Tag | Content |
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EnhancerAtlas ID | HS052-19898 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr2:27027870-27028840 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TBX21 | MA0690.1 | chr2:27027945-27027955 | TTCACACCTT | - | 6.02 | TBX2 | MA0688.1 | chr2:27027944-27027955 | TTTCACACCTT | - | 6.62 |
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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 |
GH02I026804 | chr2 | 27027789 | 27029276 |
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Enhancer Sequence | GGATTACAGG CATGAGCCAC CAAGCCCAGC CTGTTTGTTT TTTAACACAG TGACTCCATT 60 TTGATTCTGG CAACTTTCAC ACCTTCCACA GGTGAATCAT TCCTACTTCC ATATTGGAGT 120 TGGGGGCTCA CTCTGTTGCC CAGGCCGGAA TGCAGTGGTG CAATCATGGC TCACTGCAGC 180 CTGGAACCCC TGGGCTCAAG GAATTTGATC ATGCAGCCTC AACCTCCTGA GTAGCTAGTA 240 CTACAGGCAC ATGCCACAAT GCCCGGCTAA TTTCTTCTTC GGGTTTTGCT ACGTTGCCCA 300 GACTGGTCTC AAACTCCTGG CCTCAGGCAA TCCTCCAGCC TCAGACTCCT GAGTCACTGG 360 GCTTACAGGC CCCACTTTCT TCAACTGTTC TCGTTATTAT GTGGTTCAGG GCCTCTCACC 420 CCATGACACA GTTTGACTCA TCACTGCCCT TCTTAAAGTA GGTAGTGTGG GAAAAATACG 480 TGGAAAGGAA TGTAGGATTT ATAGTCAAAG TCTTATTCCT AAGTCTGGAT ATTCATCTTT 540 GTATTAGTCC ATTCTCACAC TGCTAATAAA GACATACCTG AGACTGGGTG ATTTATAAAG 600 GAAAGACTCA CAGCTGACTG TGACTGACTC ACAGCTCATC ATGGCTAGGG AGGCCTCAGG 660 AAACTTACAA TCATGGCAGA AGGGGAAGCA AACACGTCCT TCACATGGCA GTAGCAAGGA 720 TAAGTGCTGA GCAAAAGGAG GAAAAGCCCC TTATAAAACC ACCAGATCTC ATGAGAACTC 780 ACTGATTATC ATGAGAACAG CAGCATGGGG GTAACGGTTC CCATGATTCA ATTACCTCCC 840 ACTGGGTCCC TCCCATGACA CGTGGTGGGG ATTATGGGAA CTACAATTCA AGATGAGATT 900 TGGGTGGGGA CACAGCCAAA TCATATCAAT CTTCAAAATA AGGAATACTG CCCCACTTTG 960 CAGAGTCAAT 970
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