Tag | Content |
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EnhancerAtlas ID | HS101-34468 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr5:43481010-43483920 |
Target genes | Number: 12 | Name | Ensembl ID |
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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) |
RREB1 | MA0073.1 | chr5:43481942-43481962 | TGTTTGTTTGTGTTTTGTGT | - | 6.08 | ZNF263 | MA0528.1 | chr5:43482533-43482554 | TCCACTTCCTATTCCTCCCCC | - | 6.76 | Zfx | MA0146.2 | chr5:43481149-43481163 | CCCGCCTCGGCCTC | + | 6.01 | Zfx | MA0146.2 | chr5:43482188-43482202 | CCCGCCTCGGCCTC | + | 6.01 |
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Enhancer Sequence | TCTCCTGCCT CTCAGCCTCC CGAGTAGCTG GGACTACAGG TGCCCGCCAC CACGCTCAGC 60 TAATTTTTTG TATTTTTACT AGAGACGGGG TTTCACCATG TTAGCCAGGA TGGTCTCGAT 120 CTCCTGACTT CGTGATCCGC CCGCCTCGGC CTCCCAAAGT GCTAGGATTA CAGGCGTGAG 180 CCACTGCGCC CGGCTTACTT TTTTTTTTTT TTTTTTTTGA CAAGGTATCT CTGTTGCCCA 240 AGCTGAAGTG TAGTGGCACG ATCATAGCTC ACTGTAACCT TGAACTCATG GGCTCCTGCT 300 TCAGCCTCCT GAGTAGCTAG GACTACAGAA ATGCACAACT ATACTTGGCT AGATTTTTGT 360 TTTTAAAGTG TTTTGTAGAG ATGGGGTCTC ATTGTGTTGC CCGGGCTGGT CTTCAGCTCC 420 TGGCCTCAAG TGATCCTTCC ACTTTGGCCT CCCAAAGTGC TGGGACTACA GGCAGAAACT 480 ACCACACCGA ACCTACTAAC TCTACATTTT ACATGATGAG TTCAGATTTT AAAAGGATTA 540 GTTTGCTAAT AAAGTGTCGT GAGCAAAGTG AAAAATCAAA AGATTACTTG AAGTATTTAC 600 ATGATGATCC AAATTTAAAG CGACCTCAAC AAGCAAAATT TACTGTTTAC AAAAAACTGT 660 ATCACGGTTT ACGAATAGGA ACACATATAT TATATATAAT GGGTATAATG CGAATGCATT 720 TTACCAATGG AAAGTACAAA ACAGCTTGCT GATGAAAGAG GAAGGAAAAA GCTCACAGTG 780 AACTTGGAAG CAGATCCTTC AGCCCCAGTC AACCCTTCAG ATGTCCGCAG CCACTGCCGA 840 CATCCTGACT GCAACTTCAT GAGACCCTGG GCCAGAACCG CCAGCTAAGT CTTGACCCCA 900 CAGAAAGAAT AAAATTATTG TCTACTGTTT TTTGTTTGTT TGTGTTTTGT GTGAGATGGT 960 TCCTCGCTCT GTCACCCAGG CTGGAGTGCA GTGGCATGAT CTCGGCTCAC TGCAAGCTCC 1020 CCCTCCCGGG TTCACGCCAT TCTCCTGCCT CAGCCTCCCG AATAGCTGGG ACTACAGGCG 1080 CCCGCCACCA CGCCCGGCTA ATTTCTTGTA TTTTTAGCAG AGACGGGGTT TCACCCGTGT 1140 TAGCCAGGAT GGTCTCGATC TCCTGATCTC GTGATCCGCC CGCCTCGGCC