| Tag | Content |
|---|
EnhancerAtlas ID | HS069-00684 | Organism | Homo sapiens | Tissue/cell | GM18951 | Coordinate | chr1:181446360-181447680 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Esrra | MA0592.2 | chr1:181447069-181447080 | TTCAAGGTCAT | + | 6.62 | | Esrrg | MA0643.1 | chr1:181447070-181447080 | TCAAGGTCAT | + | 6.02 | | FOXA1 | MA0148.4 | chr1:181446645-181446661 | GAATAAGTAAACAAAC | + | 6.34 | | FOXP2 | MA0593.1 | chr1:181446649-181446660 | AAGTAAACAAA | + | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTCAAAGAGA TCTCTTTTGT ATTCTTCCCT TTTCCAGCTG CCTCCAGTGG GAGGGGATGG 60
CTCCCTGCTC TGTTGTCTCC CAGTACTCTC CTGTGGTGCA CTCCACATCC CGCCTTGTAT 120
TCGAGCCCTT TGTGGGTATG TTTTCCCTTC TCCTCTTTTG AACTGTAAGT TTTTAGAGGC 180
TATGACTGTG TCTAATTTAT CTCTGAGCCC CAGAATCCCT GAGAACAATG TGTGGCTCAT 240
CAAAGGGGAT TAATGAGTAT TTGTTAAATG GGTTTATGAA TTCATGAATA AGTAAACAAA 300
CACACAGCTC TCTCAGGTAT CATGGCCTTT GGGTCTCCAG ACACTGGTCT CTACTATTTT 360
TTTTTCCTTT TTTCCTCCAT TCCTCTTTCT GACCTGATCT CAGGCACTTA CATGTCTCTG 420
CTCCTCTGTC CATCCCCCGC ACAACAGAGT GTGTTCATCC CTGGCTGCAC TTCTGAAGTT 480
GGCTTTCAGA AACAGAGTCT GTAGACATGC AGTGTTTCCA GTGTGTTACC GTGGTCACAG 540
CTACTGAAGG TGAAATGTAC ATAACAAGTA CTTACGTAGC ACATACTTAT TGTGTGCAAG 600
GTACTGATCT AAGAGCTTTA TGCATATAAA CTAACTTAAT TTTCACAACA GCCCAGTGGA 660
GCAGAATGGT ATTATTCTTA ACAATTAAAC CCTCTGGGAG ACTCTCTGGT TCAAGGTCAT 720
GCCTTACCTC TCTAAAGCTC AAGATCCTGC CTATAACTTG ACTCTTAAGC AAGGAAAATA 780
TTATTTTGAC ATGCAGTATG TTAATAATGG TCACATATTG TGAAGAATCC TGTCCTTATT 840
ATTAGGAGAT CCAGCTCTGC TATTTCCTAG CTCTGTGCAC TTGGACAAGT CCCTGACTCT 900
CTGGGTGTTC AGATAACAGG ATGTGCCTCA CAGTCCTTCT GCAAAGATGC AATGAGAAAA 960
CATTACGGTT GGCACCCAGG AAGTGATGGG TTGTCATAAA TGAATGGTTT TTAAAACACT 1020
TTAAAACCAA CTTTGCTGAC CTGTGGTTAG CTGATAGCAT GTTGGAGTGT GGGGCTTCTC 1080
AGGCTTAGGT TTGAGAGATG CTGATTCTAG GGACGGACAT TACATAAGGA TGTGAAGTTA 1140
TGTTTTCACC CAAGTAAGGG CTGTGAGGTA TTGTGAAAGC CACCAGACTC CCAAGATGTC 1200
TGCATTGCCA TAATGCTCCT CTGCTCCACT ATGCATTTGC ACATGGTCTC CTGCCAACTT 1260
TTTTCTTAAG AACCCACTCC CAAATCCTCT CTGCATTATG TTCCTTAGAG CACTGCTTTG 1320
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