Variant report

Variant rs7987643
Chromosome Location chr13:96184485-96184486
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:96181200-96185800 Weak transcription Cortex derived primary cultured neurospheres brain
2 chr13:96182400-96185200 Enhancers A549 lung
3 chr13:96182600-96186400 Weak transcription NH-A brain
4 chr13:96182600-96187600 Weak transcription HSMMtube muscle
5 chr13:96182800-96184600 Weak transcription Fetal Lung lung
6 chr13:96182800-96185800 Weak transcription HepG2 liver
7 chr13:96182800-96186000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr13:96183000-96185800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr13:96183000-96186000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr13:96183000-96186200 Weak transcription Muscle Satellite Cultured Cells --
11 chr13:96183000-96187000 Weak transcription HMEC breast
12 chr13:96183000-96187200 Weak transcription Hela-S3 cervix
13 chr13:96183000-96187400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr13:96183000-96188800 Weak transcription Primary hematopoietic stem cells short term culture blood
15 chr13:96183000-96192800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
16 chr13:96183200-96185800 Weak transcription HUVEC blood vessel
17 chr13:96183400-96185800 Weak transcription Pancreas Pancrea
18 chr13:96183600-96187200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
19 chr13:96184200-96184600 Enhancers Osteobl bone
20 chr13:96184200-96187200 Weak transcription NHDF-Ad bronchial
21 chr13:96184400-96184800 Enhancers iPS-20b Cell Line embryonic stem cell

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