Variant report

Variant rs577717618
Chromosome Location chr1:245966310-245966311
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:245949200-245999600 Weak transcription Gastric stomach
2 chr1:245952000-245970400 Weak transcription Aorta Aorta
3 chr1:245955200-245970800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr1:245957000-245970400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr1:245961400-245968000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
6 chr1:245961800-245980000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr1:245962000-245972600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr1:245962600-245970400 Weak transcription HepG2 liver
9 chr1:245963400-245970400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
10 chr1:245964600-245968400 Enhancers Placenta Placenta
11 chr1:245964600-245971200 Weak transcription Fetal Heart heart
12 chr1:245964800-245970400 Weak transcription NH-A brain
13 chr1:245964800-245973800 Weak transcription Fetal Stomach stomach
14 chr1:245965200-245966800 Strong transcription K562 blood
15 chr1:245965200-245967400 Weak transcription Primary T helper cells PMA-I stimulated --
16 chr1:245965600-245967000 Enhancers Placenta Amnion Placenta Amnion
17 chr1:245965600-245968000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
18 chr1:245966000-245966800 Enhancers HSMM muscle

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