Variant report

Variant rs10899058
Chromosome Location chr11:74738814-74738815
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:74726600-74746400 Weak transcription GM12878-XiMat blood
2 chr11:74734400-74742200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
3 chr11:74734600-74739000 Weak transcription Psoas Muscle Psoas
4 chr11:74735000-74739200 Weak transcription NHDF-Ad bronchial
5 chr11:74735200-74741600 Weak transcription Left Ventricle heart
6 chr11:74735400-74742400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr11:74736400-74741800 Weak transcription Brain Angular Gyrus brain
8 chr11:74736400-74741800 Weak transcription Brain Substantia Nigra brain
9 chr11:74736400-74741800 Weak transcription Fetal Intestine Large intestine
10 chr11:74736600-74742200 Weak transcription Fetal Intestine Small intestine
11 chr11:74737800-74739800 Weak transcription Fetal Adrenal Gland Adrenal Gland
12 chr11:74737800-74741600 Enhancers K562 blood
13 chr11:74738200-74743200 Enhancers Skeletal Muscle Female skeletal muscle
14 chr11:74738400-74739600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
15 chr11:74738600-74739000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
16 chr11:74738600-74743200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
17 chr11:74738800-74740000 Enhancers Skeletal Muscle Male skeletal muscle

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