Tag | Content |
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EnhancerAtlas ID | HS165-13797 |
Organism | Homo sapiens |
Tissue/cell | Ramos |
Coordinate | chr7:2070390-2071880 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Mecom | MA0029.1 | chr7:2070592-2070606 | GGTTATCTTATCTG | - | 6.25 | SPIC | MA0687.1 | chr7:2070549-2070563 | TTCTTCCTCATTTT | - | 6.42 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 5 | Chromosome | Start | End |
chr7 | 2070800 | 2070984 | chr7 | 2070431 | 2070585 | chr7 | 2071503 | 2071576 | chr7 | 2070624 | 2071398 | chr7 | 2071625 | 2071875 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I002031 | chr7 | 2070881 | 2071030 |
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Enhancer Sequence | TGGGTCAGCG AGGGTTTCCG GGGCCCCGTG GGAGGCGCCC TGCTGTCAGA CGCGTTTCTG 60 TCCTCCTCAG CCCCCAACCT GCGCCTGGTG CTCTCGGCCA ACCTTGCTCA GAGCTTGATG 120 ATACCATGTC TCTCCCTTGT TCCCATTCCA TCCTCTCTGT TCTTCCTCAT TTTTGCCTCA 180 AGTTCCACAA GTCTCATTAC AAGGTTATCT TATCTGACCA ATAAACCCGG TTTACTGTTG 240 ACAAAGCTCT ATTTCTGCTG GGCGACTGGA TTCGGAGGAG CCCCCAGGAG AAAAAACGGT 300 CCCCAGCCTT CAGCAGCATC CTCCCTCCAG CAGCCAGCTG TGCATTCTCC ATGAACTGCA 360 CCTACGCGAG CTCTCCTGAA GGCAGCAGGA GGCTGAACAC CAGGCCGCTC AGAGAGGAAG 420 CACGGGGTCC TCTCCCACTA CTCACCCCTC TGCCTGCAGC TGCACCAGGC ACACAGAGCA 480 CGCTCCCTTC CCTGCCCCAC AGCTGTCTTG GGGTTACCCT CAGCCAGCTC CTCCTCTGGC 540 TTCCTGCCGT CACACCCTCC CCACTGGCCT CCACCACCCA CGTGTAGCTG TGGGGGAGGG 600 GGAAAAGGGG CTGTTCTGGG CTCCCCACCA GCAAGCCTGG TTTTTACAAT TTCAACCTCT 660 GATAAAAAGC TCTACAACAC CTATTGTAGG AAGGAGTGGA ATCAATTATG ATTTCCCGAG 720 GCAATTTTAC TTACATTTCA CACTGCTCTA TGACAAATTC CACTTCATTT GTGTTCGCTG 780 TATAAATGCA TTCCCCAGCA TCCACCTGAA CCAGCACCAG CCTTGTTACA GCAGCTGCTC 840 ACACCTGCGC TATGACGACG TGGGTGCCGT GCACATCTGG GAGGGCACTG GGACCATCCT 900 GACAGGAAGC CATACCCAAG CCACAGTGGC TGCAGACGGC CCCTCACCAG GGAGGAGGAC 960 GTGACCCTCG CAAGGTCTCG CCAGCATGCC TGACCCACGC GGATATGGGG CCATGGGCCT 1020 GAGACAGGCC CTGTGCCGCA TGGCTCTATT TTGAGTGCAG TTTATTTGAC AGGACAGGGA 1080 GAAAGGAGAG CAGGGCAACG TGGGAAACAG ACAGCACAGT GGAGTCACGG CTCTGGGGCC 1140 ACTACTCAGC CTGAGCAGTC AGACGGGTTC CTTTCCTCTC TAGGCCTCCA GCGTTCCTAT 1200 CAGCAAAACA GGGAATTAGA TGGACTTGGT CTTCTACAGT TCAAAAATCT TACAGTGCTG 1260 CAAAGTCTAG GTGGCTTTCT CCACCGACGG GTAACAGGCA GGCAGCCAGT GCCCAGGGTG 1320 CCAGGCACAC TCCGGGCCTT GTGCCAAGGA GTTTCCATGC ATCAGCTCCC TGACCCCTCA 1380 TTCATGCGGG ACGCCCGGCC CCAGTCCCTG TCCAGTGCCT GGAACAGAAC AGGTGCTCAG 1440 GAACTGTGTG TTCAATTAAA AAATGAACGA GTGAAACCAT CAGCCAATCA 1490
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