| Tag | Content |
|---|
EnhancerAtlas ID | HS091-01544 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:45180280-45182700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:45180817-45180836 | TGTCCAGTAGGTGGCAGGC | + | 6.29 | | MNX1 | MA0707.1 | chr1:45181894-45181904 | TTTAATTACC | - | 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 |
| GH01I044714 | chr1 | 45180241 | 45181289 |
|
Enhancer Sequence | GGTATACAGA AATCAGAGAC AGAATTAATT ACAGAATGTC AGGAAGATGG CTGACACTGG 60
TCTCTTCCTT TTTTCTTGAG GCAGGGCCTT GTTCTGTCAC CTAGGCTGGA GTGCAGTGGC 120
GCATGCACGG CTCACTGCAG CCTCAACCTC CTGGGCTCAA GTAAGTAGCT GGGACTACAG 180
GCACATGCCA CTATGCCTGG CTAATTTTTT TTTTAATTCT TTTTAGAGAT GGGATCTCAC 240
GATGTTGCCC AACCTGATTT GACTGTCCCC GGCCTTTTTT CTTTTTTTGT TGGGGGGGAA 300
ACAGTTTTAC TGTTTCCCAG GCTGGAGTTG AGTGGCTTGA CAGCTCACTG CAGCCTCAAA 360
CTCTTGGGCT CAAGCGATCC TCCCGCCTCA GCCTCTTAAA GTGTTGAGAT TGCAGGCATG 420
AGCCACCACG CCTGACTGGT CTGTTTCTTA CAGCAGTGCA ACATGCTAAA CACGTTCATG 480
CTAGTGCCCT GCTGGAAAAG GAAGCAAACC TCGGTAAGGA AGCGCACTTC TCATATGTGT 540
CCAGTAGGTG GCAGGCTTGT CTGGACCTGC AGAGAAAGAC CCGGAACCCT GGTTTTGCAA 600
GGCTCTGGGA TCAAAGAATT ATAAATGATC AGTGCTGTTA GCACCCTGGA AATGGCTGCA 660
TGGAATATCC ACAGTTCCCA GGTACAATGC CATTTCTATG GCTCCTTCTG CCAAAGGAAT 720
ACTAAGCCTG CTGCTACAGC CCTGTCTCTT GTTCATTGTG GTTTCCTGGG CAAGTCATTT 780
GTTCTTGGTT TCTTCGTCTA TTCAATGAGA TGATCAGACC AGTGATCACT GAGGTTTCCT 840
CTAATGCTGA TAGGCTGTGG ATTCCAAAGT TCCTCTTCGG ATTGGAGCAA TGAATTTGTC 900
TCCTGCACCA TTAAAGAGTT TCCATGGAGT GTGAGTGGCT AGGACCTCAC ATCTGTTTTT 960
TGTTTTTTTG AGATGGAGTC TCACTCTGTC ACCCAGGCTG GAGTGCAGTG GCACAATCTC 1020
AGCTCAATGC AACCTCTGCC TCCCGGGTTC AAGCAATTTT CCTACCTCAG CCTCCTGAGT 1080
AGCTGGGATT ACAGGCGCCC ACCATCACAC CTGGCTAATT TTTGTATTTT TAGTAAAGAC 1140
AGGGTTTCAC AATGTTGGCC AGGCTGGTCT TCAACTCCTG GCCTCAAGTG ATCATCTGCT 1200
CGCTTCAGCC TCCCAAAGTG CTGGGATTAC AGGCGTGAGC CACTGCACCC AGCCACATCT 1260
GTTTCATTTA CTGCTGTTTC ATCAGCACCA GCACTGCACC TAGCACGTGC TCAATCCCTG 1320
TTTGTCAAAT GCATGAGCAT GGGCCCCACA GAGCATCCTC TCAGCTTCAT GGGGCCTGAA 1380
CTCTCAAACA TTCAAACCCT CCTGATGATA CCTCCTCCTT GAATACTCTC ATCCTCCTTC 1440
CCAAACCCAT ACTCTCCTGG CTTCCTCCTA TGGCTCTAGA AACTGCTTCT CGGTCTTTTA 1500
TACATTCCCA TTCCTCTACC AGTCTCCTAG GTGTCAATTT TTTTTTTTCA GCATTCAACT 1560
CCAGGTCTTC TTCTCCTTCT TTGCTGTCTA TGGCACCTCG TCCGCTCCCA CAACTTTAAT 1620
TACCACGACT TTATGTACCA CCTACCACCT TGATGACAGA AACAATAGTC GCTAATCTTT 1680
ATAGAGTGTT AACTCTATGC TGGATACTGC CCTTGATCTT TACTCATTTA CCCCTCACAG 1740
CAAGCCAAGG AGGTGGGCAC TATTATTTTC CCCATTTTAT GGATGGAGGA CAGAGTAGTG 1800
GAGTGACCTC TCTATAGCTC TAGACCTGTG TGTCCATTTG CCTTCTGAAC ACCTCCCCTC 1860
AGATGTCACC AGTGGACTTC TGATATTCCA GTTCCAAAGC TTTTCTTCTC CAAGGTCCCA 1920
ATCTCAGTGG AAAGTACCCA GCTGCCCAGG CTAGAAATAT TGGTAATTGT CTTGTCTTTT 1980
TGCTTCCCAC CTTCAACCAA CTTCTAACAA GACCAGTCAA TTCTAACTCT TCAATATGCA 2040
GATGCGTTCC CTCTTCCCCA TTCTGTCTCC ACTGCTGTAA TTCAGGTCTT CATACTGCTC 2100
ACCTGCACTG GCCTCTACAC CAATCTTCAT CTGTCCAGTA TGGCGCCCAC ACACAGTTCA 2160
TTTTCCTAGT CCACCACCAG AGTGGAGGCA GTAGACTTAG TGGTGAAGAA TATGGGATTT 2220
GGAATCCGAA CTATTCTTTT TTCTTTTTTT TTTTTTTTTT GAGACGGAGT CTCACTCTGT 2280
AACCTAGGCT GGAGTGCAGT GGCGCGATCT CGGCTCATTG CAACCTCTGC TGCACAGGTA 2340
AAAGATATTC TCCTGCCTCA GCCTCCCAAG TAGCTGAGAT TACAGGCACC TGCCACTGCG 2400
CCCAGCTAAT TTTTGTAGTT 2420
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