Variant report

Variant rs10937928
Chromosome Location chr4:3469458-3469459
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:3465800-3470000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr4:3466400-3482400 Weak transcription Right Atrium heart
3 chr4:3467000-3469600 Bivalent Enhancer Fetal Muscle Trunk muscle
4 chr4:3467000-3493600 Weak transcription Aorta Aorta
5 chr4:3467200-3469600 Enhancers Fetal Heart heart
6 chr4:3467200-3470400 Enhancers Fetal Muscle Leg muscle
7 chr4:3467600-3473000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr4:3468200-3469800 Weak transcription Pancreas Pancrea
9 chr4:3468600-3469800 Enhancers Left Ventricle heart
10 chr4:3468600-3470400 Weak transcription Spleen Spleen
11 chr4:3468600-3478400 Weak transcription HSMMtube muscle
12 chr4:3468800-3475000 Weak transcription Breast Myoepithelial Primary Cells Breast
13 chr4:3468800-3486400 Weak transcription Psoas Muscle Psoas
14 chr4:3469000-3470800 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
15 chr4:3469200-3469600 Flanking Active TSS Skeletal Muscle Male skeletal muscle
16 chr4:3469200-3469600 Flanking Active TSS Skeletal Muscle Female skeletal muscle
17 chr4:3469200-3473200 Enhancers Right Ventricle heart
18 chr4:3469400-3469800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
19 chr4:3469400-3470000 Weak transcription Gastric stomach
20 chr4:3469400-3472800 Genic enhancers HSMM muscle

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