| Tag | Content |
|---|
EnhancerAtlas ID | HS098-38722 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr3:53106330-53107820 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr3:53106848-53106867 | TCCTGCCCTCTAGTGGCTG | - | 6.77 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr3 | 53107035 | 53107200 | | chr3 | 53107324 | 53107487 | | chr3 | 53106812 | 53106929 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH03I053071 | chr3 | 53105884 | 53108148 |
| Enhancer Sequence | TTCAGTCAAA TGACAGCCTC TCTTGACCCT CAGTTTCCCC AACTGCAAAA GTAGCACCCG 60
ACAACATGCA CTGACCCCCC AGGGCTGCTG GGCGTGCTTG GCTGATGGTT CACTCTCAGA 120
AGTATCTGTC CCTACCCACC TCGTAGGTGC GGTCAGGTGA GTTCTTCTCT GCCTCTGTTT 180
CCACACTGCA CCTGGAAGAA GCTGGAGGAC CTGCTCTCCT AATTGCTCCT CTACCACTGA 240
TGTTGTAAGA AGGGGACACT GACTTGTCAC TCTCTGCCAA TGTAGGAGCC AGGCACTGTC 300
TCTGTTGGCT CAGGGCTGGG CTCCCAGGAA GTAAAAGCCT AAAGGCTCAG GGAGGCCATT 360
TAAGGTCTAG GGTCCAGTGG ACTTTCGGAC GCATCGCAGC CTCCGCTGAG CCCTTCTAGC 420
AGGCTTGTGG TGACTGCACC CTGGGGCGGC TGCTCCATTG TTTCCTGTCA GTCCCGCTCA 480
TCTGCTCAAC AACCCTTTGG AGGAAACACA CAGGAGGGTC CTGCCCTCTA GTGGCTGCCG 540
GCGGCCAGGT CTCTCCTCAC AGGGCTCCGC CCGCGACCTC AGAGGAGCCC ACCGCCCTCT 600
CTGCCTGCTC TAGTGCCTGC CGCACAGCAA CAAGCAGGCA TTTCCTGGGG GTGAAGCCGA 660
GGCTGGCCCC ATGAGCTGAC ACCCAGCAAT CTTCATCTCC GAGCACCTTT GAGTCCTGGG 720
GGGCCCTGCT TCCAGATGTG AGCCCCCAGC CCGTGGGGCT GGGTGGTCCT GGGCTGTGCC 780
ACAGGGTTTC AGCCCACCGC GAAGGAGGCC TGACGGTGTC CAGGTCGAGG GCACCTGTGG 840
GCAATGATTG ACATAACACT GCAGAGAGAG AGCCTGGTGG GGCACCGGCC TCTGCCCAGG 900
CTGGGTTCCG GGGCCTTCCC CCATGTGCCC ACATCCCATG CTTCCCCCGT TACAGCCTCT 960
GCCGTCAGAC TGCGCACCAG CATCTGTGGG TGAGGAGAGA ACCTGGGCTG GGGCTTGACA 1020
CAAAAGGGGC TTTGCCTCTG GACACCCCCA CCTGTGCCGC AAGTGGAGGG GGCGGGGAAA 1080
CGGGGAGGAG GGAAAGTAAG CGGAAGTCCC GCCTCTGTGG AAGCGCCTCT GCACCCTTTG 1140
TCCCCCAAGG GAAGCACAAG TGTGTGGCCA GTCAGATAAA GCAGGCCTTT CCTTGCCTTT 1200
ATGGAGCCAC GGGCTGAGGC TGGACCAAGG GTCAGTGAGG GGTTCAGGAG GCCCCCTCTG 1260
CGCCTCTCTT CCAGGCCCTG AGCCCATCAT TCCCTTCGTT GTTAGAGTGA AACTGTGAAG 1320
AGCCGCAGCT CTGTGCCGGG CGAAGAGGAT TTGGCAGTGA AAAGGATGAG CTTGCCTTGC 1380
CCTGGGGGCA ACTGGCACCT GGGGTAAGAG GTGGCCGGTG AGAGCCTGAG CCCTCTGGAG 1440
AGCAGAGGCC CCGTTGTGCA CAGAGCCAGT ATACCCAATG CTCGGGGAGC 1490
|
| |
|
|
|
