Variant report

Variant rs563053261
Chromosome Location chr14:21778425-21778426
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:21777600-21779000 Weak transcription Small Intestine intestine
2 chr14:21777600-21781600 Weak transcription Fetal Intestine Large intestine
3 chr14:21777600-21791400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr14:21777800-21779000 Weak transcription iPS-15b Cell Line embryonic stem cell
5 chr14:21777800-21779800 Weak transcription ES-I3 Cell Line embryonic stem cell
6 chr14:21777800-21781000 Weak transcription Primary monocytes fromperipheralblood blood
7 chr14:21777800-21781400 Weak transcription Primary neutrophils fromperipheralblood blood
8 chr14:21777800-21781400 Weak transcription Monocytes-CD14+_RO01746 blood
9 chr14:21777800-21787600 Weak transcription HUES6 Cell Line embryonic stem cell
10 chr14:21778000-21779800 Weak transcription HepG2 liver
11 chr14:21778000-21780000 Weak transcription HUES64 Cell Line embryonic stem cell
12 chr14:21778000-21785400 Weak transcription GM12878-XiMat blood
13 chr14:21778000-21787600 Weak transcription Primary B cells from cord blood blood

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