Variant report

Variant rs13403781
Chromosome Location chr2:73290258-73290259
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:106 , 50 per page) page: 1 2 3
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:73259200-73291200 Weak transcription Small Intestine intestine
2 chr2:73262800-73290600 Weak transcription NHEK skin
3 chr2:73264200-73290600 Weak transcription H9 Cell Line embryonic stem cell
4 chr2:73272600-73291200 Weak transcription Fetal Heart heart
5 chr2:73275800-73297000 Weak transcription Pancreas Pancrea
6 chr2:73277800-73290400 Weak transcription HMEC breast
7 chr2:73277800-73290800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
8 chr2:73277800-73291200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr2:73284600-73290600 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
10 chr2:73284600-73296600 Weak transcription Primary mononuclear cells fromperipheralblood Blood
11 chr2:73284800-73296400 Weak transcription Fetal Kidney kidney
12 chr2:73285000-73290600 Weak transcription iPS-18 Cell Line embryonic stem cell
13 chr2:73285000-73290600 Weak transcription HSMMtube muscle
14 chr2:73285000-73290800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr2:73285000-73291200 Weak transcription Colon Smooth Muscle Colon
16 chr2:73285000-73291200 Weak transcription Fetal Muscle Trunk muscle
17 chr2:73285000-73291200 Weak transcription Lung lung
18 chr2:73285000-73291200 Weak transcription Rectal Mucosa Donor 29 rectum
19 chr2:73285000-73291200 Weak transcription Rectal Mucosa Donor 31 rectum
20 chr2:73285000-73295600 Weak transcription Primary B cells from cord blood blood
21 chr2:73285000-73295800 Weak transcription Rectal Smooth Muscle rectum
22 chr2:73285000-73296000 Weak transcription Adipose Nuclei Adipose
23 chr2:73285000-73296000 Weak transcription Gastric stomach
24 chr2:73285000-73296000 Weak transcription Thymus Thymus
25 chr2:73285000-73296600 Weak transcription Placenta Placenta
26 chr2:73285000-73296600 Weak transcription Ovary ovary
27 chr2:73285200-73290600 Weak transcription H1 Cell Line embryonic stem cell
28 chr2:73285200-73290600 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
29 chr2:73285200-73290800 Weak transcription Pancreatic Islets Pancreatic Islet
30 chr2:73285200-73291000 Weak transcription Breast Myoepithelial Primary Cells Breast
31 chr2:73285200-73295800 Weak transcription Stomach Smooth Muscle stomach
32 chr2:73285200-73296400 Weak transcription Primary Natural Killer cells fromperipheralblood blood
33 chr2:73285400-73290800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
34 chr2:73285600-73290400 Weak transcription HUES48 Cell Line embryonic stem cell
35 chr2:73285600-73290400 Weak transcription Fetal Intestine Large intestine
36 chr2:73285600-73290600 Weak transcription iPS-20b Cell Line embryonic stem cell
37 chr2:73285600-73291400 Weak transcription Duodenum Mucosa Duodenum
38 chr2:73285600-73291800 Weak transcription Fetal Thymus thymus
39 chr2:73285800-73290800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
40 chr2:73285800-73291000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
41 chr2:73285800-73291200 Weak transcription Fetal Muscle Leg muscle
42 chr2:73285800-73295200 Weak transcription Dnd41 blood
43 chr2:73285800-73295600 Weak transcription Primary hematopoietic stem cells blood
44 chr2:73285800-73295600 Weak transcription Aorta Aorta
45 chr2:73286000-73290600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
46 chr2:73286000-73291000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
47 chr2:73286000-73296800 Weak transcription Fetal Stomach stomach
48 chr2:73286200-73290600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
49 chr2:73286200-73290600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
50 chr2:73286200-73290600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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