| Tag | Content |
|---|
EnhancerAtlas ID | HS007-10211 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr20:44960850-44962180 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr20:44961422-44961443 | CTCCTCCTCTAGCCCTCCTCC | - | 6.16 | | ZNF263 | MA0528.1 | chr20:44961303-44961324 | GGGGCAGGGGAATAAGGAGGG | + | 6.21 | | ZNF263 | MA0528.1 | chr20:44961411-44961432 | TCCTCTGGCCTCTCCTCCTCT | - | 6.29 | | ZNF263 | MA0528.1 | chr20:44961583-44961604 | GGAAGAGGGGAGGGGAGGGGG | + | 6.58 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr20 | 44961427 | 44961777 | | chr20 | 44961032 | 44961397 |
| Enhancer Sequence | GGGATTACAG GCATGAGGAG AACTGACCAG GAATACAAGC AAGGATGGAT CCCGAATCCT 60
GTTTGTCTCC CTCTGCATCC CTACCCCCCA CTGCTGACTC CAGAAGGCCT GGTGGGGAGC 120
GGTGGTGGAT CTGGGGGCTA CAAAGCCGGG CAGGATTGTT TACCCTCTCC CTACCTTCCC 180
CTCACTGGCC CAACTGTGAT GGGGGTGAGA TGGCAGGCTG GGGCTGTGGG AGGCTCCCAG 240
AACAGCTGGT GGCTGTGCAG GGCCGTGGGT GGTGGCAAGT GGGGACCTGC TGGAGCAGGC 300
AAGCTAATCT CATTTGGTTG CTGCAGTCGC AAACAAGGAC TGCATGCTAA GTGGCCAGAG 360
GCAGCAGCGG GACTCAGGGC CGACCCAGGC CCCACGCATA CCTGGGAGCA CCTAGAGGCC 420
AGCCCTGGTT TGAATGAGGA GCCATGTTGG GCAGGGGCAG GGGAATAAGG AGGGGGAGGA 480
TGCGTCTTGT GGGGTAAGAG GTTACTCCCC GGGAAATACC TGCTGGGAGA TAGGGCGCCA 540
GGGTCAGCCA GCTCCTCCCA ATCCTCTGGC CTCTCCTCCT CTAGCCCTCC TCCTGTAGGG 600
TCCTGGATCA GATGCCACTG GGCAGGAGGC ATCTGGAGAG CAAGCTTCAT CCCCTTTGCC 660
AGCAGAATTG TGATTGGAGA GAGGGACCCG CCTGTTCACA GCAGAGCATG AGGGAGGCAT 720
CGGGGAAGGT GCTGGAAGAG GGGAGGGGAG GGGGCTGGGG GAGCCTTGAG CCTCGAGGCC 780
CTGCCCAGTC ACTCCACTCC TCTGAGCCTC TAGGGGCTTG TTTAGAGGCA GGGCCAGGGA 840
GGTGCAAGAA GATGCCCTGG CTGTAAAAAG GTGATTGGGC TTGCGACTCT TGTGAAATGG 900
TCTGAAACTA TCTTTAGCTT AGATGGGAGT GCCAGGCTTG CAGGGCCCAG GTTTGGCAGA 960
TGAGCCAGGC CAGAAGCCAG TGCCCTGAGG GCTTCCTGAC TGCCACCCAC ACTCTCCGCC 1020
CGGCTGCCAC TTCTCGGAGC AGCTGGTACC ATCAGCTCCC AGGGAGAATC CTGAAATCAC 1080
ACAGGTAGCT CTGGTCTTTG GGCAAAGGTT TGTGCTCTAG ACGTGGGTGG CCTGAACTTG 1140
GGGCTGCATC ATGGTAACAG ATGGATTTGA AGGCAGAGCT TGCAAGGGAG TCCAGATGGC 1200
CACAGCCACC ATCCAGGTCT GTTTTTGGTA CTTGCTGGGC CCCTGTGGGC AGCTCCATTT 1260
GCAACCCCTT TGGAGCTCCT TAGCTCAGGT CTTGCTGATA AAAATAAGCC CTGCCAATCA 1320
CAGGGGGCTT 1330
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