Tag | Content |
---|
EnhancerAtlas ID | HS182-08830 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr17:48830-51170 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REL | MA0101.1 | chr17:50224-50234 | GGAAATCCCC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 5 | Chromosome | Start | End |
chr17 | 48917 | 49379 | chr17 | 49699 | 50413 | chr17 | 49762 | 50714 | chr17 | 50723 | 51143 | chr17 | 49643 | 49733 |
| | Number: 1 | ID | Chromosome | Start | End |
GH17I000198 | chr17 | 48371 | 50927 |
| Enhancer Sequence | TGGAACTGAG ACTTCTTTTT CTTTTGTATC TGTCCTTCTC AGATCTCATA TTTGTATTTT 60 CCAAAACAAT CTAGTTGAAG AAATCCTATT TGGTATGTTT GAAATCTTTA TGCTCCCAGC 120 TCAAACTCTG GATTAACAAC AAAACAGAGG AAAACTCTTT TTCTTATTCA GCAGTCAAAC 180 TTCAAGGCAA CTTCAGCCCT GGGAACTCAG CCAGTTGCTG GGAAGTAAAG GAATCAAAGG 240 CTTCTAAACA GTAAAAAATG TCTTTAGAGC TCGGCTCAGA GGGAGCTTTG GCCTTCCTGC 300 AAATTAAGAA TAATGATTTG GTGAGCTTGT TTATCTCCCC TCCACCAGCA AGGCTTGGTC 360 TCCCCAGGGG TAACCGGCTG CAGATTCAAG AGGAAGCTGG GAGGGCTGTC TGGGGCTGGA 420 GAAGGAGGCA GCTCCAACAC GCCGCGGTCA GGCAGTGTGG GGACAAAGAG GTCTCCTTAC 480 TTCCACAGCA CCGAGTCATC GAAGTTTACA AGACACTTCT ACGTTGATCT GGAAAAAGGA 540 GGTGTTCCTA GTACATCTTA GAAAGATTTC CATAAAACGG GCTAAAAAGC AATCATAAAA 600 CCACAACAAA ACACAAACAG GCAAGGGAAA GGATAAACTT CCATCACCTG GAAGCCTCAG 660 AGACAGGAGA GGGTACACAG GTGAGAGCCT TGGCTGGGTG GGAGGTAGGA GTCAGACCGG 720 ACCCTCTGCA GAATTAGCAG TGGTGTGCGC TCACCTCTGG AGCTGCTCCT CTGAGATGGG 780 CCTGGCCCCC TAGATAATTG GAGGGTCCTG CATCTCATGG CAGTTTCCAC CATGCCCTGC 840 TGCAGCTCGC ACCCAGAGCC CTCTGATCAC GGGAGTGGGC AGCTGCCATT TACTGCTGCA 900 CCATTCTGAC CATGTGCCCC ACGTTATTTC ATGTAGCCCT CACTACTGCT GTGTCCAGGA 960 GGCTCAGAGA GGTCAAGTTA CTTACCTAAG GTCACACAGC TGGTATGTGC CAGAGCTGGG 1020 AAGAGAACGT GCACTTGTAT GACTCCGGGA TGTTGGCTTT CTGCCTTGAC GCCCCAGCCT 1080 CTTCAGCTGT GGCTGGTGGC AGGTCCTGGG CCTCTAGCGA GGACGTGCCT GGCTGTGGGC 1140 CCAGCCTGGG ATTGACCTCA CACCCTCTCT CACACCTGGG GCTTCACTGA CAGCGGCGGG 1200 CACAGTGCCT TCCTTTCTCT TTCCCTAGAC ACCAGCTCTG ACCCTCCAAT TTCCACCATG 1260 ATCACAGTGT TCTCAGAGTC AGGCAGCATA TGAGGAAAAT TGCCCTTTCC CTGGAATAAT 1320 TTACCATCTT GTAATTTCCA TTACCTGACC CTGTTGGAGC CTATTCCGTG CTGAGCTGTT 1380 TGAATTTCCA GCTTGGAAAT CCCCAGGCTG GGCGGGAAAT GCTGTTTCCT GAGGGAGGAG 1440 CAGACGAGGG AGGTGCTGCC TGCAGGCTTG GCGGAGGGTC AGGGGGTGTT TGGGACAGGG 1500 ACACAGTGGG GAGGGGGCTG AGAACAGCAA CCAGGCAGCA TTTGTGATTC TTCTGAATCC 1560 AGAGGGGCTT GTGTGATGAA ATTCCACAGG GCTCTGCCAG GCTGATACGT GGGAAGGGTG 1620 GCAGAGGGCT ACTGCGACCT ACAGGCAGGG GGTGGTCCTA GGCAGGCAAA GGCATTGGTA 1680 GGAATGCAGA GAGGGCTACA GAAAGCAAGG GGACTCCTGG GCCAGGCCCT GGACCGGGGC 1740 ACAGAGTAAG GCTGTTGAGG GTGTTGATTT CAGTTTTTGA CAAGTCGAGG ATCCTCCGGA 1800 TACCACGTGA CAACACACAG CTTAAGAGCA CGGGCCTTGG GCTCAAATCC TCGCTCTGTC 1860 ACTCGCTGGC AGTGTGGTCC TGTGCAAGTT GACGGACTTC TCTCAGCCTC AGTTTCCTCC 1920 TCTGTGAAGT GGAGGGAATG GTGTCCACCC CCCATTATTC CTTTAATGTG AGCGCTAACT 1980 CAGGGCAAGT GTGTAAAGAC CCAGTCTGGC CTCCAGCTGG GGTCCATCTG ACCCAGGTGG 2040 TGGCTGTTTA CAGGGATCAA CTCTCCCCAG TTTGCTGGGA ACTTTCCTGG TTTTAGCCCT 2100 GAAAGTCCCG CATCTTGTGA AACCCGTTGG TCCTGGAAAA CCTGGATGGT TTCTCACTCT 2160 GCCTGTGGTC TCCCGCTCCT CATTGCACTA AAAGTGCCAG GTCATGTCTG TGTCCTGGGG 2220 AAGGCCGAAG CCCTTGCTAA GGTTTCTGTA ATATCACCTG TGGCTCTGAG GCCTGCTTTG 2280 GCTGAGTTAA TTCGGTGTTG AGGTCGGTAC GTGTGCTTGC ACACGTTTCT GAACCACAGA 2340
|
| |
|
|
|