| Tag | Content |
|---|
EnhancerAtlas ID | HS187-08642 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr15:75422800-75424220 |
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 | CCTCAGCCTC CCGAGTAGCT GGGATTACAG GCATGCGCCA CCACGCCCAG CTAATTTTTG 60
TATTTTTAGT TGAGACAGGG TTTCACCATG TTAGCCAGGC TGGTCTCAAA CTTCTGACCT 120
CAGGTGATTC ACCAGCCTCA GCTCCCAAAG TGCTGGGATT ATAGGCGTGA GCCACCACAC 180
CCATGCCTGG CTCCCCTTTC CTTTTTTTTG TTGTTTTTTT TTTTTGTTTT TTTTGCATAG 240
AGTCTCACCC TGTTGTCCAG ACTGGAGTAC AGTGGTGTGA ACTCGGCTCA CTGCAACCTC 300
TGCCTCCTGG GTTCAAGCAA TTCTCCTGCG TCAGCCACCT GAGCAGCTGG GACTACAGCC 360
GTGTACCACC ACACCTGGCT AATTTTCGTA TTTTTAGTAG AGACAGGGTT TCACCATGTT 420
GGCCAGGCTA GTCTCGAACT CCTGACATCA AGTGATCCAC CTGGCTTGGT CTCCCAAAGT 480
GCTGGGATTA CAGACGTGAG CCACTGTGCC TGGCCAAAAT TTACCATCTT AACCATTTCT 540
AAGTATAGAG TTAAGTACCG TTAGTTAAAT TCGCATTGTT ATGGAAGAGC TCTCCGGAAT 600
TTTTTTAGCT TGCAAAAGTG AAACTATACC CATGAAACTA ACACCTCTGT ATTTCCCTCT 660
CCCCAGCCCC TGACAACCAC TATTCTACTT TCTGTTTCTA TGAATTTGAC TACTATAGAC 720
AACTCATGTA AGTAGAATCA CATAGTATCT GTGTTTTGGG GACTGGCTTA TTTCACTTAA 780
TAAGATGTTC TCAAGGTTCA ACCATGTTGT AGCATGTGTC AGAATTTCCT TCCTTTTTAA 840
GGCTCAATAA TATTCCGTTG TATGTATATA CCTCATTTTC TTTATCCATT TGTCAGTGGA 900
CACTTGGGTT GCTTTTGACC TCTTGGCTAT TACAACTAGT GCTGCTGTAA GCATAGTGTG 960
GAAATATCTC CTTGAGATCC TGTTTTCAAT TATTTTGGCT GTAAAACCAG AAGTGAGATG 1020
GTTGGGTCAT AGGATAGTTC TATTTTTAGT GTTTTAGGAA CTTCCATATT GTTTCCCATA 1080
GTAGCTGCCC CATTTTACAT TCCCACCAGC AGTGCAGAAG CATTCCAGTT TTCACACATT 1140
ATTGCCAACA CTTGTTATTT TCTGTTATTT TGATACTAAT TATCCTAATA CGTGTGTTTT 1200
TTTTCTTTTT TATTTTGGAG ACAAGAGTTT TGCTCTTGTC TCCCAGGCTG AAGTGCAGTG 1260
ACGCAATCTC AGCTTACTGC AACCTCTGCC TCCTGGGTTC AAGTGATTCT CCTGTCTCAG 1320
CCTCCTAAGT AGCTGGAATT ACAGGTGCCT GCCACCACAA CTGGCTAATT TTTTGTATTT 1380
TTAGTAGAGA CAGGGGTTTT ACCATGTTGG CCAGGCTGGT 1420
|
