Variant report

Variant	rs2885196
Chromosome Location	chr3:143618902-143618903
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143616800-143619600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr3:143617000-143619000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:143617000-143619600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr3:143617000-143619600	Weak transcription	NH-A	brain
5	chr3:143617200-143619200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr3:143617200-143619600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr3:143617200-143619600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr3:143617200-143619600	Weak transcription	HSMM	muscle
9	chr3:143617200-143619600	Weak transcription	NHEK	skin
10	chr3:143617200-143619600	Weak transcription	Osteobl	bone
11	chr3:143617600-143619400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr3:143617600-143619400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr3:143617600-143619600	Weak transcription	NHDF-Ad	bronchial
14	chr3:143618800-143619200	Weak transcription	HMEC	breast
15	chr3:143618800-143621400	Enhancers	NHLF	lung

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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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