Variant report

Variant rs538279228
Chromosome Location chr7:4215260-4215261
allele C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:24 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:4169200-4228200 Weak transcription Pancreatic Islets Pancreatic Islet
2 chr7:4185000-4227800 Weak transcription Cortex derived primary cultured neurospheres brain
3 chr7:4189200-4217000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
4 chr7:4189600-4228400 Weak transcription Fetal Brain Female brain
5 chr7:4196400-4216000 Weak transcription Fetal Lung lung
6 chr7:4196400-4219600 Weak transcription Fetal Intestine Large intestine
7 chr7:4207200-4216600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
8 chr7:4207800-4228800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr7:4212000-4220800 Weak transcription Fetal Intestine Small intestine
10 chr7:4212600-4216800 Strong transcription Pancreas Pancrea
11 chr7:4213200-4222200 Weak transcription Stomach Smooth Muscle stomach
12 chr7:4213600-4221000 Weak transcription Gastric stomach
13 chr7:4213800-4217400 Strong transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr7:4213800-4219400 Strong transcription Fetal Stomach stomach
15 chr7:4214000-4215600 Enhancers Esophagus oesophagus
16 chr7:4214200-4216200 Weak transcription Breast Myoepithelial Primary Cells Breast
17 chr7:4214400-4215400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr7:4214400-4215400 Strong transcription Spleen Spleen
19 chr7:4214800-4215400 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
20 chr7:4214800-4215600 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
21 chr7:4215200-4215400 Bivalent Enhancer Fetal Muscle Trunk muscle
22 chr7:4215200-4215600 Strong transcription H9 Derived Neuron Cultured Cells ES cell derived
23 chr7:4215200-4215600 Strong transcription Aorta Aorta
24 chr7:4215200-4215600 Bivalent Enhancer Fetal Muscle Leg muscle

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