Tag | Content |
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EnhancerAtlas ID | HS161-08609 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr2:20435390-20436320 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr2:20436256-20436274 | CCTTCCTTCCCACCCTTC | - | 6.03 | EWSR1-FLI1 | MA0149.1 | chr2:20436268-20436286 | CCCTTCTTCCCTCCCTCC | - | 6.04 | EWSR1-FLI1 | MA0149.1 | chr2:20436272-20436290 | TCTTCCCTCCCTCCCTCC | - | 6.16 | EWSR1-FLI1 | MA0149.1 | chr2:20436244-20436262 | CTTCCTTCCCTTCCTTCC | - | 6.1 | EWSR1-FLI1 | MA0149.1 | chr2:20436199-20436217 | CTTTCCTTCTTTCCTCTC | - | 6.24 | EWSR1-FLI1 | MA0149.1 | chr2:20436243-20436261 | CCTTCCTTCCCTTCCTTC | - | 6.33 | EWSR1-FLI1 | MA0149.1 | chr2:20436183-20436201 | CCTTTCTTCTTTCCTTCT | - | 6.47 | EWSR1-FLI1 | MA0149.1 | chr2:20436175-20436193 | CCTTTCTTCCTTTCTTCT | - | 6.64 | EWSR1-FLI1 | MA0149.1 | chr2:20436219-20436237 | CCTCCCTTCCTTCCCACC | - | 6.6 | EWSR1-FLI1 | MA0149.1 | chr2:20436227-20436245 | CCTTCCCACCCTCCTTCC | - | 6.78 | EWSR1-FLI1 | MA0149.1 | chr2:20436281-20436299 | CCTCCCTCCCTTCCTCCC | - | 6.92 | EWSR1-FLI1 | MA0149.1 | chr2:20436223-20436241 | CCTTCCTTCCCACCCTCC | - | 6.94 | EWSR1-FLI1 | MA0149.1 | chr2:20436191-20436209 | CTTTCCTTCTTTCCTTCT | - | 6.95 | EWSR1-FLI1 | MA0149.1 | chr2:20436187-20436205 | TCTTCTTTCCTTCTTTCC | - | 6.96 | EWSR1-FLI1 | MA0149.1 | chr2:20436231-20436249 | CCCACCCTCCTTCCTTCC | - | 7.03 | EWSR1-FLI1 | MA0149.1 | chr2:20436277-20436295 | CCTCCCTCCCTCCCTTCC | - | 7.08 | EWSR1-FLI1 | MA0149.1 | chr2:20436171-20436189 | TCTTCCTTTCTTCCTTTC | - | 7.18 | EWSR1-FLI1 | MA0149.1 | chr2:20436215-20436233 | TCTCCCTCCCTTCCTTCC | - | 7.25 | EWSR1-FLI1 | MA0149.1 | chr2:20436293-20436311 | CCTCCCTTCCTTCCTTAC | - | 7.82 | EWSR1-FLI1 | MA0149.1 | chr2:20436195-20436213 | CCTTCTTTCCTTCTTTCC | - | 7.85 | EWSR1-FLI1 | MA0149.1 | chr2:20436252-20436270 | CCTTCCTTCCTTCCCACC | - | 7.87 | EWSR1-FLI1 | MA0149.1 | chr2:20436297-20436315 | CCTTCCTTCCTTACTTCT | - | 7.88 | EWSR1-FLI1 | MA0149.1 | chr2:20436179-20436197 | TCTTCCTTTCTTCTTTCC | - | 7 | EWSR1-FLI1 | MA0149.1 | chr2:20436285-20436303 | CCTCCCTTCCTCCCTTCC | - | 8.06 | EWSR1-FLI1 | MA0149.1 | chr2:20436239-20436257 | CCTTCCTTCCTTCCCTTC | - | 8.32 | EWSR1-FLI1 | MA0149.1 | chr2:20436248-20436266 | CTTCCCTTCCTTCCTTCC | - | 8.57 | EWSR1-FLI1 | MA0149.1 | chr2:20436235-20436253 | CCCTCCTTCCTTCCTTCC | - | 9.72 | EWSR1-FLI1 | MA0149.1 | chr2:20436289-20436307 | CCTTCCTCCCTTCCTTCC | - | 9.83 | TFAP2C | MA0524.2 | chr2:20435652-20435664 | TGCCCTGGGGCA | + | 6.44 | TFAP2C | MA0524.2 | chr2:20435652-20435664 | TGCCCTGGGGCA | - | 7.22 | ZNF263 | MA0528.1 | chr2:20436202-20436223 | TCCTTCTTTCCTCTCTCCCTC | - | 6.12 | ZNF263 | MA0528.1 | chr2:20436227-20436248 | CCTTCCCACCCTCCTTCCTTC | - | 6.16 | ZNF263 | MA0528.1 | chr2:20436206-20436227 | TCTTTCCTCTCTCCCTCCCTT | - | 6.18 | ZNF263 | MA0528.1 | chr2:20436244-20436265 | CTTCCTTCCCTTCCTTCCTTC | - | 6.24 | ZNF263 | MA0528.1 | chr2:20436289-20436310 | CCTTCCTCCCTTCCTTCCTTA | - | 6.32 | ZNF263 | MA0528.1 | chr2:20436240-20436261 | CTTCCTTCCTTCCCTTCCTTC | - | 6.39 | ZNF263 | MA0528.1 | chr2:20436276-20436297 | CCCTCCCTCCCTCCCTTCCTC | - | 6.54 | ZNF263 | MA0528.1 | chr2:20436256-20436277 | CCTTCCTTCCCACCCTTCTTC | - | 6.61 | ZNF263 | MA0528.1 | chr2:20436211-20436232 | CCTCTCTCCCTCCCTTCCTTC | - | 6.67 | ZNF263 | MA0528.1 | chr2:20436272-20436293 | TCTTCCCTCCCTCCCTCCCTT | - | 6.85 | ZNF263 | MA0528.1 | chr2:20436285-20436306 | CCTCCCTTCCTCCCTTCCTTC | - | 6.93 | ZNF263 | MA0528.1 | chr2:20436280-20436301 | CCCTCCCTCCCTTCCTCCCTT | - | 7.27 | ZNF263 | MA0528.1 | chr2:20436268-20436289 | CCCTTCTTCCCTCCCTCCCTC | - | 7.49 | ZNF263 | MA0528.1 | chr2:20436277-20436298 | CCTCCCTCCCTCCCTTCCTCC | - | 7.9 | ZNF263 | MA0528.1 | chr2:20436223-20436244 | CCTTCCTTCCCACCCTCCTTC | - | 8.06 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_02914 | chr2:20435910-20436272 | Bladder | SE_23108 | chr2:20435429-20436301 | Colon_Crypt_1 | SE_23761 | chr2:20435435-20436241 | Colon_Crypt_2 | SE_24805 | chr2:20435425-20436239 | Colon_Crypt_3 | SE_26530 | chr2:20435190-20437204 | Esophagus | SE_35878 | chr2:20430227-20437683 | HMEC | SE_50296 | chr2:20435375-20436284 | Sigmoid_Colon | SE_56896 | chr2:20435280-20436289 | VACO_400 | SE_64257 | chr2:20435164-20437609 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH02I020230 | chr2 | 20430368 | 20437558 |
|
Enhancer Sequence | CCCCTTCTGA TGGGTGCCAT TTTTAAAGGC TTTGCTGTCA CAAACAATAC TGTTGAATAT 60 CCTCACGTGG ACATCGTCCC ACAGCTGACA AACCTTTCTT AGGACAGAAG TGGCCTGGCT 120 GCCTTGGAGG AGATTCTGAG ACCACTGCTA CATTGCTCTC CCCAAACGCT GTGTCTCCAT 180 GGTCCTTTGG ATGCTCTTAA ATTGCAGCGA GCGCCCACTC CCAGCCAGGG CCTGGGGGTG 240 CATGCTGTCC AAGGCAGGGC CCTGCCCTGG GGCAACTGCA ATCTTTGAGT CCTATGATGA 300 GATGGTTCAA GAGCCAGGGG CCCCAGTCCT GGGTTGCAGG GAGGAGTTCA GGGAAGGCTT 360 CCTGGAGGAG TTGACGTCCA GGCAGAAACC TGCCTGCTGA GTAGCAGTTT GTCAGGCAGG 420 GGAGCAAGTG GGCAGGGCTG CTCAAGCTAG GGGAGGACTT GGCCAGCTGA GGCCCTGAAA 480 GGGCCAGGGC CATCTACGCA CCGCTGAGTA ATGGTGTTCC CTAAATGCTC AGGGCAGTGG 540 CTGAAGGGAG TGGCAGTGGG TGGGGATGAC AGGAAGCTGG GGCAACCGGT GAAGGCCTTC 600 ACTGCCAAGC TAAGGAGTGG GAATGTTGCC CAGGGCAAGC GAGAGCCTGA TTACACACCT 660 GAGGAAGTGA GCCATAGGCT GGAGGGGAGA AAGGACCAGT GCCCTGGGAT GGAGGCTGGG 720 TGGGAATTCA CACCTGGCAA GAGCCCACCA GGAGCCAGGC CCTGTGTAAG GAGAAGCCCC 780 CTCTTCCTTT CTTCCTTTCT TCTTTCCTTC TTTCCTTCTT TCCTCTCTCC CTCCCTTCCT 840 TCCCACCCTC CTTCCTTCCT TCCCTTCCTT CCTTCCCACC CTTCTTCCCT CCCTCCCTCC 900 CTTCCTCCCT TCCTTCCTTA CTTCTTCCTT 930
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