Tag | Content |
---|
EnhancerAtlas ID | HS108-01663 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr1:46534590-46536960 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Mecom | MA0029.1 | chr1:46534806-46534820 | GAGACAAGATAAAG | + | 6.11 |
| | 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 |
GH01I046069 | chr1 | 46535473 | 46536672 |
| Enhancer Sequence | CTCTAGCTGC TGAGTTGAGA AAAGACTGTT CAAAGGAGGC AGCAGTAGAA GTGGAAAGAT 60 CACTTGTGAA ACTTTTATAA TAATCTAGGC AAGGCATGAT GGTGTCTTGG ATGAGGGTAG 120 CAGTAGTAGA GGTCATGAGA AATAGTGAGA TTCTTAACAT ATTTTGAAGA TAGAGCTGAC 180 AGGATTTGCT GATGGCTTGG ATACAAATAT GACAGAGAGA CAAGATAAAG ATGATTTCAA 240 GGTTTTTGTC ATAAGCAATC AGAAGAATGG AATTGTCATT TATTGACATG AAGAAGGCTA 300 TTTAAAAAGA ATGTGTTTAG ACCAGGCACG GTGGCTCACG CCTGTAATCC CAGCACTTTG 360 GGAGGCCAAG GCAGGCAGAT CACTTGAAAT CAGGAGTTCG AGACCAGCCT GACCAATGTA 420 GTGAAACCCC GTCTCTACTA AAATACAAAA ATTAGCCTGG CGTGGTGGAG GGCACCTGTA 480 ATCCCAGCTA TTCAGGAGCC TGAGGCAGAA GAATTGCTTG AATCCAGGAG GCAGAGGTTG 540 CAGTGAGCCG AGATCACGCC ACTGCACTCC AGCCAGGGGT ACAGAGTAAG ATGCCATCTC 600 AAAAAAAAAA AAAAGAATAT GTTTAAAGGG GGAAAAAGTT TGGTTTTAGA CACTTTAAGT 660 TTGAGATGCC TCCTAAACAT TCAAAAGCAG ATGATCCAGC AGGCTACTTA AAGAATCTAA 720 AGTTCAGGAG AAAGGTCTGG GCTAAAGATA GAAATTCAGG AGTTACCAGC CGATGTATGT 780 TATTTGATGG TGAGCATAGC TGGACAGAAA AAGAGGTCCA AGGCCTAAGC ACTGGGGTAT 840 GCCAATGTTT GGTGGTCAGA GACATGGAAG GAAGAATCAG CAAAGGAAAC CAAAAGGGAG 900 CAATTAATGA AGTGAGAGGA GAACTAAGAG TGTGATATCC TAAAAACCAA TACGTACAAA 960 AGCACTTCAA CAAAGAGGAA ATTATCAACC AAGTCCAATG ATAATTAGGT TTGGCAAAGT 1020 AGATAGCACT AAATGAACTG ACTAAATGGT TTCAGTGAAA TGGTAAGGAT AGAACCCTGA 1080 CTGGAATGGA TTCAAGAAAA TGAAAGAAGA TAGAAATGCC CATAGACAAG TGTCTCGAGG 1140 AACACTGCTA TAAATAAGGG CAGAGAAATA GGGAAGTATC TAGAAAGAGA TATAGGGTCA 1200 ATTATTTACT ATTCTTAAAT GGGAGATAAT AGAGTATATT TATATGCTGA TGGGAATGAC 1260 TCAATAGACA AAAATTGTTG ATCCAACAAA GAGGACAAGA TTATTCCTAG AGTGATGTCC 1320 TTGAGTAGAT TAGAGGGATG GGATGGGATC CAGTCTACAA ACAGAGAAGC AGACCCTGGA 1380 CAAGGACATG AACAGTCATC CACTGGAACA GAAAAGCGGC AGACTATTCA CATTAATGTG 1440 TAAATATGTT GATAGCTGTG GTAATAGGAG CATGAAGGAG TTCTCGTCTG ACTGTGTCCA 1500 TATATCAGTG AAATTAAAAG CAAGTTCTAT AGTTAAAAGT GGGAAGAAAG GCTGTCCTTT 1560 AAAAGAGAAA AAAAGAACAT GTGAAATTGT CATTTACGAA ACTGACGAGG AAGCAGGATG 1620 AATGCATTGT GGAAATGCAG AAGTTAAGCT GGGCAGTTTT AAAGGTCACT TAAGGTTAGT 1680 GGTCATAATT AATGTGAAAC CAGTCCATGT GGTCACGTCC CCTTCTCCAC ATTCAGCAGC 1740 TCAAGTATAG GGAAGGACTA AGTGGAGAAC TGAATTTAAT ACCGTGTTGG AATTTAGTCT 1800 GGTGACTACA CTGGAGGAAG AGAGGAGCAA GTTTGTTAAG GATATATTCA CATGGGTAAT 1860 TTTAATAATA ATGTACATGG ACTCTAAGCA GAGATGAGAG AAGGAAAGGA ACTGAAGGTC 1920 ATGCTAGTCC TCCTTGTATC TCAGCACCTA GTCCAATGCC TGGCAGATAG CAGATTCTTA 1980 AAGATTTGTT AAGTATCCAG ATTTTCTACA ACAAATACTA TTTACCAATT TAAAAAATAA 2040 GAGCTATTGA ACTGAAAAAT CTCTATTTCT TCACTACCTA CTACTCTCTG CAGTCTGGTT 2100 TTACTCTCAT TCCTCTCATT TAAGAGTCAC CAATGACTTT GAACAAATTC AGACTCTGTC 2160 CCCTTCCTTT ATCCCAGGCC CTCCTTCTCC CTCACTCTCT CCCTTCTTAA TATTTCATCC 2220 TTCCATAACT TTGATGAAAT TATTATTTTC TTTCAACCTC TCAAACCACT CTTCCTGTCT 2280 CCTCCAACCC TAGTTATTCC CTAAAAAAAA ATTTTGCCTT CAGCCTCCAC CTTTTAAATT 2340 TTATATATTT TTTTCCATAA AAATCCCATT 2370
|
| |
|
|
|