Variant report

Variant	rs62072029
Chromosome Location	chr17:15820591-15820592
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:15811001..15813774-chr17:15817788..15820656,2	K562	blood:
2	chr17:15819602..15821859-chr17:15822735..15824245,2	MCF-7	breast:
3	chr17:15820333..15822975-chr17:15833482..15836087,2	K562	blood:

Extended variants
information (count: 98 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs11654524	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11655374	0.88[ASN][1000 genomes]
rs11656489	0.88[ASN][1000 genomes]
rs11656518	0.88[ASN][1000 genomes]
rs11658370	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11658454	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs11658871	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11870637	0.85[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs12051835	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12603728	0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs12603863	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1558409	0.95[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs1613538	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1639393	0.86[ASN][1000 genomes]
rs1639394	0.91[ASN][1000 genomes]
rs17776817	0.92[ASN][1000 genomes]
rs1797453	0.91[ASN][1000 genomes]
rs1797460	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1797462	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1889021	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1974626	0.86[ASN][1000 genomes]
rs2429742	0.91[ASN][1000 genomes]
rs2535598	0.91[ASN][1000 genomes]
rs2535599	0.91[ASN][1000 genomes]
rs2586557	0.82[ASN][1000 genomes]
rs2779187	0.90[ASN][1000 genomes]
rs2787070	0.82[ASN][1000 genomes]
rs35743185	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3744329	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3744330	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3859260	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4297751	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4791653	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4792704	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4792705	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62071036	0.85[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs62071037	0.85[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs62071038	0.85[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs62072030	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62072031	0.94[ASN][1000 genomes]
rs62072032	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs62072033	0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs62072034	0.92[ASN][1000 genomes]
rs62072052	0.88[ASN][1000 genomes]
rs62072161	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62072162	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62072168	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62072173	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62072198	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62072201	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62072203	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62072205	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6502475	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs708590	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs708591	0.87[EUR][1000 genomes]
rs708593	0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7214215	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7218000	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7223657	0.89[ASN][1000 genomes]
rs7503620	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8076401	0.92[ASN][1000 genomes]
rs8079686	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8080194	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs859226	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs859228	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs859229	0.81[ASN][1000 genomes]
rs859230	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs859232	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs859234	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs859236	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs859237	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs859238	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs859240	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs859247	0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs859248	0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs859252	0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs859253	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs859255	0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs859256	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs859257	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9893636	0.90[ASN][1000 genomes]
rs9894474	0.86[ASN][1000 genomes]
rs9901375	0.88[ASN][1000 genomes]
rs9903682	0.88[ASN][1000 genomes]
rs9907878	0.80[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9912875	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916652	chr17:15093600-15856310	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	nsv1059056	chr17:15294011-15856861	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv934185	chr17:15552960-16551197	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	190 gene(s)	inside rSNPs	diseases
4	nsv1062951	chr17:15561070-15890644	Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
5	nsv1066023	chr17:15607267-16053512	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
6	esv3330182	chr17:15652014-16569534	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
7	esv3446844	chr17:15654843-16572246	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
8	nsv1061222	chr17:15672934-15999778	ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
9	nsv907706	chr17:15731923-16056442	ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
10	nsv1067555	chr17:15804228-16001117	Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
11	nsv1063459	chr17:15804228-16543593	Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
12	nsv1061987	chr17:15810017-15855135	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15809800-15820800	Weak transcription	Gastric	stomach
2	chr17:15812000-15820800	Weak transcription	Left Ventricle	heart
3	chr17:15813400-15820800	Weak transcription	Pancreas	Pancrea
4	chr17:15814600-15822400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr17:15816200-15820800	Weak transcription	Fetal Heart	heart
6	chr17:15816200-15820800	Weak transcription	Right Atrium	heart
7	chr17:15816600-15820800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr17:15817200-15825000	Enhancers	Hela-S3	cervix
9	chr17:15818600-15820600	Weak transcription	NHDF-Ad	bronchial
10	chr17:15818600-15823800	Weak transcription	Placenta	Placenta
11	chr17:15820200-15820600	Enhancers	Right Ventricle	heart
12	chr17:15820200-15820800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
13	chr17:15820400-15820600	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
14	chr17:15820400-15820600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
15	chr17:15820400-15820600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr17:15820400-15820600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr17:15820400-15820600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr17:15820400-15820600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr17:15820400-15820600	Active TSS	Cortex derived primary cultured neurospheres	brain
20	chr17:15820400-15820600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr17:15820400-15820600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr17:15820400-15820600	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
23	chr17:15820400-15820600	Bivalent Enhancer	Osteobl	bone
24	chr17:15820400-15821200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
25	chr17:15820400-15821400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr17:15820400-15821400	Enhancers	Esophagus	oesophagus
27	chr17:15820400-15821400	Bivalent Enhancer	Fetal Intestine Small	intestine
28	chr17:15820400-15824400	Weak transcription	HUVEC	blood vessel

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