Variant report

Variant rs139784546
Chromosome Location chr6:24323501-24323502
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:24316400-24326800 Weak transcription Pancreas Pancrea
2 chr6:24316600-24324800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr6:24319600-24323600 Enhancers HepG2 liver
4 chr6:24321800-24323800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
5 chr6:24322000-24324000 Weak transcription HSMMtube muscle
6 chr6:24322200-24324000 Weak transcription Fetal Intestine Small intestine
7 chr6:24322200-24324200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
8 chr6:24322200-24324800 Enhancers Fetal Kidney kidney
9 chr6:24322400-24323600 Weak transcription iPS-20b Cell Line embryonic stem cell
10 chr6:24322400-24323600 Weak transcription A549 lung
11 chr6:24322400-24325400 Enhancers HUES6 Cell Line embryonic stem cell
12 chr6:24322600-24325000 Weak transcription ES-WA7 Cell Line embryonic stem cell
13 chr6:24323200-24324400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
14 chr6:24323200-24325000 Enhancers NH-A brain
15 chr6:24323400-24323800 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
16 chr6:24323400-24324200 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
17 chr6:24323400-24324200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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