Variant report

Variant rs61834077
Chromosome Location chr1:213222564-213222565
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:213219200-213224000 Weak transcription Fetal Intestine Large intestine
2 chr1:213219600-213222800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr1:213220000-213223800 Weak transcription Fetal Intestine Small intestine
4 chr1:213221600-213222600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr1:213222000-213224200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
6 chr1:213222200-213222800 Weak transcription HUES6 Cell Line embryonic stem cell
7 chr1:213222200-213223000 Enhancers HUES48 Cell Line embryonic stem cell
8 chr1:213222200-213223000 Enhancers HUES64 Cell Line embryonic stem cell
9 chr1:213222400-213223000 Flanking Active TSS K562 blood
10 chr1:213222400-213223200 Enhancers iPS-15b Cell Line embryonic stem cell
11 chr1:213222400-213223200 Enhancers Primary hematopoietic stem cells short term culture blood
12 chr1:213222400-213223200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr1:213222400-213223800 Enhancers Monocytes-CD14+_RO01746 blood
14 chr1:213222400-213224000 Enhancers Primary monocytes fromperipheralblood blood

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