| Tag | Content |
|---|
EnhancerAtlas ID | HS080-03541 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:246957280-246959110 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr1:246958047-246958059 | CAGTAAACAGAA | + | 6.02 | | PAX6 | MA0069.1 | chr1:246958948-246958962 | CACTTATGCGTGAA | - | 6.09 | | ZNF263 | MA0528.1 | chr1:246957394-246957415 | AGGGAAGGGGGAGGGGAAGGG | + | 6.11 | | ZNF263 | MA0528.1 | chr1:246957324-246957345 | GGGGGAGGGCAGGGTGGGGAG | + | 6.3 | | ZNF263 | MA0528.1 | chr1:246957425-246957446 | AGAGCAGGGGCAGGGGGAGGG | + | 6.61 | | ZNF263 | MA0528.1 | chr1:246957365-246957386 | AAAGGAAGGGGGAGGGGAAGG | + | 6.64 | | ZNF263 | MA0528.1 | chr1:246957356-246957377 | GGGGCAGGGAAAGGAAGGGGG | + | 6.69 |
|
| | 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 |
| GH01I246794 | chr1 | 246957671 | 246958925 |
|
Enhancer Sequence | AGGGCGGGGT GGGGAGAAGG CAGGGCAGGG GCAGGGGGAG CACAGGGGGA GGGCAGGGTG 60
GGGAGAAGGC AGGGCGGGGG CAGGGAAAGG AAGGGGGAGG GGAAGGACAC GGAAAGGGAA 120
GGGGGAGGGG AAGGGCAGGG AGGGGAGAGC AGGGGCAGGG GGAGGGCAGG GTTGGGGCAG 180
GGGAAGGCAG GAGGGTGGGG TGGGGAGAGG GCAGGGCGGG GGCAGGGGGC CGGCTGAGTA 240
CCAGCTTGAA TGAAGTACTT GAGCACCCTG GTGAGCTGAG GGTCCTCGCT GAGGTTAAGA 300
AGGTGAGGGA AGGTCATCAT CTGCCGCTCC TGCAGGAGAA GTGGAGAGGG TTGGGTGTCA 360
CCAGTCCGCA CCAGCCCACT GGGGAGAGCA ACACTTCTTT CCCGTCTCTG TGCACCTTGT 420
CAACCCTCCT GGGGAGGGAG GAAAGCTGAG AGGGGCTGGG GCATTGCTGA TGGTGGGGTG 480
GAGTCTCAGG CAGGCCAGCC GTCAGGAGTC TGAGTACATC TGGACTGGAC AGTTCCAAGG 540
AGCTGTCTCC CGGCTGCCCT CCCCAGCTGT CTGCATGCCC CGCTCTGGTC CCCTGCCTGG 600
GCAGCCCCTC CCCATGTCTC CATGCAGCCT CTCATTCTCC CGAAGTGCTG CTGGCTGGCT 660
GAGAATCAGA TGTTGATGGC AAAAAGTGGG GTATGGCACG AACCCTCGCC TGGCAACCTG 720
AACATGTCAT TCGTCCACAC AAGGATTGTT GTGGCGTAGG GATTTGACAG TAAACAGAAC 780
GGGGATGATT ATGCAGCCAC GAGGAAGACT TTTACAGCTT GAAATCCTCT CTGACAAAGA 840
GTAAAGAGGG CAAAAACCCT TCCAATTTTT ACTGTATATG CAGAACCCAA AATCCCGTAT 900
TCCTCCATGT GACCTTACTT GACCCTTGAA GCTGAGAGTC CCAGCCACCA CTTACACAGA 960
ACGTGACTCA GTACAGCCCT AACTGTCTGG TTTCCTGATG CCACAGACCC CACCCTGCTC 1020
CACCCCCCAG GCCCTGAGGC CGTAGTTAGG CAGTATGAGG TTCCGGAATC CCCAGCTCCA 1080
GTCCCCTAGT ACTCCAGGTC TGATCCTCAA CTTTGGGATT TTCCCAGGGC CTCGTGGCCA 1140
CGGGGAGTGG GGTGGGGTGG AAGCCGGGGT GGCCAGGGGA GGCCGAAATT CAATCACAGC 1200
CCATTTAGGG TGTGATATCA TCAGCGAATG CCAGGATAGA CACCCGGCCT TACGCCCTGC 1260
CAGGCCCCGA GTCCTCCCCG TTTCCCTCGC TGGCATGCCC TGATGTTCTC TCCCTAGCTC 1320
TGCCAGTAGC ATCATTACCA GTCACACATT ACACATTCAC CAAAAAAGCC TCGCCACAGT 1380
CGGGCCTGGC CAGCCAGACT GCAGCCTGTG CCTGGCCCCC TGCCCTGGGC TCAGCCTCCG 1440
CAGGTGGCGG AGGTGAAGCT CACCTGGGCC CTCTCCAGCA GGTGTGCCCA GGTCACCTGA 1500
TCAGGAGTCC CCAGCTGCTG CTCTGCCTGG AGACAGGCCG ACGGCTCTGG AAGGAGGGAG 1560
GCATTTTAAG CGGCGGGTCT GCGGTGCCAG GGGGAGTCAC GGGATAGCTA GTGTGTCTCT 1620
GGCTCTGTTC TCAAAGCCCA GGATCCCGGC AGCAGCAGGA ATGCAGCACA CTTATGCGTG 1680
AAGACGAGAT CTTTCGGTAA GTCCTACAAA GAGGACTTTT AATTCCCCTC CTAATTCGTA 1740
AGACGTTAGT GCAAGAAGGT CCTTTAAGGG GGAGGCATGA GTTCAGTGTT CTGTCTCTTA 1800
TTTTTGTACT TGCTCAGGCT TGTGAGGGCG 1830
|
