| Tag | Content |
|---|
EnhancerAtlas ID | HS187-02322 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr1:212331700-212333220 | 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 | TGCTATGATT ACAAGTATGA GCCACCACAC TCAGCCAATC TCCCTATTTC AAAGTCAGTT 60
AATTAGCAAC CTTAGTTCTG CTTATAATCT AAATTCCCCC TTGCCATGTA GCATAGCAAA 120
GTCATAGCAT CTGAGGATAA GAATGTGTAC GTCTCCAGGA GCCATTATTC TGCTTACCAC 180
AGACTCCAAG CTCTGTGAGG ACAGAAATTA TATCTCACTT TTTTTTAAGA TGGAGTCTTG 240
CTCTGTCGCC CAGGCTGAAG TGCAGTGGAG CGATCTCAGC TCACTACAAC CTCCACCTCC 300
CAGGTTCAAG CAATTCTCCT GCCTCAGCCT CCCAAGAAGA TGGGATTACA GGTGTGCACC 360
ACCATGCCTG GCTAACTTTT GTATTTTTAG TAGAGGCAGG GTTTCACCAT TTTGGCCAGA 420
CTAGTCTCGA CCTCCTGACC TCAAGTGATC CACCTGCCTT GGCCTCCCAA AGTGCCGGCA 480
TTATCGGCGT GAGCCACTGC GCCTGGCCTA TATCTCACTT CTGTTATACC TGCTTCATGT 540
CTGTGCATTT CTTTCAGGTC AGGTAAAGAA TCCTACCCTA GTTCTCTGCC AGATGGCACA 600
CTGCTATCTA CTTATCAAAG CAGGCAAAGA AACCTCACTG TGGCTGTGAA AAAGGTGTTT 660
TCCCGCAACC AGTCCTCTCA CCAGCTGCAG ACTCTTTTTC TAACAACATC ATTTTTAGCC 720
TGAGAATGTT GAAGACAGGG ACAGTTACAG GTGTCTTTCA GGGCAAGAAC CACGTCATTC 780
ATCTGCGTGT TGCCTATCAC AGGGCCTGGT ACACTTTCAG AACTCAATGC TTGTATGTTG 840
AGTGGGTAGA GGTGGAGCCA GAGTCCAACT GGGGCGGCCA AGCTGATAAC AAGGTGACCA 900
GTAGGTCACT GGGTCAGAGA TCTAGAGCCC AGTTGGGGTG GCTCCTGTGT GACCACAAAC 960
TTCTGAGGCA TACAATACTG TCAATCAGAC TACCAGGGAG CCAGGTGGCC TTGGATTTGG 1020
TGAATCAGGC CAGGCAGGAA GTCAGCAGCA GGCAGACAAG GCAGTGCCCA CATAGGCACC 1080
AAGAGAGGGG TTGGGGCCAA GTGGGTTCAA GAACCTGGTG TGAGTAGAAG CTGAAATGGA 1140
AGGGGCACAT CAGAAACCTG CAGGAGAAAA GGAGCAACTT AACCAGAGGC AGCTTCCTGC 1200
ACCATGACCC AGTACTGATA TTGTCCTCTG CAGTGAGAAT CAGCTCAGCT TAGCCACAGG 1260
CTCATGGGCC ACAGCATGTG AGCGTGAGCA ACAGCTGTGA GGGTCTCTGG TAGGCAGACT 1320
CTGAAACCAG AGGTGAGCTG AAAACAGTCA CTTCAACAAG CAACAGTCAC AGTAGATACG 1380
AAACTGAATA GGACAGTCAC CACCCTTGGG AAGCTCATGG TCTAGCGCAA CAGTCAGGCA 1440
CCAAAAAACA ATCTCATATA TGGTGGTAAA TGAGAACAAA AGGCTACCAG ACTGAAAGCT 1500
TTAAAAAAAA AAAAAAGAAA 1520
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