Tag | Content |
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EnhancerAtlas ID | HS018-13993 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr20:25018340-25019960 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF2 | MA0051.1 | chr20:25018824-25018842 | GGAAAGTGAAAGTCTCTT | + | 6.18 | ZNF263 | MA0528.1 | chr20:25019622-25019643 | TCCCTCCCCTGCCCCTCCTCC | - | 7.77 |
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| Number of super-enhancer constituents: 33 | ID | Coordinate | Tissue/cell |
SE_01860 | chr20:25017701-25021723 | Aorta | SE_03453 | chr20:25017710-25019265 | Brain_Angular_Gyrus | SE_03453 | chr20:25019320-25021482 | Brain_Angular_Gyrus | SE_04126 | chr20:25016146-25021701 | Brain_Anterior_Caudate | SE_05098 | chr20:25016289-25026626 | Brain_Cingulate_Gyrus | SE_05867 | chr20:25009884-25041019 | Brain_Hippocampus_Middle | SE_06947 | chr20:25008932-25026827 | Brain_Hippocampus_Middle_150 | SE_08089 | chr20:25015965-25026562 | Brain_Inferior_Temporal_Lobe | SE_08927 | chr20:25018757-25018950 | Brain_Mid_Frontal_Lobe | SE_08927 | chr20:25019039-25019321 | Brain_Mid_Frontal_Lobe | SE_11633 | chr20:25015552-25028126 | CD20 | SE_23688 | chr20:25017698-25021595 | Colon_Crypt_1 | SE_24056 | chr20:25017780-25020014 | Colon_Crypt_2 | SE_25265 | chr20:25017710-25019730 | Colon_Crypt_3 | SE_27084 | chr20:25017735-25021719 | Esophagus | SE_29549 | chr20:25018015-25019244 | Fetal_Intestine_Large | SE_29549 | chr20:25019674-25021615 | Fetal_Intestine_Large | SE_30760 | chr20:25017959-25018862 | Fetal_Muscle | SE_30760 | chr20:25019497-25021753 | Fetal_Muscle | SE_31460 | chr20:25017655-25021710 | Gastric | SE_40636 | chr20:25016197-25021763 | Left_Ventricle | SE_41962 | chr20:25017724-25020051 | LNCaP | SE_42209 | chr20:25016477-25021748 | Lung | SE_47497 | chr20:25017799-25018933 | Pancreas | SE_47497 | chr20:25019007-25021557 | Pancreas | SE_48726 | chr20:25017715-25021736 | Right_Atrium | SE_49493 | chr20:25018255-25021555 | Right_Ventricle | SE_50687 | chr20:25017729-25021565 | Sigmoid_Colon | SE_51643 | chr20:25016516-25022884 | Skeletal_Muscle | SE_52650 | chr20:25017716-25021718 | Small_Intestine | SE_54397 | chr20:25018123-25020883 | Spleen | SE_54979 | chr20:25017519-25024711 | Stomach_Smooth_Muscle | SE_59947 | chr20:25013726-25040720 | Ly4 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr20 | 25019087 | 25019137 | chr20 | 25018384 | 25018988 |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I025035 | chr20 | 25015714 | 25021830 |
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Enhancer Sequence | CCTTAGGGAA GGGAAGCCTG GCGAGGCTGA CCCCTTCTCA CGCAGGAGGA GCGTGGAAGG 60 CCACGCAAAG CATGGATGGC CAGCTCGCAT CTCATGGACC CAGGCCTGGG GAACAGACTC 120 CTTCCCTCCT GGCAGCCTCC TCTGGCCCTG ACATTACTGT AGCCACTGAC TGTCATTCAA 180 TGGTGGTAAG ATTTGCTCAC TCTGCTGAGA GAACAGAAGA CCAGGAAGTC AGCTAGCAGG 240 GCTCATAAAC CAAGTATGAA ATTTCTCACG TCATTATTTG ATGTCATGAC CATGACATTT 300 AGCAAAGAGA AGCTGCCGTG AAAACATAAA GTGGCAGCCG CACTTGAACA TGAATGGTCC 360 CCTGGGCCAA GGCGGGCCCA GGCACAGCGA GGGCCCCCAG GAGACATGAG CTGAGTTGCT 420 AGTAGTGATG CCAGCTCAGC CAGTAACAAG ATCACTAAAG CTATGTGTGT TCTAAATTCC 480 TTATGGAAAG TGAAAGTCTC TTCCCTGAGG TTTTGCTAGA CTCTGTGGAA AGCGCTGAAC 540 CTGCAAGTTT ATCACTCAGG AGTCTCACGG GAGGCCAAAC AATGACTGAT CAGAGAGCAG 600 GGTTCCCAAC ACAGCCCCCC ACACCACTGG GGCCTGAACT GTCTCATCTG TGAAATGGCC 660 TAATAATAGG ACCCACTACC AAGGTGGTCG TGGAGACCAA ATATGAAGTT GCAGGCACCT 720 TTGAAGGTGA CCTGTAAACA GTGGCCATAA TGACTGCAGA AAATACAAGA CATGGGAAAA 780 AGAGAATTAT TGAACACTGA TGGACCTTTA AGAAAGGTGG GCACCTCAGG CACCTCCTTC 840 TCAGGAGGGC AGGTGCAAAA TGCTGGTTTG CCTTATGGAA GCTGCAGTCT CCGTGTCGCC 900 GGCTCAGGGC ACATGCACCT CAGCTGTGTG AATGCCTTGC AGGAAGCCCT CACCTGCACA 960 GCCTGCCTGC TCCATGCCCC CAAGGCAGGT GCTGAGGGCG GGAGTAGATC TGAGAAGGAT 1020 GCAGAGCCTC CTACAGTTGG GGTTGCTGCC AGTCTGGGGG TTCCAGGCAC TCAGCCCGAG 1080 GCCTGTGCTT CCAAAAGGCC AGAGGGAAGG CAGTTCCACC CCACATGCTC TGCACAGCCT 1140 ACCACCATCT GCCATGTCGT CCTGTCACTG CCCCCCTGCT GGCTACCCAA GCTTCTCCAG 1200 CCATGATTGC CTGCCACTGC CAGCACAGGA AACCTCCTCT CCAGGCCCAT GGCCTCCTAC 1260 CTCCTCTGCA TCCAGGGGGT ATTCCCTCCC CTGCCCCTCC TCCCACTTGT CCTCACCCCA 1320 CCCTCAGTTC ACAGCCCCAT CCCATGGAAC AAGGACAGAA CAGCTATCAA GCAAGTATCC 1380 TGTACCCAGG GCTGCTCCCA CAGAGCAGGT TCCCATGGAG AACCCACTTA ACCCTCACAA 1440 CAGCCCATAG GTTCTGAGCT CCCCTTCCCT TCTTCACTTT CCTGATGAGG AAATTGAGGC 1500 ATAGAGAAGT TGGGCCACTT TCTCAAGGCT ATTCAGCTGA AGGAGTCAGG GCAGGATTCA 1560 AACCCAGGCC CAGCTCCAGG GGCCTTGCTG TCAGCCAGCT CCTCAGTATC AGAACCACTC 1620
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