Variant report

Variant rs183316364
Chromosome Location chr1:180221498-180221499
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:180213600-180225800 Weak transcription Right Atrium heart
2 chr1:180216400-180221600 Weak transcription A549 lung
3 chr1:180216600-180221600 Weak transcription Primary monocytes fromperipheralblood blood
4 chr1:180217000-180221600 Weak transcription Monocytes-CD14+_RO01746 blood
5 chr1:180217400-180222000 Weak transcription ES-WA7 Cell Line embryonic stem cell
6 chr1:180217600-180222800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
7 chr1:180219000-180222000 Weak transcription iPS-15b Cell Line embryonic stem cell
8 chr1:180219200-180222200 Weak transcription HUES48 Cell Line embryonic stem cell
9 chr1:180219200-180223000 Weak transcription HUES6 Cell Line embryonic stem cell
10 chr1:180219200-180223000 Weak transcription HUES64 Cell Line embryonic stem cell
11 chr1:180219200-180223200 Weak transcription iPS-18 Cell Line embryonic stem cell
12 chr1:180219200-180224400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr1:180219400-180221600 Weak transcription HSMMtube muscle
14 chr1:180219600-180222800 Weak transcription H1 Cell Line embryonic stem cell
15 chr1:180219800-180222000 Weak transcription ES-I3 Cell Line embryonic stem cell
16 chr1:180219800-180223600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
17 chr1:180221200-180224200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
18 chr1:180221400-180221600 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
19 chr1:180221400-180222200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
20 chr1:180221400-180222800 Enhancers Primary neutrophils fromperipheralblood blood

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