Variant report

Variant rs11102631
Chromosome Location chr1:113973622-113973623
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:113940200-113987000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr1:113964400-113974200 Weak transcription A549 lung
3 chr1:113966800-113986600 Weak transcription Fetal Intestine Small intestine
4 chr1:113967400-113977400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
5 chr1:113970000-113986600 Weak transcription Esophagus oesophagus
6 chr1:113972000-113973800 Enhancers Liver Liver
7 chr1:113972200-113976800 Weak transcription Right Atrium heart
8 chr1:113972400-113973800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
9 chr1:113972600-113976800 Weak transcription Left Ventricle heart
10 chr1:113972600-113980600 Weak transcription Psoas Muscle Psoas
11 chr1:113973200-113976000 Weak transcription HepG2 liver
12 chr1:113973400-113975800 Weak transcription Pancreatic Islets Pancreatic Islet
13 chr1:113973400-113975800 Weak transcription Stomach Mucosa stomach
14 chr1:113973600-113974000 Enhancers Gastric stomach
15 chr1:113973600-113974000 Enhancers Pancreas Pancrea

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