Variant report

Variant rs60910740
Chromosome Location chr6:134399324-134399325
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:134395600-134405000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr6:134396200-134399600 Weak transcription HUES48 Cell Line embryonic stem cell
3 chr6:134396200-134400800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr6:134396600-134401000 Weak transcription HUES64 Cell Line embryonic stem cell
5 chr6:134396800-134402800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
6 chr6:134397600-134401800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
7 chr6:134398200-134399400 Enhancers HUVEC blood vessel
8 chr6:134398200-134399400 Enhancers Osteobl bone
9 chr6:134398200-134399600 Enhancers NH-A brain
10 chr6:134398200-134400000 Enhancers K562 blood
11 chr6:134398400-134400000 Enhancers Hela-S3 cervix
12 chr6:134398800-134399800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr6:134398800-134404200 Enhancers Placenta Placenta
14 chr6:134399000-134400600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr6:134399000-134400800 Weak transcription HMEC breast
16 chr6:134399200-134399600 Enhancers HepG2 liver
17 chr6:134399200-134400200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr6:134399200-134400600 Weak transcription NHEK skin

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