Tag | Content |
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EnhancerAtlas ID | HS101-00551 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:19227120-19228950 |
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) |
MEF2A | MA0052.3 | chr1:19228574-19228586 | GCTAAAAATAGA | + | 6.92 | MEF2B | MA0660.1 | chr1:19228574-19228586 | GCTAAAAATAGA | + | 6.44 | MEF2C | MA0497.1 | chr1:19228572-19228587 | GTGCTAAAAATAGAA | + | 8.55 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_26830 | chr1:19228361-19230663 | Esophagus | SE_47330 | chr1:19227817-19231739 | Panc1 | SE_53460 | chr1:19228446-19230083 | Spleen |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 19227600 | 19228507 | chr1 | 19227534 | 19227591 | chr1 | 19227777 | 19227868 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I018900 | chr1 | 19226773 | 19227369 |
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Enhancer Sequence | GTAGCCCCAA ATGCGAATAG TGGTGAGGTT GAGAAATCCT GTCTAGGGCA TGCGGCCAGC 60 TGCTGTATCA AAGGGGTAAC TTGAGCCCAG GGAACCAGCT GCAAAATGCT CTTTCTCTTT 120 CCCCTCTCAA TTCAGGAGGC CTCATAATTC AGAGCATAAA TCTGGATTTA GACCAAATGT 180 AATTTCAGTC ATATATCTCT GATGGCAGAT CGTTTCCCAT GATAATACAG GAATGAGACA 240 GTACTTACCG GCTCGGTGTT AGGCCCATGG TGCTTGATTG CTTGATAATC ATTATTGTTA 300 TCATGGGCTT ATCTTTTAGA ATATGGATTG CTTTCTACTA GATATTGGAG GGTTTTCCTA 360 TGCATTTCTC CCCTATTAAG CCGAAAACTC CTCAAAGGCC CCACCCCATG TAAATTCCCT 420 GGGTACCCCT CATCTCTAGG GTGTTTGGCA GAGCACCAGC TCACAGTAGG CACTCAGTAA 480 ACACAGGACT CTATAAGCTC CATCTTCCTG AGTCTCAGAG TGCAGGGAAG GCCTGCAAAC 540 GGGATCACAC AGGGAGTATG GCAAGTGTGG CCCCAGTCTC AGCCTAGAAG AGGAACCCCT 600 CTGTCCCATG TCCTCTTCCT GCGCCCTTTC CTATCCCCTC TTCACCCACA GAGGACACAC 660 AGCAGTGTTG CAACTCACTT GTGCTCAGAG CACCACCATG CCATCCCTTG GGGGAAGGGA 720 GAGGGCCACT GATTAACTCA GAAAGGGCAC AGCTCATCAG GAAAGACACT GCCACTAACA 780 GCCCCAGGGG TCAAGCAAAC AAACCTCAAA TGGGAGGGGG GGCTGATCCA CAGGTGGGCA 840 GCCCCACCAG ACTAGGAACC CCTCTGGGGC AGGGTCTGTG TCCCACCTAC CTCTCCAAAC 900 CTAGCTCCGA GCTGGAGGGG CTCTGAGAAT ATTTGTCATT GAGTGGGCAA GGGTCCAGGC 960 ACCTGGCTCC ACAATGTCAG GTTTGCAAAT CGGGATTTGA AGGGCAGGTC CACCCCTGAA 1020 CTGCTCCTGG GTTTCTTCAT TATTTGGAAT AATGACCTGC CTCACAGGAG TGAGAAGTTT 1080 AAATAGAGGT GATAATGATG ATGATCGTGG CAATAATAAT AACCGGGCGC TGCCTTTGTG 1140 CTGGGCACTG TTCAGTGCAC TCCCCATGTA TTAACTCATT TAATCCTCAT AAGACACCTG 1200 CCAATTGCCC GGCCAGCATT TGGTTCATTA TAAGCACTCT ATAAATATGA TTATTCCACC 1260 TACAAGAAGA AAGGAATCCT TTTTTCTGTC CAACATTTAA CTTGAAAAAA AAAAAAAAAA 1320 ACGGGCGGCG GGGTGTGTGG GGAGCGGAAA AGAGAGAGGT AGAAATCCTG GTAGAAGGAG 1380 AGGACTCGGG GAATCCGGGG CGGGATGGGG ACACTGAACG TGAGACGAGG GTGGGGAAGT 1440 GAGATGTGTG GTGTGCTAAA AATAGAAGGG CCCCTCAGGG GAAGCCAGCA AATTGCGAAG 1500 ATCCAGTATT AGGAGTGAGG TGAGTGACTA CAGAGGCTAC TTTCCGAGCG TGGGAACCGG 1560 CAGGGCCACC GAGGCACCCT ACTCGGTCGC AGGATTCGGG AAGAGGGGTC CCCTCGCTAA 1620 AGGAAGGTGA CTACCTGAGG GAGGAGGCTA AGGGATCTCA GTGGGAGAAA GGCCTGGGTG 1680 GGGGTCGGAG GGGAGCCCCT GAGGAACCCG GCGTTGACCG AGGCAGCTTG GGGGTCCGGC 1740 AGGGAGGGAG TGCGGCGCGG GGGACGCCCA GTGACTCTCA GGCTCCCGGG CCCCAGGCGC 1800 GCGCTCGGGC CGCCCCGGGC CCCGTGCTCA 1830
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