| Tag | Content |
|---|
EnhancerAtlas ID | HS061-17688 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr3:72387550-72389170 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYA | MA0060.3 | chr3:72388325-72388336 | TCTGATTGGCT | - | 6.32 | | ZNF263 | MA0528.1 | chr3:72388920-72388941 | GGAGCAGCAGGGACAGGAAGA | + | 6.47 |
|
| | 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 |
| GH03I072336 | chr3 | 72385761 | 72389151 |
|
Enhancer Sequence | ACTGGGCCAA CTGCAACTGG GCTGATGGAT TCAGTGGATT GAACATGACT GGTGAGGAGA 60
CAGGTTGACA AGGAGACCAA CTCATTGACC ACATGCATGA TGGACTGACT GGCCAGTTGA 120
TGACAATGGG TTTGGTGTAT GGTTGACTGG TTGGTTGTTT AATTCAAACT GACTGGATAA 180
CTAGGCAGCT TACTATGACT GACTATTGTG ACTGCCTGCC TGGCTGACTG AGGGAATAAC 240
TGAGTCAGTG TGACTGGCAG GCTGATTCAG ACTGACTGGA TGTCTGGATG ACTATGATCT 300
CCTAACTGAT AGCCGTCAGT GATGATCTTG ACTGACTGAC TAGCCGGCTC TGGGATTGGC 360
TGTCTCTTCC AGACTGACTT GGTAACCGTG GGTCTGACTG TGACCCCTGC GTCTTGACTG 420
ACCGCCTTGA TTGCATGCCT GACATTTTGA GATCAACTGA CTGGCTGGTT GCCTGGTGTT 480
TCATTGTGGC TGTGGCACAG CCTACGGCTA CCTGTGACTA ACCATGAAAC TGACTACACC 540
CAACTCACAG GACAGACCGG GTGGACTGAC CACCTGCCTT AGTCATGGAA AACTGACTCT 600
GGCTGACTCA ACTGCCAGAG ACTGACTGAG ATGAACAGGC CAGCCAAGAG ACAGCTGGGT 660
GACTCGTGGT GAGTGGCTTT GTCTGACTGG ATGGCTGTGA CAATGTAACT GAGTCTGGCT 720
GTGAGACAAT AACCTGTGGA TTGACTGACT TGAATGTGTT GACTGGGTGG CTGAATCTGA 780
TTGGCTATGT GGGTGACTGA TGACTCCTGG CTGACTGGCT AACCCTGCCT TGACTGACTG 840
ATTGATGGGC TGACAGATCG AGTTTGACCA GGCAGCAGGA GACCTGCTGA CCACGGCTGT 900
GACTCACTGT GTGAGCGGCC ATGTCTGACT GTGTAACACA ATCTGACCAA GAGACAATGA 960
CTAATTGACT GACCAACTGA CTGAGATTGG CTGGGTGTCT GACTGACCAG CTGTGACTGC 1020
AACTCCTGAT GTGAGTGGGC GTTGACTGGG TGGCCCTGAC TCGTATAGGC AAGTCTGGCT 1080
GTGAGACAAC AGCTAACTCC CTGACTGGCC CAGTGTGCCA ACTGGCTGAC TGCTTGAGGC 1140
TGGCCAACAG ACCAGCTGAC CGTGCCTGGG ACTCACGGTG TGCGTGGCCA TGCCTCACTG 1200
TGTGGCCCTG GCTGTGTCTC GGAGTCTGAC TGTGAGACAA GGGCAGACTG ACTGACTTTC 1260
CTGGCCAACT GCCTCCAGGT AGCCTGTCAA CACAGTCCCT ACCCTTCCCA AAACCATTAA 1320
AGTGCTGCAG TGGGAGCTGG CCCAGCCTGA GGGGACAGAG CAGCTTCTGT GGAGCAGCAG 1380
GGACAGGAAG AGGGAAGCAG GAGCCGCTGG AGGGAGAAGA GGAGTAGGCC CTGCCCAGGA 1440
ATGGGCCACA CGGAAAGTTC TCCACCTCAC CCTGGCGGGG GCTGGGTCAC AGGCACACGT 1500
TCTTGGAGCT GTGTTTTGGC TCTAGTCTTA TAGCTCCTTT GTTTGGGGGT GAGGGGGGAG 1560
GGGAGCTGGG GGAACCTATA AACATATTGA GCCAATAACT CACCTACAGG ACTCCAATTA 1620
|
