Variant report

Variant rs536491648
Chromosome Location chr7:110162044-110162045
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:110155400-110162600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr7:110159800-110170400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr7:110160200-110163000 Weak transcription iPS-15b Cell Line embryonic stem cell
4 chr7:110160800-110163600 Enhancers HepG2 liver
5 chr7:110160800-110163800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
6 chr7:110161200-110162600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr7:110161200-110163200 Enhancers Fetal Adrenal Gland Adrenal Gland
8 chr7:110161400-110163400 Enhancers Fetal Intestine Large intestine
9 chr7:110161600-110162200 Flanking Active TSS Liver Liver
10 chr7:110161600-110162200 Enhancers Duodenum Mucosa Duodenum
11 chr7:110161600-110162800 Enhancers Brain Hippocampus Middle brain
12 chr7:110161600-110163200 Enhancers Pancreas Pancrea
13 chr7:110161600-110163400 Enhancers Rectal Mucosa Donor 31 rectum
14 chr7:110161600-110163600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
15 chr7:110161600-110163800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
16 chr7:110161800-110162200 Enhancers A549 lung
17 chr7:110161800-110163200 Enhancers Cortex derived primary cultured neurospheres brain
18 chr7:110161800-110163400 Enhancers HUES64 Cell Line embryonic stem cell
19 chr7:110161800-110163400 Enhancers Fetal Intestine Small intestine
20 chr7:110161800-110163600 Enhancers Fetal Heart heart
21 chr7:110162000-110162200 Flanking Active TSS Dnd41 blood
22 chr7:110162000-110162400 Enhancers Brain Substantia Nigra brain
23 chr7:110162000-110163000 Enhancers Pancreatic Islets Pancreatic Islet

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