Tag | Content |
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EnhancerAtlas ID | HS155-07070 |
Organism | Homo sapiens |
Tissue/cell | Ovary |
Coordinate | chr19:13201200-13203870 |
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) |
Foxd3 | MA0041.1 | chr19:13202177-13202189 | GATTGTTTTTTT | + | 6.44 | RREB1 | MA0073.1 | chr19:13202847-13202867 | TGTCTGGGAGTGGTTGGGGG | - | 6.68 | Sox6 | MA0515.1 | chr19:13202424-13202434 | AAAACAATGG | - | 6.02 | ZEB1 | MA0103.3 | chr19:13203366-13203377 | GGGCAGGTGGG | - | 6.14 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_00024 | chr19:13199869-13205773 | Adipose_Nuclei | SE_01540 | chr19:13199326-13205530 | Aorta | SE_03137 | chr19:13202442-13203597 | Brain_Angular_Gyrus | SE_03859 | chr19:13200177-13205958 | Brain_Anterior_Caudate | SE_06518 | chr19:13191845-13208017 | Brain_Hippocampus_Middle | SE_06678 | chr19:13199268-13216772 | Brain_Hippocampus_Middle_150 | SE_07717 | chr19:13199946-13205923 | Brain_Inferior_Temporal_Lobe | SE_26520 | chr19:13200110-13207804 | Esophagus | SE_29770 | chr19:13200001-13205484 | Fetal_Muscle | SE_31390 | chr19:13202225-13203964 | Gastric | SE_40665 | chr19:13200250-13202182 | Left_Ventricle | SE_40665 | chr19:13202185-13205618 | Left_Ventricle | SE_41557 | chr19:13201470-13202153 | LNCaP | SE_41557 | chr19:13202271-13202931 | LNCaP | SE_41557 | chr19:13203097-13203950 | LNCaP | SE_44148 | chr19:13201563-13203052 | NHDF-Ad | SE_44758 | chr19:13202245-13202775 | NHLF | SE_46667 | chr19:13200200-13202208 | Ovary | SE_46667 | chr19:13202290-13203036 | Ovary | SE_46667 | chr19:13203071-13203857 | Ovary | SE_48143 | chr19:13202074-13203988 | Psoas_Muscle | SE_48559 | chr19:13199819-13205956 | Right_Atrium | SE_51076 | chr19:13199815-13205310 | Skeletal_Muscle | SE_54519 | chr19:13199870-13204977 | Stomach_Smooth_Muscle | SE_61813 | chr19:13190199-13217386 | Toledo |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | TCAGGTAGGA GACCCTGCCC ACCACCTGGA TGCAGGGACC AGGGGAGTAG TCAGGGTTGG 60 GGGGCATCTT GGTGTTAGGG AAGAGCCTGG AGTCCTTGGG GCTAACAGGG AGAGAGAGGT 120 CTGAGGTGGG GCTGGAGGGC CCAGGCTTTT GCACGCCCAG CTGAGCCTGT CTCCCCAGGC 180 AGCCCCCAGG CTCCCTGGCT AATCAGCTAA TTGGATAATT AGCTCTGACA GCCCTGGCCC 240 TGGGGAAGGC GGCCAAGGAC CCAAGTCTAG AGGCCCTCTG GGCCAGGCCT GGTAGAAGCA 300 AAGATGGAAG CCTGAGGCCC ATCGGGAGGA GAATAGAGTC TGCCTCACTG CTTTCACCTG 360 CCCCGACTGG AAGCCCCGGC CCCTAGCCCT CCCCTTTCCC CTGGCGTTGG GTGGGCTGGG 420 TGACGGGTGG AGGAGGGACA GAGGGCCTGG TGGGCTGCGT GCCCAGAACT GGCACTGAGG 480 GCAGGGCAGG GCAGGCCGCC ACCCTAGAGG CCCCTCACCC AAGTCTCCAG GAGTCCTGTT 540 