Variant report

Variant rs4847370
Chromosome Location chr1:93259193-93259194
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:93255800-93260000 Weak transcription HepG2 liver
2 chr1:93257800-93259400 Enhancers HUES6 Cell Line embryonic stem cell
3 chr1:93257800-93259400 Enhancers iPS-15b Cell Line embryonic stem cell
4 chr1:93258000-93260000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
5 chr1:93258000-93268400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr1:93258000-93270200 Weak transcription Right Atrium heart
7 chr1:93258200-93263000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr1:93258200-93263600 Weak transcription Cortex derived primary cultured neurospheres brain
9 chr1:93258600-93259200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
10 chr1:93258800-93259800 Weak transcription K562 blood
11 chr1:93258800-93269800 Weak transcription Fetal Heart heart

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