Variant report

Variant rs149845690
Chromosome Location chr21:40119366-40119367
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 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 chr21:40114000-40119400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr21:40115400-40129600 Weak transcription Primary mononuclear cells fromperipheralblood Blood
4 chr21:40115800-40120600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr21:40116000-40123800 Weak transcription Adipose Nuclei Adipose
6 chr21:40116400-40119400 Weak transcription Sigmoid Colon Sigmoid Colon
7 chr21:40117600-40122600 Enhancers Fetal Intestine Large intestine
8 chr21:40118400-40122000 Enhancers Fetal Intestine Small intestine
9 chr21:40118800-40119600 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr21:40119000-40119800 Enhancers HepG2 liver
11 chr21:40119000-40120600 Enhancers Rectal Mucosa Donor 31 rectum
12 chr21:40119000-40121800 Enhancers Duodenum Mucosa Duodenum
13 chr21:40119000-40122000 Weak transcription Aorta Aorta
14 chr21:40119200-40119400 Enhancers Rectal Mucosa Donor 29 rectum
15 chr21:40119200-40120200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
16 chr21:40119200-40120200 Enhancers Colonic Mucosa Colon
17 chr21:40119200-40120200 Enhancers Spleen Spleen
18 chr21:40119200-40120400 Weak transcription Small Intestine intestine

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