Variant report

Variant	rs35258395
Chromosome Location	chr9:110709927-110709928
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110702200-110711000	Weak transcription	Fetal Intestine Large	intestine
2	chr9:110704000-110714000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr9:110707400-110712600	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr9:110708600-110710200	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr9:110709000-110710400	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr9:110709200-110710600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr9:110709400-110710600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr9:110709600-110710000	Enhancers	Small Intestine	intestine
9	chr9:110709600-110710600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr9:110709600-110710800	Enhancers	Pancreas	Pancrea
11	chr9:110709800-110710600	Weak transcription	Gastric	stomach
12	chr9:110709800-110710600	Weak transcription	Stomach Mucosa	stomach
13	chr9:110709800-110712400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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

what's new

Quick links