Tag | Content |
---|
EnhancerAtlas ID | HS188-00338 | Organism | Homo sapiens | Tissue/cell | Th2 | Coordinate | chr1:35964340-35966650 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr1:35965409-35965429 | ACCCAAAACAACAACAACAA | + | 6.72 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 35964893 | 35965048 | chr1 | 35965244 | 35965960 |
| | Number: 1 | ID | Chromosome | Start | End |
GH01I035499 | chr1 | 35965001 | 35965875 |
| Enhancer Sequence | AATCACAATC CATATAGGGG TCCTCCTTGG TAAGGAACAT GCTATCCTAG TTTCTACTTA 60 ATATTAAACA ACAGTTTATA AAAATTCAGC TTTCAATACA TTTTGATTTG AGACACAATG 120 GTATTGAAAT AAAAACCCAC CACTGTCATT AATAAAAATC CTACCAATGG AAAGGAATGT 180 CTTCCTGCAG TGGCATTAGT CGGGTCTTCT TCCTGCATTA GTGGGGTCTA ATGACACACC 240 ACATCCCAAT TCTCAGCAAC TAAAGCTGAG ACTGGAGAAT ATGGCAGGGT TTATCTTTAT 300 AGAAATTAAT TAAAAGTTAG TCTTCTGAGA GTCTCCTTAG AGAAACTAAG ACCATCCACT 360 AAATAGGAAA GAGAGGGATG ACACCTGTGG TGTTAACAAG AGATGGTCAA GTTCTGCCAG 420 TTAGTAAGGA GTTGTTAAGG GACCCACACC AAAATCCCCA TCAACTCTTG CTTCGTAGGT 480 GCTACAGACT GAATGTTTGT GTTCTCCCAA AATTCGTATG TTGAAATCTA GCTAACCCCC 540 AAAGTGATGG TATTAGGAGG TAGGGCCTTT GGAAGGTAAT TAGGTCATGA AGTTGGAGCC 600 CTTGTGAATG GGATTAGTGC TCTTAGAAAA CGGACCAGAG AGAGTTTGTC TTCCTCTTCC 660 ACCGTGTGAG AACATAGCTA GAATGCAGTG TCTATGCAGA CTGGCCCCTC ACTAGACACC 720 AAATCAGCCA GCACCTTCAG CTGGGATTTC CCAGCCTCCA GAACAGTGAG AAATAAATTT 780 CTGTTGTTTA TAAACCACCC AGTTTATGGT ATTGTTACAG CAGCCTCAAT GAATTAAGAC 840 AATAAATTAG CTTACAAAGG AGCCAATAAA CGCAATTTCA AACTCACTGC ACATACTAAA 900 AACTAGATAA GTAGATTAAA GAACCAGAAC TATTAGATTA GAGGAGAAAA TGGGTAGCTA 960 TGAAGGGAAA AAAAAATAAG GAAAGGGTGT TGTGGTCCAA GAACTAACAC AACAAAAACA 1020 AGCAAACAAG TAAAAACAAG TAAAAAAAAA AAAAAACCCT GAAAAACAAA CCCAAAACAA 1080 CAACAACAAA ACATGAAGGG AAACAGCACT GCTTAGGTTT CTGTCATCAG TTACGTAAGA 1140 TTATCCCTCT GTGGCTGCCC ACACCCCACA CCTCTATCTT CTGATAAGAG GTAAGCTCAG 1200 GCTTTACATG GAGCCAGCAC AAGAGTTCTC AGAAAAAGAA GGCAGCAGAT GGCTATCTGG 1260 GTGCTTGGCT CATTTATCCT CTAAGTCATT TATTTGTTCC ACAGAAAGCC ACTGGCTTGC 1320 TAAGGGTCAA AATGCCGTGT GTGATTATTG ACTGGAAACA GGGAGACGAT GCTGTTAGAG 1380 AGAACAACAC TTCAGTCTTC CTACAGTCAA ACCTTACATG CAGGGATACC TAAGTGGACT 1440 TTCATTTCCT GCGCTCAAAT AAAGCACTTT TTTCTCTGGC ACATAGCAGG ATTGGCAGCA 1500 ATTAATTGTC AGAACTGCTT AAGCTGTACA CATTCTTATA ATGTACACAA TTAATTGGCT 1560 GAACTGCTTA TACTGTACAC GTTCCAGGAC CCAATCAACA AGCCTCTGTG CTCCTCCTGC 1620 CAACAATTCA GAGGTTCATG GTACAGAAAG GGTGCAATAC TTAAACTAAG CAGGACAGGC 1680 TTCACCCTCT TTAAGTTGAG AAACGGGAAT ATATTGATGA CATTCCTTTC TACTTTTGGA 1740 ATTGCAAAAG GTCCACAATA TCTGCCTTTG GATTCAATAT ATGTATATTT CCAAAAGAGT 1800 GAAAAATGCA GACTGACAAT CCAAATGCCT TTGCAGCTCT GCAGGCAGGC AAGACAAAAG 1860 CAATTTATGA TACAATTTCT CTCCACTTTG GATGCAGAGT TGCTTGACCT ACCTTAGTGA 1920 AAACAGCACA AACTAGAAAC TGGTGCTGCT CGCCAGTCAT CCCTAATTAG AATGAGATCT 1980 GCAGTGCATA CTTTTCTCTT CCCTTCCCTA GTGCATTAAG CAGAAGTTTG AACTCCCAAG 2040 TTCTCTCCCA AAAGAAATGC CAAGGCAATT CTCAATGCAC AAGGCAATCT TACCACCTTT 2100 CCAGAGCTAT ACATGGCCTT CAGGGTAAGA AGCTAGCTCC TAAGCATGAT ATATAAGGTC 2160 AAATATAACT TATCTGGATC TGAAGATTTC ACTTTGCCCC ATTTTTTTTT TTTTAGCAAT 2220 ACTTGCAGTT CTCAATATGT AATGCCAAGC TTTGTAATGC CTCCGTGCAA CACTGCATGC 2280 AGCAAAAGCC CACTCCCAGT CCTGGGGTTC 2310
|
| |
|
|
|