| Tag | Content |
|---|
EnhancerAtlas ID | HS091-33580 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr3:10357120-10359730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFF | MA0495.3 | chr3:10357804-10357819 | ATGCTGACTGAGCAT | + | 6.11 | | MAFF | MA0495.3 | chr3:10357804-10357819 | ATGCTGACTGAGCAT | - | 6.17 | | RREB1 | MA0073.1 | chr3:10357161-10357181 | GGTGGGTGGGTGGGGTGAGG | - | 6.43 | | RREB1 | MA0073.1 | chr3:10357153-10357173 | GCTGGGTGGGTGGGTGGGTG | - | 6.83 | | RREB1 | MA0073.1 | chr3:10357157-10357177 | GGTGGGTGGGTGGGTGGGGT | - | 8.04 | | Sox3 | MA0514.1 | chr3:10357677-10357687 | CCTTTGTTTT | + | 6.02 |
|
| | 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 |
| GH03I010317 | chr3 | 10358728 | 10360020 |
|
Enhancer Sequence | CTGCAAAGGG AGGACAGCTC GGGAAGCCTG CAGGCTGGGT GGGTGGGTGG GTGGGGTGAG 60
GGCTGTCACT ACACAGAGTC TAGTTTGGAC CAGAATCTCC CTGAAATCAA TCTGATCTCA 120
AAGTATCATC ACCCTCAGGC AGGAAGCTAG CATGTGGACA TTCTCACTTC ACCTATGGGC 180
AGTGTCTCTC TGAAATGGAC AAAGCAAGCC ATGCCCAGCT GGTGTCACAG ACCCTTTACA 240
TACCTCAGGG AAGGGCTCTT CCATTCCTGT TCCGCAGGGT GGGTATGGGA GAAAAAAAGT 300
TGGCCTAGCT GCCCTCTTCT TCCTCCATCC TCTCAGGCCC TATTCAGTTC TTAGGCTCTG 360
TGGGCTAAAG GGGAATACCC CTGGGTTCAG CTCAGCCCTA GCACCTGATG CTAATGCATG 420
GGAGCAGGCC AAAGGAGTGG GCCTCTGACT GCCTGGAGTC CCCAGTCAGG TCTTCTGTGA 480
TGCAGCTCTG GCCTGCACAC AGGGTTCCAT TCAGATATTT GGGCTCTTTC CAGCCCTGGC 540
CCTGGATCCT TTGTGGACCT TTGTTTTGGG GCTTCTGCTC GACCTTTTCC CTAGTAGTGT 600
GCCCAGAGCT TCCCAGACTT TCCACCCAAG GAACACAATG CCTTAAGTGT CGCTGCTCTC 660
ACCACTTGTG AACCGAATTC CTTGATGCTG ACTGAGCATG CAGAACTAGG CCTGGCCCCT 720
ACCTGCAGAT CCTTGTCCGC AGGGTGATGG TCTCTGAGGC ACCATGCCTC CTGCACCACT 780
GAACACCCTG GTCCCTTCTG CTTGCTGGCC CTGCCTATTC CAATGGATGT CCCTTTCCCC 840
AGCTGTCCCA CCCTGGGAGT TTCAGGACTA TCAGCTGCAC TCCCATGGCC ACCAGGGGCA 900
ATTATGCCCA TTCAAAGGCA CTCATTCTGT CTGGCTCAGA TGGGAATTCT CACCTCCCTA 960
CGCAAGGAAC ACATCCTGAT TTTTCTTTGG GAACTCCCTC CACTGTATCA GGCCTTGGTT 1020
TCTTGGAGGG CAGGCAGTAG AGGAGTGTTT CTGAAGCACT TCTCATGCTT CTCAGTGGAA 1080
GGAGGCAGGA CATAGTACCT TTCAGATCTA AATCCTATCT CCTTAGTTTA CCTGCTGTGC 1140
AAACTTTGAA AACACTTCAT CTCCTTGAGC TTCAGTTTCC TTATCTTTAT TATTTACCAA 1200
CATCCTATGG GCCTTAGTTC CCTTATCTTT AAATAAGGCT AAAGATAGCA TCTGTCTCAA 1260
CAGTTGTTAT GAAGGTTAAA CAAGATATTG AATGAAAACT CACGCCTGTA ATCCCAGCAC 1320
TTTGGGAAGC TGAGGCGGGC GGATCACCTG AGGTCGGGAG TTCGAGACTA GCCTGACCAA 1380
CATGGAGAAA ACTTGCCTCT ACTAAAAATA CAAAATTAGC TGGGAGTGGT GGCGCACGCC 1440
TGTAATCCCA GCTACTCGGG AGTCTGGGGC AGGAGAATTA CTTGAACCCG GGAGGCGTAG 1500
GTTGCGGTGA GCTGAGATCA CGCCACTGCA TGCCAGCCTG GGCTACAAGA GCGAAACTCC 1560
ATCTCAAAAA AAAAAAAAAA AAAAAAGAAA AGTACTTAGC ATGGGGCCTG ACACTCAGTG 1620
AGCATGCAAA TGTTTGTCAT TACTACTTGG CCTCATCTAG TTCTCAAACC AAACTCATAC 1680
GAGTAGGTAG CATATCCATT ATTTTTCCCG TAAGTAAATT GAGGCTGGCT CAGAAAAGTT 1740
AAGATATTGG CTAGGGAGTC TCAGACTGGG TCTTCCTGCC CATGATTCCA TGCTATCTCC 1800
AAGGAGGTGT GGTCTTACAG CTAGACCACT CATGACTGAA TCCAGAGAAC ATATACAACT 1860
CTGGGACCAG ACAACCTCTC AGAAACCCAA AAGCAACTGT TGGTGGACAG GTTGTGAGGG 1920
CAAGAACCCT GACATGAAAC ACTGTCAGCC AGCTGTCCTG GGTCTTGCTC AAAGGCTGCT 1980
TGGCCCTGAA TGAAGCAGAG TCTGTGTTTT TCCTGCGGTA GACTTTAACC TCTGGACCTT 2040
CTCCTGCAGC CCTGTCCTCT TATACTGAGC CTTGTGTTTA CCTCTCAGGA AATGCCCTGA 2100
GTGTGGACTT CTGGTTCAAA GGGCCTTGTC TGGCCTATTG TCTTGGTGGT TTGACTGGGC 2160
TCTGCCTGGG GCTTTCACTG TGGCTGCCCT CTGCCTTTGT ATTGAGTCAT CTTTCTACAC 2220
TCTCTTCTTT TCACCCCCCT TTCCAGTGGG GCTAAGAAGT GACAGCAGGA GGAAGACAGG 2280
TGGGAAGACT ATTGTCAAGC CTCCGTACCC ACTCAGCCTT CATCCGAGAG CAGGTTATTG 2340
TATTGGCTGG AAGACTGACA GCCTAGAACT ACAAATTATT CCCAGGTTCC TCCCAGCAGA 2400
GAGTGATTAG ACTGCCACAG TCCTGACAAC TCAGAGGGCA CTGCTAGGGA GCCTGCCATA 2460
CCCCGAGATT ACAGGCTGAT AGGCAACCAC TGCAAAGCCA CCCTGGATCC ATGAATGATC 2520
AACAGAAAGG GGTAATGAAA ACCCCAAATT GCTTCCCTCC CACAAAAATG CCCATGTCCA 2580
CACCCCTCCA GGGAGGGTGA TATTAATACT 2610
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