49788000-49796000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr10:49788200-49792200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr10:49788200-49792800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr10:49788200-49795600	Strong transcription	Osteobl	bone
15	chr10:49788200-49795800	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr10:49788600-49790600	Weak transcription	Ovary	ovary
17	chr10:49788600-49790800	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr10:49788600-49792600	Strong transcription	NHDF-Ad	bronchial
19	chr10:49788800-49791000	Weak transcription	Brain Cingulate Gyrus	brain
20	chr10:49788800-49791200	Weak transcription	Brain Anterior Caudate	brain
21	chr10:49788800-49791400	Weak transcription	Brain Angular Gyrus	brain
22	chr10:49788800-49791400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr10:49788800-49793400	Strong transcription	HSMM	muscle
24	chr10:49788800-49795000	Strong transcription	Muscle Satellite Cultured Cells	--
25	chr10:49788800-49797200	Weak transcription	Rectal Smooth Muscle	rectum
26	chr10:49789000-49790600	Enhancers	Primary B cells from peripheral blood	blood
27	chr10:49789000-49791000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr10:49789000-49791200	Strong transcription	HMEC	breast
29	chr10:49789000-49791400	Weak transcription	Colon Smooth Muscle	Colon
30	chr10:49789000-49793000	Strong transcription	NH-A	brain
31	chr10:49789200-49790400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr10:49789400-49793400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr10:49789800-49790400	Enhancers	Primary B cells from cord blood	blood
34	chr10:49789800-49792600	Strong transcription	HSMMtube	muscle
35	chr10:49790000-49791200	Weak transcription	Pancreas	Pancrea
36	chr10:49790000-49791600	Enhancers	Adipose Nuclei	Adipose
37	chr10:49790200-49791400	Strong transcription	Aorta	Aorta
38	chr10:49790200-49791400	Strong transcription	NHLF	lung
39	chr10:49790200-49792000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links