Tag | Content |
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EnhancerAtlas ID | HS003-16149 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr15:78719060-78720540 |
SNPs | Number: 3 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-3 | MA0672.1 | chr15:78719094-78719104 | TTCAAGTGGT | - | 6.02 |
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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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Enhancer Sequence | TATCTCAGCT CACTTGCAAG CTCCACCTCC AGGATTCAAG TGGTTCTCCC ACCTCAGCCT 60 CCCGAGTAGC TGGGATTACA GGCACGCACC ACCACGCCTG GCTAGTTTTT GTATTTTTAG 120 TAGAAACAGG GTTTCACCAT GTTGGCCAGG TTGGTCTCAA ACTCCTGACC TCAGGTGGTC 180 CACCCACCTC GGCCTTCCAA AGTGCCGGGA TTACAGGCGT GAGCCACCGT GCCCAGCCTG 240 TAATAATATC TTGAAGTCTG GTAGTGTGAT GCCTCCAGCT TTGCTCAGGA TAACTTTGGC 300 TATTTGGGAT CTTTTGTGAT TCCATATGAA TTTTAAGATT TTTTTTCTAT TTCTGTGAAG 360 AATGTCATTG ATATTTTGAT ATGGAGAGAT ATTTAAACAA AACTACATTT GTTTTTTATT 420 TATTTTTTTA CTTAAAAAAA ATTTTTTATA TTTCTTTATA CTTTTTTAAA ACAAATAAAC 480 ATGGGGTCTC ATGATGTTGC CCAAGCTGCT CTCAAACTCC TGGCTCAAGC CTCGGCTCAG 540 CCTAATTTGT TTTGTCTTTT GACACTATAA AATAAAATGA GTGTTCCAAT GAGCTGAGCA 600 GAGGAGGTTG GCTTTATGGG CAGAAAAGGG CTGAAGAAAG GTAGAAACGG AGAACGAAAA 660 GCAGACTGGT TGTTTCAAAG TTACCTTCCT TGTAAGGTAG AAGCAGAAGG GACTTCCTTA 720 TCACACCAGC TAAAGCTGGC CTGTTTGGGG ATTTGACTAC TTCTCTTTCT TGATTTCTTC 780 TAAGGTCAGG TAAACAATTT AATTTAGGCT TGGTGGCATG GAACTTCAGT GTGAGTGACT 840 CCATTATGGT TTGGTCTGTT GGGCCTAGTG CAGGAGCTCA ATTGAAACCA ATGACCTCCT 900 ATACATTTTA ACACCATAAA GGAAGTTCAT TGGCTCACAT AACTGAAGAG AATTCCAAAG 960 GAAGTTCTTG TAGAGAACAG GTAAGGCTTG ATTCAGAATC CGAAAGAATG ACACCCGGGA 1020 TCCAGAATTT CTCTCTCTTA TCTGTGCCTT CCACCGAGAA TGGCTTTATT CTCAGGTACC 1080 ACACAGTGGA GGCCACACCT CCAAACTCAC CCCTGTGGTG ATAAAATGGC TGCCGCAGTT 1140 CCAGATGTCA GAACCTCACT CTCACAACTT GTTGAGGAAA AAAGAAAGCC TCCCTTTCTC 1200 AGAAGCCCCA ACAAGTCTTG TTGTGAGTTG TTGCTTCTAA TTAGGTTACA TCCCCAATTT 1260 CTGATCTGAA TACTGGATCC ATGGTGGACC TATGGATGGG AATTGGGGAA GAGCTGAATT 1320 GCCCAGGGGA AGTTCAGAGT CATCTGAACA GGAGACACAG GAAATGACTA TCAAATGTCC 1380 ACAAAGATCT TGACCACCAA GTATCTGAGT TCAATTACTA CTGCCTCTCA GTAACATCTT 1440 TTCTGACTCC TCAGACACAT TACTACTGTC TGTTTCTCAC 1480
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