| Tag | Content |
|---|
EnhancerAtlas ID | HS095-18669 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr20:44960770-44962060 | 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 | CAGGCTGATC TCAAACTCCT GGCCTCAAGA TCAAAGTCTT GGCTTCAAGT GATCCTCCTG 60
CCTGCGCCTC CCAGAGTGCT GGGATTACAG GCATGAGGAG AACTGACCAG GAATACAAGC 120
AAGGATGGAT CCCGAATCCT GTTTGTCTCC CTCTGCATCC CTACCCCCCA CTGCTGACTC 180
CAGAAGGCCT GGTGGGGAGC GGTGGTGGAT CTGGGGGCTA CAAAGCCGGG CAGGATTGTT 240
TACCCTCTCC CTACCTTCCC CTCACTGGCC CAACTGTGAT GGGGGTGAGA TGGCAGGCTG 300
GGGCTGTGGG AGGCTCCCAG AACAGCTGGT GGCTGTGCAG GGCCGTGGGT GGTGGCAAGT 360
GGGGACCTGC TGGAGCAGGC AAGCTAATCT CATTTGGTTG CTGCAGTCGC AAACAAGGAC 420
TGCATGCTAA GTGGCCAGAG GCAGCAGCGG GACTCAGGGC CGACCCAGGC CCCACGCATA 480
CCTGGGAGCA CCTAGAGGCC AGCCCTGGTT TGAATGAGGA GCCATGTTGG GCAGGGGCAG 540
GGGAATAAGG AGGGGGAGGA TGCGTCTTGT GGGGTAAGAG GTTACTCCCC GGGAAATACC 600
TGCTGGGAGA TAGGGCGCCA GGGTCAGCCA GCTCCTCCCA ATCCTCTGGC CTCTCCTCCT 660
CTAGCCCTCC TCCTGTAGGG TCCTGGATCA GATGCCACTG GGCAGGAGGC ATCTGGAGAG 720
CAAGCTTCAT CCCCTTTGCC AGCAGAATTG TGATTGGAGA GAGGGACCCG CCTGTTCACA 780
GCAGAGCATG AGGGAGGCAT CGGGGAAGGT GCTGGAAGAG GGGAGGGGAG GGGGCTGGGG 840
GAGCCTTGAG CCTCGAGGCC CTGCCCAGTC ACTCCACTCC TCTGAGCCTC TAGGGGCTTG 900
TTTAGAGGCA GGGCCAGGGA GGTGCAAGAA GATGCCCTGG CTGTAAAAAG GTGATTGGGC 960
TTGCGACTCT TGTGAAATGG TCTGAAACTA TCTTTAGCTT AGATGGGAGT GCCAGGCTTG 1020
CAGGGCCCAG GTTTGGCAGA TGAGCCAGGC CAGAAGCCAG TGCCCTGAGG GCTTCCTGAC 1080
TGCCACCCAC ACTCTCCGCC CGGCTGCCAC TTCTCGGAGC AGCTGGTACC ATCAGCTCCC 1140
AGGGAGAATC CTGAAATCAC ACAGGTAGCT CTGGTCTTTG GGCAAAGGTT TGTGCTCTAG 1200
ACGTGGGTGG CCTGAACTTG GGGCTGCATC ATGGTAACAG ATGGATTTGA AGGCAGAGCT 1260
TGCAAGGGAG TCCAGATGGC CACAGCCACC 1290
|
| |
|
|
|
