Tag | Content |
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EnhancerAtlas ID | HS052-01154 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:43997210-43999730 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:43998859-43998877 | CCTCCCTTTCTTCCTTCT | - | 6.52 | EWSR1-FLI1 | MA0149.1 | chr1:43998851-43998869 | CCTTCCTTCCTCCCTTTC | - | 8.52 | EWSR1-FLI1 | MA0149.1 | chr1:43998855-43998873 | CCTTCCTCCCTTTCTTCC | - | 8.64 | EWSR1-FLI1 | MA0149.1 | chr1:43998843-43998861 | AATTCCTTCCTTCCTTCC | - | 8.86 | EWSR1-FLI1 | MA0149.1 | chr1:43998847-43998865 | CCTTCCTTCCTTCCTCCC | - | 9.47 | RREB1 | MA0073.1 | chr1:43998539-43998559 | ACCCCCTCCACCCCCACACA | + | 6.23 | RREB1 | MA0073.1 | chr1:43998957-43998977 | GAGGAGGGGGTGGTTGGGTG | - | 6.39 | ZNF263 | MA0528.1 | chr1:43998846-43998867 | TCCTTCCTTCCTTCCTCCCTT | - | 6.28 | ZNF263 | MA0528.1 | chr1:43998858-43998879 | TCCTCCCTTTCTTCCTTCTTC | - | 7.16 | ZNF263 | MA0528.1 | chr1:43998855-43998876 | CCTTCCTCCCTTTCTTCCTTC | - | 7.63 |
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| Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
SE_00616 | chr1:43995107-43998898 | Adipose_Nuclei | SE_00616 | chr1:43998907-44001249 | Adipose_Nuclei | SE_04240 | chr1:43997230-43998647 | Brain_Anterior_Caudate | SE_05040 | chr1:43996981-44000130 | Brain_Cingulate_Gyrus | SE_05962 | chr1:43995415-44000121 | Brain_Hippocampus_Middle | SE_07193 | chr1:43995683-43999544 | Brain_Hippocampus_Middle_150 | SE_08033 | chr1:43997264-44000544 | Brain_Inferior_Temporal_Lobe | SE_23218 | chr1:43996011-43999623 | Colon_Crypt_1 | SE_23829 | chr1:43996144-43998350 | Colon_Crypt_2 | SE_23829 | chr1:43999234-43999589 | Colon_Crypt_2 | SE_24870 | chr1:43996197-43999448 | Colon_Crypt_3 | SE_26649 | chr1:43995723-44004223 | Esophagus | SE_27645 | chr1:43995619-44017587 | Fetal_Intestine | SE_28595 | chr1:43995607-44004348 | Fetal_Intestine_Large | SE_31538 | chr1:43995971-44000533 | Gastric | SE_41575 | chr1:43998407-43998733 | LNCaP | SE_41575 | chr1:43998859-44001617 | LNCaP | SE_47657 | chr1:43998383-43998667 | Pancreas | SE_47657 | chr1:43999225-43999586 | Pancreas | SE_50363 | chr1:43995694-44004359 | Sigmoid_Colon | SE_52524 | chr1:43995689-44000339 | Small_Intestine | SE_56987 | chr1:43995814-43998375 | VACO_400 | SE_65452 | chr1:43996948-43999005 | Pancreatic_islets | SE_65452 | chr1:43999008-43999882 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 43997843 | 43998152 | chr1 | 43999309 | 43999502 |
