| Tag | Content |
|---|
EnhancerAtlas ID | HS136-01750 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr1:221840500-221841800 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arid5a | MA0602.1 | chr1:221840513-221840527 | TTTTTCAATATTGG | - | 6.72 | | FOXC1 | MA0032.2 | chr1:221841745-221841756 | TAAGTAAATAT | + | 6.14 | | FOXP1 | MA0481.2 | chr1:221841394-221841406 | ATCTGTTTACAT | - | 6.62 | | FOXP2 | MA0593.1 | chr1:221841395-221841406 | TCTGTTTACAT | - | 6.02 |
|
| | 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 |
| GH01I221667 | chr1 | 221840377 | 221841590 |
|
Enhancer Sequence | AAGTACTTTG GTTTTTTTCA ATATTGGTGT TTAAGATCTA TCAGGACAGG ACAGAGGAGG 60
CTTTATTCTA TGGCTAGCTT AAGCCCTGCT CTCAAGGCCA ACCATTTTGG AGTTTCTAAC 120
AAATGTTCCA GGTATTCAAT AATGTCTGTC TTCACTCTGG CTGTTTGGAA ATGGAATATC 180
CTCCTACTCT CTATGAACTC TGTGAATTAT TTAACTTACA GCTCTTTAGT AGTTTTTCTT 240
ATCCTGGCCT CATAGAGTTT TATTGGATGC AAGCTCAGCT TATTCAGGCA AAGACTCAAG 300
GGGATTCCTG GGCAAATGTT TGGAGTTATT TTTCTTAAAA ATTCCCTCTT CTCTGCAACC 360
CAGCCCTTCC AACTTGAGCT GCCTCGGTCT CCCTGAATTT GGTTTTACGT CTCCTCACTC 420
AGTGAGAGTG TTATGCTCTG CTTGTTCCCC CACTGTGCAT GCTAGTTCAG AAAAGGTTCC 480
CATGCAGAAA CCTCAGGTAA TTATGGGACT TGCCTTGTTA GTTTCCCTTA TCTTATGAGT 540
CACAGTCCTG CAGTTCCTAT TGCTCAAGAT CTGAACATGA TGTGTCATGT GCTTTGTCCC 600
ATATTCTAGT TGTTTACAGC AAAAGAGCAA ATCTAATATC AGTTATTCCA TAGTGGCTAT 660
AAGTGGAAGA TTTTGGAAAC AGTGCTTCTT GAATTGTTTC ATGTCTCCGC ACTGTCAGAC 720
ATACAAATTA CTGATAGCCT TGTTGGAAGG ATTGAATGGT AAGCATGCTT TATAAATTAG 780
AAATAGTAAA TTGCTCTGGA GAGATCTGAA GTTCCATCTC CATCAGAACT ATTTGCTTAC 840
ACTCTAAGAG TGATAAAAAC CTAGAGACAC CTTCCTTTCC TCTCCCCAGA GAGGATCTGT 900
TTACATTTCA GAGCAGCAAG ATCTCTTTCA TTCTCCCCTC CCTTCAGGGC AGGTAAGACA 960
CATGTGCCAG CCATCTTATA GAAGCTTCAA GCATCATAAA TAATCAATCA AGTATCAATA 1020
ATCAATATCA AATTTACCTA CTTGTGCAGC GGTTGCTTCA TAGGAGAGAA AACTAACATT 1080
AGTTTTCTCT CCTATGAAGC AACCGCTGCA CAAGTAGGTA AATTTGGCTC CCACTATGTT 1140
ACCCGCGAAA CAAGAATTGG GACATGGGGA ACTAGTGCTG CTAAGATTCT CTGAGTGAAT 1200
GATCTGTTTC TGACCCAGAG ACCTGTGTTG TCAGAAAAAA ATAGATAAGT AAATATAGGG 1260
AGATTTTTTT AAAGACTCTT TTAAAGTCTC TCGTGATTGT 1300
|
