Variant report

Variant rs74124209
Chromosome Location chr1:172465093-172465094
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172454200-172466000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr1:172457000-172465600 Weak transcription Primary monocytes fromperipheralblood blood
3 chr1:172460800-172466000 Weak transcription Aorta Aorta
4 chr1:172460800-172466800 Enhancers Fetal Intestine Large intestine
5 chr1:172462600-172466000 Enhancers HepG2 liver
6 chr1:172464000-172466000 Weak transcription Right Atrium heart
7 chr1:172464200-172466800 Enhancers K562 blood
8 chr1:172464600-172466800 Enhancers Fetal Intestine Small intestine
9 chr1:172464800-172466200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr1:172464800-172467200 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
11 chr1:172464800-172471000 Enhancers Placenta Amnion Placenta Amnion
12 chr1:172465000-172465200 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
13 chr1:172465000-172466200 Enhancers Duodenum Mucosa Duodenum
14 chr1:172465000-172467000 Enhancers Stomach Mucosa stomach
15 chr1:172465000-172467800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
16 chr1:172465000-172468600 Enhancers Breast Myoepithelial Primary Cells Breast

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