| Tag | Content |
|---|
EnhancerAtlas ID | HS060-24964 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr3:121951640-121952960 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr3:121952130-121952147 | AAGCACAGGGTGTTCCT | + | 6.29 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 121951931 | 121952115 | | chr3 | 121951825 | 121952851 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH03I122232 | chr3 | 121951241 | 121953247 |
| Enhancer Sequence | AAGTGATTGC TGAGAAAGAG AAAAGTGGCC CCTGACAACC TGGATCTGGG TGGTCCCATA 60
AGCTAGGCCT TGGCGTTCTC CTGTTAAACA TAAACAACTT CACAGAACAT CAACAGCAAG 120
CAAGATGTCT CTGTGACCAT GATAAAGACA AAAATAAGAC CACTCCACAA TCATGTCTGA 180
ACACAGACAA AAAACGTTAA CATTGTCCAA ACCATGGAAC TAACCAAACA TTTCCCTATT 240
CTGGCTCGGA GGAGTGACTG CTACTCCTTT ACCCTTACAG CTTCAGTCTC ACTTAGTCTT 300
CCTCCCTTCT AGACAAGATT TATTAAGATA TGGAATCATA GAATTTACCC CTGCTTCTGA 360
CAGCATGCAA AGCTCCACTT CCTTAAACCG TCCCCAAAAT CGCCTACCAC AAACCGCACT 420
CCTGTAAGTC CTTTCTAACA CCCTGTCGGT GAGACACCCC ACCGTTCTCC TTCTCTGCTA 480
TGTCCTGTCC AAGCACAGGG TGTTCCTCAT GCAAGTGCAG GGCTGGCCAT GAGAAGCAAT 540
GCCACCCTAC ACTTTGCTCT CCTGGTGTCT CTCTTGTCTC ACCAGTTCCA GCCCAGTCCT 600
GGGGGTCTTT GGCTGGATGG AGTTGACATC AGTCCCCTTC CCTGCTCTTC TCTAATCTCA 660
CCACAGGTAC CCTGCTCTGG GCCTCAGGGT GTTGGGGAGT AGAGCTGGGA AGTAGCGGAG 720
GAGAAAATGA GGAAGAGAAA TGCAAGAGGG CGACTTCACA GGGGAATTTT GTCCACCTGA 780
TGATGTGGGA ACGGAATTAA AACTGTCTCC AGAGCGAATG TTTCTTCTCT CACTTGAAGT 840
CTGGGCTTCC TCCTTTTATG TCTATGCCCC ACCCAGATTA CGCATGGGCT ACTTGGGCGG 900
TTGTGGTATT TCTGTTTCCC AACCAAACGC CACCACCTCC CCTTAAAGCC ATCTTCACAG 960
GAAGGTAACC AGCTCCCGGT GGAACTGACC CATTTGACAG TATCTAAGGG GAACAAAAAT 1020
TGTTGCTGCT GCTGATTCAG ATTCACAGCT TGGACTTCCC ACCCTTAGCT AAAAGTTTTT 1080
CACTGGGGGG AGTCCCCACC ACACAACCTA CTCTATTCAT GTGAGCCAGT GGTAAACAAA 1140
CCAGACTCCT GGTGCCTCCT GAGTCAGATG ATAACCAAGG GAAAGAAGTG ACCTCTATCT 1200
CTGGACACAA AACAAACTAG AGGACCCTTA CTCCTCTGAT TGAGAAAGCT GGTGAAGTCA 1260
GCTCCTTTCA ACTTGGAGAA GCCATTGCTC ACATCAGGCG CATAACTGTT TCCAAAGTCA 1320
|
| |
|
|
|
