| Tag | Content |
|---|
EnhancerAtlas ID | HS091-48749 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr9:131667250-131669430 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr9:131668355-131668370 | TGACCTTTGGTCTTC | - | 6.12 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr9 | 131667633 | 131667800 | | chr9 | 131668475 | 131668589 | | chr9 | 131668289 | 131668550 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH09I128905 | chr9 | 131667537 | 131668604 | | GH09I128906 | chr9 | 131668830 | 131669176 |
|
Enhancer Sequence | TAGGCAACAG AGCGAGACTC CGTCTCAAAA AAAAAAAAAA AAAAAAAAAA AATTAGCCAG 60
GCATGGTGGC ACACACCTGT AGCCCCAGCT ACCTGGGGGA GGCTAAGGTA GGAGGATTGC 120
TTGACCAGGA GGTTGAGGCT GCAGTGAGCC ATGATCACGC CACCGCACTC TAGTTTGGGC 180
AACAGAGCAA GATCCAATCT CTTACAAGAA AAATTATAAA ATTATAAAAT ACACAGAAAG 240
GACTGGAAGG TTATTATTCA GTGAAAAGTT AACAGTGTGT AACCCTGGTG GGGATTGTAA 300
AGCGGATTCT TCTTTTTTTG CTGCTACGCT TTTTTACAAT TTTCCGTATG TTCTCCAGGG 360
AACATCTAGT ACCTTATCCC TCCGTGACAG CCATACGTCT TTCATTGTAA GAGCAACCAG 420
CCTTGGCCGT GTGACCACGA ATGGCCACAG AGAGGCATTC TCACAGAGAT CTTGCTGCGT 480
GCCTCCTGTG TAGCACAGTC TGGGTTTCCT AATGTGGCTT CTCAGCCAGT GTTTCCCAAG 540
CTTGGCCAAT CATTAGAGTC ACCAAAGTTA TGTGTTAAAA ATCAGGTTCC CAGCCAGGCA 600
CGGTGGCTCA CTCCTGTAAT CCCAGCACTT TGGGAGGCTG AGACGGGCAG ATCAGGAGGT 660
AAAGGGATCG AGACCATCCT GGTCAACATC GTGAAACCTT GTCTCTACTA AAAAACACAA 720
AAATTACCTG GGCATGGTGG TGCAGGCCTG TAGTCCCAGC TACTCGGGAG GCTGAGGCAG 780
GAGAATCACT TGAACCCTGG AGGCAGAGGT TGCAGTGAGC CGAAATGATG CCACTGCACT 840
CCAGCCTGGC GACAGAGCAA GACTCCGTCT CAAAAAAAAA AGAAAAATCA GATTTCCAGC 900
TTCTCGCCAT AGTAGTCAAA CTAGACTCTC TCTGGGAGAG CCTGCTGTTG CTGCTGTTTT 960
TAATTCCTTT ATACACACGC AACCAGAGAT GATTTTACAT TAAGGCCTCT CTGTGATCAC 1020
CCAGTTTGTG AGGGAGGAGA GCCTTATTCT TAATCCCCTC TCTTGAGGCC GCTCCCCTAG 1080
GAGCCTGTCA TTAAGACCCA CTATGTGACC TTTGGTCTTC CGAGTGTTCC CAGAATCTTG 1140
TACACACATA ACTATACACA CATGTGGAAT TTTGTTGTTG AAGCAGGGTC TCTGTCACCC 1200
AGGCTGGAGT ACAGCGACGG GGTCATAGCT CACTGCAGCT TCAACCTCCT GGACTCAAGC 1260
GATCCTCCCA CTTCATCCTC CCAAAATGCT GGGATTACAG GCTAGGATTA CAGGCGTGAG 1320
CCACCATGCC AGCCCCCATG TGGAATTTTT TTTTTTTTTT TTTTTTTTGA GTTGGAGTTT 1380
CACTCTTGTC GCCCAGGCTG GAGTGCAATG GCACAATCTC AGCTCACTGC AACCTCCACC 1440
TCCCGGGTTC AAGTGATTCT CCTGTCTCAG CCTCCCGAAT AGCTGGGATT ACAGGCACCC 1500
GCCACTACGC CAGGCTAATT TTTGTATTTT TAGTAGAGAC CGAGTTTCAC CATGTTGGCC 1560
AGGCTGGTCT TGAACTTCTG ACTTCAGGTG ATCCACCCAC CTCGGCCTCC CAAAGTGCTG 1620
GGATTACAGA CGTGAACCAC GTGGAATTTT TAAACCTTGC TCTTTGTTTT ATGGAAGTGA 1680
GTTCATGTTG TGCCCCCTCT GCATGTTGCT TTCTTTCCTC ATATTTTGCG GGAATCCCTC 1740
CAGCCCTTTG CTGCAGCTTT ACAGCAGCTG GTTCCCAGTG AACTGGGAGT TTTAAATGTG 1800
TCCCTCTGGT CAATCTGTTC ATTAAATAGG TGGACTTTAG AAAGGAGTTC CCGATTGCTC 1860
TTACTGGAAT GCAAGGGATG GAGCAGAGAA CCCTGAGGCT GCACTGGGGA TCTGTCTAAT 1920
CTCACTGTGC TCAGTCTTCC TGTGTATTAA ATGGGGAGCC TGCCTGCCTC CCCCAGGGTG 1980
GTTTCCCAGC CAAGTGGCCA CATGCTTTCT GCAGAAGGGC TGATAAGTGG GCTGCCCCGT 2040
GGAGTAGGCA GGCTTTGGCT CCCAGCTAGA TTTGAGGTGG AATTTTGGAC AATGGAAGAA 2100
TTTTCATTGT CTTCTTCCCC TGACCCCTGG TCCTAGGAAA GCCAGGCCAC CCTGTGCTAA 2160
CCCCCCTCCT ATGGCTCCCT 2180
|
