| Tag | Content |
|---|
EnhancerAtlas ID | HS091-20031 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:43908310-43910500 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr17:43909663-43909682 | AAGCTCCACCTGGTGGTGA | - | 6.23 | | SOX10 | MA0442.2 | chr17:43909603-43909614 | AAAACAAAGCA | + | 6.02 | | SREBF1 | MA0595.1 | chr17:43908663-43908673 | GTGGGGTGAT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 43910137 | 43910232 | | chr17 | 43909559 | 43910125 |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH17I045834 | chr17 | 43909601 | 43909750 | | GH17I045833 | chr17 | 43909781 | 43909790 | | GH17I045832 | chr17 | 43909801 | 43909930 |
|
Enhancer Sequence | GTCATCTCCT TTCCCTTCCT GACCCCAAGG TTTAGGCTCC CAGCCCAGCT TGGTGACACT 60
CCCCACGGGC ATTGGCCATG CTGGCTTTTT CCCCTCAGGA CCATGGTTTC TGCATCTATA 120
AAGGGAGAGA TCTGGGGGCT GGACTCATTC AGAGGGTCCC TGCCTGTGCT CTGCCTGGGT 180
GGGGCTGGAC AAGCAGGACC CAGCCTCCTT TATCTGCCTT GAGCTTACAC AGGAAGCAGC 240
CTGGAGCCAG ACTGCCCAGG TTCAAATAGC TGTGTGACCT TGGACAGATT ACTGCAGTGT 300
GCCTCAGTTT CCTCATCTGT AAAATGGACA TGCTACTGCC TCAAAGGGCT GTTGTGGGGT 360
GATATGAGTC CATCTATATT AAGCATTTAC AATAGCTCCT GGCACATAGA GTAAATGCTA 420
TATAAATGTG TTCTATTAAT ATTAAGACAT CTTAATAAAA GAGTCCATGA ATTTAATAGA 480
AGTGGACCTA GATGATCTCA GAGGCTTCTT CCAGCTCTGA AGTTCTTTGG TTCCTTATGA 540
AATGGACTCA GATGTTTCCA ATCGTGCCTG GAAACTTGAT TTCTGCTGCA GTGGAGCTCA 600
ACTTTGGCTC ACATTAGAAT CACCTGGAAT GCTTGGAAAA GTACCAATGC CCAGGCTTCA 660
CCCTCAGAGA ATCAGGCGCA ATTGGTCTGG GGTGTGGCCT GGCACCCAGA AGTCTTGAAA 720
ACTGCCCAGG TGATTCTAAT GTGCAGCTCA GATTGAGAAC CACTGAGAGA GAGCGGGGCA 780
GAAAAGGTGG ACATGGATGG CAGGGGAGCC CCAGGACCTT CTTTGCCAAA CAAGTGTTCC 840
CGGGAACCTA TCTGACTGAC GGACCTGGCG TCCAAGTGGC CTCCACCACA GTGACAAGCC 900
CTCTCCTCCC CCATGGAGGG GAGGGGGCCT GCACGGCTTC ATTGGGCTGA AAGAGGAGCC 960
TGGAAGATTA TCTTGCGTGT TTATGTGGTT GACTCCCTCC TGACTCCCTC CTGACTCAGG 1020
CTGGCTGAGG CCTTGGGAAG CCGAGGCAGG CGGATCACTT GAGGTCAGGA GTTTGAGACC 1080
AGCCTGGCTA ACATGGTGAA ACCCCGTATC TACTAAAAAA AAAACAAAAA AACAAAAATT 1140
AGCTGGGTGT GGTGGTGCGC ACCTGTAGTC CAGCTACTCG GGAAGGCTGA GGCAGGAGAA 1200
TCTCTTGAAC CCAGGAGGCA GAGGTTGCAG TGAGCCAAGA TCGTGCCACT GCACTCCAGC 1260
CTGGGCAACA GAGTGAGACT CCATGAGTCT CAAAAAACAA AGCAAAACAA AAACTGTTTG 1320
GGCTAAAGGA GAAAGTGAGT CTGAGCGGCT CTGAAGCTCC ACCTGGTGGT GAGAATTCAA 1380
CACTGCAACA GAGAGGATCT GGGTGTGAGA AACCAGAAAC GAACTTGCAG ACCAGAGGCC 1440
CGAGGACTGG ACCCGGCCCT CAGAAGCTGT GTGTGGCCAG CATGGTGTTT TCTGAAAACT 1500
CGATTTTGTA GCCAACCTTT AAAAAATCCA AAGGTTTCAT TTACAAATCT CAATTTCTGG 1560
CTTATGAGAT CTAGCCACTG GGGGTCTTCA TACCCACGAG GACATAAGGG CTTCCAGTTT 1620
GTCTGGTCCC CACCCACTCC CCAGGCCTCC CTGGAGCTTG CTGGAGGGAC ACTCGGGAAA 1680
ATGCAAAGCA ATTACCTCCT GCAGCAGGTA GAACCTGTGC AAGTATTCCT CTCAAGGTTG 1740
TTCAGGCTGT GACTGGACAG ATTCAGGCTG AGATTGCGAA CTGCTGGGTG CCCACTGGGT 1800
GACAGGTGTG GTGCCACTCC CACCAGCAGC CCCCCAGAGG GCATGCTGGG CCTCAGCCAC 1860
TGCCAGGGGA CTGTGAGGAG GAGCCGAGGA TGCAGCCTCG TGTTGGGCCC ATGCCCGTTC 1920
CCAGCCACTC AGTCTTTCCC ACTGTCTACC TCCTGCCCCG GTGCTTGCTT CCAACTTTGC 1980
ATCTCATCAC AGAGGATGCT GTCCGTTCTG CAGATGGGAC AATTGAGGCA TGGCAGTGGG 2040
ATCAAGTGAC TTGACCTTCT GCCAGGGTTG GAATTGGGAC ATCTACCTCT TGGCCTCCAG 2100
CCCCAGTCCT GTCCTGGCCA AGCACTGTCC CTCCCCATGC CATCGAGGTG GACGCAGATG 2160
ACCCTTCCTC CCCTTTCCTC TGTGGCCTTC 2190
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