| Tag | Content |
|---|
EnhancerAtlas ID | HS050-06726 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:246957400-246958880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr1:246958047-246958059 | CAGTAAACAGAA | + | 6.02 | | ZNF263 | MA0528.1 | chr1:246957425-246957446 | AGAGCAGGGGCAGGGGGAGGG | + | 6.61 |
|
| | 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 | GGGGGAGGGG AAGGGCAGGG AGGGGAGAGC AGGGGCAGGG GGAGGGCAGG GTTGGGGCAG 60
GGGAAGGCAG GAGGGTGGGG TGGGGAGAGG GCAGGGCGGG GGCAGGGGGC CGGCTGAGTA 120
CCAGCTTGAA TGAAGTACTT GAGCACCCTG GTGAGCTGAG GGTCCTCGCT GAGGTTAAGA 180
AGGTGAGGGA AGGTCATCAT CTGCCGCTCC TGCAGGAGAA GTGGAGAGGG TTGGGTGTCA 240
CCAGTCCGCA CCAGCCCACT GGGGAGAGCA ACACTTCTTT CCCGTCTCTG TGCACCTTGT 300
CAACCCTCCT GGGGAGGGAG GAAAGCTGAG AGGGGCTGGG GCATTGCTGA TGGTGGGGTG 360
GAGTCTCAGG CAGGCCAGCC GTCAGGAGTC TGAGTACATC TGGACTGGAC AGTTCCAAGG 420
AGCTGTCTCC CGGCTGCCCT CCCCAGCTGT CTGCATGCCC CGCTCTGGTC CCCTGCCTGG 480
GCAGCCCCTC CCCATGTCTC CATGCAGCCT CTCATTCTCC CGAAGTGCTG CTGGCTGGCT 540
GAGAATCAGA TGTTGATGGC AAAAAGTGGG GTATGGCACG AACCCTCGCC TGGCAACCTG 600
AACATGTCAT TCGTCCACAC AAGGATTGTT GTGGCGTAGG GATTTGACAG TAAACAGAAC 660
GGGGATGATT ATGCAGCCAC GAGGAAGACT TTTACAGCTT GAAATCCTCT CTGACAAAGA 720
GTAAAGAGGG CAAAAACCCT TCCAATTTTT ACTGTATATG CAGAACCCAA AATCCCGTAT 780
TCCTCCATGT GACCTTACTT GACCCTTGAA GCTGAGAGTC CCAGCCACCA CTTACACAGA 840
ACGTGACTCA GTACAGCCCT AACTGTCTGG TTTCCTGATG CCACAGACCC CACCCTGCTC 900
CACCCCCCAG GCCCTGAGGC CGTAGTTAGG CAGTATGAGG TTCCGGAATC CCCAGCTCCA 960
GTCCCCTAGT ACTCCAGGTC TGATCCTCAA CTTTGGGATT TTCCCAGGGC CTCGTGGCCA 1020
CGGGGAGTGG GGTGGGGTGG AAGCCGGGGT GGCCAGGGGA GGCCGAAATT CAATCACAGC 1080
CCATTTAGGG TGTGATATCA TCAGCGAATG CCAGGATAGA CACCCGGCCT TACGCCCTGC 1140
CAGGCCCCGA GTCCTCCCCG TTTCCCTCGC TGGCATGCCC TGATGTTCTC TCCCTAGCTC 1200
TGCCAGTAGC ATCATTACCA GTCACACATT ACACATTCAC CAAAAAAGCC TCGCCACAGT 1260
CGGGCCTGGC CAGCCAGACT GCAGCCTGTG CCTGGCCCCC TGCCCTGGGC TCAGCCTCCG 1320
CAGGTGGCGG AGGTGAAGCT CACCTGGGCC CTCTCCAGCA GGTGTGCCCA GGTCACCTGA 1380
TCAGGAGTCC CCAGCTGCTG CTCTGCCTGG AGACAGGCCG ACGGCTCTGG AAGGAGGGAG 1440
GCATTTTAAG CGGCGGGTCT GCGGTGCCAG GGGGAGTCAC 1480
|
