| Tag | Content |
|---|
EnhancerAtlas ID | HS060-28090 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr5:134212440-134213910 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr5:134213108-134213129 | TTTATCTTTCAGTTTCACTTG | + | 7.07 |
| | | 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 |
| GH05I134876 | chr5 | 134212368 | 134213329 |
| Enhancer Sequence | CTGCAGAGGA TGCCACTGGC AGATTATGCT GGCCTCAGGT GCTGAGGCCC TGAGAGACTA 60
AGCAACCTGG AGGTAGCAAT GCTATCCAGG TGTCTAGGAA TGGAAGCAAA CTCCTGGCTT 120
CAATACCCCT ATGCCACTCT TCCCTAGGCA GTCAGCTAGC AAATTCTTAC TGAGCACTCA 180
TCATATGCTA AACACTGTGC TGAGCACTGG GGATCCAGTG GTGAGTTAGA GCAGCAGGCC 240
TTTGGGGAAG GCAGCCACTA AATAACTACA AATTACTAAG AAAATTGCAA GACTGAGAAA 300
TGCATCAAGG AGAGTCCCAG GGCGTTTTTG GGAACTGTAA TGGGAGACCT CCCACCCTGG 360
TCTGAGGGTC AGGGAATGTG TCCTTACAGA GGTGACATTT AGGGTGAGAT CTGAATGAGG 420
AGGATGAAGG ATTTGGCAGG AGGAAGCTTC CCAGCAGAGA AACAGCCCTC AGGAAGGCTC 480
TAAGGCAGGT GGGGATAGGA GGAGTGTAAA TGATCAGGGA CTAGAGGGAT CTGATGGCCA 540
CAGGTGAGAG TGCAGACAGA GGCCACATTG GGGCCTGGTA GCTCTGCTAC AGAATGCAGA 600
TGCATTCACA GGGTAGGGGA AGCCACTGAA AGAGTTTTAG CAGGGGAGTG ACATGATCAG 660
ATATGCCTTT TATCTTTCAG TTTCACTTGT ATTGCTGTGA AGGTCAGGGT CTGGAGGGGG 720
GATAGCAGGC TGACCAGGGA GACCAGTTTA GGTGGCTACA GTAGTTGCCC AGACAAGAAT 780
TGGCTGTGGC CTTTGCTGAG AAGTGTTAGT TGGGATGGGG AAAGTAGATG GATTGTGAAT 840
GTGTTTAGCA GGTGAAATTT TTTTTTTTCT TTTTGAGAAG GAGTCTTGCT CTTGTCACCC 900
AGGCTGGAGT GCAGTGGCAC CATCTTGGCT CACTGCAACC TCCACCTCCT GGGTTCAAAT 960
GATTCTCCTG CCTCAGCCTC CCGAGTAGCT GGGATTACAG GCATGCGCCA CCATGCCTGG 1020
CTAATTTTTT TTTTTTTTTT TGAGATGGAG TTTTGCTCTT GTTGCTCAGG CTGGAGCAAT 1080
GGTGCGATCT TGGCTCATTG CAACCTCTGC CTCCCGGGTT CAAGCGATTC TCTTGTCTCA 1140
GCTTCCTGAG TAGCTGGGAT TACAGGCACC CGTCACTACA CCCCGGCTAA TTTTTGGTAT 1200
TTTTAGTAGA GATGGGGTTT CGCCATGTTG GCCAGGCTGG TCTCGAACTC CTGACCTCAG 1260
GTGATCTGCC CGCCTTGACC TCCCAAAGTG CTGGGATTAC AGGCGTGAGC CACTGCGCCT 1320
GGCCTAATTT TTGTATTTTT TAGTAGAGAT GGGGTTTCAC CATGTTGGCC AGGCTGGTCT 1380
TGAATTCCTG ACCTCAAGTA ATCTGCCTGC CTTGGCCTCC CAAAGTGTTA GGATTACAGG 1440
TATGAACCAG CAAGCCCAGT GTGCAGGTTA 1470
|
| |
|
|
|
