Tag | Content |
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EnhancerAtlas ID | HS060-29888 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr6:42954930-42956270 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CEBPA | MA0102.3 | chr6:42955978-42955989 | ATTGCACAATC | + | 6.32 | ESR2 | MA0258.2 | chr6:42956066-42956081 | AGGTCACCAAGCCCC | + | 6.32 | ZNF263 | MA0528.1 | chr6:42955837-42955858 | CCTTTCTTCCTCCCCACCTCC | - | 6.37 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH06I042987 | chr6 | 42955044 | 42958425 |
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Enhancer Sequence | TTAATTGTGG ACAAGACTTT TCTTCCCCTT TGAGATAATA ACTAAGTTTC ATTTTGGTTT 60 GACAACTCCT TTTCACACGG TAAGTACGTG CTTAGTGGAT AGGTGCTAAG ATAATCTCTT 120 GGAGGGATTC GCATCTCTCC TCTTCCTTCA TGTTCTCCTC TGGGACTTAC CTCTTTTATT 180 TTCCTGAGTA GGGTGCCCCT GCCCCCTCCG ATTTTTTTCT TGTTCATAAT AATAGTAATA 240 ACATTGACCA GCACTACGGT TTTCATGTGC CTTAACACTG TGCTGAGGGA AGAGGGTATT 300 ATGATTGTCA TCATCTAATA GATGAGGAAA CTGAGGCTCA GAGAGGCTAG TTAACTTGCC 360 TGTGATTACA CAGCCAGTAA GAGTTGGGCC CAAAACACAG GGCTGAGTCC AAACATGTTC 420 TTTTAACCTC TGTGCTACAC AGCATTTGAC TACTGAGCTG GGCTGAAATG TGTGTGCTTC 480 ACCTGTTCTG CAGGAGCCAG GGAGCAAGGG TGGTAGGCCT GGTTCCTCCA TGCCCACTCA 540 CACCCACACA CTAAGGCAGC TGGATCTCTC TTAGGCTCAT TCTTTGAAAG ATACGTCTGA 600 GGCATCATGC TGAGTGCTGT AGGGTGGGTG GAGGGGTACA AAAAAGAATA AGCAGCTTAT 660 GGTCTAATAG ATTGGAGATG TATGAAGATG GGTCAGCTTT GTTCAAGGGG TTCATGTCTG 720 GGGTGTGTGC AGACACCTCA ATGTTGTGTC CTGCCTGCAC CCTGCCCCCG GCCTATTTCT 780 CTCCACCCCA TGCTCTCAGC CACTGATAAG GGTCAGTGTG GCCAGCTGGG TTAGTATACA 840 GCAGGAGCGT GCTCAGGCCA AAGAAGGAAC TCCTTCCCCC TACTGCATGG AGCTGCTCTA 900 CACCACACCT TTCTTCCTCC CCACCTCCAA GAAGCCTTCC CCCTACTCCA GCCCACACAG 960 AGCTCTCTTC TCCCTGAAAT CCTTTTGCCC CCATAGTCAC AATAACTCGA TTTAACACTT 1020 CTCACTGAAG GGGCTTGGCT GCTATTGAAT TGCACAATCT CAGAGCTGGA AGTGATTTCC 1080 AAGATCCTCC AGTCCTCATT AAAGGCTTGA ATTTCTTTTG CAACATGCCT TACAGGAGGT 1140 CACCAAGCCC CTGCTTGAAT GTTCTCAGGG GTTGGGGAGC TTTCGGCTTC ACTAGGTGGC 1200 CAGTTTTAGT GCAATTGCTC CATGATAAAA TTCTTCCTTG TTTGGAGCTT CAGGTGGCTT 1260 GCAACTTCAG CCCATTGCTC TCGTGCCTCT GGTCCATATG GACAAGTTGC ATCCAAGGCA 1320 TCCAAGTTGC ATCTTCATTT 1340
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