Tag | Content |
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EnhancerAtlas ID | HS024-16490 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr9:136910940-136913040 |
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) |
KLF16 | MA0741.1 | chr9:136911139-136911150 | GGGGGCGTGTC | - | 6.32 | PRDM1 | MA0508.2 | chr9:136912215-136912225 | TCACTTTCAC | + | 6.02 | RREB1 | MA0073.1 | chr9:136912583-136912603 | GCACCCACCACCACCCCCCA | + | 6.06 | SP2 | MA0516.2 | chr9:136912743-136912760 | GAGGGGGTGGGGCTTGG | - | 7.01 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_41736 | chr9:136909947-136915745 | LNCaP | SE_65515 | chr9:136910784-136912761 | Pancreatic_islets |
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| Number: 2 | ID | Chromosome | Start | End |
GH09I134045 | chr9 | 136910785 | 136912761 | GH09I134047 | chr9 | 136912832 | 136913710 |
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Enhancer Sequence | AAAGTCAGAC TCCACCAACA ACAGGGGGCC TGCTCAGTCT ACACAAGGAA ATGTAATTTT 60 TTCCCTCGAG GAAGCCAGTA GCTGTTAGCC AGCTTGCGTC TTACAGAAGC ACCCTGGTAT 120 CCCAGGGGCC TAGCTGGACC TAAGGGACTC CACGCTGTGT CCAGCGGCAG CTCCTGAACC 180 CCACAGGGGT GGAGGCAACG GGGGCGTGTC GGCTGACACC CACCCACGTT TACTCGGCCA 240 CACAGAGACC CTACAGCAAA ACCCACCGCA GGTCCCACCT GGCTCTGGCA AGCAGAGAAC 300 TGAGGCCAAG GCCTGGGTAG ACAGTGCCAG GCGGCAGGGG TAAGGAGGGG CACACAGTCA 360 GTCCCCAGAG CTGGGAGGTG CAGGTGGCTC TGCCAGGGAG TGGCCAGAGG CAGGATCGTC 420 GAGGGACGCT TCAAGGTGGC CACTGGGAAC ACACTAGTTG GGGCAAAGAG AGGTCACGCT 480 GTGCCCGAGG GAGTGAGTTT CCCATCCTGG GATGGCTTCA AGGAGAGGCA CCTTGTCGGG 540 GACCTCGAGG GACGACACAC GCAAGGGCAA GGCAAATCTA CCCCGACCGC TCTGTGGGGT 600 CCAGGCTGCA TTTGTCCAGG TGCCAGTGAG ATGGAGGGGC CGGGTCCTAA CCCGCAGAGG 660 GCGCCCCCAA CTCAGGGCCC GTACCCTATG CACTCAGACA TGAGACCCAT CCAGAAGGAA 720 GGGCTGGCAG AAAGAACCCG GGGGCACAGT GGGACCTGGA AGCCTCTGAT GTTGGGGGAA 780 AAGCTAGTTT TCCGTTTTAG CATGTGCCGG GATAAACCAT CCCCAAAAGC TCCATCTGTA 840 TAATCTAGAG GTCCTGAGGC CTCTCTCCCT GATTCACTGC CCCTTTTCCG CAGCGTCCGG 900 GCCACAGTCG CGGGCAGCAA GTGCTGCCAC TGCACCTGGC TTCTCCCCAT GCCATGCCAG 960 GACAGATAGA GGTGGGAAGC TCCGAACAAA GCAGATCATG ACTTTAAAGT GAATTGTTTT 1020 TCTAGAGCTT CTTTATTATG GTTTCAAGGG CAAATCAGAC CCTTTGACCA AAATGGAATT 1080 AAGCTGAGCT TGAGTCCAGC CCAAACACTG GAACCCCCCA TGATGTTCCA GAAATTCCTG 1140 TTAACTGTGC TATGGTAGAG ACACACAAAC CCCAGCCCTG GAGGCTGCAG CCGAGGCTCC 1200 TGGCAGCTTC TGGGCTGCGT GGCTCTGGCC CTCAGCTTCC CCACCCACGG CAGTGGAGCC 1260 AGGCGGCCCC GCTCGTCACT TTCACCTGAC TGTGCACCGG GCTCTGGGGC CTGGGCCAGC 1320 CAGGTCTGTC CTGCCCGAGA TCCAGTCAAT CAAGGAAGAA AAGGGTTTCA TCAGCAGATC 1380 CTGCCTCAGG TAGGCAGAAT GACTGCGACT GGCTTCCCAG GATGAAAACA ACTGCCCAAC 1440 AGGGCTGCCA GCAGCTCTTC CCAGGGCCGC ACGGCAGTTG GCGGAGGAGG CAGGTCACAC 1500 CTCTGCCAAC TGCCTGCACG TCCCTGGGAG CTGGCTTGGA GCTCTCCCAG AGGGAGGGCA 1560 GGTGCCAGCC AGGAGTCTGG AAAGGTGCTC AGGGAAGACC CGGTGGAGCT CACCCTGGCT 1620 TGGGGCGGTG CAGCTCAAAT GCCGCACCCA CCACCACCCC CCATAGGGAC CAGACTCACT 1680 CTGACCTGCT GTGAGGCACA CAAGAGCCCA GGCAGAGGCT GCCGCCTTGA GAAGACTGGC 1740 ATGGGGGAGG CCAGGCTCTC GGTCTCAGCT CTGCCACCCA CCCAGGTCCC GCTTCCGTCT 1800 TGTGAGGGGG TGGGGCTTGG AGGCACTTAG GGGACAGAAG CCAGGCCATC CCCACTGGCC 1860 GCCTCACTCC TGTCTGCTGT GAGGCGCCTG TATCCGGGGC TTGAGGGAAG CAAAGTGCAG 1920 CTTTAAAACT TTGCCAACTG TGAGAGTGGC CCAGCTCTAG GGACCCCCTG ACCTGATGAT 1980 ACAGAATGGG AGGTAGGAAT GAAATCAATG AAATCACTAA ACGGGTTCGA TGGGAATAAA 2040 CAACAACAGA GCCACAGACT CCGGGACCCA CAGGCAGAGC ACGCCTTCCT CGCTGAGCCT 2100
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