Variant report

Variant	rs17161562
Chromosome Location	chr5:108250768-108250769
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10036583	1.00[JPT][hapmap]
rs10037675	1.00[JPT][hapmap]
rs10039132	1.00[JPT][hapmap]
rs10039544	0.82[EUR][1000 genomes]
rs10039951	1.00[JPT][hapmap]
rs10041657	1.00[JPT][hapmap]
rs10042152	1.00[JPT][hapmap]
rs10042569	1.00[JPT][hapmap]
rs10050547	1.00[JPT][hapmap]
rs10052208	1.00[JPT][hapmap]
rs10052531	1.00[JPT][hapmap]
rs10054086	1.00[JPT][hapmap]
rs10061811	1.00[JPT][hapmap]
rs10064960	1.00[JPT][hapmap]
rs10065605	1.00[JPT][hapmap]
rs10065611	1.00[JPT][hapmap]
rs10070327	1.00[JPT][hapmap]
rs10072148	0.84[EUR][1000 genomes]
rs10077917	1.00[JPT][hapmap]
rs10477428	1.00[JPT][hapmap]
rs10477429	1.00[JPT][hapmap]
rs10477432	1.00[JPT][hapmap]
rs10477931	1.00[JPT][hapmap]
rs11741855	1.00[JPT][hapmap]
rs11748534	1.00[JPT][hapmap]
rs12719099	1.00[JPT][hapmap]
rs13358881	1.00[JPT][hapmap]
rs13359423	1.00[JPT][hapmap]
rs13360253	1.00[JPT][hapmap]
rs1396444	1.00[JPT][hapmap]
rs1423456	1.00[JPT][hapmap]
rs1423459	1.00[JPT][hapmap]
rs17161466	1.00[JPT][hapmap]
rs17161505	1.00[JPT][hapmap]
rs17161540	1.00[JPT][hapmap]
rs17161593	0.82[CHB][hapmap];0.85[JPT][hapmap]
rs17163941	1.00[JPT][hapmap]
rs17450138	0.82[CHB][hapmap];0.85[JPT][hapmap]
rs2009646	1.00[JPT][hapmap]
rs2081128	1.00[JPT][hapmap]
rs2113001	1.00[JPT][hapmap]
rs2229085	1.00[JPT][hapmap]
rs2900037	1.00[JPT][hapmap]
rs35141056	1.00[JPT][hapmap]
rs3805600	1.00[JPT][hapmap]
rs3805601	1.00[JPT][hapmap]
rs41508849	1.00[JPT][hapmap]
rs4358573	1.00[JPT][hapmap]
rs4361568	1.00[JPT][hapmap]
rs4479887	1.00[JPT][hapmap]
rs4560594	1.00[JPT][hapmap]
rs4560595	1.00[JPT][hapmap]
rs4957796	0.85[JPT][hapmap]
rs6594341	1.00[JPT][hapmap]
rs6869591	1.00[JPT][hapmap]
rs6873130	1.00[JPT][hapmap]
rs6873917	1.00[JPT][hapmap]
rs6884637	0.84[EUR][1000 genomes]
rs6888173	1.00[JPT][hapmap]
rs7711892	1.00[JPT][hapmap]
rs7715658	1.00[JPT][hapmap]
rs7719329	0.82[JPT][hapmap]
rs7720808	0.82[CHB][hapmap];0.85[JPT][hapmap]
rs7728920	1.00[JPT][hapmap]
rs889269	1.00[JPT][hapmap]
rs9326750	1.00[JPT][hapmap]
rs9326752	1.00[JPT][hapmap]
rs9326753	0.84[EUR][1000 genomes]
rs975056	0.82[CHB][hapmap];0.85[JPT][hapmap]
rs9885265	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882689	chr5:107595383-108299744	Enhancers ZNF genes & repeats Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv1016343	chr5:108220116-108364687	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv882691	chr5:108229760-108366473	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:108183800-108260400	Weak transcription	Ovary	ovary
2	chr5:108194600-108260000	Weak transcription	Fetal Intestine Large	intestine
3	chr5:108197000-108268200	Weak transcription	Fetal Muscle Trunk	muscle
4	chr5:108199200-108271400	Weak transcription	Aorta	Aorta
5	chr5:108203800-108323400	Weak transcription	Primary B cells from cord blood	blood
6	chr5:108208200-108268800	Weak transcription	Primary T cells from cord blood	blood
7	chr5:108214200-108272200	Weak transcription	Gastric	stomach
8	chr5:108217400-108253200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr5:108217600-108323200	Weak transcription	Left Ventricle	heart
10	chr5:108221400-108280600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr5:108229600-108269800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr5:108230200-108302400	Weak transcription	HSMM	muscle
13	chr5:108230600-108260000	Weak transcription	Fetal Intestine Small	intestine
14	chr5:108235000-108253200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr5:108235200-108252400	Weak transcription	NHEK	skin
16	chr5:108235200-108253000	Weak transcription	Adipose Nuclei	Adipose
17	chr5:108236800-108253400	Weak transcription	NH-A	brain
18	chr5:108240400-108252800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr5:108242200-108271000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr5:108242800-108252800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr5:108244200-108295000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr5:108246600-108251000	Weak transcription	Psoas Muscle	Psoas
23	chr5:108246800-108253000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr5:108247000-108252800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr5:108247200-108277600	Weak transcription	Fetal Lung	lung
26	chr5:108248400-108255400	Weak transcription	Stomach Mucosa	stomach
27	chr5:108249200-108253200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr5:108249600-108253000	Weak transcription	HMEC	breast
29	chr5:108250400-108255000	Weak transcription	Fetal Heart	heart
30	chr5:108250400-108277600	Weak transcription	Brain Hippocampus Middle	brain

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