Variant report

Variant rs9899977
Chromosome Location chr17:37891653-37891654
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:37887200-37891800 Weak transcription Lung lung
2 chr17:37887200-37892000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr17:37887200-37892000 Weak transcription Fetal Intestine Small intestine
4 chr17:37887200-37892000 Weak transcription Pancreas Pancrea
5 chr17:37887200-37892200 Weak transcription H9 Cell Line embryonic stem cell
6 chr17:37887200-37892200 Weak transcription Stomach Mucosa stomach
7 chr17:37887200-37892400 Weak transcription ES-I3 Cell Line embryonic stem cell
8 chr17:37887200-37892400 Weak transcription iPS-20b Cell Line embryonic stem cell
9 chr17:37887200-37892400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr17:37887200-37893600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
11 chr17:37887200-37893800 Weak transcription HUES64 Cell Line embryonic stem cell
12 chr17:37887200-37893800 Weak transcription HMEC breast
13 chr17:37887200-37894200 Weak transcription Small Intestine intestine
14 chr17:37887400-37892400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr17:37887800-37892000 Weak transcription Rectal Mucosa Donor 31 rectum
16 chr17:37888000-37892200 Weak transcription Hela-S3 cervix
17 chr17:37891600-37892000 Weak transcription Esophagus oesophagus
18 chr17:37891600-37892400 Enhancers HepG2 liver
19 chr17:37891600-37893800 Enhancers Placenta Placenta

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