Tag | Content |
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EnhancerAtlas ID | HS161-00136 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr1:8471660-8474120 |
Target genes | |
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) |
Foxq1 | MA0040.1 | chr1:8472704-8472715 | AATAAACAATG | - | 6.02 |
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| Number of super-enhancer constituents: 38 | ID | Coordinate | Tissue/cell |
SE_00045 | chr1:8465614-8485937 | Adipose_Nuclei | SE_02022 | chr1:8471864-8473073 | Aorta | SE_02685 | chr1:8471679-8473108 | Astrocytes | SE_03407 | chr1:8472178-8472509 | Brain_Angular_Gyrus | SE_03947 | chr1:8466807-8473327 | Brain_Anterior_Caudate | SE_04978 | chr1:8472168-8473408 | Brain_Cingulate_Gyrus | SE_07042 | chr1:8471442-8473593 | Brain_Hippocampus_Middle_150 | SE_07921 | chr1:8471677-8473585 | Brain_Inferior_Temporal_Lobe | SE_11329 | chr1:8466472-8473455 | CD20 | SE_23717 | chr1:8471892-8473171 | Colon_Crypt_1 | SE_25808 | chr1:8466353-8473444 | Duodenum_Smooth_Muscle | SE_27457 | chr1:8471373-8473141 | Esophagus | SE_28078 | chr1:8471067-8473500 | Fetal_Intestine | SE_29095 | chr1:8467196-8473478 | Fetal_Intestine_Large | SE_29887 | chr1:8471530-8472949 | Fetal_Muscle | SE_31622 | chr1:8471348-8473131 | Gastric | SE_31622 | chr1:8473574-8474325 | Gastric | SE_37218 | chr1:8470307-8473795 | HSMMtube | SE_40658 | chr1:8471226-8474591 | Left_Ventricle | SE_41679 | chr1:8471818-8472621 | LNCaP | SE_41679 | chr1:8473602-8473935 | LNCaP | SE_42166 | chr1:8471250-8473174 | Lung | SE_42166 | chr1:8473399-8473862 | Lung | SE_44612 | chr1:8466766-8473359 | NHDF-Ad | SE_45170 | chr1:8471272-8473290 | NHLF | SE_45677 | chr1:8466378-8473709 | Osteoblasts | SE_47251 | chr1:8465934-8485673 | Panc1 | SE_48103 | chr1:8466858-8473292 | Psoas_Muscle | SE_48600 | chr1:8471253-8473209 | Right_Atrium | SE_50481 | chr1:8471784-8473126 | Sigmoid_Colon | SE_51176 | chr1:8466318-8473509 | Skeletal_Muscle | SE_52016 | chr1:8471071-8473292 | Skeletal_Muscle_Myoblast | SE_52725 | chr1:8471316-8473303 | Small_Intestine | SE_54752 | chr1:8471019-8473384 | Stomach_Smooth_Muscle | SE_58576 | chr1:8455425-8501956 | Ly1 | SE_60758 | chr1:8454848-8500160 | DHL6 | SE_62661 | chr1:8450826-8509851 | Tonsil | SE_63725 | chr1:8470591-8473292 | HSMM |
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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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| Number: 2 | ID | Chromosome | Start | End |
GH01I008415 | chr1 | 8474111 | 8474386 | GH01I008406 | chr1 | 8466449 | 8473883 |
