| Tag | Content |
|---|
EnhancerAtlas ID | HS106-00025 |
Organism | Homo sapiens |
Tissue/cell | iPSC |
Coordinate | chr1:15059520-15060630 |
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 | TCAAAAATGT AGCTCCAAAC AGCTCCCTGG GTGGTTCAGA CATGAGCAAC CACTTTCTTA 60
GAAGACAAGT GCGCTGAGTG TTTCTCGGGG ATCTGTGGCT GCAAAGCGGA TCAGCTCTGA 120
TTTCAGCCCC AGACTTTCTG ACAGAGGGAC TTTCCGCCCA CTGCCCCAGG CTTGGTAATT 180
AAGCAGTCTG AGTGATTGCA GAATTCTCGC ATGTTCCCGG CAGCCTGTGC TTGGAGTTAC 240
CATGAAAGCA AGTCAGGACA AGTCCCAGAG AAACTTAGCT GGTGAAGAGG AAATGGCATT 300
TATTTCAAAT ACACAACCCA GAGTTTGAAG TTGATGAAAT GGGAACAGAG AAGTTCTTTC 360
CCGTTGCCCC ACCCGCCGTG CAATATTGAT TTGCAAATTT TCCAGCAGCC ACCGCCGCTG 420
CAACACTTCA GCAATAGTTG AATTAATGAC CGTGGCAGTG CAGCCTCGTG CCGTAGGGTG 480
GGACCTCCTG GAGCCTTCAG AGTCGGGCAG AGATGCTTCC TGGGAGGTGT CCGGATGACC 540
TCTCTTTCGG GGAGTGGGGG AGTTCTGGAA GTTTCCATAC AAGGAGCAGT TCAAGTGTTG 600
GAGGCCCCCG GTTCTCCCAG GGCCCCTTTG ATGTTCAGCG TGGGGACTCG GGGGTCATAG 660
CAGCTTCCTG GATGTGTCTG AGTCATCAAA GCTCTGCTTA GTAACCTTAA CCTTAGTGCC 720
TTAACCTTGC TAAGGCACAG GTTTCTCGCA TCTGAACCAC CTGCGAGCTG TTTGGGAGCT 780
ACATTTTTGA AGAGGAAACT CCACTTTTAT TCTCTGGGGT TTGGCCCCCC GATCAGCCTC 840
TCCAGATGGG ATCTCCCTCC TTGCCCAATC TGCAGCCCAC GCCCCAGCCA GTCCAGACTG 900
CTGTCGGTTC CCGGCACACC ATAGGGCTGC GCACAGCTCC TGCCCTGGCT TCGGCCCTTC 960
CCTCTGCCCA GGATGCCCTT CATCTGGATA TCTACGCCTA ACAGGTTCAA CTCAGGGGTT 1020
CCCTCCTGCC GGGTGAGCAG TGGGAATCAC AGTCCAAGGA ACTTTGGTCT TGGAAGTATC 1080
TGAGTTCCAG TGCTTACTAA GCCCTCGAGC 1110
|
