Variant report

Variant rs4625695
Chromosome Location chr15:78118495-78118496
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:78114800-78118800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
2 chr15:78115800-78119200 Enhancers Fetal Intestine Small intestine
3 chr15:78117200-78119000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
4 chr15:78117800-78118600 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
5 chr15:78118000-78119000 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr15:78118000-78119000 Enhancers ES-WA7 Cell Line embryonic stem cell
7 chr15:78118200-78118600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
8 chr15:78118200-78119000 Bivalent Enhancer Fetal Intestine Large intestine
9 chr15:78118400-78118600 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
10 chr15:78118400-78118600 Enhancers Fetal Brain Female brain
11 chr15:78118400-78119000 Enhancers H1 Cell Line embryonic stem cell
12 chr15:78118400-78122400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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