Tag | Content |
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EnhancerAtlas ID | HS047-07889 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr12:50950290-50951560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr12:50950771-50950782 | CATGAGTCACC | - | 6.62 | JUND | MA0491.1 | chr12:50950771-50950782 | CATGAGTCACC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr12:50950711-50950726 | TGAACTCCTGACCTC | - | 6.22 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_64405 | chr12:50950779-50951334 | NHEK |
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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 |
GH12I050557 | chr12 | 50949989 | 50951486 |
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Enhancer Sequence | GGAGTTAGAA GGGCTGTTTA TTGACTTAAA TGACACTATG TATTGTGAGA CTTTTTTTTT 60 TTTTGAGATG GAGTCTCGCC CTGTCGCCCA GGCTGGAGTG CAGTGGCTCA CTGCAATCTC 120 TGCCTCCCGG GTTCAAGCGA TTCTCCTGCC TCAGCCTCTC CAGCAGCTGG GACTACAGGC 180 GCATGCCACC ACACCTGGCT AATTTTTTGT ATTTTTTTTG AGACAGAGTT TTGCTCTTGT 240 TGTCCATGCT GGAGTGCAGT GGTGTGATCT TGGCTCACTG CAACCTCCAC CACCCAGGTT 300 CAAGTGATTC TCCTGCCTCA GCCTCCCAGG TAGCTGGGAT TACAGGCATT CGCCACCACA 360 CCCAGCAAAT TTTTGTATTT TTAGTAGAGA CAGGGTTTCT CCATGTTGGT CAGGCTGGTC 420 TTGAACTCCT GACCTCAGGT GATTCACCTA CATCGGCCTC CCATAGTGCT GTGATTACAG 480 GCATGAGTCA CCGCGCCCGG TGCATTTTTT TGTATTTTTA ATGAAGACAG GATTTCACCA 540 TGTTGGCCAG GCTGGTCTTG AATTCCTGAC CTCAAATGAT CTGCCTGCCT CCGCTTCCCA 600 AAGTGCTGGG ATTACAGATT TGAGCCACCT GGTCGGTATT GTGAGACTTT CTGAATCACT 660 GAGCCTTGAT TCTTTATCTA TAAAATGGAG ATAATAAGCT CTTCCTACTT TATAGGACTT 720 GAAGAAGCAA ATGGGAGAGG GTGAGTGAAA GTGGGAAGCT CTGAAATGAT TTTTAATTTG 780 TGTGCCCCAC ACACCTTGCC TTCCATAGAT GGTCCAGGCT GTGGTCTGGT TGCTGCTTTC 840 CTGTGTGTGG TGCATGGACA CAGGCAGGAG TGAGTAGATT CCCAGAGGAC CTACTATGGC 900 TTGGATGATC TCTCCACTTT GGGGCGGGCA CCATCCCCTC CATGTCTTCT TAGATTGTTA 960 GATATAAAGC ATCGGCTGTA CATTCTTACT TTACACACTA ATGTTCTCAC AACAGTGGCA 1020 GGGCCTTCCT AGGCAGAGGA CATCTACAAA GAGTGGATGA TGGTGGCTGC CACCTGCTGA 1080 ACTGTGGCTA ATGGGCTGCT GGGTGGGGGG ATATTGCCTG AGGGATCTGC TGGAGCCCAT 1140 GGCAGGCAAA AGCCAGCAAA AATTTGTTAC TGTTATTGTG ACTACATCTG TATGCATGAA 1200 CCACTTAGCT CTAGAGGAAT TTTGGTTACA TAAGCTTAGT GGTGGCTTAG TAAATGGATT 1260 CTGCAGTTCT 1270
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