Variant report

Variant rs561391776
Chromosome Location chr14:104742974-104742975
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104734800-104745600 Weak transcription Ovary ovary
2 chr14:104736200-104746000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr14:104736800-104745600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr14:104736800-104754800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
5 chr14:104741400-104743400 Enhancers Fetal Stomach stomach
6 chr14:104741600-104743000 Enhancers Rectal Mucosa Donor 31 rectum
7 chr14:104741600-104743000 Flanking Active TSS Hela-S3 cervix
8 chr14:104741800-104751000 Enhancers Fetal Brain Male brain
9 chr14:104742200-104743000 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr14:104742200-104743000 Enhancers Rectal Mucosa Donor 29 rectum
11 chr14:104742200-104743400 Weak transcription Fetal Adrenal Gland Adrenal Gland
12 chr14:104742200-104743600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
13 chr14:104742600-104745800 Weak transcription Colon Smooth Muscle Colon
14 chr14:104742800-104743000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr14:104742800-104743000 Enhancers NHEK skin
16 chr14:104742800-104743600 Weak transcription Fetal Brain Female brain
17 chr14:104742800-104743800 Bivalent Enhancer Fetal Muscle Leg muscle
18 chr14:104742800-104744600 Weak transcription Fetal Lung lung

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