Variant report

Variant rs61431903
Chromosome Location chr12:8852631-8852632
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:104 , 50 per page) page: 1 2 3
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:8849200-8852800 Active TSS Aorta Aorta
2 chr12:8849400-8852800 Active TSS H1 Cell Line embryonic stem cell
3 chr12:8849600-8852800 Active TSS Brain Cingulate Gyrus brain
4 chr12:8849600-8852800 Active TSS Rectal Mucosa Donor 29 rectum
5 chr12:8849600-8853000 Active TSS Brain Inferior Temporal Lobe brain
6 chr12:8851000-8852800 Active TSS Brain Germinal Matrix brain
7 chr12:8851400-8852800 Flanking Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr12:8851400-8852800 Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr12:8851400-8852800 Flanking Active TSS HUVEC blood vessel
10 chr12:8851400-8853200 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr12:8851400-8853200 Enhancers Fetal Heart heart
12 chr12:8851400-8862000 Weak transcription Gastric stomach
13 chr12:8851600-8852800 Flanking Active TSS iPS-18 Cell Line embryonic stem cell
14 chr12:8851600-8853000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr12:8851600-8855600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr12:8851600-8862000 Weak transcription Lung lung
17 chr12:8851800-8852800 Weak transcription Primary neutrophils fromperipheralblood blood
18 chr12:8851800-8852800 Enhancers Primary T helper naive cells from peripheral blood blood
19 chr12:8851800-8852800 Enhancers Primary T helper cells fromperipheralblood blood
20 chr12:8851800-8852800 Enhancers Fetal Intestine Large intestine
21 chr12:8851800-8852800 Enhancers NHDF-Ad bronchial
22 chr12:8851800-8853000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
23 chr12:8851800-8853000 Enhancers Primary monocytes fromperipheralblood blood
24 chr12:8851800-8853000 Enhancers Primary T helper memory cells from peripheral blood 2 blood
25 chr12:8851800-8853000 Enhancers Primary T helper naive cells fromperipheralblood blood
26 chr12:8851800-8853000 Enhancers Primary T killer naive cells fromperipheralblood blood
27 chr12:8851800-8853000 Enhancers Monocytes-CD14+_RO01746 blood
28 chr12:8851800-8853200 Enhancers Fetal Intestine Small intestine
29 chr12:8851800-8853200 Enhancers Fetal Thymus thymus
30 chr12:8851800-8853200 Weak transcription Right Atrium heart
31 chr12:8851800-8853200 Enhancers Thymus Thymus
32 chr12:8851800-8853200 Enhancers Osteobl bone
33 chr12:8851800-8853400 Enhancers Fetal Stomach stomach
34 chr12:8851800-8854600 Weak transcription Brain Substantia Nigra brain
35 chr12:8851800-8855600 Weak transcription Brain Angular Gyrus brain
36 chr12:8851800-8859800 Weak transcription Spleen Spleen
37 chr12:8851800-8862000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
38 chr12:8851800-8862000 Weak transcription Left Ventricle heart
39 chr12:8851800-8862000 Weak transcription HSMM muscle
40 chr12:8851800-8862000 Weak transcription HSMMtube muscle
41 chr12:8851800-8863400 Weak transcription Right Ventricle heart
42 chr12:8851800-8873200 Weak transcription Fetal Muscle Trunk muscle
43 chr12:8851800-8877200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
44 chr12:8852000-8853000 Enhancers Primary T cells from cord blood blood
45 chr12:8852000-8853000 Weak transcription Primary T killer memory cells from peripheral blood blood
46 chr12:8852000-8853000 Flanking Active TSS Ganglion Eminence derived primary cultured neurospheres brain
47 chr12:8852000-8853000 Enhancers A549 lung
48 chr12:8852000-8853200 Enhancers Breast Myoepithelial Primary Cells Breast
49 chr12:8852000-8853200 Enhancers Primary B cells from cord blood blood
50 chr12:8852000-8853600 Enhancers Duodenum Smooth Muscle Duodenum

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