| Tag | Content |
|---|
EnhancerAtlas ID | HS101-29092 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr22:43670820-43672880 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr22:43671836-43671854 | GGGAGGCAGGAAGGCAGC | + | 6.18 | | EWSR1-FLI1 | MA0149.1 | chr22:43671259-43671277 | GGAAGGGAGCAAGGTGGG | + | 6.36 | | MYB | MA0100.3 | chr22:43672213-43672223 | GACAGTTGGT | - | 6.02 | | ZEB1 | MA0103.3 | chr22:43672173-43672184 | GGGCAGGTGGG | - | 6.14 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I043275 | chr22 | 43671581 | 43671990 |
|
Enhancer Sequence | ACAAGCAGTG GCGCTCACTT CCTCTCCCTC AGCTGTGCAT GAGGGGCGGC AGCGGGTACT 60
TCTCATGGCC CTTCGAGGAC AAAAGGGGCT CATGGGCTCG GGGCACAGTA GGTACGTTTG 120
GATCATCGGC AGGTACAGCC ACTTTGGGGA CATAAGCCAA TTCCCGCCAC CGACTCAAAC 180
TTAGTCTGGT GACTTGTCGC TGCACTCAAC AGACAAACGT GTGGGCGATC TGTGATGTGC 240
CCTGGGGGCA CAGGAGTCAG GCGCTCTGTG ATGTGGAGGC GAGGCTGGGC AGCGGGAGGG 300
AAAGGTGTTC TGGAGCAGGA ACAAGCCCAT GCAGAGGCCT GGGGAGTGAG GCTGGGGGTC 360
TCTGCGCTTC TGACAGACAA ACTGGGGCTG GAGAGGCCTC GTGGAGAGAA GCCGGCAGAC 420
CTGCAAGCTG ACCAGCTGTG GAAGGGAGCA AGGTGGGACA GCAGTGCAGG ACCCAGCAAA 480
CCACGACGCG CTGGGCGTCC CTCTCCTGGC GGTGGGCTGG GCACACTGCT CTGCACGAGG 540
GGTGTGAAGG CACTTTGTGA ACGGATGATG CACACACTTC GGGCATGAGT CCCTCATGAG 600
ATGGTCTCAT CTCCTCTACA CTCCCATGCG GCATGTTTTC CTCTGCACCC TGCCCTGTGT 660
GAGACGTGAG AAACACAAGG ATGACTTAAA CACATCCCTG CCCTTCTTGG GAGCTCATGG 720
ACTGGTCCTG CAGTAGAGGG CTGAACCATT TCAAACACAT GAGTGCAAGT AAAGAGGAAG 780
ACGTGCACGC CTGCCTAAGA GTCAGAGACA GCTTCAGAGA GGAGGTGAAA GTGCGCTGGG 840
TTTTGATGGA TGACTAAGAG TTCTCCAGGA AGGGAGGGGA ATGGGAAATG GCAGTAAAGG 900
CAGAGGATGA CACATACCGA GGTTGTAATC AGTAAAGGGC ACGTGTGCCG TAACAGGGAG 960
AACAACAGGC AGATGGGGAG GAACCAGGAG AGAGGAACTG GACTGTGGGA GGCCTTGGGA 1020
GGCAGGAAGG CAGCAGTGCC TGACAATGGA GGAACTCGGA GGGGGGCGGA GAAAGCGCCC 1080
CGGCTGCAGG ATGCAGGAGG GAAGGGGGAT GAGGCGGAGG TAGGGACACC AATTAGCAAC 1140
CACAACCTTT GAAGAAGGCA GGGCAACAGG GGTGAGGAAG CTGGCTGGGT TTGGGAGGTG 1200
AGTAGAGCTC GGACGTGGGA TCCGGTCACA CTAGGATGTG GGAGCCACAC AGGGGAAGGG 1260
TGAAGGCAGC ACCCCAGCGC TGGTGCCCCA CTGATGGGGG ACGCGCTAGG AAGCACAGGT 1320
CTGGGAGGAT GGGAAGATGC TGCGTTTGGT TTTGGGCAGG TGGGAATTCT GTAGCTGGGG 1380
TCCCCGTCTA GGGGACAGTT GGTACTGGGG TCAGAGCTGG AGAAGTGGCC ACTGCTGGTC 1440
AGCAAGGAGA CTCAAGAAGC TTAGGGGAGA GCTAGGAGAG GGCTGAGGCA GAGGAGGAGC 1500
CAGGATCGGG GGCTGAGGAG GAAGGGAAGA AGTCCCATGG GACGTACATG CTGAAAGAGT 1560
CTGGTGACAT AATCAAGCAG CCACCAGGCC GGGAGACAAA AACCCACCTG GCTGGCCTCA 1620
GGCGGGTGAC GAGGACCTGG GGAATGCTGC GGCCAGGGGT GGCCAGGCAG ACGTCCCACC 1680
AGGAGATTGG CCTTGTGGCC ACAGTCACAA CCCAATTTCC CTAATGAGGC TAGGGAGGGC 1740
TCACACCACT CCCTAATGAC CCAGGATGAC CTCGGCTGCT TCCCCACTCT GCCAACCAGG 1800
CATCTGCCCG GTGGTTTCCG AACCCACACT CCAGATCTGC ATGACTTTCC ATGCGTAGGG 1860
CCTGTGCCCA CAAACCCCAG GTGGGAAGCC AGGCTGTGGG CTACGGTGTA GGGGGTGGGC 1920
ACTGGTCTGG AGCCTAGGGG CCTGGGACAA GTTCCAGCTC TGCCCCCAAC ATGCTAAGTG 1980
ACCTCTGACA GGACACATGG TGTTTCCAGG GCCTCTGCTA CTTCACTCTA GAACAGGCGT 2040
GCAGGCCAGC TTCCCTCCAG 2060
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