Variant report

Variant	rs17096290
Chromosome Location	chr10:119242379-119242380
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:119237600-119248600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr10:119238400-119247400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr10:119238600-119242600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr10:119239400-119252200	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr10:119240600-119243000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr10:119240800-119243600	Enhancers	NHDF-Ad	bronchial
7	chr10:119241200-119242400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr10:119241200-119242600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr10:119241800-119242400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr10:119242000-119243600	Enhancers	Esophagus	oesophagus

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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