Tag | Content |
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EnhancerAtlas ID | HS034-14753 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr19:13201600-13204010 |
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 | CTGGCGTTGG GTGGGCTGGG TGACGGGTGG AGGAGGGACA GAGGGCCTGG TGGGCTGCGT 60 GCCCAGAACT GGCACTGAGG GCAGGGCAGG GCAGGCCGCC ACCCTAGAGG CCCCTCACCC 120 AAGTCTCCAG GAGTCCTGTT AGGGAGAAGG CCAGCATGCT GGAGACCTCA TCCTTGCTCC 180 TATCCCCTGC TGACACCACC CTTAGTTCTC ACCAGGAGAC AGATCCCCGT CACAAGCAGG 240 GCATAAGACT ACTCTTAGCC CTCCAGGTGG AGACCCCAGA GGCCAGTGCC CACAGAGCCC 300 AGTGCCCTTG GGGGCACAGG GAAGACCCAT CTCAGGAGGA GGACAGAGGC AGCTTTAGGG 360 GGCCTGAGGC TTTTACCACC CAGGGTTTTG AAAAAGAACA TGCAAAGATC TTTCTTTTGC 420 ACATTTTACA AAAACACCAC CTTGGAGGTG TCCTCAGCCC GGGGAAATCC ACCTCTCTCA 480 AGAGCCCCTG GGGCCACCTC TCATCTCCTG CTCTGCCTCT GTTCTGGGGC CTGAGTCCAG 540 AGAAAGTTGG TGGATGGAAG TTGTGTGTGT GGTTTGAGAT TGTTTTTTTT TTTTTCTTTT 600 CCTTTCCTTC CCTCAAAAAA AAAAAAAAAA AAAAGCCAAA AAACTTTGTC AAACTTCAAA 660 CTTCAGAGCT CCCTAGTGGC AAGGAGGGGA GGGGAAGAGA ACTTCAACCC CCTCCAGCTT 720 CCCACCCCCT TTCCCCAGAG TCACGTCTGA CCCGTCTGGT TTCCAGGAGC AACCAGACAT 780 GATGTAACAC CCAGATGAAC TTGAACTTGG GGGTGCTGAG AAGAAAAACA ATGGCTCCGA 840 GCAGGGGCTG GAGCCAGCCC CCTCTGCTCT GTGCCAGGGA GGCCGAGAGA GCCCTGCTGG 900 CAGAGGCGGG AGGGGGTGCG AGAGGAAGGG ACAGCAGGCG GGCCTCCCCT CCCAGCTCTG 960 GGCTGGCACC AGGCTTCAGG GTTCCATCGC TCCCTCCCTC CTGCTGCCTG CCTGGGCTGC 1020 TCACAGCTCT GCGGTCGTGC GCTCCGAGGA CCACTGCCAC GAGCCGTCCC TGCTAACCCT 1080 GTTTCCGCTG CCTCCTTTAC TTTCTTTGCT CACTTTGCTT GGACGTTTGG GGGCCAAGTC 1140 AGAGTTTAGG GAAAGTTTGT CTCCCCCCAT GTTCCCTGTG TCTTAGGCTC CAGGAGGTAG 1200 GAGGAAGGAG TCCCAGCGGG GGTCCAGGGC CCCTGAGCAG GCAGGTGTGT CTGGGAGTGG 1260 TTGGGGGAGC GGAAGCTGGA CAAGCGGAGC TGGAGCCCTC GGGCCTGGGG GCAGGCAGGC 1320 GGCTGCAACG GGCGGGCGCA GGGGGTACAG CCGGGGGTGG TTTCCACAGT AACCAGTGAC 1380 TTTAGCTGAT CTCTGGAGCA CCAGATGGAG AGAGAACAAT AGAATGAGGG AAGAAAAGAG 1440 AATTTTAGCA ATTTTGTCAT TCCCTGGGCA GCGCTTTTTA CTTAGTTTTA ATCAATTTTG 1500 GACCTGGCTC AGGAAGTAGG GAGGGGTGAG CAGAGAAAGC CACTCTGTGC TTGGCAGCAG 1560 ATCCCCCATT TCTGGGACCT GTGGGGAGGT GCCGGGGAGC CCCCTTGGGG CAGCCTTTGT 1620 CCCTAACTCC AGACCTGGAA CCAGAGTCTT CCTTCCCTGA GGAGGACCCC CCAGTCTGAG 1680 CATTGGCAGT TGTCCCCAAC TGTACAGCTC AGGAGACCCC AAAGGGGCCA GTGTGAGGCC 1740 CTGGCATGAT CTGCCAGGAG CAGATAGGGC AGGTGGGGCC CTCCCTGTCC TATTGTCCAC 1800 AAGCCTCATT TGCCTGGTGA GGAGAGGGGT GGGCTTACCA CCAGAGTCAG CCTCCCCCTC 1860 AACCTCGGGG CAATGGCACA GGGTTCCTGT ATAGTCTCCC CTTGGGAAGG GGGTCCCAGG 1920 GAACAGGCCC AAGCCTGTGG CAGGTGGGGG TCACCCAGCC CAGGCGCTTC CCACCCCCGG 1980 GCCTGGGCCA GAAGCCCAGG AGCTGGCTGC GGGCCGGTTC TCCCCCACCC ACTCTGGGGA 2040 TGCCTCAGGC CTGGGTTTCC GCCTTAGCCT CGCCAGGCCC CAATGAGCCT CTGTTTGGCC 2100 TGTAGTCAAT TGACCGGTTG GACTTGGGGC AGGTGCTCGA GGAGCCCCAC TGAGGGAGGG 2160 CAGGTCTCTT GTGCGTACTG TCCAGCACAT ACAGGAAATT TAGCATTTCT GCCCACCCAG 2220 CAGCGCCTGC TCATTGTGGC AATCCCAAAC CGCCACATTT CCAGATGCTC TTGATCTGCA 2280 CTGTCCATTG TGGTAGCCAC GGGCCACGTG TGGCTGTTTA CATTTAAATT ATTAACTAAA 2340 GAAAAATTTA GTTCCTCAGT TACAGTAGCC ACATTTCAAG TGCTTAGAAA CCACTTGTGG 2400 CTAGTGGCTA 2410
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