Variant report

Variant rs56974964
Chromosome Location chr21:46654230-46654231
allele -/CAGGCGGAAGCGG
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:46637800-46668600 Weak transcription Right Atrium heart
2 chr21:46643800-46664600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr21:46648800-46654600 Weak transcription Fetal Brain Male brain
4 chr21:46648800-46656400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr21:46652200-46654800 Weak transcription Cortex derived primary cultured neurospheres brain
6 chr21:46652800-46655800 Weak transcription Primary T helper 17 cells PMA-I stimulated --
7 chr21:46654000-46654400 Flanking Bivalent TSS/Enh Placenta Placenta
8 chr21:46654000-46654400 Active TSS GM12878-XiMat blood
9 chr21:46654000-46654600 Bivalent/Poised TSS Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr21:46654200-46654400 Bivalent/Poised TSS Primary T cells fromperipheralblood blood
11 chr21:46654200-46654600 Active TSS Primary T helper cells fromperipheralblood blood

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