Variant report

Variant	rs10237017
Chromosome Location	chr7:116959845-116959846
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	7:116957165-116964911..7:117326534-117332210	H1-hESC	embryonic stem cell:	embryo

Variant related genes	Relation type
ENSG00000001626	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10230259	1.00[ASN][1000 genomes]
rs10242827	1.00[ASN][1000 genomes]
rs1025342	1.00[ASN][1000 genomes]
rs10255092	1.00[ASN][1000 genomes]
rs10258791	1.00[ASN][1000 genomes]
rs10264450	1.00[ASN][1000 genomes]
rs10278953	1.00[ASN][1000 genomes]
rs10487364	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12536356	1.00[ASN][1000 genomes]
rs17139821	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17450482	1.00[ASN][1000 genomes]
rs17544734	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17545644	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17547485	1.00[ASN][1000 genomes]
rs177071	1.00[ASN][1000 genomes]
rs1800503	1.00[ASN][1000 genomes]
rs213972	1.00[ASN][1000 genomes]
rs2518872	1.00[ASN][1000 genomes]
rs254537	1.00[ASN][1000 genomes]
rs254538	1.00[ASN][1000 genomes]
rs34268361	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34420782	1.00[ASN][1000 genomes]
rs34654194	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35003065	1.00[ASN][1000 genomes]
rs35130797	1.00[ASN][1000 genomes]
rs35415299	1.00[ASN][1000 genomes]
rs35715578	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35820454	1.00[ASN][1000 genomes]
rs35987553	1.00[ASN][1000 genomes]
rs36082161	1.00[ASN][1000 genomes]
rs39308	1.00[ASN][1000 genomes]
rs39309	1.00[ASN][1000 genomes]
rs39310	1.00[ASN][1000 genomes]
rs39311	1.00[ASN][1000 genomes]
rs39314	1.00[ASN][1000 genomes]
rs39320	1.00[ASN][1000 genomes]
rs39321	1.00[ASN][1000 genomes]
rs39322	1.00[ASN][1000 genomes]
rs39325	1.00[ASN][1000 genomes]
rs4285411	1.00[ASN][1000 genomes]
rs6466610	1.00[ASN][1000 genomes]
rs6943509	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6961545	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6963669	1.00[ASN][1000 genomes]
rs73480763	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7795896	1.00[ASN][1000 genomes]
rs7802924	1.00[ASN][1000 genomes]
rs916727	1.00[ASN][1000 genomes]
rs916728	1.00[ASN][1000 genomes]
rs9886209	1.00[ASN][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	nsv608256	chr7:116928371-117040117	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:116931800-116961600	Weak transcription	Placenta	Placenta
2	chr7:116952400-116960600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:116955400-116960200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr7:116958800-116960000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr7:116958800-116960400	Genic enhancers	Fetal Lung	lung

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