| Tag | Content |
|---|
EnhancerAtlas ID | HS041-00156 | Organism | Homo sapiens | Tissue/cell | EWS502 | Coordinate | chr1:7551800-7552950 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP2 | MA0593.1 | chr1:7551887-7551898 | TTTGTTTACTT | - | 6.62 |
| | | 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 |
| GH01I007490 | chr1 | 7550829 | 7552540 |
| Enhancer Sequence | AAGAGGATAA TAATGTTTAA AAACGAAGTC ACTCATACCA TTTCCTGTCG CGAAGCCAGC 60
TCAGTGATGG GCAGAGCTTC CTCTGGGTTT GTTTACTTGC TCCATGATGG AAAATGCAAA 120
CTTAATGGGC TCCCTTCTGC CGAGGCTTTG GTGTTCCGAC GAAACAAAGA CCCATGCTGC 180
TGCCGAATCT GTGTCCACAG CTCTGGCCAG CTCACCCTGG AAGTCTTGAT TGCCACATTG 240
TGGATGTCAG AATGTCACCT GCTTGGTTAG AGCTTCTAAA CAGGAGGCTC AAGGCCACTC 300
CCTGGCTCTA GGGTGGAGTC GAGGAAACCT GTCTAGGATG GGACACGCTC CCACTAGGCT 360
CAGGGTGCCC TCCCGTCCAA GAGCATGATG GTCACCCCAG CTGGGAAGTT GCTAAGCAAG 420
TCCTCCTTGG TAGAGCGTCT TTCCCATCAT CCTCTGCGAG GAAGGCCAGG GCGATACACT 480
CAGCTTATAG AGTGAAGTCG GCAGAAAGCA CAACTTCTCA GTGAAGAGGA TAAAAGGAAG 540
GCACTACGGG GGCCCAGGAC CTGCTCTGCC CTGCTTAGGG CTGGGCAGGG CTTACGGGCG 600
TGACATGCAT AGAGGCTCAG AAGAGCTGGC TCCGGCCTTT TGCAGTCTGG GATCCTCAGC 660
TGGGGTGTGC ACATGAGCAA GGGTGCTCTA TGCCCCTGCC ACCAGCCCCC GGGCTGCTCA 720
GGAGGCAGCA GTGAAGGATG GAAAGGGTTT CCATGGCCAT GAAAGAGAGA GAGCTCATCC 780
GCTCCTGCAT AGCACTGTGA GGGCTTGAAC ACACACACGC ACGCACATAC AAACGCAAAC 840
CTACATACAC ACACGCGTGC ACACACACAC ACAAATGTAC ATACACGCGC ACACAAACAC 900
ATACAATCAC ACAAACACAA ACATACGAAC ACACACACAC AAACACAAAC CTACAAACAC 960
ACACGCAGGC ACACACACAA ACACAAACCT ACATACACAC ACGCGCGCAC ACACACACAA 1020
ACCTACATAC ACAAGTGCAC ACACAAACAC AAACCTACGT ATACACATGC GCGCACAGAC 1080
ACACAAACAT ACAAACACGC ACACGCACAA ACACAAACCT ACAAACACAC GCGCACATGC 1140
ACAAACACAA 1150
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