Variant report

Variant	rs185813531
Chromosome Location	chr6:150581424-150581425
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830843	chr6:150517411-150691173	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	esv2763602	chr6:150581193-150720666	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150574800-150590800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:150577400-150585200	Weak transcription	Right Ventricle	heart
3	chr6:150577400-150585400	Weak transcription	Left Ventricle	heart
4	chr6:150577400-150588200	Weak transcription	Psoas Muscle	Psoas
5	chr6:150578000-150589000	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr6:150578400-150588000	Weak transcription	NH-A	brain
7	chr6:150579200-150587600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr6:150579400-150584200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr6:150579400-150587200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr6:150579400-150587200	Weak transcription	NHEK	skin
11	chr6:150580200-150581600	Enhancers	K562	blood
12	chr6:150580400-150590800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr6:150580600-150586000	Enhancers	Fetal Heart	heart
14	chr6:150580600-150587000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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