Variant report

Variant rs3733350
Chromosome Location chr4:1020129-1020130
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:112 , 50 per page) page: 1 2 3
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:1005000-1020200 Weak transcription Primary T helper naive cells from peripheral blood blood
2 chr4:1006600-1027600 Weak transcription Right Atrium heart
3 chr4:1013400-1026600 Weak transcription Brain Germinal Matrix brain
4 chr4:1014200-1021600 Weak transcription ES-WA7 Cell Line embryonic stem cell
5 chr4:1014400-1021400 Weak transcription Monocytes-CD14+_RO01746 blood
6 chr4:1014400-1023000 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
7 chr4:1015400-1020800 Strong transcription Ganglion Eminence derived primary cultured neurospheres brain
8 chr4:1015400-1020800 Strong transcription Fetal Stomach stomach
9 chr4:1015600-1020200 Strong transcription Cortex derived primary cultured neurospheres brain
10 chr4:1015600-1020800 Strong transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr4:1015800-1020200 Strong transcription Liver Liver
12 chr4:1015800-1022200 Weak transcription Primary Natural Killer cells fromperipheralblood blood
13 chr4:1016400-1020600 Weak transcription Psoas Muscle Psoas
14 chr4:1017000-1021200 Weak transcription Stomach Mucosa stomach
15 chr4:1017800-1021000 Genic enhancers Fetal Muscle Leg muscle
16 chr4:1018000-1020200 Strong transcription Primary hematopoietic stem cells short term culture blood
17 chr4:1018200-1020200 Strong transcription HUES64 Cell Line embryonic stem cell
18 chr4:1018200-1020200 Strong transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
19 chr4:1018200-1020200 Strong transcription Brain Anterior Caudate brain
20 chr4:1018200-1020200 Strong transcription Stomach Smooth Muscle stomach
21 chr4:1018200-1020200 Strong transcription Thymus Thymus
22 chr4:1018200-1020200 Strong transcription NHLF lung
23 chr4:1018400-1020200 Strong transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
24 chr4:1018400-1020400 Strong transcription Fetal Brain Female brain
25 chr4:1018800-1020200 Transcr. at gene 5' and 3' Foreskin Fibroblast Primary Cells skin02 Skin
26 chr4:1018800-1020400 Genic enhancers Spleen Spleen
27 chr4:1019000-1020200 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
28 chr4:1019000-1020200 ZNF genes & repeats Fetal Brain Male brain
29 chr4:1019000-1020200 Strong transcription Rectal Smooth Muscle rectum
30 chr4:1019200-1020200 Strong transcription iPS-20b Cell Line embryonic stem cell
31 chr4:1019200-1020200 Genic enhancers Esophagus oesophagus
32 chr4:1019200-1020200 Strong transcription HepG2 liver
33 chr4:1019200-1021000 Genic enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
34 chr4:1019400-1020200 Strong transcription Primary hematopoietic stem cells blood
35 chr4:1019400-1020200 Strong transcription NHDF-Ad bronchial
36 chr4:1019400-1020200 Strong transcription Osteobl bone
37 chr4:1019400-1020400 Genic enhancers Pancreas Pancrea
38 chr4:1019600-1020200 ZNF genes & repeats H9 Cell Line embryonic stem cell
39 chr4:1019600-1020200 Genic enhancers ES-UCSF4 Cell Line embryonic stem cell
40 chr4:1019600-1020200 Genic enhancers Breast Myoepithelial Primary Cells Breast
41 chr4:1019600-1020200 Enhancers Primary T helper memory cells from peripheral blood 2 blood
42 chr4:1019600-1021800 Weak transcription Colonic Mucosa Colon
43 chr4:1019600-1027200 Weak transcription Brain Inferior Temporal Lobe brain
44 chr4:1019800-1020200 Genic enhancers H1 Cell Line embryonic stem cell
45 chr4:1019800-1020200 Strong transcription H9 Derived Neuron Cultured Cells ES cell derived
46 chr4:1019800-1020200 Genic enhancers HUES6 Cell Line embryonic stem cell
47 chr4:1019800-1020200 Genic enhancers iPS DF 6.9 Cell Line embryonic stem cell
48 chr4:1019800-1020200 Genic enhancers Adipose Nuclei Adipose
49 chr4:1019800-1020200 Genic enhancers Fetal Kidney kidney
50 chr4:1019800-1020200 Transcr. at gene 5' and 3' Gastric stomach

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