Variant report

Variant rs4730086
Chromosome Location chr7:105086631-105086632
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:105080000-105093000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr7:105080000-105094400 Weak transcription NHLF lung
3 chr7:105080000-105108400 Weak transcription Spleen Spleen
4 chr7:105080000-105161200 Weak transcription Pancreas Pancrea
5 chr7:105080200-105104600 Weak transcription Stomach Smooth Muscle stomach
6 chr7:105080200-105126800 Weak transcription Placenta Amnion Placenta Amnion
7 chr7:105082000-105088000 Enhancers Primary neutrophils fromperipheralblood blood
8 chr7:105084800-105090000 Enhancers Primary B cells from cord blood blood
9 chr7:105084800-105091200 Enhancers Primary B cells from peripheral blood blood
10 chr7:105085200-105088200 Weak transcription Primary hematopoietic stem cells blood
11 chr7:105085400-105087000 Weak transcription Primary T regulatory cells fromperipheralblood blood
12 chr7:105085400-105088000 Weak transcription Primary mononuclear cells fromperipheralblood Blood
13 chr7:105085800-105088000 Weak transcription Primary T helper cells fromperipheralblood blood
14 chr7:105086000-105087000 Weak transcription K562 blood

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