| Tag | Content |
|---|
EnhancerAtlas ID | HS065-03362 | Organism | Homo sapiens | Tissue/cell | GM18508 | Coordinate | chr20:44959390-44960700 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr20:44959481-44959492 | CCACACCCTCC | + | 6.32 | | Klf1 | MA0493.1 | chr20:44960361-44960372 | AGCCACACCCT | + | 6.02 | | ZNF263 | MA0528.1 | chr20:44959929-44959950 | GGAGTAGGGGAAGGAGGGGAA | + | 6.04 | | ZNF263 | MA0528.1 | chr20:44959935-44959956 | GGGGAAGGAGGGGAAGGAGAC | + | 6.19 | | ZNF263 | MA0528.1 | chr20:44959934-44959955 | AGGGGAAGGAGGGGAAGGAGA | + | 6.29 | | ZNF263 | MA0528.1 | chr20:44959926-44959947 | GGGGGAGTAGGGGAAGGAGGG | + | 7.61 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGAGTGGGGG AGCAATTCAA TTTCCAGAGT TGGCCCTGGC AATACCGGTT GTGTCGTGAT 60
AAGAAAGCCA TTTCCCGTGA TGGCTCCTAA TCCACACCCT CCTGCCTTTG CATGCAGCAG 120
CTCCCTTCAT CTGCCTGTGG CCAGAGGCTG GAAGGGATCC CTGTCCACTA TGGAAGGGGC 180
CATGTCTGCT CCAAATGAAC CATGCTGAGC AGCATCTGTG TGGCCGGGAC AAAGACCCAT 240
GCCGAAATCT ACAAGCCCAG GAGAAGCCGT CAAACCCGAT GAATAATCCC TCGGACTGTT 300
CTAAATTCAG ATGGACATGC ACAGCTGTGA TCTAATTTGA GCCATACATC TGCCCTTGAG 360
AGAAGTAGGG ATCACTCCCA TTTTACAGAT GGGGAAAGTG AGGCTCAAAG TGGTTCAGTG 420
ATTTGCCCGA AGCTACACAG CAAGTGCGTG TAGAGAGAAG CGCAAGTTGA TGTGTGCAGG 480
GCTGAAGTGT GAGGTGAGGG TGCAGTGCGG GAGCCGCAGC CTGGGCTTCG AAGGTCGGGG 540
GAGTAGGGGA AGGAGGGGAA GGAGACAGGC AGGGAGTATG AGGAGAGGTG AGGAGAGGTG 600
TGTGCTGGGC AGCAGCTCGG TGGGAGCCCA GCTAGGAAAG GAGCCTCGGG GTGGCCTCGA 660
GAGGATTTTA GTGCTGTCTG GGCAGGGGGT CTGTGGGATA CAGACCTGGG AGGGATGGGG 720
GCATGGTGGT CAGAGAAAGA AGCTGCTGGA GGACACAGGC GAGCCAGGAC CACAGTCAGG 780
GAGGCAGCTG TGACTGTCAG CAGGAACACG GGAATCCTCT ACGAGACACC TACACCTGAG 840
TCCTGACATC AAAGGGGTTT CTCGCCTCTC CGGTCGCCTG GTTTGGAGCT CAGCTTTCTT 900
GAAAACTTTC TTCCTGCCAG TCTCCTGCAC AGGCCCTGGA CACTCCTTGG GCTGGACTGG 960
GCCCCTTTTC CAGCCACACC CTTCACTGGC TGGGAGGGTT GCAGGGAGGC CTCGGGCTGA 1020
GCCAGGCCCT TCTGCTGGCT CCCCTGTGGC CCGCAGGGGC AGAGGAGGGA GGGCAGCTGG 1080
GCTGGGGATT CAACAGGAGG GGCAGTCTAG GTGAAGCCAG CCAGGCCCTC CTGATTTGCT 1140
CCCCACCAGG AAGTTTTCTT TGTTTGTTTT GGTTTTTCCT TTTTGTTTTA TTGAGACAAG 1200
GTGTTGCTCT GTCGCCCTAG CTGGAGTGCA GTGGTGTGAT CACAGCTTAC TGCAGCCTTG 1260
ACCTCCCAGG CTCAAGTAAT CCTCCAGCCT CAGCCTCCCA AGTAGCTGGA 1310
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