Variant report

Variant rs4465577
Chromosome Location chr15:78118343-78118344
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:78114600-78118400 Weak transcription Fetal Brain Female brain
2 chr15:78114800-78118800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
3 chr15:78115800-78118400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr15:78115800-78119200 Enhancers Fetal Intestine Small intestine
5 chr15:78117200-78119000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
6 chr15:78117800-78118600 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
7 chr15:78118000-78119000 Enhancers ES-I3 Cell Line embryonic stem cell
8 chr15:78118000-78119000 Enhancers ES-WA7 Cell Line embryonic stem cell
9 chr15:78118200-78118600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
10 chr15:78118200-78119000 Bivalent Enhancer Fetal Intestine Large intestine

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