Tag | Content |
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EnhancerAtlas ID | HS026-00498 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr1:21644470-21646120 |
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) |
ESR2 | MA0258.2 | chr1:21644930-21644945 | AGGTCAGCCTGGCCT | + | 7.13 | SREBF1 | MA0595.1 | chr1:21645053-21645063 | GTGGGGTGAT | - | 6.02 |
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| Number of super-enhancer constituents: 39 | ID | Coordinate | Tissue/cell |
SE_00105 | chr1:21640019-21654616 | Adipose_Nuclei | SE_00854 | chr1:21642962-21648227 | Adrenal_Gland | SE_01643 | chr1:21642185-21648218 | Aorta | SE_02944 | chr1:21644056-21645524 | Bladder | SE_02944 | chr1:21645843-21646528 | Bladder | SE_03598 | chr1:21644394-21645277 | Brain_Angular_Gyrus | SE_04518 | chr1:21643279-21645748 | Brain_Anterior_Caudate | SE_04518 | chr1:21645844-21646711 | Brain_Anterior_Caudate | SE_05710 | chr1:21643177-21645586 | Brain_Cingulate_Gyrus | SE_05944 | chr1:21639044-21646536 | Brain_Hippocampus_Middle | SE_08398 | chr1:21643228-21645720 | Brain_Inferior_Temporal_Lobe | SE_08982 | chr1:21644985-21645172 | Brain_Mid_Frontal_Lobe | SE_26127 | chr1:21642960-21646679 | Duodenum_Smooth_Muscle | SE_26770 | chr1:21642974-21647847 | Esophagus | SE_28486 | chr1:21644573-21646764 | Fetal_Intestine | SE_29337 | chr1:21644662-21646709 | Fetal_Intestine_Large | SE_31433 | chr1:21643029-21648183 | Gastric | SE_39164 | chr1:21643088-21645576 | IMR90 | SE_42174 | chr1:21642958-21646742 | Lung | SE_44380 | chr1:21642937-21647054 | NHDF-Ad | SE_45045 | chr1:21643168-21646698 | NHLF | SE_46660 | chr1:21643459-21645622 | Ovary | SE_46660 | chr1:21645855-21646940 | Ovary | SE_47592 | chr1:21643574-21645731 | Pancreas | SE_47592 | chr1:21645786-21646790 | Pancreas | SE_48583 | chr1:21642944-21648219 | Right_Atrium | SE_50108 | chr1:21643010-21645670 | Sigmoid_Colon | SE_50108 | chr1:21645842-21646761 | Sigmoid_Colon | SE_52633 | chr1:21642919-21645734 | Small_Intestine | SE_52633 | chr1:21645749-21646973 | Small_Intestine | SE_53334 | chr1:21642938-21645903 | Spleen | SE_54639 | chr1:21639148-21648300 | Stomach_Smooth_Muscle | SE_56171 | chr1:21642916-21645508 | u87 | SE_56171 | chr1:21645755-21646598 | u87 | SE_65263 | chr1:21643359-21649820 | Pancreatic_islets | SE_67931 | chr1:21642916-21645508 | u87 | SE_67931 | chr1:21645755-21646598 | u87 | SE_68932 | chr1:21643728-21645709 | H9 | SE_68932 | chr1:21645866-21648182 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I021312 | chr1 | 21638973 | 21657659 |
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Enhancer Sequence | AGTGGGGACA AAACACATGC AAAGCAGGGC CTGCCCCTCC AAGGTGCACC TTGAAGGTAT 60 CAGACGGCAT GGACGAGGTC CCCTCGCTGG CTGCTGTGAC GGTTAAACGA TTCTTCCCAG 120 CTCTGCACAA CTCAAGTGAT AGCTGTTGGA CTCGGAGATG AACAAGAGTG AGGGAAACGG 180 TGGGGGAGAG CAGTGGGCAA GACCTGGCGT GGCAAGTGGG GAGCAGGAGG CCCTCGTGTG 240 GACTCGCAGA GACCCAAACC CAATGAAACA AGTACCCTGC TGGCGCATGT GCAGGAACTG 300 ATCAGCGTTC CTGAGGGCCC AAGGACATTT CCAGGGCACA GCTTGGGGAG GGCAGCAGAG 360 TGGGAGCAGC TGTGAAATTG GGTTTCAGGT CATGACGCAG TTGGGGAACT TATTTCCTTC 420 ATCCCTGCCC TTTCCTGACC CTGTCCCACT CCCTTAACAA AGGTCAGCCT GGCCTAGGGG 480 TGTCCTCCCT GGAGACCTCC CCTCCCTTGT GCCTCAGCCT CTCACTGTCT TTGGGGCAGA 540 CATTTCTCCG CTCTGGGCTT CAGTTTCTCT ATCTGTAAAA TGGGTGGGGT GATATTTCAG 600 GCCTTAGCAA CTTCTAAAAT CCCATTTTTT GAAGATTTAG AACCAGTGAG CCTTCCTGAG 660 GCCCACTTCA CAAGCCTATC CAAGCAGAGG TGGCAAAATC CTCCTCCCTG GGTGAGAGGC 720 AGGCGACACC CCTGAGTTGG TCACACCAGC CTTCCAAGGA GCTAACCCGA CCTGACAGTC 780 ACTTCAGCCT GGCCAGGCCC CCAGGCAGTG TGCCAAAAAG CGGACGGGGG AGGGGATTTG 840 CAGCAAGAGC TACAGCTCCC CAGAGGCCGC ACTTCTGTCG GGGGAGACGC TGAGCGAGGG 900 TCAGAAGAAA GTCAGCATGG GAAATGTGAC GTCAGCAGAG GCAGATGCGA AGGAATACTA 960 TCCGAAAATG CTTCCGTAAA CTCACCCTCC CAGGAAGCCA AATTCTGTGG GTTTTCAGTG 1020 GAGCTGGGTC TGTACAATCT CCCGGGCTCC GTTTTCTCAT CAGCTAAGTC AAAATAATAA 1080 AGTGAGGCCA GGCACGGTGG CTCAAGCTCG TAATCCAAGC ACTTTGGGAA GCCAAGGTGG 1140 GTGGATTGCC TGAGCTTAGG AGTTCGAGAC CAGCTTGGGC AACATGGTGA AACCCCGTCT 1200 CCACTAAAAT ACAAAAAAGT AGCCAGGCGT GGTGGTGTGC GTCTATAATC CCAGCTACTT 1260 GGGAGGCTGA GGTGGGACAA TCGCTTGAAC CCGGGAAGTG GAGGTTGCAG TGAGCCGAGA 1320 TCGCATCACT GCTTTCCAGC CTGGGAGACA GAGCGAGACT CCGTCTCAAA ATAATAATAA 1380 TCATAATCAT AATCATAATC ATAATCATAA AGTGGACTAC GCAGGGCTTT TCTAGAGACA 1440 TGATAAGACC TCGTGTCTAA ATGGCCTGGT ACATACTAGG GCCTCCATAA ATGCCGGCTC 1500 CATGCTGCCC CCACCTCTGT CCACCAGGGC ACCCCCGGCA CCAAGGGCCA GACTCCCTCT 1560 GCTGCCCCCA ATCTGCTTCT CAGACTTTCT GCTCCTGGCC TTCCTGGGAG CCCTCCAAGC 1620 CAGCAGCTGT GCCCTCCCCT CTGTGAACTG 1650
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