| Tag | Content |
|---|
EnhancerAtlas ID | HS052-03308 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr1:204732560-204733720 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TBX20 | MA0689.1 | chr1:204733202-204733213 | CTTCACACCTA | - | 6.62 |
| | | 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 |
| GH01I204763 | chr1 | 204732729 | 204733387 |
| Enhancer Sequence | GTTATTCAGG CACTAATGTG TAAGGCTGTG ATTCTAAGGC AGACTGACTG ACTACAAAGC 60
TAATGTTCTT AATCCCTAGA TGCTCCCACC TTCCAAATGT CCTGGCTCCT AGAATTACAT 120
CTGTTCTACT CCCTCCATGG CTCCATGGAA CCTGGACATC TCAATTTCCT CCCCAAAAGC 180
TGGAGTTCTC CAAGATGCAG AAGCCAGAGG GCTGATGTTC CTGTGCAGGA AGAAGCAACG 240
CCCAGGCCCA CTGCCCCCAC TCTCTCAGCA GATTCTCATT TTCAGAATCC TGGAAACCAG 300
AGCTAGAAAT CTGCCTCCCT CTGTTTACCC TGAGTTCCAA TGTCACCAAC CCCCTTAATT 360
AATGCTAGGG TGCTGGGTCA TGCATAGCAC GGTCAGCTTG GTCTCCAGTT CTGGCAGCAG 420
CTGCAGCCAA GGTCAAGAAC AACGGGGGCT GGGTTAGCTC TTACTCATCC ACCTAAATGC 480
CACTGCCCAC GCTCTCCGCT CTCGCCCCTC CCGCTGAGCA GTGGCTGCCA GGGCGGCAGG 540
AAGTCCTTCT TCCTGGGCCT GGCGCCCTCC AGCGGTGGGC GCAGAGCACT AGGCTCCAAA 600
ACTAGGAAGC CGGCTCAGCC TGCAGCAGGG CAGCTTGGGC AGCTTCACAC CTAAACCAGC 660
CTCTAAACGG GCGCACCTGG ACAAAACCCA GTAATTTAGA AAAGCCTGTG TTTCTAGACA 720
TCTCGCACTG CCAGCATTCT CCATGAGAAA GGAGCTAATA GGATCAACTT TTCCTATACG 780
CTGGAGACTT AATGAGTCCC TCACCGACCC AAGGCTGACC TGTAATCTGA CAGATGACCA 840
CGAAAAAGAG GCAATTTCAA GCCTAAAGAA AGGACCCCAT TATGTTGACA TTTAGGCATG 900
AGTGTGGGTG GCATTGGGGC AGGAGTCCTA TGTGCTGCTC AAATCCCACC GTAGAGTCAA 960
CTGGCAGTGT GGCCTCTGTC TGACACAGCT CAGGCTCTCC TGCTCCGAGG GAGTTTAGCA 1020
GAAGGTCCCT TACCCCACCC AGTTCTGCAG CCCCTCTGAG AAGTCACATA GCTGATGCCC 1080
ATGGGGGCTG GCGGTGTGCC TTCTCACACC TCTCACATTG CCTGTGGTTC CAGGAGCCAG 1140
CTGCGTTTAG TCTGATCTCT 1160
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