| Tag | Content |
|---|
EnhancerAtlas ID | HS105-11349 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr10:100019460-100020670 |
Target genes | |
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 | GGGAGCATTT AGGGAGGGCC CAAGAGAAGG GGCCCTCTGG GGACAGGTGG GAGGTGAAGG 60
CCTTGCTGGT GGGGGCGGCC CGCCCAGAGA CACCCAGGCT ACCATCAGGC CTGCCCTCCT 120
CATGGGTGGC AGGCAAGTCA GCGAGACCCA GGTGTGCAAT TACCAGGCAG GGGGAGTCAG 180
GCTGCATCCC AGGATCCCCA AGGATGGAGC CAGAGGCTGA CCAGCACCCC TGTTTCCTCA 240
GAACGGGGTT CCTCTAAGTC ACTGCAACAA GGGCCTTCTA ACCCTTTAGG GAAGCAGGAT 300
CAAACTGATT GGGGTGGCAG ATGACTCAGA CGTACTACGG GAGACTTCTC ACTTGATGGG 360
AAACACACAA GTCCTCCCTG ACACGGATCT GGCAGAACCA TGACTGTGGC TGTCGTTTAC 420
TGGTTGATGC AATCAGTTGT GACAGTTCCG CCTTGTTTCT GACAGAATAT TTTTATGTCT 480
CCTCTCTCCA GGTGCCCCAC CCCACGCCTC ACTTACACAC AACCCAGTCA CAGCCTGGCT 540
TGATCAGAGC TGAGGAAATT CAGGAGGGAA GCGTTGGGAT ATTCGCAGTG GAATTGAGGA 600
TGGAGGCTCA GAGGCCCTCC CCAAAGCCCT AACGCCAGTC ACTGGCTGAG CTGAGGCCAG 660
AACAGTTTGT CTAAACTCTA CACGTGGGTG TCACTGCAAG TATCTGCAGG AAAGTCTAGT 720
GTTTTAACCA AGGACACGCG GTTTTATGTT CAACTGTTTT CACCGGGGGC GGGGGGTGGG 780
GGGGCGTTCT GTACCTAGTT AATTCTGTTT ACATAATTCG AGAGTGCAGT GTTTGTTTTC 840
TGACTGTTTC TAGGTATTTC CCAGGATCCT GAAGGTCCTC CTTATTCACT TTCCTGTTTA 900
TTATTCTGAG GCACCCGTGA AGCAAGAAAT CTGGGCACAT TCCTCAGTAG GGCCTGTTTT 960
CTCTCCCCCA ATCCCAACAC CTGCTGGATG TCCTGCCACA GACAACACCA CTGCCAGTCA 1020
GTACTCACTG AACTCTGCGA GGTCCCACAT GCCACACACA TCACACACTC GCCTGTGTGC 1080
ATACTTACTT GCCCCTCACA TGAGTCCACA CTCAGACTCA TGCACACACC CTACATCACA 1140
TGCACGCACA TGAACACACA CTCAGTCCCT GCCCCACAAC CCTGCCTCCT GTGGGGCCTA 1200
CGCCAGCCGC 1210
|
