Variant report

Variant rs571973770
Chromosome Location chr14:104745986-104745987
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104736200-104746000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr14:104736800-104754800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr14:104741800-104751000 Enhancers Fetal Brain Male brain
4 chr14:104743000-104747800 Weak transcription Rectal Mucosa Donor 29 rectum
5 chr14:104743800-104747200 Enhancers Fetal Brain Female brain
6 chr14:104744400-104746600 Enhancers Brain Germinal Matrix brain
7 chr14:104744600-104746600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr14:104744600-104750000 Enhancers Fetal Lung lung
9 chr14:104745400-104746400 Bivalent Enhancer Fetal Stomach stomach
10 chr14:104745400-104751200 Enhancers Fetal Muscle Leg muscle
11 chr14:104745400-104752400 Bivalent Enhancer Fetal Muscle Trunk muscle
12 chr14:104745600-104746000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
13 chr14:104745600-104746200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr14:104745600-104746400 Enhancers Ovary ovary
15 chr14:104745800-104746000 Enhancers Colon Smooth Muscle Colon
16 chr14:104745800-104746000 Enhancers Hela-S3 cervix
17 chr14:104745800-104747800 Weak transcription Fetal Adrenal Gland Adrenal Gland

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