Variant report

Variant rs368817569
Chromosome Location chr12:104060128-104060129
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:104033200-104062200 Weak transcription Spleen Spleen
2 chr12:104059200-104060200 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr12:104059200-104061600 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr12:104059400-104060200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
5 chr12:104059600-104060200 Enhancers HUES48 Cell Line embryonic stem cell
6 chr12:104059600-104060200 Enhancers iPS-18 Cell Line embryonic stem cell
7 chr12:104059600-104060200 Enhancers iPS-20b Cell Line embryonic stem cell
8 chr12:104059600-104060200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
9 chr12:104059600-104060200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
10 chr12:104059600-104060400 Enhancers H9 Cell Line embryonic stem cell
11 chr12:104059800-104060200 Enhancers H1 Cell Line embryonic stem cell
12 chr12:104060000-104060200 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
13 chr12:104060000-104063400 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
14 chr12:104060000-104063600 Weak transcription HUES6 Cell Line embryonic stem cell
15 chr12:104060000-104064000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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