Variant report

Variant rs11206935
Chromosome Location chr1:57385076-57385077
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:57377800-57386000 Weak transcription NHDF-Ad bronchial
2 chr1:57382200-57390200 Weak transcription Right Ventricle heart
3 chr1:57383000-57386200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr1:57383200-57390800 Weak transcription iPS-18 Cell Line embryonic stem cell
5 chr1:57383400-57385400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr1:57383400-57386200 Weak transcription Gastric stomach
7 chr1:57383600-57386000 Weak transcription Fetal Muscle Leg muscle
8 chr1:57383600-57386200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
9 chr1:57383600-57386200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
10 chr1:57383600-57386400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
11 chr1:57384200-57387400 Enhancers Liver Liver
12 chr1:57384600-57385400 Enhancers Fetal Intestine Large intestine
13 chr1:57384600-57385400 Enhancers Fetal Kidney kidney
14 chr1:57384600-57386600 Enhancers Pancreas Pancrea
15 chr1:57384800-57385400 Enhancers Fetal Intestine Small intestine
16 chr1:57385000-57385400 Flanking Active TSS HepG2 liver
17 chr1:57385000-57385600 Enhancers Pancreatic Islets Pancreatic Islet
18 chr1:57385000-57385800 Enhancers Duodenum Mucosa Duodenum

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