Tag | Content |
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EnhancerAtlas ID | HS017-21829 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr22:29479300-29480740 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr22:29479319-29479334 | TCTGCTGAGTCAGTG | - | 6.01 | NKX2-3 | MA0672.1 | chr22:29479731-29479741 | ACCACTTGAA | + | 6.02 | Stat4 | MA0518.1 | chr22:29480001-29480015 | TTTCCGGGAAGGGG | + | 6.25 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_33639 | chr22:29479987-29481193 | H2171 |
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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 |
GH22I029083 | chr22 | 29479590 | 29480715 |
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Enhancer Sequence | GAAATATTTT TCTTAGAGTT CTGCTGAGTC AGTGACTTTT GACTATTTGA ATGAGTCCAT 60 TCTTTAACTG AAGTTTAATC TCTACATATT ATAGACCTGA ATGCTGATAG GTTAATGGAC 120 ATTTTTTTCT CAAAAAGTGT CTTTTGGACT TCAATTTGAT GGTTGTGATA CGAGAAAGGG 180 GTCCTGATCT AGACCCCAAA AGGGGGTTCT TGGATCTTGC ATAAGAAAGA ATTCAGGGGT 240 CCGGCACAGT GGCTCACGCC TGTAATCCCA ACACTTTGGG AGGCTGAGGC CGGCGGATCA 300 CTTGAGGTCA GGAGTTTGAG ACCAGCCTGG CGAACATGGG GAAACCCTGT CTCTACTAAA 360 AATACAAAAG TTAGCCAGCC ATGGTGGTGG GTGCCTGTAA TCCCAGCTAC TAGGGAGGCT 420 GAGGCAGGAA AACCACTTGA ACCTAGGAGG CGGATGTTGC AGTGAGCTGA GATTGCGCCA 480 CCGCACTCCA GCTTGGGCGA CAGAGTGAGA CTCATCTCAA AAAAAAAAAG AAAGAATTCA 540 GGACAAGTCC ACAGAGTAAA GTGAAAAGGA GTTTATTAGA GAAGTAAATC AACAAAAGAA 600 TGGCTACTCC ATAGGCAGAG CAGCCCCGAG GGCAGCTGGT TGGCTATTTT TATGGTTATT 660 TCTTGACCAT ATGCTAAACA AGGGGTAGAT TACTCATGAG ATTTCCGGGA AGGGGGTGAG 720 GAGGTCCCGG AACTGAGGGA TCCTCTTTTT TTTAGGTCAT ATAGGGTAAC TTCTGGATGT 780 TGCTGTGGCA TTTGTAAACT GTCATGGTGC TTGTAGGAGT GTCTTTTGGC ATGCTAATAT 840 ATTATAATTA GTGTGTAATG AGCTGTGAGG ATGACCAGAG GTCACTTTCA TCACTATCTT 900 GGTTTTGGGG GGTTTTGGCT GGCTTCTTTA CCACATCCTG TTTTATCAGC GAAATCTTCG 960 TGACCTGTGT CTTGTGCTGG CCTCCTATCT TATCCTGTGA CTAAGAATGC CTAAACTGGG 1020 ATGTATCCCA GCAGGTCCCA GCCTCATTTT ACCCATCTGC TGTTCAAGAT GGAGTGGCTC 1080 TGACTCAAAT ACCTCTATTT TATGGGTTTA TAATATGGTA AATGATAAAT AAAAATTCCT 1140 GAACACTAAT GCATATTCAG GATGACTATT CCTGGCAGAA ACACACATGC TTCACAGTGA 1200 CAAGCATGGC ATGTTTTCCA GGGGGCCCTG CCTGGGTAGG AGTGGAGCAT ATGCAAGATG 1260 AGAGCCAGAT GGGAAAAGAG TGGTACCCAA GCCACTGCAT TCTGGACCTT CTCTGCCTTG 1320 ATAATTATTT GTTTTTTGAA TTTTTATTTA ACAAATAAGG CCTTCTCTCC GAAGCGTTTT 1380 CATGGTTCTT CTGAATTCAA ACATCTGGTC TTATGCTTAC CCTGTAAGTT CAGTTTTTCT 1440
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