Tag | Content |
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EnhancerAtlas ID | HS101-28767 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr22:30182740-30184450 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata1 | MA0035.3 | chr22:30184275-30184286 | TCCTTATCTGT | + | 6.14 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_27345 | chr22:30182911-30184477 | Esophagus | SE_31847 | chr22:30182746-30184651 | Gastric | SE_34183 | chr22:30182849-30184241 | HCC1954 |
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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 |
GH22I029786 | chr22 | 30182837 | 30184246 |
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Enhancer Sequence | TCGTGCCAGT GCACTCCAGC CTGGGTGACA GAGCAAGACT CCGTCTCAAA AAAAAAAAGA 60 GACAAGGTCT CACTCGTTGC CCAGGCTGGA GTGCAGTGGC ATGATTATAG CTCACTGCAG 120 CCTCCAACTC CTGGGTGCAC CCTCCAACTC CCGGGCTCAA GTGATCCTCC AGCCTCAGCC 180 TCCTGCGTAG CTGGGACTAC AGGTGTGCAC CACCATACCC ACCTTATTTA TTATTTTCTG 240 GAGGGATCGG GTCTTGCTAT GTTGCACAGG CTGGAGCAGC TGCCAATGTT AATTAAACCT 300 TGGGATCTCC TCAGAGGATT TAACTGGCAC CAGGTGGAAA GATTTCATCT GGTCCAACAG 360 GATCACTGTA CAGATGGGAA AACTGAGGCC CTGAGAGATG AGGCAGTAGG CGTAGGAACA 420 CCATTCTGGA TGGCCCCTGA GCTGTTTTCA AAGCACCTCT GAAAGAGTGC TTTCAAGATC 480 TGAAATGAGA AAGTAGTAGA TCCTCAAGGG AGATGAAGTT TGACCTGGCA CTACATTCTG 540 AAAAATTTGA AAAACTGACT CCTTCTCAAA TACTTTAAAC CAGGATTTTC ACATGAGGCC 600 TGAACACCAG TCCAGGTGGG TGGGAGGTAT AGATGACTAA GAGAATGTGA GAGGGGCCGT 660 GTGAACAGGA ACAGGTAAGA CCAGTAAATC CTGGGAACTC CCAACTCACC TTGCCTTGCT 720 CCAGGGACAA GCACTGGACC TGAGGAGTTT AGGGAGGTCC CTGGCAAATG CCTCCAGGAG 780 GAAACAGAGT CTTCCTGCTG CCTGTCAGGA CGGCTGACCC TGGGCCTGAT CTCAGCTAAT 840 TCAGCAGCTC AGGGGGAGGA CACCACCCCC GTATCTGCTC TGCATCTCAA ATACACCAAG 900 AGGGCTGGCC AGGCAGAGGG ATTGCTATTG ATTTTCACTT GTGCGGGCTG ACCTAACAAA 960 ACCAATCCAT CAAGTGCCTG TCTGCCTCTG CTTCAGACTC TCATCCTAAG CACGTGCAAA 1020 TAAATTGCAC CAGCATCCAG GGTGATTTGT CAAGGTCCAG CCAGGCATGG GCCCTGGCTT 1080 CCACTGATAG GATGGGGCTC CAGGCTAGGC TGGGCTAGGG TCAGCCCAGT CAATGCCCCG 1140 CTGTTGACTC GCCATTGAGT GACAACACGC AGTGTGGCCT GGCATCTGCT GCCACGCTAG 1200 GAACTGGTTG GCCATGCCTG GGAAGGGGCT TTGAGGAAAC AGGCCCAAGT CCCACTCACT 1260 TTGACAGGGC TTGGCAGCGA CATTCTCACT TGTTTCTTAA GGTTTCTGTC CGAACTCTAG 1320 ATTTGGGGGG ATTTATTACA ATGTAGATAC AACCATGAGG TGCTGAGTTT GGGTACTGCC 1380 TCTGCCACTG GCTGAATGTC CTTGGGCCAG TTGTGAGATG GAGATGACAC CACCTACAGG 1440 GGTCTAGAAC CCTGTAAAGG CCAGGGTCCA ATCCCTGTTC TGCCACTTCC TAGCTGTGGC 1500 CGGGGCAGGT GCCTTCAGCC CTCGGTGCCT CATTTTCCTT ATCTGTACTA CCGGGCTGAA 1560 AATGGTACCT ACCTCTTACA GTGGAGCTGT CATAACTGAA TGAGAAAATG CAAAGGACCA 1620 CAGGGGCTCA CCCCACCCAG CCCTTCATTC CACTAGCAAG GACTGGAGGC TCAGAGAAGG 1680 GGGTGATGTT CTGGGGTCAC ACAGCAAGGC 1710
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