Tag | Content |
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EnhancerAtlas ID | HS094-17542 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr17:79333280-79334430 |
Target genes | Number: 28 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr17:79333283-79333301 | TCCTCCTTCCCTCCCTCC | - | 6.4 | Foxd3 | MA0041.1 | chr17:79334357-79334369 | AATTGTTTGTTT | + | 6.22 | ZNF263 | MA0528.1 | chr17:79333296-79333317 | CCTCCCTCATTCCCTTCCTCT | - | 6.09 | ZNF263 | MA0528.1 | chr17:79333287-79333308 | CCTTCCCTCCCTCCCTCATTC | - | 6.89 | ZNF263 | MA0528.1 | chr17:79333283-79333304 | TCCTCCTTCCCTCCCTCCCTC | - | 8.43 | Zfx | MA0146.2 | chr17:79333569-79333583 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_27741 | chr17:79334036-79334801 | Fetal_Intestine | SE_68308 | chr17:79314112-79339705 | TC32 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I081359 | chr17 | 79333607 | 79335099 |
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Enhancer Sequence | CCTTCCTCCT TCCCTCCCTC CCTCATTCCC TTCCTCTCTC TCTCTCTTTC TCTCTTTCTT 60 TTTGAAACAG AGTGTCACTC TGTCACCCAG GCTGGAATGC AGTGGCGCTA TCTCAGCTCA 120 CTGCAACCTC TGTCTCCCGG GTTCAAGTGA TTCTCCTGCC TCAGCCTCCC AAGTAGCTGG 180 GACTACAGGC ACCCACCACC ACACCCGGCT AATTTTTGTA GTTTTAGTAG AGATGGGGTT 240 TTGCCATATT GGCCAGGCTG GTCTCGAACT CCTGACCTTA AATGATCCGC CCGCCTCGGC 300 CTCCCAAAGT GCTGGGATTA CAGGCGTGAG GCACCGTGCC TGGCCAAGAG CTCATTCATT 360 TCTTTGTTGA GTGATATTCC AGGGTGTGGA GGTACCACAG TGTCTTTGAC CATTCACCCA 420 CTGAAAGGCA TCTGGGTTCT TTCTGCTTTC AGCTCTTATG AACAGAGCTG CTGTGTACAT 480 TGATGTTCAG GATTTTGTGT GAACATAAAT CTTTGCTCTG GGACAAATGC CTAGGAATAC 540 AATTGCAGGG CTGTTTAGTA GTTACAAGTT TAATTTTTTT TTTTTTTTTT TTTTTTGAGA 600 TGAAGTCTCA CTCCGTCACC CAGGCTGCAG TGCAGTGGCG CGATCTCCAC TCACTACAAC 660 CTTCGCCTCC CAAGTTCAAG TGATTCTCCT TTCTCAGCCT CCTGAGTAGC TGGGATTACA 720 GGCATGCACC ACCATGCCGT GCTAATTTTT GTATTTTTAG TAGAGATGGG GTTTCTCCAA 780 TATGTTTAAT TTTTAAAGAA ACTGCCAAAC TATCTTCTGG AGAGGTTGTG TCATTTTACA 840 TTCCCACCAG TAACACACAA GTAATTCGGT TTCTCCACAT CCTTGCCAAC ATTTGGTTTC 900 ATGACTATTT TTTACTTTAA CCATCCTGAT AGGCGTGTGC TGGTATCTCA CTGTGTTTTT 960 TAGTTTGCAT TTTCCTGACC ACTGATGATG TTGAACATCT TTTCACGTGC TTATTTGCCA 1020 TCTGTATAAC CTCTCTAGTG AAATGTCTGT TCATGTCTTT AGCTCACTTT CCAATTGAAT 1080 TGTTTGTTTT TTCACCTTTG AGCTTTAAGC ATTCTTTACA TATTTTAGAT ACTAGCCCTT 1140 GGTTTGATAT 1150
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