| Tag | Content |
|---|
EnhancerAtlas ID | HS060-29713 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr6:35316120-35317570 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr6:35316793-35316814 | TTCTCCTTTCTTTTTTTTTTT | + | 6.05 | | MEF2A | MA0052.3 | chr6:35317245-35317257 | GCTAAAAATAAA | + | 6.04 | | MEF2C | MA0497.1 | chr6:35317243-35317258 | GAGCTAAAAATAAAA | + | 6.5 | | ZNF263 | MA0528.1 | chr6:35316567-35316588 | GAGGGAGGAAGAAGGGGGGAG | + | 7.47 | | Zfx | MA0146.2 | chr6:35317045-35317059 | CCGGCCTCGGCCTC | + | 6.28 |
|
| | 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 |
| GH06I035347 | chr6 | 35315772 | 35317360 |
|
Enhancer Sequence | GTTTCTTCCA TCTCTGCAGG GGTAGGAGGT TCTCACCAAG AGTCTGAACA ATGCTCTGGG 60
TTCCCATTGC TGTTTCCATG TTCTCAGGAT GCCTGGCAGG TTTTATAAAC TCTCAGAAGT 120
GGAGCTCCAG GGAATACAAT GTTCATTGTC CTATTTGGAA GGCTGGGTTG TTGTGGGTCC 180
CTGCTGGGGG CCGGGGAAAC GTGGGCCTCC TGCCTGATTT GTTTTAATCT CTGAAGTTCA 240
GTGGTTCCAG TAGCTGTTTG TGGGCTTCAC TTCCCCTTCT CTGCCTTTAA CACCCTGCAG 300
GTTTTCCTGT TGTCAGACAG GGTGGTGAGT CCCTGTGTCT CTCTGTCTGT GGGGGTCAGG 360
TTGTTTGTAG ATCTTTCAGG AAGGTCCTGG GTGGGGGGCC CTCCTGCTTT CAAACCCATA 420
CCAAGTGCTT TCCTCTGAAG GGAATGTGAG GGAGGAAGAA GGGGGGAGTT TCAGAGACTT 480
CTGAGGTTCC CCAAGAGGGA AGAGGTCAAA GTACCTCCTG AGCGGGGAGA GCTACTGAGT 540
TGAACTGATT TGCTTTGCCA TTTGCTTTAG CAGCAGCCAG GCCCAGTGGC AGCAATTGTA 600
CGTGCATTTC CAGGGGTCAG TTGTCCAGTT CATCCCTGAG CCTTGAGCTC CCAGTCGCAG 660
GTAGGAACTT CTCTTCTCCT TTCTTTTTTT TTTTTTTTTT GAGACGGAGT CTCGCTCTGT 720
CACCCAGGCT GGAGTGCAGT GGCGCGATCT AGGCTCACTG CAAGCTCTGC CTCCTGGGTT 780
CACACCATTC TCCTGCCTAA GCCTCCTGAG TAGCTGGGAC TACAGGCGCC CGCCACCACG 840
CCCGGCTAAT TTTTTGTATT TTTAGTAGAG ACGGGGTTTC ACCGTGTTAG CCAAGATGGT 900
CTCGATCTCC TGACCTCGTG ATCCACCGGC CTCGGCCTCC CAAAGTGCTG GGATTACAGG 960
CGTGAGCCAC CGCGCCCGGC CTCTTCTTTC TTTCTTGATT GGGTACTGCT ATATCACCTA 1020
GGACCAGGGG TGTGTCCAAT CTTTTGGCAT CCCTGGGCCA CATTGGAAGA AGAATTATTA 1080
TCTTGGGCTA TACATAAAAT ACACTAACAC TAACAATAGT GATGAGCTAA AAATAAAAAT 1140
GGCAAAAGAA TCTCATGTTT TAATAAAGTT TACGTATTTG CGTTGGGATG CATTCAGAGC 1200
TCTCCTGGGC TGCATGCAGT CATGGGCCAT GGGTTGGATA AGCTTGGCCT CCCTAGGCAG 1260
TCCTCTCACC ACAGCCTCCC AAGTAGCTGG GACTACAGGT GCACACCACT GTGCCTGGCT 1320
AAGTTTTTTT TTTGTTTGTT TTTGTTTTTT TTTAATTTAA TGGGTACATA GTAGTAGGTG 1380
TATATTTCTT TTTTTCTTTT CTTTTTTGTT TTTTTGAGAT GGAATCTTGC TCTTGTCACC 1440
CAGGCTGGAG 1450
|
