Variant report

Variant rs76003397
Chromosome Location chr15:42173313-42173314
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:42138200-42173400 Weak transcription Right Atrium heart
2 chr15:42141200-42191200 Weak transcription Aorta Aorta
3 chr15:42148200-42174400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
4 chr15:42157400-42179200 Weak transcription HSMMtube muscle
5 chr15:42163200-42174000 Weak transcription Placenta Amnion Placenta Amnion
6 chr15:42165400-42184800 Weak transcription HMEC breast
7 chr15:42168600-42173400 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr15:42168800-42173400 Weak transcription Gastric stomach
9 chr15:42169400-42173600 Weak transcription Fetal Heart heart
10 chr15:42169400-42173800 Weak transcription Pancreas Pancrea
11 chr15:42169600-42174000 Enhancers Esophagus oesophagus
12 chr15:42170200-42173800 Weak transcription Lung lung
13 chr15:42171000-42173600 Weak transcription Right Ventricle heart
14 chr15:42171000-42173600 Weak transcription Skeletal Muscle Female skeletal muscle
15 chr15:42172000-42178400 Enhancers Liver Liver
16 chr15:42172400-42173600 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
17 chr15:42172600-42174000 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
18 chr15:42172600-42175800 Strong transcription HUVEC blood vessel
19 chr15:42173000-42173600 Active TSS Spleen Spleen
20 chr15:42173000-42174000 Strong transcription HSMM muscle
21 chr15:42173000-42174400 Bivalent Enhancer Stomach Smooth Muscle stomach
22 chr15:42173200-42173600 Genic enhancers H1 Derived Mesenchymal Stem Cells ES cell derived

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