| Tag | Content |
|---|
EnhancerAtlas ID | HS108-03882 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr1:204732510-204733600 | 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 | TTACTGATGA GGAAACTGAG GCAATGTATA ACAGGTATAA GTAGCCCAAG GTTATTCAGG 60
CACTAATGTG TAAGGCTGTG ATTCTAAGGC AGACTGACTG ACTACAAAGC TAATGTTCTT 120
AATCCCTAGA TGCTCCCACC TTCCAAATGT CCTGGCTCCT AGAATTACAT CTGTTCTACT 180
CCCTCCATGG CTCCATGGAA CCTGGACATC TCAATTTCCT CCCCAAAAGC TGGAGTTCTC 240
CAAGATGCAG AAGCCAGAGG GCTGATGTTC CTGTGCAGGA AGAAGCAACG CCCAGGCCCA 300
CTGCCCCCAC TCTCTCAGCA GATTCTCATT TTCAGAATCC TGGAAACCAG AGCTAGAAAT 360
CTGCCTCCCT CTGTTTACCC TGAGTTCCAA TGTCACCAAC CCCCTTAATT AATGCTAGGG 420
TGCTGGGTCA TGCATAGCAC GGTCAGCTTG GTCTCCAGTT CTGGCAGCAG CTGCAGCCAA 480
GGTCAAGAAC AACGGGGGCT GGGTTAGCTC TTACTCATCC ACCTAAATGC CACTGCCCAC 540
GCTCTCCGCT CTCGCCCCTC CCGCTGAGCA GTGGCTGCCA GGGCGGCAGG AAGTCCTTCT 600
TCCTGGGCCT GGCGCCCTCC AGCGGTGGGC GCAGAGCACT AGGCTCCAAA ACTAGGAAGC 660
CGGCTCAGCC TGCAGCAGGG CAGCTTGGGC AGCTTCACAC CTAAACCAGC CTCTAAACGG 720
GCGCACCTGG ACAAAACCCA GTAATTTAGA AAAGCCTGTG TTTCTAGACA TCTCGCACTG 780
CCAGCATTCT CCATGAGAAA GGAGCTAATA GGATCAACTT TTCCTATACG CTGGAGACTT 840
AATGAGTCCC TCACCGACCC AAGGCTGACC TGTAATCTGA CAGATGACCA CGAAAAAGAG 900
GCAATTTCAA GCCTAAAGAA AGGACCCCAT TATGTTGACA TTTAGGCATG AGTGTGGGTG 960
GCATTGGGGC AGGAGTCCTA TGTGCTGCTC AAATCCCACC GTAGAGTCAA CTGGCAGTGT 1020
GGCCTCTGTC TGACACAGCT CAGGCTCTCC TGCTCCGAGG GAGTTTAGCA GAAGGTCCCT 1080
TACCCCACCC 1090
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