Variant report

Variant	rs62305515
Chromosome Location	chr4:86860504-86860505
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs189395	0.85[ASN][1000 genomes]
rs189396	0.91[ASN][1000 genomes]
rs2043647	0.91[ASN][1000 genomes]
rs2136782	0.91[ASN][1000 genomes]
rs2575681	0.82[ASN][1000 genomes]
rs2575682	0.82[ASN][1000 genomes]
rs2665869	0.91[ASN][1000 genomes]
rs2665876	0.89[ASN][1000 genomes]
rs346469	0.86[ASN][1000 genomes]
rs346470	0.86[ASN][1000 genomes]
rs346472	0.82[ASN][1000 genomes]
rs346473	0.82[ASN][1000 genomes]
rs346477	0.82[ASN][1000 genomes]
rs346482	0.89[ASN][1000 genomes]
rs346483	0.82[ASN][1000 genomes]
rs346486	0.89[ASN][1000 genomes]
rs346487	0.89[ASN][1000 genomes]
rs346489	0.89[ASN][1000 genomes]
rs346490	0.89[ASN][1000 genomes]
rs346491	0.89[ASN][1000 genomes]
rs346493	0.89[ASN][1000 genomes]
rs346494	0.89[ASN][1000 genomes]
rs346495	0.91[ASN][1000 genomes]
rs346496	0.91[ASN][1000 genomes]
rs346501	0.84[ASN][1000 genomes]
rs62305513	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62305514	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62305516	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	nsv830000	chr4:86745341-86909059	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv879519	chr4:86786204-86871282	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv879520	chr4:86829529-86918232	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:86851200-86863200	Weak transcription	Psoas Muscle	Psoas
2	chr4:86851400-86861600	Weak transcription	Primary B cells from peripheral blood	blood
3	chr4:86851400-86865800	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr4:86851400-86874600	Weak transcription	HSMMtube	muscle
5	chr4:86851600-86870000	Weak transcription	HSMM	muscle
6	chr4:86851600-86874800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr4:86853800-86864400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:86854000-86867400	Weak transcription	Fetal Lung	lung
9	chr4:86854000-86874200	Weak transcription	Fetal Stomach	stomach
10	chr4:86854000-86893000	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr4:86854200-86863000	Weak transcription	HUVEC	blood vessel
12	chr4:86854200-86863200	Weak transcription	Pancreas	Pancrea
13	chr4:86854200-86880200	Weak transcription	Gastric	stomach
14	chr4:86854200-86893000	Weak transcription	Fetal Muscle Trunk	muscle
15	chr4:86854200-86915800	Weak transcription	Left Ventricle	heart
16	chr4:86854400-86860800	Weak transcription	Adipose Nuclei	Adipose
17	chr4:86854600-86863000	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr4:86854800-86863200	Weak transcription	Fetal Muscle Leg	muscle
19	chr4:86856000-86863200	Weak transcription	Right Atrium	heart
20	chr4:86858400-86863600	Enhancers	Fetal Kidney	kidney
21	chr4:86858800-86876600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr4:86859600-86861000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:86859600-86861200	Weak transcription	Stomach Mucosa	stomach
24	chr4:86859600-86874200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr4:86859800-86860600	Enhancers	Liver	Liver
26	chr4:86860000-86861600	Enhancers	Ovary	ovary
27	chr4:86860200-86867400	Weak transcription	Primary B cells from cord blood	blood
28	chr4:86860400-86861000	Active TSS	NHDF-Ad	bronchial
29	chr4:86860400-86861200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr4:86860400-86861400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr4:86860400-86861600	Active TSS	Pancreatic Islets	Pancreatic Islet
32	chr4:86860400-86861800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr4:86860400-86863200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr4:86860400-86867600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr4:86860400-86874800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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