| Tag | Content |
|---|
EnhancerAtlas ID | HS105-05764 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr1:179996480-179997970 | 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 | CATTAAGTAA CAGAATACTA TTCTGTTTTG GCTTTTTTTG TTTTGTTTTT TGAGATAGGG 60
TCTCACTCTA TCACCCAGGC TGGAGTACAG TGGTGTGATC ACGGCTTATG GCTCACCGTA 120
GCCTCAACAT CCTGGGCTCC ATCAGTCCTT CCACTCAGCC TCCCAAGTAG CTGGGACTAC 180
AGGCACACAA CACCCCACCT GGCTAATTTT TCTATTTTTT TGTAGGGATG GCTTCTGCCA 240
TATTATCTAG GCTGGTCTCA AACTCCTGGG CTCAAGCAAT CCACCTGTTT TAGCTTCCCA 300
GAGTGCTGGG ATTATAGGCG TGAGCCACTG CACCTGGCTT GTTATTTGAA TATATTATAA 360
TTTATTTAAC TCTTTCCCCA TTGCTGGATA TTTAGGTTAT TTTCTTTTTT CTTTATTCCA 420
TTATAAATAC TACTGCATTG AATATCCTTG TAAATACACC TTTATGCATT AGTCTGTTTT 480
TTTCCTATAG GGGAAAATCC TAGAGATAAG ATAATGGGGC AAATAATATG CCATGTTTAA 540
AATGTGGTAC ATTTTGTCAA ATAGCCTTTC AGAAAGTTAG TGCCAGTTTA TACGTCCAAT 600
GAGAATGCTA GGAGAAATTA TTTTTAAATC ATTAACCTAA TATAAACAGT TTAGAAGTGT 660
TCTGAAAGTC TTTGTAGGAC ATTTAGACAT CATTTTACCA GCACTTCCGA AACTGTATTT 720
TCTTGTGAAA TACAAGTTTA GTGGTATAGA CTGTTTCATA AGTGTTCTGA GAATAAAAGA 780
GCTCCATGGT TCCAGAAATT TGGGAAATTC TTTTAGAGTG AAACAAGATT CTTTCCTGTA 840
AGACTCATCA ACACTGTAAT ATGCTAGTGC ATTACTTATT TTAGGATAAG GATGAGGCTG 900
TAGTATGAAG CATTTTCCAA GTGTATTTTG ACTACTGAAT CATCAATCAT CATTTTATGG 960
CATTAGAATT CAGCTGAACA CAGTTTGGGA AATGCTGATC TTGCTCAATT CTTATTTTGC 1020
AATTGTTAGC GTTTGCTAAG TTAGTGTCTC ACCTAAGGTC ACTAACTTGT TATTGGCAAA 1080
GCCCAGATTC TGACTTCTGA CTCCCAAATC CAGTCTATCT TCTGGTATGA TATACTGCAC 1140
AATTTTGAAA TATCATGATA TAGGTTGGGC ATGGTAGCTC ACTCCTATAA TCTCAGCATT 1200
TTGTGAGGCT GAGGTGGGTG GATCGTTTGA TGCAGGAGTT CAAACTCCTG GAGTTCGAGA 1260
CCAGCCTGGG CAACATGGTG AAGCCCTGTC TTTAGAAAAA ATAGAAAAAT TATCCAGGCG 1320
TGGTGGCGCA CACCTGTAGC TCCAGCTACT GGAGAGGCTC AGGTGGGAGG ATCAGTTGAG 1380
TCCCCAAAGT TGAGGCTGCA GTGAGCCATG ATCATGCTAC TGCACTCCAG CCTGGGCAAC 1440
AGAGCTAGAC CTGTCTCAAA AAAAAAGAAA AAATCATGAT TTATTGAGTA 1490
|
| |
|
|
|
