Variant report

Variant	rs190171559
Chromosome Location	chr4:166553486-166553487
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830141	chr4:166502908-166689626	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1028337	chr4:166544699-166659468	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv537338	chr4:166544699-166659468	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv3448287	chr4:166553452-166556850	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:166545200-166555200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:166551800-166553600	Enhancers	Muscle Satellite Cultured Cells	--
3	chr4:166551800-166553800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr4:166551800-166554000	Enhancers	HMEC	breast
5	chr4:166552000-166553600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr4:166552000-166553600	Enhancers	Fetal Heart	heart
7	chr4:166552000-166554000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:166552200-166554000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr4:166552400-166554000	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr4:166552600-166553600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:166552600-166554000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr4:166552800-166554000	Enhancers	Fetal Stomach	stomach
13	chr4:166553000-166553600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr4:166553200-166553600	Enhancers	Rectal Smooth Muscle	rectum
15	chr4:166553200-166554000	Enhancers	Psoas Muscle	Psoas
16	chr4:166553400-166553600	Enhancers	NHEK	skin
17	chr4:166553400-166555800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr4:166553400-166556400	Weak transcription	Fetal Thymus	thymus
19	chr4:166553400-166556600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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