Variant report

Variant	rs17528257
Chromosome Location	chr5:58538848-58538849
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:58532712..58534586-chr5:58538179..58539997,2	K562	blood:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10036406	0.81[CEU][hapmap];1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs10038599	0.84[CEU][hapmap];1.00[CHB][hapmap];0.80[JPT][hapmap]
rs10055446	0.89[CEU][hapmap];1.00[CHB][hapmap];0.80[JPT][hapmap];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10059709	0.88[CHB][hapmap];0.91[EUR][1000 genomes]
rs10061600	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10061786	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10064893	0.90[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10068836	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10070294	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10070436	0.91[CEU][hapmap];1.00[CHB][hapmap];0.80[JPT][hapmap];0.89[ASN][1000 genomes]
rs10075364	0.98[ASN][1000 genomes]
rs10440630	0.89[CHB][hapmap]
rs11740402	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11747413	1.00[CEU][hapmap];1.00[CHB][hapmap];0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13328160	1.00[CHB][hapmap];0.85[JPT][hapmap]
rs13328226	1.00[CHB][hapmap];0.85[JPT][hapmap];0.88[ASN][1000 genomes]
rs13354210	0.82[CEU][hapmap]
rs13360907	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17444059	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs17528285	0.90[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17528473	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs17780740	0.81[CEU][hapmap]
rs2112959	1.00[CHB][hapmap];0.85[JPT][hapmap];0.88[ASN][1000 genomes]
rs28529077	0.98[ASN][1000 genomes]
rs28647633	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60453299	1.00[ASN][1000 genomes]
rs6861842	1.00[YRI][hapmap]
rs6881054	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs6888386	0.82[AFR][1000 genomes]
rs72765932	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72765942	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72765953	0.98[ASN][1000 genomes]
rs72765961	0.98[ASN][1000 genomes]
rs7717248	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2830363	chr5:57893949-58555491	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv598252	chr5:58487764-58618889	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv881703	chr5:58517918-58540847	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1025807	chr5:58520050-58548231	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv520721	chr5:58520735-58558388	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:58527400-58549800	Weak transcription	Aorta	Aorta
2	chr5:58532600-58540800	Weak transcription	Fetal Muscle Leg	muscle
3	chr5:58532600-58541000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr5:58533200-58540800	Weak transcription	HSMMtube	muscle
5	chr5:58533600-58541000	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr5:58535400-58539000	Enhancers	Colon Smooth Muscle	Colon
7	chr5:58535400-58541000	Weak transcription	Fetal Intestine Large	intestine
8	chr5:58535600-58540800	Weak transcription	Brain Hippocampus Middle	brain
9	chr5:58535600-58540800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr5:58535600-58541000	Weak transcription	Right Ventricle	heart
11	chr5:58535600-58551800	Weak transcription	HUVEC	blood vessel
12	chr5:58537200-58540800	Weak transcription	Fetal Intestine Small	intestine
13	chr5:58537200-58540800	Weak transcription	Right Atrium	heart
14	chr5:58537200-58541000	Weak transcription	Osteobl	bone
15	chr5:58537200-58541400	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr5:58537200-58542600	Weak transcription	Fetal Kidney	kidney
17	chr5:58537400-58540800	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr5:58537400-58541000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr5:58537400-58542200	Weak transcription	Brain Cingulate Gyrus	brain
20	chr5:58537400-58543600	Weak transcription	Left Ventricle	heart
21	chr5:58537600-58540800	Weak transcription	Brain Angular Gyrus	brain
22	chr5:58537600-58541000	Weak transcription	Fetal Heart	heart
23	chr5:58537600-58548600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr5:58537600-58553000	Weak transcription	Duodenum Mucosa	Duodenum
25	chr5:58537800-58540800	Weak transcription	Adipose Nuclei	Adipose
26	chr5:58537800-58541000	Weak transcription	Brain Substantia Nigra	brain
27	chr5:58537800-58542600	Weak transcription	Hela-S3	cervix
28	chr5:58538000-58541000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr5:58538200-58540800	Weak transcription	Fetal Lung	lung
30	chr5:58538400-58539000	Genic enhancers	A549	lung
31	chr5:58538400-58541000	Weak transcription	Psoas Muscle	Psoas
32	chr5:58538600-58539000	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr5:58538600-58541000	Weak transcription	Rectal Smooth Muscle	rectum
34	chr5:58538800-58539000	Enhancers	Small Intestine	intestine
35	chr5:58538800-58540800	Weak transcription	Skeletal Muscle Male	skeletal muscle

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