| Tag | Content |
|---|
EnhancerAtlas ID | HS105-72285 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr7:3220880-3221750 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr7:3221408-3221419 | GGCCACACCCA | + | 6.62 | | Rxra | MA0512.2 | chr7:3221006-3221020 | CGGTTCAAAGGTTA | + | 6.01 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_67016 | chr7:3217720-3225109 | H2171 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 3221000 | 3221495 | | chr7 | 3220929 | 3221545 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I003181 | chr7 | 3220655 | 3221931 |
|
Enhancer Sequence | TTGCCATGTT GGCCAGGCTG GTCTCGAACT CCTGATCTGA AGTGATCCAC CTACCTCGGC 60
CTCCCAAAGT GCTGGTATTG CAGGCATGAG CCGCTGCGCC TGGCCTGTAA CAAGTTCCCT 120
TTGAAGCGGT TCAAAGGTTA AAACTTCCGA GGGCTGCCAG TTATCGTCCT GGTGAGTGCC 180
CCTTCCCGGG TCCGATTCCA AGGTCTCCAC TGCAGGCTCT GGTATGTTCA GACGCAGTTC 240
CTGGAGGAGA GGCCCTGCTG GCTCTGAGCC GGGAACCCGC CACGACGTGC AAAGTCGAGA 300
TTGCAAAGAC AGCGCAGGTC ACACATCCTG CCTGACTCCA GATTGCACGT CACCGTTTAT 360
TTTCTGTGCC CTGTGCCAGA AAACGAGATA TGTGCCATAT GCTCGCTTAC TTGTGAAGAC 420
TCAGGGATTC TACACACATT GCTGGCATTC GCACGCATAG GGAGGTGTGA TCGTCGCTGA 480
CACTGGAGCT TCCGTGTCTG TGTGCCAGGA GGCTCCGAGA TCTTTCCCGG CCACACCCAG 540
CACTCACATA TGGTGTTGAA GGTGCTGTAA TTCTAGACAC AGAGCATATG TCCTCGGAGC 600
AGACAGGGTG CTAAATTAAT TCTAAACGTC CGTTGTAAGT TTCTTGCCGA GATGCTCCCT 660
CCCTGTATAA ATAGCGTCTG TGCTGCACTT TCCTACAGCA GGCTCCACGG AAGCCTAGAT 720
AACCTGATTT CAGCTTTATT TTATAGTATT GAACATTCTT CAAAACAGCC CATCTCCATA 780
AAGGGAAACT GGGGGAAATG ATGATATGCT AAGCCGAGGG ACATTTGCTA AGTCTAACTG 840
GGTGTTCTCT CCTCTTGTTT CAATAGTGGG 870
|
