Tag | Content |
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EnhancerAtlas ID | HS091-08828 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:118065130-118067440 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF14 | MA0740.1 | chr11:118067379-118067393 | AGCCACGCCCACCA | + | 6.09 | SP1 | MA0079.4 | chr11:118067377-118067392 | CCAGCCACGCCCACC | + | 6.27 | SP3 | MA0746.2 | chr11:118067379-118067392 | AGCCACGCCCACC | + | 6.78 | SP4 | MA0685.1 | chr11:118067377-118067394 | CCAGCCACGCCCACCAC | + | 6.04 | SP8 | MA0747.1 | chr11:118067380-118067392 | GCCACGCCCACC | + | 6.62 | Sox3 | MA0514.1 | chr11:118065499-118065509 | AAAACAAAGG | - | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_28986 | chr11:118065065-118066748 | Fetal_Intestine_Large | SE_28986 | chr11:118067107-118068176 | Fetal_Intestine_Large | SE_35395 | chr11:118064424-118066958 | HepG2 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 118065482 | 118066498 | chr11 | 118067135 | 118067194 |
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| Number: 2 | ID | Chromosome | Start | End |
GH11I118194 | chr11 | 118064725 | 118066852 | GH11I118196 | chr11 | 118067108 | 118068176 |
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Enhancer Sequence | TGCTGTGGGG GAAGGGCAGA AAGAAACAAA ACATGCTTGT AAGAAGTAGT TCCATAATCA 60 TAGCAGCTGC TGTTCATTGA GCTCTTCTCA TGAGCCCGGC CCAGTACTGA ATTTCATATG 120 CATTATCTCA TGTGATCCTT ACCACCAGGA GGTAGGTATT ATTATTGCCT TTCTAAGGAT 180 AAGGAAACTG AGGCTCAGAC AGGCCAAGTT ACTGCCCAAG ACCATCTGGC TGCAACACAG 240 AGTTAGAATT TGGACCCAGG TCTGTCTAAC TCCACAGCTT GTGATCTTAA CCTCTGTGTG 300 TACAGCCTCA GAAAGGGAAA ACAGCAAGGT GCCACTACAT TTACATGAAT TTCATCAATT 360 CAACAACAAA AAACAAAGGC TCTTTGTTAC CCCTGCTCCC TATCAGAGAA CACCTTTATA 420 AATGCAGTCT CAAACAAGTG GCCTGCAGTC CCAAATTCAC CAACAGCCTT ATTTAACTTG 480 GCACATCATA TTTTAAAATA ACTTGACTGG CCCCTGCCAG CCTTTGAGTT TGCAGCCCAG 540 GCCTCTTCTC TTACTCTATT GGATCTAGAT CAAGAGGACA GGAATGGTGT TTTCAACAGA 600 ATCAAAACCA TAATCGCCTA GCATTAAACC TGGGGAAGTT AGCTGTGAAG ACAATTGTTC 660 CTCCTGCATC ATCTCCACCT CGGAGACGTT CTGCAAACAG TGCCACCCTG GCTGGTGACC 720 CACTCAGCAG TAGCCACAAG GCAGCTGTAT CAGCAGGTCT CCAGGAGCCA GGATGAGGCC 780 TCGCAAGTTA CTGCAGCATC ACATAACAGT ATGGGAGAAA GATACAGAGG GAAAATGATT 840 CCATTCAGCT GCAACTTCAG GGTGGAGTTA ATGTTTCACT CGGTGGATCC AGGCCAGGCC 900 TCTGATCTCA CACTTCCCTG GCAGACCTCT CTCTGCTGCA ATCAGCTGGG AGTCATGTGT 960 CCTCAGGGCT GGTACGATAG GAACAAACAA AGCCCATCAT TCCACAAGCA GAGGAGGCCA 1020 GCCTTCCCAA ACCCACAGAA CACTGCTCCT TAATAGGCTG GGTGCCTATA ATTAGTCTAC 1080 AAATAGCACC GTGCTCATCG CCAGCTCACT CCTTTTGTCC CTACCCCCAC TCACTGCACG 1140 CCCCGAGGTG CCTTTTCCAG GCACTGCAGT TCTCTAAGGG GCTACAGAAG TCTAAGCAAA 1200 GGGAAATTAG GAATCAGACT CCAAAATATT GTATGAGATC CAGCATGCAG CCTGCCTGGC 1260 AGTTAGGTTA TGAGAAGGTA TAATAAGTCA CAAAGTTAAG AAACAAAATC TAAGCATTGG 1320 AAGGAACCCT ACTTTGACCT TTTGATAGCA AGGAAAACGA CTCACAGCAA CACAATACTT 1380 GCCCAAGGAT CTTATCCTAT TTATCCTATT TTCTTTGTTG TTGTTGTTGT TTTGAGACAG 1440 GAGTCTCGCT CTGTTTCCCA GGCTGGAGTG CAGTGGCGCG ATCTTAGCTC ACTGCAACCT 1500 CCACCTCCCA GGTTCAAGCA ATTCTCCTGC CTCAGCCTCC CAAGTAGCTG GGATTACAGG 1560 TGCCCGCCAC CATGCCTGGC TAATTTTTTT GTATTTTTAG TAAGACAGTG TTTCACCATG 1620 TTGGCCAGGC TGGTCTCAAA CTCCTGACCT CAAGTGATCC ACCTGCCTCA GCCTCCCAAA 1680 GTGCTAGGTT TACAGGTGTG AGCCACCATG CTCGGCCTTT TTTTTTTTTT TTGAAACAGA 1740 GTCTTACTCT GTCTCCCAGG CTGGAGTGTA GTGGTGGATC TCGGCTCATG TAACCAACGC 1800 CTTCCAGGTC CAAGCAATTC TCGTGCCTCA GCCTCCCAAG TAGCTGGGAT TATAGGCACG 1860 CATCTCCACA CCTGGCCAAT TTTTGTATTT TTAGTAGAGA GGGAGTTTTG CCACATTGGC 1920 CAGGCTGGTC TTGAACTCCT GGCCTCAAGC AATCCGCCCA CCTCGGCCTC CCAAAGTGCT 1980 GGGATTTCAG GCATGAGCCA CCACACCCGG CCGTGTTTTC TTTATTAGAT TGAACTGATG 2040 AGGCAAAAGA CGTCCTCCCT GCCCTCAGTA AAAGCCACTC TTCACTTCTT TTCACCACTA 2100 ATATAAATAA TCTCTGGTGA TAACCTTTAA TCCTTGAGCT TGGGTAAGAA AGTTTGATAT 2160 CACTCTTCTA TCCAGCAGAA CTTCAGTTTC TCAGACTTTT CTGCTACTTA GAAAAATCAC 2220 CGCCCTCAGC AGCCTCCCTT GGGCAACCCA GCCACGCCCA CCACCACCAC CACCTGAGCC 2280 TCTGACACCT GGCTCAGCTG AGGCCAGAAT 2310
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