Variant report

Variant rs11879116
Chromosome Location chr19:21757881-21757882
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:21752000-21769600 Weak transcription Fetal Heart heart
2 chr19:21752800-21766200 Weak transcription Fetal Intestine Large intestine
3 chr19:21753000-21768000 Weak transcription Fetal Intestine Small intestine
4 chr19:21753200-21762800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
5 chr19:21756800-21762400 Weak transcription Primary T helper cells PMA-I stimulated --
6 chr19:21757000-21764400 Weak transcription Pancreas Pancrea
7 chr19:21757400-21762800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr19:21757800-21759400 Weak transcription Dnd41 blood

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