| Tag | Content |
|---|
EnhancerAtlas ID | HS023-00727 | Organism | Homo sapiens | Tissue/cell | CD8+ | Coordinate | chr1:35964600-35965970 | 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 | TAAAGCTGAG ACTGGAGAAT ATGGCAGGGT TTATCTTTAT AGAAATTAAT TAAAAGTTAG 60
TCTTCTGAGA GTCTCCTTAG AGAAACTAAG ACCATCCACT AAATAGGAAA GAGAGGGATG 120
ACACCTGTGG TGTTAACAAG AGATGGTCAA GTTCTGCCAG TTAGTAAGGA GTTGTTAAGG 180
GACCCACACC AAAATCCCCA TCAACTCTTG CTTCGTAGGT GCTACAGACT GAATGTTTGT 240
GTTCTCCCAA AATTCGTATG TTGAAATCTA GCTAACCCCC AAAGTGATGG TATTAGGAGG 300
TAGGGCCTTT GGAAGGTAAT TAGGTCATGA AGTTGGAGCC CTTGTGAATG GGATTAGTGC 360
TCTTAGAAAA CGGACCAGAG AGAGTTTGTC TTCCTCTTCC ACCGTGTGAG AACATAGCTA 420
GAATGCAGTG TCTATGCAGA CTGGCCCCTC ACTAGACACC AAATCAGCCA GCACCTTCAG 480
CTGGGATTTC CCAGCCTCCA GAACAGTGAG AAATAAATTT CTGTTGTTTA TAAACCACCC 540
AGTTTATGGT ATTGTTACAG CAGCCTCAAT GAATTAAGAC AATAAATTAG CTTACAAAGG 600
AGCCAATAAA CGCAATTTCA AACTCACTGC ACATACTAAA AACTAGATAA GTAGATTAAA 660
GAACCAGAAC TATTAGATTA GAGGAGAAAA TGGGTAGCTA TGAAGGGAAA AAAAAATAAG 720
GAAAGGGTGT TGTGGTCCAA GAACTAACAC AACAAAAACA AGCAAACAAG TAAAAACAAG 780
TAAAAAAAAA AAAAAACCCT GAAAAACAAA CCCAAAACAA CAACAACAAA ACATGAAGGG 840
AAACAGCACT GCTTAGGTTT CTGTCATCAG TTACGTAAGA TTATCCCTCT GTGGCTGCCC 900
ACACCCCACA CCTCTATCTT CTGATAAGAG GTAAGCTCAG GCTTTACATG GAGCCAGCAC 960
AAGAGTTCTC AGAAAAAGAA GGCAGCAGAT GGCTATCTGG GTGCTTGGCT CATTTATCCT 1020
CTAAGTCATT TATTTGTTCC ACAGAAAGCC ACTGGCTTGC TAAGGGTCAA AATGCCGTGT 1080
GTGATTATTG ACTGGAAACA GGGAGACGAT GCTGTTAGAG AGAACAACAC TTCAGTCTTC 1140
CTACAGTCAA ACCTTACATG CAGGGATACC TAAGTGGACT TTCATTTCCT GCGCTCAAAT 1200
AAAGCACTTT TTTCTCTGGC ACATAGCAGG ATTGGCAGCA ATTAATTGTC AGAACTGCTT 1260
AAGCTGTACA CATTCTTATA ATGTACACAA TTAATTGGCT GAACTGCTTA TACTGTACAC 1320
GTTCCAGGAC CCAATCAACA AGCCTCTGTG CTCCTCCTGC CAACAATTCA 1370
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