| Tag | Content |
|---|
EnhancerAtlas ID | HS127-04519 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr10:100019180-100020670 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr10:100020262-100020274 | TTCTGTTTACAT | - | 6.92 | | FOXP2 | MA0593.1 | chr10:100020263-100020274 | TCTGTTTACAT | - | 6.02 | | PLAG1 | MA0163.1 | chr10:100019488-100019502 | GGGGCCCTCTGGGG | + | 6.37 | | TCF3 | MA0522.2 | chr10:100020435-100020445 | AACACCTGCT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr10 | 100019640 | 100020631 | | chr10 | 100019677 | 100020107 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH10I098259 | chr10 | 100019378 | 100020430 | | GH10I098260 | chr10 | 100020569 | 100021624 |
|
Enhancer Sequence | ACTTTCCTGT TATGGGAGAA AACAGATAGG AGGTGGAAGG GGTGTGGAAG TCCCACCCCC 60
TGCCACCTGG TTCCTCATAG TTGTCCTTAA GTTTGCACAG GACTTTACAT TTTGTAAACT 120
TATTCACTAA TCTGATTTCA ATGCTGAGCT TCACAGCAGC CCTGACGGGG TGGCCACCTC 180
ACAAATAACC ATTTTACAAG GAAGGCAAGC AAGGTCCCTC GGCCAGTCCT AGAGTGGGGG 240
CAGGTGGATC AGGCTTGCCC TCTCCGAAGT CCAGAGGAAG GGGAGCATTT AGGGAGGGCC 300
CAAGAGAAGG GGCCCTCTGG GGACAGGTGG GAGGTGAAGG CCTTGCTGGT GGGGGCGGCC 360
CGCCCAGAGA CACCCAGGCT ACCATCAGGC CTGCCCTCCT CATGGGTGGC AGGCAAGTCA 420
GCGAGACCCA GGTGTGCAAT TACCAGGCAG GGGGAGTCAG GCTGCATCCC AGGATCCCCA 480
AGGATGGAGC CAGAGGCTGA CCAGCACCCC TGTTTCCTCA GAACGGGGTT CCTCTAAGTC 540
ACTGCAACAA GGGCCTTCTA ACCCTTTAGG GAAGCAGGAT CAAACTGATT GGGGTGGCAG 600
ATGACTCAGA CGTACTACGG GAGACTTCTC ACTTGATGGG AAACACACAA GTCCTCCCTG 660
ACACGGATCT GGCAGAACCA TGACTGTGGC TGTCGTTTAC TGGTTGATGC AATCAGTTGT 720
GACAGTTCCG CCTTGTTTCT GACAGAATAT TTTTATGTCT CCTCTCTCCA GGTGCCCCAC 780
CCCACGCCTC ACTTACACAC AACCCAGTCA CAGCCTGGCT TGATCAGAGC TGAGGAAATT 840
CAGGAGGGAA GCGTTGGGAT ATTCGCAGTG GAATTGAGGA TGGAGGCTCA GAGGCCCTCC 900
CCAAAGCCCT AACGCCAGTC ACTGGCTGAG CTGAGGCCAG AACAGTTTGT CTAAACTCTA 960
CACGTGGGTG TCACTGCAAG TATCTGCAGG AAAGTCTAGT GTTTTAACCA AGGACACGCG 1020
GTTTTATGTT CAACTGTTTT CACCGGGGGC GGGGGGTGGG GGGGCGTTCT GTACCTAGTT 1080
AATTCTGTTT ACATAATTCG AGAGTGCAGT GTTTGTTTTC TGACTGTTTC TAGGTATTTC 1140
CCAGGATCCT GAAGGTCCTC CTTATTCACT TTCCTGTTTA TTATTCTGAG GCACCCGTGA 1200
AGCAAGAAAT CTGGGCACAT TCCTCAGTAG GGCCTGTTTT CTCTCCCCCA ATCCCAACAC 1260
CTGCTGGATG TCCTGCCACA GACAACACCA CTGCCAGTCA GTACTCACTG AACTCTGCGA 1320
GGTCCCACAT GCCACACACA TCACACACTC GCCTGTGTGC ATACTTACTT GCCCCTCACA 1380
TGAGTCCACA CTCAGACTCA TGCACACACC CTACATCACA TGCACGCACA TGAACACACA 1440
CTCAGTCCCT GCCCCACAAC CCTGCCTCCT GTGGGGCCTA CGCCAGCCGC 1490
|
