| Tag | Content |
|---|
EnhancerAtlas ID | HS101-00789 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:25192870-25193970 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:25193083-25193104 | ACAAGGAAACTGAAACCCAGG | - | 6 | | IRF9 | MA0653.1 | chr1:25193085-25193100 | AAGGAAACTGAAACC | + | 6.66 | | NKX2-3 | MA0672.1 | chr1:25193653-25193663 | TTCAAGTGGT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AATTACTCAC CAAACCAGCA GTGGGTGCCA GGAGCTCATT CACTTTGTGT GTCATTATAA 60
TTTTTTGTAA CTAGAATGGA TGGAGCAACC ACTTTGGTAG TGAAAATATT TTAATATCCG 120
CATGTGCATA AAGTGACACG AATAACAGTT CCCGTTTACT GGGCTCTGAT GCTGTAGCAG 180
GCTGTGGGGA TGGCTACTGT GCTCATTTTA CAGACAAGGA AACTGAAACC CAGGCAGGCG 240
AAGTGGCTTG CCCAGGCTCA CACAGCCAGA ACGGGATGAA GCAGGTTCTG ACCTCCAAGC 300
AAGACTGACT CCAGTGGGGA ATTATGGGTT CCCAAATGAC ACTGATCACA GCAACAACGG 360
GCAGGACAGG ACAGGTGACT CAGAGCAGAC TCCTCATGCA AGGGGAGATG TTGCCCAGTG 420
CCGAGGGCAC CGGGGCAGGG TTCATGCCTT CCCCTGGGAG AGCAAGAGGT TCAGAGTCAG 480
AAAGACTGGG GCTTGTGGTC CCAGCTCTGC CACTTTCTGG TTGTGTAACT TCTGCCAAAT 540
CCCTTCACCC CTCCGAGCCT CAATGTGCTC ATATGCAAAA GGGGCGAGTA ACCACCTACC 600
TTGCAGGCTT GTGTGGACTG AGTGTGTTAC GGCCATGAAA ACACCATGTG CTCTATAAGG 660
TGCGCTTTAT TCATTCCTGA AGTGAGCATT TATCATGCAC CCACGTTCAT GCCAAGCCCT 720
TCTCTGGGAT CTGGGGAGAC AGCAGCAAAC ACAGCAGATG AGGTCCTGGT CCCTGGAGTT 780
ACTTTCAAGT GGTTGGAGCC AGATAATCAA CCGAGAAAGC CTGACACAGT TCAGACGGCG 840
TTGAGTGCCG TGGAGAACCC ACGCCGGACA GCGTGACGGA GCGGCCTCGG GGCTGGGCTA 900
CTGAGCAAGG GAGGGGCCTC TCTGACTTTG TGATGTCTGC ACAGAGGCTG AGCGGTGTGG 960
TGCAGGTCAG TGATGGAAAG CTGTTTATGG GAAGTGTCAA GGGATAGCCC CAAGGAAGGG 1020
AGGAGCTACA GCGGGTGAGG AACAGAAGGC TAGGGCAGGG AGAATGGGCA AGGGGCCCAC 1080
CGGGCAGTGC CTGTGCACTA 1100
|
