Variant report

Variant	rs181723969
Chromosome Location	chr6:13877194-13877195
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3421604	chr6:13877064-13877269	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13874400-13877200	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr6:13874600-13877200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr6:13874600-13877200	Weak transcription	NH-A	brain
4	chr6:13874600-13877200	Weak transcription	Osteobl	bone
5	chr6:13874600-13877400	Weak transcription	HMEC	breast
6	chr6:13874600-13878600	Weak transcription	Esophagus	oesophagus
7	chr6:13874800-13877200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr6:13874800-13877200	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr6:13874800-13881800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr6:13875000-13877200	Weak transcription	K562	blood
11	chr6:13875000-13880400	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr6:13876800-13877800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:13877000-13877600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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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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