Tag | Content |
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EnhancerAtlas ID | HS018-02024 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr1:212359600-212360840 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF8 | MA0652.1 | chr1:212360135-212360149 | TGTTTCAGTTTCGT | - | 6.49 | IRF9 | MA0653.1 | chr1:212360135-212360150 | TGTTTCAGTTTCGTC | - | 6.1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 212359666 | 212360400 | chr1 | 212359997 | 212360427 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I212186 | chr1 | 212359743 | 212360831 |
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Enhancer Sequence | ACCGAGATTG TGCTACTCTA GTCTGGGTGA CAGAGTGAGA CTCTGTCTCA AAATAAAATA 60 AAAAATCAAC CTTGGACCTT CGTTTGTCAC CCAGAAATTC AGTCAACGGG TCAGTCCATC 120 AGACCAATAG CAGTAGTGAG CACCACTTGC ATAGAGAAAA AAGCCAGCCC GCCAGGATAA 180 AATAGGAGGG TCCCGAGGCC TTAACTGTGC AGAAGTGCTT CCCACACAAA GGTTTCCTCA 240 CCTGTCAGTG TCTACCCCAA CAAGCACCAG AGAACCATCA TGAAAATGTA CAGTGAATGT 300 GAGGGAGGGC CAATCACATT AACATTAAAT GTGAGGGAGG GCCAATCACA TTAACATTAA 360 ATGTGAGGGA GGGCCAATCA CATTAACATT AGCAGGACTG TACCTTGAAA CCGTTAACCC 420 TGGGAGAAAG AATGGTTGAA CAGTAAGCTT TCTGCATTGT TGAGATGAAG CCAGCAACAG 480 TAGGCAAGAA GGTCGTAGCA GGAAGAAGGA AGTATTCTCT GGAGACCAAC TCTCCTGTTT 540 CAGTTTCGTC CCTGGGGCTA GTCCTGCTGA GTCCTGTAAG GTAGTAGTGT GGTGGTTCTT 600 AATCTTTTTT TTTTCTTTTC GTGTTGGAGG CACATCTTTG ACTATTAGAA TTTGGTGTAG 660 CAGATTTGAA AAAATATGTA TTGTAAAACT GAAAATGATA CCAAAGTAAG CAGTAATTTC 720 ACCTGCAGTC ATTGCCAAAA TATTAAGTTC TCACAGCATT TACAGCACTC ATAGAGGCAG 780 CACCAGTTTT CGGTCCTTCT ATAATACATC ACCATCTAGA AACGGCCTGT TTATAGACCC 840 CTAAAGCCAT CTCTTACATA CTCTAGAGAC AAAGTTCTCA TGTGTTCCAG TCAACACAGG 900 AGTTTTTTTG TTGATTTGTT TAGGGTGGGG GTGGTGGGTG CTGGCTCCAT GTCATATTAT 960 TTCCTCCTCT ATCTAGAAGA AAGTTTACGT CGCTCTCTGT ACCCATAATG TGAACCCCTT 1020 GAGTCAGCAG TGAGTATTCT GACATACACT GAATCCTCAG TTGTAGCAAA AAGTGATTTT 1080 TTTTTTTTGA GATGAAGTCC CACTCTTGTC ACCCAGGCTG GAGTGCAGTG GCACAATCTC 1140 AGCTCACTGC AACCTCCGCC TCCCGGGTTC AAGTGATTCT CCTGCTTCAA CCTCCCAGGT 1200 AGCTGGGATT ACAGGTGGCC TGCCACCATG CCCAGCTAAT 1240
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