Tag | Content |
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EnhancerAtlas ID | HS045-12232 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr11:75176670-75178000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr11:75177174-75177192 | GGAAGGAATGCAGGCAGG | + | 7.59 | POU2F2 | MA0507.1 | chr11:75177838-75177851 | CTAATTTGCATAA | + | 6.13 | Pou2f3 | MA0627.1 | chr11:75177837-75177853 | GCTAATTTGCATAAAG | - | 7.18 | RREB1 | MA0073.1 | chr11:75177138-75177158 | GAGCTGGTGGTGGTTGGGGG | - | 6.58 |
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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 |
GH11I075465 | chr11 | 75176892 | 75177831 |
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Enhancer Sequence | GAGAGATTCC CCTGAGGCTT AACACCCAGT TCCCACAAAA AAGTACCTAG TCTTCTATAG 60 AGCCCACGCT GGCAGTGTTA GATGGCTGTC TGTCCACAGA GACCACTTTG CCTCCTCAGG 120 GGCAAGGCCT GTGTGCCTCT GACCAGCAGA GAAGGTTCTG AGAGGGACCT AGGCGAGGGG 180 TGAGCCTCGG CCTAGGATGG GTCTGGTCCC AGGCAAGTAG CCTGGAGGCG GGAAGGTAAA 240 GCACCTCCTG TAGGCGCTGG GAAGACGACC TGTGACCGGG GTGATGCAGG GCCCAGGGGC 300 AAGGCTGACA GGGGGCCAGG AAGACCACAG GGGCCGGGAG GGCCCATGGC AGCCAGGGTC 360 CTATGCCCTA AAGGCCATTG TCCTCAAGTG TCCAGATCCT TACAGTGGAG CAAGGCAGGG 420 CAGGAATGAG GGGCTGCACC TCCCACTCCT GGGAACCAGC CAAGACCAGA GCTGGTGGTG 480 GTTGGGGGTG AGGCATCCAG GCATGGAAGG AATGCAGGCA GGGCCTAAGC AACAAGGAGC 540 CAGGAACCCC ATGATCAGAA CTAGTGCATG AGCTGGGGTT GGGGCAACCT AGGGATTAAA 600 GCCCTGGGAG CTGAAGCCGG AGGCCACAGT GAGCCTGTAG ATGGGGATGA AGAGGCCCCA 660 GCACAGAGGG AGGCAGGCAG CGGGGGTCAC TCTAAGAACA ATCAGAGGAA AACACTGAAT 720 GGCAGGGACT GGAAGGAAGG GAAGGGGAAG GTGAGGAAGT AGCCAGAGGA AGTGGCCTGG 780 GGAGCAGCTC CACTGATAAA GAGGCCCCAA TAGCACTAAT GGTCCTTGTC AGGGCACATT 840 ACAGCAGAGA GAGGCCTGCC CGCTCCACCC ATTAGCAAGC CAATCTGGCC CTGCTCCCAG 900 AGACGTGGAG CAGTGATCGC TGCCTCAATG CCCCGGCCAC GGCCCTCCTT CATCTCTCAC 960 AGTCTGCATA ACACTAGGGG TTGTTTATTT AGGGGTATCT ACCCCCATTG CACAGAAGCT 1020 CAGAGAAGGG CCACCACATA TGGCTGAGCA AGTTGTGCAC TGCCCCCTAA GAAGTGCCAC 1080 TCACATCATG GTGACCATCA ATGTGCATAT TATGACGATT TGCTGGCACA TGGCGGGCGG 1140 GTGTGTCCTA GAAAATGGGT GCTTTTTGCT AATTTGCATA AAGGCTCAAC ACGGGTGAGT 1200 GGAGGGGAGT CAGAGGGGTC AGCAGGTAGG GGAGGAGTGG GGATAAGATT TGAACCCAGG 1260 CATACTGACT GGACTCTGCA GGCCCCCTTG GGAGGCAGCC TGAACAGCTC CCCTCAAAAC 1320 CCACCTTGCC 1330
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