Variant report

Variant	rs1357820
Chromosome Location	chr7:12781816-12781817
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	chr7:12752442..12758611-chr7:12777091..12782449,9	K562	blood:

Extended variants
information (count: 97 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs10227444	0.98[EUR][1000 genomes]
rs10228478	0.94[EUR][1000 genomes]
rs10228692	0.96[EUR][1000 genomes]
rs10229334	0.97[EUR][1000 genomes]
rs10230505	0.97[EUR][1000 genomes]
rs10232476	0.97[EUR][1000 genomes]
rs10232482	0.98[EUR][1000 genomes]
rs10232492	0.97[EUR][1000 genomes]
rs10233392	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs10241274	0.94[EUR][1000 genomes]
rs10251149	0.95[EUR][1000 genomes]
rs10251270	0.97[EUR][1000 genomes]
rs10253749	0.97[EUR][1000 genomes]
rs10266373	0.97[EUR][1000 genomes]
rs10271036	0.98[EUR][1000 genomes]
rs11973922	0.95[EUR][1000 genomes]
rs11973968	0.93[EUR][1000 genomes]
rs11980726	0.95[EUR][1000 genomes]
rs11980770	0.96[EUR][1000 genomes]
rs11981654	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs11984319	0.95[EUR][1000 genomes]
rs11984405	0.89[EUR][1000 genomes]
rs13242844	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1357821	0.98[EUR][1000 genomes]
rs1404521	0.96[EUR][1000 genomes]
rs1524936	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs1830019	0.98[EUR][1000 genomes]
rs1917489	0.96[EUR][1000 genomes]
rs1917490	0.90[EUR][1000 genomes]
rs2058046	0.97[EUR][1000 genomes]
rs2108471	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2140745	0.94[EUR][1000 genomes]
rs2204398	0.97[EUR][1000 genomes]
rs2884002	0.98[EUR][1000 genomes]
rs34478352	0.93[EUR][1000 genomes]
rs34687763	0.97[EUR][1000 genomes]
rs34903132	0.95[EUR][1000 genomes]
rs35983470	0.94[EUR][1000 genomes]
rs4428564	0.97[EUR][1000 genomes]
rs4721128	0.96[EUR][1000 genomes]
rs4721129	0.97[EUR][1000 genomes]
rs4721130	0.97[EUR][1000 genomes]
rs4721131	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs4721132	0.97[EUR][1000 genomes]
rs4721133	0.98[EUR][1000 genomes]
rs55864612	0.98[EUR][1000 genomes]
rs55899328	0.88[EUR][1000 genomes]
rs56309306	0.96[EUR][1000 genomes]
rs57452384	0.98[EUR][1000 genomes]
rs59470504	0.98[EUR][1000 genomes]
rs6460975	0.97[EUR][1000 genomes]
rs6460976	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs6949193	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs6954600	0.98[EUR][1000 genomes]
rs6955313	0.98[EUR][1000 genomes]
rs6956267	0.97[EUR][1000 genomes]
rs6961147	0.97[EUR][1000 genomes]
rs6965183	0.98[EUR][1000 genomes]
rs6965250	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6965370	0.93[EUR][1000 genomes]
rs6971540	0.98[EUR][1000 genomes]
rs6973261	0.97[EUR][1000 genomes]
rs6977767	0.97[EUR][1000 genomes]
rs6978369	0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6978451	0.97[EUR][1000 genomes]
rs6979212	0.97[EUR][1000 genomes]
rs7787729	0.94[EUR][1000 genomes]
rs7789825	0.92[EUR][1000 genomes]
rs7789972	0.97[EUR][1000 genomes]
rs7790314	0.97[EUR][1000 genomes]
rs7790399	0.96[EUR][1000 genomes]
rs7792091	0.91[CEU][hapmap];0.87[EUR][1000 genomes]
rs7792774	0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7802097	0.91[EUR][1000 genomes]
rs7806690	0.92[EUR][1000 genomes]
rs9690109	0.88[EUR][1000 genomes]
rs9690689	0.98[EUR][1000 genomes]
rs9690691	0.98[EUR][1000 genomes]
rs9691242	0.98[EUR][1000 genomes]
rs9692011	0.94[EUR][1000 genomes]
rs976215	0.80[CEU][hapmap];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 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	nsv830907	chr7:12661239-12818250	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
4	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
5	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
6	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
7	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
8	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
9	nsv887641	chr7:12747443-12782062	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
10	esv2763623	chr7:12777205-12813460	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv464380	chr7:12777308-12805000	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	nsv606233	chr7:12777308-12805000	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
13	nsv464381	chr7:12777308-12826398	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
14	nsv470077	chr7:12777308-12826398	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
15	nsv606234	chr7:12777308-12826398	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
16	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

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12771200-12789400	Weak transcription	Psoas Muscle	Psoas
2	chr7:12778600-12782200	Enhancers	K562	blood
3	chr7:12781200-12782000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr7:12781200-12782000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr7:12781200-12782200	Enhancers	Muscle Satellite Cultured Cells	--
6	chr7:12781400-12782000	Weak transcription	HMEC	breast
7	chr7:12781400-12782400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr7:12781600-12782400	Enhancers	NH-A	brain

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