Tag | Content |
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EnhancerAtlas ID | HS148-18044 | Organism | Homo sapiens | Tissue/cell | NHLF | Coordinate | chr8:80199850-80200860 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LMX1B | MA0703.2 | chr8:80200246-80200257 | GTTTTAATTAA | + | 6.14 |
| | 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 |
GH08I079287 | chr8 | 80199519 | 80201870 |
| Enhancer Sequence | ACCTTGAAGG TCTTGATGCA TGTTGAGAAG GGAAAGAGAG GCTACACGAA GAGGTGGGAG 60 AAGGTGAGAG GAATACTCAT GGAAAGCCTT CATATGCTCG CAAAAACAGC AGCCCTAGGA 120 TTCGAGAGGA GACTTATTTG CCCTCTTGAC ATAAACTACT AACCTCTGGA GGATTTGGGG 180 CTTGGGGTAA GAACTCACAA ATGGAAAACA AATAATTTCC CCTCATCCAA AAGGGGTGCT 240 AACTCAAAAA AGGCAAGTAG GTGGGATCCT TAGAAGGCCA GAGTGAGGTC TTACGCAGCT 300 GGACAAACTG CTTCAAAAGC CACCAGAAAA CTCGGCCCTA GGGCATAACA GGAATGAAAA 360 GCATATGATA AGTCATAAGG ATCTGGCAGA GCCGGAGTTT TAATTAATGT CTGTCCCAGC 420 AATGTGCCAG GAGACAGGGG GAGGGTTGCA GGTCATCCGA GCTGGTAGGG TAAGAACAAG 480 TATAAATCTC GGGGGATATC TGCAAGGGAG CCTGAGTCTT TGCTGTCACA CAATGCAATT 540 AAGAGCTGCA GGCTCATGAA TAACAGGGAG TGTGTGTTTT TAAGGCAGAG AAGGAAGTCA 600 CGCAGCATGC CATATGAAAC CAAAGAAAAG GCCGACTTGC CCTCTGAGTC AGACAGTCTG 660 GCTGGTGCGC AAGGCTATTT CAGAACACAC ACACAGAAAA CAGAATAGGC AGTGCAGGTT 720 CTTGGGAAAG AGCCGATTTT AGTTGAAAAA TGCAGAGAAA ACCCCAGACA TTGCACGGTT 780 TTAGGGTTTT AGGCTTTAGC CCTACCACCC TGGCAAGCCT CCTAAGAGGG CCATTAATGC 840 CTCAGTACCA CTCGGTGCAG ACCCCACAGT CCTTCCAGAC CCCGCGAGCC CATTCAGGGT 900 GAGCTGAAGA TCCGCCGAAG GAGCAGAGTC ACTTATCCCC GAGAAGAATT GTTCTGGGGG 960 CTGGATAGTG AACAGGAGAG TGAAAGGGGA GAAGAAAGCC ATGTACAGGG 1010
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