Tag | Content |
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EnhancerAtlas ID | HS145-25836 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr8:134306400-134308090 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFF | MA0495.3 | chr8:134306693-134306708 | ATGCTGAGTCATCAC | - | 6.63 | MAFF | MA0495.3 | chr8:134306693-134306708 | ATGCTGAGTCATCAC | + | 6.64 | NFE2L1 | MA0089.2 | chr8:134306692-134306707 | GATGCTGAGTCATCA | - | 6.47 | Nfe2l2 | MA0150.2 | chr8:134306694-134306709 | TGCTGAGTCATCACG | - | 6.75 | Sox3 | MA0514.1 | chr8:134306430-134306440 | AAAACAAAGG | - | 6.02 | ZNF740 | MA0753.2 | chr8:134306914-134306927 | GGGGGGGGGGCAG | - | 6.33 |
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| Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
SE_00425 | chr8:134301340-134311366 | Adipose_Nuclei | SE_03285 | chr8:134306114-134307169 | Brain_Angular_Gyrus | SE_03285 | chr8:134307354-134309528 | Brain_Angular_Gyrus | SE_04229 | chr8:134301793-134311272 | Brain_Anterior_Caudate | SE_04976 | chr8:134295645-134311554 | Brain_Cingulate_Gyrus | SE_05911 | chr8:134295053-134311486 | Brain_Hippocampus_Middle | SE_07206 | chr8:134302445-134311277 | Brain_Hippocampus_Middle_150 | SE_07895 | chr8:134295546-134311683 | Brain_Inferior_Temporal_Lobe | SE_09628 | chr8:134301461-134311725 | CD14 | SE_19655 | chr8:134305278-134311331 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_24176 | chr8:134305824-134307346 | Colon_Crypt_2 | SE_24176 | chr8:134307418-134311074 | Colon_Crypt_2 | SE_26786 | chr8:134301474-134311822 | Esophagus | SE_27791 | chr8:134300251-134313000 | Fetal_Intestine | SE_28981 | chr8:134300073-134313069 | Fetal_Intestine_Large | SE_31524 | chr8:134300227-134311122 | Gastric | SE_35245 | chr8:134304945-134311975 | HeLa | SE_36421 | chr8:134305230-134312008 | HMEC | SE_41455 | chr8:134299416-134311207 | Left_Ventricle | SE_42343 | chr8:134299449-134311251 | Lung | SE_49373 | chr8:134301634-134311208 | Right_Atrium | SE_50820 | chr8:134301340-134311288 | Sigmoid_Colon | SE_52812 | chr8:134301376-134312556 | Small_Intestine | SE_65084 | chr8:134305754-134311208 | NHEK | SE_65489 | chr8:134304326-134310961 | Pancreatic_islets | SE_67840 | chr8:134304577-134311557 | u87 |
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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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Enhancer Sequence | TCAGGCGCCC CAACATGTTG TCATGGAAAA AAAACAAAGG CTCTGAAGTC CAACTGTCCG 60 GGTTCAAAGT CTGGCTCTCC CACCTGAGCC ATATGGCAAC AGGCAAATCC TGAAACTCTC 120 CTGGCCTCAG TTGCCTCATC CATTCAATGG AGCAATACGA TCCAGGCAAC GTTCTTGCGA 180 GGATGAAGGC AGATGGAGGG AGACAGTGGC TGCTCTGGAG GGAGAGAGAT GTCGTGTCCC 240 TCCCTGGCCT TCCTTCCAGG CTGAGTCAAA CCTGAACCCT GCTTGAGTCT CAGATGCTGA 300 GTCATCACGC TTTCTCTCCC AGGACAAGGC CTCTGAGTCA CATCTGGAAT GGGATTCTCT 360 GGGGTTGGGT CCCAAGGAAG AACTGCAGCT TTGGGCCACC CGAAAAACAC AATGCTATCT 420 TTCTTTCAGG TCCATGAGGA GGCAAGTTCA GGCCAGCGGA TTTCAACGTA ACCCAGGGGG 480 GCCCTCAGCT CAGTTGAGAT CTGTCTTCTG TCATGGGGGG GGGGCAGCCC CATTCAGTCA 540 AAGGCCAACT CAGGGGGCTG CAGCCTCTAA GCCCCTGCCC TTCAGGCTGG CTTTGCTAAT 600 CTCTCAAGAA CACCTGATTT ACACTTAAAA AAAATCATTC CGCTCTGCCC CTTTGGCCTC 660 AAAAGTTTCC TCACCAGAAA TTCAATGAAG ATGCAATTTC CTTTCGCCCC TCCATAGCAG 720 GCAGGCAAAA TCCTGCCAGG AACCCTTTCC ACTGCCTTCA GTCCCACCCA GGAGCCTCTC 780 ACAAAGCTGA GCTCCAGCTC AGTTCGGCCT GGGCACATCC CTCCCCATCC CTGTGCCTCA 840 TTTTCCATCT GTAAAATGGA AAGAAGTTGG ACTAGGTAGG TCCTGTGTGA GTTTTTTATT 900 CCATTCCAAA TGATCAAACT TTGTTGCTCC AAAAGAACTT CCTCACAAGA GACCCAAACA 960 GACACTCCAG GATCCCTCAA AAGCAAAAGC CAACACCTCC ACCCATGCAC AGTCTATTAC 1020 CTCGCCCGAA ACTCAACCTG CTGGTTCACA GGAGAATGGG GCAGAAGACC CAGAGCCATC 1080 CACTTCATCC CATGTGCATA TTTCAACTCC TCCCACCTGC CAGGCGCTGG GCCAGGGGCC 1140 AGGTTACAGG GCAGGGCAGG CAAATCCTCC TCCTTGCCCA GATGCAGTGG GAGACACGGT 1200 CCCACAAAGC TAAGAAGTCA CAGGTCAGGG GAACACCCAG TTTTCCATCC ACACCAAAAC 1260 CCTCTCTCTC CCTTACACCT TCCTTCATCC CCGACACTGT GCCACCCCAG CCTGGGGCTG 1320 GCTCTGCCGC CACACACACC ACACAGAACC GGTCTGCGTC TCCAGCCGTG TGTCTTCCCC 1380 ACCAGAAGGC AGCCCTTCCA AGAAAGGCGC TGGGGTTTGC CCCCTCTGTA CCTTGCTTAT 1440 TTCAATCACA TTTGTGAAAC TCAATAAGAA CGCCAGAATT TCTCAACAGG AAGAGTCTAG 1500 ACTGAAAAAT TCGCCTTGAA ACTACATTTC TGCAGCAAGA ACAGGGGGTT TGTATTTAGA 1560 TATGTTCTTT TGAGGCAGCT TAGGAGAAGG TCCCGTGCAG CTGATGGGTA TTATAAGGAT 1620 GTCTACCGCC CTCCTGCCTG GCCACTGGCT GACTTCTGAA TATTAGATAT TTCCCAGTAG 1680 CTTAAAGAAA 1690
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