| Tag | Content |
|---|
EnhancerAtlas ID | HS101-37196 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr6:31820160-31820990 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYB | MA0502.1 | chr6:31820463-31820478 | AAACGCACCAATCAG | + | 6.73 | | NFYB | MA0502.1 | chr6:31820512-31820527 | AAACGGACCAATCAG | + | 8.25 | | NFYB | MA0502.1 | chr6:31820488-31820503 | AAATGGACCAATCAG | + | 9.03 | | NFYB | MA0502.1 | chr6:31820536-31820551 | AAATGGACCAATCAG | + | 9.03 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AAGGGCTGAA GAGTGCAGGC GCATGGGGCA GGACTGGCAA GCAGCTCCAC CTGCGGCCCC 60
AGTGCGGGAT CCACTGGGTG AAGCCAGCTG GGCTCCTGAG TGTGGTGGGG ACTTGGAGAA 120
CCTTTATGTC TAGCTAAGGG ATTGTAAATA CACCAATCGG CACTCTGTAT CTAGCTCAAG 180
GTTTGTAAAT ATACCAATCA GCATCCTGTG TCTAGCTCAG GGTTTGTAAA TGCACCAATC 240
GACACTGTAT CTAGCTAATC TAGTGAGGAC ATGGAGAACT TTTGTGTCTA GCTCAGGGAT 300
TGTAAACGCA CCAATCAGCA CCCTGTCAAA ATGGACCAAT CAGCTCTCTG TAAAACGGAC 360
CAATCAGCTC TCTGTAAAAT GGACCAATCA GCAGGATGTG GGTGGGGCCA GATAAGGGAA 420
TAAAAGCAGG CTGCCTGAGT GAGTAGTGAC ATCCCGCTCT GGTCATTTTC CATAGAGTGG 480
AAAGTTTGTT ATTTCCGTTT TTGCAATAAA TTTTATTGCT ATTTGTTCTT TGGGTCCACA 540
CTACTTTTAT GAGGTGTAAC ACTCACCGCA GGGGTATGCA GTTTCACTCC TGACGCTAGC 600
GAGAGCACGA ACCCCCCGGG AGGAACAAAC AACTCCAGAG GCGCCGCATT TAAGAACTGT 660
AACACTCCCC GTGAGGGTCT GCGGCCTCAT TCTTTAAATC AATGAGACCA AGAACCCACC 720
AATTGTGAAC ACAGAACAAT GTTGAAATTC TAAGTTTCCA TAAACTTTCT GTTTATATAA 780
GCGATTCCAA ACTTCTACAC TTTTGGAACA TAGACTAATA TTCTTTGGAA 830
|
