Tag | Content |
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EnhancerAtlas ID | HS101-34071 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr5:518020-519700 |
Target genes | Number: 15 | 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) |
PPARG | MA0066.1 | chr5:519561-519581 | GGAGGTGAAGGTGACCCACA | + | 6.33 | PPARG | MA0066.1 | chr5:519560-519580 | AGGAGGTGAAGGTGACCCAC | - | 7.44 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_25092 | chr5:518284-522681 | Colon_Crypt_3 | SE_27965 | chr5:518031-524615 | Fetal_Intestine | SE_29117 | chr5:518106-524444 | Fetal_Intestine_Large |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I000518 | chr5 | 518332 | 524328 |
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Enhancer Sequence | ATCCATCCAT CCATCCATTC ACTCCATTCA TCCATTCGCT CATCCACCCT TCCATCCATT 60 TACTCATCCA TTCATCCATT CATCAATCCA CGCATCCATC CATCTATCTA TTCACTCATC 120 CATCCATCCA TCCACATGTC CATTCACGTG CTCAGATCTG CAGGACTCTG CTGGGGACAG 180 GCACTGGGGA CACAGGAGGA ATAAGACAGA CAACCTCTGC CATTGTGGCA TCAACCTGGT 240 TGAGCCAAAA GACCTTGGAG GAGGAGGTGT CCTCAGGAGC TCAGAGGAGG AAGGCTCCGA 300 GCTCAGGAAA GGTGGAGCAG GAGAGATGCT GAGTGTGAAG GGATGAAGCT GGGGTGAGTG 360 CATGATTTGG GGGAGGGTGG AGTCTGGCAT CCCAGGACCT GGTACCCTGA GACCTGGCAC 420 CCTGAGACCT GATACCCTGA GATCTAGCAC CCTGAGATAT GGCACTTCGC GACCGGGCAC 480 CCTGAGGCCT GGCACTTGGA GATCTGGCAT CCTGAGACCT GGCACCCTGA GACCTGGTAC 540 CCCAACACCT GGTACCCAGA AACCTGGCAC GCCAACACCT GGCACCCTGA CACCTGGTAT 600 CCTGAGACTC TTGTCTCAAG GGTGGGTGAG GAAAGCCTTG GTGGCTTCAT CGTGCACTGA 660 GACTCCTGGT TGTGGGACTC AGCCCAGACG CTGGGCAGAT GATGTGCAGG ATGGGAACCC 720 CAACTCTAAA CATGCCCCAG TGCAGCCCCT GGCTCCTGGA GAAGCCGGCA GTGGGGGTGG 780 CCACGCTGGG AGAGCTCAGC CATTTCTGCA GTAGACATGA GGCTGGTTGG GTGCTGGAGC 840 TTGGGCCCAG ACAGGCATCT TAACAAGCCT GTGTGGTCAC AGGGAGCGCC ACACACGCCC 900 AGAGGCGGGG AGCTCCTGGG GTGGCAGGGA GTGGGCTGGG GGGGCTGGCG GCCAAGAGTG 960 ACTCACCATC CCTGTCTCTC TCTCAGCCTC TGGCGGAGCT GCCAGGTACC CACAGGGAGC 1020 CCTGGTGGTT CCTTCCCTGC CCCGATGCTA TCAGCACTTC CCAACCTTTG CCCCTTTCCT 1080 CAGGATTCTC CCGGGCGACA CCTTAGCTCC AAACGCCATG GATTGTTTTA TAGCCTACAG 1140 CTGATTCTCC GTGGGCAGCT CCTGGAAAAT GAAACTTCAC CCCTTCAGGG CCAGACCCTC 1200 CCCTGTGGAG ACTCCTGGGA GAGTCTTTGC TTCCAGGCCT CCCGTGATGG CTCCTGACTC 1260 CAAACCCACT GAGCATACCT CTCCTGCCAG GACTGGGGTC CACAGGGCCC ACTCACTGGT 1320 CCTCTCCTGG GAGGACTGGG TCCCCTGGGG ACTTTGCTGA CCACCCTGGC CTTCTAGGCC 1380 ATCCTTGTCC CCAGAACCTC CTTTCCTATG CTTCTTCAAG GAGAACCTAA GGGCAGTTCA 1440 GCTGGAGTGG GTAGCAGATA TGGTGAAGGG GTAGGTGCTG TGCGCATTGA GGGATTCCTG 1500 CCTCCAGGAC CAGAGCACAT GCAATAAAAC CATTCACCCC AGGAGGTGAA GGTGACCCAC 1560 AGCTGCCCTC ACAGCCTGGG CACTGAGTGC CCGGTGGAAG GCTGCACCTG GGAGAAATCC 1620 ACAGCTTAGG CAGGTGGTCT AGGCAGTGTC ACACCCCCAG TGGCGGAGGC TCCCTGGGAC 1680
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