| Tag | Content |
|---|
EnhancerAtlas ID | HS091-39869 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr5:179729580-179731770 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr5:179731204-179731215 | GGCTGTGATTT | - | 6.02 | | Myog | MA0500.1 | chr5:179731583-179731594 | GACAGCTGCGG | + | 6.32 | | NR2C2 | MA0504.1 | chr5:179730688-179730703 | TGAACTCTGCCCTCC | - | 6.03 | | SCRT2 | MA0744.1 | chr5:179731356-179731369 | TTGCAACAGGTGC | + | 6.13 | | ZBTB18 | MA0698.1 | chr5:179730639-179730652 | CAACATCTGGATG | - | 7.34 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr5 | 179730890 | 179731056 | | chr5 | 179730391 | 179730531 | | chr5 | 179730791 | 179730849 | | chr5 | 179731597 | 179731657 |
|
Enhancer Sequence | GACCCTAGAG CAGAGAAATA GCATCATAAA ATAGACCCTC TCTGAAAGAA GCTATCCCTG 60
ATGCATACAG AGTATCTGGA AGCTACATTA CTGTGATGAG AACAGTCCTC TTTTGCATTT 120
GCTGGAGTCA TGGGTGAGGT GGTATGTGTG GGACACAAAT GCTTGGAAAG GATAAAGTGT 180
CTGATGCTTT TTGGGGGTTT CTTCCCCTTC CCTGGTAAGG AGATTGCCAT CCTGCTGCAT 240
CATTTGGCAC CCATTTGTGC CTTGCCGAGA GCGGGGCAGA CTCACTCCTA ACTCTAGCGG 300
GGCTCATAGT CTAGTGGTAG AAAACAAAAA CCTAGACAAG CAAACCAAGA AATAAAGATG 360
AATTCCAGGC CGGGCGTGGT GGCTCACGCC TGTAATCCCA ACACTTTGGG AGGCTGAGGC 420
GGGTGGATCA CGAGGTCAGG AGATCGAGAC CATCCTGGCT AACATGGTGA AACCCTGTCT 480
CTACTAAAAA ATACAAAAAA TTAGCCGGGT GTGGTGGCGG GGGCCTGTAG TCCCAGCTAC 540
TGGGGAGGCT GAGGCAGGAG AATGGCGTGA ACCTGGGAGG CGGAGCTTGC AGTGAGCCGA 600
GATGGCGCCA CTGCACTCCA GCCTGGGCGA CAGAGCCAGA CTCCGTCACA AAAAAAAAAA 660
AAAAATGAAT TCCAAAGAAA TGCCACCAAG GCTAGAAAAC AGGATAATGT CATTGGGAGA 720
CTGGTGAGGT CTCCAAAGCT CTCTCAAAAA CAGGAGACAT CTGGACTGAA CCCTAAATGA 780
TGAGGGGACA ACCCTCGGCG GAGCATTCTG TGGGAAGGGC ATTCCAGACA GCAGGAGCGG 840
CCAGCGCAAA GGCCCGGAGG CGGGCGCGGG CGCAATGAGA GTGGGACGCA GAAGGAAAGC 900
TGGAGTGCCT GGAACTCACT GAAACAGGAG GAAAGGGCCA GATAACGCAG GACTGTGGGT 960
CTCTGTGGCT TGACAGGCAG GTATGGGAGG GTTTTAAGTG GGGAAATGAT GCCATTGTGT 1020
TTTATACCCT CACTCTGACC TCTGTGCTGA GCCAGGTGGC AACATCTGGA TGGGGCACCT 1080
CATTGGATTT CACCTCCCCG AAACTTCATG AACTCTGCCC TCCTACCTCA GGGCAGCTGC 1140
TGTGTACAAA GCATTTGGTT GGTCTTTGTG GCCGGTTCCA GGAAGGGAGC TCCTGGCTTC 1200
TGGACTTTCC CATGTGACAA AAGCATCTTT GTTATTTATG GGAGGTCCCT TGGACTATAC 1260
CTAACTTTAT GCTAAGGTGA CGACTCGTGG TGGGCCTGTA GATAGTTCCA GGATGGCGTC 1320
TGGCCCTGCT AGAAAGGCCA GCCACATGAT TAGAAGGTTG GGGCTTTGAG ACATGAGCCT 1380
GTCAGTCTGA CCTCCCAACC TCCAAGGACA AAAGTGGGGC TGGCGACTGA GTTTGATCAC 1440
ATGGCCAATG GTTCACTCCA TCCTGCCTAC TTAATAAAAC CACAATACAA ACTCTGGACA 1500
CTGGAGCTAG CAGCTCAGGG GAGCTCCCGG GCGACACACA GTGACGTGCT GGGAGGGTGA 1560
CACATCCTGA GGACACAAGC TTCACATCTG GGGCCCTCAA ACTAGGGGTC TCTTCTTTTG 1620
GGTTGGCTGT GATTTATATC TTTTATAATA AAACTGTAAT CATATAGTCA TCTCCTGAGT 1680
TCTATGGGTC GTTCTAGAAA ATTACTGAAC TTCAGGGGAG AGTGGGAATC CTTGGATTCA 1740
TAGTCAGTTG CTCAGATGTG TGGGTGGACC CCTGGCTTGC AACAGGTGCC TGAATCGAGG 1800
GCAGTCTTAT GGAAAGCTGT GCCCCTGCCC TATGAGACCT GACCTAACTC CAGGTAGTTC 1860
CCATCGGAGC TGCTTGGCCG CAGAACCTGG GGAAACCCTG CCCCAGGGAT GTCCACCAGG 1920
AGTACCTCCC CTGAGCTCCA GGCTAGGATC TGGTGCTGCT CACAGCAGTG TGGGTCCCTG 1980
GGCCCCACCA AAGAGCTGTG TGGGACAGCT GCGGGCTGAC CAGCTCCTTT CCAAGTGTGT 2040
GCACTCCCCA CAGGCGGCCC GGGGGAGGGT GTGTGGTCAC AGCCACTCAC TGGCCAGACC 2100
ATCCATCACT GGTACTGGCA GACAGTGGTG AGGTGGGCAT GCATGGGGAA AAGCAGGAGA 2160
GAGCTGGCCC AGTCCAGTGG AGAGCCCTCA 2190
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