Tag | Content |
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EnhancerAtlas ID | HS184-14254 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:73553090-73554230 |
Target genes | Number: 14 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr17:73553238-73553249 | CATGAGTCACT | - | 6.14 | Znf423 | MA0116.1 | chr17:73553867-73553882 | GGCCCCCTGGGGTGC | + | 6.42 | Znf423 | MA0116.1 | chr17:73553867-73553882 | GGCCCCCTGGGGTGC | - | 6.57 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_23798 | chr17:73553213-73554927 | Colon_Crypt_2 | SE_28701 | chr17:73551300-73554667 | Fetal_Intestine_Large | SE_41669 | chr17:73553153-73554910 | LNCaP | SE_47745 | chr17:73553056-73554946 | Pancreas |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I075555 | chr17 | 73551481 | 73554876 |
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Enhancer Sequence | CAGAGTGAGA CTCTGTCTCA AAAACTTTTT TTTTTTTTTT TTTTTTTTTT GTGGAGACAG 60 GGTCTTGTGA TCTTGCCCAG CCTGGTCTTG AACTCCTGGG CTCAAGCAAC TCTCTCGCCT 120 TGGCCTCTCA AAATGCTAGG GTTACAGGCA TGAGTCACTG CACTCCCAGC CTGCAGTTTT 180 GTTTTTTAAC CTATCTCGAT AAGAATCAGA GGTGGACTGG CCCCAGGGCC CTATCCACAA 240 GCAGAGATGG GGTGGCCTTG GGCCAGGAGA GCAGGGCTCG GCAGCTGTCT TCCAAATTCC 300 ACCCCCACTC CCACAGGCGG CAGAGAGTGG AGAGGGCTCT GCCTGGCAGG GACAGTCCTT 360 CCCCGGCCTG AGGCTGGATG TTGTCCAGTT GGGTCATCTT TTATCCAGAG CACTGGTTCT 420 GGCCGACTGG GGGCTCCCAG TGTTTTCAGA GATGAAAAAC CGGATCAGGT TGGGCACCCC 480 GCCAGTCTGA TCTGTGCTCC CCTCAGGGCA GGGCCCAAGG GAGTTGAGAG ATGAGGGACC 540 ACCTCCAATA GCTTGGCTGC CACCTCCAGC GGAGCCTGAC CTCCCTCTTC CCCTCTGCCC 600 GGTGTGGGGG AGGGGTATGG AGCACTCGAG TTCCAGGCTG GGCTGGTGTA CACAGGGGGC 660 CAGGGCCTTG CTGCGGGCTC AGCCTTCCCT CGGCTGGTTA ATCATTGCCA GGCCACAGCC 720 AGACTCTAGT TACCAATCCC TGGTGCCAAG ACTAATGGGC CAAGGCTGTT GGTGATAGGC 780 CCCCTGGGGT GCCGTGTGTT TTTTCACAGG TGCTACCAAG CGACAGCCAA CATGTCTTTT 840 GCAGCTCAGG ATCAGGGTGG CAGCCTGACA GTTGCCAGGG TAGGGCTTCG CCTTTCTATG 900 GAGTTGCTCC CACCGGCCTG ACTGGGAAAA ATCTCCCAGG GATCAGGTCA CTGGCCTGGT 960 GCCCCAGGGC CAGGGCTGCT GTGTCTCCTC CCCACCCTAG GCTCCATGCA TGGGTCCTGC 1020 TGCCTCGGGG GAGGGCAGCC CCTCTCTGTG TTTGCATCAT TGCACATGGG CCCCGAGGGC 1080 CTGGCACTCA AGGCAGGCAG GGGATGGTGT CCGACCTTCC AGAGCTTTCC TGAGCCTACT 1140
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