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Enhancer Sequence | CAGGTGATAC TACAGAGTGA GCTTTGGATA CATGACATGG AAACAAATGG CCAGCTGAGT 60 CCCACCTAAA TTCCTGATCT ACAAAATTAT TAAAACTATA ATATTTATAG TTTTAAGCCA 120 GTAAATTACA TATACTAAAA GGTTTTGGTT TTTAGAAATT TATTTAAAAG TTTTAGGGTT 180 TTTCTTTTTA GGCTCACATT ATCCAAAACG TGTAGTTTGC CCCCAGTTCA CTGGCTCTGT 240 GCTTTACTTT GCGAAACTAG CCATCTATAC AGATTCATCG GGCCTATTTC CTTTAGAACT 300 TAATCCTATT GTTCCACAAA TTACAGATTC TCGCCAAATG AAAACACCTC CCTCGACAAC 360 TTAAGGCCAC AAACCTCTGA CATAATTCAA TGTGTGTCAT TAGCACATTT CCAAAACAGA 420 GCACTTGTGG GAAGAAGAAC CAAGTTCTGA TCTTAGAAGC CCTGTGCCTA AGTCAATAAC 480 CACCAAATCC CAAAGGTGCT GGACAGATGC TGCTCCGGCC CCGAAAATAA TCAAACACAC 540 AAAAGTTACT ATTAATATTT CTTGCCAAAC AACAATCAAA AAAATCCAAC TCCTGCACAT 600 GGGAACAAAG CGACAATGGC AGCAGCTGCA AATACATAAG CGAAGCATCA CTGAAGAAAG 660 TCTCCAGCTT AATATTGCTC CCGACACCCT CTGTGGTGGT TCACTCATAC AGCAAAGACA 720 CGGGATAAAA AATTCCACAG ACTGTTTTCA AGATAATAAA ATGGCATATG ATGATGACTC 780 ACTAACAGAC TAAAAGGAAA AAATATCCGT CAACAGTCAT AGGAAGCTTA CAAAGCTGCA 840 GAGATCTGGC ACCACTAAAG CTCCTCCACC TCCCCTGGCT CTCACCTCCA GTACACACAT 900 GTATGTGGGA CATACAAAGT GTGTGTGTTC ATGTGCACAC CCTTTAGGGA TTAATTTGAA 960 GCCAAGTTGC AATTGGCTAA TGGCTTACTC TACTGCTTAA GACAGTATTT TATTCTTGAC 1020 TGGCTCAATA AACCTGCTGA GAAAAATAAA CAATGGATTT CAATCTTATA AATAATCTAG 1080 AACACAGAAC CGCTGCGCAA ACAGGAGAGT TGATTTACTG CGCACAATAA ACAGAACAGG 1140 AAGGACCAGT GTGGCAGAGT GAACCCCAAG TCCTAGACCC ATTGTCCTGG GACAGTAGAG 1200 TTCACAGGGG TTTTCTGTCT ATTACACAAA GTCTAAGGCC TGGGATATCC AGGTTTCAAA 1260 CTGGTCTTAA AAAGAGCATT TCAAAGCAGA TCAGGTGGAG AAGCTTTGGT GGTGCCAGAT 1320 CTCCGAAGCT TTGTAAGCTT CCTATGACTG TTGATGGATT TTTTTTTCCT TTGGTCTGTT 1380 AGATTTTGCT CACACTGAAG AGCAAAAGAT GAGGAAAATG TTCGTTTAAA AACAATGAAG 1440 AGTTTTCACG TCTTAGGACC ATTAATTATC TACCCATGAT TACAATGTAT TTCGAACCTA 1500 TTATTTATAC ATGCGTGAAC ACACACACAC ATACTTCATT TTAAGCAAAT AAAAAGTAAG 1560 GGCTGTTACA GGACTCTAAG GGTGCCATAA AGAGGTATTA AAATGAGGTC CCTGCCCAGA 1620 AGGCTTTATA TTCTATATAA ATACATATAT GCATTCATGC ACACATGTGT GCAGAGTAAA 1680 AATGCATGGA AAAGAGGAAT CAGAGTCAAG TCCAAGAATA AAATAAAATA AATTTTAATT 1740 TTGTTTTTTG TTGTTGTTGT TGTTTTTGAG ACTACTCTGT TGCCCAGGCT GGAGCATAGC 1800 AGCGTGATCT TGGCTCACTG CAGCCTCGAC CTCCTGGGCT CAAGTGATCC TCCCACCTCA 1860 GCCTCCCGAG TAGCTGTAAC TACAGGTGCG TGTCACCATA CCCAGCTAAT TTTTTGTATT 1920 TTTTGTAGAG ATGGGGTTTC ACCATGTTGC CTAGGCTAGA CTTGAACTCC TGGGCTCAAG 1980 TGATCCTCCC ACCTCAACCT CCCAAAGTGC TGGGATTACA GACATGAGCC ACTGTACCTG 2040 CCCAATCTTA ATTTGAAGAG GGTGGAACAA AACCCAACTC TGCTGAGATG AAATGGGCCC 2100 TTTGTGTAAC AGCAACCAGC CTGGGGAGGA GCAGAGGCAG CCCCAGCAAG ACCGTTAGAA 2160 ATGAGGGAAC TTTAGCAGGG CACCATGGCT CATGCCTGTG ATCCCAGCAC TTTGGGAGGC 2220 CAAGGTGGGT GTATCATCTG AGGTCGGGAG TTCAAGACCA GCCTGGCCAA CACAGTGAAA 2280 CCTCATCTCT ACTAAAAATA CAAAATTAGC CAGGCATGGT GGCGCATGCC TATAATCCCA 2340 GCCATTCGGG AGGAAGAGGG AGGAGAATTG CTTGAACCCG GGAGACGGAG GCTGTGGTGA 2400 GCTGAGATTG TGCCATTGCA CTCCAGCCTG GGCAACAAGA GTGAAACTCC ATCTCAAAAA 2460
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