| Tag | Content |
|---|
EnhancerAtlas ID | HS108-30027 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr4:9692430-9693800 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr4:9693307-9693317 | GCCCCGCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr4:9693586-9693596 | GCCCCGCCCC | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr4 | 9692600 | 9693454 | | chr4 | 9693473 | 9693800 |
| Enhancer Sequence | TTTAGACTTT GAACACAGTT CAGATTTCAG GGGCAGTACT GAAATATGAA CTGTGTTGCT 60
AACTGCCCTG CCTTTCAACT CAAGACACAA TAACTTTGAA CTAAAATAAT TATATTTTTG 120
TTGTTTTCCA CTCTGTCCCC AAGTCTATAT CACCACCACC GCTAATCCCA CCCCGCAGGA 180
GCTAACTCCT CCTTCCTGTC CCTGCAAGAT CAAAACTCCT CCTGGAAGCC CCGCTAGCTC 240
TGTCTGCTCA CCTTCATGGC AGATATCGCT ATTGTACTTT TATATTCATT TGTATCATAA 300
GTACTTCAAT GTCCACTTCT TCCACGAGCC CCTGAGACCC TGGAGGGTCT GGACCACACC 360
TAGTTTTTCT CACTGTTACA TCTGCCTTGC CAGGCGCATG GTAGGCGCTT AGTAAGTATT 420
TGGTGAACGA ATGGCTTGTT TGGTGACAGT CCAAAGGCTG GAGGACAGAG GGAAAGCTCC 480
CTCCTGTCGG GCCCCAGACG GGTGGCGCTG ATGGAGAGGC GGCTGGGATA AGGCCTCCAG 540
GACCGAAGCG CGCACCCATA AGGCCCCTGC CAAAAAGACC TTCCTGAAGG CGGAGGAACT 600
GCGAGAGTGT CTACTTTGGC CCAAGGCCTG ACTCGACGAT CCCAGGGACC CTTGCCCTAA 660
CCGGCCCCGC CTCCCGGGCC CCAAACCCGT ACTCGGCCCC GCCCAAAGCT CCGGCTCCTA 720
GGGCCCGCCC CTGGCCCCGC CTCGGCCGAC CATGGCCTTG CTCCTGGGCC TGCCTCAAAC 780
CCTCCGCAGG TAACGCCTCC CGAACGTGAG CCACACTCCG ATTCCCTCCT CAAACCCCTC 840
CCCGTTTCCC ACACCCTGGA CCCCTCGCTC CGTCTCGGCC CCGCCCCAAG CCCAGCTCCG 900
TCTCGGCCCC TGAGCCCAGC CCCGACCCAC CTCCCAGTCC CTGGGTTCCT CCCGACACCG 960
GCGCCTCCCT AAGCTCCGCC TCCCAGGGCC CGAGCAGCGC CTGGCCATAC CCCCATGGCC 1020
CGCCTCCTGA GCGTAGCCCG CAGCCCAGAC TCGGACCCGC CTCCCGGACC CTGGGCCCCT 1080
CCCCACGTCG GCCCTCCCTA AGCTCTGCCT CCCAGAGTCC GAGCACCGCC TGGTCATGTG 1140
CTACGACATA GTCAACGCCC CGCCCCGGCC CCGCCTCCTG AGCCCTTCTC TGTGCTATTG 1200
TTTTCTTCTT AATAAAATGG GGGATATAAT GATAGCTACC TCTTAGGGTT GTTGTCAGAG 1260
TTGAGTACAA AAGCCTGTGG ATCAGTGCCT GGCTCATGGT AAATGCATGT CGGTGTTAGC 1320
TACTGTTTTT ATTCGGTCTG AAAATGTTTA ATAAATGCCT TTCGTGAGCC 1370
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