Variant report

Variant rs4945207
Chromosome Location chr11:71460555-71460556
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:71451000-71464200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
2 chr11:71459400-71461600 Enhancers Duodenum Mucosa Duodenum
3 chr11:71459400-71462000 Enhancers Fetal Intestine Small intestine
4 chr11:71459600-71460600 Enhancers iPS-20b Cell Line embryonic stem cell
5 chr11:71459600-71461400 Enhancers Fetal Intestine Large intestine
6 chr11:71459600-71461600 Enhancers HUES6 Cell Line embryonic stem cell
7 chr11:71459800-71460800 Enhancers HUES64 Cell Line embryonic stem cell
8 chr11:71460200-71460600 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
9 chr11:71460200-71460600 Enhancers iPS-18 Cell Line embryonic stem cell
10 chr11:71460200-71460800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr11:71460200-71460800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
12 chr11:71460200-71460800 Enhancers HUES48 Cell Line embryonic stem cell
13 chr11:71460200-71460800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
14 chr11:71460200-71460800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr11:71460200-71460800 Enhancers Fetal Adrenal Gland Adrenal Gland
16 chr11:71460400-71460800 Flanking Active TSS K562 blood

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