Tag | Content |
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EnhancerAtlas ID | HS102-07091 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr14:35842440-35844930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr14:35842494-35842512 | GGAAGGAAGAAAGAAAGA | + | 6.81 | EWSR1-FLI1 | MA0149.1 | chr14:35842490-35842508 | GGAAGGAAGGAAGAAAGA | + | 8.26 | EWSR1-FLI1 | MA0149.1 | chr14:35842482-35842500 | GAAAGAAAGGAAGGAAGG | + | 8.57 | EWSR1-FLI1 | MA0149.1 | chr14:35842486-35842504 | GAAAGGAAGGAAGGAAGA | + | 8.73 | FOSL1 | MA0477.1 | chr14:35842589-35842600 | GGTGACTCATG | + | 6.62 | Foxd3 | MA0041.1 | chr14:35844274-35844286 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr14:35844278-35844290 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr14:35844282-35844294 | GTTTGTTTGTTT | + | 6.32 | HES2 | MA0616.2 | chr14:35843055-35843065 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr14:35843055-35843065 | GGCACGTGCC | - | 6.02 | IRF1 | MA0050.2 | chr14:35842467-35842488 | AAAGAGAAAGAAAAAGAAAGA | - | 6.42 | IRF1 | MA0050.2 | chr14:35842505-35842526 | AGAAAGAAAGAGAAAGAAAGA | - | 6.76 | IRF1 | MA0050.2 | chr14:35842523-35842544 | AGAAAGAAAGAGAAAGAAAAG | - | 6.95 | IRF1 | MA0050.2 | chr14:35842461-35842482 | AGAGAGAAAGAGAAAGAAAAA | - | 7.25 | IRF1 | MA0050.2 | chr14:35842447-35842468 | AAAAAGAAAGAGAAAGAGAGA | - | 7.38 | JUND | MA0491.1 | chr14:35842589-35842600 | GGTGACTCATG | + | 6.02 | NFE2L1 | MA0089.2 | chr14:35843718-35843733 | AGGTGACTCAGCACT | + | 6.52 | Nfe2l2 | MA0150.2 | chr14:35843716-35843731 | AGAGGTGACTCAGCA | + | 6.01 | Nr2f6(var.2) | MA0728.1 | chr14:35844496-35844511 | CGAACTCTTGACCTC | - | 6.24 | ZNF263 | MA0528.1 | chr14:35842495-35842516 | GAAGGAAGAAAGAAAGAAAGA | + | 6.18 | ZNF263 | MA0528.1 | chr14:35842491-35842512 | GAAGGAAGGAAGAAAGAAAGA | + | 6 |
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| Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
SE_00565 | chr14:35843272-35844215 | Adipose_Nuclei | SE_23298 | chr14:35843682-35844131 | Colon_Crypt_1 | SE_26613 | chr14:35843283-35844147 | Esophagus | SE_27693 | chr14:35843478-35844369 | Fetal_Intestine | SE_28626 | chr14:35843099-35844408 | Fetal_Intestine_Large | SE_34130 | chr14:35843135-35844391 | HCC1954 | SE_34831 | chr14:35843037-35844498 | HeLa | SE_42211 | chr14:35843627-35844121 | Lung | SE_50091 | chr14:35843441-35844139 | Sigmoid_Colon | SE_52425 | chr14:35843629-35844140 | Small_Intestine | SE_53368 | chr14:35843176-35844364 | Spleen | SE_56156 | chr14:35843675-35844477 | u87 | SE_67556 | chr14:35843675-35844477 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr14 | 35842569 | 35842689 | chr14 | 35843199 | 35843268 | chr14 | 35843478 | 35844086 | chr14 | 35844529 | 35844624 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I035373 | chr14 | 35843141 | 35845605 |
