Variant report

Variant rs549782688
Chromosome Location chr21:40118970-40118971
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:40102600-40124800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr21:40113800-40119200 Weak transcription Spleen Spleen
3 chr21:40114000-40119400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr21:40114200-40119000 Weak transcription Duodenum Mucosa Duodenum
5 chr21:40114400-40119000 Weak transcription Rectal Mucosa Donor 29 rectum
6 chr21:40114400-40119000 Weak transcription Rectal Mucosa Donor 31 rectum
7 chr21:40115400-40129600 Weak transcription Primary mononuclear cells fromperipheralblood Blood
8 chr21:40115800-40120600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr21:40116000-40123800 Weak transcription Adipose Nuclei Adipose
10 chr21:40116400-40119400 Weak transcription Sigmoid Colon Sigmoid Colon
11 chr21:40117600-40122600 Enhancers Fetal Intestine Large intestine
12 chr21:40118400-40122000 Enhancers Fetal Intestine Small intestine
13 chr21:40118800-40119000 Enhancers Aorta Aorta
14 chr21:40118800-40119200 Enhancers Small Intestine intestine
15 chr21:40118800-40119600 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --

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