The 2.0 version of rSNPBase

Variant report

Variant esv3388704
Chromosome Location chr4:9899016-9899128
allele n/a
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:9882600-9903600 Weak transcription Fetal Intestine Large intestine
2 chr4:9888800-9905800 Weak transcription Duodenum Mucosa Duodenum
3 chr4:9889000-9906200 Weak transcription Liver Liver
4 chr4:9890600-9905600 Weak transcription Primary mononuclear cells fromperipheralblood Blood
5 chr4:9892200-9903600 Weak transcription Fetal Intestine Small intestine
6 chr4:9892800-9903600 Weak transcription NHEK skin
7 chr4:9893400-9900200 Weak transcription HMEC breast
8 chr4:9893800-9899400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr4:9894000-9917800 Weak transcription Lung lung
10 chr4:9894800-9903400 Weak transcription HepG2 liver
11 chr4:9895800-9906800 Weak transcription Right Atrium heart
12 chr4:9897000-9924600 Strong transcription Breast Myoepithelial Primary Cells Breast
13 chr4:9897600-9899800 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr4:9898000-9902000 Strong transcription Monocytes-CD14+_RO01746 blood
15 chr4:9898400-9899800 Strong transcription Primary monocytes fromperipheralblood blood
16 chr4:9898800-9899400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links

Copyright © 2015, Bioinformatics Lab, Institute of Psychology, Chinese Academy of Sciences. All Rights Reserved Feedback
Last update: Aug 31, 2015