Variant report

Variant	rs12253715
Chromosome Location	chr10:118542443-118542444
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:118531400-118547200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr10:118534800-118547400	Weak transcription	Esophagus	oesophagus
3	chr10:118538600-118547200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr10:118539000-118542600	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr10:118539000-118547400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr10:118539400-118542600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr10:118539600-118546600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr10:118540600-118542600	Weak transcription	HSMM	muscle
9	chr10:118541000-118542600	Weak transcription	Osteobl	bone
10	chr10:118541200-118542600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr10:118541200-118542800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr10:118542000-118543200	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr10:118542000-118543200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr10:118542200-118543200	Enhancers	HMEC	breast
15	chr10:118542400-118543000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr10:118542400-118543400	Enhancers	HSMMtube	muscle
17	chr10:118542400-118543800	Enhancers	Breast Myoepithelial Primary Cells	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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