| Tag | Content |
|---|
EnhancerAtlas ID | HS176-13124 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr14:100085890-100087390 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
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 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_52517 | chr14:100086322-100087047 | Small_Intestine | | SE_65289 | chr14:100085650-100087565 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I099619 | chr14 | 100085769 | 100087363 |
|
Enhancer Sequence | TCAGTGGGAT ACTTGCTTGC CCAGGGTCCC CTACCTAGAG ATGGAAGTCA CCACCTCTGA 60
GTTCTGGAAC ATGTCTGTTT GCCAGTGTCA GAGTAGGGAT CAGGCTGGGA TGTCAAAGTT 120
CAGGAAGCCT AGAGTGCTAA GCCAGGACCT CCAAGCCCCC CCGCCCCCCA TCCTCCCCAT 180
TTGCCCTATG TCACAGCCAG GTGATATTTA GCCCAGCCGT GGTGCGTGGC TGTTCCCGCT 240
GCTGAGCGCC AGTTCTGTTA TACAGAACTC CTATGGGGAC GTGTTTGTGC ACAGCTTTGC 300
TTTCCTGTTG GATTGTTTCC TTGGGGTAAG TTCCCAGAAG TGGGATTCCT GAGTGGAAGG 360
AGGGATATTT TCCCACCCCC AATCCACATC CTTAGCAGAG GCTGGCCCCA GGATGAGGAT 420
CCGGCCTTTC TCCGGCTTCA AGGAGGGGCA GCCAGCAATC CCCGCCTGGC ACTTCCGGAG 480
GAAAATGACA GACCTTTTCC TTTCCTGTAA GAGCTAATTA CCAGCTGGAT GATGCGTTCA 540
CGGCTGTCAG GGCAATGAGG GCCCAGGTGA CTCAATGCCA TCTTTCTTGG ACCCTCCTGG 600
ATTGCTCAGC CAGCCGGTGA TGGATTTTTC TCTGTGGAGG TCACAGGAAA CAAGAAAAGA 660
GTCCCTCAGC TCCCCAGGGA GTCAGGTCTG TCAGCAGCTT TGGGAGAGGG CAGAAAGGAG 720
GCCTTGAAAT CCACTGGGCA GATAATCCCT CTGCCCTTCC AGACAACGAA GGGCTTCTGG 780
CCCCTGGCCT CTCCAACCTG CTGGACAGGA ATGGCTGGCT GAGGGTCCAG GAGCCCCTGC 840
CCTGACCTGG GCTTCTTGCA GGGAGTGCCC TCCCCCTTTT TCTCGCTCCC CATCCCAGCA 900
TCCCTACATC CAGGTCAGGG TCCCTGGCTG GATCCAGCCT CTGAGGGGCA CGAGAAGAGG 960
GGTGTCCAGG CTCCTCCTTA AGGAAGCCCC TTCCTCCCCG CAGGGGGGCT AAGGGCAGAC 1020
ATCAGCCCCT CCCAGCTGTC ACCACTCAGG TGGGGGGCGG GTCAGGAGCA GTGAGGGAAA 1080
GGGGGACAGG GGCCACTGTG GGAAAGTCAC TTGTGGGCAG TGGCCTACCA GCTTTCCACA 1140
GGAAGGAGGG GTCTTGGCTT CCCAGGGCTC TGGCTGGCTG CCTGAGCCTA AGGGCCACTC 1200
TCCCTCTGCC TGCAGAACGT AGGGGGGCCA GGCCTCTGGG CAGGGCCCAT CTCTGGAGCA 1260
CTCTAGCCCA TTTCCCTCTG GGGACACCCT CTGAAGGAGC AGCAGGAGTC AGACCTGGAG 1320
GCCGGCCCCG CCACTGCCAC CAGCTCACTT CCCCATGAGA GTGCGGATTC TCTGAAGGCA 1380
ACACTCGGGT CTGCCCTGTC CCAGGCTCAA GGTAGTGAGT TCCCTGTCCC TAGAGGTGAA 1440
CAAGCTAAGA GAGCATGGCC ATCTCACAGA GGTATAGAGG AAGTGCTTGC TGTGAGCACC 1500
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