Variant report

Variant rs1797758
Chromosome Location chr12:32025996-32025997
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:32020600-32027400 Weak transcription Primary T helper cells fromperipheralblood blood
2 chr12:32021000-32027000 Weak transcription Primary T cells fromperipheralblood blood
3 chr12:32022400-32027600 Weak transcription Ovary ovary
4 chr12:32022600-32028000 Weak transcription H9 Cell Line embryonic stem cell
5 chr12:32023000-32027400 Weak transcription iPS-18 Cell Line embryonic stem cell
6 chr12:32023800-32027800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
7 chr12:32024200-32028000 Genic enhancers Primary B cells from peripheral blood blood
8 chr12:32024800-32026200 Strong transcription Primary Natural Killer cells fromperipheralblood blood
9 chr12:32025200-32027800 Weak transcription Small Intestine intestine
10 chr12:32025400-32026600 Enhancers Liver Liver
11 chr12:32025400-32027800 Weak transcription iPS-15b Cell Line embryonic stem cell
12 chr12:32025600-32026000 ZNF genes & repeats Primary T cells from cord blood blood
13 chr12:32025800-32026000 Enhancers Spleen Spleen
14 chr12:32025800-32026200 ZNF genes & repeats Thymus Thymus
15 chr12:32025800-32026400 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
16 chr12:32025800-32026600 ZNF genes & repeats Primary B cells from cord blood blood

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