Variant report

Variant rs9390049
Chromosome Location chr6:143376520-143376521
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:143356800-143377000 Weak transcription HepG2 liver
2 chr6:143372000-143380400 Weak transcription K562 blood
3 chr6:143373600-143380800 Weak transcription GM12878-XiMat blood
4 chr6:143374800-143380800 Weak transcription Primary T cells from cord blood blood
5 chr6:143375200-143380000 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr6:143375200-143381200 Weak transcription Aorta Aorta
7 chr6:143375600-143379600 Weak transcription Fetal Intestine Small intestine
8 chr6:143375800-143377200 Enhancers HUES48 Cell Line embryonic stem cell
9 chr6:143375800-143377200 Enhancers HUES6 Cell Line embryonic stem cell
10 chr6:143376000-143380600 Weak transcription Adipose Nuclei Adipose
11 chr6:143376200-143380800 Weak transcription Duodenum Smooth Muscle Duodenum
12 chr6:143376400-143377200 Enhancers H9 Cell Line embryonic stem cell
13 chr6:143376400-143378600 Enhancers ES-I3 Cell Line embryonic stem cell
14 chr6:143376400-143380200 Weak transcription Fetal Intestine Large intestine

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