| Tag | Content |
|---|
EnhancerAtlas ID | HS062-03736 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr12:47700530-47702130 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EN2 | MA0642.1 | chr12:47700544-47700554 | GCTAATTGGG | - | 6.02 | | NFYB | MA0502.1 | chr12:47700594-47700609 | AAACGCACCAATCAG | + | 6.73 | | NFYB | MA0502.1 | chr12:47700644-47700659 | AAACGCACCAATCAG | + | 6.73 | | NFYB | MA0502.1 | chr12:47700669-47700684 | AAATGGACCAATCAG | + | 9.03 |
|
| | 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 |
| GH12I047306 | chr12 | 47700701 | 47702647 |
|
Enhancer Sequence | GTGCTCTGTG TCTAGCTAAT TGGGTGGGGA CTTGGAGAAC TTTTGTGTCT AGCTAAAGGA 60
CTGTAAACGC ACCAATCAGC ACAATCAGCA CTCTGTGTCT AGCTAAAGGT TTGTAAACGC 120
ACCAATCAGC ACTCTGTCAA AATGGACCAA TCAGCTCTCT GTAAAATGGA ACAACCAGCA 180
GGATGTGGGT GGGGCCATAC AAGGGAATAA AAGCAGGTCA CCCAAGCCAG CAGCCACAAC 240
GCGGGTACCG TTGCACGCTG TGGAGGGTTT AGCTCTTTGC AATAAATCTT GCTGCTGCTC 300
ACTCTTTGGG TTGGCACTGC CTTTATGAAC TGTAACACTA ACCACGAAGG TCTGCAGCTT 360
CACTCCTGAA GCCAGCGAGA CCACGAACTC ACCAGGAGGG ACGAACAATT CCAGATGGGA 420
GGAACAAACA ACTCCGGACA CGCCACCTTT ATGAACTGTA ACACTCACCG CGAAGGTCTG 480
CAGCTTCACT CCTGAGGCCA GCAAGACCAT GAACCCACCG GGAGGAAGGA ATAACTCCAG 540
ACGCATCGCC TTTAAGAGCT GTAACACTCA CCACAAAGGG ATGCAGCTTC ACTCCTGATG 600
TCAGCCACGA ACCCACCAGA AGGAAGAAAC TCCGGACCCA TCTGAACATC TGAAGGAACA 660
AACTCCGGAC ACACCATCTT TAAGAACTGC AACACTCACT GCGAGGATCC GCGGCTTCAT 720
TCTTGAAGTA AGCGAGTCCA AGAACCCACC AATTCTGGAC ACACTTCCAC ATTTGTGACG 780
TCTCTCCCCT CATTCTGACT GGTATCAAGC ACAAGAAATA ATTTCCCCCA ACTCAGTTTC 840
TCACTGGAAA AAATGAGGTT GAGGTGGATA ACCAACTTCA TCATCCTGGG TTCCATGGCA 900
AGAGACCCAT CCCTACCTTA GAGCCACAGG AAGCACTGTG AGTGCCTGAA AAGAGAAATA 960
TCCCTGAGAA CAGTCAGAAC CGGTGGGGAG GGAAGACTAC CATCCCCTGC CCTGGGAACT 1020
GCTTTGTAAA TCAGCCAAAC AAGACACCAA ATCAGAGTGA CTGTTCAGCA GCACCATACT 1080
GCAGAAGGTT TGTTCCACAG GTCTCCTGGG GACGAACTTC TAGCCAACCT TCCTACACTG 1140
CCAGGATATC CCCTTAGGGA CCTCTGCCAC TCAGAAAGGG CATGCTCTGA TCATTTACTA 1200
GAGCTGAGGT GAACCTGGCG TAAAGACGCC ACCTAGAGCT GAAAAGAAGA CAGTCCATAG 1260
CAATAAAGAA CCTTTAAGCA ATTGTAGCCA ATAAAAATCA AAACAAGCCA GACAGAGAAG 1320
ACTGGAATAA ATAATTAATC CTTCAATGTA AAGACATAGA CATACATCCA CAAGAAACAA 1380
CAGCAAACAG GAAACCAAGG TCTCCCCAAA TGGACAAAAC AAGAAACCAG TGACTGACCC 1440
TAAACGGCAG TTTTAAGGAA ACTCAGTGAT CGCCAAGATA ACACGGAAAA CAAATTTCAG 1500
AAATTTATCA GAGCAATTTA ACAAAGAAAT CTAAATAATT TAGAAAAACA AAAATTTTGG 1560
AACTTAGAAA AATATTTGGT GAACTGAAAA ATTCATTAGA 1600
|
