Variant report

Variant	rs112224264
Chromosome Location	chr6:25039894-25039895
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022966	chr6:24763776-25154212	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv538160	chr6:24763776-25154212	Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv1023989	chr6:24930362-25285679	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
4	nsv1030634	chr6:24938277-25040161	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv830610	chr6:24951741-25124239	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
6	nsv830611	chr6:25039374-25199112	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:25035200-25041200	Weak transcription	Fetal Kidney	kidney
2	chr6:25035200-25044600	Weak transcription	Right Atrium	heart
3	chr6:25035800-25040600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr6:25035800-25041000	Enhancers	Fetal Thymus	thymus
5	chr6:25036000-25042400	Weak transcription	Lung	lung
6	chr6:25036400-25040600	Enhancers	Primary B cells from peripheral blood	blood
7	chr6:25036400-25041000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:25036400-25041000	Weak transcription	Duodenum Mucosa	Duodenum
9	chr6:25036600-25040600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr6:25036600-25041200	Weak transcription	NH-A	brain
11	chr6:25036600-25041800	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr6:25037000-25041000	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr6:25038400-25040600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr6:25038600-25040000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
15	chr6:25038600-25041200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
16	chr6:25038600-25041400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
17	chr6:25038600-25042200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
18	chr6:25038800-25040000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
19	chr6:25039000-25040200	Flanking Active TSS	Primary hematopoietic stem cells	blood
20	chr6:25039000-25040200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
21	chr6:25039000-25041400	Enhancers	Primary B cells from cord blood	blood
22	chr6:25039000-25041400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr6:25039000-25042000	Flanking Active TSS	Dnd41	blood
24	chr6:25039000-25043800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr6:25039400-25040200	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr6:25039400-25040600	Enhancers	Fetal Lung	lung
27	chr6:25039400-25041400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
28	chr6:25039400-25041800	Weak transcription	Small Intestine	intestine
29	chr6:25039600-25040000	Enhancers	Fetal Heart	heart
30	chr6:25039600-25040000	Flanking Active TSS	Thymus	Thymus
31	chr6:25039600-25040200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr6:25039600-25041000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
33	chr6:25039600-25041200	Weak transcription	Spleen	Spleen
34	chr6:25039600-25041200	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr6:25039800-25040200	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr6:25039800-25040200	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr6:25039800-25040400	Flanking Active TSS	GM12878-XiMat	blood
38	chr6:25039800-25041000	Enhancers	Primary T cells from cord blood	blood
39	chr6:25039800-25041000	Enhancers	Primary T helper naive cells from peripheral blood	blood
40	chr6:25039800-25041400	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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