Variant report

Variant rs74132409
Chromosome Location chr1:180216161-180216162
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:180211800-180216400 Weak transcription H9 Cell Line embryonic stem cell
2 chr1:180212600-180216200 Weak transcription iPS-15b Cell Line embryonic stem cell
3 chr1:180213600-180225800 Weak transcription Right Atrium heart
4 chr1:180214200-180216200 Weak transcription iPS-20b Cell Line embryonic stem cell
5 chr1:180214200-180216400 Weak transcription iPS-18 Cell Line embryonic stem cell
6 chr1:180214400-180216200 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr1:180214400-180216400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr1:180214400-180216800 Weak transcription HUES64 Cell Line embryonic stem cell
9 chr1:180214400-180217200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
10 chr1:180214600-180216200 Weak transcription ES-WA7 Cell Line embryonic stem cell
11 chr1:180214600-180216200 Weak transcription HUES6 Cell Line embryonic stem cell
12 chr1:180214600-180216800 Enhancers HepG2 liver
13 chr1:180214800-180216800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
14 chr1:180215800-180216400 Enhancers A549 lung
15 chr1:180215800-180216800 Enhancers Hela-S3 cervix
16 chr1:180216000-180216600 Enhancers Primary monocytes fromperipheralblood blood
17 chr1:180216000-180216800 Flanking Active TSS Primary neutrophils fromperipheralblood blood
18 chr1:180216000-180216800 Enhancers GM12878-XiMat blood
19 chr1:180216000-180217000 Enhancers H1 Cell Line embryonic stem cell
20 chr1:180216000-180217000 Enhancers HUES48 Cell Line embryonic stem cell
21 chr1:180216000-180217400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin

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