Tag | Content |
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EnhancerAtlas ID | HS161-08131 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr19:41112430-41113270 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr19:41113156-41113176 | GCACCCACCAACCCCCCACC | + | 6.06 | RREB1 | MA0073.1 | chr19:41113164-41113184 | CAACCCCCCACCCCCAACCC | + | 6.18 | RREB1 | MA0073.1 | chr19:41113160-41113180 | CCACCAACCCCCCACCCCCA | + | 6.95 |
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| Number of super-enhancer constituents: 15 | ID | Coordinate | Tissue/cell |
SE_19562 | chr19:41108845-41112793 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_23361 | chr19:41107982-41112714 | Colon_Crypt_1 | SE_23361 | chr19:41112780-41114625 | Colon_Crypt_1 | SE_23880 | chr19:41110524-41112653 | Colon_Crypt_2 | SE_23880 | chr19:41112899-41114599 | Colon_Crypt_2 | SE_24744 | chr19:41106882-41112618 | Colon_Crypt_3 | SE_24744 | chr19:41112813-41114756 | Colon_Crypt_3 | SE_26743 | chr19:41105087-41114655 | Esophagus | SE_31942 | chr19:41105610-41112707 | Gastric | SE_31942 | chr19:41112892-41114639 | Gastric | SE_34376 | chr19:41106131-41114683 | HCT-116 | SE_35142 | chr19:41107199-41114860 | HeLa | SE_50342 | chr19:41104847-41112785 | Sigmoid_Colon | SE_50342 | chr19:41112849-41114801 | Sigmoid_Colon | SE_52682 | chr19:41107240-41114649 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I040606 | chr19 | 41112681 | 41114310 |
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Enhancer Sequence | CTGTGAGCAA CCAGCAGGGA GCTGAGGCTG GGTCCCGCCC TCCCTGCCCT CAGAAGTCCC 60 AGAGCATCCT GGGGCCTTTA ATTCCCTCGG ACCCCCCCAG ACTCCCGGGT TCCTCTGTCA 120 GCCTTAGAGC CCCCTCAGAA CTTCTCAGAT TCTTATACAG CTTCAGCATC CCTGGACCAC 180 CTTTAGACCT TTCAAGCCTT TTGGATCCAG ATCCCTCCAG ACTCCCAGAC TTTTTTTTTT 240 GGAGATGGAG TCTCGCTCTG TCGCCCAGGC TGGAGTGCAG TGGCGCGATC TCGGCTCACT 300 GCAATCTCTG CCTCCTGGTT TCAAGTGATT CTCCTGCCTC GGCCTCCCGA GTAGCTAGAA 360 CTACAGGCGG GCACCACCAT GCCCGGCTAA ATTTTTTTGT ATTTTTGGTA GAGACAGGGT 420 TTCGCCACGT TGGCCAGGCT GGCCTCAAAC CCCTGGCTTC AAGTGATCTG CCCACCTCAG 480 CCTCCCAAAG TGCTGGGATT ACAGGCGTAA GCCACTGCGC CCAGCTCTCC CAGACTTTCT 540 GGAATCCTTC TCAGACCCCC AAATCCTCTC GTCCCCCTCA ACGACTCGAC TATCTTCAGA 600 TCTTGAGATC CTTCTCAGAG TCTCTCATTC ACCACTGACA CCCCATTGAG GCTCCAAGCC 660 CTTCTCAGAC CTCCAGAGCC CACTGCTCTC CTTCAGACCC TCTCAGACCT CTCCCAAATG 720 CCCCTCGCAC CCACCAACCC CCCACCCCCA ACCCCAGAAC CATTCCCCTC TCTCCCAAAT 780 CCCTCAGTGC TACAGCATTC CCAGCCCCGC CCTGAAGGAT TTCCTCCCTG CTCCTCGCAG 840
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