Variant report

Variant	rs4719339
Chromosome Location	chr7:12865818-12865819
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:12725501..12727537-chr7:12863824..12866814,2	K562	blood:

Variant related genes	Relation type
ENSG00000122644	Chromatin interaction

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10229134	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10238211	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10243288	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10243324	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10246359	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10256191	0.91[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs10269634	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10278442	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12669053	0.89[ASN][1000 genomes]
rs1476815	0.83[ASN][1000 genomes]
rs17619124	0.80[EUR][1000 genomes]
rs17619332	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1978246	0.91[CHB][hapmap];0.87[JPT][hapmap]
rs1990346	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2109290	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2191265	0.81[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2191267	0.92[ASN][1000 genomes]
rs2215333	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2215337	0.91[ASN][1000 genomes]
rs2357049	0.81[CEU][hapmap];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2357052	0.91[CHB][hapmap];0.87[JPT][hapmap];0.87[ASN][1000 genomes]
rs2357053	0.82[CEU][hapmap]
rs28433921	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28610292	0.90[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2884084	0.96[ASN][1000 genomes]
rs35490471	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4260793	0.84[ASN][1000 genomes]
rs4288267	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4721148	0.91[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs4721153	0.85[CEU][hapmap];0.91[CHB][hapmap];0.87[JPT][hapmap];0.86[ASN][1000 genomes]
rs62448164	0.89[ASN][1000 genomes]
rs6460985	0.85[ASN][1000 genomes]
rs6942839	0.81[EUR][1000 genomes]
rs6944255	0.91[ASN][1000 genomes]
rs6947361	0.88[ASN][1000 genomes]
rs6948576	0.82[CHB][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs6948718	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6949476	0.91[ASN][1000 genomes]
rs6950280	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6950340	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6953097	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6961897	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6962633	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6965712	0.88[ASN][1000 genomes]
rs6969461	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6976082	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs758675	0.82[CEU][hapmap];0.91[CHB][hapmap];0.87[JPT][hapmap];0.87[ASN][1000 genomes]
rs7787464	0.88[ASN][1000 genomes]
rs7790527	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7793560	0.93[ASN][1000 genomes]
rs7800218	0.89[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7800522	0.85[ASN][1000 genomes]
rs7800580	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7803338	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7809081	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7810511	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7811356	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	nsv932020	chr7:12676890-13239551	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv830908	chr7:12695007-12870475	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
5	nsv868830	chr7:12712753-13517417	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
6	esv2422346	chr7:12739291-12883550	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1027501	chr7:12743592-12927109	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv606235	chr7:12781381-13205950	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv1020568	chr7:12802640-13183737	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	nsv1027806	chr7:12842708-12875714	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12854800-12867200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:12861200-12868600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr7:12861800-12866000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr7:12861800-12871200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr7:12862000-12867200	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr7:12865800-12866000	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr7:12865800-12866000	Enhancers	K562	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links