Variant report

Variant	rs10260677
Chromosome Location	chr7:25874991-25874992
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:25874523..25877275-chr7:25878833..25881768,2	K562	blood:

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10225976	0.95[ASN][1000 genomes]
rs10238703	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10241634	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10241659	0.91[ASN][1000 genomes]
rs10242536	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10245353	0.91[EUR][1000 genomes]
rs10262483	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10267498	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10271088	0.91[ASN][1000 genomes]
rs10271460	0.91[ASN][1000 genomes]
rs10274306	0.91[ASN][1000 genomes]
rs10282436	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1055144	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10951112	0.95[EUR][1000 genomes]
rs11770186	0.86[ASW][hapmap];1.00[CEU][hapmap];0.98[GIH][hapmap];0.91[JPT][hapmap];0.94[MEX][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12666961	1.00[CEU][hapmap];0.86[JPT][hapmap];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1451382	0.89[ASN][1000 genomes]
rs1451385	0.82[CEU][hapmap]
rs2391168	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28392961	0.91[EUR][1000 genomes]
rs28473292	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28858973	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2893220	0.91[ASN][1000 genomes]
rs2893221	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35766302	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4141278	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs41469349	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4722530	0.94[EUR][1000 genomes]
rs56376645	0.95[ASN][1000 genomes]
rs57246313	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs60643312	0.93[ASN][1000 genomes]
rs61140461	0.91[ASN][1000 genomes]
rs62447896	0.89[ASN][1000 genomes]
rs7782246	0.91[ASN][1000 genomes]
rs7782292	0.91[ASN][1000 genomes]
rs7798002	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7798130	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7798431	0.89[ASN][1000 genomes]
rs9987000	0.94[EUR][1000 genomes]

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	nsv1016813	chr7:25405859-26150509	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	108 gene(s)	inside rSNPs	diseases
2	nsv538803	chr7:25405859-26150509	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	108 gene(s)	inside rSNPs	diseases
3	nsv830928	chr7:25820147-25965014	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region lncRNA	11 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	chr7:25869600-25881800	Weak transcription	Right Atrium	heart
2	chr7:25871200-25885400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:25871800-25879400	Weak transcription	Psoas Muscle	Psoas
4	chr7:25872000-25876000	Weak transcription	Rectal Smooth Muscle	rectum
5	chr7:25872000-25881600	Weak transcription	Stomach Smooth Muscle	stomach
6	chr7:25872200-25881400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr7:25872200-25886200	Weak transcription	NHLF	lung
8	chr7:25872400-25885200	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr7:25873200-25876000	Weak transcription	Fetal Kidney	kidney
10	chr7:25873400-25876200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr7:25873600-25876600	Weak transcription	Aorta	Aorta
12	chr7:25873800-25875200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr7:25873800-25875400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr7:25874000-25879200	Weak transcription	Fetal Heart	heart
15	chr7:25874200-25875200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr7:25874400-25875000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr7:25874400-25875000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr7:25874400-25875000	Enhancers	Colon Smooth Muscle	Colon
19	chr7:25874400-25875200	Enhancers	NHEK	skin
20	chr7:25874400-25875400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr7:25874400-25875400	Enhancers	Muscle Satellite Cultured Cells	--
22	chr7:25874400-25875400	Enhancers	HSMM	muscle
23	chr7:25874600-25875000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr7:25874600-25875000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr7:25874600-25875000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr7:25874600-25875000	Enhancers	NHDF-Ad	bronchial
27	chr7:25874600-25875200	Enhancers	HMEC	breast
28	chr7:25874600-25875400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr7:25874600-25875400	Enhancers	Osteobl	bone
30	chr7:25874800-25875800	Weak transcription	Fetal Stomach	stomach

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