| Tag | Content |
|---|
EnhancerAtlas ID | HS059-00409 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:15059140-15060610 |
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 | AAAGGAAAAG AACAAAATGA AACTTATTTT TTTTCTTTCA ACATATATGT ATTATTTTTT 60
CAACTGGCTA TTACAATGTT AGAACATAAA TACTTAGTAA GTTGTTTGGC CCTACCTATT 120
TAGTAAACGA AGTGGTTAGG GATTTCTTTT GGCCCTACGG TGCCATGAGA AAAATTACTG 180
AGACTCTAAG AGTGCCATAA ACTGAGAAAA TATCAGGACA CCTGCCCTGT GGCACACTCA 240
GTGACTCAGT GTTCGTTTCA AACTCCTTTA ACCGATAGGT ATTTTCTGAA TGAACAGGGA 300
AATGGAAGCA CATCTTCCCT CCTTCCCCTA TGTTCACGGA GCAAGCAGAA GAGTTTGCTG 360
CATGAGATTT GGGAAGAAAT TCAAAAATGT AGCTCCAAAC AGCTCCCTGG GTGGTTCAGA 420
CATGAGCAAC CACTTTCTTA GAAGACAAGT GCGCTGAGTG TTTCTCGGGG ATCTGTGGCT 480
GCAAAGCGGA TCAGCTCTGA TTTCAGCCCC AGACTTTCTG ACAGAGGGAC TTTCCGCCCA 540
CTGCCCCAGG CTTGGTAATT AAGCAGTCTG AGTGATTGCA GAATTCTCGC ATGTTCCCGG 600
CAGCCTGTGC TTGGAGTTAC CATGAAAGCA AGTCAGGACA AGTCCCAGAG AAACTTAGCT 660
GGTGAAGAGG AAATGGCATT TATTTCAAAT ACACAACCCA GAGTTTGAAG TTGATGAAAT 720
GGGAACAGAG AAGTTCTTTC CCGTTGCCCC ACCCGCCGTG CAATATTGAT TTGCAAATTT 780
TCCAGCAGCC ACCGCCGCTG CAACACTTCA GCAATAGTTG AATTAATGAC CGTGGCAGTG 840
CAGCCTCGTG CCGTAGGGTG GGACCTCCTG GAGCCTTCAG AGTCGGGCAG AGATGCTTCC 900
TGGGAGGTGT CCGGATGACC TCTCTTTCGG GGAGTGGGGG AGTTCTGGAA GTTTCCATAC 960
AAGGAGCAGT TCAAGTGTTG GAGGCCCCCG GTTCTCCCAG GGCCCCTTTG ATGTTCAGCG 1020
TGGGGACTCG GGGGTCATAG CAGCTTCCTG GATGTGTCTG AGTCATCAAA GCTCTGCTTA 1080
GTAACCTTAA CCTTAGTGCC TTAACCTTGC TAAGGCACAG GTTTCTCGCA TCTGAACCAC 1140
CTGCGAGCTG TTTGGGAGCT ACATTTTTGA AGAGGAAACT CCACTTTTAT TCTCTGGGGT 1200
TTGGCCCCCC GATCAGCCTC TCCAGATGGG ATCTCCCTCC TTGCCCAATC TGCAGCCCAC 1260
GCCCCAGCCA GTCCAGACTG CTGTCGGTTC CCGGCACACC ATAGGGCTGC GCACAGCTCC 1320
TGCCCTGGCT TCGGCCCTTC CCTCTGCCCA GGATGCCCTT CATCTGGATA TCTACGCCTA 1380
ACAGGTTCAA CTCAGGGGTT CCCTCCTGCC GGGTGAGCAG TGGGAATCAC AGTCCAAGGA 1440
ACTTTGGTCT TGGAAGTATC TGAGTTCCAG 1470
|
