Variant report

Variant	rs2897244
Chromosome Location	chr5:119723294-119723295
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	chr5:119721254..119725042-chr5:119751252..119754462,3	K562	blood:
2	chr5:119719801..119721845-chr5:119723016..119725406,2	K562	blood:

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10036322	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10036536	0.90[EUR][1000 genomes]
rs10052468	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10058597	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10059974	0.83[EUR][1000 genomes]
rs10072828	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1108712	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13158141	0.84[EUR][1000 genomes]
rs13161485	0.84[EUR][1000 genomes]
rs13171950	0.83[AMR][1000 genomes]
rs13172224	0.83[EUR][1000 genomes]
rs13357775	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13435941	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1347070	0.95[CEU][hapmap];0.83[EUR][1000 genomes]
rs1368182	0.85[CEU][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1368189	0.95[CEU][hapmap];0.85[EUR][1000 genomes]
rs1368191	0.90[EUR][1000 genomes]
rs1394115	0.86[EUR][1000 genomes]
rs1432454	0.90[EUR][1000 genomes]
rs1432456	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1432457	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1432458	0.83[EUR][1000 genomes]
rs1432464	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17146485	0.85[EUR][1000 genomes]
rs17146501	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17422462	1.00[ASN][1000 genomes]
rs1835870	0.85[EUR][1000 genomes]
rs2082356	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2116606	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35399227	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4499860	0.83[EUR][1000 genomes]
rs4895246	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4895247	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4895248	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4895249	0.88[EUR][1000 genomes]
rs4895250	0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs58274987	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs59264625	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59336675	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6595225	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6595232	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6863943	0.82[EUR][1000 genomes]
rs6865215	0.95[CEU][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6895493	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6896794	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6899092	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72784177	0.83[EUR][1000 genomes]
rs7446731	0.84[EUR][1000 genomes]
rs753641	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7709140	0.81[EUR][1000 genomes]
rs7713691	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7714965	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7718509	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7722765	0.81[EUR][1000 genomes]
rs7727978	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9327141	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs982827	0.82[AMR][1000 genomes];0.83[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	nsv532200	chr5:119317901-120102513	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1018955	chr5:119679918-119802014	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv527509	chr5:119697716-119724069	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:119721000-119725800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr5:119721000-119725800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr5:119721200-119725800	Enhancers	NHDF-Ad	bronchial
4	chr5:119721600-119723800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr5:119722400-119723400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr5:119722400-119723400	Enhancers	Aorta	Aorta
7	chr5:119722400-119723400	Flanking Active TSS	Dnd41	blood
8	chr5:119722400-119724600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr5:119722400-119724800	Enhancers	HSMM	muscle
10	chr5:119722400-119725000	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr5:119722400-119725200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr5:119722400-119725600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr5:119722400-119725600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr5:119722400-119725800	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr5:119722400-119725800	Enhancers	Primary hematopoietic stem cells	blood
16	chr5:119722400-119726000	Enhancers	Muscle Satellite Cultured Cells	--
17	chr5:119722600-119724800	Enhancers	HMEC	breast
18	chr5:119722600-119725000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr5:119722600-119725000	Enhancers	NHLF	lung
20	chr5:119722800-119724600	Enhancers	Hela-S3	cervix
21	chr5:119722800-119725000	Enhancers	Osteobl	bone
22	chr5:119722800-119727400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr5:119723000-119723400	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr5:119723000-119724800	Enhancers	HUVEC	blood vessel
25	chr5:119723000-119725000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr5:119723200-119723400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr5:119723200-119724200	Enhancers	NHEK	skin
28	chr5:119723200-119724800	Enhancers	NH-A	brain
29	chr5:119723200-119725000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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