Tag | Content |
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EnhancerAtlas ID | HS045-11273 | Organism | Homo sapiens | Tissue/cell | Fetal_lung | Coordinate | chr11:34880820-34882540 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIL3 | MA0025.1 | chr11:34881378-34881389 | TTATGTAACCT | + | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TACTTCTTAT TTATATGTTT TAAAATGTTG GTGACTGCAC CCTCTTGCAT TGTTCTGCAT 60 TTGGCAGGAA GGTCAGTTGA TATATGTTTC ATGGATTTAA CTTTCCATAA CACTCCAAAC 120 TAGGATTCTG GGAAGAGGGA GGAGAGTGAA GAACTTGACC ATGATACGCT GGAGCTGCAG 180 GTCAAAGATG GCTCAGGAGG TTACTGCTTC TTCCCACCTG CTGGTGTGGA GCCAAGGCAC 240 CAGCCTCCCT GCAGGACAGG CAGGTGGAAG AGAACATGAT TCTAGGGAAA GATGTGCATT 300 GGAGCTCCTT GGAAGACTTA TGTTTACACG CCTTTCCCAA TGCTGCCTTT TTGTTTAATT 360 AAACCCAGAG ATAAATGTTG TGAAACTCCT GTCTGGCCTC AGTTTGCTTA CAACCCTGAG 420 TATGTGTCCC CTGACACATT CCAACATGTA AGTAATCTTC GCTGACCCTA ACTGGAGCAA 480 AGCTTTTGCT GAAAGGAATG AATTATGTAC CTATTTTTAG TGAAGTATCT GGTATCTGTC 540 TGCTTTGGTT TAATATGCTT ATGTAACCTC ATTGAAGGGC TGATTTCCTC AGTTAATAAG 600 GATGCAAAAG ACCAGAGTGC CCACTTAAGA GAGACTATGT TTAGACCTCT CAAGGAATAA 660 TTAATAAAGG GAATCAAGGG TCAAAGATTA TTTCAACTGA CAAGTCTAGG CCCTTCTCAT 720 TAGTAAAAAC TGCCCGGTTG CCTTGCAGTA TTTTCTTTGC CAGGAGACAA CACCTATCCT 780 AAATGTTTAA GTGACTTCTT GTTGGGCTGG TTTCGGAGGA TTAAGCTCAG TGTAATTTCA 840 TCCTTCCCAG GTGTGAGACA CTTGCGTGTG CAGTAATATG ATTCTGTACT GTCAGGGAAA 900 AGAGTGTGTC TTTGTCAGCA GTGTTTGGCA GTCAAACCCC TGAATCATGA CCTCACTTTC 960 AGGTAATCAC TCTTTGCAGG CTTAAAACCC CTGGCGTTAC CACTTGCTCT TATGCTGAGA 1020 GACTTAAAGG TTTGGCTGCT GGCACGTGGT CCTGCTGGTC AGCAGAATGG AGATGATCTG 1080 TGCTGGCAGC CCAACTGGAC TTCAGAAAGC ATTCCCTCCC CAGCTGTTTG GATTCAGTTT 1140 CTAAGTGCTG AGCAATACCA TCTCTATGTT CAAGAAGGGC AAAAACCAAA ATGAGTAGTA 1200 ATTATTTGGA TTTGCTTTAG CCTGTAGTTA GATCAATTCT TCTTCTGATG CTTTGGGTAA 1260 TGTCCTCAAA ATGATTTCCT ACTGAATGTT TACAATTTCA ACATGTAATA CATACTCTGG 1320 ATAAAGCAGT AGCTCACAAA TCATCTGATC AACAAGGTGA ATCCTATCTC TGTCTTGGTC 1380 CACATGGAGA CTAGCACATG TGATTGACAG GCAGATAAGG GCCGTATTGT CATTTGGTTG 1440 CACCTGTCCA TATGGCGAGG GATCGGAAAT GAGAAATGGC TGTATTCTAA GCTGGGGATT 1500 ATAGAGCTGT GTTACTCTAA GTCTTACTGT CTTACAGTAG CAAGGAGCAA GAAGAGTCTT 1560 GAAAGAACGG AGCCTTAAAT ATCATAGGTC AAGCCCTATA GTTTCACAGA TGAGGAACTA 1620 TTGCCTCAGA GACAGAAAGC AACTTACACA AAATCACAGA GAAAATGCGA GTGGCCTTGC 1680 TGGGGTTAGA GTCAAAGTTT CCTGACACCC ATCTAGTGGT 1720
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