| Tag | Content |
|---|
EnhancerAtlas ID | HS062-11300 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr3:53106270-53108530 | 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 | CATGCAGGCT CAGCATCATC CTGCCCGGGC GGGAACCCTG GTCCACCCTT GCTGTAGGAC 60
TTCAGTCAAA TGACAGCCTC TCTTGACCCT CAGTTTCCCC AACTGCAAAA GTAGCACCCG 120
ACAACATGCA CTGACCCCCC AGGGCTGCTG GGCGTGCTTG GCTGATGGTT CACTCTCAGA 180
AGTATCTGTC CCTACCCACC TCGTAGGTGC GGTCAGGTGA GTTCTTCTCT GCCTCTGTTT 240
CCACACTGCA CCTGGAAGAA GCTGGAGGAC CTGCTCTCCT AATTGCTCCT CTACCACTGA 300
TGTTGTAAGA AGGGGACACT GACTTGTCAC TCTCTGCCAA TGTAGGAGCC AGGCACTGTC 360
TCTGTTGGCT CAGGGCTGGG CTCCCAGGAA GTAAAAGCCT AAAGGCTCAG GGAGGCCATT 420
TAAGGTCTAG GGTCCAGTGG ACTTTCGGAC GCATCGCAGC CTCCGCTGAG CCCTTCTAGC 480
AGGCTTGTGG TGACTGCACC CTGGGGCGGC TGCTCCATTG TTTCCTGTCA GTCCCGCTCA 540
TCTGCTCAAC AACCCTTTGG AGGAAACACA CAGGAGGGTC CTGCCCTCTA GTGGCTGCCG 600
GCGGCCAGGT CTCTCCTCAC AGGGCTCCGC CCGCGACCTC AGAGGAGCCC ACCGCCCTCT 660
CTGCCTGCTC TAGTGCCTGC CGCACAGCAA CAAGCAGGCA TTTCCTGGGG GTGAAGCCGA 720
GGCTGGCCCC ATGAGCTGAC ACCCAGCAAT CTTCATCTCC GAGCACCTTT GAGTCCTGGG 780
GGGCCCTGCT TCCAGATGTG AGCCCCCAGC CCGTGGGGCT GGGTGGTCCT GGGCTGTGCC 840
ACAGGGTTTC AGCCCACCGC GAAGGAGGCC TGACGGTGTC CAGGTCGAGG GCACCTGTGG 900
GCAATGATTG ACATAACACT GCAGAGAGAG AGCCTGGTGG GGCACCGGCC TCTGCCCAGG 960
CTGGGTTCCG GGGCCTTCCC CCATGTGCCC ACATCCCATG CTTCCCCCGT TACAGCCTCT 1020
GCCGTCAGAC TGCGCACCAG CATCTGTGGG TGAGGAGAGA ACCTGGGCTG GGGCTTGACA 1080
CAAAAGGGGC TTTGCCTCTG GACACCCCCA CCTGTGCCGC AAGTGGAGGG GGCGGGGAAA 1140
CGGGGAGGAG GGAAAGTAAG CGGAAGTCCC GCCTCTGTGG AAGCGCCTCT GCACCCTTTG 1200
TCCCCCAAGG GAAGCACAAG TGTGTGGCCA GTCAGATAAA GCAGGCCTTT CCTTGCCTTT 1260
ATGGAGCCAC GGGCTGAGGC TGGACCAAGG GTCAGTGAGG GGTTCAGGAG GCCCCCTCTG 1320
CGCCTCTCTT CCAGGCCCTG AGCCCATCAT TCCCTTCGTT GTTAGAGTGA AACTGTGAAG 1380
AGCCGCAGCT CTGTGCCGGG CGAAGAGGAT TTGGCAGTGA AAAGGATGAG CTTGCCTTGC 1440
CCTGGGGGCA ACTGGCACCT GGGGTAAGAG GTGGCCGGTG AGAGCCTGAG CCCTCTGGAG 1500
AGCAGAGGCC CCGTTGTGCA CAGAGCCAGT ATACCCAATG CTCGGGGAGC TCCCAACAAC 1560
CCTACCCAGC CCTGCGGGAG ACCACAAAGC TCTAGGGAAG AGCCTGTCCC AGGAAGCACA 1620
GGGCTTCGAA GTTCTGACAA GGACATCGGA GTTCCAGGCC CACCCCACAC ATGCACACAC 1680
TTCCTGCTTC CAATTAGCAC TAATTGGACG ACTGGGAAAA CCCACAGACC ATGAAGCAGA 1740
AGCAGTTAGG TCTGCGGGGC CCCGGTGAGG CAGGCCCTGC GAGGGCCCAG GTGAGCCAGG 1800
CTCTGGGGGA TGGGCCCTGG GGTCTCTGTC TCTCTGAGAG GGGATCAGGT GATCAGGGCC 1860
ACATCTGCCA GGATCCCTAC TGGCCCCTCT GGAAGACGGA AATTGTCCCA GGGCCAGGGC 1920
AGAAGCTGGG TGTGGGGGAG CCTGACAAAC ACCCCCTCTC AGCCTGGCAT TTAAGGCTCC 1980
CCTAAACCTG GCCCTACCAG CATCCCCCCT CCCAACCTGG TCTCTTTCAT TTCTTCTGCT 2040
CCTAGTTCTC ACTGCCTAAG TCACCCACTG ATTAATTCTT TATGTCACTC CATCTATTCA 2100
TGTATTACGT GTCCAGGAGC CCTCCTGTGG CCAGATCCTG GGACCACAGA GATGGATGTG 2160
CCAGGCTTGG CTGGTCAGGT GGACCTTGGA GCCAGGACCT TTTCCAGGGT CCCCAGAGCA 2220
CTGGATGGTC AGAATCAAAA CAGGGCTAAG GCAGGTCCAG 2260
|
| |
|
|
|
