Variant report

Variant rs529119339
Chromosome Location chr1:113611117-113611118
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:113600400-113614400 Weak transcription iPS-15b Cell Line embryonic stem cell
2 chr1:113600400-113614800 Weak transcription H9 Cell Line embryonic stem cell
3 chr1:113600400-113615000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr1:113602400-113615000 Weak transcription Right Atrium heart
5 chr1:113602600-113614800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr1:113610600-113611200 Enhancers Fetal Intestine Large intestine
7 chr1:113610600-113611200 Enhancers Fetal Intestine Small intestine
8 chr1:113610600-113611200 Enhancers HepG2 liver
9 chr1:113610800-113611200 Enhancers A549 lung

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