Tag | Content |
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EnhancerAtlas ID | HS003-04105 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr1:233679100-233680420 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Crx | MA0467.1 | chr1:233679394-233679405 | AAGAGGATTAA | + | 6.14 | ESR2 | MA0258.2 | chr1:233679277-233679292 | GGGTCACTCTGCCCT | + | 6.43 | FOSL2 | MA0478.1 | chr1:233679604-233679615 | GGATGACTCAT | + | 6.62 | IRF1 | MA0050.2 | chr1:233680281-233680302 | CTCAGGTTTCACTTTTGTTCT | + | 6.1 | JUNB | MA0490.1 | chr1:233679604-233679615 | GGATGACTCAT | + | 6.62 | MEF2C | MA0497.1 | chr1:233680252-233680267 | TTTTATTTTTAGTAT | - | 6.12 | PPARG | MA0066.1 | chr1:233679275-233679295 | CTGGGTCACTCTGCCCTCCA | + | 6.21 |
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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 |
GH01I233542 | chr1 | 233678544 | 233680459 |
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Enhancer Sequence | AAGATGCTAT ATAAGCTTCT GTACCCACTG TGGGGCTGTA TCTTCATTCT GAAGCTTCCC 60 GTGTATATAT ATTAGATAGA TGTGTATACC TTTTATCCTC TTAATCAGCC TTTTGTGAGT 120 TGATTTTTCA GTGAACCTTC AGGAGGCCCA GGGCCTGGTC CCCTGCAAGG CAGTGCTGGG 180 TCACTCTGCC CTCCACCACC AGGCAAGGCT TCTGTGTGTA AACTTCTGCA GGGCTGACAG 240 TAATCAACAA TACGTTCTCT CTGCAGTCAG GTTCCCTTTC AAAAAGGAAA GAATAAGAGG 300 ATTAAAATAA TGCCTTACTT TTCTTCCAAA CTCCCAATCA AGGAAGACTC TCACTTTCCC 360 TGGGTGAGGC TGGGAGTGTT TTGCTGACGG AGCTCCATCT ACGTGGGAGT AGGGATGACA 420 CATCCCTCCC ATTAACATTC TCTGCGATCA GGCTTGACAG TCCTTGACTC TCCACACCCG 480 GGCTTGTTCA GCCTCTGGAA GCAAGGATGA CTCATGTGTT GCTCTAGTCA TCCCTAGTAC 540 TGTCTTCCTG TTGCAAATCC TTTCCATTAA ATAACCCTGA TTTGATCACC TATCTTCTCG 600 GCACTATGTG TATACCACAG AGACTTTTTT TTTCTCATGT GCCAGGTGGT ATCTTCTGCC 660 TCTTAGTAGA CCTTAGTGGA ACCAGGGAGG CAGTATCCTG GCACAGTTGA GGCTCTGGAG 720 TCAGACCAGG TTTGGATCTC ATTTCCAGCA CTGCTTATCA ACATCAGCTG GGACAAGCGC 780 CTTAACACCC CCTGTGCTTA ACTTTCCTCA TTTGTACAAA TGGGATAATC ATAGTCCTTA 840 CTTCACAGGT TTGTTCTGGC ATATAACAAG TGCTCCATAA ATGTGGTCCT CCCCCAAAAA 900 ACTCTAGTCC CATGCAAGGA ACACACTATT TGGCATATTG GTTAGACCCT TCTTTCATCT 960 TTTGCAGTGT TCGAGTTTCT ATCTTCCCAG TCCCTAACTC CTTGATGCCT TTGGCTTTCC 1020 CTAATTTATG CCCTTATGCA AACTGTGACT TCGAGCACCT TGGGCTCTTG GCATCACCTA 1080 GCAGCTCCCA GCCTCCTCCT GATACCTTGT GACTCTGATT TTGGACCACA GCCTTGGACC 1140 TGGCTGCTGA TTTTTTATTT TTAGTATCGA CTTCGTGTGC CCTCAGGTTT CACTTTTGTT 1200 CTAGGCTGCT CAGCAAGGTA CTTGTCTCTT TGTTCTAAGG AAGAGGTACT TCTGTCTGAC 1260 TTTTGTTGAA AACTCCTTCC CTCTGCTCCT GATTCACATC CTCCAAGTTT TCCTGGTTCC 1320
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