Variant report

Variant rs1401455
Chromosome Location chr11:16309385-16309386
allele A/G
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 chr11:16303000-16310800 Weak transcription K562 blood
7 chr11:16308600-16309600 Enhancers iPS-20b Cell Line embryonic stem cell
8 chr11:16308600-16310000 Enhancers Pancreatic Islets Pancreatic Islet
9 chr11:16308800-16309600 Enhancers iPS-18 Cell Line embryonic stem cell
10 chr11:16308800-16309800 Enhancers iPS-15b Cell Line embryonic stem cell
11 chr11:16309000-16309800 Enhancers HUES64 Cell Line embryonic stem cell
12 chr11:16309000-16310000 Enhancers HUES48 Cell Line embryonic stem cell
13 chr11:16309000-16310000 Enhancers Fetal Intestine Small intestine
14 chr11:16309200-16310000 Enhancers Fetal Intestine Large intestine

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