| Tag | Content |
|---|
EnhancerAtlas ID | HS062-11344 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr3:58517760-58519170 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr3:58518650-58518669 | GGCCGCCACCTGGTGGCCA | - | 8.59 |
| | | 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 |
| GH03I058532 | chr3 | 58518328 | 58518928 |
| Enhancer Sequence | TATTAATGAA TTACTCTGTC ATCAACCTTA TAATAATGAA TACAGATAAT TATCATTTAT 60
CAAAATCTAG GTGGCGCTAG ACCCTGTGAT AGATGCTTTC CAGTTCTTGC AGGGGAGAGA 120
GGATGATGAG TCCCATTTTC CAGTTAAGGA AACAGGCTCA GAGAGTAGAG TGACACACTG 180
AAGGTCATTG GCCTGGAGGG GCAGAGCTAG GATTCATCTG TACCCTGGTC TGTCTGATCT 240
AAAAGGCTGG TTTCTTTTGT CTTCATTTTT GACAGTGGTC ATTTATTTTC TCTCTCTCTT 300
TCTGTCATCA CTCTCTCATC TCTCTCTCTC TTTTTTTTTC TTTTTCTTCT TTCTTTCTTT 360
CTTTTGTTTT TGAGACAGAG TCTCACTCTT TCGCCAGGCT GGAGTGCAAT GGCCTGAGCT 420
CGGCTCATTG CAGCCTCTGC CTCCCAGGTT CAAGCAATTC TCCTGTCTCA GCCTCCCGAG 480
TAGGTGGGAC TACAGATGCC CGCCACCACA CACGACTAAT TTTTGTATTT TTAGTAGAGA 540
TGAGGTTTAA TGATATTGGT CAGGCTGGTT CAAACTCCTG ACCTCAGGTG ATCCACTCAC 600
CTCGGCATCC CAAAGTGCTG GGATTATAGG CATGAGCCAC CGCACCCGGC TCATGTCTCT 660
CTCTTATGTC TCTGGTCTCT GCCTGTGTCT CCCTCTCTCT ATGTGTCTCT CATCTCTGTC 720
ACTCTCCTGC TTTAGTTGGG CTCAGCATAT TTGTTTTAAT TTTTTCCACA CAAGGTGTGG 780
GTCCCCAAGT GCCACAGATG TGTCCTTGGA GGTGAAATTC TCAAGTTTGA GGAAGGGGAA 840
ATCCCTCGTT GGGGCTTGGT AAATCACCAA GCCTCAGGGA CGCTTGATGT GGCCGCCACC 900
TGGTGGCCAC AGCAGGAGGT ACGGCGTTGG TGGCCTGATG GGGGCTGGTG ATGGGCGTGA 960
GCCTTCCTGG GTGTCTGCAG CAGGGGCAGG CAGGCGTATT CTTTCCACTG TGTCATCACA 1020
GGGCCTGTGC TCTGGCTGGT GGCAAGCTCT GCCACTAACT CGGGAGATGA GAGGAACCGG 1080
GGTTGTGAGG AGTGCCTAGG ACTAGACCAA GTGTGTGTGT TTGTGCGTGT GTGTGTGAGT 1140
GAGGCCTTGT CTCTCATGGA TCGATTGTCT CCTCTACTTC AAAGTTCCTT TGGGGACTTT 1200
CCAGCCACTC ACTAATGAAA TGTTTAATAT CCCACCTATT TTACAGAGTA AGAACCTGAG 1260
GCTCAGGTTG GTGAACTGAC TTGCCCAAGG TCAGCAGCCT AGAACAGAAA ATCAATCTGA 1320
GGTCTGTTGG ACCTCAAAGC CAGTGCTACT CTGCCCTCCA ACATTCTTCT ACTTGGGGAG 1380
AGTTAAGGAA GGGGGGTGGA TGTATACTCA 1410
|
| |
|
|
|
