Variant report

Variant	rs61386675
Chromosome Location	chr4:86795926-86795927
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 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	esv3376337	chr4:86795153-86797901	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
4	esv3448281	chr4:86795328-86797751	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
5	esv3354642	chr4:86795628-86797526	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
6	esv2565886	chr4:86795761-86797344	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
7	esv3358909	chr4:86795874-86795988	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:86750000-86809200	Weak transcription	Fetal Muscle Trunk	muscle
2	chr4:86779800-86800200	Weak transcription	Primary B cells from cord blood	blood
3	chr4:86788000-86797000	Weak transcription	Ovary	ovary
4	chr4:86788000-86804000	Weak transcription	Aorta	Aorta
5	chr4:86788000-86807400	Weak transcription	Left Ventricle	heart
6	chr4:86788000-86810800	Weak transcription	Primary B cells from peripheral blood	blood
7	chr4:86788000-86812400	Weak transcription	HSMM	muscle
8	chr4:86788200-86812000	Weak transcription	Fetal Muscle Leg	muscle
9	chr4:86790800-86835400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr4:86791000-86803600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr4:86791000-86804200	Weak transcription	HSMMtube	muscle
12	chr4:86791200-86844400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr4:86791600-86802000	Weak transcription	NHDF-Ad	bronchial
14	chr4:86794600-86804800	Weak transcription	HUVEC	blood vessel
15	chr4:86794800-86805600	Weak transcription	Pancreas	Pancrea
16	chr4:86795800-86796800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr4:86795800-86797000	Weak transcription	Stomach Mucosa	stomach

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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