Variant report

Variant rs201346608
Chromosome Location chr20:26299841-26299842
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:26293800-26300000 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
2 chr20:26293800-26300000 Weak transcription Colon Smooth Muscle Colon
3 chr20:26293800-26300000 Weak transcription Fetal Kidney kidney
4 chr20:26293800-26300000 Weak transcription Left Ventricle heart
5 chr20:26293800-26304400 Weak transcription NH-A brain
6 chr20:26293800-26309600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr20:26294000-26300000 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
8 chr20:26297000-26301200 Weak transcription Primary T helper naive cells fromperipheralblood blood
9 chr20:26298200-26309600 Weak transcription K562 blood
10 chr20:26299600-26300000 Weak transcription Primary T helper 17 cells PMA-I stimulated --
11 chr20:26299800-26300400 ZNF genes & repeats ES-I3 Cell Line embryonic stem cell
12 chr20:26299800-26300400 ZNF genes & repeats H1 Cell Line embryonic stem cell

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