Variant report

Variant rs17158362
Chromosome Location chr7:110777373-110777374
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:110753000-110778000 Weak transcription Ovary ovary
2 chr7:110764800-110777800 Weak transcription Primary T cells from cord blood blood
3 chr7:110771400-110777800 Weak transcription Aorta Aorta
4 chr7:110773200-110777400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr7:110773400-110777600 Weak transcription Muscle Satellite Cultured Cells --
6 chr7:110773400-110777600 Weak transcription HUVEC blood vessel
7 chr7:110773400-110777800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr7:110773400-110778000 Weak transcription HUES48 Cell Line embryonic stem cell
9 chr7:110773400-110778000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
10 chr7:110773600-110778000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr7:110773800-110778000 Weak transcription A549 lung
12 chr7:110776600-110779800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr7:110776800-110777800 Enhancers Hela-S3 cervix
14 chr7:110776800-110780000 Enhancers Primary T helper cells PMA-I stimulated --
15 chr7:110777000-110777800 Enhancers Primary T helper 17 cells PMA-I stimulated --
16 chr7:110777000-110778000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
17 chr7:110777000-110778400 Enhancers Small Intestine intestine
18 chr7:110777200-110779000 Enhancers HUES64 Cell Line embryonic stem cell

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