| Tag | Content |
|---|
EnhancerAtlas ID | HS105-25632 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr14:94507920-94509390 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr14:94508829-94508849 | GGTTTGGGGGTGGGAGGGGG | - | 6.82 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 2 | ID | Chromosome | Start | End |
| GH14I094041 | chr14 | 94508262 | 94508390 | | GH14I094042 | chr14 | 94508441 | 94508590 |
| Enhancer Sequence | CCGAGACCAT GTCACTCCCA AGCTTGAAAT ATGCCCCTGA CCTCTAGGAG CAGTGGAAAC 60
CCCTGACACC AACGCCCTCC ACACCAGGCC CCTGCCTCTC CTGCCCCGTT GCCTACCCAC 120
CCTGAGTTCT AGGCACAGGG ACTCACTTAT CCTACACACA CCAGAGCTTG CAGGCATGAC 180
ATGCCGCCTG ACGCTGCCTG GGCCTAGGTA GCCCTGCTTC TGACCCGGCT GTGGGTTCCT 240
TGGGCCCCAG GCAGGCTGCT TCACTCACTC CTCTGTAGCT CCTTTCCCCA GTTGAACAGT 300
GGCCATAGCC CTGTCACGGA CATTAAGTGA TTGACTCGTG AGCACTTGGA ACACTGACCT 360
GGGGTGTTCC GTGCTAGCTC TTAGCGTCAG CGTCATGCAT CCTCCACAAG CCACTGTCTC 420
CCTGTGTGCA GTGAGCCCAG AGCCACCCAG GCAGACACTT GTTCTCTGCT CAGTGCTGCT 480
GCAGGGCTGG AGCAAGCGTG TTGCAGCAGT ATGCTTGTTC CAGCCCTGTA TCTTGCATAC 540
TTGCTCTAGA AGTATGCGAA GTACTTGTGT GTGCCAGAGG CTTGGAGAAC ACGCGCCGCC 600
TCTGAGGGCA GCCACTGTTA CTACCACATC TGATGAGCAA ACAGAGCCTC ATAGAGGTCA 660
AATGACTTGC CAGAGGTCCC ACACAGGCTT GTGTGCAGCC CCAGCGGTCT GAACTTGCAC 720
CCCCTCCAAG CCCCAGTGCT ATCCTTCTCC CTATCCCTGG CTTGCCTCTC GGGGGTGCAT 780
GTCCTGGCCT GGGGGCTTGC CCCCTTCTGA CAGAGCCTAC GACTGCATGC TGCTTATCTC 840
CGTGCCCCAG TGCCTGGCAC AGAGGGGCCC ACAAGTCACT GGCGAGGAAT GAATGTGGAA 900
TGAGGCAGAG GTTTGGGGGT GGGAGGGGGG GCAGGAGAGC TGGGAGCAGA GCAGTGCACT 960
TCATGGCCAT GCAGGGACAG AGTGGCTAGA AGAGGGTGCC GGCCCTTGGA GCAGCCCTGG 1020
AGGACTGCAG CTGCTTCCTG GAGCTGCTTC TAGTACTCTG GCCATGGGCC ACCTAGCCGC 1080
AGCTGAAGAC TGAACAGGGG GTGCTGATGA GGGTGGCTCC TGAGTGAGAG GCGTTAGCCA 1140
GCACTGACCA TCAGATCCTT GCCCTGGCCA GGAGGGGAAA CCTAGGCAGC AGGTACCACT 1200
GCAGTGGAGG CCTCGTCCTC CCAGGCAGCT CTCCGTTCGC CCTCAGCACC CCTGCAGTCA 1260
AGGCGTCATC ACCATCCACA CTTGCGCCAA AGTGGAGCTT ATGGCCAAAA GCCACAGGGG 1320
GACTTGACAG GGCTGGAGGG GACTGCGGCT AGAAGCCAGC ACAGGCTCCA TCCCTCCAAT 1380
CCAGGCACCT CACCCTGCAA TCAGGACAAA CTAGTCCTGG CCCAGGCAGG ACTGTTAGAT 1440
ATGCCAGGAC CAGGCAGGGG CAAGCGGCAT 1470
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