Tag | Content |
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EnhancerAtlas ID | HS092-32199 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr5:131654110-131654890 |
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) |
CDX2 | MA0465.1 | chr5:131654642-131654653 | AGGCCATAAAA | + | 6.02 | NFE2L1 | MA0089.2 | chr5:131654592-131654607 | ACTGCTGTGTCATCT | - | 6.07 | Nr2f6(var.2) | MA0728.1 | chr5:131654778-131654793 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_09625 | chr5:131653988-131654910 | CD14 | SE_27887 | chr5:131653835-131654911 | Fetal_Intestine | SE_28847 | chr5:131653891-131655264 | Fetal_Intestine_Large | SE_40097 | chr5:131653490-131654882 | K562 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH05I132317 | chr5 | 131653665 | 131655210 |
|
Enhancer Sequence | AGGTTCTCCC CGTGCCAGAT GGAGGACACT CCTAGCCCAT GGTTCCTGGG TCTCGCCTCA 60 TATCCTGGCA GCTGCACTAC AGTCTTGTTT CTTGAGCTGG GGTCTACTGA GAGCCTATGT 120 TGGTCATTTA TGAAGGTGCA TGTCCTGCCT CTGTGTGGAA TGGGCCCAGC GGTTCCTGGG 180 GCAGGTACTG CTCTACATGG AAGGCAGCCT GGCCCTCTCT GAGTCACTCC CTCTTGGAGA 240 GAGTGCTCAG ATTCAGAGGG GTGTGACAGG TGGTGGGCAA TACTCCTAGG GCTATGCTGG 300 CCCTCATCCT AGCCAGGTCA TGTCCCTTTG GCTTAGATGT CAAAGTTTCA CTCCCAGGAG 360 AAACTCAGAA GCCCAGCCAG ACCAAGACCA ACCAGGCTTT GCCCTAGAAG CAAAGCAGGC 420 AGAAGAGGCA GATAGAGCAT AGGGGGCCAG GACAGGGATC CCCCGTCAGC ACAGCAGGAG 480 TCACTGCTGT GTCATCTGTT TCACTGCCAC ATGGAAAGCT CATGGCAGCT GCAGGCCATA 540 AAAGATCTGT GTAATCAGGG TTCTCTCCTA GCATTACTCA GAGGGGTCTG GCTGGCTTCC 600 AGTGACAAGC CAAGGAAGGG AAAATGTAAA TCCACTTCTG AAAGGGGGAT AAGGTGGGTG 660 GATCACCTGA GGTCAGGAGT TCAAGACCAG CCTGGCCAAC ATGGCAAAAC CCCGTCTCTA 720 CTAAAAATAC AAAAATTAGC CGGGCATGGT GGCAAGCGCC TGTAGTCCTA GCTACTTGGG 780
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