Tag | Content |
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EnhancerAtlas ID | HS047-31989 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr7:151076870-151077980 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr7:151077055-151077076 | TTCAGCACGATGGAAAGGTCC | + | 6.74 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_61550 | chr7:151064397-151109664 | Toledo |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 151077400 | 151077482 | chr7 | 151076877 | 151077484 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I151379 | chr7 | 151076837 | 151080022 |
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Enhancer Sequence | GTGGGGACTG GAGCTGACGT GTCAGTGAGG GGCTGCTCAG GCCAGAGCGC AGCATCACCA 60 AGCAGCAGTG TCTTCGGCAA GCAGGAGTCA GTGTGAACGT CTGTGCAGGC TCAGGGCCGG 120 CCGGCAGCAC TGCCCGCAGG CAGCACTCAA GGCGGTTCTC TGGCCTGCGC CACCGGAACC 180 GTCCCTTCAG CACGATGGAA AGGTCCTCTC TGGTAGGTAT GCCCCTTGTG GCAGCCACAG 240 GCCCCAATGG CTCCGGGACG CAGCAAGACC TGGCCACCCC CGAGGTCTGT GTGTGCTTAA 300 GTCTCACCCG GAGAACAGTG CATGGTGCCG TTTCTGCGGG TTCTCCTGCA CCGATCTGCT 360 TGCCTCCCAA CAGGCCCATT TTCCTGGGGT GGGGGTCGGG GGCACTTTGG TTCCCAGGGT 420 TTGGAGGTTT GGCCTAGAGG AGTTACAGCG CCTGCGTCCT TTCCTTCCTA CTGCCCACAG 480 TGCAATCCCT ACCTGTTCAT CCGCGCCCGA GGGCGGACCC GCCCATCACC TAGCAGGTGA 540 TCCCTGGCGG CCCCGGCCGT CTCTGATGAA GTATCTTCTG CATTAAGACT ATGAAGCGCA 600 TGCTGCTCTA CCTGAAAGGG CTGCTCCACT TGAAGGGGCT GCTCCACTTG AAGGGGCTGC 660 TCCTGCAGCA GGTGCTTCTC TCTGCAGCGA GATGATGAGC TCTCCACGGC AGACACTGTC 720 ACCTGCAGCT TCTCTCCTGG CACCCGGGCC AACCGGGGCA CATGGATGCA GAAAGTGGCA 780 CCATCAAGGG ACTGAAGAGC ACCCCGCTCA GGTGCTGTGA GGGGTGCTGA GGGGTCTCCT 840 GCAGGGCCCC TCGGCAGACT GAGCCCCACT GGCCCCTCGA GCCCCTGGGC ACAGGGCTCC 900 CCTTGGGTGC CCGGTGGCTC TGGCATGTGT GTTGCGCCTT CCAGCACCAG GCGCTGCCCT 960 GGCTCCTGTG CACGAGCCCG GGGTGGGGCT GCTGCCCGCC CCCACCCCTC CTTCCACTCC 1020 AGGCCCTGAA CGGACTTCCT AGATTCATGC CAGAAAATGA CATGCCAGAA AATGACCCTG 1080 CTCCCAAGCA GGGTCCCCGC TGTCACCTGC 1110
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