Variant report

Variant rs9425575
Chromosome Location chr1:172332231-172332232
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172320800-172332800 Enhancers Fetal Intestine Small intestine
2 chr1:172323000-172333000 Enhancers Fetal Intestine Large intestine
3 chr1:172328000-172332400 Enhancers Cortex derived primary cultured neurospheres brain
4 chr1:172328400-172334000 Weak transcription Aorta Aorta
5 chr1:172329000-172332400 Weak transcription Fetal Brain Male brain
6 chr1:172329200-172334600 Weak transcription Primary hematopoietic stem cells blood
7 chr1:172329800-172334000 Weak transcription Left Ventricle heart
8 chr1:172329800-172334000 Weak transcription Osteobl bone
9 chr1:172330400-172336600 Weak transcription Colon Smooth Muscle Colon
10 chr1:172330400-172343000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr1:172331000-172336400 Weak transcription Small Intestine intestine
12 chr1:172331200-172347200 Weak transcription Fetal Kidney kidney
13 chr1:172331800-172332400 Bivalent Enhancer HUES64 Cell Line embryonic stem cell
14 chr1:172332000-172332400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
15 chr1:172332000-172332800 Weak transcription Sigmoid Colon Sigmoid Colon
16 chr1:172332200-172332800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
17 chr1:172332200-172334800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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