| Tag | Content |
|---|
EnhancerAtlas ID | HS091-08117 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:68643800-68646720 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr11:68644324-68644338 | AGTCCCAGGGGATT | - | 6.44 | | EWSR1-FLI1 | MA0149.1 | chr11:68646556-68646574 | CTTTCCTTCCTTCCTTCC | - | 10.53 | | EWSR1-FLI1 | MA0149.1 | chr11:68646548-68646566 | TTTTCTTTCTTTCCTTCC | - | 6.18 | | EWSR1-FLI1 | MA0149.1 | chr11:68646581-68646599 | CTTTCTTTCCTTCCCTTC | - | 6.23 | | EWSR1-FLI1 | MA0149.1 | chr11:68646595-68646613 | CTTCCCTTCCTCCCCTCC | - | 6.25 | | EWSR1-FLI1 | MA0149.1 | chr11:68646572-68646590 | CCTTCTTTCCTTTCTTTC | - | 6.98 | | EWSR1-FLI1 | MA0149.1 | chr11:68646599-68646617 | CCTTCCTCCCCTCCTCCC | - | 7.39 | | EWSR1-FLI1 | MA0149.1 | chr11:68646568-68646586 | CCTTCCTTCTTTCCTTTC | - | 7.97 | | EWSR1-FLI1 | MA0149.1 | chr11:68646552-68646570 | CTTTCTTTCCTTCCTTCC | - | 8.46 | | EWSR1-FLI1 | MA0149.1 | chr11:68646560-68646578 | CCTTCCTTCCTTCCTTCT | - | 9.09 | | EWSR1-FLI1 | MA0149.1 | chr11:68646564-68646582 | CCTTCCTTCCTTCTTTCC | - | 9.47 | | Foxd3 | MA0041.1 | chr11:68644937-68644949 | AAACAAACAAAC | - | 6.32 | | Myod1 | MA0499.1 | chr11:68645166-68645179 | TCCAGCTGTCCCC | + | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr11:68643974-68643989 | GAGGTCAGGAGTTCA | + | 6.22 | | ZNF263 | MA0528.1 | chr11:68646552-68646573 | CTTTCTTTCCTTCCTTCCTTC | - | 6.03 | | ZNF263 | MA0528.1 | chr11:68646548-68646569 | TTTTCTTTCTTTCCTTCCTTC | - | 6.1 | | ZNF263 | MA0528.1 | chr11:68646587-68646608 | TTCCTTCCCTTCCCTTCCTCC | - | 6.27 | | ZNF263 | MA0528.1 | chr11:68646556-68646577 | CTTTCCTTCCTTCCTTCCTTC | - | 6.48 | | ZNF263 | MA0528.1 | chr11:68646590-68646611 | CTTCCCTTCCCTTCCTCCCCT | - | 7.04 | | ZNF263 | MA0528.1 | chr11:68646598-68646619 | CCCTTCCTCCCCTCCTCCCTC | - | 7.61 | | ZNF263 | MA0528.1 | chr11:68646595-68646616 | CTTCCCTTCCTCCCCTCCTCC | - | 8.09 | | ZNF263 | MA0528.1 | chr11:68646602-68646623 | TCCTCCCCTCCTCCCTCCCTC | - | 8.11 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_28338 | chr11:68644801-68645914 | Fetal_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I068876 | chr11 | 68644228 | 68646038 |
|
Enhancer Sequence | CTCTAAATAA ATAAATAAAT AACCCAGTCT GGGGTATGTC TTTATTAGCA ACGTGAGATA 60
CATGGGTACT GGGCTTAATA CCTGGGTGAT AAAATAATCT GTACAACAGG CCGGATGTGG 120
TGGCTCAAGC CTGTAATCCC AGCACTTTGA GAGGCGGAGG TGGGAGGATC ACCTGAGGTC 180
AGGAGTTCAA GACCAGTCTG GCCAACATGA CAAGACCCCA TCTCTACTAA AAATACAAAA 240
ATTAGCTGGG CGCGGTGACA GGTGCCTGTA ATTCCAGCTA CCTGGGAGGC TGAGGCAGGA 300
GAATCACTTG AACCTAGGAG GCAGAGGTTG CAGTGAACCA AGATCATGCC ACTGAACTCT 360
GGCCTGGGGG ATAGAACGAG ACTCTGTCTC AAAAAAAAAA AAAATCTGTA CAACAAACCC 420
CTGCGACATG AGTTTATCTA TGTAACAAAC CTTCACATGT ATCCCTGAAC CTAAAATAAA 480
AGTTAAAAAA AACATCCAGC AGCTCCTCAC ACAGTTCCAG AGTCAGTCCC AGGGGATTCT 540