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Enhancer Sequence | AAGAAGAAAA AAGAAAGAGA AAGAGAGAAA GAGAAAGAAA AAGAAAGAAA GGAAGGAAGG 60 AAGAAAGAAA GAAAGAGAAA GAAAGAAAGA AAGAGAAAGA AAAGAAAAGA AAAGAAAAGA 120 AAAGGGAGGG AGGGAGAGAG GCCAGGCGCG GTGACTCATG TCTGTAATCC TAGCACTTTG 180 GGAGGCTGAG GCAGGCAGAT CACGAGGTGG GTGGATCACG AGGTCAGGAG TTCGAGACCA 240 GCCTGACCAA CATGGTGAAA CTCCGGCTCT ACCAAAATTA CAAAAATTAG CCAGGCGTGG 300 TGGTGTGCGC CTGTAATCCC AGCTACTCAG GAGGCTGAGG CAGGAGAATC GCTTGAACCC 360 GGAAGGCGGA GGTTGCAGTG AGCAGAGATT GTGCCATTGC ACTCCAGCCT GGGTGACAGA 420 GTGAGACTCT GTCTCAAAAA AAAAAAAAGA AAAAAGAAAG AGATAGAGGA CAGGCGCGGT 480 GGCTCACGCC TATAATCCCA GCACTTTGGG AAGCTGAGGC AGGTGGATCA CCTGAGACCA 540 GGAGTTCGAG ACCAGCCTGG CCAATACGGT GAAACCCCAT TTCTACTAAA AATACAAAAA 600 TTAGCCGGGC GTGATGGCAC GTGCCTGTGA TCCCAGCTAC TCAGGAGGCT GAGGCAGGAG 660 AATTGCTTGA ACCTGGGAGG TGTAGGTTGC AGTGAGCTGA GATCGTGCCA CTGCACTCCA 720 GCCTGGGCAA CAAGAGTGAA ACTCCGTCTC AAGAAAAAAA AAAAAAAAGA GAGAGAGAGA 780 GAAAGAGACA GGTTCTGTTT CAAAGCCCCC TGTGCTGCAC CTGAAGGAGT CCCAGCTGTT 840 AACACCTATG TCTCCCTACC TTCTGTGATA TTGACTAGGC TACCATTTTT TTTTTTTTTT 900 TGAGACAGGG TCTCGCTCTG TCACCCAGGC TGGAGTGCGG TGGCACAATC TCAGCTCACT 960 GCAGCCTCTA TCTCCCAGGT TCAAGCAATT CTCCTGCATC AGCCTCCCAA GTAGCTGGGA 1020 CTACAGTCAT GTACCACCAC ACCCAGCTAA TTCTTTTAAT TCTTTTGTAT TTTTTGTAGA 1080 GATGGGGTTT CACCATGTGA CCCAGGCTGG TTTCGAACAC TTGAGCTCAA GTGATCCTCC 1140 CTCCTTGGCC TCCCGAAGTG CTAGGATTAC AGGCATGAGC CAACACACCC GGCCTGCACT 1200 CATTTCTTAA TCAAGGAAAA ATGAATATAA AAGGAGGCTT GGGAAATCTA GGAAGCTCAT 1260 TACAGGAATT CCTCATAGAG GTGACTCAGC ACTTCATTTC ACAAGGAGGA CCAGAAGTGT 1320 CGCAAACACA GTGTTCTTCC CTTTAAAGAG TCAGATCGAA CCAAGATCTC CCTGCGTAAC 1380 TCTCTCTGCA GGAGACCCGG GCTCAGTTAC AAAAGACTCT GGGTTGGCAG AAACAGTGCT 1440 CCCACTTTTT CAGAAGTGAT TGGGTCTGGA ATGGCTGAAT TACATGATGT GCTTCTGCGA 1500 GAGGATGGCA GACTAGCTGG GGCCAGGTAG CCAGGGCTAC CTGAAACACC AGGAAATAAC 1560 TATTAGTTCA TCTCATGAAC CAGACACAAT AGTGCTAACA GAAAATTTGC CTCTAAATAG 1620 GTCATAAAAT CCCAGCCAAA CTTTCGCACA CAGCATGATC AATGGCATCC TAGTTTTTTA 1680 TTAATATTCA TTATTAATTT AATATTGATA TTATTAATAT TCATTTGAGC TTATAAATGT 1740 ATATAAAATG TATATGAACA CTATAGTCAA GAAATTGAAA GGATGGAATG TCTTTATAGT 1800 AGCTTGTTTT GCCAAATTAC CTAAGGGTTT TTTTGTTTGT TTGTTTGTTT GTTTTTGAGG 1860 CGGAGTCTTG CTCTCTCGCC AGGCTGGAGG GCAGTGGCAC AATCCTGGCT CACTGCAACC 1920 TCTGCCTCCC GGGTTCAAGC GATTCTCTTG CCTCAGCCTC CCAAGTAGCT GGGACTACAG 1980 GTGCACGCCA CCATGCCCAG CTAATTTTTG TATTTTTAGT AGAGCTGGAG TTTCACCATG 2040 TTGGCCAGGC TGGTCTCGAA CTCTTGACCT CGTGATCTGC CCGCCTCGGC ATCCCAATGT 2100 GCTGGGATTA CAGGTGTGAG CCACTACACC TGGCCAAGTT TTTTTTTTTT TTTTTAAAGT 2160 ACTTTCCAGG CCGGGTGAGG TGGCTCACAC CTGTAATCCC AGCACTTTGA GAGGCCAAGG 2220 CAGGTGGATC ATGTGAGGTC AGGAATTCGA GACCAGTCTG GCCAACATGG TGAAACCCCA 2280 TCTCTATTAA AAATGCAAAA ATTAGCTGGG CATGGTAGCA CATGCCTGTA ATCCCAGCTA 2340 CTCAGGAGGC TGAGGCAGGA GAATCACTTG AACCTGGAAG GCAGAGGTTG CACTGAGTGG 2400 AGATCATGTC ATTGCACTCC AGCCTGGGGA ACAAAGAGCA ACACTTCATC TCAAAAAAAA 2460 AAAAAAAAAA AAGGTACTTT CCCAGATGTC 2490
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