Variant report

Variant	rs368526791
Chromosome Location	chr6:24951805-24951806
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 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	nsv1019504	chr6:24869174-24994758	Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv883482	chr6:24926730-25035920	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	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
6	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
7	esv2763543	chr6:24951199-24951809	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	inside rSNPs	diseases
8	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

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:24947800-24953600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr6:24948400-24954600	Enhancers	Fetal Thymus	thymus
3	chr6:24948400-24955800	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr6:24949200-24952800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
5	chr6:24949200-24952800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
6	chr6:24949200-24953400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
7	chr6:24949400-24953200	Flanking Active TSS	Primary T cells from cord blood	blood
8	chr6:24949600-24952800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
9	chr6:24949600-24952800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
10	chr6:24949800-24952000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr6:24949800-24952400	Weak transcription	Colonic Mucosa	Colon
12	chr6:24949800-24952800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
13	chr6:24950200-24952000	Enhancers	Duodenum Smooth Muscle	Duodenum
14	chr6:24950200-24952200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
15	chr6:24950200-24952400	Enhancers	Fetal Lung	lung
16	chr6:24950400-24952000	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr6:24950400-24988600	Weak transcription	Dnd41	blood
18	chr6:24950600-24953200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
19	chr6:24950800-24952800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
20	chr6:24950800-24952800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
21	chr6:24951000-24952800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr6:24951200-24952800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr6:24951200-24953200	Flanking Active TSS	Primary B cells from cord blood	blood
24	chr6:24951200-24960800	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr6:24951400-24952600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
26	chr6:24951400-24952800	Flanking Active TSS	Primary hematopoietic stem cells	blood
27	chr6:24951600-24952000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
28	chr6:24951600-24952000	Enhancers	Rectal Mucosa Donor 29	rectum
29	chr6:24951600-24952800	Flanking Active TSS	Primary B cells from peripheral blood	blood
30	chr6:24951600-24952800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
31	chr6:24951800-24952000	Active TSS	Primary T cells fromperipheralblood	blood
32	chr6:24951800-24952400	Flanking Active TSS	Thymus	Thymus
33	chr6:24951800-24952800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr6:24951800-24952800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
35	chr6:24951800-24952800	Flanking Active TSS	GM12878-XiMat	blood
36	chr6:24951800-24961600	Weak transcription	Spleen	Spleen

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links