Variant report

Variant rs10766318
Chromosome Location chr11:16310895-16310896
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16286800-16314800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr11:16300200-16313400 Weak transcription Brain Germinal Matrix brain
3 chr11:16300800-16314200 Weak transcription Cortex derived primary cultured neurospheres brain
4 chr11:16302200-16314200 Weak transcription Fetal Muscle Leg muscle
5 chr11:16302200-16321600 Weak transcription Left Ventricle heart
6 chr11:16309600-16314800 Weak transcription iPS-18 Cell Line embryonic stem cell
7 chr11:16309800-16314800 Weak transcription HUES64 Cell Line embryonic stem cell
8 chr11:16310000-16311200 Weak transcription Pancreatic Islets Pancreatic Islet
9 chr11:16310000-16314000 Weak transcription Fetal Intestine Large intestine
10 chr11:16310000-16314000 Weak transcription Fetal Intestine Small intestine
11 chr11:16310400-16313400 Weak transcription Fetal Kidney kidney
12 chr11:16310800-16311000 Enhancers K562 blood

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