Variant report

Variant rs1495932
Chromosome Location chr12:117311989-117311990
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:117300000-117314200 Weak transcription Thymus Thymus
2 chr12:117303000-117312200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr12:117303000-117313600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr12:117306400-117312400 Weak transcription Primary B cells from cord blood blood
5 chr12:117311400-117312000 Enhancers Fetal Thymus thymus
6 chr12:117311400-117312000 Enhancers Dnd41 blood
7 chr12:117311600-117312200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
8 chr12:117311600-117312600 Enhancers Placenta Placenta
9 chr12:117311800-117312000 Bivalent Enhancer Primary T cells from cord blood blood
10 chr12:117311800-117312800 ZNF genes & repeats Right Atrium heart

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