AGGGAGAAGG CCAGCATGCT GGAGACCTCA TCCTTGCTCC TATCCCCTGC TGACACCACC 600 CTTAGTTCTC ACCAGGAGAC AGATCCCCGT CACAAGCAGG GCATAAGACT ACTCTTAGCC 660 CTCCAGGTGG AGACCCCAGA GGCCAGTGCC CACAGAGCCC AGTGCCCTTG GGGGCACAGG 720 GAAGACCCAT CTCAGGAGGA GGACAGAGGC AGCTTTAGGG GGCCTGAGGC TTTTACCACC 780 CAGGGTTTTG AAAAAGAACA TGCAAAGATC TTTCTTTTGC ACATTTTACA AAAACACCAC 840 CTTGGAGGTG TCCTCAGCCC GGGGAAATCC ACCTCTCTCA AGAGCCCCTG GGGCCACCTC 900 TCATCTCCTG CTCTGCCTCT GTTCTGGGGC CTGAGTCCAG AGAAAGTTGG TGGATGGAAG 960 TTGTGTGTGT GGTTTGAGAT TGTTTTTTTT TTTTTCTTTT CCTTTCCTTC CCTCAAAAAA 1020 AAAAAAAAAA AAAAGCCAAA AAACTTTGTC AAACTTCAAA CTTCAGAGCT CCCTAGTGGC 1080 AAGGAGGGGA GGGGAAGAGA ACTTCAACCC CCTCCAGCTT CCCACCCCCT TTCCCCAGAG 1140 TCACGTCTGA CCCGTCTGGT TTCCAGGAGC AACCAGACAT GATGTAACAC CCAGATGAAC 1200 TTGAACTTGG GGGTGCTGAG AAGAAAAACA ATGGCTCCGA GCAGGGGCTG GAGCCAGCCC 1260 CCTCTGCTCT GTGCCAGGGA GGCCGAGAGA GCCCTGCTGG CAGAGGCGGG AGGGGGTGCG 1320 AGAGGAAGGG ACAGCAGGCG GGCCTCCCCT CCCAGCTCTG GGCTGGCACC AGGCTTCAGG 1380 GTTCCATCGC TCCCTCCCTC CTGCTGCCTG CCTGGGCTGC TCACAGCTCT GCGGTCGTGC 1440 GCTCCGAGGA CCACTGCCAC GAGCCGTCCC TGCTAACCCT GTTTCCGCTG CCTCCTTTAC 1500 TTTCTTTGCT CACTTTGCTT GGACGTTTGG GGGCCAAGTC AGAGTTTAGG GAAAGTTTGT 1560 CTCCCCCCAT GTTCCCTGTG TCTTAGGCTC CAGGAGGTAG GAGGAAGGAG TCCCAGCGGG 1620 GGTCCAGGGC CCCTGAGCAG GCAGGTGTGT CTGGGAGTGG TTGGGGGAGC GGAAGCTGGA 1680 CAAGCGGAGC TGGAGCCCTC GGGCCTGGGG GCAGGCAGGC GGCTGCAACG GGCGGGCGCA 1740 GGGGGTACAG CCGGGGGTGG TTTCCACAGT AACCAGTGAC TTTAGCTGAT CTCTGGAGCA 1800 CCAGATGGAG AGAGAACAAT AGAATGAGGG AAGAAAAGAG AATTTTAGCA ATTTTGTCAT 1860 TCCCTGGGCA GCGCTTTTTA CTTAGTTTTA ATCAATTTTG GACCTGGCTC AGGAAGTAGG 1920 GAGGGGTGAG CAGAGAAAGC CACTCTGTGC TTGGCAGCAG ATCCCCCATT TCTGGGACCT 1980 GTGGGGAGGT GCCGGGGAGC CCCCTTGGGG CAGCCTTTGT CCCTAACTCC AGACCTGGAA 2040 CCAGAGTCTT CCTTCCCTGA GGAGGACCCC CCAGTCTGAG CATTGGCAGT TGTCCCCAAC 2100 TGTACAGCTC AGGAGACCCC AAAGGGGCCA GTGTGAGGCC CTGGCATGAT CTGCCAGGAG 2160 CAGATAGGGC AGGTGGGGCC CTCCCTGTCC TATTGTCCAC AAGCCTCATT TGCCTGGTGA 2220 GGAGAGGGGT GGGCTTACCA CCAGAGTCAG CCTCCCCCTC AACCTCGGGG CAATGGCACA 2280 GGGTTCCTGT ATAGTCTCCC CTTGGGAAGG GGGTCCCAGG GAACAGGCCC AAGCCTGTGG 2340 CAGGTGGGGG TCACCCAGCC CAGGCGCTTC CCACCCCCGG GCCTGGGCCA GAAGCCCAGG 2400 AGCTGGCTGC GGGCCGGTTC TCCCCCACCC ACTCTGGGGA TGCCTCAGGC CTGGGTTTCC 2460 GCCTTAGCCT CGCCAGGCCC CAATGAGCCT CTGTTTGGCC TGTAGTCAAT TGACCGGTTG 2520 GACTTGGGGC AGGTGCTCGA GGAGCCCCAC TGAGGGAGGG CAGGTCTCTT GTGCGTACTG 2580 TCCAGCACAT ACAGGAAATT TAGCATTTCT GCCCACCCAG CAGCGCCTGC TCATTGTGGC 2640 AATCCCAAAC CGCCACATTT CCAGATGCTC 2670
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