| Tag | Content |
|---|
EnhancerAtlas ID | HS184-18342 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr20:47139580-47140540 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr20:47139728-47139749 | CCCAGCTTTCTCTTTCTCTCT | + | 6 | | REST | MA0138.2 | chr20:47139884-47139905 | TGAGCTGTCCTAGGTGCTGAA | - | 9.26 | | ZNF263 | MA0528.1 | chr20:47140278-47140299 | CCTCACTTTCTCCCCTCCTCC | - | 6.53 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH20I048523 | chr20 | 47139801 | 47139970 |
|
Enhancer Sequence | ACCAGGAAAA CTGGGCTTTT CTTGACCCTA AAGTGCTGGT TTATCGGCCC AGCACTGAAG 60
TTATACCTCA CGCACAGCCC TGACTTTTGG ATGGAAACTA CCGTTATCCT ATTTGGGGTC 120
GCTTCCCAGT GGCTCCCATG TCCAAGACCC CAGCTTTCTC TTTCTCTCTT CACCCACTTT 180
GGATTGGGAG CCTCAAAACC ACTGTGCTGA AACCACTTCT AGGCATCAGC ACCATTCACT 240
AACAGCACAC TGGCCTTTGT TCTAAGACAG GGATTCAGCA GTTACATAGA TGTGCACTGA 300
GCACTGAGCT GTCCTAGGTG CTGAAATGAT TTCATCAGGA GCAATCAGAG GCTGCCTAGT 360
CCAGGAATCT CAGACATTTG ACCCTGGCTG AATGCCCTTA TTGGAGCAGG AAAGAAGTGC 420
AACAGTTTGC AATAAAATAG GCCCCTCATT TGCCATCCAG GGACACACAC AAAGAAGCAA 480
CAGTGAACAG TCAGTACTTC ACCCAGATTC AAGCAACACA TCCCGACCTA TGTGGTATCC 540
TCCCTGTGAC ACAGGAACGG GGTGGGAGAG GAGTTCTCTA GCCACTTGCC TCCCAAGCTC 600
ATCCATGGGA AAGCATCTTG CTCCCAAGCT GTCAGGGAGA ACCACAAAAC CCCCCTCAGC 660
CGGCAGGAAG CTTGCCCCAC CCTCTTCCCC ATTCACCCCC TCACTTTCTC CCCTCCTCCA 720
CTGACACTCC TCAACTCCCT GGACTGTCCA CTCAGCCCCA GACCTTCTCT CTTCTGCCCC 780
CACTGTGTCG TGACTGTCAG CCATTCCTCC CTAGTCCAGA AATGTCCATG AGGGTGAGAG 840
AGCAGGGGGA GGACAGGACC CTCCAGGATG ACCTGGCCTC AGAAAAAGAG CATCTAAAAC 900
ACATCGGAGG CATCGCCTTG TGAAGCTTCA ACTGCCAGCA AGTCCCATCC ACAGATTCTG 960
|
