Tag | Content |
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EnhancerAtlas ID | HS081-01991 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr1:228973790-228974740 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr1:228974358-228974369 | AGTGACTCATG | + | 6.14 | HNF1A | MA0046.2 | chr1:228973872-228973887 | TGTTAATCTTTAACC | - | 6.36 | HNF1B | MA0153.2 | chr1:228973873-228973886 | GTTAATCTTTAAC | - | 6.18 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_23450 | chr1:228971657-228975640 | Colon_Crypt_1 | SE_27943 | chr1:228970281-228975761 | Fetal_Intestine | SE_28861 | chr1:228970139-228975730 | Fetal_Intestine_Large | SE_52925 | chr1:228971171-228975530 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I228834 | chr1 | 228970561 | 228975769 |
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Enhancer Sequence | GGGCCTGCCC CGCACAGCTC CTTCACCCCG GAGAGGTGAC AGCAGACTAC ATTAGGCCCT 60 GCCAGGCCCA AAGACTCCAG CCTGTTAATC TTTAACCAGA GCTCTGGACA AAGGTAGCCC 120 TTCTGACCTC CTGAGAGTTT CTGAATAGCT CGGAGGCTTC TGTGACAGAG CCACACGTTA 180 GCAATGACAT ATATTTAGTG CAGGGAGGCA TGTTGAGTAC AGTTCTAAAT TCTGTTGTGA 240 ATTGTGCCCA GGGAACAAGC ACAGAGAACA TTTTCACCAT GGATATGTAT GTACTTGTAA 300 GAAGCAGCTG GGTGGTTCCT TCAGCAATCT GCTGAGCTGT GGCGATTACA TCACACACTG 360 GTGCAAAGGC CTTGAACCAT TAATGTGCTG CCTCTGCGAG GGTGACCAGG ATTCCAGCAA 420 TGAACAGAGA AGGTGCTTGT CCCCACTGCT CACTGGGTGC CTTCAGATTC TTAACTTTTG 480 TCTTTTTCTT TTTTCTTTCA CTTCTTACCT GTATCTATAA AACAGGACTC TGTTTGCTTT 540 GAAAAGAGCC AGAATGACCT CAGGGGTCAG TGACTCATGC TGTTGGCTCT GTGAACACAA 600 TCGAGTGCCC CTTACGTAAG AAGCTCCTGC TATCTGAGGG AAGGGAGGTC CGAGCCATTA 660 TTCCTTGGTT ATAAACACTC CATGTGGTTT TGTTTGGTGG TTTTAAAAAA GGTGTGTCCA 720 CAGGGTTGGT GTTCTAGAAT CGTGGGCAGA AAGAAGTCTA GCTCCTTTCA TCCAAGGTTC 780 TAAAGGGTTC TCTGAGCTGT AACTCAGCTC TAACTGGACA AAGAGGCAAC AATTCCCCTC 840 ATTTCCTGTG CGCTGTCACC ACAGGAGGCT ACACTTAAGG AGGTCAACTC AAGTTGTTTG 900 GACCAAGCTT CCGCAGTTGT TCCCATTATC CTGTTTGAAT CCATTCACTC 950
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