Variant report

Variant rs35106858
Chromosome Location chr6:166608020-166608021
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:166587800-166608400 Weak transcription Pancreas Pancrea
2 chr6:166605600-166609000 Weak transcription Spleen Spleen
3 chr6:166607200-166609800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
4 chr6:166607800-166609600 Enhancers Primary B cells from cord blood blood
5 chr6:166607800-166609600 Enhancers Primary B cells from peripheral blood blood
6 chr6:166608000-166608200 Bivalent Enhancer iPS-20b Cell Line embryonic stem cell
7 chr6:166608000-166608200 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
8 chr6:166608000-166608800 Bivalent Enhancer Placenta Placenta
9 chr6:166608000-166609400 Bivalent Enhancer Fetal Muscle Trunk muscle
10 chr6:166608000-166609600 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
11 chr6:166608000-166609600 Enhancers Fetal Intestine Large intestine

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