Tag | Content |
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EnhancerAtlas ID | HS141-01848 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:231938720-231940090 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HOXA13 | MA0650.2 | chr1:231939911-231939922 | GTTTTATTGGT | - | 6.32 | YY1 | MA0095.2 | chr1:231938973-231938985 | CAACATGGCTGC | + | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 231939533 | 231939668 | chr1 | 231939296 | 231939383 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I231803 | chr1 | 231938843 | 231939979 |
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Enhancer Sequence | TCCAGATACC AAAATCTATT TTCATTATCT ACTGCTGCCT AATAAAAAAT AAGTCACTTT 60 AAGACGTAGT GACTTAAAAT ATTACCAGTT ATTTATTTTG CCCATGGAAA TACAATTTGG 120 GCAGGGCTTG GCAGGGACAG CTAGGGTGGC TCAACTGGGG TGGGAGAATC CACACCCAAG 180 ACGGTGCATA CATATGGTCT GGCTGTTGAG TGCTCTCTAT GTGGGCCTCT CTATAGGCAG 240 CTTGGCTTCC TTACAACATG GCTGCTGGGT TCCAAGAGCA AGTGTCCCAA GAGAAAGGAA 300 ATGGAAATTT CTTATTCTTA AGGTCTGAAT TCAGACACTG GTATGCATCT CTATTAATGT 360 GTAATAAGTG GCTCCTCAAA CTTCATAGCT TGAAACAACA AACCTTTATC TCTCACAGTC 420 TCTGAGAGAC AGGAGTCCAG AGTGACTTAG CTGGGTGGCT CTGACTCAGG GTCTCATAAG 480 GTCGCTGTTA AGACACACTT TGGAGCTGCA GTCGTCTAAA GGCTTGGCTG GGGCTGAAAG 540 ATCTGCTTCC AAACTCATGC ATGTGTTGTT AACAGACGGC TTCAGTTCCT TGCCACAAGA 600 GCTGTGCCCT AGGACCTCTT GCAACATAGC AGCTGATTTC CTCAGAGCCA GTGATCTGAG 660 GGAGAGAGAC CAAATAAGAC AGAAGCCACA GATGCCAGGC GCGGTGGCTC ACGCCTATAA 720 TCCCAGCACT TTGGGAGGCC GAGGTGGGTG GATCACGAGG TCAGGAGATC AAGACCATCC 780 TGGCTAACAT GGTGAAACCC CGTCTCTACT AAAAATACAA AAAATTAGCT AGGCGTCATG 840 GCGGGCGCCT GTAGTCCCAT CTACTCGGGA GGCGGAGGCA GGAGAATGGC ATGAACCGGG 900 AGGCGGAGCT TGCGGTGAGC CCATATCGCG CCACTACACT CCAGCCTGGG TGACAGAGCA 960 AGACTCCGTC TCAAAAAAAA AAAAAAAAAA AAAAAAAAAA GCCACAGTGT CTTGTTAGGA 1020 CTTAGCCTTC AAAGTCACAC AGCATCACTT CTGCTTAGTG ACTAGAAGCA AGTCACTAAG 1080 TTCAGTTCAG CCCACAGGCA AGGGGAAGGA AACAGGTTTT ACCCCAAAGG AGGAGTATTA 1140 AAGAATTTGG TGGGCATATT TTTATAACCA CTGCAGTGTT ACTTCCATTG TGTTTTATTG 1200 GTCCAGCATT CCTGGTGTGC TGATTCAAGG GAAGGGCCAC TATAACAAGT CTCAATGAGA 1260 GGTGTGTCAA AGAGTTTCAG TGCCATGCTC TAAAAAGTGC CACAGTATTT ATTGAGACAG 1320 AAGGATTTTG AGAACTGAAG ACCTGGACAG AGAGCTTTTC AGTCAGAGGA 1370
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