Variant report

Variant	rs17619626
Chromosome Location	chr7:12871627-12871628
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	chr7:12869802..12871805-chr7:13260631..13263120,2	K562	blood:
2	chr7:12867009..12868914-chr7:12869062..12871956,2	K562	blood:

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10240689	0.88[EUR][1000 genomes]
rs10254295	0.92[EUR][1000 genomes]
rs10256191	0.85[EUR][1000 genomes]
rs10259240	0.91[EUR][1000 genomes]
rs10259524	0.93[EUR][1000 genomes]
rs1476815	0.90[CEU][hapmap]
rs17166415	0.84[EUR][1000 genomes]
rs17681457	0.94[EUR][1000 genomes]
rs1978246	1.00[CEU][hapmap]
rs2191266	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs2191267	0.81[EUR][1000 genomes]
rs2215337	0.82[EUR][1000 genomes]
rs2356698	0.94[EUR][1000 genomes]
rs2357046	0.91[EUR][1000 genomes]
rs2884084	0.83[EUR][1000 genomes]
rs28873158	0.92[EUR][1000 genomes]
rs35469032	0.80[ASN][1000 genomes]
rs4288268	0.88[EUR][1000 genomes]
rs4721148	0.96[CEU][hapmap];0.83[EUR][1000 genomes]
rs55991971	0.94[EUR][1000 genomes]
rs6460980	0.93[EUR][1000 genomes]
rs6460986	0.80[ASN][1000 genomes]
rs66817397	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6944255	0.81[EUR][1000 genomes]
rs6948576	1.00[CEU][hapmap]
rs6949476	0.82[EUR][1000 genomes]
rs6959404	0.86[ASN][1000 genomes]
rs6959543	0.87[ASN][1000 genomes]
rs6959850	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6978013	1.00[CEU][hapmap];0.92[CHB][hapmap];0.84[JPT][hapmap];0.81[YRI][hapmap];0.86[EUR][1000 genomes]
rs758676	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.85[YRI][hapmap];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7783477	0.93[EUR][1000 genomes]
rs7787728	0.87[EUR][1000 genomes]
rs7791902	0.92[EUR][1000 genomes]
rs7793560	0.82[EUR][1000 genomes]
rs7793747	0.81[EUR][1000 genomes]
rs7795573	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7808814	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 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	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
5	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
6	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
7	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
8	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
9	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:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12867600-12873400	Weak transcription	Pancreas	Pancrea
2	chr7:12868200-12877200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:12871400-12871800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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