Variant report

Variant rs6902732
Chromosome Location chr6:143375887-143375888
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:143356800-143377000 Weak transcription HepG2 liver
2 chr6:143372000-143380400 Weak transcription K562 blood
3 chr6:143373600-143380800 Weak transcription GM12878-XiMat blood
4 chr6:143374800-143380800 Weak transcription Primary T cells from cord blood blood
5 chr6:143375200-143380000 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr6:143375200-143381200 Weak transcription Aorta Aorta
7 chr6:143375600-143379600 Weak transcription Fetal Intestine Small intestine
8 chr6:143375800-143376000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
9 chr6:143375800-143377200 Enhancers HUES48 Cell Line embryonic stem cell
10 chr6:143375800-143377200 Enhancers HUES6 Cell Line embryonic stem cell

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