Variant report

Variant	rs17665337
Chromosome Location	chr7:12239693-12239694
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:12237815..12240381-chr7:12248250..12250812,3	K562	blood:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10488193	0.85[CEU][hapmap];0.92[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[ASN][1000 genomes]
rs11980425	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs12699320	1.00[ASN][1000 genomes]
rs1468800	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs16877361	0.82[JPT][hapmap]
rs17165706	0.85[JPT][hapmap]
rs17165736	0.91[ASN][1000 genomes]
rs17165737	0.91[ASN][1000 genomes]
rs17165744	0.85[CEU][hapmap];0.92[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs17165746	0.85[CEU][hapmap];0.92[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs17165750	0.85[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs17594223	1.00[ASW][hapmap];0.82[CEU][hapmap];0.91[GIH][hapmap];0.84[MKK][hapmap];0.91[TSI][hapmap];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17595150	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17595402	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17605315	0.82[ASN][1000 genomes]
rs17652223	0.81[AMR][1000 genomes]
rs3807864	0.98[EUR][1000 genomes]
rs60495893	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60699002	0.87[ASN][1000 genomes]
rs6947990	1.00[ASW][hapmap]
rs6978684	0.91[ASN][1000 genomes]
rs73284389	0.87[ASN][1000 genomes]
rs73299019	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73299021	0.96[EUR][1000 genomes]
rs73301035	0.89[ASN][1000 genomes]
rs73677511	0.89[ASN][1000 genomes]
rs73677523	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs73677558	0.87[ASN][1000 genomes]
rs73678692	0.91[ASN][1000 genomes]

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	nsv606199	chr7:11506143-12486659	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv1023608	chr7:12064114-12247520	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv534432	chr7:12148960-12693032	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv1021710	chr7:12164993-12251790	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
5	nsv1024554	chr7:12214722-12967418	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
6	nsv538735	chr7:12214722-12967418	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12236800-12239800	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr7:12237000-12239800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:12238400-12240600	Enhancers	Hela-S3	cervix
4	chr7:12238600-12240000	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr7:12238600-12240000	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr7:12238800-12239800	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr7:12238800-12239800	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr7:12238800-12240800	Enhancers	HepG2	liver
9	chr7:12239200-12239800	Enhancers	NH-A	brain
10	chr7:12239400-12240000	Enhancers	A549	lung
11	chr7:12239600-12240000	Enhancers	H1 Cell Line	embryonic stem cell
12	chr7:12239600-12240000	Enhancers	H9 Cell Line	embryonic stem cell
13	chr7:12239600-12240000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr7:12239600-12240000	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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