Tag | Content |
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EnhancerAtlas ID | HS091-02998 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:154993700-154995590 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr1:154994781-154994792 | AGCCACACCCA | + | 6.14 | TP53 | MA0106.3 | chr1:154993763-154993781 | ACCATGCCCTGGCAAGTT | + | 6.04 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_23265 | chr1:154995241-154996031 | Colon_Crypt_1 | SE_26626 | chr1:154993852-154994425 | Esophagus | SE_35099 | chr1:154994490-154995927 | HeLa | SE_41600 | chr1:154995264-154996095 | LNCaP | SE_52379 | chr1:154995118-154996014 | Small_Intestine |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 154993889 | 154993975 | chr1 | 154994223 | 154994276 | chr1 | 154994727 | 154994863 |
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| Number: 3 | ID | Chromosome | Start | End |
GH01I155021 | chr1 | 154993853 | 154994425 | GH01I155022 | chr1 | 154994721 | 154994870 | GH01I155023 | chr1 | 154995340 | 154996090 |
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Enhancer Sequence | TCCTGACCTT AAGTGGTCCT CCCGCCTCAG CCTCCCAAAG TGCTGGGATT ACAGGCGTGA 60 GCCACCATGC CCTGGCAAGT TTTTGTATTT TTAGTAGAGA TGGAGTTTTG CCATGTTGCC 120 CAGGCTGGTC TCGAACTCCT GGACTCAAGT GATCGGCCCA CCTCGGCCTC CCAAATTGCT 180 GAAATTACAG GTGTGAGCCA CTGTGCCCAT CCCCCTACTT GATTTCATAT GTTTGGCTCT 240 CCTGCTTTCT TGAGCCTCTC CCCTCCCTGT CCCCTCCCAC TCTCCTGCCA TGCCCTCTGC 300 CAGGATGATC TAGCTCATCC TCTCTCTTAC AGTCTCTAAC TTAACCCCCC AAAAATATAC 360 CTCCAGCCCG GATCCCTGCC CTTTTCTAAC TGCCCCCCTG GGCATCTCCA GCTGGATGCC 420 CTACAGACAC CTCAAAGATC TCAAACTGGG CCAGTCGTCT TTCCCCAGAA CCTGTTTATC 480 TTCCTGCCCT AACACCTGCC CAGGCCCAAG CATAGAAATC CCAGTCACGC TCAGCACTTC 540 AGTACTGAGG CCATCACGAA CTTCTCCTAG ACTAAGACAA GCTTCTCTCT GACCTCCCTG 600 CTCCTGCCCA ACCTCCACTC TGCCTTCTTT GCTTATGGTC TTTTTTTTTT TTTTGGAGAC 660 TGAGTCTCAC TCTATCATCC AGGCTGGGCT GGAGTGCAGT GGTGTGATCT TGGCTCACTG 720 CAATCTCTGC CTCCTGGGTT CAAGCAATTC TCCTGCCTCA GCCTCCCGAG TAGCTGGGAC 780 TACAGGCATG CACCACCAAA CCCGGCTAAT TTTTGTATTT TTAGTAGAGA TGGGGTTTCG 840 CCATGTTGGC CAGGCTGGTC TCGAACTCCT GACCTCAGGT GATCCACCCA CCTCGGCCTC 900 CCAAAGTTCT AGGATTACAG GCATGAGCCA CCGTGCCCGG CCCGCTTATG GTCTTAAAAG 960 ACAAATATGA GCATATCACT TTCCAACCTA AGCTTTTCAA ATGACAAGTT AAGGTTCTTG 1020 CCCATCTCTT CCCACCTTGA CTTCCAACCT CATCTCCCAG CATTCTCTGA GGTCTCTACC 1080 CAGCCACACC CATCCCTTGG GCTCTACCCT TCTGAATGCC TCACATTCTC CAAACCCACA 1140 CAGGCCTCCC CTTGGAATGC TTTCCTCTAC TTCTCAGCCT AACAAACCAC CAAGTTGCCC 1200 CCAAAATCCA GCCCGTGGCC AGGCACCATG GCTCACACCT ATAATCCCAT AATCCCAGCA 1260 CTTTGGAAGG CCAAGGCGAG AGGATGGTTT GAGCTCAGGA GTTTGAGACC AGCCTGGGCA 1320 ACATAGTGAG ACCCCCGTCT CTACAAAATA ATAATAATAA CAAAATAATA ATAATAAGGC 1380 AGGTGTGATG GTGTTCCTGA CATCCCAGCT ACCCAGGAGA CTGAGGTGGG AGGATCACTT 1440 GAGCCCAGGA GGTCGAGGTT GCAGTGAACT GGGATTGCAC CACTGCATTC CAGCCTGGGT 1500 GACAGAGTGA GACCCTGTTT CAAACAAAAC AAAACAAAAC AAAAATCCAG CTCATGTATC 1560 ACCTCTTCTA TGAAGCCTTC ATTAATATGC CCCTTTTCCC AAATTGGCTG TTGTGTCCTC 1620 TGTGCTGTCC AGAGTGTACT TCACTCCTTT ATCAGGGTGC TGTCCACCCT GTTATCTATT 1680 CGATGTCACT CTCCCCAAGG GCATGGTGAG CTCCTCCTGG GCCACGGTGC TGACACAGAG 1740 CAGCCGCTTG GCAAACCTCA GTTACTTCCC CTCCCCTCAT GTCTGTTTCA AGCCCTGGCA 1800 AAGGTCCAGA CACCCAGGAA GGCCTTTGCA AATGGAACAG AACATGCTTA GGACTCACAA 1860 TTCCCAGGTG CCAACTCCTG CTTCCTGCTC 1890
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