| Tag | Content |
|---|
EnhancerAtlas ID | HS061-00262 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr1:15059270-15060740 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF7L2 | MA0523.1 | chr1:15060142-15060156 | CCCCTTTGATGTTC | - | 6.29 | | TP63 | MA0525.2 | chr1:15059766-15059784 | AGCAAGTCAGGACAAGTC | + | 6.38 |
|
| | 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 |
| GH01I014731 | chr1 | 15058041 | 15060857 |
|
Enhancer Sequence | AGTGGTTAGG GATTTCTTTT GGCCCTACGG TGCCATGAGA AAAATTACTG AGACTCTAAG 60
AGTGCCATAA ACTGAGAAAA TATCAGGACA CCTGCCCTGT GGCACACTCA GTGACTCAGT 120
GTTCGTTTCA AACTCCTTTA ACCGATAGGT ATTTTCTGAA TGAACAGGGA AATGGAAGCA 180
CATCTTCCCT CCTTCCCCTA TGTTCACGGA GCAAGCAGAA GAGTTTGCTG CATGAGATTT 240
GGGAAGAAAT TCAAAAATGT AGCTCCAAAC AGCTCCCTGG GTGGTTCAGA CATGAGCAAC 300
CACTTTCTTA GAAGACAAGT GCGCTGAGTG TTTCTCGGGG ATCTGTGGCT GCAAAGCGGA 360
TCAGCTCTGA TTTCAGCCCC AGACTTTCTG ACAGAGGGAC TTTCCGCCCA CTGCCCCAGG 420
CTTGGTAATT AAGCAGTCTG AGTGATTGCA GAATTCTCGC ATGTTCCCGG CAGCCTGTGC 480
TTGGAGTTAC CATGAAAGCA AGTCAGGACA AGTCCCAGAG AAACTTAGCT GGTGAAGAGG 540
AAATGGCATT TATTTCAAAT ACACAACCCA GAGTTTGAAG TTGATGAAAT GGGAACAGAG 600
AAGTTCTTTC CCGTTGCCCC ACCCGCCGTG CAATATTGAT TTGCAAATTT TCCAGCAGCC 660
ACCGCCGCTG CAACACTTCA GCAATAGTTG AATTAATGAC CGTGGCAGTG CAGCCTCGTG 720
CCGTAGGGTG GGACCTCCTG GAGCCTTCAG AGTCGGGCAG AGATGCTTCC TGGGAGGTGT 780
CCGGATGACC TCTCTTTCGG GGAGTGGGGG AGTTCTGGAA GTTTCCATAC AAGGAGCAGT 840
TCAAGTGTTG GAGGCCCCCG GTTCTCCCAG GGCCCCTTTG ATGTTCAGCG TGGGGACTCG 900
GGGGTCATAG CAGCTTCCTG GATGTGTCTG AGTCATCAAA GCTCTGCTTA GTAACCTTAA 960
CCTTAGTGCC TTAACCTTGC TAAGGCACAG GTTTCTCGCA TCTGAACCAC CTGCGAGCTG 1020
TTTGGGAGCT ACATTTTTGA AGAGGAAACT CCACTTTTAT TCTCTGGGGT TTGGCCCCCC 1080
GATCAGCCTC TCCAGATGGG ATCTCCCTCC TTGCCCAATC TGCAGCCCAC GCCCCAGCCA 1140
GTCCAGACTG CTGTCGGTTC CCGGCACACC ATAGGGCTGC GCACAGCTCC TGCCCTGGCT 1200
TCGGCCCTTC CCTCTGCCCA GGATGCCCTT CATCTGGATA TCTACGCCTA ACAGGTTCAA 1260
CTCAGGGGTT CCCTCCTGCC GGGTGAGCAG TGGGAATCAC AGTCCAAGGA ACTTTGGTCT 1320
TGGAAGTATC TGAGTTCCAG TGCTTACTAA GCCCTCGAGC CTGCCCCAGC TACTTTCTCC 1380
TCACCCGTGG AATGAGGATA AAGTAGCACC TAACTCAGTG TTTCTCAAAC TGTACAGTGC 1440
GCCTGAAGCA CTCCGGGATC TGGATAGACT 1470
|
