Tag | Content |
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EnhancerAtlas ID | HS145-10764 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr18:12005100-12006430 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLI2 | MA0734.2 | chr18:12005727-12005742 | CCGCGTGGGTGGTCT | - | 6.46 | STAT1 | MA0137.3 | chr18:12006134-12006145 | TTTCTAGGAAA | + | 6.14 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_23131 | chr18:12004661-12007002 | Colon_Crypt_1 | SE_23828 | chr18:12004773-12006909 | Colon_Crypt_2 | SE_25040 | chr18:12004601-12007001 | Colon_Crypt_3 | SE_26608 | chr18:12004648-12006956 | Esophagus | SE_31757 | chr18:12004501-12007585 | Gastric | SE_47528 | chr18:12004997-12005401 | Pancreas | SE_47528 | chr18:12005519-12006001 | Pancreas | SE_47528 | chr18:12006071-12006900 | Pancreas | SE_50470 | chr18:12004706-12007618 | Sigmoid_Colon | SE_65647 | chr18:12004952-12013930 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr18 | 12005208 | 12005369 | chr18 | 12005666 | 12005763 |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I012004 | chr18 | 12004667 | 12007576 |
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Enhancer Sequence | CGCTGCAGCC ACACAGTGCA GAAGCCTGCT CCCTGCTGCC CACAAGCATG AGGCAGGTGG 60 GAAGGGGGAT GCTCGTGCCA CCTTGTAGGC GGGCAGGCAG TCTCATGGGC AGAGGTGTAC 120 ACAAGGTGGG TGATGAGGAA GACAGCTCTA GGGTATGAAT GATCAGCTGC TGAAAAACAT 180 CCAGTGCTCA GTGTGGGTAC TTAGAGTTAT TCTCATAAAA AATGTGAGGC AGAGTTAGTC 240 AGGTGTGGTG ATGCATGCCT GTGGTCCCAG CTACTCAGGA GGCTGAGGCA GGAGGATTGC 300 TTGAGCCCAG TGGTTTGTGG CTTCAGTGAG CCATGATTGT GCCACTGCAC TCCAGCCTGG 360 CTGACAAAGC GAGACCATGT CTCCAAGAAA AAAAAAAAAA ATTTCTAAAA GTACTTGCTG 420 GGTTACACTA AATGAAACCT AAAAAACAAA TAGATAAATA ATAAAGGTTA CACACAGCAG 480 AAGCTTTGTT AACAAATTAA CTTATATTAA TAGTTGCTGC TGGGAAAACA AGCTGCTTGG 540 TGACTTCCCT AAAGGGTGTC CCACGCATCT GGCGAATGAA CAGACAGAGC TCCTGCTCCC 600 GAGTGTCCTG GGAGGCACGT GGGCATGCCG CGTGGGTGGT CTGGGTGCTG CAGCGTGAGT 660 TGTCCTGGGT GTGGAGTGTC AGTGCCTGCA GACCCACACT GCCTCCTCCT TCAGGGCTCA 720 CTGGCAGTTT TCTTTCCACC GCTTCAGTTT CCTACTTGAA GTCAGGTTTA AAAAGGAGAA 780 GAATTGCACA TTCCTCCTCA GTTTCTTAGA AACTTACCTT TGTGCCTGAG TCATTTCTAG 840 TCCCTCTGGA CCTGAGTCAT ATCTGTTCGC TGCTTTGTCA ACCTTGTGCC CAGTTTAAGC 900 TTTCGTAGTT GCTCCTTGTA TGTGTGTTTT CAGGGTGTGG AGCGTTTTCT TTAAAAACGT 960 CATTGCAAGC CATTACAGAA GAGGAAAGTC ACATAGCTAC AGAAGACATG GAAAAACAGA 1020 TTTAGTGCCT GAAGTTTCTA GGAAAACTGG CAGTGCTGAC AGCACTTATG ATCACGCCCT 1080 AAGTGGAATC ATCACCTGTG TGTCTCCTGC AGGCTGCTGT TGTCAGGAGG CAGCCTCTCC 1140 ACCCCCTGCC CCGGCTGCCA TTGTGGCTTC TACCCACCAT TTTTCCTCCT AGATCTGTTT 1200 GGGGAGCACC AGTTCCTGAG CAGGGGCTCT GGCTGGTGGG CCTGTGCATC ACCTGACCTA 1260 GAAGCATGTG GACAACTGAG AGTGGAGAGG CAGTTCCTGC AAGGAGCAAG GCGTGCAGTG 1320 TAGATGAAGA 1330
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