Variant report

Variant rs568965511
Chromosome Location chr6:24332661-24332662
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:24327400-24339200 Weak transcription Pancreas Pancrea
2 chr6:24330200-24338400 Weak transcription Fetal Intestine Large intestine
3 chr6:24331000-24334200 Enhancers A549 lung
4 chr6:24332000-24333800 Enhancers HMEC breast
5 chr6:24332200-24332800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr6:24332200-24333200 Enhancers Fetal Kidney kidney
7 chr6:24332200-24333400 Enhancers HSMMtube muscle
8 chr6:24332200-24333400 Enhancers NH-A brain
9 chr6:24332200-24333600 Enhancers NHEK skin
10 chr6:24332200-24334400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr6:24332400-24333200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr6:24332400-24333200 Enhancers HSMM muscle
13 chr6:24332400-24333400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr6:24332400-24333400 Enhancers Hela-S3 cervix
15 chr6:24332400-24335200 Genic enhancers HepG2 liver
16 chr6:24332600-24333200 Enhancers ES-WA7 Cell Line embryonic stem cell
17 chr6:24332600-24338600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived

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