Variant report

Variant rs188389268
Chromosome Location chr1:216982358-216982359
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:216979000-216986200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr1:216979400-216983000 Weak transcription Psoas Muscle Psoas
3 chr1:216979600-216983200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr1:216979800-216985000 Weak transcription Fetal Heart heart
5 chr1:216979800-216985200 Weak transcription Brain Substantia Nigra brain
6 chr1:216979800-216988800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
7 chr1:216979800-216989000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
8 chr1:216980000-216984800 Weak transcription Cortex derived primary cultured neurospheres brain
9 chr1:216980200-216986400 Weak transcription Fetal Muscle Leg muscle
10 chr1:216980200-216987400 Weak transcription HUES64 Cell Line embryonic stem cell
11 chr1:216980400-216988000 Weak transcription Skeletal Muscle Male skeletal muscle
12 chr1:216981200-216986000 Weak transcription HSMMtube muscle
13 chr1:216982000-216983000 Weak transcription Gastric stomach

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