| Tag | Content |
|---|
EnhancerAtlas ID | HS108-27692 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr3:32740080-32741540 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ALX3 | MA0634.1 | chr3:32740100-32740110 | TCTAATTAAA | + | 6.02 | | IRF1 | MA0050.2 | chr3:32741457-32741478 | TATCAGTTTCTTTTTTTTTTT | + | 6.48 | | MEF2C | MA0497.1 | chr3:32740277-32740292 | TTTTATTTTTAGTTT | - | 6.1 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGCTATATTT ATTTAGCATC TCTAATTAAA AACAGGCCAA AGGACGACTG GACTGAAGAT 60
GTGACTGATT CTAAGACTTG TGCTCTTTTA ATTATGTCAT ATTGCCTTCT TGGAAAAGGG 120
AAGTTGGGAA TCTTCACTGA CTGCTGACAT GTGCCAGGCT AGGACTTCCC AAAGTTAGTT 180
CTGTTGACAA CTGGTTCTTT TATTTTTAGT TTATTAAGAT GGGGTCTTAC TCTGCTGCCC 240
AGGCTGGAGT GCTTTGGCAC AATCTCAGCT CACTGCACAC TCCACCTCCT GTGTTCAAGC 300
AATCCTCCCA CCTTCGCCTC GCTTGTAGCT GGGACTACAG ATGCATGCCA CCATGCCCAG 360
CTAATTTTTG TATTTTTTGT AGAGACGGGG TTTCACCATG CTGCCCAGAC TGGTCTTGAA 420
CTCCTGGGCT CAAGTGATCC ACCCGCGTTG GCCTCCCAAA ATGCTGGAAC TACAGGTGTG 480
AGCCACCACA CCTGGCCAAC AACTGGTTCT TTGAGATGCT CCTGTTGTCT AGGCAGTTAT 540
CAAAAAGTGC CCAGATCATA AGTGCACATA CAGTTTGGTG AATAGTTTGC TGTGTATCCT 600
TGTAGACTTT ATACTTATTC AGAGGTACAT ATTTGTGTAT ATATTTTTAT AAAACATGGG 660
ATTCAGTTGT ACAAAGCAGT TTGCAATCTG TTTCTTTTAT TTAACAACAT GTTGTAAATA 720
TTTTTCCACA TCAAGTTATA TAGACTTAAT AACTGTTAAT GTGCCATTGT ATTCCTATAC 780
CATGATTTAG TTATCAAATC TCTTGAAGAA TATTTATTTC TAGACATTTA GTATTATCGT 840
TTTAATTTAC AATTATTTAA TAAATAATGA GGCTGAATTT CATTTCACGT TATTAAGCCA 900
TTCATATTTA CTCTTCTTTC AGCAAGTTTC TGGTGTTTGA GGAACACTGT GAAGGACTGT 960
GGCAGGGTTC TTGAAGATAA GGGAGTTTGT TTATCTAGGC AACTCCTGGA AGCCATTATA 1020
GAGGGAGTCA CACTTCCCAG TATCCTGGAA GGGGGCTTGT GATGGATGAG GTGCGAAAGT 1080
GGAGGCTACT ATGACAGATG CAACTCTAGG GCACCATACT GGGGGAGCAT TCCACTAGCT 1140
CTAGCCCCAA CTTGAGTCCA TGTTGGCAGA TCTATAGAAG GAGAGGGAAG AATGGAAAGG 1200
AGCCAGTAAG CAAAAGAACC CCATAACCAG TGTGATTCTT GACAACTTTC TGGAAAGTTG 1260
GTTGTAGGCA CTCTTGAGGG GTAAACTTGG GGACAAGGTG GTCTACTATT TCTCATGTGG 1320
GTATTTGTCT TCCATAGAAA CCTTAATTGG ATATGAGTGC TGCTTTAGGA ACAAACATAT 1380
CAGTTTCTTT TTTTTTTTTT TTTTTGAGAT GAAGTCTTGC TCTGTCACCC AGGCTGGAGT 1440
GCAGTGGCAT GATCTCGGCT 1460
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