CCCTGCTTGT GAGTCTCCTC CTTGCCTTCC CCAGCAAGGA GTCCCCATCC TTGCCTTCAT 600
ATAGGATGGT TCACCATCCT ATATGAACCA TTTTCGTGTT GTTACGGAAC TTTTCTTGGC 660
GCTGTCATCT CCATTAGAGG GTTTCTGTGA TGTCACCCAA GGTATTGTAG GTATTTCAGG 720
TTTCAAGATT ATTTTATGTC CTTCAGTCAT GAGGTAGCTT CAATTAATGT CTAACAGCAA 780
GTTAGTAAAT GCCCCTCCAA TGGAAATTTT CTAGTCCAAA GTCCCAGGTA GACTGGGTGT 840
GATGGCTCAT GCCTGTAATC CCAGCACTTT GGGAGGCCAT AGTGAGAGGA TTGCCTGAGT 900
CTAGGAGTTT GAGACCAGCC TGGGCAATAT GATTAAACCC TATCTCTACT ACAAATACAA 960
AAATTAGCTG GGCATGGTGG TGTGTGCCTG TAGTCCCAGC TACTCAGGAG GCTGAGGCAG 1020
GAGAATCGCT AGAACCCGGG AGGCAGAGGT TGCAGTGAGC TGAGATCATG CCACTGCACT 1080
CTAGCCTGGG CAACAGAGAG AGACTCTGTC TCAAACAAAA CAAAACAAAA CAAAACAAAA 1140
CAAACAAACA AGCACCCTTA CACACAGCGT TTTCCATGAC CTGGGTAATG GGCATGTCCA 1200
GTAGAAACAC ATTCTGTTCA TCACAAAGCC AACATCAAAT GGCTTGTGTT CAAATCTGAT 1260
GAGCTGCTCC GTCTGAGACA TTTGACTTGG CATGTAGACG AGGAAAGGAA CAGGGACCTT 1320
TCTCAGGGTA CACAGACCCT ACAGTGACTT TTACCCAGTC CAGCAGTCCA GCTGTCCCCT 1380
TGGGAGTCAC CTCCTGCGTG TCTGAATCAG GGACAGCTCC CCGTGATTGT CCCATGGTGA 1440
GCTGCGGGTG CTGTGTCAAC CCAAACACAC TCTTCCACCC TGCAGCATTT AAAACTGAAG 1500
ACACTGATCC TAAATCAGCT ACTGCCAGAA TCCATTTTCC TAAAGGCGCC CCAGGAAGCA 1560
GAAAACATGG AGCTACAAAA TGAAACCCTT CCGTCACACT CCACGGCCTG GCTTTGGCAG 1620
TCGCTTGGTT CTGTCCTCCC TGCTGTGGAC CACCTTGTTG GTGACCAGAG TTCTCAGAGG 1680
CACTTTCTGT TATTCCTGCG TCATTTTGCC CTTGGGAGTC AGCTCTGAGG CTAGCAGCCT 1740
GTCGTCCAAA AGGCCACCAG GATGGCCAGA TAGTAGAAAG AGCTGGACTG GTGATTTCAG 1800
CTTGCAAATC AGGGAGAGGT CATCTCCGGT GTGGACTGAA GGTTTGCTGT CTTCCAAGAG 1860
GGAAAGGGCA GGTGAGGTTG ATGACTCACA GGGCCCGTAT CACACAGCAG AGTCACACGT 1920
ATTCAGCAGG TTTGGAGGAA AAGCTATATT TGTTCATAAT GGGGGTTGAG TGCACGTGCG 1980
ATGGGTAAAC ATGCATGTAA CATACATTCC ATGTTCACTT TGGGGTGGGG CTCTGGCTTT 2040
AAAATGAGGT GGAATGTGGC TCTTTTCATC AAAATGTGAG CTATAAGGCT GGGTGTGGTG 2100
GCTCACGCCT GTAATTCCAA CACTTTGGAA GGCTGAGGTG GGAGGACTGC TTGAGGCCAG 2160
GAGTTCAAGA CCGACCTGGG CAACATAACA AAACCCTGTC TCTACAAAAA AAAAATTAAA 2220
AAAATTAAAA AGAAAAAGGG CAGGGCTGGG CACGGTGGCT CATGTCTGTA ATCCCAACAC 2280
TTTGGGAGGC CAAGGTGGGC AGATCATTTG AGGTTGGGAG TTTGACACCA GCCTGGCCAA 2340
CATGGTGAAG CCCCATTTCT ACTAAAAATA CAAAAATTAG CTGGGTGTGG TGGTGGGCAC 2400
CTGTAGTCCC AGCTCCTCAG GAGGCTGAGG CAGGAGAATA GCTTGAACCT GGGAGGTGGA 2460
GCTTGCAGTG AGCCAAGATC ATGCCATGGC CCTCCAGCCT GGCCCACAGA GCCACCATCT 2520
CAGAAACAAA ATGAAACGAA ACAAAACGAA ACAAAACAAA ACAAAAAAAG AGGGAGGGTA 2580
CAGTCACATT GTTTTGAGGT CTTGGTTAAA CCTACTGAAT CCACACGTTG CATGTGAAAA 2640
GGAGGCAGAG GAACAGTCCA TTATGTATTC TTCTCGAGCT CAATAAAACT ACATTTTTAT 2700
GAGAAAGAAG TCAAATATGC ATTGAGGTGG GTGGTGATGG CAGGTATCTT TTCTTTCTTT 2760
CCTTCCTTCC TTCCTTCTTT CCTTTCTTTC CTTCCCTTCC CTTCCTCCCC TCCTCCCTCC 2820
CTCTCTCTCT CTCTCTTTCT TTCCAATCTC GACTCACCGC AACCTCTGCC TCCCGGGTTC 2880
AAGCGATTCT TCTGCCTCAG CCTCCTGAGT AGCTGGGATT 2920
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