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Enhancer Sequence | CGCGCCCCCG CCCCCGCCGC ACAGGCGCCC CCTCCCAGCC GGCGGGGGAT CCGCAGCCGG 60 CGCGCCCGGG TCTCGCTCGC GGCCCCGGCG CACGTGCGGT CCCGGGCTGC GCCGGGCGCG 120 AGTTTGAAGC CCCCCCACCC CCTTCGTTCG CGAGCACGGG ATGGGGAGGG GCCGAACGGG 180 CTGTACCCGC CCCCAACCGG GTGCAACGCC CTGGAGGCCC TGGAGCGACC TGTCCCGTGA 240 GGACGTGGCC ACTCGGACCC TCTCCGAAAG TTCACTCAGT GGCCGCCCCG CGTCCCGTCC 300 CGTCCCGTCC CGGCTCCCCA TCGCCGTGCC GGCGTCTCTG TCTCGGCTGC TTTCTGTTTT 360 CCTCGGCGTC TCTGCCTCCC CGTGTCAGTG CCTCCCAATC TCACGCCCCT GCAATCCCAG 420 GGTCTCTCCA GCTGTCTCCA TTCTTTTTCC CCAGGTCACT CTGTTCTTTC TCCCCAGGTC 480 TCTCGATTCT GTCTCCCTGG GTCGTCTTGT TCCCTGTCCC TGAGTCTGTT CTCTCCGCTT 540 GGGTCTCTCT ATTTCCTCTC CCTGGGTCTC TGTCTCCCTC CTTAAGTCTC TGCCTCTTGT 600 CTCTCACCCA TCTCTTGGTG TCTCTGCACT CTCTGTGCTA GGCGCCCCCC CATTTCCCTG 660 GAATGCTGCC CCTCTGGTTC TTCCACCCCG GAGGGGGAGG GGCTAGACTT TCTCCCCATT 720 TCAAGCCCCC CTGCCCCCCA GTGCACGGCC CCTGAGTTGG AGCAGGTTGG GGGTGGGGAG 780 CGCTACCTGC CTGAGCTGTG AAATGGGAGA GGGAGGCTGC CCCAGCCTGG GGGTTGTCTG 840 GATCTCCCTG AGGGGCCACA GGGCAGGGCC GGGAGGCTGG ATTAGGTTGA GGAAGGCTCC 900 ACTTTTGAAG GAACAGGGGC AGGGATCCAG AGCGATCTGG TGTCGGATCT GGCCTGAGAA 960 GCAGGGAAGT GCACTGGGGT GAGAGGCGTA GAAAAGGATG TGGGGTGGTG GTTCCAGGCG 1020 GGTGCTCATG GGGAGGAATC TGCTGAGAAG GGAAGATCTG GTGGGGAATC CTTTGGGAGG 1080 CTTCGGGGAT CTGAGGGATC CAGAAGAGAG TTCTGACAGG CTATCTAAGG AAATTTCTGT 1140 GCTTAGCTCC TTATTAACTC TTGCTTCAGG GAGCATGAAA ATCCCTGTTT TTTTACTGAT 1200 TATATGAATG AGCCTAGGGC TTCAAGAAGG AGCAGGTGTA ACTCCCCAAG TACAACCCCC 1260 TACATTCTCA GCCCCAGGCA CAGGCCACAC TTTCTCGTAC CCTCTTGCCT TCATTTCCAC 1320 ACTCAGCTCA CCCCCTCCAC CCCCACACAC ACTCCCTATT CAGCTGCTTT CTTGCCCCCT 1380 CTCGCATACC TGGGCCCGCA TGCCGGCCAG GGCTCAAGAA ATCTGTGCCT GCACACTCTC 1440 GCAGCATACC TGTGCACATG CACAGTCATC CTTGTGTATT TTTGTATATG CACTTTCTTG 1500 CACATTTTAC TTGCTCAGTC TCTTATTTGA AATGTCTTTA TAGTGTTTTT TTTAGTTTCC 1560 TTTATAGTTT CCTTTTCCAG CTGCTCTTCC TCTTCCCTCT TTCTTTCCTT TAACAAGAAA 1620 ATTGTTTTAA CATAATTCCT TCCTTCCTTC CTCCCTTTCT TCCTTCTTCT TGCAACTACT 1680 GATACCTCCC CTTTATCCAG CTTTGTGTGC CCTGGGCGGG TTGGCTTGGT GTACAAGGCT 1740 GCCAAGAGAG GAGGGGGTGG TTGGGTGTTG GTGAAGGAAT TTGGCGGGGC AGAGTTAGAC 1800 TGCAGCAAAC GGAAACTAGC TACACATCTT TTACTGGGAA GTGTATGGAT ACGCAGCAAA 1860 ATACTAGCCC TGGCAGTTTG GGCACAGTCC ACCCTTTTTT CCATCAGCCT GAACTATGGG 1920 AGTCTAGCTT TGAGGGTCCT CCCTGGGGGC GGGGAGGAGG GGACCCAGAC CTCCTGCAGT 1980 AGAGGGGTTG TGATACACAC CACGGCTCCT CCACTTTCCA GCTTCAGGCC TCAAAGAGGC 2040 CCCTTTCTCC CTGAGTCTCA ATTTCACTCC CTGTAAAATG GGGTAGCTAA TCCAACCCGG 2100 ACTGGGTCCC AGGGCTGTTG TAAGAATCCA AGGGAACTGT GTGGCAGTGC ATCGTCAGCA 2160 GTGGCAGTCA CTTCCCTTGT GACTGACACT GCTGTGTGCT TGGTTCCAGC TTGCAGTCAG 2220 GGCCCTACCC TCGAGAAGCT CGTGGTCCTT GGGGGAGCAG GTTGCACCAT GGGATTGCAA 2280 AAGCAATTCA GTTACCTGTC ATTGATTGCT GACTGTGTGC CAGACCCCGG GGTAGGCGCT 2340 TTCGGCCCCG GCTGCCTTTC TTCCTTTGGG ACTAACAGCT ATGTAGAAGA GGCAGCCCAC 2400 CCCTAAGGTT CAGGCATCTG CTCAACTAAA GCAGCTGCGG TTCTGAGTTG GGTTAGAACA 2460 TTGCAAGAGT TCATCAAGAG ACGGGGGAGA GTTCGGAGGT CAGGGTGAGG TGAGTCCCAG 2520
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