Tag | Content |
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EnhancerAtlas ID | HS105-72079 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr7:510890-512530 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr7:511838-511853 | TCTGCTGAGTCAGTC | - | 6.08 | Zfx | MA0146.2 | chr7:511667-511681 | CAGGCCGGGCCCGC | - | 6.01 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28669 | chr7:510970-512701 | Fetal_Intestine_Large | SE_68824 | chr7:510820-511938 | H9 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I000471 | chr7 | 510921 | 512657 |
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Enhancer Sequence | CCCTCCCCCA CCACCCTATA GCTCCCCCAT GCCCCTTCTC CCCTTTCATG CTGTTCGGGG 60 CGTGTCCATC TGTTGACCGT CTGTCTCCCC CGCCAGGATC CTGTGCACCC CTGCACACGC 120 CCAGCCTGGG CACACTCGGC AGACCGCTGA TGATCTACTG GAAGAGCAGA CGAGGGTCTG 180 ACTTCCTAAG TCATGGTGTC AGCCTCGAAC AGGAGTGTTC TGGGTCCAGG GAGATGTCAT 240 GGAGTGAGCT GGGCCTGGGC TGGAGGCCTG GCTCTGCTGG CGGGGCTGAG CCCATTCACC 300 CATCAAGCCC CCGTTTCTCA TCTGTATGAT GGGAGGCTCC CCGCACCACC CTCTCTTCCC 360 TATCACCTTT CCGACTGACC TGGGTGGGGG CCAGGTGTGA CTGTGGCCAG GGTCTATGGG 420 GGATCACTGA GGTCCTCAAG ATGGCCCCGG ACAAGGAGGG GCATCAAAGC AGGGGAGACA 480 GAGGAGCTCT GGCCCCGTCT TCCCCAGCAG CCCATGAGCC ATGGATCAGC CGGGGGCGCC 540 CATGTTGAGC AGTCCCAGGG AGCCCGCTGC CCTGAGCCAT TTGACCAGAG GGGTGGCCCG 600 GCCAGCTCGG CACAGTGCTG AATTCTGGGG ACCTCATCGC TCCTGCCGGT CCCCTAGGGG 660 CTCACAGTGG GGCTGGAACG AAAGGGAGCC TGATGGAGCC TGCAGCTGAC TGCCCAGGAA 720 GCTTCCGGAA CGCAGCCACG TGGGAGCGGT TGCTGGAACT TCCTCACACT GCCTGTTCAG 780 GCCGGGCCCG CATTCCCCCT CCAAGGGAAG GGAGGGCCAG AGCCGGTGCG AAATCTGTCC 840 TGGCAGCTCC CCAGGGACTC CCGGGGCAGG CTCAAGTTTC TAAGGAGCAT AAACTATGTC 900 TTACAAGTCG AGATAGTGAC TCCAGTGACT GAAAACATCA GAAATAGCTC TGCTGAGTCA 960 GTCCCTTCCC AAAGTTCTGT GGGAAAGAGT CTGTCGGCCA GAGGGCTGAC CCCACAGGCC 1020 CCAGCTCACT TGCAACAGCT CCTGCAGCCC AGGGAGAAGG CATGGGAGGG ACCCGGGTGG 1080 TGGCACCTGG CAGCTGGTGA GCAGCCCTGA ACCGTCCCTG GTGACAAGGA GGGGACACAG 1140 CTTAGAGGCA CCCGCCATGC CACCTTTGTG GAGCTGGGCA GGCCTGGGGT TTAGGGACTC 1200 GGCGCAGGTC CCCCGGCCCC CTCATCCTGA CACTTCTTTT CCTGGAGCTG CCTTTTCACA 1260 GCCTTCCCCC GAGGAGGAGT GACCTTTGGC TTGTTTGGAT GTTAAGCGGG GAATCCGCAC 1320 ACAAGCCACA GTGTATGCGC ACACACACAG AGGCACTGAC GCACGGTGGC TTTACATGAA 1380 GGAGGTGCGT TATATCACAT GACAGGAAGT TCAAGGTGTG CACTCAGTGA TTCTGTGATA 1440 CCACAGGAGC TGGGATTCCT CCTCCTCTCT ACCCTGCCAT TCTCAATTGG CCTCACACCT 1500 CATAATTGTC CCCTCGTGGT CACAAGAGGA CTGCCATAGC TCCAGGCATC ACGTCCTCAT 1560 CCACCACCCT CTAAAGGCAT CCCTGCCTTC TGCCCCTTTT ATGACTTTTT ATTTTTATTT 1620 TTATTTTTAT TTTTAAAGAT 1640
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