Tag | Content |
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EnhancerAtlas ID | HS003-29568 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr20:33276900-33278600 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr20:33277410-33277422 | GTCTGTTTACTT | - | 6.52 | FOXP2 | MA0593.1 | chr20:33277411-33277422 | TCTGTTTACTT | - | 6.32 |
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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 |
GH20I034689 | chr20 | 33277341 | 33277490 |
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Enhancer Sequence | TCCAGAGAGG ATTTACATTT ATTTCTTCCA GGCATCTGAG AGATCATTTC AGAGTGGGTC 60 GCTTTTTATA TTAATTTCTC AGCTTCGAGA TTCCCAGCCA TGCAGGTGAT GCAAATGTGA 120 ACGCCAGACT CATGGAGGGT AGGCATGTGG TTTCAAATTC TCAGGAGATT ATTTTCCCTC 180 TTACCCAAAG ACCAGGTCAA GATGGACACA TCCTTTTTGT CTCCCTTCGC TAGTAGGTGT 240 TGGTTTTTCC CCTAGTTTGT TCTTTCACTG TGGGTGTAGC CCTTCAAGGG TCCTAGATTT 300 ATCAAGGGTC TCAGTTGCAA CCTCTAATTT CATATAAGCC CAAAGCTTCA ACTCCCCAAA 360 TGTTTCTTTA AAAACACAAG CTATTGCAGA TTCAGTTGTG CCTTTTAAAG GATGTTTGTT 420 GTTTTTATTT CCAGCATCTC CTTGGGTTGT GTAGCAGGAA GTTCCTGATA TTGTCAGAAA 480 AGGAAGTCCA ACTCAGTATT TAGTACAACT GTCTGTTTAC TTGTCTATTT TCTCCATGAG 540 TGTCAAGCTC TGGGAGGTCA GGAACTAAGG CTGACTCATC TCTGGGACAA AACACCAGGC 600 CCAAGATCTG GCACAAAGTA AATGCTCAGT GCGTTTGTTG ATACTGAACC TCCACTTGGT 660 CACTTCTAAT GATGGGGAGC TCACTTTCTC CCAAGGTGGC CTCTTTCCTT TAGAGAGGGT 720 GTGTGACCTG AGTGACCACC GGGCTAATGG GGGACAGCCT GCCCCTCATT TATGTACAAC 780 CTTCCCAATA CTTAGCTTGT CCATCCAGAT TCTGCAGAAG GGGGCTCAAG GCCTAGACAT 840 CCCAGTAATA ACTGAGACTT TGAGCTTTGA CTCAGAGGGA AGCACACGGG CCAGTTCCAG 900 ATGACACCCT AAGGCTCATC TTAGGGTGGA AGTCTAAAGT GGTACAGCAT TTTGGGAGAG 960 TAATTTGACA GCATCTGTTA AATTTGAAAT GTACATACCT ATCAATCTTG CAGTTCACTT 1020 CTCTGAAACT ATTCTGTATA TCCAAGGATA GTCACTGTAG CATTATTTGT GGCAGCAAAC 1080 AATTGAAAAC CACCCAAATG TCTGTCAATA AGAATAACTA AATAAATTCT CTAAAGTCAA 1140 GTCATACAGT GGAAAACTGT GAGCCTTTTA TTTTTGTTTT TTTGAGACAG GGTCTCACTC 1200 TGTTGCCCAG ACTAGACTGC AGTGGCGCCA TCACGGCTTA CTGCAGCTTC AACCTTCTGG 1260 GCTCAAAGGA TCTTCCCACC TTAGCCTCCC AAGTAGCTGG GACTACAGGT GCACACTACC 1320 ACACTTGGCT AATTACTTTT TATTTTTGTA GAGATGAGGT CTCACTATAT TGCCCAGGCT 1380 GGTCTCAAAC TCCTGGGCTC AAGAGATCCT CCAACCTAGG CCTCCCAAAG TGTTGGGATT 1440 ACATGCGTGA GCCACCACAC CTGGCCTATG TTTTTTTTTG GTTTTTTTTT TTGAGATGGA 1500 GTCTCGCTCT TGTCACCCAG GCTGGAGTGC TGTGGCGCGA TTCCGGCTCA TTGCAATCTC 1560 TGCCTCCCGG GTTCAAGTGA TTCTCCTGCC TCAGCCTCCT GAGTAGCTGG GATTGCAGGC 1620 GCCTGCCACC ACGCCCAGCT AATTTTTTTA CTTTTAGTAG AGATGGGGTT TCGCTATGTT 1680 GGCCAGTCTT GTCTCAAACT 1700
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