| Tag | Content |
|---|
EnhancerAtlas ID | HS050-34930 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr2:1971250-1972190 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr2:1971498-1971509 | GGAGGGTGTGG | - | 6.32 | | Klf1 | MA0493.1 | chr2:1971500-1971511 | AGGGTGTGGCC | - | 6.32 | | REST | MA0138.2 | chr2:1971851-1971872 | GGCTGTGTCCAGGGTGCTCAG | - | 6.03 | | ZNF263 | MA0528.1 | chr2:1971481-1971502 | GGTGGAAGAGGATGGGGGGAG | + | 6.12 | | ZNF263 | MA0528.1 | chr2:1971759-1971780 | AGGGGAGGAGGGGGCAGAAAA | + | 6.31 | | ZNF263 | MA0528.1 | chr2:1971762-1971783 | GGAGGAGGGGGCAGAAAAGAG | + | 6.59 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCTCCTTTGC TGCGCCTTCA CATCCTCCCC CTTTCCTCCT TTATTAGAAA TCAATTTGGG 60
TTAATTTAAG AAGCTTCTCT GCCAAAACCA TACTGGCCTC AGGGAAAGTT CAGTTCATTA 120
GTCACTCAAA GCAGGTGCAC CTTATTCTAA TAATGTGATG AGTGCCTTCT GCGCAGCTGC 180
AGCAGGGACT TCAGGCCTGA CTGGAGCTGG AGGAAGAAAA GGTCGTTCCA GGGTGGAAGA 240
GGATGGGGGG AGGGTGTGGC CAAAGAGGGG GTGTTTTGCT GCGCAGGCGA GACGAGGTGC 300
AGCGAGGCCG CAGGCCCCGA GCCCTGCCTG GGAACAGCGA GTGCTTCTGG GACGTTGCTG 360
TTATTACCAG AAGGGCCTCC TGCAGGGGAG GGCAGGAGCC TAGACTCCAC TTCCGCAAAG 420
AGTCCTGCTG TCTGTGTGTC CTCAGGGAGC CTGGGAGGAG AGGAGCTTCC TCGGGCCCCT 480
GCACTGCTCC CTGCTCACTG CACCCCAGGA GGGGAGGAGG GGGCAGAAAA GAGAGGAGAG 540
GCCCAAGATC TGCATTCCTG GACACAGTCA ACTCCACCCA CCTGGCAAGG AGTGGCAAGG 600
AGGCTGTGTC CAGGGTGCTC AGGGAAGCCC AGCCCCAGGG CCCGCAGCTG GGCCCCTCTA 660
GCAGCACCAC TCTCTGCTCT CAGATCTTAT CCCCGTTGAG GTTGGACTAA AGCTCTGGAC 720
TCTCCAGCCT TCCTGACGAT AAATGCAGCC ATTAGGATTC ACTACCCTCT GCCCTCTCCG 780
CATGCCCGCT TCCCTTCCTG GCTCCCCAGA GCGTCTGCAC TTCATTCAGA AGCGTGAGAA 840
GCCGCAGGAT TGGTCGAGGG AATAACAAGG TGATCCAGGC ATCGCTGAAT TGCTATGTAT 900
TATTTATGAA TAAAATTTCT TCCAAGATGT TCATTTTCCC 940
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