Variant report

Variant rs7083926
Chromosome Location chr10:97163050-97163051
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:77 , 50 per page) page: 1 2
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:97146800-97168400 Weak transcription Small Intestine intestine
2 chr10:97150200-97163600 Weak transcription Stomach Mucosa stomach
3 chr10:97151000-97166200 Strong transcription Liver Liver
4 chr10:97151800-97168800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
5 chr10:97152000-97164200 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr10:97154400-97190800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr10:97154600-97168000 Weak transcription ES-I3 Cell Line embryonic stem cell
8 chr10:97155400-97168000 Strong transcription Fetal Intestine Small intestine
9 chr10:97155400-97170800 Enhancers Right Atrium heart
10 chr10:97156000-97166200 Weak transcription Pancreatic Islets Pancreatic Islet
11 chr10:97156800-97163600 Strong transcription Lung lung
12 chr10:97156800-97164400 Weak transcription Psoas Muscle Psoas
13 chr10:97156800-97173400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr10:97156800-97182600 Weak transcription Esophagus oesophagus
15 chr10:97157000-97173200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr10:97157000-97174000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
17 chr10:97157000-97183200 Weak transcription Colonic Mucosa Colon
18 chr10:97157000-97190400 Weak transcription Spleen Spleen
19 chr10:97158200-97163800 Weak transcription K562 blood
20 chr10:97158600-97199600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
21 chr10:97158800-97163600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
22 chr10:97158800-97163600 Strong transcription Skeletal Muscle Male skeletal muscle
23 chr10:97158800-97164400 Weak transcription Sigmoid Colon Sigmoid Colon
24 chr10:97158800-97165800 Weak transcription Brain Germinal Matrix brain
25 chr10:97158800-97166400 Weak transcription Brain Substantia Nigra brain
26 chr10:97159000-97164400 Weak transcription H1 Cell Line embryonic stem cell
27 chr10:97159000-97164400 Weak transcription Rectal Mucosa Donor 31 rectum
28 chr10:97159000-97164800 Weak transcription iPS-18 Cell Line embryonic stem cell
29 chr10:97159000-97165400 Weak transcription HUES48 Cell Line embryonic stem cell
30 chr10:97159000-97165600 Weak transcription HUES6 Cell Line embryonic stem cell
31 chr10:97159000-97165600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
32 chr10:97159000-97165600 Weak transcription Fetal Lung lung
33 chr10:97159000-97166000 Weak transcription Brain Angular Gyrus brain
34 chr10:97159000-97166400 Weak transcription Rectal Mucosa Donor 29 rectum
35 chr10:97159000-97166800 Weak transcription Duodenum Mucosa Duodenum
36 chr10:97159000-97167800 Weak transcription iPS-15b Cell Line embryonic stem cell
37 chr10:97159000-97168000 Weak transcription H9 Cell Line embryonic stem cell
38 chr10:97159000-97168000 Weak transcription HSMM muscle
39 chr10:97159200-97163600 Weak transcription Brain Inferior Temporal Lobe brain
40 chr10:97159200-97163600 Weak transcription Pancreas Pancrea
41 chr10:97159200-97187000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
42 chr10:97159400-97163800 Strong transcription Fetal Adrenal Gland Adrenal Gland
43 chr10:97159400-97165400 Weak transcription iPS-20b Cell Line embryonic stem cell
44 chr10:97159800-97167800 Weak transcription HUES64 Cell Line embryonic stem cell
45 chr10:97160000-97166000 Strong transcription Fetal Stomach stomach
46 chr10:97160400-97164000 Strong transcription Aorta Aorta
47 chr10:97160400-97166600 Weak transcription Fetal Brain Male brain
48 chr10:97160800-97166200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
49 chr10:97161600-97164000 Weak transcription Gastric stomach
50 chr10:97161800-97163200 Strong transcription Fetal Brain Female brain

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