Variant report

Variant rs564683789
Chromosome Location chr7:4215146-4215147
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 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 chr7:4191400-4215200 Weak transcription Aorta Aorta
6 chr7:4196400-4216000 Weak transcription Fetal Lung lung
7 chr7:4196400-4219600 Weak transcription Fetal Intestine Large intestine
8 chr7:4202000-4215200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
9 chr7:4207200-4216600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr7:4207800-4228800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr7:4212000-4220800 Weak transcription Fetal Intestine Small intestine
12 chr7:4212600-4216800 Strong transcription Pancreas Pancrea
13 chr7:4213200-4222200 Weak transcription Stomach Smooth Muscle stomach
14 chr7:4213600-4221000 Weak transcription Gastric stomach
15 chr7:4213800-4217400 Strong transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr7:4213800-4219400 Strong transcription Fetal Stomach stomach
17 chr7:4214000-4215600 Enhancers Esophagus oesophagus
18 chr7:4214200-4216200 Weak transcription Breast Myoepithelial Primary Cells Breast
19 chr7:4214400-4215400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
20 chr7:4214400-4215400 Strong transcription Spleen Spleen
21 chr7:4214800-4215400 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
22 chr7:4214800-4215600 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell

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