Variant report

Variant rs77359975
Chromosome Location chr20:26300212-26300213
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:26293800-26304400 Weak transcription NH-A brain
2 chr20:26293800-26309600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr20:26297000-26301200 Weak transcription Primary T helper naive cells fromperipheralblood blood
4 chr20:26298200-26309600 Weak transcription K562 blood
5 chr20:26299800-26300400 ZNF genes & repeats ES-I3 Cell Line embryonic stem cell
6 chr20:26299800-26300400 ZNF genes & repeats H1 Cell Line embryonic stem cell
7 chr20:26300000-26300400 ZNF genes & repeats iPS-20b Cell Line embryonic stem cell
8 chr20:26300000-26300400 ZNF genes & repeats Primary T helper memory cells from peripheral blood 1 blood
9 chr20:26300000-26300400 ZNF genes & repeats Primary T helper cells PMA-I stimulated --
10 chr20:26300000-26300400 ZNF genes & repeats Primary T cells effector/memory enriched fromperipheralblood blood
11 chr20:26300000-26300400 ZNF genes & repeats Liver Liver
12 chr20:26300000-26300400 ZNF genes & repeats Brain Hippocampus Middle brain
13 chr20:26300000-26300400 ZNF genes & repeats Colon Smooth Muscle Colon
14 chr20:26300000-26300400 Active TSS Psoas Muscle Psoas
15 chr20:26300000-26301400 ZNF genes & repeats Primary hematopoietic stem cells blood
16 chr20:26300200-26301000 Weak transcription Fetal Kidney kidney

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