Variant report

Variant	rs4713715
Chromosome Location	chr6:33867897-33867898
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:33862211..33864928-chr6:33866922..33868481,2	K562	blood:

Variant related genes	Relation type
ENSG00000249346	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10807129	0.94[EUR][1000 genomes]
rs1324579	0.93[EUR][1000 genomes]
rs1408503	0.91[EUR][1000 genomes]
rs1535940	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1535941	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1535943	0.85[EUR][1000 genomes]
rs1535944	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1535945	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1535946	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1535947	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1969843	0.89[EUR][1000 genomes]
rs2093907	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2147423	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2147426	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2147427	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2181916	0.90[EUR][1000 genomes]
rs2477228	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2477231	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2477232	0.94[EUR][1000 genomes]
rs2477235	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2477236	0.93[EUR][1000 genomes]
rs2477237	0.94[EUR][1000 genomes]
rs2499681	0.80[EUR][1000 genomes]
rs2499737	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4711364	0.90[EUR][1000 genomes]
rs4711365	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4713716	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4713717	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4713721	0.95[EUR][1000 genomes]
rs6457747	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6921366	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9296103	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9368781	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs942506	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs942508	0.95[EUR][1000 genomes]
rs942509	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs942510	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916210	chr6:33804111-34144062	Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33850000-33871800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:33864000-33870800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr6:33864800-33869600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:33865000-33871200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr6:33865200-33868200	Weak transcription	Primary hematopoietic stem cells	blood
6	chr6:33865200-33868800	Weak transcription	K562	blood
7	chr6:33865400-33868800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr6:33865400-33869400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr6:33865400-33870400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr6:33865600-33868200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr6:33865600-33869800	Weak transcription	Primary T cells from cord blood	blood
12	chr6:33865600-33870200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr6:33865600-33870400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr6:33865600-33870400	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr6:33865600-33870600	Weak transcription	Primary T helper cells PMA-I stimulated	--
16	chr6:33865600-33870600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr6:33865600-33871600	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr6:33865600-33883000	Weak transcription	Esophagus	oesophagus
19	chr6:33866000-33870200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr6:33866000-33871800	Weak transcription	Pancreas	Pancrea
21	chr6:33866400-33871800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr6:33866600-33871600	Enhancers	Fetal Thymus	thymus
23	chr6:33867000-33868600	Enhancers	Spleen	Spleen
24	chr6:33867600-33868200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr6:33867600-33869800	Enhancers	Thymus	Thymus
26	chr6:33867800-33868000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
27	chr6:33867800-33868000	Bivalent Enhancer	Fetal Muscle Trunk	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links