Variant report

Variant rs2001129
Chromosome Location chr1:172333248-172333249
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172328400-172334000 Weak transcription Aorta Aorta
2 chr1:172329200-172334600 Weak transcription Primary hematopoietic stem cells blood
3 chr1:172329800-172334000 Weak transcription Left Ventricle heart
4 chr1:172329800-172334000 Weak transcription Osteobl bone
5 chr1:172330400-172336600 Weak transcription Colon Smooth Muscle Colon
6 chr1:172330400-172343000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr1:172331000-172336400 Weak transcription Small Intestine intestine
8 chr1:172331200-172347200 Weak transcription Fetal Kidney kidney
9 chr1:172332200-172334800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr1:172333000-172333400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain

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