Variant report

Variant rs13230832
Chromosome Location chr7:100995535-100995536
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:100991000-101006000 Weak transcription Right Atrium heart
2 chr7:100993400-100995600 Weak transcription HUES6 Cell Line embryonic stem cell
3 chr7:100993400-101005400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr7:100994000-100995600 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr7:100994800-100996000 Enhancers Stomach Mucosa stomach
6 chr7:100994800-100996400 Enhancers K562 blood
7 chr7:100995000-100996400 Enhancers Liver Liver
8 chr7:100995000-100996400 Enhancers Rectal Mucosa Donor 31 rectum
9 chr7:100995000-100996600 Enhancers HepG2 liver
10 chr7:100995200-101005600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
11 chr7:100995400-100995800 Enhancers Fetal Intestine Large intestine
12 chr7:100995400-100995800 Enhancers Fetal Muscle Leg muscle
13 chr7:100995400-100996000 Enhancers Primary T helper cells fromperipheralblood blood
14 chr7:100995400-100996000 Enhancers Fetal Intestine Small intestine
15 chr7:100995400-100996000 Flanking Active TSS A549 lung
16 chr7:100995400-100996200 Flanking Active TSS Hela-S3 cervix

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