Variant report

Variant	rs17100317
Chromosome Location	chr1:77788462-77788463
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	chr1:77786657..77790465-chr1:77794165..77797983,5	K562	blood:
2	chr1:77781240..77784199-chr1:77786063..77789429,3	K562	blood:

Extended variants
information (count: 115 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:107)

rs_ID	r²[population]
rs10493536	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10493537	0.80[AMR][1000 genomes]
rs10493602	1.00[CEU][hapmap];0.92[CHB][hapmap];0.85[JPT][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10873932	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11162312	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11162317	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11162319	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1167198	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1167205	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12057706	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12059542	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12061595	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12062754	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs12070404	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12070567	1.00[CEU][hapmap];0.92[CHB][hapmap];0.92[JPT][hapmap];0.87[EUR][1000 genomes]
rs12071077	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12072100	0.83[ASN][1000 genomes]
rs12076479	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12079185	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12079206	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12079234	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12079316	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12088702	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12089562	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12097728	0.83[ASN][1000 genomes]
rs1502526	0.82[CEU][hapmap]
rs1615404	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1616272	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1670611	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1670612	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1670614	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1670617	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1670618	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17098286	0.83[TSI][hapmap]
rs17099982	0.82[CEU][hapmap]
rs17099983	1.00[ASW][hapmap];0.82[CEU][hapmap]
rs17099986	0.82[CEU][hapmap]
rs17100001	0.82[CEU][hapmap]
rs17100002	0.82[CEU][hapmap]
rs17100005	0.82[CEU][hapmap]
rs17100021	0.82[CEU][hapmap]
rs17100075	1.00[AFR][1000 genomes]
rs17100133	0.80[AMR][1000 genomes]
rs17100172	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17100185	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17100198	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17100204	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17100319	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17100422	1.00[CEU][hapmap];0.92[CHB][hapmap];0.93[JPT][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17100440	1.00[CEU][hapmap];0.92[CHB][hapmap];0.93[JPT][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1721163	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1721164	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1721165	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1721168	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1779177	0.81[CHB][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1779178	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1779180	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1779181	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1966873	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2054017	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2054018	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2054019	0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2154090	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2602953	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2799551	0.95[ASN][1000 genomes]
rs2799552	0.84[ASN][1000 genomes]
rs2799553	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2815313	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28476720	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28605112	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2996486	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3962875	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.83[TSI][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4033035	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.83[TSI][hapmap];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4033036	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4033037	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs41292262	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4949653	0.92[CHB][hapmap];0.93[JPT][hapmap]
rs60401394	0.83[ASN][1000 genomes]
rs6661765	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6665543	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6668328	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6669724	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6680763	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6683829	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[MEX][hapmap];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6685087	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6691415	0.84[CHB][hapmap];0.93[JPT][hapmap];0.85[ASN][1000 genomes]
rs6693999	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6698996	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6703688	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs721514	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72677859	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72677889	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72679506	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72679513	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72679514	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72679531	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72679538	0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72679540	0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72679542	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7367731	0.84[ASN][1000 genomes]
rs7511768	1.00[CEU][hapmap];0.91[CHB][hapmap];0.92[JPT][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7517796	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7529083	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7531431	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7534033	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7537603	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7545096	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005183	chr1:77728990-77949309	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv535010	chr1:77728990-77949309	Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv932557	chr1:77730247-77958687	Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1003714	chr1:77756861-77949309	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv470719	chr1:77774413-78269207	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
6	nsv546591	chr1:77774413-78269207	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
7	esv2756848	chr1:77775014-77788462	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	esv2758945	chr1:77775014-77788462	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77774000-77790400	Weak transcription	Brain Substantia Nigra	brain
2	chr1:77777000-77794600	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr1:77779400-77794400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr1:77779600-77794600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr1:77781400-77790000	Enhancers	NHDF-Ad	bronchial
6	chr1:77785000-77789800	Enhancers	Muscle Satellite Cultured Cells	--
7	chr1:77785200-77789600	Weak transcription	Brain Anterior Caudate	brain
8	chr1:77785200-77794400	Weak transcription	Primary T cells from cord blood	blood
9	chr1:77785200-77799200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr1:77786800-77789000	Enhancers	NHLF	lung
11	chr1:77786800-77790400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr1:77787200-77788600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr1:77787200-77790600	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr1:77787400-77788600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr1:77787400-77788600	Enhancers	NH-A	brain
16	chr1:77787400-77789000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr1:77787600-77788600	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr1:77787600-77788800	Enhancers	NHEK	skin
19	chr1:77787600-77789200	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr1:77787600-77790600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr1:77787800-77788600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr1:77787800-77788600	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr1:77787800-77788600	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr1:77787800-77788600	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr1:77787800-77788600	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr1:77787800-77788600	Enhancers	Brain Angular Gyrus	brain
27	chr1:77787800-77788600	Enhancers	HepG2	liver
28	chr1:77787800-77788800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr1:77787800-77788800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr1:77787800-77789000	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr1:77787800-77789000	Enhancers	Brain Cingulate Gyrus	brain
32	chr1:77787800-77790600	Enhancers	Brain Hippocampus Middle	brain
33	chr1:77788000-77788600	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr1:77788000-77788600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr1:77788000-77788600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr1:77788000-77788600	Enhancers	HMEC	breast
37	chr1:77788000-77788600	Enhancers	HSMM	muscle
38	chr1:77788000-77788600	Enhancers	K562	blood
39	chr1:77788200-77788600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr1:77788200-77788600	Flanking Active TSS	A549	lung
41	chr1:77788200-77788600	Enhancers	Hela-S3	cervix
42	chr1:77788200-77788600	Enhancers	HSMMtube	muscle
43	chr1:77788200-77788800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr1:77788400-77788600	Enhancers	Osteobl	bone
45	chr1:77788400-77789000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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