| Tag | Content |
|---|
EnhancerAtlas ID | HS092-05031 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:228973470-228975000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr1:228974358-228974369 | AGTGACTCATG | + | 6.14 | | Gata4 | MA0482.1 | chr1:228974957-228974968 | TCTTATCTCCT | + | 6.14 | | HNF1A | MA0046.2 | chr1:228973872-228973887 | TGTTAATCTTTAACC | - | 6.36 | | HNF1B | MA0153.2 | chr1:228973873-228973886 | GTTAATCTTTAAC | - | 6.18 |
|
| | 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 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I228834 | chr1 | 228970561 | 228975769 |
|
Enhancer Sequence | ACCTTCCTGT GGATGGAACT TGCCAGAACT TCCTCAGCAA CCCTGAAGAG GAAAGCTGGA 60
GGCCCCAACA GACGCAGAAG TGGGCTGCAC TGCTGTGCTT CCATGGGGCA GTCAGGGCTC 120
AGGGCCCCAG CAGCAGGCCA AACCCCAGCC CAGCTCCCTT GCAAACCTCC TCTGTCATGT 180
ACCCTGGGAG TCAGGTCCAA CCCCACTATG TCACAACTGA GGAAACAGAG GCCCCGAGAA 240
GTTCAGGGAG AGCTGGGGTC AAGATGCTAG ATCCTGCCTC TGGGTGTGGT GGCTTTTGTT 300
CTTGTCATCC GGTGGGCACT GGGCCTGCCC CGCACAGCTC CTTCACCCCG GAGAGGTGAC 360
AGCAGACTAC ATTAGGCCCT GCCAGGCCCA AAGACTCCAG CCTGTTAATC TTTAACCAGA 420
GCTCTGGACA AAGGTAGCCC TTCTGACCTC CTGAGAGTTT CTGAATAGCT CGGAGGCTTC 480
TGTGACAGAG CCACACGTTA GCAATGACAT ATATTTAGTG CAGGGAGGCA TGTTGAGTAC 540
AGTTCTAAAT TCTGTTGTGA ATTGTGCCCA GGGAACAAGC ACAGAGAACA TTTTCACCAT 600
GGATATGTAT GTACTTGTAA GAAGCAGCTG GGTGGTTCCT TCAGCAATCT GCTGAGCTGT 660
GGCGATTACA TCACACACTG GTGCAAAGGC CTTGAACCAT TAATGTGCTG CCTCTGCGAG 720
GGTGACCAGG ATTCCAGCAA TGAACAGAGA AGGTGCTTGT CCCCACTGCT CACTGGGTGC 780
CTTCAGATTC TTAACTTTTG TCTTTTTCTT TTTTCTTTCA CTTCTTACCT GTATCTATAA 840
AACAGGACTC TGTTTGCTTT GAAAAGAGCC AGAATGACCT CAGGGGTCAG TGACTCATGC 900
TGTTGGCTCT GTGAACACAA TCGAGTGCCC CTTACGTAAG AAGCTCCTGC TATCTGAGGG 960
AAGGGAGGTC CGAGCCATTA TTCCTTGGTT ATAAACACTC CATGTGGTTT TGTTTGGTGG 1020
TTTTAAAAAA GGTGTGTCCA CAGGGTTGGT GTTCTAGAAT CGTGGGCAGA AAGAAGTCTA 1080
GCTCCTTTCA TCCAAGGTTC TAAAGGGTTC TCTGAGCTGT AACTCAGCTC TAACTGGACA 1140
AAGAGGCAAC AATTCCCCTC ATTTCCTGTG CGCTGTCACC ACAGGAGGCT ACACTTAAGG 1200
AGGTCAACTC AAGTTGTTTG GACCAAGCTT CCGCAGTTGT TCCCATTATC CTGTTTGAAT 1260
CCATTCACTC TTACACTGGC CATGCAAATA GACACTCCCC AAGGAAAGAA GGACCTTAGA 1320
AAATAAGTGA TCTCAGTTTT CATCTGACTT TCTTCTGGGG TGTGGGGCTG GTCATGGGTC 1380
TATATTCCCT GCTGTGGTCA GGGCCCTGTG GGACATGTGG CTGTGTCCCA GCCCTCTAGC 1440
ACAATCTGCC GTCACTCCTG GGCTTTTGTA TGCCTGCTCC CATTTGCTCT TATCTCCTCA 1500
ACAACCACGT CAGGTAGATA ATACATACCA 1530
|
