Tag | Content |
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EnhancerAtlas ID | HS161-00412 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr1:27173520-27175090 |
Target genes | Number: 18 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr1:27174587-27174602 | GAGGTCAGGAGTTCA | + | 6.22 | ZNF263 | MA0528.1 | chr1:27175068-27175089 | TTCCCCATCTTTCTCTCCTCC | - | 6.25 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_23384 | chr1:27173604-27174629 | Colon_Crypt_1 | SE_23384 | chr1:27174699-27178454 | Colon_Crypt_1 | SE_24351 | chr1:27174710-27177316 | Colon_Crypt_2 | SE_26621 | chr1:27173970-27186608 | Esophagus | SE_34526 | chr1:27174651-27176664 | HCT-116 | SE_50491 | chr1:27174691-27177388 | Sigmoid_Colon | SE_53016 | chr1:27174654-27177272 | Small_Intestine | SE_57686 | chr1:27174839-27175963 | VACO_503 | SE_64263 | chr1:27174693-27178982 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I026847 | chr1 | 27174110 | 27178056 |
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Enhancer Sequence | GGACTACAGG CACACGCCAC CACAACCGGT TAATTTTTTG TATTTTTAGT AGAGACGGGG 60 TTTCACCGTG TTGGTCAGGA TGGTCTCGAT CTCCTGACCT CATGATCCGC CCGCCTCGGC 120 CCCCCAAAGT GCTGGGGTTA CAGATGTGAG CCACCACACC TGGCCAATTG TTCCCTAATT 180 TTTGTTTGTT TTTAGAGACA GGGTCTTGCT CTGTCACCCT GGCTAGAGTG CAATGGAGTG 240 ATCCTGGCTC ATGCTCACTG CAGCCTGGAA CTCCTGGGCT CAAATGATCC TCCCACCTCA 300 GCCTCCTTAG TAGCTGGGAC TATAGTCACA CGCCGTCATA CCCGGCTAAT TTTTGTCATT 360 TTTTATAGAG ATAGGGTCTT CCTATTTGCC CAGGCTCATC TTGAACTCCT GGGCTCAAGC 420 AGTCCTCCCA TCTTGGCCTC CCAAGGTGCT GGGACTACAG GCATGAGCCA CTGCATTCGG 480 CCTGTTTCGT AGTTTTTAAT CTGTAGTCAG ATTTCCACAG TTGCCCTCCA AATGTCTTTT 540 GTTGCTGTGT TTTGTTTTGT TTTTCAAAAT AAGATCCATG ATGTATTGCA TTTGTTTATG 600 TCTCTTAAAT CGCTTTTAAT TTAGAATCAT CTCCTCTCTG CCTCTCTTTC TCTCTCTCTC 660 TTTTTTTTTT AAGACAGGTT CTGGCTTTGT TGCCCAGGCT GGAGTGCAGT GGCGTGATCT 720 TGACTCACTG CAGCCTTCAC CCCCTGGGCT CAAGTGATCC TCACTCCTCA GCCTCCCAAA 780 GTGCTGGGAT TACAGGTGTG AGCTACTGCA CCCGACCTCC TCTCTCTTTT TATAAATGAC 840 ATTGACTTTT GTTAGAGATC AGGCCAGCAG TCTTGTAAAT GTCTCATATT CTAGATCTGA 900 CTTTTTCCTC ATTGTGTTAC TCACTTTGTT CCTCCATCTC CTGAACCTCC TGTAAACTGG 960 GACATAGGTC TAGGCTTGAT GAGATGCAAA TAAACCTCAC TGGCTGGGCG CGGTGCATCA 1020 CTCCTATAAT CCTGGCTGTT TGGGAAGCCA AGGTGGGCAG ATCACCTGAG GTCAGGAGTT 1080 CAGACCAGCC TGGCCAACGT GGTGAAACTC TGTCTCTACT AAAAATACAA AAATTAGCTG 1140 GGCGTGGTGG CACACTCCTG TAATCCCAGC TACTCGGGAG GCTGAGGCAT GAGAATCGCT 1200 TGAACCTGCG AGGTGGAGGT TGCAGTGAGC TGAGATTCAC GCCACTGTAC TCCAGCCTGG 1260 GCGACAGAGT GAGACTCTGC CTCAGGAAAA AAAAAAAAAC CCTCACTAAG CTTTCTGGGA 1320 GTCTCCTTCT CTGACAGCCC TTCTTAGAGT GGGTAAGGCC GGCAGGTGTA TGAACAGAGG 1380 CAGTCTCAGT ACATGGTGGC AGTTCCTAAT ATTTGTCCCT GCCTTAGGCC AGACATTTTA 1440 CTCCAATGTT TGTTCCTGGG AACCTGTTAC CCTGAGGCTT CTCCTGGACT GGCCAGGCAG 1500 CAGTAGCTTT CCCCTGCTGG GGATCCGGGC CCTGGGCTGC CTTGGGCATT CCCCATCTTT 1560 CTCTCCTCCT 1570
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