| Tag | Content |
|---|
EnhancerAtlas ID | HS059-37147 | Organism | Homo sapiens | Tissue/cell | GM12878 | Coordinate | chr5:78431250-78432700 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr5:78431686-78431699 | TGTTAATTAATTA | - | 6.12 | | Lhx3 | MA0135.1 | chr5:78431689-78431702 | TAATTAATTATTC | + | 7.12 | | POU4F2 | MA0683.1 | chr5:78431688-78431704 | TTAATTAATTATTCCC | - | 6.07 | | RUNX1 | MA0002.2 | chr5:78431843-78431854 | GTCTGTGGTTT | + | 6.62 | | SREBF1 | MA0595.1 | chr5:78431508-78431518 | ATCACCCCAC | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAGCTGAATA TCTTTTTAAA TAGTTCAGAC TTTTTCTCAA GTCAGCCTGG TCATTCTTCC 60
AATTATTCTG ACTTAATGAG ATTTTACTGT TCTTTGCAAA AGTTAACGTC CTAAACACCT 120
GAGGTAGCTT AGTGGAATTC ACCTATGGCT CAAAAACACT AGTGGCACAT AGCAGAAAAA 180
GCAAGGAAGA CATTTAGAAT CAAGACTTTG GGGTGCAAGT CCTAGCTTTG CCCCAACTCC 240
CTGCAGAACA TTGGGTAAAT CACCCCACTT CTCTGTCCTT CAATTTTCTC AACTGTAGGA 300
TAACAAGTTT CTAATGCCTT GCTGGAAAAC TCCACAGTTG TTTGCGATTT GATGATATAA 360
ATAAATAATA GCCTCATCAT TGTCAATAAA TATTTACTGA ATGCCACTTG GTGGTATGTT 420
TCCAGCGGAC TGAAATTGTT AATTAATTAT TCCCCTGGCT AAACAGACAG CCGACTAAAA 480
CAAGTAACAC TGTTCAGAGG GCAGGGAAAA TGTTACTACC CTAGACTCAG CCTGGTGCTG 540
AAAAATGAAA ATGTCATTCC TCCCCACAGG TACTGTTTTC TAAGGAGACT TGGGTCTGTG 600
GTTTTTCATA TTATGAACTG TTTCTATTTT CAAGGTTCAG AATTCTTTGT AGATTTGCAT 660
AAGCTAAATA TTCTAAAAAT CATCAAGTGA GTAATTTTTG GTTTAGAGTC CTTCATCTAC 720
CTAGGAAGGG AGAGAGCTGG CTTCTCACAT TTTGAGAATA GGAGAGTGGA ATTTGGGAGC 780
TAGACACCTC AGGATTTTTT TCCTTCCATC AGGCCATTCT CAGCAGCTTG ATGACTCCCA 840
GATTTCTCTC TCCAGCCTGG ACTACTCCCC AGCATTCAGG CACATGATAT CAGCCTGGCC 900
TGTAGACCCA AGCCAGCGGT CCGTGGCCCG GACCCTGTAC CTCAGGCCCC AAGCCACTTC 960
CCATGGCCAT TCAGGCAGAT GCCCCAGGTC TGGAGCAGGT CCCACATGGA TCCTGGTTGT 1020
CAGAGGCACC TTCCTCAAAA TTGTTTACAT CCTCCTCCAG TGGCTGAGAG CAGCCAGGGC 1080
CAGCTGTGCC ATCTAGGAAG GGAACCCCAA GCCTGGACCA GTCAGCATGG GACCCAGTCC 1140
TCATTTGTCT CCTTCTGAGT GTTCAGTGAC CCTGTACATC CCCGTACCAT GTCCCTCACA 1200
CCCACCCCAC TCCTGGAGTG ACCAAGTGCC CTAAGAAGCC TAAGGCTTTA TGTTGGTCCT 1260
GGTTCCAGGA GGGAGCCCTG GTGATAGGAT GGCTTCTGCT GGCAGGAACT GTATTTTATC 1320
CCAAGATCTG GTGAGATTGG GCTACCCAGT ATGGTGCTGA CACTCTGATT TTGGCTGACT 1380
CACATCAGAC ACAGGACAAG TTCAGGACCT TTGCCCCTTG CCTTGAGCAG TGAACGTAGG 1440
CCTTCATTGG 1450
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