Tag | Content |
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EnhancerAtlas ID | HS045-11818 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr11:63728920-63729940 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SP2 | MA0516.2 | chr11:63729420-63729437 | CTCTGTCCCGCCCCCTC | + | 6.4 | Znf423 | MA0116.1 | chr11:63729262-63729277 | GGAACCCTGGGGTGC | + | 6.42 | Znf423 | MA0116.1 | chr11:63729262-63729277 | GGAACCCTGGGGTGC | - | 6.57 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr11 | 63729600 | 63729651 | chr11 | 63728931 | 63729786 | chr11 | 63729474 | 63729600 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I063960 | chr11 | 63728399 | 63730471 |
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Enhancer Sequence | TGGGGACCTG CCCTAAGCTG ATCAGGGGTC CAGAAACAAG AGAGGCCCAT GGGTATTGGA 60 GCTATGAGCG CAGGCTAGGG GCTCAGAAGG CAGAGGGGCC TGGATGTGGT TCCAGCCTGG 120 TAGGGGTGAG TCTGGGGGCC AGCCCATGAT GGAGGGAAAC GTGGCCTGAG AAGCCAGTCT 180 TCACCAAGCT GGAGCCACCG TCCCACATGG GTGCAAATGC GGTGATCTCG CCCTTACCAC 240 ACAGGGCTGC TGGCTGTGGA CTGCGTTCCG GAAGGGGTTA ACCACCACAG GCTCTCGGCA 300 GGCCCGCCCA GCCCTCAGCT TGCACCCTTC CCTCCCGCTG CTGGAACCCT GGGGTGCCCC 360 AGCCAGTACA GCTGTGCCTG CCTAGAGAGC AACCCCTCCA CCCCCAACCC CGCCCCCGAC 420 AGCTGTGTCT GGGCCTGTCC CCTGGATGCC TGGCAACAGC TGTATCCCAG GAAGAGCAAA 480 CACTCCTCTA AGATCCTTGT CTCTGTCCCG CCCCCTCCCT TGACCGTTGC CTGGTTAGGT 540 TTCCCAAACT AGCTCTTCCA GTGATGCCGT CTCTCCCTCC ATCTTCTCCT GGAGTTTGCA 600 TTAGCGCCCC CATTTTGCAG ATGGGGAAGC TAAGGCCCAC GGAGGGAAAG GTGCATTCTC 660 GAGGTACCCA GCACCCCAGT GTTAGGCCTG TATCTCCTTC CCCGAGGCCC TTGTTCACCC 720 TCCACCTCTG GGCACTGGGC CCTTCCTGCA GCTTCACTAG AGTCTCCTGC TGCTGCCGTC 780 ACCCCAAGAG TCATTCCCCA CCCACAGGCA GATGAAGAGG CCCCAGCTGC CCTCTGAAAG 840 CACAGGGCTG GCTTCTTTGC ATCCTCACCA TGCAGCCCTC CTGGCCAGCC CCAGGGCTCA 900 GTGCCTGGCA CCCACCTGAT GTGCCAGGAG GAGAGACCAG GCCAGGTAGG GAAACTGGAT 960 ACCCAAAGCT CAGGTTCTTA CCAGCTCCAG ATCAGATGCT TTGGGAGGTG GCAAGCTCTA 1020
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