Variant report

Variant rs10184382
Chromosome Location chr2:20277070-20277071
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:20272000-20280600 Weak transcription H1 Cell Line embryonic stem cell
2 chr2:20272400-20277200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
3 chr2:20273000-20279600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr2:20273200-20281800 Weak transcription Hela-S3 cervix
5 chr2:20274200-20281800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr2:20274400-20278000 Enhancers HepG2 liver
7 chr2:20274600-20280600 Weak transcription Placenta Amnion Placenta Amnion
8 chr2:20275000-20277400 Weak transcription Placenta Placenta
9 chr2:20275000-20278000 Weak transcription Left Ventricle heart
10 chr2:20275000-20280000 Weak transcription K562 blood
11 chr2:20275000-20280200 Weak transcription Ovary ovary
12 chr2:20275000-20280200 Weak transcription Pancreas Pancrea
13 chr2:20275000-20280400 Weak transcription Spleen Spleen
14 chr2:20275200-20280600 Weak transcription Fetal Adrenal Gland Adrenal Gland

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