| Tag | Content |
|---|
EnhancerAtlas ID | HS150-00366 | Organism | Homo sapiens | Tissue/cell | NT2-D1 | Coordinate | chr1:50824000-50825480 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr1:50824411-50824421 | GGGGCGGGGC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGGCAATTGA GAGGAAAGCG TGGGGCAATT AGTGGCATAT ATTAGGGAAT AGGGTGAGTC 60
ACTAAGTTTA CAAGCAAATG TCTGAACGTC CATTTAAAGG AAGTGGCAGG AAAGTAAGGA 120
CCCCACTCTG CTGGCAGGGA GAAATGTCTC AAAGAACTTC TCTCTGAACA CTGGCTTGGG 180
CCATTTGGGT GTGGTGTAGA CCTGGAAGCT GTCAAGGGTG ACTGAGCCCT GTTCCTATTA 240
TGGGAAATTT AAACTTATAT TCAAAATGAA TGCAGAGGGC CGGGCACAGT GGCTCACGCC 300
TGTAATCCCA GCACTTTGGG AGGCCGAGGC AGGCAGATCA CTTGAGGTCA GGAATTCAAG 360
ACCAGCCTGG CCAACATGGT GAAACCCTGA CTCTACTAAA ATACAAAAAT TGGGGCGGGG 420
CCAAGATGGC CGACTGCAAG AGCCAAAACA GCATGCAAAT CCTGCACCAG CAACTGAAGT 480
GTCCAGGTTC TGTCATCAGG TCTGACTAGG CGATTGGCAT GACCCATGGA GAGGAGGGAA 540
GAGCAGGGTG GTGCGTCAGC CCACCCGAGA GCCACACGGG GCAGGGGAGC CCCTACCCGC 600
AGCCAAGGGA GGCAGTGAGT GAGCATGGTA CCCAGCCAGG GAAACAATGC TTTTTACTTG 660
GAATTGTGAG GCCACACCAC CGGGCCTTGG GTCCCAACCA CGGAGCCACG CAGATTGTCA 720
ATAGCCACTC GGCTGGAATC TGTCTAAGAC CACCCAGTTC CCAGTGGGAG GGGCGGCCAT 780
TAACAGTGCT GCTGCCTGCT GCTGAAGCCA TCTGAGCTCC TTGGGGGAGG GGCGGCAGCC 840
ACCACTGCGG CTGTCTGAGA CAACCGAGCT CCCTGACTGA GAGGCGGCCC TCACCACTGC 900
TACTGCCTGC TGTCTAAGCC GTCTGAGCTC CCTGAGGGAG GGGCAGCAGC CATCACTGCT 960
GCTGGCTGCT GCTAGCTACC TAAGACACTA AGTTACCAGG GGGAAGAGCG GCAGCCATCA 1020
CTATAGTTCC AGGCCGCGCT TTTCCCCTTC TGGAGCCGGG GAGACTGGAC AGCTTGGTCC 1080
AAGAGGTATT CCCCACAGCA CAGCACACTG GCTGTGGCAG GCCGTGACCA CATTGCCTCT 1140
TTAGGCCAGA CCCTGGCTCA TCCCTCCTCA CTGGGCAGGG CCTCCCGGCA GGAACTCCAA 1200
CGACTCCAAC CAAGGGCTCA GGGACAGAAC TCTGATCTCT CTGGGCCTGA GCCCCTAGTG 1260
GGAGGGTTGG CCATGGTCTC CAAGGACCAG CAGTCTTAGT CTTTCCTCCT GCAAGCTCTG 1320
AGGAATCCAG GCAACTTAGA CAAGTGCGTT TCCCCCCAGC ACAGCACATC CCCTCCACCA 1380
AGGGACAGCC AAAGTGCTTT GTTAAATGGG TCCTGGTTCC TGTACCCTGC AACTGAGTGA 1440
GACTACCCAA CAGGGGTCAC CAGACACCCT ATACAGGAAT 1480
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