Tag | Content |
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EnhancerAtlas ID | HS101-39784 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr7:30904010-30905340 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr7:30904542-30904562 | CGGGGGTGGGTGGTTCGTGG | - | 7.21 | ZNF263 | MA0528.1 | chr7:30905257-30905278 | GGAGCTGGAGGTGGAGGAGAG | + | 6.21 | ZNF263 | MA0528.1 | chr7:30905266-30905287 | GGTGGAGGAGAGAGGGAAAGG | + | 6.75 | ZNF263 | MA0528.1 | chr7:30905263-30905284 | GGAGGTGGAGGAGAGAGGGAA | + | 6.79 | Zfx | MA0146.2 | chr7:30904264-30904278 | CAGGCCTGGGCTGC | - | 6.2 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_01927 | chr7:30900837-30904654 | Aorta |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I030864 | chr7 | 30904284 | 30905305 |
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Enhancer Sequence | GCCAGTGTAA GCAGAAACAA AGCTACTGAC TGATTCCTAT CAGAAGCCCA GGCTTTAAGA 60 GGGGCTGGAT CCAGGAACCC AGACATTGTC TTTGGGAATT GGTGTCTGTT CTTTTGTCTC 120 TTCACTTTTG GCTCCTCTGT CCCAGCTGCA TTCTCAGGAA GGTCCTTCTG CACGGTGGGC 180 TCAAGGGAGC CCTTCTCCAG CAGCTCCTCA GCCTGCTGGG TGCTGGGTGC CATTCCTGGT 240 GTGATTGCCG TGGCCAGGCC TGGGCTGCAC CATCACATAT ATATGGACAT GGGGTATCCC 300 CAAAAGGCAG TCACTGCCCA GAGAAGGCCA CCACATCTGC TAGCAAAGGG ATAGGGCAGA 360 GTCAGGAAAC AGGTATCTGA GAACAGGAGA GCAGATGTGG GTTTGGGGTG GGCTGAGCCT 420 TCATGGAGGC CCCCAGGCTC CTCTCAGTAA TGGAGAAAAG AGATCACCAA GCTTTCTGTT 480 CCAGCAATTG TGGGCAGTGC TCACCCCGTC AGAGACCCTC TGGGGGGAAT CACGGGGGTG 540 GGTGGTTCGT GGGGTGAGAT GTGAACAGGG GCTGTTCCCC TTGAGAATCA CGGGCTCTTG 600 GAGGTTTAAG TGTGCTGTTC TGAACGGGAG GGGTCCATGG GATGCTCGTC AGCTTACCTG 660 GGACTCTGCT GAGCCTCTGC CAGCCCAGAA TAATGAATAA TGAGGTGTGA ACAGAGCCAC 720 CCAGACCAGG AGCCTGACCC ATGGGCTCCC GTCTCTGCAC CGACACCTGG CTTTGTGGCT 780 CACTTGCCCT CTCTCACCTG AATCTTCCCC CAGGTCACAT GTGAGGCAGG GTGGGTTGGG 840 TAAGTGTCCT TCCTACCCAG CATGCTAAGA CCTTTTGAAG CTTAGCTGGG AAACAGGAGA 900 AGAGGAACTT CCTCAATAAA CTCCAGCCGA ACTTTGACAC TGATTCAGAT TAGGGCAGAG 960 GCCCCACTAA TGAAGATTTT CAGCAATGTC TCAAGAGACC AAGGTGACAA TGGAAGGTGG 1020 ACCCACGGGG GCATGGATGC CAGTGTCATG GAAATAGTGG GCCCACCACT GAGACTCCAC 1080 TTCCTTCCAC TGACTCTGTC TCTCTCCCTG GTCCCGTCCC TGGGAGCCAC CTGCTCCTTT 1140 GTCCCCAGGC CCCTTTACAG GGAACCAAAT TCTGTCCTGT AGATCTCTGC CTCGCTTCCT 1200 CTGGAGACCC TGTGCAGACA CCTGAATCTG GAGGCTTAGC CTCAGCGGGA GCTGGAGGTG 1260 GAGGAGAGAG GGAAAGGGCC CTTGCTGCCA TCTTAGGCCT TTGTTGTCTT GTGGCAACCC 1320 AAGGGATGGG 1330
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