| Tag | Content |
|---|
EnhancerAtlas ID | HS091-07188 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:17561520-17563920 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr11:17561911-17561929 | CTTTCCTTCCTCGCTTGC | - | 6.06 | | HNF1A | MA0046.2 | chr11:17562940-17562955 | AATGAATGATTAACA | + | 6.04 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28323 | chr11:17561810-17566455 | Fetal_Intestine | | SE_29229 | chr11:17561648-17566493 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGTGCACAAC ACCACACCTG GCTAATTTTT GTATTTTTTG TAGAGATGGG GTCTCGCTAT 60
GTTGCCCAGG CTGGTCTCAA ACTCATGGAC TCAAGTGATT CTCCCACCTC AGCCTCCCAA 120
AATGCTGGGA TTTCAGGCGT GAGCCGCCAC ACCTGACTTC TTTTCTTTTT CTGGAACCAC 180
TTTATTGAGG TATGCCTGAC ATGTAAAGCG CTGTATATAT TTAGTGTATA CAACCTGATG 240
AGTTTGGGGA TAAATGTGCA CGTGTGAAAG CATCACCACC ATCAAGGACA TAGACAGTGC 300
CCTTCATCTT TTCAGAGGCT CTTGACATGT CAGCTAGTTT GTAGTATTTC ACCCTGTGCC 360
TGGCACAGCA ATCACGCCCT GCTTCTCCTT GCTTTCCTTC CTCGCTTGCT GCTCCTTCTC 420
CTCCAAAAGT TGAGGTACCC CGGGCTCTGT CCTAGGTCTC CTCTCCATCT GCACTGTCTC 480
TCTAAGTGAC CTCATTCATC TCAGGGGTTT AAATACCACT CACACCCCCA AGGACCTACC 540
GATGCTTATC TCCAGGCCAG ACCTACAGCC TTCTCAGTCA CCTCTAGCAG GCGTCTCAAA 600
CTTACAGCAT TCGAAGTGGA ACGCTAGGTT TCCACCACCT CCTGCTCCGT CTCCACCAAC 660
CTGCTCCGTC TCCACCAAAT GTGGATTCAC CCTTGATGCC TCTCTTTCTA CGCTCGCAGC 720
CAATCCATCA GCAAAGCCTG TCAGTTTTTC CTTTAACATG TATCCTGAAT CCGACCCATT 780
CTCACCCGAG TCCGAGCCCC TGCCTCTGGC CTGGGCTCCT GCAGGAGCCT CCTGACTGAG 840
GTCCCCTTCT ACTCTTGGGC CCCTCAGTGG ATTCTCTACA GAGCAGCCAG AACAATTCCT 900
TTTAAATGTA AATCATTCAC ACTTACAAGA AAATCCTGAC CTGACCATGG CCTACCAGGC 960
CCCTACCACC CCTCCGACCC ATTTCTCACC ATTCTCCACT CACGATTCCT CTGGGACACA 1020
CTGTCCTACT TGCTGTTCCA TACAGGCGGG CATCTGCTTG CCTCAGGGCC TTCACACTTG 1080
TTGCTTCCAC TTTAGGGAAT GCTCTTCTAC ATGTATCTCT GTGGCTCCTT CTCCTCACTT 1140
CTTCTAGGTC TCTGCTCAGA TGTCACCTCT TCAGAGAGGC CTTCGTGACT GCCTACCTTG 1200
TCACTTACTA TCTCTCTCTC CCCATCTTAG TTTATTTTTT CATAGAATTT ATCACTATCT 1260
GGCATTGTAT GATACTTTTG TTGATTTCCT TTTAACTACC TGTCTTCCCT ACTGGAATGT 1320
ACTGTCTAAG ACAGCAAGGG CTTTATTTTG TTTTTTGATG CTTAGAGTAC TGCCTGGCAT 1380
ATATTAAGGG CTCAGTCAAT ATTTATTGCC TATGTGAATA AATGAATGAT TAACAAATTC 1440
CTAGAGAGTG GTGGCTCTTT CTGATCTTAT TCATCCCAAC CGGTTGTCAG ATGCCTGGCC 1500
TCAGGCAGAA TACACAGCTA TGCTCATAAA TGCATGATTG CTGAAGAGGC AATAAATACT 1560
TTTAAGCCAA TGAGTAACCA AGTTCCTACC CTGTGCTGGT GCTGCGAACA GAAGAGCAGT 1620
CTCCCTTTGA AAGCTGGTTC TCTGAGGGAG AAAACAGTCT CTGACCAAGC CCTGCTCCCC 1680
CACATCCTGG CCCAAGGTTG CTACTAGTTA CTGGAAGGGT ATGCAAGTGC TCCTGGCGGC 1740
CTTGGGGTAA CTTCACAAAT CAAAGGGAGT CGATGCCTGG AGCCTGTTGG CTCCCACTGG 1800
ACACTCTGCA GGTATCAGCT GGAAACAGTG TGGTTACTGT GGGCCCAGAG CAGCCAGTAC 1860
TTTAATTGCT AGTTAGTTTT GACTGTCTTG TGAGGTAAGT TCTACAAACT CCATCTCATA 1920
GCTGAAGAAA CTAAAACTCA GGGAGAGTGG GTGGCTTGGT CAAGGTCTTC CTGACAGTGA 1980
CAGGGCTAAG ATTTGGTCCC AGTTCTGCTA ACTCCAGATA ATAATCAACA TGGACATTTC 2040
TTGAGAGCTC CCTAAGTGCC AGGGTCTATT TAAGCTCCCC ACACACATGT AGGTCTCATT 2100
CAGCATTCAT GGTAACCTTA TTCGTTAAAT ATTGTTATCT CTTTTCACAA GTAAGAGCAC 2160
TGAGGCACAG AGAGATTAAG TAACTTGCTC AAGGTCACAG AGCACTTTCC ATTATAACAC 2220
ACTACCTTAA ATATTACTTC CAACAACTAA GGATTTAGAT CACAAACCAT TTCTTCCAAA 2280
ACACTAAGGA AGGGACCCCT ACAAAGCAAA CAACAGCAAG CTGTAAATTT CTCCCAGCAT 2340
GTCTGTGTGC CTCCTTTCTA TCCTCTGTGC TTCATCCTCT CTCCCCAGTT CCTGGATGAT 2400
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