Variant report

Variant rs1106372
Chromosome Location chr19:39233221-39233222
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:39227400-39234600 Weak transcription Placenta Amnion Placenta Amnion
2 chr19:39228400-39234600 Weak transcription Placenta Placenta
3 chr19:39228600-39234400 Weak transcription A549 lung
4 chr19:39228800-39233800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr19:39229800-39233800 Weak transcription Fetal Intestine Small intestine
6 chr19:39230800-39234400 Weak transcription K562 blood
7 chr19:39231000-39234400 Weak transcription Primary T helper 17 cells PMA-I stimulated --
8 chr19:39231000-39234400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
9 chr19:39231000-39234600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr19:39232400-39234400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
11 chr19:39232600-39234200 Weak transcription Spleen Spleen
12 chr19:39233000-39235200 Enhancers HepG2 liver
13 chr19:39233200-39236000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived

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