Tag | Content |
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EnhancerAtlas ID | HS098-50997 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr7:577290-580230 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr7:577927-577938 | CAGCAGCTGTC | - | 6.14 | PLAG1 | MA0163.1 | chr7:578362-578376 | CCCCCCAGGGCCCC | - | 7.03 | RREB1 | MA0073.1 | chr7:579358-579378 | TGGGGTGGGGTGGGTGGTGA | - | 6.06 | RREB1 | MA0073.1 | chr7:579324-579344 | GGGGTGGGGTGGGGTGGGGT | - | 6.22 | RREB1 | MA0073.1 | chr7:579329-579349 | GGGGTGGGGTGGGGTGGGGT | - | 6.22 | RREB1 | MA0073.1 | chr7:579334-579354 | GGGGTGGGGTGGGGTGGGGT | - | 6.22 | RREB1 | MA0073.1 | chr7:579339-579359 | GGGGTGGGGTGGGGTGGGGT | - | 6.22 | RREB1 | MA0073.1 | chr7:579344-579364 | GGGGTGGGGTGGGGTGGGGT | - | 6.22 | RREB1 | MA0073.1 | chr7:579349-579369 | GGGGTGGGGTGGGGTGGGGT | - | 6.22 | RREB1 | MA0073.1 | chr7:579362-579382 | GTGGGGTGGGTGGTGAGGGG | - | 6.35 | RREB1 | MA0073.1 | chr7:579353-579373 | TGGGGTGGGGTGGGGTGGGT | - | 7.06 | RREB1 | MA0073.1 | chr7:579323-579343 | GGGGGTGGGGTGGGGTGGGG | - | 7.67 | RREB1 | MA0073.1 | chr7:579328-579348 | TGGGGTGGGGTGGGGTGGGG | - | 7.67 | RREB1 | MA0073.1 | chr7:579333-579353 | TGGGGTGGGGTGGGGTGGGG | - | 7.67 | RREB1 | MA0073.1 | chr7:579338-579358 | TGGGGTGGGGTGGGGTGGGG | - | 7.67 | RREB1 | MA0073.1 | chr7:579343-579363 | TGGGGTGGGGTGGGGTGGGG | - | 7.67 | RREB1 | MA0073.1 | chr7:579348-579368 | TGGGGTGGGGTGGGGTGGGG | - | 7.67 | Tcf12 | MA0521.1 | chr7:577927-577938 | CAGCAGCTGTC | - | 6.02 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_01848 | chr7:577087-579344 | Aorta | SE_24307 | chr7:576843-580879 | Colon_Crypt_2 | SE_24737 | chr7:576639-580996 | Colon_Crypt_3 | SE_54197 | chr7:577039-579785 | Spleen | SE_57553 | chr7:577219-578035 | VACO_503 | SE_57553 | chr7:578064-580880 | VACO_503 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr7 | 579451 | 580185 | chr7 | 577367 | 579185 | chr7 | 579426 | 579712 | chr7 | 577876 | 578141 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I000537 | chr7 | 576992 | 580503 |
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Enhancer Sequence | CACCCTCCTG AAGAGTCCCC CCCCCAAAAA AGACATTGGC CAACCCAGCT CCCAGGCTTT 60 CACTCTCCTG GTCCCCGCCA AAAAAAGACA TCGGCCCACC CGGCTCCCAG GTGGGAGAGG 120 GACCTGATCC ACCTCCGGGG CCAGCCTGCC AGGGACCTGG CCTTACCACG ACTGCCCTCA 180 GCGTCCTCAG CTGTGAAGTG GGGCTGATTT GCCTACACTC CAGGGAAATC AGGAATAGAG 240 AGAGTGAGTT AATCCATGGA GAGGGCTGGG AACAGCGCTG GGCACAGGAA GCACCAGGAA 300 ATCGACTCCC CCACCAGGCT GTGGCCCTCA CTCACACGCC CCCCTCCCTC CACGCCTGGC 360 CGCCGGCCTT GGGTGCAGGG AACACACCCA CCCCAGCTCC GTGGTTGTGG GCGGCCCGGC 420 CAGGCCCTGC TTAGGTTCTG GGGTGCACTG CAGGGGTGCA CAGCAGGAGT GCGCTGCGGT 480 GGATCAGGGC CGTGGAGGGC CCAGCCTGGG GCTGACCTGA CCAGAGCCCA GGGGAGCCGG 540 GGTCCCTGGA GGAGGGCGCC CCTGGTCCAG GGGCTGCAGA GGAATCTGAG GCGGCTTCCA 