Tag | Content |
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EnhancerAtlas ID | HS010-03565 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr5:77147130-77147930 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6B | MA0731.1 | chr5:77147611-77147628 | TCCTTTCTAGGACTCCC | + | 6.13 | EHF | MA0598.2 | chr5:77147636-77147648 | CACCCGGAAGTG | + | 6.18 | ELF1 | MA0473.2 | chr5:77147636-77147648 | CACCCGGAAGTG | + | 6.14 | ELF4 | MA0641.1 | chr5:77147636-77147648 | CACCCGGAAGTG | + | 6.18 | ELF5 | MA0136.2 | chr5:77147637-77147648 | ACCCGGAAGTG | + | 6.32 | RELA | MA0107.1 | chr5:77147919-77147929 | GGAAATTCCC | - | 6.02 | SOX10 | MA0442.2 | chr5:77147675-77147686 | AAAACAAAGCA | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_56404 | chr5:77147523-77149806 | u87 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH05I077851 | chr5 | 77147025 | 77149236 |
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Enhancer Sequence | GGACCTCTCC CGAGGACACA CACAAAGGCC AGGGAGCGCG AGTGCGCGTT CCCTCTCCCA 60 GAGTGTGTGT ATGTGTGTGT CTATGTGTGA CTGTGCCCGT GGGACACTGT GCGCGCGACC 120 ATCGCAGGAC CCTCCATCCA GCAGTTAACC CTTGGCAGGC CGGCTCAGGA GAGAGGAACT 180 CCGAGGGGGC GCGCTTCTGC TCTACTCCAG CAAGGCTTTT ACAGGCCGGC GCGAGGTGCG 240 GGCGGTCCCG TGCGCGCGCG CGCGTGTATG TGGGTGTGTG TCTGTGTGGT GGGTGTGTAA 300 GAGGGACAAT GTGTGTGCCT GCACGTGGCG TGTGCGCGTG TGATCAAGTG TCTATGTGGC 360 GTGTGCGTGT GTGGTGTGGG TGTGCGCGGC GTGCATGTGT GCGTGTGTGC ACGCGCGAGA 420 AGTGCGTGTG TAGGCGCGTG TGCAAGTGCG CGCGCGTGTG TTTACACTTC CAGAAGTCAA 480 ATCCTTTCTA GGACTCCCCC TTGCTTCACC CGGAAGTGTT CGGTGACCCC TCCACCCAAT 540 TAATGAAAAC AAAGCAAAGG GCCCGAGCGG GCCTCCGACA GCCCGGGGCT TGCGGAGCTG 600 GACGCCGACA GGGCGTCAGC CCGGTCGCTC GCGGCGCGGA GGCTGCTGCG GTTCGGAGCT 660 GGGGTTCTGC ACTCTCGCTC CCGGCTCCCG GCTCCCGGCT CCCCGCCACC CGCAGCCTCC 720 TCGCGCCGCC GCCGCGGGCA CCGCCGGGGC TTCAGTGACA CCAGGCACCC GCCCCGGGCC 780 GCGGGAGGAG GAAATTCCCT 800
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