Tag | Content |
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EnhancerAtlas ID | HS145-18016 | Organism | Homo sapiens | Tissue/cell | NHBE | Coordinate | chr3:131983570-131984710 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr3:131983654-131983666 | CTCTGTTTACAT | - | 6.32 | FOXP2 | MA0593.1 | chr3:131983655-131983666 | TCTGTTTACAT | - | 6.02 | NFE2L1 | MA0089.2 | chr3:131984012-131984027 | ACTGCTGAGTCATGT | - | 7.26 | Nfe2l2 | MA0150.2 | chr3:131984014-131984029 | TGCTGAGTCATGTGG | - | 6.75 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TAACAAGCAA GATTCTGCTA TGATTTTTGT ATTCATACTT TATCAGATTG GACATCAAAA 60 TTATGCTAAA TTCATTAAAT GAGTCTCTGT TTACATAAAA TGGTGTCTAA GACTGGAATT 120 ACTTGTTTTA CAAATGTTTG ATAGAGCTTA CTGGCTAAAC CCTTGGAGCC TGTGACCACA 180 CTTGTTGGAC AACTCAAGTT TTTACCCACT CTGAACATGT CCACAAATGA CTGTGAAAGC 240 ATCACAACTG TTGATTTGGG AGTTACAAAT AAATTTGTAT CAAGTAAGTA TATTCACAAA 300 TATGGAATCT GCAAATAGTA AAGATTGACT CTATCTAACA AGTGGTAGGG TAAGAGCATT 360 AACAAACCAG AAGAGTTGCA AATCACATTA TTTAAGATCC TAGGGACTCC TGATGTGCCA 420 GGCAAGAATA CCTTGATTGC AGACTGCTGA GTCATGTGGA GCTCTAGGGA GAGTCCAAAG 480 GAAGAGCTGG GCAGCTGGGG TGGCATAGGG ACAGCAGCTA TTTACCAATC CATTAGGGAA 540 GAATTGCAAT ATCTTGTATT CATCACTTTA ACTAAACTGG CCCTTCCTGA TACCAAAGTA 600 ATACCAGGCT GAGAAATTCC AAATTTCTCC TATTACTCAT TATTTTGTAA ATCTGTTTGA 660 CCCACTTACA TTGGAAACTG TATTATCCCT CCTCCAGACA GAAAACCTAA TTATATCTTA 720 AGAAAGGGGA AATCTGACAC TGAAATGATT TTAATAGCAA TCTGTTGGTA CTAGCAAACT 780 GATTATATTT CATATGGTAC CTCTCCCAGT CTTCATGGAC AGGAGCAGAG TCTTCTCTGT 840 AGAAACTGCA ATGTTGTCCA AATTTGCAAA ATGCCAATTC TAGATAATGA CACTCAAGTG 900 CTGAGGGAAG TGGAAGGAAC AGCCTGTTAC CTTCTACTTC AGTGCTTTGA TGGCTGAAAT 960 GGGAGGAGTC ATAGACTGGC TCTGGCTCAA TGCCCTTCAA GGGATAATCT AGTCTAGAGC 1020 AGTGCTTTGC AAAATACAAT GTGCTTACAA ATCGCATGAG AATCTTGGTA AAGTGCAAAT 1080 ACTGATTTAG TAGGTTTGGA CTGGGGCCTG AGACTTTACA TTTCTAACAA GCTCCGAGCG 1140
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