Variant report

Variant rs2699437
Chromosome Location chr4:3486819-3486820
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:88 , 50 per page) page: 1 2
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:3467000-3493600 Weak transcription Aorta Aorta
2 chr4:3476800-3490800 Bivalent Enhancer Fetal Muscle Trunk muscle
3 chr4:3481000-3489200 Enhancers Fetal Heart heart
4 chr4:3481200-3488800 Enhancers Left Ventricle heart
5 chr4:3481400-3491200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr4:3482400-3487200 Bivalent Enhancer Fetal Muscle Leg muscle
7 chr4:3483200-3489600 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
8 chr4:3485000-3489400 Bivalent Enhancer Placenta Placenta
9 chr4:3485200-3487400 Enhancers Pancreas Pancrea
10 chr4:3485200-3487400 Bivalent Enhancer Sigmoid Colon Sigmoid Colon
11 chr4:3485200-3487400 Enhancers Spleen Spleen
12 chr4:3485200-3488200 Flanking Active TSS HMEC breast
13 chr4:3485200-3489400 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
14 chr4:3485200-3489600 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
15 chr4:3485400-3487600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr4:3485400-3488200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
17 chr4:3485400-3488600 Flanking Active TSS Primary B cells from peripheral blood blood
18 chr4:3485400-3489800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
19 chr4:3485600-3487000 Bivalent Enhancer Fetal Thymus thymus
20 chr4:3485600-3488000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
21 chr4:3485600-3488600 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
22 chr4:3485800-3487000 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
23 chr4:3485800-3487000 Bivalent Enhancer GM12878-XiMat blood
24 chr4:3485800-3487000 Flanking Bivalent TSS/Enh NHEK skin
25 chr4:3485800-3487200 Bivalent Enhancer Adipose Nuclei Adipose
26 chr4:3485800-3487600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
27 chr4:3485800-3487600 Flanking Bivalent TSS/Enh Foreskin Keratinocyte Primary Cells skin02 Skin
28 chr4:3485800-3487600 Flanking Active TSS Esophagus oesophagus
29 chr4:3486000-3487000 Flanking Active TSS Hela-S3 cervix
30 chr4:3486000-3487600 Active TSS Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
31 chr4:3486000-3488000 Bivalent Enhancer Placenta Amnion Placenta Amnion
32 chr4:3486000-3488200 Flanking Active TSS Primary Natural Killer cells fromperipheralblood blood
33 chr4:3486000-3489000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
34 chr4:3486200-3487000 Bivalent Enhancer Primary T cells effector/memory enriched fromperipheralblood blood
35 chr4:3486200-3487000 Bivalent Enhancer Fetal Intestine Large intestine
36 chr4:3486200-3487000 Bivalent Enhancer Fetal Intestine Small intestine
37 chr4:3486200-3487000 Flanking Bivalent TSS/Enh Rectal Mucosa Donor 31 rectum
38 chr4:3486200-3487200 Flanking Bivalent TSS/Enh Skeletal Muscle Male skeletal muscle
39 chr4:3486200-3487400 Bivalent Enhancer Primary T helper memory cells from peripheral blood 1 blood
40 chr4:3486200-3487400 Bivalent Enhancer Primary T helper cells PMA-I stimulated --
41 chr4:3486200-3487400 Enhancers Right Atrium heart
42 chr4:3486200-3487400 Flanking Active TSS Right Ventricle heart
43 chr4:3486200-3487800 Bivalent Enhancer Primary T helper cells fromperipheralblood blood
44 chr4:3486200-3487800 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
45 chr4:3486200-3488600 Bivalent Enhancer H1 Cell Line embryonic stem cell
46 chr4:3486400-3487200 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Female --
47 chr4:3486400-3487200 Enhancers Psoas Muscle Psoas
48 chr4:3486400-3487400 Flanking Active TSS Primary B cells from cord blood blood
49 chr4:3486400-3487400 Enhancers Primary T helper naive cells from peripheral blood blood
50 chr4:3486400-3487400 Bivalent Enhancer Primary T helper naive cells fromperipheralblood blood

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