Variant report

Variant rs41399553
Chromosome Location chr15:51595829-51595830
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:51591400-51602800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr15:51591800-51604600 Weak transcription Gastric stomach
3 chr15:51592200-51615000 Weak transcription Spleen Spleen
4 chr15:51593400-51596600 Strong transcription Placenta Placenta
5 chr15:51594600-51602200 Weak transcription HepG2 liver
6 chr15:51594800-51596200 Enhancers Fetal Muscle Leg muscle
7 chr15:51594800-51596800 Enhancers Fetal Intestine Large intestine
8 chr15:51595200-51596200 Bivalent Enhancer GM12878-XiMat blood
9 chr15:51595200-51596800 Enhancers Fetal Intestine Small intestine
10 chr15:51595800-51596200 Enhancers Primary B cells from peripheral blood blood
11 chr15:51595800-51596200 Enhancers Pancreas Pancrea
12 chr15:51595800-51596200 Enhancers Right Atrium heart
13 chr15:51595800-51596400 Weak transcription Fetal Lung lung
14 chr15:51595800-51596400 Bivalent Enhancer Stomach Mucosa stomach

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