| Tag | Content |
|---|
EnhancerAtlas ID | HS062-01401 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr1:204732600-204733660 | 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 | AGACTGACTG ACTACAAAGC TAATGTTCTT AATCCCTAGA TGCTCCCACC TTCCAAATGT 60
CCTGGCTCCT AGAATTACAT CTGTTCTACT CCCTCCATGG CTCCATGGAA CCTGGACATC 120
TCAATTTCCT CCCCAAAAGC TGGAGTTCTC CAAGATGCAG AAGCCAGAGG GCTGATGTTC 180
CTGTGCAGGA AGAAGCAACG CCCAGGCCCA CTGCCCCCAC TCTCTCAGCA GATTCTCATT 240
TTCAGAATCC TGGAAACCAG AGCTAGAAAT CTGCCTCCCT CTGTTTACCC TGAGTTCCAA 300
TGTCACCAAC CCCCTTAATT AATGCTAGGG TGCTGGGTCA TGCATAGCAC GGTCAGCTTG 360
GTCTCCAGTT CTGGCAGCAG CTGCAGCCAA GGTCAAGAAC AACGGGGGCT GGGTTAGCTC 420
TTACTCATCC ACCTAAATGC CACTGCCCAC GCTCTCCGCT CTCGCCCCTC CCGCTGAGCA 480
GTGGCTGCCA GGGCGGCAGG AAGTCCTTCT TCCTGGGCCT GGCGCCCTCC AGCGGTGGGC 540
GCAGAGCACT AGGCTCCAAA ACTAGGAAGC CGGCTCAGCC TGCAGCAGGG CAGCTTGGGC 600
AGCTTCACAC CTAAACCAGC CTCTAAACGG GCGCACCTGG ACAAAACCCA GTAATTTAGA 660
AAAGCCTGTG TTTCTAGACA TCTCGCACTG CCAGCATTCT CCATGAGAAA GGAGCTAATA 720
GGATCAACTT TTCCTATACG CTGGAGACTT AATGAGTCCC TCACCGACCC AAGGCTGACC 780
TGTAATCTGA CAGATGACCA CGAAAAAGAG GCAATTTCAA GCCTAAAGAA AGGACCCCAT 840
TATGTTGACA TTTAGGCATG AGTGTGGGTG GCATTGGGGC AGGAGTCCTA TGTGCTGCTC 900
AAATCCCACC GTAGAGTCAA CTGGCAGTGT GGCCTCTGTC TGACACAGCT CAGGCTCTCC 960
TGCTCCGAGG GAGTTTAGCA GAAGGTCCCT TACCCCACCC AGTTCTGCAG CCCCTCTGAG 1020
AAGTCACATA GCTGATGCCC ATGGGGGCTG GCGGTGTGCC 1060
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