Tag | Content |
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EnhancerAtlas ID | HS105-21269 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr12:133067450-133069410 |
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) |
Arntl | MA0603.1 | chr12:133069231-133069241 | GGTCACGTGC | + | 6.02 | Hnf4a | MA0114.3 | chr12:133068191-133068207 | GCTGGACTTTGACTCC | - | 6.16 | SREBF2 | MA0596.1 | chr12:133068211-133068221 | ATCACCCCAT | - | 6.02 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_06575 | chr12:133067312-133070596 | Brain_Hippocampus_Middle | SE_24669 | chr12:133066701-133067997 | Colon_Crypt_2 | SE_32237 | chr12:133066699-133068967 | Gastric | SE_32237 | chr12:133069017-133072622 | Gastric | SE_41687 | chr12:133067304-133073689 | LNCaP | SE_47660 | chr12:133069127-133069484 | Pancreas | SE_65399 | chr12:133067333-133086073 | Pancreatic_islets |
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Enhancer Sequence | GGTGGACGGG TGCGGCTTCG CAGGCGTTGA GGCGAGAACG GGGCCCGGAG TTGACGCGTC 60 GGGCGATCCC GGGACCCCTG GGCTTGCGAC CGCCCGCGCC GTGGGCAGCC CTGAGGGAAG 120 CCCCGGCCAC TTGGTACCCG TTCCAGGGAC CCTGGGTGCC CACCGCTCGC CCAGACCGTC 180 GCATCTGGAA GACCCAGCAG CGTCGGGTGG GTTTGGGGAC GTTTTAAGTT GCAGAGGCAA 240 AAAAATCTAC GCTTCGAAAT TGGGGGCTGT CTGACAGCAC CGTCGGCCTT TTATCAGTTG 300 TGTTTCTGTG GCCAGCATAT CGCTCTGCCT GGTTCAGGAC GTGCTAGGGA GCAGTGCTGG 360 ATCTTAGGGA GGTGGTGATA AAATGGATAC TCCGCGGGCC ATCCCGTTCC CTCCTCCCTT 420 CGAGGGCTCT GCTGAGAAGG GGAGAAGGAG GGTTAATCTC AAGACCCCTC TTGGTGACTG 480 CTGCCTGCTG CATGGTTAAT AGATTGGCCA AAAATATTGC TTGTCTGGCT GACGGACAGT 540 ATTTGCTGAG CAAATACTGC TCCTCTTACA TGAACTCAGC TGAGCAGAGA AGGAAATTAA 600 ATGCTGTCTG AGAGTTGGGG CAGGCGCTGT CTCCCCAGGA CTGGCATGGG CAGGAATGCT 660 AGCAAGTTGC CCTGCACCAG GGCCGAGACC CGCCCAGCGA GGTGTGCCCC GTGCAGCACT 720 TACTTTGGGG GACCCTCATC TGCTGGACTT TGACTCCCAG AATCACCCCA TTTCCAACCC 780 CTCTCACTTT TCCAGGGGCT TGGGAGCCCA TGGCCTGGGA TCCCCCAGTC TCAGAAGCTG 840 AGCTTTGGGA AAAGGGGAGA TGCCTACTGC AGGCCCCTGA AGCAGCAAGT CCTCTTCAAG 900 TTCTCATCCA AACTCTGGGG ACTGTAGAGA GCCTTGGGTC AGGGCCGGTG GCCAGGGAAG 960 TGGCCCCAGA ACAGGTGCCG CATCGTGTCC CGAGTGCACA GTCAGAGCTG GGGCTTCGTG 1020 TCCCAAGTGC ACGGACAGAG CTGGGGCTCC TGTGGGCCCA GGACGGGGTG GGTGGTGGCC 1080 AGGCTCATCA CACAGGCTGG CCATCCTCTG TCCTGCACAT TATTAGATGG CTCCAGGGCT 1140 GGCACACGCC ATTGCTCTGT GCTGGGACGG GATGGCCCTG GGGCTGTCTT CTGCCCTCTC 1200 AGTGGTGATA ATGACACAGA CTGTACGTGT ACTGAGCAAT ACTGCAAGCC AGGCCCTGCG 1260 CTCGGCTCCT GCACTGCAGC TGAGACCACG AGGATGCCCA CTTTCCAGAG CTGTCGCCAC 1320 CCACCTGCAC CTCCTGGGTC CCTAACCGCG GCTTCCTCAC TGCTCCGAGC GGGTCAGCCC 1380 TTGTACCCTG CCGTTCTCTG TCTGCTTTAT GTTTGGTGCC ATTGTGTCTT TGCAAAAACG 1440 TCACCTCAGA CTCCTCTGAA GTGGTGCCCC CCACCCCCGT CGACGTTGCC CACCTTCTTT 1500 TTGTCATCCC CACTCTGCAA AGCTGTTTTA GAATGTCTTT GCTCTCCATT TTCGTCTCCC 1560 ACAAGAACTT GTAAGCTGAA AGAGAGCAGA CACTGTGCTG TCCTGTGTGT CTCCTATGGG 1620 GTCTGGTGCC GGGAAGAGCT CGATGTGTAG AAAGTGCCCC AGATGCGTGT GTCAGGAATC 1680 TGAGTGAGGA GATGAACTGT ACTCAGGAGA TCCAGGGCCA ATCCCAGGCC CACGTGTTTT 1740 GCCCGCAGCG GCTCTGACTG GCTGTCCACC TGCTCTGGCA GGGTCACGTG CCCCCAGCCT 1800 GCAGGCAGTG GGTTCAGTGG GTTTTGGTGA CTTCGGCTTA GACCAGCTGG CCCCTCAGGT 1860 CATAGTGAGA CAAGTCTGCT GCTGCGTGGC GTTAACACAG CCACAGCACC CCAGGGTGGT 1920 TTCATGTCCC TTCCTCTGCC CTTCGGAGCC TGCCTGGGAA 1960
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