Variant report

Variant	rs34065581
Chromosome Location	chr2:114023046-114023047
allele	-/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv508162	chr2:113983043-114099966	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv535895	chr2:114015492-114037018	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv874901	chr2:114022569-114079565	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113999600-114028400	Weak transcription	Ovary	ovary
2	chr2:114010200-114030400	Weak transcription	GM12878-XiMat	blood
3	chr2:114015800-114023600	Weak transcription	HSMM	muscle
4	chr2:114016200-114023600	Weak transcription	HSMMtube	muscle
5	chr2:114016200-114028000	Weak transcription	Fetal Brain Female	brain
6	chr2:114016400-114026000	Weak transcription	Fetal Heart	heart
7	chr2:114018800-114023800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr2:114019200-114024000	Weak transcription	Fetal Muscle Trunk	muscle
9	chr2:114019200-114026800	Weak transcription	Primary hematopoietic stem cells	blood
10	chr2:114019400-114028200	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr2:114019600-114026000	Weak transcription	Spleen	Spleen
12	chr2:114020000-114027800	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr2:114020400-114023800	Enhancers	Liver	Liver
14	chr2:114021000-114024200	Strong transcription	Placenta	Placenta
15	chr2:114021200-114024000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr2:114021200-114024000	Strong transcription	Lung	lung
17	chr2:114021200-114028200	Strong transcription	Duodenum Mucosa	Duodenum
18	chr2:114021400-114023600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr2:114021400-114024800	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr2:114021600-114026200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr2:114021600-114028200	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr2:114021800-114024000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr2:114022000-114024600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr2:114022200-114023400	Enhancers	Pancreas	Pancrea
25	chr2:114022200-114026400	Strong transcription	Primary T cells from cord blood	blood
26	chr2:114022200-114027600	Genic enhancers	Fetal Kidney	kidney
27	chr2:114022400-114023400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr2:114022400-114023800	Strong transcription	Adipose Nuclei	Adipose
29	chr2:114022400-114025000	Strong transcription	Fetal Thymus	thymus
30	chr2:114022800-114023200	Enhancers	Colon Smooth Muscle	Colon
31	chr2:114022800-114023200	Enhancers	Fetal Intestine Large	intestine
32	chr2:114022800-114024200	Genic enhancers	Fetal Muscle Leg	muscle
33	chr2:114023000-114023200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr2:114023000-114023200	Enhancers	Gastric	stomach
35	chr2:114023000-114023800	Enhancers	Fetal Intestine Small	intestine
36	chr2:114023000-114026800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr2:114023000-114027200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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