Tag | Content |
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EnhancerAtlas ID | HS118-18077 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr8:18533860-18535430 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LMX1B | MA0703.2 | chr8:18534541-18534552 | TTAATTAAATT | - | 6.32 |
| | 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 |
GH08I018676 | chr8 | 18533892 | 18534561 |
| Enhancer Sequence | ACAGGAGTGG GACGCGGCTT CTCCTTCATG TATTTCTTTC TTCTTCTCTT CACAAAACCC 60 ACACCTCTAC CACCTCACTG ATGCCATACC CGCTAACCCT GAGGACTTAG TCACACAAAG 120 AAAAGAGCCA TTCTCTCTGC TCTCATAATG TTTAAATATG TTTCACTTAG TCCAGAAACT 180 GGCCTTAGGA GATTTAACAG GAAACCAAGA TTGTGGAGTG TCCTATCCTG AGTAGGAAAT 240 GCCGAACAAT TGATTTACAG CCTTGTTGCT GCTGGCCAGA CCAGCGAGGA GCCCATCACT 300 CGAGATAACT ATTACAACCA GATATGCTGA CCCGCATACC CTACCCCTCT TTTGTGCTTT 360 GCCCAGCCAA GCCTGTATAC TTTAGCCTTG ATAACAATAT CTGTGCTTTG CCTAATAAAA 420 AAACACCTAC CAGCTTCCCC CTGCTGCTTC CTGCAGAGCC AGTCAGAGGA CCCTGTGCCT 480 CACCTCCACT GTCTCCCTTG TGCTTGAGCA CAAGCCCTGA TTTGAAAGCC TCATCTGGGA 540 AATCTGCTCG GCTCCATGTT AATTTCCATT ACATGGGAAG CCAAAGAGCC TGCGGTCTGT 600 AACAGAGACA TCCAAACCAA ACACATCACC TACACTTTAC TCAAGTGAAA ATGGGTAAAC 660 AGTGATCGTA AAGATCTGCT ATTAATTAAA TTCAAGGGTC AAGAAATATC ACTCTATCAG 720 GAGCATAGTG TGCTCAACAT TTACTCCTAA GTAATCATTT GAGCAATCTT AAAAAAGACA 780 TTTATTTATA TGAAAGTACC AGCAGGATTT GAGAAATTCA CAGATACAGA GGAACTAGAG 840 GAAGGAGGGA AATTAAGAGG TGGGCAGCAG GGGGTAGCTC TAACAAACCA ACCCAGTAAC 900 AAAAACCATT GTCACTTTGC TAGGTTTCCT AACAAAAATA AAACCAGGTC AGCGCAGTGG 960 CTCATGCCTT GAATGCCAGC ACTTTTGGAG GCCAAGGAGT TCAGATCACA CGAGGCCAGG 1020 AATTAAAGAC CAGCCTGGCC AACATGGCAA AAACCCATCT CTATTAAAAA TAAAAAAAAA 1080 ATAGCTGGGT GTGGTGGTGC ATGAGAATTG CCTGAACCCA GGAGGCAGAG GTTACAGTGA 1140 GCCCAGGTCA GGCCATTGCA CTCTGGCCTA GAAGACAGAG CAATATTGTG TAAGGAGTGA 1200 AAGTTTTTAT TTTGGGGCAA GTCTGACTCA AGTCATCAAC TTAAGGGGAA TAAACAGTTA 1260 TCGATAATAT GAAAATGATA CAGATAATGA TAATCTGTAG AACTACGTCC CTGAAGAAGT 1320 CAGGTCTCTT TTTAAGATCT CCTTTGGCTA AGGATCACAG TAAAACATTA GAACATGTTG 1380 ACTGGGCACG GTGGCTTACG CCTGTAATCT CAGCACTGTG GGAGGCGAGG CGGCCAGATC 1440 ACGAGGTCAG GAGATCAAAA CCATCCTGGC TAACACGGTG AAACCCCATC TCTACTAAAA 1500 ATACAAAAAA TTAGCCAGGC GTGGTGGCGG GTGCCTGTAG TCCCAGCTAC TCGGGAGGCT 1560 GAAGCAGGAG 1570
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