Variant report

Variant rs55858763
Chromosome Location chr4:9869970-9869971
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:9845000-9874800 Weak transcription NHEK skin
2 chr4:9861600-9874400 Weak transcription Stomach Smooth Muscle stomach
3 chr4:9862600-9871600 Weak transcription Fetal Intestine Small intestine
4 chr4:9862600-9880400 Weak transcription HMEC breast
5 chr4:9862600-9883000 Weak transcription Esophagus oesophagus
6 chr4:9862800-9871800 Strong transcription Breast Myoepithelial Primary Cells Breast
7 chr4:9862800-9880000 Weak transcription Fetal Intestine Large intestine
8 chr4:9862800-9887400 Weak transcription Duodenum Mucosa Duodenum
9 chr4:9863600-9887600 Weak transcription Liver Liver
10 chr4:9864800-9877000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr4:9865800-9876200 Strong transcription HepG2 liver
12 chr4:9867000-9876400 Strong transcription Primary monocytes fromperipheralblood blood
13 chr4:9867800-9876400 Strong transcription Monocytes-CD14+_RO01746 blood
14 chr4:9868400-9871000 Weak transcription Lung lung
15 chr4:9868800-9873200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr4:9868800-9873600 Enhancers Fetal Muscle Leg muscle
17 chr4:9869800-9870000 Bivalent Enhancer Fetal Muscle Trunk muscle
18 chr4:9869800-9870000 Active TSS Gastric stomach
19 chr4:9869800-9870000 Bivalent Enhancer HSMMtube muscle
20 chr4:9869800-9874800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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