Tag | Content |
---|
EnhancerAtlas ID | HS003-41612 | Organism | Homo sapiens | Tissue/cell | A549 | Coordinate | chr7:47702870-47705230 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr7:47703445-47703465 | CCCCAAAACACACCCCCAAG | + | 6.87 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH07I047664 | chr7 | 47703641 | 47707305 |
| Enhancer Sequence | TGAAGAAACC GACATTTAAG TAACAAATTA GTAGGAGAAG GAATGAACTT TTGAACATGG 60 GGCTTTCCTT CCCATTTCAG GTCTCATTCT TTCCATCATG CCACATGCTT TGCAGAGTCT 120 GTGAACTACT AGAAGATGAG TAGCTAACCC GTATGCCTCA GGGTTCATAA AAGTAACAAA 180 GAAGGGTCTC TTAAATTCCT TAAGAAATAC TTTTTCAGGC GTATCGGAAT TCATAAATGT 240 GGTAACATCC CATTAAAATG TCAAGCATCT GCTTTTGGTT GAAATTGTGT CTAACTTTTT 300 AAATACCAAT TGACACCAGC GATTAGTTTT TGGTGAATTG TGTTGCCTCT GGAGATATAG 360 TTTCCAGAGC CACAGCTCAG GTATCAAAGT TCCTGAAATG AAATTGATCT AGCTGGGGAT 420 CAGGCCAAGC ATATTAAAAT AGGGTGGCTA TGAGGACAGC GAGGTCGGGG GAGGAAGAGG 480 GCAGAGACGG GCAAGAATAT AACTTAGGCC TGACCTTGAC TCCCCAAGGC CCCCGATCTG 540 ATGTCCCCCT CATGTCTCAG TCTTGCAAGA CATTGCCCCA AAACACACCC CCAAGCTCCT 600 TTCTTCAGTT TTTAGAAAAT TAGCAAATAT TGAGCTGGAA TAACCATTAG CGACCATCTG 660 GTCCAAACTC ATTATCTGAA ATTGGAAGAC ACTGAAACAC AGGGGAAAGA ATGACATTTC 720 TGCTGTTCCT GTTGCTGGCT GTGCAGAATA CAATGCTTCC TGCATGGACA ATAGCAGGAA 780 TTATTTTACA TGGGAAGAAA CTGAAGCTCA GCAAGGTTTG CTAATTTTCT CAAGACACTC 840 AAGATGTTCA TTTTCCACAG GACAGCCTCT CTGGGTCTCT TCCAACCTCT CTCTGTCCAA 900 TTCTGAGCTG GAGGCTAAGT CTAAGAATGG GACCAAATTC CCTACATAGA AGTGAGATTT 960 TAACCCAGGT CTTTTGGTTT TAGGGTTTAT TCCCTTTTCA TTGTCTTTAA AGGATTGCTA 1020 TAACTGAATA ACCTCAACAA TAAAATTAGA TTCATTTTTA AGGCATTGAA AGATATTTAT 1080 CTGAGGAATG CATTTATTTG CTGTTTACTG AAGAACAACT CTAGATGCTA ACAGTATCAA 1140 GATGACTAAG AGATAGTTCT GGGCCAGGCG CAGTGGCTCA TGCCTGTAAT CCCAACACTT 1200 TGGGAGGCCG AGGTGTGCAG ATCACAAGGT CAGGGGTTCG AGACCATCCT GGCTAACATG 1260 GTGAAACCCT GTCTCTACTA AAAATACAAA AAAATTAGCC GGGCATGGTG GCGGGCGCCT 1320 GTAGTCCCAG CTACTCAGGA GGCTGAGGCA GGAGAATGGC GTGAACCCGA GAGGCAGAGC 1380 TTGCAGTGAG CTGAGATTGC ACCACTGCAC TCCAGCCTGG GTGACAGAGC AAGACGCCGT 1440 CTCAAAAAAA AAAAAAAGGC AGTCCTTAGA TCCACGGAGA ATGTAGACCT TTACCACCCT 1500 CACAGCTCAA TCCAACAAAT AGACATTCAT CCTATCACTT ATTGGTTACT TATTAAATCC 1560 TCATGGCATA CCAGACATTG TGCGAAGACA CAGGGCTGTC AGACAGAGAC TTACAAGAAG 1620 CTTAGGGGGA GCAAGCGCTG GGGCACAAGT TACTGTTGCA ACAGAGGGAG CTCGTGGTGG 1680 GCAGCATGGG GATACTGGGG CCTCTCTGAC TATGGACTGG GCAATGGGAG AGGTCTCAGC 1740 AGTCCAGGGA CTTCTCAAGG GACATCATCT GACAACATGT GAGCCAATTG TCCCCGCCTC 1800 ATTTCTCTCT GCATGTTCCT TTAGAGAAAA AAGAGATGGA ATTACACCTA CAAAAGTGTT 1860 GCAACAAACA GGCTAATTCA CCAAGAAAGA CTTTTCTGGG ACTTTTCCCT GTCACTTGCA 1920 CCAGCTCCTA GTGGGAGATA GACCCATATA TGGGGCCATG TTGCCCAAAT CCAATCACCA 1980 TCTGTGGCTC AAGTTCTGTT CTTTGCTGGT CTGAGCAGGT GCTAAAGAGG ACTGGAAATT 2040 AGAATTTGAC AGTACTGAGG AAACTGGGTT TTCCAATTCA TTCTTTCGTC GGTGCATTCA 2100 TTCATCAGCA CTATGAGCAG TTCGCAAGGG TCAGGCATGG ACGGATGCCT GGGGATACAG 2160 ATACAGACGA AAACAGACTG TGCCCGGGAG AAATGCTTAC TCTCATGGGA CCAGTGGAAG 2220 GGCTGAGGGG CAATTGTGGT TGAGTGCTGC TCTGTTTTTT TTTGTTCTTT TTTTTTTTTT 2280 TGAGACAGAG TCTTGCTCTG TCACCCAGGC TGGAGTGCAG TGGCGCCATC TCGGCTCACT 2340 GCAAGTTCTG CCTCCCACGT 2360
|
| |
|
|
|