| Tag | Content |
|---|
EnhancerAtlas ID | HS118-01658 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr1:212331590-212333140 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEOX1 | MA0661.1 | chr1:212331757-212331767 | GTTAATTAGC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 212332200 | 212332373 | | chr1 | 212332400 | 212333133 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I212158 | chr1 | 212331801 | 212333049 |
| Enhancer Sequence | GCCTGGTTAA TTTTTTTAAA AAAATTTGCA GAAACGAGGT CTCACTATGT TGCCTAGCTG 60
GTCACGGAAC TCCTGACCTC GCGGGATCCT CCCACCTCAG CCTCCCAAAG TGCTATGATT 120
ACAAGTATGA GCCACCACAC TCAGCCAATC TCCCTATTTC AAAGTCAGTT AATTAGCAAC 180
CTTAGTTCTG CTTATAATCT AAATTCCCCC TTGCCATGTA GCATAGCAAA GTCATAGCAT 240
CTGAGGATAA GAATGTGTAC GTCTCCAGGA GCCATTATTC TGCTTACCAC AGACTCCAAG 300
CTCTGTGAGG ACAGAAATTA TATCTCACTT TTTTTTAAGA TGGAGTCTTG CTCTGTCGCC 360
CAGGCTGAAG TGCAGTGGAG CGATCTCAGC TCACTACAAC CTCCACCTCC CAGGTTCAAG 420
CAATTCTCCT GCCTCAGCCT CCCAAGAAGA TGGGATTACA GGTGTGCACC ACCATGCCTG 480
GCTAACTTTT GTATTTTTAG TAGAGGCAGG GTTTCACCAT TTTGGCCAGA CTAGTCTCGA 540
CCTCCTGACC TCAAGTGATC CACCTGCCTT GGCCTCCCAA AGTGCCGGCA TTATCGGCGT 600
GAGCCACTGC GCCTGGCCTA TATCTCACTT CTGTTATACC TGCTTCATGT CTGTGCATTT 660
CTTTCAGGTC AGGTAAAGAA TCCTACCCTA GTTCTCTGCC AGATGGCACA CTGCTATCTA 720
CTTATCAAAG CAGGCAAAGA AACCTCACTG TGGCTGTGAA AAAGGTGTTT TCCCGCAACC 780
AGTCCTCTCA CCAGCTGCAG ACTCTTTTTC TAACAACATC ATTTTTAGCC TGAGAATGTT 840
GAAGACAGGG ACAGTTACAG GTGTCTTTCA GGGCAAGAAC CACGTCATTC ATCTGCGTGT 900
TGCCTATCAC AGGGCCTGGT ACACTTTCAG AACTCAATGC TTGTATGTTG AGTGGGTAGA 960
GGTGGAGCCA GAGTCCAACT GGGGCGGCCA AGCTGATAAC AAGGTGACCA GTAGGTCACT 1020
GGGTCAGAGA TCTAGAGCCC AGTTGGGGTG GCTCCTGTGT GACCACAAAC TTCTGAGGCA 1080
TACAATACTG TCAATCAGAC TACCAGGGAG CCAGGTGGCC TTGGATTTGG TGAATCAGGC 1140
CAGGCAGGAA GTCAGCAGCA GGCAGACAAG GCAGTGCCCA CATAGGCACC AAGAGAGGGG 1200
TTGGGGCCAA GTGGGTTCAA GAACCTGGTG TGAGTAGAAG CTGAAATGGA AGGGGCACAT 1260
CAGAAACCTG CAGGAGAAAA GGAGCAACTT AACCAGAGGC AGCTTCCTGC ACCATGACCC 1320
AGTACTGATA TTGTCCTCTG CAGTGAGAAT CAGCTCAGCT TAGCCACAGG CTCATGGGCC 1380
ACAGCATGTG AGCGTGAGCA ACAGCTGTGA GGGTCTCTGG TAGGCAGACT CTGAAACCAG 1440
AGGTGAGCTG AAAACAGTCA CTTCAACAAG CAACAGTCAC AGTAGATACG AAACTGAATA 1500
GGACAGTCAC CACCCTTGGG AAGCTCATGG TCTAGCGCAA CAGTCAGGCA 1550
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