Tag | Content |
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EnhancerAtlas ID | HS136-10529 | Organism | Homo sapiens | Tissue/cell | Monocyte | Coordinate | chr2:68889150-68890540 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SPI1 | MA0080.4 | chr2:68889788-68889802 | TACTTCCTCTTTAT | - | 6.45 | SPIC | MA0687.1 | chr2:68889788-68889802 | TACTTCCTCTTTAT | - | 7.08 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCTTAAGAAC AGAGGGTATT TTGGTTGCAG GGAAGCACAA AGAAACATCC TGTAAAAGCA 60 GCATTGCAGA TTTACTTACC AAAACTATTG CTTTACCCTC TTACTTATTG CTTTTTGTTC 120 TCACATGAAT TATTTTGCTT CCGCTGGCCT CATTTGGATT TTGCTGGCCT TTTCACATGT 180 TCTTGAGTAG AGTGATAGAC TTATTTTATT TTTATTTTTT CTCGTAGCTT AAGCAATTAA 240 GGGAGTGAGT TTTCCTTTGA GCAGAGTTTT ACGTTTGGAC ATGTAGAGTC TCTTTAGCTC 300 TGACATGGCC CTTTTTATTC CATTATATTT GATATATGTA TTGATTAGTT CATACTTTCC 360 ATATTCTCTT TATGTATTTA AGAGTTGAAA CATTGTCATT TCTTTATTTT ATTATTTCCT 420 TTTGTTTTCC ATGATTTTTT TTTCTTCCAG GGTAGACTGC TCATTTTTCT TTCTGTTCCT 480 TTGTGTCTCT CTCTCTCTCA TTGTTTGATT TCTTTTCGTT TGTCATAATT CTGCATAGCT 540 TTCCTGTTGT GATTATTTTT ATTTTATTCA TCTTGGACAG ACCCAGCTCT GTTCCCCAGT 600 GTGTTGACCA AATCAGGGTG ACTGAATTTC CCTTATTCTA CTTCCTCTTT ATCTGGTTGC 660 TTCCTCTGTT TATAGCTTCA ATTAGAGAGT TGGTGCTCCA CATTTCATAT TGCTGGGGAT 720 GGAAGTGAGA GAACTCTTTG TAGCCATGAT TGGTGGGCTG TGTCTTCGTT GTGTTATTTT 780 TTTAAAAGTT CTATTCTGGA ATTCAGTTTT GCTGGCACTG CATATCCCAT CCTTGGGGGT 840 GATGCCCAGG GTTTTGGATT ATTTTTTCAA CTCAGAACTA CTGAGCCTTC CATTCCATCA 900 GTGATGATCT GCTCTAGATG AGTTATTCTT AGTTTTATCT ACTTTTTTTT CCCCGGTCTA 960 CATCTCTTTC TACTCTCCCA CTCATTTGGT GAGAAAATTT GAAGGCTTCT GGGTAGAGTA 1020 TTTTACTCTT GCTTGTGTAG ATCCCCTCTC TACCTTGCTG TATCACCTAG AGACTGACTT 1080 TTGGACTATA CCATTGAGCA ACGTTTCCCT CTAGTTTCTT TCTGGATTAG ATCAATGGCA 1140 GGCACCAATG GGACATTAGA GGATAAAGCA GAGTGAGGTG AGGATTTGTT CAGTTGAGTC 1200 CCAACTTTCC AGATCATGAG GGCTGGCAGC CCCCACCACT ACTGGGCAGC TAACAGCTAT 1260 AGCTGTTGGT CTCTTTGGGT CCTGGTAGCT GTTCCTCCCC TTTGCCCTCA GGCCTAGGGC 1320 TGGTGGGCTC CCTTTTTAAT GACCTCAGGG CACTCCCTGT CTCTTGTTGG TTCATCTTAG 1380 CTCTAGCCAT 1390
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