Tag | Content |
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EnhancerAtlas ID | HS182-00387 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:21643490-21645750 |
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 | KLF4 | MA0039.3 | chr1:21644137-21644148 | CCACACCCTCC | + | 6.32 | Klf1 | MA0493.1 | chr1:21644135-21644146 | AGCCACACCCT | + | 6.02 | MITF | MA0620.2 | chr1:21644318-21644336 | ACAGGTCATGTGACTTCT | + | 6.53 | MITF | MA0620.2 | chr1:21644318-21644336 | ACAGGTCATGTGACTTCT | - | 6.53 | SREBF1 | MA0595.1 | chr1:21645053-21645063 | GTGGGGTGAT | - | 6.02 |
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| Number of super-enhancer constituents: 31 | 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 | chr1:21642987-21644019 | Bladder | SE_02944 | chr1:21644056-21645524 | Bladder | SE_03598 | chr1:21643482-21644096 | Brain_Angular_Gyrus | SE_03598 | chr1:21644394-21645277 | Brain_Angular_Gyrus | SE_04518 | chr1:21643279-21645748 | 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_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_47592 | chr1:21643574-21645731 | Pancreas | SE_48583 | chr1:21642944-21648219 | Right_Atrium | SE_50108 | chr1:21643010-21645670 | Sigmoid_Colon | SE_52633 | chr1:21642919-21645734 | Small_Intestine | SE_53334 | chr1:21642938-21645903 | Spleen | SE_54639 | chr1:21639148-21648300 | Stomach_Smooth_Muscle | SE_56171 | chr1:21642916-21645508 | u87 | SE_65263 | chr1:21643359-21649820 | Pancreatic_islets | SE_67931 | chr1:21642916-21645508 | u87 | SE_68932 | chr1:21643728-21645709 | 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 | CAGTCACTGA AGAGTCTCTC CCAGTCTCTT CCCCTGGGAG AGAGAGTGGT AAGAAACGGA 60 CTGGGGGTGT GGGGGTATGG GGGATTCAAC TGCATTTGGG ATGTTTTATT CCTTAAGCTG 120 AACACTTACA TACCAGTGTT TGGTTTTACT GAGCCTGATG CTTTTAATAT GTCTGAGATA 180 TTTTGCTACC CACCAGAATA GGTCAGACAG ACTTGGGCTT CGAGCCAGCC CTGTGCTTTG 240 CTGCCATGCG ATCCTAGTCT TCTCTGTGAA GTGGGAATCC TATCGCCCAC TGTTAGCTCC 300 CGGGACTCTT CTGAGAATTA AACAAGGTCG TGTCTGCAAA GGGCCTGGCA TCCGGTGGCT 360 GCCATTGTTC CTGCTGCTGT TGGGAGGGTC TCCCAAAATG AACAGACAGA GGGGAAGGCC 420 AGCTCGCAGG CCTCAGATGG GGAAAAGGGT TTGCTTGTCA CAAGGCCAGT CCAGCCCGCG 480 GCGACGCTGA GCTGGTGACG CATCTGCAGC TCTGGGGATT GAGCAATCTT GGTCCCCTGA 540 CCGGGATGGA GTCATGGGCC CAGGCTGGCT GGAGCCCCTC TACTGCTCCC CACCCGCTTC 600 TCAGACTTTG TGTTCCTGGC CTTCTTGGGA CCCCTCCAGG CTGGCAGCCA CACCCTCCCC 660 TCTGTGAGCT AGGCAGGAAA GCCCGGTTCC ATTCCTGCCC AGTTCTCTTC GGCCTCTCCT 720 GAGCCCCTGC TCCCCAACTC AAGGTGGGGT CCTAACCACC TTGCATCCAA ACAGATCCTC 780 TGGAGACGCA CGAGTGGGTC AGGGCAGTCA AGAGCTGTGC AGGCTCAGAC AGGTCATGTG 840 ACTTCTGTAG GTCCCTGGCT TTAGCAGGTG TGGCCGAAGG TGTGGGGTGC CAGTGTCTGT 900 CTCCTGGTTC AAATCCAGGC TCGGGGTGTG ACCCCAATGT TCTTGAACTT AAATCAGAGC 960 CACCGCGATC TCTTTCTCGA AGTGGGGACA AAACACATGC AAAGCAGGGC CTGCCCCTCC 1020 AAGGTGCACC TTGAAGGTAT CAGACGGCAT GGACGAGGTC CCCTCGCTGG CTGCTGTGAC 1080 GGTTAAACGA TTCTTCCCAG CTCTGCACAA CTCAAGTGAT AGCTGTTGGA CTCGGAGATG 1140 AACAAGAGTG AGGGAAACGG TGGGGGAGAG CAGTGGGCAA GACCTGGCGT GGCAAGTGGG 1200 GAGCAGGAGG CCCTCGTGTG GACTCGCAGA GACCCAAACC CAATGAAACA AGTACCCTGC 1260 TGGCGCATGT GCAGGAACTG ATCAGCGTTC CTGAGGGCCC AAGGACATTT CCAGGGCACA 1320 GCTTGGGGAG GGCAGCAGAG TGGGAGCAGC TGTGAAATTG GGTTTCAGGT CATGACGCAG 1380 TTGGGGAACT TATTTCCTTC ATCCCTGCCC TTTCCTGACC CTGTCCCACT CCCTTAACAA 1440 AGGTCAGCCT GGCCTAGGGG TGTCCTCCCT GGAGACCTCC CCTCCCTTGT GCCTCAGCCT 1500 CTCACTGTCT TTGGGGCAGA CATTTCTCCG CTCTGGGCTT CAGTTTCTCT ATCTGTAAAA 1560 TGGGTGGGGT GATATTTCAG GCCTTAGCAA CTTCTAAAAT CCCATTTTTT GAAGATTTAG 1620 AACCAGTGAG CCTTCCTGAG GCCCACTTCA CAAGCCTATC CAAGCAGAGG TGGCAAAATC 1680 CTCCTCCCTG GGTGAGAGGC AGGCGACACC CCTGAGTTGG TCACACCAGC CTTCCAAGGA 1740 GCTAACCCGA CCTGACAGTC ACTTCAGCCT GGCCAGGCCC CCAGGCAGTG TGCCAAAAAG 1800 CGGACGGGGG AGGGGATTTG CAGCAAGAGC TACAGCTCCC CAGAGGCCGC ACTTCTGTCG 1860 GGGGAGACGC TGAGCGAGGG TCAGAAGAAA GTCAGCATGG GAAATGTGAC GTCAGCAGAG 1920 GCAGATGCGA AGGAATACTA TCCGAAAATG CTTCCGTAAA CTCACCCTCC CAGGAAGCCA 1980 AATTCTGTGG GTTTTCAGTG GAGCTGGGTC TGTACAATCT CCCGGGCTCC GTTTTCTCAT 2040 CAGCTAAGTC AAAATAATAA AGTGAGGCCA GGCACGGTGG CTCAAGCTCG TAATCCAAGC 2100 ACTTTGGGAA GCCAAGGTGG GTGGATTGCC TGAGCTTAGG AGTTCGAGAC CAGCTTGGGC 2160 AACATGGTGA AACCCCGTCT CCACTAAAAT ACAAAAAAGT AGCCAGGCGT GGTGGTGTGC 2220 GTCTATAATC CCAGCTACTT GGGAGGCTGA GGTGGGACAA 2260
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