| Tag | Content |
|---|
EnhancerAtlas ID | HS130-02903 |
Organism | Homo sapiens |
Tissue/cell | MDA-MB-231 |
Coordinate | chr1:228973360-228974790 |
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 | TCAGGTTGCT CCCCTGAGCA AGGCCAAGCT CAGTTTTCAC CTGGTGGTCC CATGGGGAGC 60
TTCCTGTGGC TTAGTGTTTG CGTCTGCCAT TTGCTATCCC TCCCCAGCAC ACCTTCCTGT 120
GGATGGAACT TGCCAGAACT TCCTCAGCAA CCCTGAAGAG GAAAGCTGGA GGCCCCAACA 180
GACGCAGAAG TGGGCTGCAC TGCTGTGCTT CCATGGGGCA GTCAGGGCTC AGGGCCCCAG 240
CAGCAGGCCA AACCCCAGCC CAGCTCCCTT GCAAACCTCC TCTGTCATGT ACCCTGGGAG 300
TCAGGTCCAA CCCCACTATG TCACAACTGA GGAAACAGAG GCCCCGAGAA GTTCAGGGAG 360
AGCTGGGGTC AAGATGCTAG ATCCTGCCTC TGGGTGTGGT GGCTTTTGTT CTTGTCATCC 420
GGTGGGCACT GGGCCTGCCC CGCACAGCTC CTTCACCCCG GAGAGGTGAC AGCAGACTAC 480
ATTAGGCCCT GCCAGGCCCA AAGACTCCAG CCTGTTAATC TTTAACCAGA GCTCTGGACA 540
AAGGTAGCCC TTCTGACCTC CTGAGAGTTT CTGAATAGCT CGGAGGCTTC TGTGACAGAG 600
CCACACGTTA GCAATGACAT ATATTTAGTG CAGGGAGGCA TGTTGAGTAC AGTTCTAAAT 660
TCTGTTGTGA ATTGTGCCCA GGGAACAAGC ACAGAGAACA TTTTCACCAT GGATATGTAT 720
GTACTTGTAA GAAGCAGCTG GGTGGTTCCT TCAGCAATCT GCTGAGCTGT GGCGATTACA 780
TCACACACTG GTGCAAAGGC CTTGAACCAT TAATGTGCTG CCTCTGCGAG GGTGACCAGG 840
ATTCCAGCAA TGAACAGAGA AGGTGCTTGT CCCCACTGCT CACTGGGTGC CTTCAGATTC 900
TTAACTTTTG TCTTTTTCTT TTTTCTTTCA CTTCTTACCT GTATCTATAA AACAGGACTC 960
TGTTTGCTTT GAAAAGAGCC AGAATGACCT CAGGGGTCAG TGACTCATGC TGTTGGCTCT 1020
GTGAACACAA TCGAGTGCCC CTTACGTAAG AAGCTCCTGC TATCTGAGGG AAGGGAGGTC 1080
CGAGCCATTA TTCCTTGGTT ATAAACACTC CATGTGGTTT TGTTTGGTGG TTTTAAAAAA 1140
GGTGTGTCCA CAGGGTTGGT GTTCTAGAAT CGTGGGCAGA AAGAAGTCTA GCTCCTTTCA 1200
TCCAAGGTTC TAAAGGGTTC TCTGAGCTGT AACTCAGCTC TAACTGGACA AAGAGGCAAC 1260
AATTCCCCTC ATTTCCTGTG CGCTGTCACC ACAGGAGGCT ACACTTAAGG AGGTCAACTC 1320
AAGTTGTTTG GACCAAGCTT CCGCAGTTGT TCCCATTATC CTGTTTGAAT CCATTCACTC 1380
TTACACTGGC CATGCAAATA GACACTCCCC AAGGAAAGAA GGACCTTAGA 1430
|
