Tag | Content |
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EnhancerAtlas ID | HS092-30379 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr4:87824950-87825830 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYB | MA0502.1 | chr4:87825114-87825129 | CTGATTGGTGCGTTC | - | 6.34 | NFYB | MA0502.1 | chr4:87824957-87824972 | CTGATTGGTGCGTTT | - | 6.73 | NFYB | MA0502.1 | chr4:87825073-87825088 | CTGATTGGTGCGTTT | - | 6.73 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_28924 | chr4:87825051-87825881 | Fetal_Intestine_Large |
|
| Number: 1 | ID | Chromosome | Start | End |
GH04I086903 | chr4 | 87824954 | 87825953 |
|
Enhancer Sequence | CAGGGTGCTG ATTGGTGCGT TTATAAACCT TGAGCTAGAC AGAGTGGTGA TTGGTGCATT 60 TACAATTACT TAGCTAGACA CAAAATTTCT CCAAGTCCCC ACTGACTAGC TAGACACAGA 120 GCGCTGATTG GTGCGTTTAC AAACCTTTAG CTAGACACAG AGCGCTGATT GGTGCGTTCA 180 CAAACCTCTA GCTAGACACA GAGTGCTGAC TGGTGCATTT ACAATCCTTT AGCTAGGCTG 240 AAAAGTTCTC CAAGTCCCCA CCCATCCCAG AAGCCCAGCC AGCTTCACCT CTCACTGGCA 300 CGCTGGCACT CGCCGGGACT TTGCGTCACC CAGCCTGGGC ACTCCGGTAG CCCAGAAGGA 360 GCTCATCCCG AGATCAAGCC CAGCAGGAAC CGGCCGCCGC GCCCAGTGCG GGGCCAGCCG 420 AGCCTGCGCC CACCCGGAAC CCGCGCCGGC TAGCGAGCGC CTTGCGCAGC CCTGGCTCCG 480 CCCGCGCGTT TCTCTTCACA CTTCCCCGCG AGCACAGGGA GCCGGCTCCG GCCTCGGCCA 540 GCCCCAGAGA GGGGCCCTCA TAGCGCAGCG GCGGGCTGAA GGGCTCCTCG AGTGCGACCA 600 GAGCGGACGC CAAGGCCGAG GAGGCGCGGA GAGTGAGCGA GGGCTGGTAA CACGTTGTCA 660 CCTCTCACCA GCAACTCAGG AGGCTGAGGC AGGGTAATCG CTTGAACCTC GGAGGGGGAG 720 GTTGCAGTGA GCCAAGATCG CGCCACTGCA CTCCAGCCTG GCGACAGAGC AAGACTCTGT 780 CTCAAAAAAA AAAAAAAAAA AAAAAAAAGT TGTAAGCTGG CAGCAGTGGT GTACACCTGT 840 AGTCCCGCCT ACTCAAAAGG CTGAGGCAGG AGAATTGATT 880
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