Tag | Content |
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EnhancerAtlas ID | HS182-06842 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr14:100085830-100087340 |
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) |
FOXH1 | MA0479.1 | chr14:100086267-100086278 | CCCAATCCACA | + | 6.14 | ZNF263 | MA0528.1 | chr14:100086954-100086975 | GGAGCAGTGAGGGAAAGGGGG | + | 6.22 | ZNF263 | MA0528.1 | chr14:100086045-100086066 | CCCCCCCGCCCCCCATCCTCC | - | 7.54 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_52517 | chr14:100086322-100087047 | Small_Intestine | SE_65289 | chr14:100085650-100087565 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I099619 | chr14 | 100085769 | 100087363 |
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Enhancer Sequence | AAATGCATCC TTGAAGCTGC AATGTAAGCA GGGGTTCTCA CACCTGCGTG ATGATAAGAC 60 TCAGTGGGAT ACTTGCTTGC CCAGGGTCCC CTACCTAGAG ATGGAAGTCA CCACCTCTGA 120 GTTCTGGAAC ATGTCTGTTT GCCAGTGTCA GAGTAGGGAT CAGGCTGGGA TGTCAAAGTT 180 CAGGAAGCCT AGAGTGCTAA GCCAGGACCT CCAAGCCCCC CCGCCCCCCA TCCTCCCCAT 240 TTGCCCTATG TCACAGCCAG GTGATATTTA GCCCAGCCGT GGTGCGTGGC TGTTCCCGCT 300 GCTGAGCGCC AGTTCTGTTA TACAGAACTC CTATGGGGAC GTGTTTGTGC ACAGCTTTGC 360 TTTCCTGTTG GATTGTTTCC TTGGGGTAAG TTCCCAGAAG TGGGATTCCT GAGTGGAAGG 420 AGGGATATTT TCCCACCCCC AATCCACATC CTTAGCAGAG GCTGGCCCCA GGATGAGGAT 480 CCGGCCTTTC TCCGGCTTCA AGGAGGGGCA GCCAGCAATC CCCGCCTGGC ACTTCCGGAG 540 GAAAATGACA GACCTTTTCC TTTCCTGTAA GAGCTAATTA CCAGCTGGAT GATGCGTTCA 600 CGGCTGTCAG GGCAATGAGG GCCCAGGTGA CTCAATGCCA TCTTTCTTGG ACCCTCCTGG 660 ATTGCTCAGC CAGCCGGTGA TGGATTTTTC TCTGTGGAGG TCACAGGAAA CAAGAAAAGA 720 GTCCCTCAGC TCCCCAGGGA GTCAGGTCTG TCAGCAGCTT TGGGAGAGGG CAGAAAGGAG 780 GCCTTGAAAT CCACTGGGCA GATAATCCCT CTGCCCTTCC AGACAACGAA GGGCTTCTGG 840 CCCCTGGCCT CTCCAACCTG CTGGACAGGA ATGGCTGGCT GAGGGTCCAG GAGCCCCTGC 900 CCTGACCTGG GCTTCTTGCA GGGAGTGCCC TCCCCCTTTT TCTCGCTCCC CATCCCAGCA 960 TCCCTACATC CAGGTCAGGG TCCCTGGCTG GATCCAGCCT CTGAGGGGCA CGAGAAGAGG 1020 GGTGTCCAGG CTCCTCCTTA AGGAAGCCCC TTCCTCCCCG CAGGGGGGCT AAGGGCAGAC 1080 ATCAGCCCCT CCCAGCTGTC ACCACTCAGG TGGGGGGCGG GTCAGGAGCA GTGAGGGAAA 1140 GGGGGACAGG GGCCACTGTG GGAAAGTCAC TTGTGGGCAG TGGCCTACCA GCTTTCCACA 1200 GGAAGGAGGG GTCTTGGCTT CCCAGGGCTC TGGCTGGCTG CCTGAGCCTA AGGGCCACTC 1260 TCCCTCTGCC TGCAGAACGT AGGGGGGCCA GGCCTCTGGG CAGGGCCCAT CTCTGGAGCA 1320 CTCTAGCCCA TTTCCCTCTG GGGACACCCT CTGAAGGAGC AGCAGGAGTC AGACCTGGAG 1380 GCCGGCCCCG CCACTGCCAC CAGCTCACTT CCCCATGAGA GTGCGGATTC TCTGAAGGCA 1440 ACACTCGGGT CTGCCCTGTC CCAGGCTCAA GGTAGTGAGT TCCCTGTCCC TAGAGGTGAA 1500 CAAGCTAAGA 1510
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