Variant report

Variant rs7113955
Chromosome Location chr11:16373664-16373665
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16319400-16377600 Weak transcription Psoas Muscle Psoas
2 chr11:16367000-16376400 Weak transcription HepG2 liver
3 chr11:16368800-16374000 Weak transcription Skeletal Muscle Male skeletal muscle
4 chr11:16369000-16375000 Weak transcription Brain Germinal Matrix brain
5 chr11:16369800-16374400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
6 chr11:16369800-16375000 Weak transcription Fetal Intestine Large intestine
7 chr11:16370000-16374200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr11:16370000-16375200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
9 chr11:16370000-16375800 Weak transcription Fetal Heart heart
10 chr11:16370400-16374400 Weak transcription Skeletal Muscle Female skeletal muscle
11 chr11:16370600-16373800 Weak transcription Cortex derived primary cultured neurospheres brain
12 chr11:16370600-16373800 Weak transcription Pancreatic Islets Pancreatic Islet
13 chr11:16372000-16374400 Weak transcription K562 blood
14 chr11:16372200-16377400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
15 chr11:16372400-16374200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
16 chr11:16373400-16374400 Weak transcription Fetal Intestine Small intestine

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