| Tag | Content |
|---|
EnhancerAtlas ID | HS074-00191 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr1:24677310-24678480 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:24677816-24677834 | TCCTCCTTGGTTCCTTCC | - | 6.21 | | EWSR1-FLI1 | MA0149.1 | chr1:24677802-24677820 | CCTGCCTGCCTTCCTCCT | - | 6.26 | | IRF8 | MA0652.1 | chr1:24677956-24677970 | AGTTTCGGTTTCCA | - | 6.46 | | IRF9 | MA0653.1 | chr1:24677956-24677971 | AGTTTCGGTTTCCAT | - | 7.16 | | RREB1 | MA0073.1 | chr1:24678154-24678174 | GGGGGGTGGGAGGGTGGGGT | - | 6.41 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_26747 | chr1:24676495-24677610 | Esophagus |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I024350 | chr1 | 24676496 | 24677610 |
|
Enhancer Sequence | GTGCCTGGCT GCCTACCATG GGCTCCTGGG CACCAGAGTA CCTTTGTTGT CTGCTCAGAA 60
GATCCCTTGG GAAAGGGAGG TAGGGTCACA TGGTAACTGT CCTCCAGACA TCAGTCCCCT 120
GGTCAGAGCT AGTGAGCCTG TCCTCTGCAG CCCTTCCTGA GTAGGTGACT TCACCAGCCT 180
GGCATAGGGC CCCCAGACAG TGAGGAATTG TCATTGCTGT TGCCAGCCCA GAGGCCCCAG 240
AACCAGAGCC CTGGGAAATG CACTCCTAGC CCCTCTGCCC ACAGCTCCAA TCTGATCCTC 300
TTGCTGTGGA TAGTCTAACT CGAGCGACAT TTGCTAGTAG CCCCTTGGAG GTGCTCAGCC 360
ACTTGCCCCG TGGCTACTGC AAGTGGATCT TCCTTTGTAG AAGACTTTGC AAAGCGAGGC 420
AAGTTTTGTA CTCAAGCTGA ATCCCCATCT CATCAGGCCT AGGGGCCTGG CCGCCTTCCT 480
CACAGGCCCA GCCCTGCCTG CCTTCCTCCT CCTTGGTTCC TTCCTAGCCT TCCATAGAAG 540
GCTGAGGGTG GGGGAAGGTG TCCATCCCTG CAGCCCCTGG GAAGGGGGTT TTTTTTGGTT 600
TTAGCTGCAT GCATGTCTAG AGTTTTTCGT GTGTCTTTTT TTTCCAAGTT TCGGTTTCCA 660
TCTGAGTCTC ACATGCTCTG TAGAGTGAAA TCCACTTCAC GGCAAAGGGC AGGCTCTGCT 720
TTCCCCAGAC AAGCCCAGCC CCACTCTCCC TTCAGCTCCA GTGCCCATGC CCCCTGGCTC 780
CAGCCCCACC TGTGGCAGGC CTCCCTTACC AATCCCACTC CAGGCCAGGC TGTGTGATTG 840
CATGGGGGGG TGGGAGGGTG GGGTGTGTGT ACAAGGATGT TCCCCAGCCC CACTGGCTGA 900
GTTGCCAGAG GCTTCCCCTT AAGCCCCAGC CAGCTATTGA AATCATAATT CTAAAACCTT 960
CCATTTATGG GGCACTTCCT ACATGCCAGG CACTGGGCTG CATCACTCCC AAGCATCATC 1020
TCGTTGACCC TTTGAGCTGG GTATCATTAT CTCTGTTTGT ACGTATGGGG AAACTGAGGT 1080
CTGCAGTAGT TACAAGGTCA TGAGTTAGGA ACTGGCAGAA GCATCTTGGA CTTCTAAAGC 1140
CTGTACAGGC ATCCACTCTG TTATCCTGCC 1170
|
