Variant report

Variant rs568855703
Chromosome Location chr5:180060492-180060493
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:180040000-180061200 Weak transcription Gastric stomach
2 chr5:180046200-180071800 Weak transcription Liver Liver
3 chr5:180046400-180072200 Weak transcription Right Atrium heart
4 chr5:180056800-180068400 Weak transcription H9 Cell Line embryonic stem cell
5 chr5:180057400-180061400 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
6 chr5:180057800-180063000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr5:180058400-180061200 Enhancers Spleen Spleen
8 chr5:180058600-180060600 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin02 Skin
9 chr5:180058800-180061200 Bivalent Enhancer Fetal Muscle Trunk muscle
10 chr5:180059000-180060600 Enhancers Right Ventricle heart
11 chr5:180059600-180065000 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
12 chr5:180059800-180061000 Weak transcription HUES6 Cell Line embryonic stem cell
13 chr5:180060000-180063200 Weak transcription Fetal Muscle Leg muscle
14 chr5:180060200-180060600 Weak transcription Left Ventricle heart
15 chr5:180060200-180061000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
16 chr5:180060200-180061000 Weak transcription Lung lung

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