Variant report

Variant rs28371764
Chromosome Location chr7:99277593-99277594
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:46 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:99243000-99278800 Weak transcription Brain Angular Gyrus brain
2 chr7:99273800-99290400 Weak transcription Primary T cells from cord blood blood
3 chr7:99275000-99277600 Active TSS Duodenum Smooth Muscle Duodenum
4 chr7:99275000-99277600 Active TSS Stomach Mucosa stomach
5 chr7:99275400-99277800 Active TSS Pancreatic Islets Pancreatic Islet
6 chr7:99275600-99277800 Active TSS Rectal Mucosa Donor 29 rectum
7 chr7:99275800-99277600 Active TSS Colonic Mucosa Colon
8 chr7:99275800-99277600 Active TSS Rectal Mucosa Donor 31 rectum
9 chr7:99276000-99277600 Active TSS Duodenum Mucosa Duodenum
10 chr7:99276000-99277600 Active TSS Esophagus oesophagus
11 chr7:99276000-99277600 Active TSS Gastric stomach
12 chr7:99276000-99277600 Flanking Active TSS A549 lung
13 chr7:99276000-99278200 Enhancers HepG2 liver
14 chr7:99276400-99277600 Active TSS Fetal Lung lung
15 chr7:99276400-99277800 Enhancers ES-WA7 Cell Line embryonic stem cell
16 chr7:99276400-99277800 Enhancers Hela-S3 cervix
17 chr7:99276600-99277600 Active TSS Colon Smooth Muscle Colon
18 chr7:99276600-99277600 Active TSS NHDF-Ad bronchial
19 chr7:99276600-99277600 Active TSS NHLF lung
20 chr7:99276600-99277800 Enhancers iPS-15b Cell Line embryonic stem cell
21 chr7:99276600-99277800 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
22 chr7:99276600-99278200 Flanking Active TSS K562 blood
23 chr7:99276800-99277600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
24 chr7:99276800-99277600 Flanking Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
25 chr7:99276800-99277600 Flanking Active TSS Fetal Intestine Large intestine
26 chr7:99276800-99277600 Active TSS Sigmoid Colon Sigmoid Colon
27 chr7:99276800-99277600 Active TSS Stomach Smooth Muscle stomach
28 chr7:99276800-99277800 Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
29 chr7:99276800-99277800 Flanking Active TSS Adipose Nuclei Adipose
30 chr7:99276800-99277800 Enhancers Skeletal Muscle Male skeletal muscle
31 chr7:99276800-99278400 Enhancers Psoas Muscle Psoas
32 chr7:99277000-99277600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
33 chr7:99277000-99277800 Active TSS Liver Liver
34 chr7:99277000-99295800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
35 chr7:99277200-99277800 Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
36 chr7:99277200-99277800 Enhancers Lung lung
37 chr7:99277200-99277800 Active TSS Rectal Smooth Muscle rectum
38 chr7:99277200-99278000 Enhancers Skeletal Muscle Female skeletal muscle
39 chr7:99277200-99281200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
40 chr7:99277200-99282800 Weak transcription ES-I3 Cell Line embryonic stem cell
41 chr7:99277400-99277600 Enhancers Fetal Adrenal Gland Adrenal Gland
42 chr7:99277400-99277600 Enhancers NHEK skin
43 chr7:99277400-99277800 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
44 chr7:99277400-99277800 Flanking Active TSS Pancreas Pancrea
45 chr7:99277400-99277800 Weak transcription Small Intestine intestine
46 chr7:99277400-99278400 ZNF genes & repeats Fetal Intestine Small intestine

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