Variant report

Variant rs10876696
Chromosome Location chr12:38032721-38032722
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:37989800-38041200 ZNF genes & repeats HUES64 Cell Line embryonic stem cell
2 chr12:37990000-38040800 ZNF genes & repeats HUES48 Cell Line embryonic stem cell
3 chr12:38026800-38038800 ZNF genes & repeats iPS-18 Cell Line embryonic stem cell
4 chr12:38029200-38035000 Weak transcription Primary T killer naive cells fromperipheralblood blood
5 chr12:38029200-38035000 Weak transcription Ovary ovary
6 chr12:38029200-38035000 Weak transcription Thymus Thymus
7 chr12:38029200-38035000 Weak transcription K562 blood
8 chr12:38029200-38035000 Weak transcription NHDF-Ad bronchial
9 chr12:38029200-38038000 Weak transcription NHEK skin
10 chr12:38029400-38035000 Weak transcription Hela-S3 cervix
11 chr12:38031000-38034600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr12:38031600-38035000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr12:38032000-38033800 ZNF genes & repeats HUVEC blood vessel
14 chr12:38032000-38041000 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr12:38032600-38035000 Weak transcription Colon Smooth Muscle Colon
16 chr12:38032600-38035000 Weak transcription HSMMtube muscle

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