| Tag | Content |
|---|
EnhancerAtlas ID | HS073-01392 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr1:228973280-228974770 |
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 |
|
| | 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 | ATCATGCCAT TGCACTCCAG TCTGGGCGAC AGAGCAAGAC TGTCTCAAAA AAAACCCCAA 60
AAAAACAAAA AAAACCCATG TCAGGTTGCT CCCCTGAGCA AGGCCAAGCT CAGTTTTCAC 120
CTGGTGGTCC CATGGGGAGC TTCCTGTGGC TTAGTGTTTG CGTCTGCCAT TTGCTATCCC 180
TCCCCAGCAC ACCTTCCTGT GGATGGAACT TGCCAGAACT TCCTCAGCAA CCCTGAAGAG 240
GAAAGCTGGA GGCCCCAACA GACGCAGAAG TGGGCTGCAC TGCTGTGCTT CCATGGGGCA 300
GTCAGGGCTC AGGGCCCCAG CAGCAGGCCA AACCCCAGCC CAGCTCCCTT GCAAACCTCC 360
TCTGTCATGT ACCCTGGGAG TCAGGTCCAA CCCCACTATG TCACAACTGA GGAAACAGAG 420
GCCCCGAGAA GTTCAGGGAG AGCTGGGGTC AAGATGCTAG ATCCTGCCTC TGGGTGTGGT 480
GGCTTTTGTT CTTGTCATCC GGTGGGCACT GGGCCTGCCC CGCACAGCTC CTTCACCCCG 540
GAGAGGTGAC AGCAGACTAC ATTAGGCCCT GCCAGGCCCA AAGACTCCAG CCTGTTAATC 600
TTTAACCAGA GCTCTGGACA AAGGTAGCCC TTCTGACCTC CTGAGAGTTT CTGAATAGCT 660
CGGAGGCTTC TGTGACAGAG CCACACGTTA GCAATGACAT ATATTTAGTG CAGGGAGGCA 720
TGTTGAGTAC AGTTCTAAAT TCTGTTGTGA ATTGTGCCCA GGGAACAAGC ACAGAGAACA 780
TTTTCACCAT GGATATGTAT GTACTTGTAA GAAGCAGCTG GGTGGTTCCT TCAGCAATCT 840
GCTGAGCTGT GGCGATTACA TCACACACTG GTGCAAAGGC CTTGAACCAT TAATGTGCTG 900
CCTCTGCGAG GGTGACCAGG ATTCCAGCAA TGAACAGAGA AGGTGCTTGT CCCCACTGCT 960
CACTGGGTGC CTTCAGATTC TTAACTTTTG TCTTTTTCTT TTTTCTTTCA CTTCTTACCT 1020
GTATCTATAA AACAGGACTC TGTTTGCTTT GAAAAGAGCC AGAATGACCT CAGGGGTCAG 1080
TGACTCATGC TGTTGGCTCT GTGAACACAA TCGAGTGCCC CTTACGTAAG AAGCTCCTGC 1140
TATCTGAGGG AAGGGAGGTC CGAGCCATTA TTCCTTGGTT ATAAACACTC CATGTGGTTT 1200
TGTTTGGTGG TTTTAAAAAA GGTGTGTCCA CAGGGTTGGT GTTCTAGAAT CGTGGGCAGA 1260
AAGAAGTCTA GCTCCTTTCA TCCAAGGTTC TAAAGGGTTC TCTGAGCTGT AACTCAGCTC 1320
TAACTGGACA AAGAGGCAAC AATTCCCCTC ATTTCCTGTG CGCTGTCACC ACAGGAGGCT 1380
ACACTTAAGG AGGTCAACTC AAGTTGTTTG GACCAAGCTT CCGCAGTTGT TCCCATTATC 1440
CTGTTTGAAT CCATTCACTC TTACACTGGC CATGCAAATA GACACTCCCC 1490
|
