Tag | Content |
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EnhancerAtlas ID | HS108-07942 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr11:68444680-68445930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr11:68445188-68445199 | GATGAGTCACC | - | 6.32 | FOSL2 | MA0478.1 | chr11:68445189-68445200 | ATGAGTCACCC | - | 6.14 | JUNB | MA0490.1 | chr11:68445189-68445200 | ATGAGTCACCC | - | 6.32 | JUND | MA0491.1 | chr11:68445188-68445199 | GATGAGTCACC | - | 6.62 | KLF16 | MA0741.1 | chr11:68445325-68445336 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr11:68445326-68445336 | GGGGCGGGGC | - | 6.02 | SP2 | MA0516.2 | chr11:68445323-68445340 | TGGGGGGCGGGGCTGGG | - | 6.55 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 68445769 | 68445924 | chr11 | 68445644 | 68445704 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I068677 | chr11 | 68444926 | 68445570 |
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Enhancer Sequence | GGGTGTGGTG GCGGGTGCCT GTAATCCCAG TGACTCCGGA GGCTGAGGCA GGAGAATTGC 60 TTGAGCCTGG GAGGCGGAGG TTGCAGTGAG TCGAGGTTGT GCCACTGCAC TCCAGCCTGG 120 GCAACAGAGC AAGACTCTGT CTCAAAAAAA AAAAAAAAAA AAAAAATATG TTGGGTCCCT 180 GAGAAGCAGG TCAGAGCTTT TCCTGCACAG CTCAGGCCTC CAGGTGGAAG CACCCCTCTC 240 TCTTCCCACT GCCCCTCCTT GTGGCCCCCC AGCTGCCTGT CCTCCTCCTG CACACCCACA 300 TCCTGGTAGC CAGACGGGTT CCCATATGGC CCTGGGTGCT GCTGATGGGC CTGACTCAGG 360 GCCAGGAAAC AGGGGCAGCT GTCCAGGGCC TGTCGCTGAG TCACCTACTT CCCGCCCCCA 420 CCCCTCCCAA CTGCAGGCGT CAGCCTCTGG CAAGGCCATT AGCAGCCCCT CTTCCTCCAG 480 GCTGAGCTAC CCAGAAAACC CCCAGCTGGA TGAGTCACCC AGGGCACAGG TGGATTCACG 540 GACTCCCGGC TGTGACCCTG CCTCTGACCA GCAAGGAGGT CCCTGAGGAA GCTCATCTCC 600 CATGGGATGA GTTCACCAAG GAGCAGGAGG GGAGGCTACA TGGTGGGGGG CGGGGCTGGG 660 GGCTGGGAAG GAGAGGCTTC CCTGGCACAG AGCCCAGGGC AGTGAAGGAG CGGGCCGGGG 720 GTGGTCTGTT GGAGAAAGAA GATGCAGGTG GTGGGTTTAG GGAGGAGAGA GTGCCACACT 780 GCAGACAAGG ATGGCTCCAG CTAAAGAGCC CAGGACTTGT GAGCTGAGCA AAGCAAGACA 840 TCAAAAGCGA CATCCCCCCT CCACTCACCC TGGAATTGGA GGGGAGAGTT GAGCTTGCGT 900 GGAACTGCGT CTGGGGTGGG AGGTTGCAGG GGCTTCCTGA GAAGCCACCG TGGCTCCCAA 960 GACGCTGGTA GAATGTGTCC ACTAATAAAA AGCTGACTAA ACACTTTTCA AAGATGCAGC 1020 TCTCCAAATT ATCCTAGTGA CCCCAGGCTT GTCTCAAGCC CATCTCCCTG GGAGACGACA 1080 GCTTTCCACG AGGGCTGTGC CACCAACGCT GCAGCATGCG TGCCAGCCAC ACAGCTCGTG 1140 TTCCAGTGCT AGGGGAGCGG GTGCTTGGGC AGCGGGGCAC TCCTAGAACT ATTCCCACAG 1200 CAGACGGCGA GCGGCAACTC AGCCATCCTA TGCAAGTGAG ATCAATACAT 1250
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