Tag | Content |
---|
EnhancerAtlas ID | HS052-02964 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr1:179995490-179998000 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Mecom | MA0029.1 | chr1:179996982-179996996 | GAGATAAGATAATG | + | 6.42 |
| | 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 |
GH01I180026 | chr1 | 179995387 | 179997878 |
| Enhancer Sequence | GCTGGTCTCG AACTCCTGGG CTCAAGCAAT CCTTTTGCCT CCGCCTCCCA AAATGTTGGG 60 ATTGTAGGCA TAAGCCATTG CCCTCTGCCT ATTTTAATTG TGGTAAAATA TACATGACAT 120 AGAATTTATC ATTTTAACCA TTTTCAAATA TACAGTTCAG TGACATTAAG TACATTCACA 180 TTATTGTTGC AAGCATCACC ACTGTCCTTC TCCAGAAATT TTTCATATTC CCCTACTGAA 240 CTCTGTATCC ATTAAATAAT AACTCCATTC TTCTGTCCAT CAGCCGCTGG TAACCACTGT 300 TCTGTTTTCT GTCCCTATCA ATTTGACTAC TCTGCGTACT TCATATAAGT GGAATAATAG 360 AGTATTTGTC CTTTTTATCT TGCTTATTTC ACTTAGCATA ATATCTGACT CACCGTTCAT 420 CTATGTTGCA GCATGTATCA GAATTTCCTT TCTTTCTATT GCTGAATAAT ACTCCATGCT 480 GTGTGTATGC CATATTTTGT TTATCCATTC ATCTGTTGAT GGACATTTTG GTATTTTCCA 540 CCTTTTAGCT ATTGTGAATG ATGTTGCTAT GAACATTGGT GTACAAATAC CCTATTTGAA 600 TCCCTGCTTT ACCCAGATAC AGAATTGCTA GATCAAATGG TAATGCCATG TTTAATTTTT 660 TGAGGAACTG CCATAATGTT TTCTATAGCA GCTGTACCAT TTTACTTTCC CACCAGCAAT 720 GCACAGGGTT CTATTTTGTC TACATTTATG CCAGCACTTT ATATTTTCTG CTTTTTTGAT 780 AATAGGACAT CCTAATGGGC GTGAAATGTT AACATTTTTA GCAAGAGTCC TTCCAGACAA 840 TTTGTAGGCA CACACAAATA GGCAATTTTA TGTGTATGGG ATCACATTTT ACATGCAATT 900 TTATTCTGTC TGTAGGGTAT GGGTATCTTT TTCTGTCAGT AAATATGGAT TACCATTTGT 960 AAGGATTACC CACTAAATAA ACTCTAGACC CATTAAGTAA CAGAATACTA TTCTGTTTTG 1020 GCTTTTTTTG TTTTGTTTTT TGAGATAGGG TCTCACTCTA TCACCCAGGC TGGAGTACAG 1080 TGGTGTGATC ACGGCTTATG GCTCACCGTA GCCTCAACAT CCTGGGCTCC ATCAGTCCTT 1140 CCACTCAGCC TCCCAAGTAG CTGGGACTAC AGGCACACAA CACCCCACCT GGCTAATTTT 1200 TCTATTTTTT TGTAGGGATG GCTTCTGCCA TATTATCTAG GCTGGTCTCA AACTCCTGGG 1260 CTCAAGCAAT CCACCTGTTT TAGCTTCCCA GAGTGCTGGG ATTATAGGCG TGAGCCACTG 1320 CACCTGGCTT GTTATTTGAA TATATTATAA TTTATTTAAC TCTTTCCCCA TTGCTGGATA 1380 TTTAGGTTAT TTTCTTTTTT CTTTATTCCA TTATAAATAC TACTGCATTG AATATCCTTG 1440 TAAATACACC TTTATGCATT AGTCTGTTTT TTTCCTATAG GGGAAAATCC TAGAGATAAG 1500 ATAATGGGGC AAATAATATG CCATGTTTAA AATGTGGTAC ATTTTGTCAA ATAGCCTTTC 1560 AGAAAGTTAG TGCCAGTTTA TACGTCCAAT GAGAATGCTA GGAGAAATTA TTTTTAAATC 1620 ATTAACCTAA TATAAACAGT TTAGAAGTGT TCTGAAAGTC TTTGTAGGAC ATTTAGACAT 1680 CATTTTACCA GCACTTCCGA AACTGTATTT TCTTGTGAAA TACAAGTTTA GTGGTATAGA 1740 CTGTTTCATA AGTGTTCTGA GAATAAAAGA GCTCCATGGT TCCAGAAATT TGGGAAATTC 1800 TTTTAGAGTG AAACAAGATT CTTTCCTGTA AGACTCATCA ACACTGTAAT ATGCTAGTGC 1860 ATTACTTATT TTAGGATAAG GATGAGGCTG TAGTATGAAG CATTTTCCAA GTGTATTTTG 1920 ACTACTGAAT CATCAATCAT CATTTTATGG CATTAGAATT CAGCTGAACA CAGTTTGGGA 1980 AATGCTGATC TTGCTCAATT CTTATTTTGC AATTGTTAGC GTTTGCTAAG TTAGTGTCTC 2040 ACCTAAGGTC ACTAACTTGT TATTGGCAAA GCCCAGATTC TGACTTCTGA CTCCCAAATC 2100 CAGTCTATCT TCTGGTATGA TATACTGCAC AATTTTGAAA TATCATGATA TAGGTTGGGC 2160 ATGGTAGCTC ACTCCTATAA TCTCAGCATT TTGTGAGGCT GAGGTGGGTG GATCGTTTGA 2220 TGCAGGAGTT CAAACTCCTG GAGTTCGAGA CCAGCCTGGG CAACATGGTG AAGCCCTGTC 2280 TTTAGAAAAA ATAGAAAAAT TATCCAGGCG TGGTGGCGCA CACCTGTAGC TCCAGCTACT 2340 GGAGAGGCTC AGGTGGGAGG ATCAGTTGAG TCCCCAAAGT TGAGGCTGCA GTGAGCCATG 2400 ATCATGCTAC TGCACTCCAG CCTGGGCAAC AGAGCTAGAC CTGTCTCAAA AAAAAAGAAA 2460 AAATCATGAT TTATTGAGTA TATGTGTATT AATAATATGA TTTAATGTAG 2510
|
| |
|
|
|