Tag | Content |
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EnhancerAtlas ID | HS182-11961 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr2:27286370-27287590 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr2:27286660-27286671 | TCTGACTCATT | + | 6.32 | ONECUT1 | MA0679.1 | chr2:27287564-27287578 | AGTATCGATTTTTT | - | 7.95 | ONECUT2 | MA0756.1 | chr2:27287564-27287578 | AGTATCGATTTTTT | - | 7.42 | ONECUT3 | MA0757.1 | chr2:27287564-27287578 | AGTATCGATTTTTT | - | 6.76 | ZBTB18 | MA0698.1 | chr2:27286741-27286754 | GAACATCTGGCTG | - | 6.32 |
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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 |
GH02I027062 | chr2 | 27285209 | 27287190 |
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Enhancer Sequence | GAGAATGGCG TGAACCCAGG AGGCGGAGCT GGCAGTGAGC CCAGATCGCG CTACTGCACT 60 CCAACCTGGG CGACAGAGCG AGACTCCGTC TCAAAAAAAA AAAAAAAGAA TGCTTGTCCC 120 ACCTTTCTAC CCCTCAGAGG GCATAAATCA GGTCTGTGAT TGTCCCAGGG ATTCACTAAG 180 ATCTGGAGTG CTAGGGACGG TTCCAAAGAC GTTCAGGGAG GATGACACAC AGGACCTTGG 240 CACAAGTCAA GTAACTGCTG CTGTAAACAG TGAGACCTTA GAACACCCAT TCTGACTCAT 300 TCAAGGGGAG ATCAGTCTCC CCTCAGACCT CTTAGACCTT TGCCCAGTAC TATCCTACCA 360 CCCCCAAAAT GGAACATCTG GCTGGTTGCC ATAAGATACC ATTTCATAAC CTCTGGAAGC 420 AGAGCTGATC ACATCACTCT TGCACTCTTG CTTGTTCTTT CTCACTTGCT TTTACCCTTT 480 CCTGGGGTAG GGTGAAGGTT TGTCCCTTAA TATGGTTTCA GCATGCCTGT GTGTGTAGAT 540 ATTTCTCAAA TTATCTAAAC TATTTCCTCT ATCAAGTTCA TGATTTCTGC CTACTGTGCA 600 CTGTCAGCTG GACATCATCC TGACATCCAT TTTAATCACA GAATTACTTG GCTCTGGGCC 660 CTAGACTATC TCTGTCATTG GTGGTAGCTA ATGTTTTAGG TTATTTGACT ATGGCCACGA 720 GTCTTGACTT CTGTTATCCT ATTGGCAACC TGTGCCAACA ACTCTCACTA GCCCCCTAAC 780 ATCTGGTTGT TTTTGACTTT TTTTTTTTTT TTTGAGACAG TCTCGCTCTG TCACCCAGGC 840 TGGAGTGCAG TGGCGTGATC ACAGCTCACT CCAACCTTCG TGTCCCTGGC TCAAGTGATC 900 CTCCAGCCTC AGCCTCCCTA GTAGCTGGGC CTACAGGTGC ACACCACCAC ACCTGGCTGA 960 TTTTTGTATT TCTTTTTTTA GTAGAGATGG GGTTTCACCA AGTTGCCCAG CCTAGTCTCA 1020 AGCTCCCGGA CTCAAGTGAT CCAGCCGCCT CAGCCTCCCA AGGCACATGA GCCACCGTGC 1080 CTGGCGTTTT TGACTCTTGA CCACCGTCTT AACCTATAAT TGGTACCCAG CATATCTCCT 1140 CATAATAGAG TAGCTTCCAT CCTGAGATCT CTCCCTTTCT TCTTTATTCA TACAAGTATC 1200 GATTTTTTTT TTCCATTCAA 1220
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