Tag | Content |
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EnhancerAtlas ID | HS170-03570 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr7:117474760-117475940 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr7:117475002-117475018 | ATTTGTTTACTTAGAG | - | 6.81 | FOXP2 | MA0593.1 | chr7:117475003-117475014 | TTTGTTTACTT | - | 6.62 | GFI1 | MA0038.2 | chr7:117475474-117475486 | CCAATCACAGCA | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_60976 | chr7:117409842-117480596 | HBL1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 117475000 | 117475923 | chr7 | 117475113 | 117475672 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I117834 | chr7 | 117474866 | 117475728 |
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Enhancer Sequence | TTTTTAGTGC GAGTCATAAA CTTCTCCATT TTACATTAAG AGAAATCTTA TTTAGAACAT 60 TCAATATTGC TTTCAAGAAG TGATGAGATT TTATAATTTA TTCTATTTTG TTTAAACATA 120 GGGATAGAAA TGCATGTACT AATTCTTTAG TCCACACCGA AGGTGCTAGG TTGGGTTTAC 180 TTACTCAAAA CAAAATAATT CTGGCCCTTC AAAAGCTACA CAGGAAAATT GCTTCAGGTT 240 TCATTTGTTT ACTTAGAGTT GCCTCTTGGA AATGCCTCAA AATGATGCAG CAGTGTTCCA 300 ATTTTCCTAA ACTCTTCAGA TAATTGCCAG CGTCAATAAA AGCAAAAACA GCTTGCAGTG 360 CACACCTCCG TAGGTGGAAT TCTAAACCTG AGCAGCTCAG CTGCCACACA TGAATGGATG 420 CTCTCAACAC TAAGCCTCCC ACAGGGGACG GCTGAAGTTG CAGTTTAAAA GTGTTTGCAG 480 AAATAGGAAT GAGTCTCTCT CTGAGCCCTA AGGATGGCAT GGTGAATTAT CAGTGTGTCT 540 TGTCCACATG AAAGATATGC ACACTAATTC ATGTTTAATT AAGTTTAGAC CAAAGCTGAC 600 ATCTTATATG TTTTAAGTTC AGCCTAAAGG TTTCTCTGTA TGTAGTGAAC TGTGACCCAA 660 CTTAATGTGT AAACAGACTG GAACCTACTT TTCTAACAAG TAGCCAAGGC TCAGCCAATC 720 ACAGCAGCCA AACTTCAGTC AACCACAGGG GGTCAACAGT TAGAAGCAGA TTCAAACAAG 780 GCAAACACTC AGCTGTAACC TATCCAGCTG TTTCCCTCAC TTCCCTTTTC TCTCTCTAGT 840 CACTTTCCTT TTTCTGTCCA TAAATGTTAT CGACCATGTG GCCACTCTGG AGTTCTACCA 900 AACCTATACT GGTTCAGGGG CTGTCCAATT TGAGAATCAT TCTTTGCTCA ATTGAATTGT 960 TAAATTTAAT TTGTTTAAAG TTTTCAACAC GCATTCGTCT TGATTAAAGC CAGAGGGTCT 1020 GGTCGTGCAT CTGGAAAGAG ACTGGAGATT ATAAGGATGC AGAGCCACAT AATTCAGTCC 1080 ACAACGGGGG CTCTGGTTTT CAACTGCCTA GATTTGAGTT TTGGCTCTAA AGTTCCTAGC 1140 TCTGTGATCT CTGCCAAGTT GCTAACCACT CTAAGCCTCA 1180
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