Variant report

Variant rs9316359
Chromosome Location chr13:48695831-48695832
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:48686600-48700000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr13:48691200-48698400 Weak transcription Adipose Nuclei Adipose
3 chr13:48692200-48697800 Weak transcription HepG2 liver
4 chr13:48694800-48696200 Enhancers Duodenum Mucosa Duodenum
5 chr13:48695000-48696200 Enhancers Fetal Kidney kidney
6 chr13:48695200-48696400 Enhancers Fetal Heart heart
7 chr13:48695400-48696400 Enhancers Small Intestine intestine
8 chr13:48695400-48696600 Enhancers Colon Smooth Muscle Colon
9 chr13:48695600-48696400 Flanking Active TSS Stomach Smooth Muscle stomach
10 chr13:48695800-48696000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr13:48695800-48696000 Enhancers Ovary ovary
12 chr13:48695800-48696000 Enhancers Rectal Mucosa Donor 31 rectum
13 chr13:48695800-48696000 Enhancers Right Ventricle heart
14 chr13:48695800-48696000 Enhancers Sigmoid Colon Sigmoid Colon
15 chr13:48695800-48696000 Enhancers HSMMtube muscle
16 chr13:48695800-48696200 Enhancers ES-I3 Cell Line embryonic stem cell
17 chr13:48695800-48696200 Enhancers Right Atrium heart
18 chr13:48695800-48696400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
19 chr13:48695800-48696400 Enhancers Rectal Smooth Muscle rectum
20 chr13:48695800-48698000 Weak transcription Fetal Adrenal Gland Adrenal Gland
21 chr13:48695800-48699600 Weak transcription HUVEC blood vessel
22 chr13:48695800-48700000 Weak transcription Duodenum Smooth Muscle Duodenum
23 chr13:48695800-48701200 Weak transcription Fetal Intestine Small intestine

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