Variant report

Variant rs1401925
Chromosome Location chr19:21765015-21765016
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 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 chr19:21760200-21768000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr19:21760400-21769000 Weak transcription Fetal Kidney kidney
6 chr19:21762600-21766800 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
7 chr19:21763400-21767200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr19:21763400-21767400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr19:21763400-21768000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr19:21764000-21767400 Weak transcription Primary T cells from cord blood blood
11 chr19:21764000-21767400 Weak transcription Primary T helper cells PMA-I stimulated --
12 chr19:21764400-21765200 Enhancers Pancreas Pancrea
13 chr19:21764400-21765600 Transcr. at gene 5' and 3' Dnd41 blood
14 chr19:21764400-21767600 Enhancers Primary T cells fromperipheralblood blood
15 chr19:21764600-21768000 Weak transcription Primary T helper naive cells from peripheral blood blood
16 chr19:21764800-21766200 Weak transcription Gastric stomach
17 chr19:21764800-21769000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
18 chr19:21765000-21767200 Weak transcription Primary T helper naive cells fromperipheralblood blood

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