| Tag | Content |
|---|
EnhancerAtlas ID | HS129-02091 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:150867790-150868590 |
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 | chr1:150867806-150867827 | TTTTTCTTTTTTTTTCTTTTT | + | 6.07 | | NFE2L1 | MA0089.2 | chr1:150868229-150868244 | GCATGACTCAGCCTT | + | 6.13 | | Nr2f6(var.2) | MA0728.1 | chr1:150868038-150868053 | TGAACTCCTGACCTC | - | 6.22 |
|
| | 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 |
| GH01I150895 | chr1 | 150867849 | 150868735 |
|
Enhancer Sequence | GTTTGGGGAA ATCTTTTTTT TCTTTTTTTT TCTTTTTTTA ATTTTGTGTG ACGAAGTCTC 60
TTTCTGTTGC CCAGGCTGCA GTGCAGAGAC GCGATCTCAG CTCACTGCAA CCTCCACCTC 120
TCAGGTTCAA GTGATCTTCC TACCTCAGCA TCCCAATTAT CTGGAATTAT AGGTGCGCAC 180
CACTACGCCC AGCTAATTTT TGTATTTTCA GTAGAGATGG GCTTTCACTA TGTTGACTAG 240
GCTGGTCTTG AACTCCTGAC CTCAAGTGAT CCACCTGCCT CGACCTCCCA AAGTGTTGGG 300
ATGATTACAG GCGTGAGCCA CTGCACCCGG CCATGAAGAA GTCTTTCTTC ACATGAATCT 360
GTCAGAAACA ATTCCCACTG CGGAGGCCTA GAGAAATCAA ATATTCCCTC TTCCACCCTC 420
TGGCAGCCAA GGTGTTAGTG CATGACTCAG CCTTGACCAG TCAGATGCTC TAGCCAGAGA 480
CTAGACTATT GAGTGACACA AAGATGACAC AATTTATAAT TCAGCCATGC CAGAGGCAGC 540
AGTATCCAAT GACAGTAGCA GCAGTGCTCG GCAACAGCAG TGTCTGGTGG TGGCAATGTC 600
TAATGCCAGC ATTGCCCTAA CCAGACTTTT CCTGTGCTCT CCCTGGCTAT GGTTCCTGAT 660
GGCTGGCTTC TCTTGATTTC TGTCTGTTTA TAAGACTAGT TCTCTTTCTG AGAGCTATCT 720
GACCTCTTTA CAATAAATAT ATTTTCTGTT TAACGGAGAA TCCGTTCCTG TTGCTTGCAA 780
ACAAGAATGT GTTCTTTTTT 800
|
