| Tag | Content |
|---|
EnhancerAtlas ID | HS060-12919 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr16:31012920-31014000 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr16:31013494-31013505 | TCTTCCCGCCC | - | 6.14 |
| | | 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 |
| GH16I031001 | chr16 | 31012944 | 31015399 |
| Enhancer Sequence | TCGCCTGGGG ACAAGGAAGG CTGAGTCCAT GAGCAGGCCC TACCTGGGTC CCCAAGGCTG 60
GCTCTCCAGC TCTCCCACCC TCTCCCTGCT ATGCACACAC AGGTGCTCCC AGCTCTAGGC 120
TCAGAGGAGG GGTCCTGGGA GGGGTCCCAT GCAGGGTAGA TGGCAAAGGC ACCAAAAGTG 180
TTTGTCAGCC CAAAGGATTC CTTAGAAGGA ATTGGAAAAA GACCCCCTCT CAGGGTGGAT 240
GTGGCCTTGG GGGCGCAGAG CCAGCCTTGA CCAGCCAATA GGGATGATTT CAATATTTCA 300
ACAACGGCTC AACGTCAGGC TTGCAGTAAC TGACCCTGGG CTCCATGAAG GGTCCTGGAC 360
TAGAGTCCCG GGAGCCTGGA TCTCCCTACT GTTCCTGCTC TCCTGCCCAG ATCTCACTTT 420
ACTCCTTCTC TTCCTCTCCT GCCCCACCTG ACCAGACATG TCCCCTGTGC AAGGTCACTT 480
CACTGCCAGC GGCAGGCGCC AAGTTGAGCA AGCAGTGAGG GCTGGATAAG AGATACGGGC 540
AGCACCCCGA CCTCCCTCGC GCCCTGTGCC CCCCTCTTCC CGCCCACTCT CCCTCCCCTC 600
CCAGCCGGCT CTCCCTCGCA GTGGATTCAC TTGCTTTCAT CCAGCCCCTT CCAACTTCAC 660
ACCCACCTAC TCTTGCTGGC TTGGATTTCC CAGTTGCAAC CTGCAGCTGC TCAACCCTCC 720
ACCCGCAGGG CTCAGAGACA CAAAGAGATT TACCCACCCA CAGCACCACT GCCACCGACA 780
GACAGACTCG AGACACAGAC AGAAGAGCTG ACACCCAAGG CACACAGGAA TAGGCCCCCC 840
CGACACCCAC ACGGAGATGC ACTGATGCTG GCGTTCACCC GCACGCAGAC TCACAGCTGA 900
GCCGCACTGA CATGTGTGGA CACACTGGCT TTCAGCTGCA CCCCTGAGGA CATTTGGGAG 960
GGCTCACTGG GCTTGTTCTT CCAGCTTCTC CGAGCCTCAT GTCTGCACAC ACACTCAGAG 1020
CTGGACAGGA GAGGCTGTAG GGGAGGTGCC CTGTGCTACA CACACCTGAG TCCTTCTCTG 1080
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