Variant report

Variant rs4886928
Chromosome Location chr15:78124923-78124924
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:78119800-78126800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr15:78122200-78125600 Enhancers Fetal Stomach stomach
3 chr15:78123600-78128000 Weak transcription Fetal Brain Male brain
4 chr15:78124200-78125000 Bivalent Enhancer Fetal Intestine Large intestine
5 chr15:78124200-78125200 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr15:78124200-78125400 Enhancers Fetal Lung lung
7 chr15:78124400-78125200 Enhancers Fetal Intestine Small intestine
8 chr15:78124400-78125200 Bivalent Enhancer Fetal Muscle Leg muscle
9 chr15:78124400-78125600 Enhancers Fetal Muscle Trunk muscle
10 chr15:78124400-78126000 Enhancers Fetal Thymus thymus
11 chr15:78124600-78128600 Weak transcription Fetal Brain Female brain
12 chr15:78124800-78125400 Enhancers Fetal Adrenal Gland Adrenal Gland
13 chr15:78124800-78125600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr15:78124800-78126200 Enhancers Primary hematopoietic stem cells short term culture blood
15 chr15:78124800-78132800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell

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