Tag | Content |
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EnhancerAtlas ID | HS076-18668 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr14:100658000-100660370 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr14:100660295-100660315 | GGGGTGGGGGTGGGGGTGGG | - | 6.27 | RREB1 | MA0073.1 | chr14:100658428-100658448 | CCACCACCCACCCACTTCCG | + | 6.57 | RREB1 | MA0073.1 | chr14:100658424-100658444 | CCCCCCACCACCCACCCACT | + | 7.63 | ZNF263 | MA0528.1 | chr14:100659731-100659752 | CCTTTCCCCCCTTCCTCTCCC | - | 6.21 | ZNF263 | MA0528.1 | chr14:100659733-100659754 | TTTCCCCCCTTCCTCTCCCCC | - | 6.41 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_23822 | chr14:100658575-100659390 | Colon_Crypt_2 | SE_23822 | chr14:100659435-100660335 | Colon_Crypt_2 | SE_24776 | chr14:100658405-100660543 | Colon_Crypt_3 | SE_27982 | chr14:100658545-100660323 | Fetal_Intestine | SE_29025 | chr14:100658411-100660318 | Fetal_Intestine_Large | SE_31574 | chr14:100658310-100661006 | Gastric | SE_35748 | chr14:100658539-100659393 | HepG2 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I100192 | chr14 | 100658488 | 100660354 |
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Enhancer Sequence | GAAACCCCGT GTGTACTAAA AATACAAAAA AATTAGCTGG ACGTGGTGGC AGGTGCCTGT 60 AATGCCAGCT ACTCGGAAGG CTGAGGCAGG AGAATCGCTT GAACCCGGAA GGCGGAGCTT 120 GCAGTGAGCC AAGACTGCGC CACTGCACTA GAGCCTGGGC AACATAGTGA GACTCTGTCT 180 CAAAGGAAAA AAAAGAATTA TAACTGGGGA CAGACTTTTC TTCCCTTTTA GAGCTGACCT 240 TCTCTGGGAG AGGCTATCAC CAAGATAAAT CGGTAAGGCT TAATTCCATG TCCAGTGTTT 300 TTGGCAAAAC CCTTGTTCCC GAGGGGGTGA GTGGCCTTCC CAGCAGGCTC TGCTGAATTC 360 TGGAAGAGCC TGTTTCCAGA AACTTTGTTT TGTACATGTC TTGGCAAATG ATCACCACCC 420 CCCTCCCCCC ACCACCCACC CACTTCCGAA GTGGTCTAGG GCTTAAGTCC AGATGCGGAT 480 GGGCTCAGGG CGGGGTGGGA GAAGTCAGGG GAAAAAAAAA AAGAAAAGAA AAAAAAGATA 540 AAGAAATAAA TTTCTTCTGC CAGATACCTT AATTAATCAA GGTCGGCCTT CCATCAAGGT 600 CGGCTTCTCG GCTCCCCAGC CCCCGCGCCT CACGGGGACC TCAGGCCTCG GCAGGGTCCT 660 CTCCCTTTGC ATCTCCTACT AGTCAGCTGT CGGTGGTGAT GGCCCGTGCC AAGTTCACGG 720 TCTCAGCCTG ACGAAAGGCG GCCTTTACCA GCCTCAGGAC CCCCAACGAA CCTGGGGCCA 780 TGGCTGGGGA GGGGGCTCTG CCCAGGCTCT GCGTTCTGGG ACAGGGGTCC CCAGATGGCC 840 ATGCGTCAAG GCCCAGGGAC CTGTTTGTGG GCCCGAGAGC ACGGGGGTCA GGGGTGGGGC 900 TCGAGTCTCG TCCCAGGGCT CCGGGACAAG CTTCCTGGAG GAGGCAGCGT GAGCTCTGGG 960 AGGTAGAGGT CAAGACCTCA AAAAATGGGG GGACATGGGC GGAGGGGGCA TTTTGTAACT 1020 CCTACGTCCC TGCAGAAGCC CAGACCCTCA GAGACTAGGA ACTGAGGCCT GGCAGAGTGG 1080 GGTGGGCCAG CAATCACGCG CCAGGCCACA CGAGGAGAGC CCACTGCCCC GGGGATGTCA 1140 GACGCGGGGC GGCCTCGGCG ACCGCACACG CCATAGAAAG GTCACCGAAC TTGGCCGCCC 1200 GGCCGTCCCG GAAATCGCTA CTGCCCGGCA GCCCTGGGGC CTCCACAACC GCGTCCCGGC 1260 GGCTCAAGTT GCCCTTTGTC GCCCCCTGCC GACCAGTCTC CCTGCGGCTC CCGCGCGGGA 1320 CAATCAGGCG GGCCGGGCTC GGAAATAGTG GGCATGGGTC CCTGAGGCGC GGGGATTGGC 1380 CGCTCTGTGT CATGTGTCCT CGGCTCGGGC CAACCAGCGA GGGAGGCAAA GTCCCATCCC 1440 GCGCGTCCCG TAGCCCTTCA GCGAGCTGTG GGCGGGGCGT CAGGCCTGAC ACCTCGGCCA 1500 GAGGGCGGGG CCGGAGACCT GAGCGGCGCC GCTTCCGCTC TTTCGCCCAG GTGCCTTGGA 1560 GCCGCTGCTC TCGCCTCCCT TCTCCACCTA GCGGCGGTGT TTCACACCCC GGAGTGGCTT 1620 TTTGGGGATA AAGGCACAAA TCTTTGCCAG ACCTCCCGCC AGGCCCCCTG GCCTGCCACG 1680 TGCTCCTTGC CGGCCTAGAC TCACCCAGGC TGTGCCCTCT GCTCAGAACG ACCTTTCCCC 1740 CCTTCCTCTC CCCCTCGCTT GCTCCGACTG TTCTTTGCAA TCCCGGCTGG GGTTGGGTTA 1800 AGGGCCTTCT GGGGCTTCTT CATACCCTGT GCATCTTCCT CCTACTGGCA CCGACCACCC 1860 CACACTGGGC TGCCATCTGC TTGTCTACAC CCACTGACTT TTCATCTCTG TATCTCCCCA 1920 GTAAGCAGGA GTGGCTCACA GAAGGCACGT TAATACCTGT GTGTTAATAT AAACCAAGGA 1980 GCGGGACGAT AGCTAGGAAG TAACATCCCT GGGCATCATC TGAGTACCAG GCCCCCTGCC 2040 AGGTACTTTA GAGGCTACTT GATGTTCAGG CCCATGGCAG CCCTGGGAGG GAGGCACAAA 2100 GGCTCTTTTG TTCCTGGGGA GTCAGTGGAG GCCCCTAGAG GCTGAATGAC TGTCTGGGTC 2160 CCCCAGCTGG ACTGTTTGGG GACAGGCCTG GGGAGCTGAG GGCACCCTCA TACCAGGCAG 2220 CCTTGCGCCT GAAGCTCTGC TGGTGAAAAC TGATGGGCAG GGCCCTGGAA GGGAGAGTCA 2280 GCGCCTGCGG GGGCGGGGGT GGGGGTGGGG GTGGGAAGGC AAGCGGAGGG GAAAGGTGAG 2340 CATAGACAGG CATTTGTGAT GGCCACAGGC 2370
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