Variant report

Variant	rs1613538
Chromosome Location	chr17:15796805-15796806
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:15791472..15794195-chr17:15796023..15798848,3	K562	blood:
2	chr17:15791535..15794057-chr17:15795691..15797755,2	MCF-7	breast:
3	chr17:15794765..15797289-chr17:15822819..15824762,2	MCF-7	breast:
4	chr17:15782611..15786264-chr17:15794710..15797679,3	MCF-7	breast:
5	chr17:15786537..15789462-chr17:15796062..15797687,2	MCF-7	breast:
6	chr17:15787293..15789868-chr17:15796195..15798125,2	K562	blood:

Extended variants
information (count: 103 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11654524	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11655374	0.82[ASN][1000 genomes]
rs11656489	0.82[ASN][1000 genomes]
rs11656518	0.82[ASN][1000 genomes]
rs11658370	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11658454	0.87[ASN][1000 genomes]
rs11658871	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11870637	0.81[ASN][1000 genomes]
rs12051835	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12603728	0.87[ASN][1000 genomes]
rs12603863	0.87[ASN][1000 genomes]
rs1558409	0.80[ASN][1000 genomes]
rs1639393	0.83[ASN][1000 genomes]
rs1639394	0.88[ASN][1000 genomes]
rs17776817	0.81[ASN][1000 genomes]
rs1797453	0.88[ASN][1000 genomes]
rs1797460	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1797462	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1889021	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1974626	0.80[ASN][1000 genomes]
rs2429742	0.88[ASN][1000 genomes]
rs2535598	0.88[ASN][1000 genomes]
rs2535599	0.88[ASN][1000 genomes]
rs2586557	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2779187	0.87[ASN][1000 genomes]
rs35743185	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3744329	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3744330	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3859260	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4297751	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4791653	0.87[ASN][1000 genomes]
rs4792704	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4792705	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs481648	0.90[CEU][hapmap]
rs62071036	0.81[ASN][1000 genomes]
rs62071037	0.81[ASN][1000 genomes]
rs62071038	0.81[ASN][1000 genomes]
rs62072029	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62072030	0.87[ASN][1000 genomes]
rs62072031	0.87[ASN][1000 genomes]
rs62072032	0.87[ASN][1000 genomes]
rs62072033	0.87[ASN][1000 genomes]
rs62072034	0.86[ASN][1000 genomes]
rs62072052	0.82[ASN][1000 genomes]
rs62072161	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62072162	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62072168	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62072173	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62072198	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62072201	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62072203	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62072205	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6502475	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs708590	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs708593	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7214215	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7218000	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7223657	0.83[ASN][1000 genomes]
rs7503620	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8076401	0.86[ASN][1000 genomes]
rs8079686	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8080194	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs859226	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs859228	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs859229	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs859230	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs859232	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs859233	0.85[EUR][1000 genomes]
rs859234	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs859236	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs859237	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs859238	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs859240	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs859247	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs859248	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs859252	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs859253	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs859255	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs859256	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs859257	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9893636	0.84[ASN][1000 genomes]
rs9894474	0.80[ASN][1000 genomes]
rs9901375	0.82[ASN][1000 genomes]
rs9903682	0.82[ASN][1000 genomes]
rs9907878	0.84[ASN][1000 genomes]
rs9912875	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 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	nsv1993	chr17:15759198-15799029	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv510700	chr17:15788617-15798726	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	esv1830799	chr17:15789513-15796959	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
13	esv1801208	chr17:15789804-15807280	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
14	esv1810041	chr17:15789804-15807280	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
15	esv1826171	chr17:15789804-15807280	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
16	esv1829876	chr17:15789804-15807280	Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
17	esv1811790	chr17:15790320-15807280	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15782600-15799000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr17:15790600-15797600	Weak transcription	Lung	lung
3	chr17:15790600-15800000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr17:15790800-15800800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr17:15795000-15798200	Enhancers	Pancreas	Pancrea
6	chr17:15795600-15797600	Enhancers	HepG2	liver
7	chr17:15795800-15797200	Enhancers	Fetal Kidney	kidney
8	chr17:15795800-15797400	Enhancers	NH-A	brain
9	chr17:15795800-15797600	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr17:15796000-15797000	Enhancers	Duodenum Smooth Muscle	Duodenum
11	chr17:15796000-15797200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr17:15796000-15797800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr17:15796000-15798000	Enhancers	K562	blood
14	chr17:15796000-15811600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr17:15796200-15797000	Enhancers	Esophagus	oesophagus
16	chr17:15796200-15797200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr17:15796200-15797200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr17:15796200-15797200	Enhancers	Fetal Heart	heart
19	chr17:15796200-15797400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr17:15796200-15797800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr17:15796200-15797800	Enhancers	HUVEC	blood vessel
22	chr17:15796200-15798000	Enhancers	Fetal Lung	lung
23	chr17:15796200-15798800	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr17:15796400-15797200	Enhancers	Colon Smooth Muscle	Colon
25	chr17:15796400-15797200	Enhancers	Osteobl	bone
26	chr17:15796400-15797400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr17:15796400-15797400	Weak transcription	Stomach Smooth Muscle	stomach
28	chr17:15796400-15797600	Weak transcription	Placenta	Placenta
29	chr17:15796400-15798600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr17:15796600-15797000	Weak transcription	Fetal Intestine Large	intestine
31	chr17:15796600-15797000	Weak transcription	Gastric	stomach
32	chr17:15796600-15797600	Enhancers	A549	lung
33	chr17:15796600-15801000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr17:15796800-15797000	Enhancers	Fetal Muscle Leg	muscle
35	chr17:15796800-15797200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
36	chr17:15796800-15797200	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr17:15796800-15797400	Enhancers	HUES6 Cell Line	embryonic stem cell

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