Variant report

Variant	rs538841204
Chromosome Location	chr9:92854911-92854912
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:92219469..92221520-chr9:92854815..92856417,2	MCF-7	breast:
2	chr9:92219124..92221595-chr9:92854778..92859945,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000130222	Chromatin interaction

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv482303	chr9:92752928-92890226	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv614852	chr9:92786722-93100550	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv893563	chr9:92816727-92967125	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv3390661	chr9:92854836-92855168	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:92839200-92855200	Weak transcription	Pancreas	Pancrea
2	chr9:92848400-92858000	Weak transcription	Right Atrium	heart
3	chr9:92848800-92855000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr9:92848800-92857800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr9:92848800-92862200	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr9:92849000-92856000	Weak transcription	Fetal Brain Female	brain
7	chr9:92851800-92855000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr9:92854200-92856200	Enhancers	Fetal Thymus	thymus
9	chr9:92854400-92855400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr9:92854400-92856200	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr9:92854400-92856400	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr9:92854600-92855200	Enhancers	Duodenum Mucosa	Duodenum
13	chr9:92854600-92855400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr9:92854600-92855800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr9:92854600-92856000	Enhancers	Dnd41	blood
16	chr9:92854600-92856200	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr9:92854600-92856400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr9:92854800-92855200	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr9:92854800-92855600	Flanking Active TSS	Primary T cells from cord blood	blood
20	chr9:92854800-92855600	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
21	chr9:92854800-92855800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr9:92854800-92856000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr9:92854800-92856400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
24	chr9:92854800-92856400	Enhancers	Primary T helper naive cells from peripheral blood	blood

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