Tag | Content |
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EnhancerAtlas ID | HS108-34131 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr6:26389440-26390170 |
Target genes | Number: 31 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFF | MA0495.3 | chr6:26389960-26389975 | GTGCTGACTCAGCAT | - | 7.99 | MAFF | MA0495.3 | chr6:26389960-26389975 | GTGCTGACTCAGCAT | + | 8.03 | MAFG | MA0659.1 | chr6:26389957-26389978 | GCTGTGCTGACTCAGCATGGC | - | 6.12 | MAFG | MA0659.1 | chr6:26389957-26389978 | GCTGTGCTGACTCAGCATGGC | + | 6.2 | MAFK | MA0496.2 | chr6:26389958-26389977 | CTGTGCTGACTCAGCATGG | + | 6.17 | MAFK | MA0496.2 | chr6:26389958-26389977 | CTGTGCTGACTCAGCATGG | - | 6.4 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | CACATGGTGA CGAGCATGTA GGAAAAATTA AGCAAAGAGA AAATAGAGAG TTCCAGGGGT 60 GTGAGGCATC AGAATTATTA ACAAGGTGGT CAGGGAAGAC TTCACTGTAA AGATGGAAAT 120 TGAGCAATCA AGACAAGGAA CCATCAGATG CTTAAGGACT GAGCAGCCAA GGTACAGGAA 180 GAGCATATGC AAAAGGCCTG AGGAAGGAGC TTGTCTGGCA GTTTCCAGGA CTCCCAGGAG 240 GTGATGCTGG TGTGGCTGAA ATGGAGTGAG TTCAGGAAGT AGGGGGAGAT GAATTCACAG 300 AGTGATGCAA CTACGTTATA TATGGCAGCA CAGGCCACAA ACAGGCTTTG GCTTTTAGAG 360 TGAGTGAGTG GGAAGCATTG GAAGGTTTTG AGCAAATAAT TAACATGATC TCACTTGGGC 420 TGCTCTGCTG AGAGTAGATT ACAGAATAGA GCAGAACAAG AAGGAGGGCA CTCTAGTATT 480 CCAGGCGTGA GTGATGGTGG TTTGAGGCAG GGTGATGGCT GTGCTGACTC AGCATGGCTG 540 GTTAGTTTTA TGCACTCTGG TCCTTTCCAT GGTGACTCCA GATGTTTCTG CTTTGCCCCC 600 TTCTGGGCCC GGCCCTGGCA GTCACTGAGG TGTCAGCCAG TGTTGAGCCA GCATCGCTTT 660 CTCCATCTAA GGTTTCTGAG GGAGAAGCCA ACAGAACAGG TGGCTGAGGA GCTCTTCAGA 720 TGTGCTCTTA 730
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