| Tag | Content |
|---|
EnhancerAtlas ID | HS196-04730 |
Organism | Homo sapiens |
Tissue/cell | ZR75-1 |
Coordinate | chr1:228973560-228974910 |
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 | TGCTGTGCTT CCATGGGGCA GTCAGGGCTC AGGGCCCCAG CAGCAGGCCA AACCCCAGCC 60
CAGCTCCCTT GCAAACCTCC TCTGTCATGT ACCCTGGGAG TCAGGTCCAA CCCCACTATG 120
TCACAACTGA GGAAACAGAG GCCCCGAGAA GTTCAGGGAG AGCTGGGGTC AAGATGCTAG 180
ATCCTGCCTC TGGGTGTGGT GGCTTTTGTT CTTGTCATCC GGTGGGCACT GGGCCTGCCC 240
CGCACAGCTC CTTCACCCCG GAGAGGTGAC AGCAGACTAC ATTAGGCCCT GCCAGGCCCA 300
AAGACTCCAG CCTGTTAATC TTTAACCAGA GCTCTGGACA AAGGTAGCCC TTCTGACCTC 360
CTGAGAGTTT CTGAATAGCT CGGAGGCTTC TGTGACAGAG CCACACGTTA GCAATGACAT 420
ATATTTAGTG CAGGGAGGCA TGTTGAGTAC AGTTCTAAAT TCTGTTGTGA ATTGTGCCCA 480
GGGAACAAGC ACAGAGAACA TTTTCACCAT GGATATGTAT GTACTTGTAA GAAGCAGCTG 540
GGTGGTTCCT TCAGCAATCT GCTGAGCTGT GGCGATTACA TCACACACTG GTGCAAAGGC 600
CTTGAACCAT TAATGTGCTG CCTCTGCGAG GGTGACCAGG ATTCCAGCAA TGAACAGAGA 660
AGGTGCTTGT CCCCACTGCT CACTGGGTGC CTTCAGATTC TTAACTTTTG TCTTTTTCTT 720
TTTTCTTTCA CTTCTTACCT GTATCTATAA AACAGGACTC TGTTTGCTTT GAAAAGAGCC 780
AGAATGACCT CAGGGGTCAG TGACTCATGC TGTTGGCTCT GTGAACACAA TCGAGTGCCC 840
CTTACGTAAG AAGCTCCTGC TATCTGAGGG AAGGGAGGTC CGAGCCATTA TTCCTTGGTT 900
ATAAACACTC CATGTGGTTT TGTTTGGTGG TTTTAAAAAA GGTGTGTCCA CAGGGTTGGT 960
GTTCTAGAAT CGTGGGCAGA AAGAAGTCTA GCTCCTTTCA TCCAAGGTTC TAAAGGGTTC 1020
TCTGAGCTGT AACTCAGCTC TAACTGGACA AAGAGGCAAC AATTCCCCTC ATTTCCTGTG 1080
CGCTGTCACC ACAGGAGGCT ACACTTAAGG AGGTCAACTC AAGTTGTTTG GACCAAGCTT 1140
CCGCAGTTGT TCCCATTATC CTGTTTGAAT CCATTCACTC TTACACTGGC CATGCAAATA 1200
GACACTCCCC AAGGAAAGAA GGACCTTAGA AAATAAGTGA TCTCAGTTTT CATCTGACTT 1260
TCTTCTGGGG TGTGGGGCTG GTCATGGGTC TATATTCCCT GCTGTGGTCA GGGCCCTGTG 1320
GGACATGTGG CTGTGTCCCA GCCCTCTAGC 1350
|
