Variant report

Variant rs4729690
Chromosome Location chr7:100995632-100995633
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:100991000-101006000 Weak transcription Right Atrium heart
2 chr7:100993400-101005400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr7:100994800-100996000 Enhancers Stomach Mucosa stomach
4 chr7:100994800-100996400 Enhancers K562 blood
5 chr7:100995000-100996400 Enhancers Liver Liver
6 chr7:100995000-100996400 Enhancers Rectal Mucosa Donor 31 rectum
7 chr7:100995000-100996600 Enhancers HepG2 liver
8 chr7:100995200-101005600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
9 chr7:100995400-100995800 Enhancers Fetal Intestine Large intestine
10 chr7:100995400-100995800 Enhancers Fetal Muscle Leg muscle
11 chr7:100995400-100996000 Enhancers Primary T helper cells fromperipheralblood blood
12 chr7:100995400-100996000 Enhancers Fetal Intestine Small intestine
13 chr7:100995400-100996000 Flanking Active TSS A549 lung
14 chr7:100995400-100996200 Flanking Active TSS Hela-S3 cervix
15 chr7:100995600-100995800 Enhancers HUES6 Cell Line embryonic stem cell
16 chr7:100995600-100995800 Enhancers Primary T helper memory cells from peripheral blood 2 blood
17 chr7:100995600-100996000 Enhancers ES-I3 Cell Line embryonic stem cell
18 chr7:100995600-100996000 Enhancers Duodenum Mucosa Duodenum
19 chr7:100995600-100996200 Enhancers Fetal Adrenal Gland Adrenal Gland

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