Tag | Content |
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EnhancerAtlas ID | HS161-03099 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr11:74878820-74880210 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr11:74878930-74878951 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_04383 | chr11:74879055-74880204 | Brain_Anterior_Caudate | SE_24620 | chr11:74879211-74880718 | Colon_Crypt_2 | SE_27748 | chr11:74877568-74883704 | Fetal_Intestine | SE_28613 | chr11:74860563-74883833 | Fetal_Intestine_Large | SE_50381 | chr11:74877676-74879003 | Sigmoid_Colon | SE_50381 | chr11:74879111-74881291 | Sigmoid_Colon | SE_52534 | chr11:74877670-74881343 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I075166 | chr11 | 74877673 | 74882414 |
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Enhancer Sequence | CAGAGAGGGG AGGAACTGCC CCAAGGACAC ACCCAGGTAG CCCTGCCTTA GCTGCTGTTC 60 TGAACTGCCG AATTCTTCCA CTTCTGAATT CCTTATCTGG AGAACTTTGT TCTTTCTTTC 120 TTTTTTTTTT TTTTTTGAGA TGGAGTATCA CTCTGTCACC TAGGCTGGAG TGCAGTGGCT 180 TGAACTTGGC TCACTGCAAC CCCTGCCTCC CAGGTTCAAG CAATTCTCCT GCCTCAGCCT 240 CCTGAGTAGC TGGGATTACA GGCATGTGCC ACCACTCCCG GCTAATTTTT GTATTTTAGT 300 AGCGATGGGA TTTCTCCATG TTGGCCAGCC TGGTCTCAAA CTCCTGATCT CAGGTGATCC 360 ACCCTGCTCG GCCTCCCAAA GTGCTGGGAT TACAGGCATG AGCCACAGCG CCTGGCCAAA 420 TTTTGTTCTT TCTTTCATTT GAAAGATGAA GAAACCAAGG CCCAGAGTGG GTAAGGGCCT 480 CTGTCAAAGT CACACAGCAA GTCCCAGGCA GCCTCCGTGG AAGGCTTCTT TCACGTTCTT 540 GACCTTGGTT CACATGGCTC TTTGCAGCCC AAGGGAGTGG CTCTCCGTGC TGGGTTGACA 600 CAGCTCAGAG TCCCAGCTCC ATAAATGGAG GGCCGCAGAG AGAAGGCTGC TTCTACAGCC 660 ACATTTGGGA TAATAATAGT GTGAGGGTCT CCTCAAGTTT GCTCACCAAA TATTGGTGAG 720 CTCCAGGGAA CAAATGTCAG GTACTAAATT AAGAAATTCT TTTCTGTACT CTGCATCTGT 780 GTCCCAAGCT GACACTGAAC CCTCCCCCAA AGTGAATGCC AAGGGCCCCA GGGCCCTCCA 840 CAATCCAGCC CCAGCTGCCC CACCCTGTTC CACTGTGCCT TCAGCCCTGG CCTTGCCCTC 900 ATACTTTGTG ATCTAGCCAT TCTGAGCTTC TCATTCTCCC GGCACGGTGC CCTTTCAAGT 960 CCCTGGGTTT TGCGTGTACT GTGACCTCTC CCTGGAACAC CCCTCCCCTC CCTCTTTTTC 1020 TGGAAAATTG TGTTTATTCT TCCGGACCCA GTTCAAACTA CACCACCTTT GACCACCCCG 1080 CCCCACCCAG GGGCCACCGT TGCTATGGCA CTTGCAAATG CCTCAGCTCA GAAAGGTGGT 1140 GTAGGGCAGT TTAAGAGCAT GGACTCTGAA GCCAGACCTC CTGAGTTCCA ATCCTGGCCC 1200 TGTCACCTTA CTAGTTGCTG TCTAAGCATC AGTTTCCTCA CCTATGAAAC AGGCATAATG 1260 AGAGCACTCA CCCTTGAGGT TTGTTGTGGG GCTCAAATTA TTTTTATACA CAGCACTTAG 1320 AACAGTACCT TCCCCCGGGG TAAGCGCTAT TTAAGTCTTA GCTATTGTTA TAATATTTTT 1380 TCATTGTCGT 1390
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