Variant report

Variant rs571651167
Chromosome Location chr1:216983087-216983088
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 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 chr1:216979600-216983200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr1:216979800-216985000 Weak transcription Fetal Heart heart
4 chr1:216979800-216985200 Weak transcription Brain Substantia Nigra brain
5 chr1:216979800-216988800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
6 chr1:216979800-216989000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr1:216980000-216984800 Weak transcription Cortex derived primary cultured neurospheres brain
8 chr1:216980200-216986400 Weak transcription Fetal Muscle Leg muscle
9 chr1:216980200-216987400 Weak transcription HUES64 Cell Line embryonic stem cell
10 chr1:216980400-216988000 Weak transcription Skeletal Muscle Male skeletal muscle
11 chr1:216981200-216986000 Weak transcription HSMMtube muscle
12 chr1:216983000-216983200 Genic enhancers Gastric stomach
13 chr1:216983000-216983200 Enhancers Right Atrium heart
14 chr1:216983000-216983600 Enhancers Psoas Muscle Psoas

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