600 GGAGGAGGTG GCATTTGAAT CCAGCCTTGA AAGACAGCAG CAGCTGTCCC AGGCCTGGAA 660 TTTCCTCTTC CCATGCAGCC AGGCCCCACC CCTCTTATCT GCCTCCTCGG GGAGCTGGAT 720 CCCAGGGACC TTCCCGAGAA GGGCAGCCCA GCCTGGCCCC ACCCCACCCC AAGGCCGCAG 780 GCTGTGTCAC CCGCCTGGAA TGCACTTTCC AGTCCTCCCC TCCCTCCCCC ATGCCAGCCC 840 TTCACTTCCT GACCCAGCCG GCCAGGCCAG CCCCCAGGCC TCAGAAAATC TGGGGGCCCC 900 CCCGGGCCTG TCACCCCAGA AAGGTGGGGG GAAGGGGGCA CCCCCTAGAC AGGAGGAAGG 960 AGCTCCTGAG AGTCTCACCT TACAACCTCC CCATGGGGAC AGCAAGCCCT CAGTGTCCCC 1020 TCCTAGGCCC CCAAGGAAGC CAGACTTGCT GAGAGGAACA CAACTCACAC ATCCCCCCAG 1080 GGCCCCCACT TCCTCACCAA CCCAATGGGG GCTCTAGGGG CGTCAGCATC CTGCGGTTTC 1140 TTAAAGACGC TGGCGACCCT CCTTCACTCC GGTGGCTCCT CCAAGCCTCT CTACAGCCCA 1200 ACTGGACAGA TGGGCATGGC CCCAAGGTGT TTCGAGCCAG CCAGAGTCCA GAGCTGGGGT 1260 CCCCTCTCGG GCACAGTTGC CCGCCCTACC CTTTCCTTCC CCATCCCTCA GACTGGTAGG 1320 GTCCCAGGAG CCGGCCTGGA GGTCAGACCA GGAATGCCCA GAAGCCAGTG GAGTCAGCAG 1380 GGCTCTGAGC ATTCCCCACA CGGGACCCTG CCTGCCACAT AGGACCCCGC CTGCCACACA 1440 GTCACCTCCC CAGGCCCTGA GCTCAGAGCA GTTGCCCTCT GTCGCCTGCA CAGGGGGTCC 1500 TGTCTGCCTC CCCTGGACTT GGAAGGACCC TTCCAGCTGG CGGGGGGCTC CCGTTTGGGG 1560 ACAAGTGCCT CAGCTACGCC GGTGGAGCCT TGGTGAGGAA CCCCTGTGCC CCCACTCACT 1620 GCGGGCAGAG GCACCACCTC TGGGGGCCGG TGTGAAGCCA GACTCCTAGC CAGCCCTGCA 1680 GCCTGTCCCA GGGGCCAGTA GAACCGGGAG GGGGCCGGGT GTGTAACTGC CTCCTGAGGC 1740 CGGCGAGTAG ATTCCTGAGG CTCAGGGCGG TGCCCTCCTC TACCTGCCCA CACACTCCAA 1800 GGGAGCTTCA GTCCCCACCT GCCAGCTGGA ACAGGGGCTC CCTGAGGGCC CGAGTCCCCA 1860 ACGCTAACAC AGGAGGCACC AGGGAGCGTC TGCGGAATTA AACCAACACT CTGTGTGCAC 1920 GTCACACGTT TAGCGGACAC AGGCCCAGGC TCCCTACACT GGGGTCCCCG CCCCTGCTCT 1980 CCGGCGTTCC GAGCCTAGAC GTGGAGGTGA ACAGACACGT GGCCTCCTGC GCCGGGGGTG 2040 GGGTGGGGTG GGGTGGGGTG GGGTGGGGTG GGGTGGGGTG GGTGGTGAGG GGGTGTGCAG 2100 GGCTGCCTGG ATGCACTCGG CCTAACGGCC CGGGAAGAGC CTGGGGCCTG AGAATTCCAG 2160 CCACCACCAC CCCAGGGGTG CCGCCCACTG CTCACAGGGC CACCCACACC TCTAGCCACC 2220 TCATCGGGCC TCCAGGCGGC TGCCCTGTGT GGTGTGGGGG GACTCCCAGA GGGAGTGAGC 2280 CCGCCCTCCT AGGAGAAGCC TGGCCAGGTT CCAGTGGGGT GGTGGCCCGG CCCATAAACA 2340 GGAGGGGTTT ATGGCCCAGT GACAGGCAAA ACTGGTGGGG CAAGCCCAGG CTAGATCCCA 2400 ACCCTGAGCC AAGGACAAGA GGATTCCAGA GTGGGAGCAG GAAGGCAGGG GTCCGTGGAA 2460 CCAGCCTGCT CCCCTGCTCC CTACGGGCCT CCTCCACCCT ATCTCAGGGA CCCAGGCCCC 2520 AGTCCCAGAG CACCCAGGGG CCACCCCCAC CCCGTCCCTG GCCAAGCCTC ACCCCCTCCA 2580 GAGCGGCCTG TCACCACCTC GGGGTGGGAG CAGCCTCTCT GCTCTCCATC AATGCGGAGA 2640 GTTGATACCA GGGTTGTCTA CCTTCATGAA AGTTACTTGT TGTGATTTCT TCGGCCTACA 2700 GAAAAATATA AACGTGGGCT CCTAGGAGCA CCAGCACATG ACCAGGACCT CGTCCTTCTA 2760 AAGCGTGTAA AGTTTGCTTT ACTGTATTGA CAGCAACAAT AATCAGACCA AAAGCAAGAT 2820 GACAAGACTC CTTCTCACTC GGGTAGTTCG GAGGAGCAAA GTGTGAGAGG CCCAGCGGGG 2880 CTGCAGCCTC AGCTCTGATA CCCCAGCCAG ACCCGCTGTC TCCCAGACTC AGTTTCCCCA 2940
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