Tag | Content |
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EnhancerAtlas ID | HS003-18227 | Organism | Homo sapiens | Tissue/cell | A549 | Coordinate | chr16:87027460-87029200 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr16:87028323-87028338 | ACAGCTGAGTCATTG | - | 6.31 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH16I086993 | chr16 | 87027518 | 87029163 |
| Enhancer Sequence | CTTAGGAGGT CACGGTGGGA CTGCACCCCG TGCCCCAGCA GCGACGTCAA TCGCACAGCC 60 TGCTCCTCCT GACTTGCCAC TGAACCCATG CGCCCTGGAC AACCTCCCAA GGAACCCACC 120 ACTGCTCCAC GGGCAAGTTG CCGGCTGCCT TTGGGGAGCC CAAGATAAGA GCAGGGGTGG 180 ATTAGAAGGA TGGTGGGGGA ACGAAAGCCA CGTGTGGGAC AAAAGACGAT CATGAAAGCT 240 CGTCTAGACC CAGGAAGGAA ACCTAAGTGT CCAGATGAAC ACCGCTCCAC AGAGAAGTGG 300 CAGCAGAGCA GCGGACGGCA GAAACCACGC CTTGCCGAGC TCCCACGGGG CCAGAATCTA 360 CCCCACAATT CGGCTTCATC TTAATCTACT AAGCCTCCCT GCAAAGACTT TTATCACTTC 420 TTTGATTTTA CAAATTTGGA AACTAAGGCT CAGAGAAGTG TGGTTTTACC TCTGAAACAC 480 GCAACTTCCC ACCCACCCAA AATGAGTGAT GGAGAAAGAA CCAACAGGAT TGGGCAACTG 540 TTGGATGTTG AGCAAGAGGG AGAGAAGAGT TGACTCGGAG GTTGGTATAC TCCAAGAAGG 600 CTTCCTGGAG GAAGTGGACA ATTCAGAACA CAGGACCCTT TATCCAAATC AAATACAAAT 660 AGGGAACACT ATTATTAAGT ATTATCTCCT ATCTCTGTAA AAAGCCTTGT GGCCAGGGGG 720 TGTTCTGGAA ATGCTAGTTA ATTTCTGGTT AAATATTGGA TCCCTGGGAG TTCTTTAAAG 780 GCTCGTTTAC CCAGCCTGGA AGTTAAGCCT GTAACTTAAA CGCATTGTCA AAACCAGGAA 840 ACATTTACCC CCCAGTCCAG ACCACAGCTG AGTCATTGGC CAGGAGAAGC TCAGTCTGTG 900 TGCAGAGAGC TGGAGATTAT CTCATCTTCC AGGCACTTGT AGACATCCAA TCTGGACAAA 960 TCATGTCCCA CTCCCAAGAA TCTGCAAGAA ATGGCCTGAT GTGTCTCCCA CAGAACAGCC 1020 GATGATGATA ACTCATTGTC ACTCGAGCCA GTGGGCAGAT AATGACCCCG CTGACAGGGT 1080 CCAGCCTGCT GCTCCGCCCC AGCAGACATG CTCCAACAAT GGCTTCATCA TCCTCCCCAC 1140 CGGGACTGTG TAGATGAGGG AGGTGCCTCC CGCGGTGCAG GCTGTGAGCT CTAAGCAGTC 1200 ACGCTGGACG CTGGACCAGT GCCCTGGGCT GCTCCTCCCT GCAGCCCCAC GAGCCCAGGT 1260 AGGGATCACC AGAGGTCGTT TCACTCCCAA GTGGAGTGAT AAGTCAGTCC TTCTACAGGA 1320 AGATTTCTCA CAAAGTGCCC TACTGCACTG TCAAAGGGTA AAAAGGAGAA AAAAAATAAT 1380 AAAGCCAGAG GCAAGGGCTC CAGGCAAGAG CAAGATGACA ATATTTGTAC AGCGGGGTTT 1440 GGAGAGGAGC CCCCGTGAGA GCCCAGCGTC TGAGAGAGCC AGTCCTTTGA ACTGTCCCAC 1500 CCTTTGTTAT GACAAGAGAC TTGATAAGCC CACCCAGCAC AGAGACCCTT AGAATCCAGG 1560 CATATGGACT CCATTAATCT GCCCTTGCAC CTTTTAAGTA CTTTGCAGCT CCTGCCGCCC 1620 ACAAAATCCA AGCAGAGTGA GAGTCGCAGG GTTAATTTTC TTAAATGGAT TTTAGTCAGG 1680 CAAGCCCCGG ATTTCTTTGG AGGGCAGAAG TTGACAGCTC ACTGCTGGCC CCAATCTGTC 1740
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