Variant report

Variant rs1455101
Chromosome Location chr11:16177318-16177319
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16172400-16191400 Weak transcription Cortex derived primary cultured neurospheres brain
2 chr11:16172600-16191400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
3 chr11:16174200-16191200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr11:16174800-16178400 Enhancers Stomach Mucosa stomach
5 chr11:16174800-16180000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr11:16175000-16178400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr11:16175000-16180800 Enhancers NHEK skin
8 chr11:16175200-16177400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
9 chr11:16175200-16177800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr11:16175200-16180600 Enhancers HMEC breast
11 chr11:16175400-16179000 Enhancers Pancreatic Islets Pancreatic Islet
12 chr11:16175600-16177600 Flanking Active TSS A549 lung
13 chr11:16176000-16177600 Enhancers Fetal Intestine Small intestine
14 chr11:16176200-16178000 Enhancers Fetal Intestine Large intestine
15 chr11:16176200-16178400 Enhancers HepG2 liver
16 chr11:16177000-16180000 Weak transcription Hela-S3 cervix
17 chr11:16177200-16179800 Weak transcription Muscle Satellite Cultured Cells --

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