Tag | Content |
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EnhancerAtlas ID | HS161-14119 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr7:76638840-76640900 |
Target genes | |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr7:76639672-76639687 | AGATGACTCAGCAGG | + | 6.66 | Nr2f6(var.2) | MA0728.1 | chr7:76640759-76640774 | GAGGTCAGGAGTTCA | + | 6.22 | TCF7L2 | MA0523.1 | chr7:76639689-76639703 | AAACATCAAAGGAA | + | 8.12 | Zfx | MA0146.2 | chr7:76640735-76640749 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_26739 | chr7:76638557-76640122 | Esophagus | SE_68923 | chr7:76639200-76640242 | H9 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I077009 | chr7 | 76639119 | 76640130 |
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Enhancer Sequence | ATGCCCAGTT TCTGATGTGG CCTGGGCGTG AATGCAAAAA TTGGGGTCTT CTGTGCTTTG 60 CAAGTGAGTG CACCACCACA GTTTGCTTTA CGGCAAGGCC CCAGGAAAAG GGGTTCTGGG 120 GATGTCATCT CAACGGCAGG TGTGTTCCAC AAGAACATTA ATACATCGTT AATATTTTTG 180 AAAGACAAGA CTGGGCATGG TGGCTCACAC CTGTAATCCC AGCCCTTTGG GTGGCTGAGG 240 CAAGTGGATC ACTTGAGCTC AGGAGTTTGA GACCAGCCTG GGCACCATGG CAAAACCCCG 300 TGTCTACTAA AAATACAAAA AATAGCCAGA TGCGGTGGCT CGTGCCTGTA GTCCCAGCTA 360 CTCGGGAGGC TGAGGCAGGA GAATCGCTTG AATCTGGGAG GCAGAAGTTG TAGTGAGCCG 420 AGATCACACC ACTGCACTCC AGCCTGGGCA ACACAGCGAG ACTCCATCTG AAGATAAAAA 480 AAAAAAAAAA AGAAGAACCC AAGGGAGGGG GCACTGCCCA GCACAGGCAC AGTCCCATCA 540 GGCCCTGGGG AGCCATGCCA GGGCGTTCTG CCCAGCACAG TCACACCTAA AAGGGTCCTC 600 AGCCGAACCC CATCCCCTTG AATACCAGCT CATGACGGCT TTGAGCAGAA CATGTCACGG 660 GAACGGCATT GTGTAGAACT TTTTATTAAA TGGCATTTAA AATATTCCCC AGGACTGTGT 720 AGCTGGGGAA ACACCACAAA ATCCATTGGC CCGGAACATA ATGGCTCAAT GGTACGAAAC 780 AAATGCATTG TTAAAAAGGA AAAACAGCAA CTGTTGCGGG GTAATGACTT GCAGATGACT 840 CAGCAGGCCA AACATCAAAG GAATTCGGAT GGCAGCAGGT GGGCACAGGC AGCCAGGAAG 900 CACCCCTCCC TCGCTCTCAC TTCCAGCGAT CGCTTTACCT CCCTGGAGTG TCTAAGCCAC 960 CCATTTCTCT CCATCATCCC TGCAATCCCC AAGCAAGAAC CACCTTGGTC TCCCGCTGGG 1020 ATGTCCGTGG TTCCTCTCTA GCTGAACTCT CCATGTCCAC TCCTGCCCGT CGCCCATTCC 1080 CCTCTCAGTA TCCAGAGGGA CCAGGTTCTT TGTTCTTTTT TTTTTTTTTT TTTTAAGATA 1140 GAGTCTCACT CTGTTGCCTA GGCTGGAGTG CAGTGGTGTG ATCTCGGCTC ACTGCAACCT 1200 GCAGCTTCAG GTTCAAACGA TTCTCCTGCC TCAGCCTCCC AGGTAGCTGA GACTATAAAC 1260 GTGCGCCACC GTGCCTGGCT AATTTTTTTG TATTTTTAGT AGACGGGGTT TCACCATGTT 1320 GACCAGGCTG GTCTCAAACT CCTGACCTCA GGTGATCCAC CCACCTCGGC CTCCCAAAGT 1380 GCTGGGATTA CAGGTGTGAG CCACTGCACC CAGCCAGGAC CAGGTTCTAA ACCTGATCAC 1440 ATCACACCTC TGCTCCCAAC ATTCAGGAAC TTCACACTGC AAGAACAGAA TCTAGGTTCA 1500 GACAGGTGTG GCGGCTCACA TCTGCAATCC CAGCACTTTG GGAGGCCAAG GCAGGCGGAT 1560 CACTTGAGGC CAGGAGTTCG AGACCAGCCT GGCCAGCATG GTGAAATGCC ATCTCTACTA 1620 AAAATACAAA AATTAGCCAG GCATGGTGAT GGGCGCCTGT AATTTCAGCT ACTTGGGAGG 1680 CTGAGGCAGG AGAATTGCTT GAACCTGGGA GGCGGAGGTT GCAGTGAGCT GAGATCACAC 1740 CACTGCACTC CAGCCTGGAC GACAGAGCGA GGCTCTGTCT CAAAAAAAGC AAAACAAAAT 1800 AAAACATACC AACATCTAAT CTCTATAAAA TATTTTTAGA AGTTATCCAG GTGGGCCGGG 1860 TGCAGTGGCT CATGCCTGTA ATCCCAGCAC TTTGGGAGGC CGAGGCGGGT GGATCACTTG 1920 AGGTCAGGAG TTCAAGACCA GCCTGGCCGA CGTGGTGAAA CCCCATCTCT ACTAAAAAAA 1980 AAATACAAAA ATTAGCCGAT TACAGGCATG AGCCACCCCA CCAGGCCATG CTTTCAGTTT 2040 TCAAGAAAGA AGACACCATT 2060
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