Variant report

Variant	rs6987417
Chromosome Location	chr8:92210246-92210247
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:92208641..92211587-chr8:92213183..92215216,2	K562	blood:
2	chr8:92185616..92187449-chr8:92210169..92211682,2	K562	blood:
3	chr8:92155872..92157525-chr8:92209191..92211411,2	K562	blood:

Extended variants
information (count: 46 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10111323	0.82[CEU][hapmap];0.80[CHB][hapmap]
rs10956794	0.85[CEU][hapmap];0.80[AMR][1000 genomes]
rs11778758	0.85[CEU][hapmap]
rs11779990	0.85[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs11783034	0.86[CEU][hapmap]
rs11784415	0.85[CEU][hapmap]
rs11785003	0.84[CEU][hapmap]
rs11787225	0.86[JPT][hapmap]
rs12540975	0.85[CEU][hapmap];0.80[AMR][1000 genomes]
rs12544236	0.85[AMR][1000 genomes]
rs12545986	0.96[CEU][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12546574	0.88[YRI][hapmap]
rs12546650	0.85[CEU][hapmap];0.94[CHB][hapmap];0.81[JPT][hapmap];0.85[AMR][1000 genomes]
rs12549426	0.96[CEU][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs34520902	0.80[AMR][1000 genomes]
rs34548877	0.80[AMR][1000 genomes]
rs35066004	0.81[CEU][hapmap]
rs35606777	0.80[AMR][1000 genomes]
rs3885969	0.81[CEU][hapmap]
rs3923174	0.96[CEU][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4129720	0.81[CEU][hapmap]
rs4259383	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4419777	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap]
rs4431560	0.89[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.85[AFR][1000 genomes]
rs4501551	0.92[CEU][hapmap];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4524748	0.83[AMR][1000 genomes]
rs4577919	0.85[CEU][hapmap];0.80[AMR][1000 genomes]
rs4596614	0.92[CEU][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4620242	0.85[CEU][hapmap];0.80[AMR][1000 genomes]
rs5029071	0.82[AMR][1000 genomes]
rs55762572	0.80[AMR][1000 genomes]
rs55779688	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61279214	0.80[AMR][1000 genomes]
rs62526682	0.80[AMR][1000 genomes]
rs62526683	0.80[AMR][1000 genomes]
rs62526686	0.80[AMR][1000 genomes]
rs62526707	0.85[AMR][1000 genomes]
rs62526730	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6471268	0.85[CEU][hapmap];0.82[AMR][1000 genomes]
rs6987764	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[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	nsv1028628	chr8:91680968-92418954	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv539672	chr8:91680968-92418954	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	esv2758623	chr8:91974499-92273724	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	esv2759629	chr8:91974499-92273724	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	esv35058	chr8:92127463-92218776	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
6	nsv982091	chr8:92203990-92240482	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6987417	SLC26A7	cis	Adipose Subcutaneous	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:92202600-92211400	Weak transcription	Right Atrium	heart
2	chr8:92209600-92210400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
3	chr8:92209600-92210400	Active TSS	Fetal Intestine Large	intestine
4	chr8:92209600-92210400	Active TSS	K562	blood
5	chr8:92209600-92210600	Active TSS	HUES6 Cell Line	embryonic stem cell
6	chr8:92209600-92210600	Active TSS	HUES64 Cell Line	embryonic stem cell
7	chr8:92209600-92210600	Active TSS	iPS-20b Cell Line	embryonic stem cell
8	chr8:92209600-92210600	Active TSS	Fetal Intestine Small	intestine
9	chr8:92209600-92210800	Active TSS	ES-I3 Cell Line	embryonic stem cell
10	chr8:92209800-92210400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr8:92210000-92210400	Active TSS	H1 Cell Line	embryonic stem cell
12	chr8:92210200-92210400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
13	chr8:92210200-92210400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
14	chr8:92210200-92210400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell

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