Variant report

Variant rs4296926
Chromosome Location chr6:109808526-109808527
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:109804400-109814200 Weak transcription Gastric stomach
2 chr6:109805000-109817000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr6:109805200-109809200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr6:109805400-109808800 Weak transcription Fetal Adrenal Gland Adrenal Gland
5 chr6:109805400-109812000 Weak transcription H9 Cell Line embryonic stem cell
6 chr6:109805600-109812400 Weak transcription Brain Angular Gyrus brain
7 chr6:109806000-109811400 Weak transcription Dnd41 blood
8 chr6:109806200-109812200 Weak transcription Primary hematopoietic stem cells blood
9 chr6:109806800-109812200 Weak transcription Fetal Muscle Leg muscle
10 chr6:109807400-109812800 Weak transcription Placenta Placenta

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