| Tag | Content |
|---|
EnhancerAtlas ID | HS064-05107 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr15:75422900-75424280 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr15:75423412-75423430 | CAAAAGTGAAACTATACC | + | 6.53 | | MEF2A | MA0052.3 | chr15:75423838-75423850 | TCTATTTTTAGT | - | 6.27 | | MEF2B | MA0660.1 | chr15:75423838-75423850 | TCTATTTTTAGT | - | 6.32 | | MEF2C | MA0497.1 | chr15:75423837-75423852 | TTCTATTTTTAGTGT | - | 6.03 |
|
| | 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 |
| GH15I075129 | chr15 | 75421961 | 75424509 |
|
Enhancer Sequence | TGGTCTCAAA CTTCTGACCT CAGGTGATTC ACCAGCCTCA GCTCCCAAAG TGCTGGGATT 60
ATAGGCGTGA GCCACCACAC CCATGCCTGG CTCCCCTTTC CTTTTTTTTG TTGTTTTTTT 120
TTTTTGTTTT TTTTGCATAG AGTCTCACCC TGTTGTCCAG ACTGGAGTAC AGTGGTGTGA 180
ACTCGGCTCA CTGCAACCTC TGCCTCCTGG GTTCAAGCAA TTCTCCTGCG TCAGCCACCT 240
GAGCAGCTGG GACTACAGCC GTGTACCACC ACACCTGGCT AATTTTCGTA TTTTTAGTAG 300
AGACAGGGTT TCACCATGTT GGCCAGGCTA GTCTCGAACT CCTGACATCA AGTGATCCAC 360
CTGGCTTGGT CTCCCAAAGT GCTGGGATTA CAGACGTGAG CCACTGTGCC TGGCCAAAAT 420
TTACCATCTT AACCATTTCT AAGTATAGAG TTAAGTACCG TTAGTTAAAT TCGCATTGTT 480
ATGGAAGAGC TCTCCGGAAT TTTTTTAGCT TGCAAAAGTG AAACTATACC CATGAAACTA 540
ACACCTCTGT ATTTCCCTCT CCCCAGCCCC TGACAACCAC TATTCTACTT TCTGTTTCTA 600
TGAATTTGAC TACTATAGAC AACTCATGTA AGTAGAATCA CATAGTATCT GTGTTTTGGG 660
GACTGGCTTA TTTCACTTAA TAAGATGTTC TCAAGGTTCA ACCATGTTGT AGCATGTGTC 720
AGAATTTCCT TCCTTTTTAA GGCTCAATAA TATTCCGTTG TATGTATATA CCTCATTTTC 780
TTTATCCATT TGTCAGTGGA CACTTGGGTT GCTTTTGACC TCTTGGCTAT TACAACTAGT 840
GCTGCTGTAA GCATAGTGTG GAAATATCTC CTTGAGATCC TGTTTTCAAT TATTTTGGCT 900
GTAAAACCAG AAGTGAGATG GTTGGGTCAT AGGATAGTTC TATTTTTAGT GTTTTAGGAA 960
CTTCCATATT GTTTCCCATA GTAGCTGCCC CATTTTACAT TCCCACCAGC AGTGCAGAAG 1020
CATTCCAGTT TTCACACATT ATTGCCAACA CTTGTTATTT TCTGTTATTT TGATACTAAT 1080
TATCCTAATA CGTGTGTTTT TTTTCTTTTT TATTTTGGAG ACAAGAGTTT TGCTCTTGTC 1140
TCCCAGGCTG AAGTGCAGTG ACGCAATCTC AGCTTACTGC AACCTCTGCC TCCTGGGTTC 1200
AAGTGATTCT CCTGTCTCAG CCTCCTAAGT AGCTGGAATT ACAGGTGCCT GCCACCACAA 1260
CTGGCTAATT TTTTGTATTT TTAGTAGAGA CAGGGGTTTT ACCATGTTGG CCAGGCTGGT 1320
CTCGAACTCC TGACCTCAGG TGATCCACCT GCCTCAGCCT CCCAAAGTGC TGGGATTACA 1380
|
