| Tag | Content |
|---|
EnhancerAtlas ID | HS184-22500 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr4:6762960-6764200 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZBTB18 | MA0698.1 | chr4:6763848-6763861 | GCACATCTGGAAT | - | 6.03 |
| | | 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 |
| GH04I006761 | chr4 | 6763328 | 6763604 |
| Enhancer Sequence | ACAGTGGTTG TTAGAATTAA ATAAGTGCCT ACAGTGCTAA TCCAGAAAGG GTACTCCAGG 60
GTCAGTGTTC ACAGCCACAC TCCCCTGACC CTATAACTTT CTGTTTTGGG CTTCAAACTG 120
GTGGGCTTGT AACATGGAAG GCAGTTCACA ACAACGCAGG GTCCTGGGTG CAGGCCAGAC 180
CAACCCGTGG CAGCCTGGGC TCATGTGTGT GACCTCAGAA AAATCCTTTT TGTCTCCTGA 240
CTTCAGCTTC CCCATCTGAA AAAGGAGAGG GCTGGACTGA AGGATGCCCA ATGTCCCCAG 300
GTGTCTTCCT CATCAACATC CCTTCTTGTC CCAGATGGTA ACGGCTCTAT CTCGTTTCTC 360
AACTGTCTGT GGACAGGGAT CTTGTAAAGT AACCTCCATG TGGCCCTTAA CATCCTGCTC 420
TCCCATTCTT TCAGCCACCC ACCCCCAACA GAACAGGGAA ACCGTTTCCC TCTAGCCTGC 480
AGCCCTGGCC TCCCGCCACT GAAGGAACAC CGTGTCACCA GGGCCGGCAG GCGGAGGACA 540
AAGGCGGCTC TGTCCCCCAG GGCAGTGGTT ATCCACTGTC ACCATGCAGC CCGGACCATC 600
ATCGTATGCC CCTTGTCTCC CACCTTAGGG CGCTGAGGGT GGGCTGACGC TCACATTTCC 660
GCACTGGCCC CATTTCTTGC TGCAGAAACG CACTGACTGC CTTCACAGGC TTCCTGCAGC 720
TGAGCTGGGG GCCTCCGCCT GGCAGCCAGG GAGGAGGCGG GCAGCGAGGA GGCGGGCAGC 780
GAGGAGGCGG GCAGGAGGAG GCGGGCAGCG AGGAGGCGGG CAGGAGGAGG CGGGCAGCGA 840
GGAGGTGGGC AGGAGGAGGC GGGCAGGAGG AGCTGCGCAG CCCTCAAGGC ACATCTGGAA 900
TGGAGCAGCC CGGAGGCCTG ATGCGGGTGG AAGTGGCCAG CAGCCGGCCA GCTTTGGGGG 960
CTGGGCCAGG CACGGGGAGG GTGGGTGCAG GGGTGAAGTG GGCTCCCAAA CTGTGATGGC 1020
CTGTGACCAG TCTGTCTAGT GGAACAGGCA CAGCTCCTGA AACATTGATG TGCATGGTCT 1080
CGCTTTTACG TTCATTTATG TACATGTTAA CTATAAATGT ATCTTCTGCA TCAAGTTATC 1140
CACAGCACCT GGCTCTGAGT AAGCACTGAA TGAATGTTAG CTATTTTTTC ATTGCTCTGA 1200
TGTGCTACAG TGGTTTTAAA GCATGGCCCT GAAATCTTCC 1240
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