Tag | Content |
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EnhancerAtlas ID | HS111-04407 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr7:577200-579950 |
Target genes | |
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: 3 | Chromosome | Start | End |
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 | TGGGTGTGGT GGAGGGGGAC CTTGTTCAGG GGCCAGGGGG CACTCACCTT CATGGTGCTG 60 GAAGCCCCCA GGGACAGTGA GCCTGGCTTT CACCCTCCTG AAGAGTCCCC CCCCCAAAAA 120 AGACATTGGC CAACCCAGCT CCCAGGCTTT CACTCTCCTG GTCCCCGCCA AAAAAAGACA 180 TCGGCCCACC CGGCTCCCAG GTGGGAGAGG GACCTGATCC ACCTCCGGGG CCAGCCTGCC 240 AGGGACCTGG CCTTACCACG ACTGCCCTCA GCGTCCTCAG CTGTGAAGTG GGGCTGATTT 300 GCCTACACTC CAGGGAAATC AGGAATAGAG AGAGTGAGTT AATCCATGGA GAGGGCTGGG 360 AACAGCGCTG GGCACAGGAA GCACCAGGAA ATCGACTCCC CCACCAGGCT GTGGCCCTCA 420 CTCACACGCC CCCCTCCCTC CACGCCTGGC CGCCGGCCTT GGGTGCAGGG AACACACCCA 480 CCCCAGCTCC GTGGTTGTGG GCGGCCCGGC CAGGCCCTGC TTAGGTTCTG GGGTGCACTG 540 CAGGGGTGCA CAGCAGGAGT GCGCTGCGGT GGATCAGGGC CGTGGAGGGC CCAGCCTGGG 600 GCTGACCTGA CCAGAGCCCA GGGGAGCCGG GGTCCCTGGA GGAGGGCGCC CCTGGTCCAG 660 GGGCTGCAGA GGAATCTGAG GCGGCTTCCA GGAGGAGGTG GCATTTGAAT CCAGCCTTGA 720 AAGACAGCAG CAGCTGTCCC AGGCCTGGAA TTTCCTCTTC CCATGCAGCC AGGCCCCACC 780 CCTCTTATCT GCCTCCTCGG GGAGCTGGAT CCCAGGGACC TTCCCGAGAA GGGCAGCCCA 840 GCCTGGCCCC ACCCCACCCC AAGGCCGCAG GCTGTGTCAC CCGCCTGGAA TGCACTTTCC 900 AGTCCTCCCC TCCCTCCCCC ATGCCAGCCC TTCACTTCCT GACCCAGCCG GCCAGGCCAG 960 CCCCCAGGCC TCAGAAAATC TGGGGGCCCC CCCGGGCCTG TCACCCCAGA AAGGTGGGGG 1020 GAAGGGGGCA CCCCCTAGAC AGGAGGAAGG AGCTCCTGAG AGTCTCACCT TACAACCTCC 1080 CCATGGGGAC AGCAAGCCCT CAGTGTCCCC TCCTAGGCCC CCAAGGAAGC CAGACTTGCT 1140 GAGAGGAACA CAACTCACAC ATCCCCCCAG GGCCCCCACT TCCTCACCAA CCCAATGGGG 1200 GCTCTAGGGG CGTCAGCATC CTGCGGTTTC TTAAAGACGC TGGCGACCCT CCTTCACTCC 1260 GGTGGCTCCT CCAAGCCTCT CTACAGCCCA ACTGGACAGA TGGGCATGGC CCCAAGGTGT 1320 TTCGAGCCAG CCAGAGTCCA GAGCTGGGGT CCCCTCTCGG GCACAGTTGC CCGCCCTACC 1380 CTTTCCTTCC CCATCCCTCA GACTGGTAGG GTCCCAGGAG CCGGCCTGGA GGTCAGACCA 1440 GGAATGCCCA GAAGCCAGTG GAGTCAGCAG GGCTCTGAGC ATTCCCCACA CGGGACCCTG 1500 CCTGCCACAT AGGACCCCGC CTGCCACACA GTCACCTCCC CAGGCCCTGA GCTCAGAGCA 1560 GTTGCCCTCT GTCGCCTGCA CAGGGGGTCC TGTCTGCCTC CCCTGGACTT GGAAGGACCC 1620 TTCCAGCTGG CGGGGGGCTC CCGTTTGGGG ACAAGTGCCT CAGCTACGCC GGTGGAGCCT 1680 TGGTGAGGAA CCCCTGTGCC CCCACTCACT GCGGGCAGAG GCACCACCTC TGGGGGCCGG 1740 TGTGAAGCCA GACTCCTAGC CAGCCCTGCA GCCTGTCCCA GGGGCCAGTA GAACCGGGAG 1800 GGGGCCGGGT GTGTAACTGC CTCCTGAGGC CGGCGAGTAG ATTCCTGAGG CTCAGGGCGG 1860 TGCCCTCCTC TACCTGCCCA CACACTCCAA GGGAGCTTCA GTCCCCACCT GCCAGCTGGA 1920 ACAGGGGCTC CCTGAGGGCC CGAGTCCCCA ACGCTAACAC AGGAGGCACC AGGGAGCGTC 1980 TGCGGAATTA AACCAACACT CTGTGTGCAC GTCACACGTT TAGCGGACAC AGGCCCAGGC 2040 TCCCTACACT GGGGTCCCCG CCCCTGCTCT CCGGCGTTCC GAGCCTAGAC GTGGAGGTGA 2100 ACAGACACGT GGCCTCCTGC GCCGGGGGTG GGGTGGGGTG GGGTGGGGTG GGGTGGGGTG 2160 GGGTGGGGTG GGTGGTGAGG GGGTGTGCAG GGCTGCCTGG ATGCACTCGG CCTAACGGCC 2220 CGGGAAGAGC CTGGGGCCTG AGAATTCCAG CCACCACCAC CCCAGGGGTG CCGCCCACTG 2280 CTCACAGGGC CACCCACACC TCTAGCCACC TCATCGGGCC TCCAGGCGGC TGCCCTGTGT 2340 GGTGTGGGGG GACTCCCAGA GGGAGTGAGC CCGCCCTCCT AGGAGAAGCC TGGCCAGGTT 2400 CCAGTGGGGT GGTGGCCCGG CCCATAAACA GGAGGGGTTT ATGGCCCAGT GACAGGCAAA 2460 ACTGGTGGGG CAAGCCCAGG CTAGATCCCA ACCCTGAGCC AAGGACAAGA GGATTCCAGA 2520 GTGGGAGCAG GAAGGCAGGG GTCCGTGGAA CCAGCCTGCT CCCCTGCTCC CTACGGGCCT 2580 CCTCCACCCT ATCTCAGGGA CCCAGGCCCC AGTCCCAGAG CACCCAGGGG CCACCCCCAC 2640 CCCGTCCCTG GCCAAGCCTC ACCCCCTCCA GAGCGGCCTG TCACCACCTC GGGGTGGGAG 2700 CAGCCTCTCT GCTCTCCATC AATGCGGAGA GTTGATACCA GGGTTGTCTA 2750
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