Variant report

Variant rs7998822
Chromosome Location chr13:111254899-111254900
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:111249200-111255200 Enhancers Placenta Placenta
2 chr13:111249800-111262400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr13:111253400-111255200 Weak transcription Placenta Amnion Placenta Amnion
4 chr13:111253600-111255400 Enhancers K562 blood
5 chr13:111254000-111255200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
6 chr13:111254000-111255200 Enhancers Fetal Adrenal Gland Adrenal Gland
7 chr13:111254000-111260400 Weak transcription HepG2 liver
8 chr13:111254000-111262600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr13:111254600-111256000 Enhancers Ovary ovary
10 chr13:111254800-111255000 Enhancers Fetal Intestine Large intestine

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