Tag | Content |
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EnhancerAtlas ID | HS018-22475 | Organism | Homo sapiens | Tissue/cell | CD19+ | Coordinate | chr8:38733310-38734820 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr8:38734171-38734183 | ATGTAAACAGAC | + | 6.44 | FOXP2 | MA0593.1 | chr8:38734171-38734182 | ATGTAAACAGA | + | 6.02 | Nr2f6 | MA0677.1 | chr8:38734413-38734427 | TGACATTTGACCTT | - | 6.37 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCGTCTTGAA CTCCTGGCCT CAAGTTCCTC CTACTTCAGC CTCCCAAATT GCTGGGATTA 60 CAGGTGCAAG CCACCATGTC CGGCTTTAGC AGGAATTATG AAGTGACAAA TTCTGTCTCT 120 GACAGTCCTG CTTCAAGCAG CTAATGCATC CCCTGGTACC ATCTGTGATT GGATGAGGAC 180 TGTGGAAATG GTGCGGACAC TGTAGAATGA TGAGAGGTGG CTAACAAGTA AATAGGCTTC 240 AAAATAGCTT GTGCCCCATA GGTATTTTTA CTTGCTCAAA CTCCTTCCAA GTTCCCTCCT 300 TGCCAATGGG GCTCAACGTG TGGATGTAGC TTATGTTGGG AATACTGGCA GCTCAAAGAC 360 AGATCTGCTA TAAGTCTCAA CTGACATGTT CATTAAAATC CTCATGTTTG TAATCCTAGC 420 ACTTTGGGAG GCTGAAGCAG GTGAATCACT AGGTCAGGAT GGCCAACATG GTGAAATCCC 480 ATCTCTACTA AAGATACAAA AAAAAAAAAA AATTAGCAGG GCGTAGTGGC GGGTGCCTGT 540 AATCCCAGCT ACTCAGGAGG CTGAGGCAGG AGAATTGCTT GAACCTAGGA GGCGGAGGTT 600 GCAGTGAGCT GAGATCATGC CACTGCACTG CAGCCCGGGT GACAGAGTAA GACTCCATAT 660 AAAAAAAAAA AAAATAGAAA TTCTCACTGA GCTTCAAGCA TCTGGTTTCC TGCTCCTTTG 720 GCAAAACTAT CATGTGTAAT CTAAATATGC AAAACAGGGG AAATCCGTTC TTTTTACACA 780 ATAAAGTACT CCAAGCTCTG TGCTCAATGG TAGGGAATAA ATATGAGTAA CAAAGGGTCA 840 TGTGTGAACA GGGAGAGATG CATGTAAACA GACACGTGCT GTCAAACATT GAGGATGCAG 900 AGGAGGGAAT CATCCATTTA AAACAATTTT TTTTTCTTTA GTGATGGGGG TCTCACTATG 960 TTGCCCATGC TGGCCTCCAA CTCCTGGGCT CAAGCTATCC TCCTCCCTCA GCCTGCCAAG 1020 TAACTGGGAT TACAGACATG AGCCACCATG CCCTGTGGGA ACAGTCCATT CTATCTGGGG 1080 GGTAGTGATC AGGAAAGATG AGGTGACATT TGACCTTCGG CTTGCAGGAT GTGTAGATTT 1140 TTGTTTGATG ATGGATGGCG TAGGGAATGC TGTACCCAGA GAGATGCATC CTGAGAAAAG 1200 ACATGGCAGA ACCCACGAGG CAACCTGGAA GTTGCTTGGC ATGGCCAGGC AAAGGAGATA 1260 AAGAGACACA AGGAAAAATA AGGATGGAGC GAAACATGGG GCGAGAGCAT TCAGGGCCTT 1320 GTAGGCCAAG CTAAGCAGTT TAGGTGTTAA CAGCAGGCAA ATGGGAGCCA CTGGAAATTT 1380 TTAAAACCCA GAGAGACATG ATCAGATACT TGTCCTGGAA AGACCAACCT TGAAGCCATG 1440 TTGAAGAAGG ATTGAAGAGA TATGGAAGGC CCAGGGAGAC AGGTCACCCT CCTGATTAAC 1500 ACTTTTCAAC 1510
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