Tag | Content |
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EnhancerAtlas ID | HS118-00235 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr1:21643230-21645460 |
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 | ACATCATGGG ATGGAATACT ACACGGTAAT GAAAACCAAG TGGCTGCAAC TCAAACAACA 60 GGAAGACAGA AAAGCTGCAG AAGTCAACAT GGAGCCTCCA ATCAATTATT GAAAGTTCAA 120 AAACAGTGAG CAACATCATA CCTATGTATC ATTTAGGGAG GCAGAATCAG GCTGCGCTTG 180 GTGGCTCACA CCTGTAATCC CAGCACTTTG GGAGGCCGAG GTGGGCGGAT CACCTGAGGT 240 CAGGAGTAAC AGTATCAAGA CAGTCACTGA AGAGTCTCTC CCAGTCTCTT CCCCTGGGAG 300 AGAGAGTGGT AAGAAACGGA CTGGGGGTGT GGGGGTATGG GGGATTCAAC TGCATTTGGG 360 ATGTTTTATT CCTTAAGCTG AACACTTACA TACCAGTGTT TGGTTTTACT GAGCCTGATG 420 CTTTTAATAT GTCTGAGATA TTTTGCTACC CACCAGAATA GGTCAGACAG ACTTGGGCTT 480 CGAGCCAGCC CTGTGCTTTG CTGCCATGCG ATCCTAGTCT TCTCTGTGAA GTGGGAATCC 540 TATCGCCCAC TGTTAGCTCC CGGGACTCTT CTGAGAATTA AACAAGGTCG TGTCTGCAAA 600 GGGCCTGGCA TCCGGTGGCT GCCATTGTTC CTGCTGCTGT TGGGAGGGTC TCCCAAAATG 660 AACAGACAGA GGGGAAGGCC AGCTCGCAGG CCTCAGATGG GGAAAAGGGT TTGCTTGTCA 720 CAAGGCCAGT CCAGCCCGCG GCGACGCTGA GCTGGTGACG CATCTGCAGC TCTGGGGATT 780 GAGCAATCTT GGTCCCCTGA CCGGGATGGA GTCATGGGCC CAGGCTGGCT GGAGCCCCTC 840 TACTGCTCCC CACCCGCTTC TCAGACTTTG TGTTCCTGGC CTTCTTGGGA CCCCTCCAGG 900 CTGGCAGCCA CACCCTCCCC TCTGTGAGCT AGGCAGGAAA GCCCGGTTCC ATTCCTGCCC 960 AGTTCTCTTC GGCCTCTCCT GAGCCCCTGC TCCCCAACTC AAGGTGGGGT CCTAACCACC 1020 TTGCATCCAA ACAGATCCTC TGGAGACGCA CGAGTGGGTC AGGGCAGTCA AGAGCTGTGC 1080 AGGCTCAGAC AGGTCATGTG ACTTCTGTAG GTCCCTGGCT TTAGCAGGTG TGGCCGAAGG 1140 TGTGGGGTGC CAGTGTCTGT CTCCTGGTTC AAATCCAGGC TCGGGGTGTG ACCCCAATGT 1200 TCTTGAACTT AAATCAGAGC CACCGCGATC TCTTTCTCGA AGTGGGGACA AAACACATGC 1260 AAAGCAGGGC CTGCCCCTCC AAGGTGCACC TTGAAGGTAT CAGACGGCAT GGACGAGGTC 1320 CCCTCGCTGG CTGCTGTGAC GGTTAAACGA TTCTTCCCAG CTCTGCACAA CTCAAGTGAT 1380 AGCTGTTGGA CTCGGAGATG AACAAGAGTG AGGGAAACGG TGGGGGAGAG CAGTGGGCAA 1440 GACCTGGCGT GGCAAGTGGG GAGCAGGAGG CCCTCGTGTG GACTCGCAGA GACCCAAACC 1500 CAATGAAACA AGTACCCTGC TGGCGCATGT GCAGGAACTG ATCAGCGTTC CTGAGGGCCC 1560 AAGGACATTT CCAGGGCACA GCTTGGGGAG GGCAGCAGAG TGGGAGCAGC TGTGAAATTG 1620 GGTTTCAGGT CATGACGCAG TTGGGGAACT TATTTCCTTC ATCCCTGCCC TTTCCTGACC 1680 CTGTCCCACT CCCTTAACAA AGGTCAGCCT GGCCTAGGGG TGTCCTCCCT GGAGACCTCC 1740 CCTCCCTTGT GCCTCAGCCT CTCACTGTCT TTGGGGCAGA CATTTCTCCG CTCTGGGCTT 1800 CAGTTTCTCT ATCTGTAAAA TGGGTGGGGT GATATTTCAG GCCTTAGCAA CTTCTAAAAT 1860 CCCATTTTTT GAAGATTTAG AACCAGTGAG CCTTCCTGAG GCCCACTTCA CAAGCCTATC 1920 CAAGCAGAGG TGGCAAAATC CTCCTCCCTG GGTGAGAGGC AGGCGACACC CCTGAGTTGG 1980 TCACACCAGC CTTCCAAGGA GCTAACCCGA CCTGACAGTC ACTTCAGCCT GGCCAGGCCC 2040 CCAGGCAGTG TGCCAAAAAG CGGACGGGGG AGGGGATTTG CAGCAAGAGC TACAGCTCCC 2100 CAGAGGCCGC ACTTCTGTCG GGGGAGACGC TGAGCGAGGG TCAGAAGAAA GTCAGCATGG 2160 GAAATGTGAC GTCAGCAGAG GCAGATGCGA AGGAATACTA TCCGAAAATG CTTCCGTAAA 2220 CTCACCCTCC 2230
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