Variant report

Variant rs10785471
Chromosome Location chr12:44311998-44311999
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:44307000-44315600 Weak transcription NHDF-Ad bronchial
2 chr12:44307400-44324000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr12:44308400-44318400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr12:44308600-44314800 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr12:44311200-44312800 Enhancers Fetal Heart heart
6 chr12:44311200-44313000 Enhancers Fetal Adrenal Gland Adrenal Gland
7 chr12:44311400-44324600 Weak transcription Left Ventricle heart
8 chr12:44311800-44312000 Enhancers Pancreatic Islets Pancreatic Islet

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