TCCCAAAGTG 1200 CTGGGATTAC GGGCGTGAGC CACGGCGCCT GGCCCCTACT GTCTACTGTT TTAAGCCTCT 1260 AAGTTTTGGT GTAATTTATT ACACAATAGA TACGTAGAAG AGAACTATTT CTATTTTTAA 1320 GGAAGGTATA ATTGCAGTTC CAGAACCCCA CATTTCTGGC ATCTATTCTA CTCCAACTTT 1380 TGGTGCAGAT ATTTAACATC TGGCTCAGAG TCTGAGTATT AGAAAAAGAG AAATTTACTA 1440 AGTGTTCTTC CTGTATTACT TATTGTCTCT GAATAATACA CCTAAGGGTA CCCATTTTTC 1500 TTCTTAAACT TTTTATTTCC TTTTCCACTT CCTATTCCTC CCCCTACAAA TAAAACGGAC 1560 TCCCGAACCT CCTTTTACAT ATTCACTTTT GTTGATAAGG TTCCTTAAGA GTAGTGATCT 1620 CTTTTAAACT TGTCATGTTT AAAAATCCAG TGTGCTCAAG GTATTTAATA AATATTCCAT 1680 TTTACTAATA CAAGAGATAA TCACATAATA AATCCGCAGC CTATGAACTA AAGATACTGT 1740 TTGGGATAGC TTCTCTGACA TAACTGACAT ATTATAAATT CCTCCCTATG ACTCGCAGAA 1800 GCCATTTTCT GCAATGGCCA AACTTTGTCA CACCCCATCC CCCTTATAGC AAATACCACT 1860 AACTTTGGGG CCTTCAGAGT ATACATAACA GTACTTTTCT CCTTCCTGAA TTCCACAAAC 1920 ATATAATTAG CTGGTCACTT TAATTATACG CTATCATGTA TTGTTTGCTA ATAATCTCTT 1980 AGACATTATT TCTGTCAAAA CAAATAAGAG CTGATACATT CTCTAAGTAA GTGTCATCTG 2040 TTTTAACTTT CCCTCTTCCC CACCAACCTT ACACATTATA TGCAAAAACC CAAGGTCAAA 2100 ACACGGTCCA AATTCCAGAA ACCGCCTTTA TTATGCTTTA CCAGTAAGTC TTCTTCACTG 2160 AACTGTAGTT GCTGTAAACT TAATATATTT AATTTCTTTA ATGGAAAAAT ATCAAAAGCA 2220 GATGCCAAAT CTGATGCAAC TAACTGACAA AGGAAACACA AATCTTGCTT ACTTTCACTG 2280 AAACTTTTTA TAGCCATCAG ATGTCTGCAC TTAAAATGTT TAGTTCCTAT GCCCATTACG 2340 AATAAAACAA AATTCTGTAT TTCAACATGT TTCAAGCCTC AGAAGTTCCC AGACATCCTT 2400 TTCTGAGTCT GGTGTGATGC AATAATTTTT CAAATGTCAT TTAAAAAAAT GGGCCAGGCT 2460 GCAGGGAAAG GACCATGTCA CACTCTCAGC ATTCAAGCCT CAAAGGCTCC GGGGCACGAA 2520 AGGCTCTTAC AACCGGTTAA GGACGGCAAT GGGCTCCTTC GGCACGACTC CCGGAACCCC 2580 ACCCTGGGCC AGAAAAAGGC CAGGGGCGCG GAGCGTAGGC GGAGGGCTGG GGTTCTAGGG 2640 ATCTAGAAAA AGCGCGAAGC CGGAGGGCGG CGCCAGGGCT CCTCGCAGAC CCCAGGGCCG 2700 CGGGACGGTG CCGGCTCGTG GGTCACACGC ACCCAGGAGG CTCCTGGCTC CCGCGTGGCG 2760 GCTGTTCCAG CACGCCCTCC GACCCGCAAC CGGACCCTCC AGACATCAGA CTCAGTGGTC 2820 CCCCACCTCC GGTCTCCCAC CTCAGGACGC AGTTCCGCGG CGTCCACCCG GCCCCCTCCC 2880 CTCAGTCCCA CGCAGCGGCT CAGCCATACC 2910
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