Variant report

Variant	rs190811054
Chromosome Location	chr2:173445428-173445429
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	nsv533927	chr2:173161637-173796894	Active TSS Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	esv2760591	chr2:173396905-173719520	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv3035	chr2:173419058-173463901	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	nsv875415	chr2:173444462-173501069	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv875416	chr2:173444462-173504674	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:173421600-173453400	Weak transcription	Pancreas	Pancrea
2	chr2:173421800-173465200	Weak transcription	Small Intestine	intestine
3	chr2:173422200-173451000	Weak transcription	Rectal Smooth Muscle	rectum
4	chr2:173423400-173451000	Weak transcription	Colonic Mucosa	Colon
5	chr2:173424600-173447800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr2:173426200-173460600	Weak transcription	HSMMtube	muscle
7	chr2:173430600-173461600	Weak transcription	Right Ventricle	heart
8	chr2:173431400-173480600	Weak transcription	Gastric	stomach
9	chr2:173432000-173462400	Weak transcription	Colon Smooth Muscle	Colon
10	chr2:173436000-173445600	ZNF genes & repeats	GM12878-XiMat	blood
11	chr2:173437000-173451000	Weak transcription	Thymus	Thymus
12	chr2:173437000-173451800	Weak transcription	Spleen	Spleen
13	chr2:173437400-173449600	Weak transcription	Left Ventricle	heart
14	chr2:173437400-173452000	Weak transcription	Lung	lung
15	chr2:173437600-173449800	Weak transcription	Fetal Stomach	stomach
16	chr2:173437800-173447000	Weak transcription	Placenta	Placenta
17	chr2:173438000-173445800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr2:173438600-173445600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
19	chr2:173439200-173445600	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr2:173439800-173458000	Weak transcription	NHDF-Ad	bronchial
21	chr2:173440200-173458200	Weak transcription	Osteobl	bone
22	chr2:173440200-173467600	Weak transcription	NH-A	brain
23	chr2:173441400-173445600	ZNF genes & repeats	K562	blood
24	chr2:173441400-173447800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr2:173442800-173448400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr2:173442800-173451000	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr2:173443000-173446800	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr2:173443000-173451000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr2:173443000-173451000	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr2:173443200-173446200	Weak transcription	Liver	Liver
31	chr2:173443200-173447000	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr2:173443200-173449800	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr2:173443200-173451000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr2:173443200-173451000	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr2:173443200-173454400	Strong transcription	HUES6 Cell Line	embryonic stem cell
36	chr2:173443200-173455200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr2:173443200-173472200	Strong transcription	Primary neutrophils fromperipheralblood	blood
38	chr2:173443400-173447000	Weak transcription	Hela-S3	cervix
39	chr2:173443800-173445800	Weak transcription	Fetal Intestine Large	intestine
40	chr2:173443800-173446000	Strong transcription	Primary T cells from cord blood	blood
41	chr2:173443800-173446200	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr2:173443800-173446600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr2:173443800-173446800	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr2:173443800-173446800	Weak transcription	Stomach Smooth Muscle	stomach
45	chr2:173443800-173451800	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr2:173443800-173453600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr2:173443800-173463200	Weak transcription	A549	lung
48	chr2:173444000-173446600	Weak transcription	Brain Anterior Caudate	brain
49	chr2:173444000-173446800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr2:173444000-173446800	Weak transcription	Aorta	Aorta

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