Variant report

Variant rs549859156
Chromosome Location chr14:104746136-104746137
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104736800-104754800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr14:104741800-104751000 Enhancers Fetal Brain Male brain
3 chr14:104743000-104747800 Weak transcription Rectal Mucosa Donor 29 rectum
4 chr14:104743800-104747200 Enhancers Fetal Brain Female brain
5 chr14:104744400-104746600 Enhancers Brain Germinal Matrix brain
6 chr14:104744600-104746600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr14:104744600-104750000 Enhancers Fetal Lung lung
8 chr14:104745400-104746400 Bivalent Enhancer Fetal Stomach stomach
9 chr14:104745400-104751200 Enhancers Fetal Muscle Leg muscle
10 chr14:104745400-104752400 Bivalent Enhancer Fetal Muscle Trunk muscle
11 chr14:104745600-104746200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr14:104745600-104746400 Enhancers Ovary ovary
13 chr14:104745800-104747800 Weak transcription Fetal Adrenal Gland Adrenal Gland
14 chr14:104746000-104746200 Flanking Active TSS Hela-S3 cervix
15 chr14:104746000-104746800 Active TSS H1 Derived Mesenchymal Stem Cells ES cell derived
16 chr14:104746000-104750000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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