| Tag | Content |
|---|
EnhancerAtlas ID | HS091-02136 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:85748920-85751200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYB | MA0502.1 | chr1:85750041-85750056 | CCGTGAACCAATCAG | + | 6.1 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_25309 | chr1:85749315-85749985 | Colon_Crypt_3 |
|
| | 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 |
| GH01I085283 | chr1 | 85749316 | 85749985 |
|
Enhancer Sequence | GATTACAGGC GTGAGCCACC GCGCCCGGCC AGGCCAGTGT TCTTAATTAC TAGCTGTAGA 60
CTGAGCTAAG TGCTTCAGGA CATAATGATT CAGAGAAGCT AGGATGCTTG AGCATTCTCT 120
GAATCATTAT ATCCTGAGCC TCACAAATGA TGTATCTGCT CCAGCTTAGG ATCCATGAAG 180
GGCACTGTGC AACAATGAGA GTAGCTGAAG ACTGGCAATG TTAACTAATG CAAGTCTCAG 240
AAAGAGGAAG ATGATATTTG CAAACTCCAG GTGGGGTTCG ATGGCAAGCA TAATTCCAGA 300
AAATAACTTT TTTTTTTTGA GACAGGGTCT TGCTCTGTTG CCCAGGCTGG AGTTCAGTGT 360
TGCAATCTTG GTGATGGCGT GGGTGGCCCT TCTGGAGTGG CTGCTATCAT GACACTGGCT 420
GCAGTGGGGG AGGCGTGGCC AGGGCTGCGA GCTCTACAGG GCTGGGAGGA GCCGGGAACT 480
GTGGAAGCCC TGCCCACTTC CAAGTTGGCA GGGCGGGAGC CTTGTGCTCC CTGGGTGCAG 540
CTGCAGCTGC CCAGGCACAG CTCCAGACCT GGACATCCCT GTGCTCTTGG GGGCCAGAAT 600
CAGGCAGGAG CCCTGCCCTC TCAGGCACAG CTGCAGCCAT CCAGCCATGG CTGTGGACCC 660
GGGCATCTCT TGGGGGCCAG GGAAGCCTCC CTGCCCCTGC AGGCTCAGAA GTACCTGCTC 720
CTGTTGCCTG GTCTCTCCCC ACTCCCGGTG CCGACTCTGA TTTTGGAGCA AAGTTGAGGC 780
CAAGCCCAGG CCCTCTTGCA ACCCAGCCAG GTGTATGCAT GCTCAGAGCA GCACTGACAT 840
GCCAGACCCC TGCCGCCTTG GCTCCCCTCC AGGCTTTGGG CACTGACGAG CACAGGAGGG 900
AGGCTGAGGG AGCACTGAGG GTGGCTCAGC ATGGGCCTGC AGGAGCCCCT CAACACAAAT 960
AGCTTGGGCA GTGGCAGGAG GCAGACAAGC TCCTGGGCAG AAAGGGGCAG GTCCCTGGTG 1020
AAGCCTCACC TTCAAGCCAG GGATGGCCTA AAGCCTGGTG GTGGGGCTGA TGGGCCAGAA 1080
TGGGAACTTA TGGTGCTATT TTCAGGCCCA CCCATTGCCA CCCGTGAACC AATCAGCATG 1140
TACTTCCTCC CCTCTGAAGC CCATAAAAAC CCCTGGACTC AGCCAGACTC CGATGACCAG 1200
ATGACCTGCC TTTGGAGAGG AGCTACCTGC TCCAGGATCT CCTCTCTGCT GAGAGCTGGG 1260
CATAAGTTGG GACTACCAGC TGCAGAGAGG AGCTGCCCAC TCTAGGGTCT CCTCTGCTGA 1320
GAGCTGAACA CTGTTGGGAC AACCTGCCTG TGGAGAGGAG CTGCCTACTC TAGGGTCTCC 1380
TCTGCTGAGA GCTGAACACT ATTGGGACAA CCTGCCTGTG GAGAGGAGCT ACCCACTGTG 1440
GTTTCCTCTA AGCTGTTCTG TCACTCAATC AAACTCCTCT TTGACTTGCT CACCCTCCAC 1500
TTGTCTGCGT ACCTCATTCT TCCTAGACAC AGGACAAGAA CTTGGGATGC GCTGAATGCC 1560
TGGGCTAAAA GAGCTATAAC ACAAATGGGT CTGAAATACA CCCCTTGCTT ACCACGTTGT 1620
GGGCAACAAG AAGGAGAGAG AGCTGCAGCC CTTCTGGGAG CCCAGACCTA GGAGCTCCCC 1680
AAGCCAGGGC TGTAACACCC TCTCTGGGGC TCTGTGGTTC CCGGCATCTC CAAGCTTCCA 1740
AGTTCCACTG CGTTCCTCAG TGCCAGCCAT GGAAGCTGCT TGTGGTCCAC CTGGTCCAGC 1800
CACAGCCTCA CAGGGAGCTG GCGCCTGTGC TGGTGCTTGG AACTGCCTGC CCCACCACAG 1860
CCAGTGTGCC TGGCTGTGCT CAGTGGCCGG GCACCATGCT TGCTCACTCA CACACCCCTT 1920
GCTGCTCTGT GCCTGGCTCT CCCTTGGCAG GCATGAGATT CAGGCCAGTA GTGCAAGCTG 1980
AGCACAGCCT GCCAGGCTGA TTGGGTGGAA CAAGCCCAGC GGGCCTAAGT AAAAACTCAG 2040
GGAAAAGCGC CACTGGCCAC ACAGGTTTCC GGCTGGTGAA GTGACACCCA CAGGATCCCA 2100
TGACATCAGC TCACTGCAGC CTCAACCTCC TGGACTCAAG TGATCCTCCC ACCTCAGCCT 2160
CCCAAGGTGC TGGGACTACA GGCATGCACC ACCATGCCCA GCTAATTTTT GTATTTTTTT 2220
GTAGAGATGG GGTTTCACCA TATTGCCCAG GCTAGTCTTG AACTCCTGGG CTCAAGTGAT 2280
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