Variant report

Variant rs561798477
Chromosome Location chr6:11834506-11834507
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:11831000-11835400 Weak transcription Left Ventricle heart
2 chr6:11833800-11834600 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
3 chr6:11833800-11834600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr6:11833800-11834800 Enhancers HUES48 Cell Line embryonic stem cell
5 chr6:11833800-11834800 Enhancers iPS-15b Cell Line embryonic stem cell
6 chr6:11833800-11835200 Flanking Active TSS K562 blood
7 chr6:11833800-11835600 Flanking Active TSS GM12878-XiMat blood
8 chr6:11833800-11835800 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr6:11833800-11835800 Enhancers Liver Liver
10 chr6:11833800-11836000 Enhancers Fetal Muscle Leg muscle
11 chr6:11834000-11834600 Enhancers H1 Cell Line embryonic stem cell
12 chr6:11834000-11836000 Enhancers Fetal Heart heart
13 chr6:11834200-11834600 Enhancers HSMMtube muscle
14 chr6:11834200-11834600 Enhancers NHEK skin
15 chr6:11834200-11834800 Enhancers iPS-18 Cell Line embryonic stem cell
16 chr6:11834200-11835200 Weak transcription Pancreas Pancrea
17 chr6:11834200-11835400 Weak transcription Esophagus oesophagus
18 chr6:11834200-11835400 Weak transcription Gastric stomach
19 chr6:11834200-11836400 Enhancers Fetal Lung lung
20 chr6:11834400-11834600 Enhancers Spleen Spleen
21 chr6:11834400-11835800 Enhancers Skeletal Muscle Male skeletal muscle

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