Variant report

Variant rs11023904
Chromosome Location chr11:16313295-16313296
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 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 chr11:16310000-16314000 Weak transcription Fetal Intestine Large intestine
9 chr11:16310000-16314000 Weak transcription Fetal Intestine Small intestine
10 chr11:16310400-16313400 Weak transcription Fetal Kidney kidney
11 chr11:16312400-16314200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
12 chr11:16312600-16313600 Weak transcription Pancreatic Islets Pancreatic Islet
13 chr11:16313000-16314000 Enhancers K562 blood
14 chr11:16313200-16319800 Enhancers Fetal Heart heart

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