| Tag | Content |
|---|
EnhancerAtlas ID | HS041-01453 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr1:90222760-90224120 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr1:90223491-90223506 | CAGGGACAAAGTTCA | + | 6.12 |
|
| | 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 |
| GH01I089755 | chr1 | 90221267 | 90225158 |
|
Enhancer Sequence | TGACACTGAC AACTGAAGAA CTTAAGTCAC TGGGGCATAA GACAGCATGA CAGACGCTAC 60
CCCAGTCCTA GGCATGCGGA CTTGCCTCGA GCACACTGTA AGTGTTCAGA CAGCTTTGGA 120
CAAATGCTGT CTTGAACTGC CAGATCGTAC CTTCGTATTT AAGAGACCAT TGCTCGGCAC 180
AACATGGCAG CTAATATTTA AAACAAATGG TAAAGAGGAA AGGCAATCAT TTCCTCACTA 240
AATGAAAAAG GAGATATGAA TCTGAGGAAC ACAATCCGGC ACTGATTGAA AGTAAATTAC 300
CAGTTGATTA GACGGCTGTA AATTCAGGGA GAGAAGCCTC AACCGGCAGC TGGATTTTGT 360
AAGGAAGAGG GCAATTAGAG AGGGCACAGG CGAGGCAGAG CACAGAGAGG GCTCTGCACA 420
GAGCAGACAG GGCAGCTTTG CAACACTAGG ATTACAAAGG CAGGAAGGGG TTTGTAGGAA 480
GTGTTCTGTG GATGGAGCCT GCAAGAAAGG GGAGCTCCCC ACTCCCACTC GCCCTGCCCC 540
ACCTCCCTAG TGAGCAGGAA GAGGTTAAAC TGCCAGTTCC CTGTCTAGCA GCAGTTAGGA 600
CGGGTGTTTG TTATTGCAAC ACAGGAAGTA TCACGATTTC TCTTCCTTTT TCAGGCTGTA 660
CTCAATCTAG AAGCTTTTTG CTTCCTATCA AAAGCCAGGG ACTTGAAAAC TACTCAGGTC 720
CCTGCAGCCC ACAGGGACAA AGTTCATGCA GATTTCAGTG GGAGATGCCA TCTCCGGATA 780
GCAACTGGGG CCAGTTTTTG CAGATGGCAA GCGCTTAAAG ATGCAAGCCT CCATGATTAC 840
CACGAACTGA GAAATCTCTG CAATTAGCAG GAGTGTAACT GGAAAACCAA GGGCTCCTCT 900
GTGCCTTACC AAAAGACATT CCCTCTTCCT CTGGCAAGTT GAAGAAGATA ATTTGGCCAG 960
CCTAGGAGGA AGTGATTGAT TGAGACAGAA ATGGTGGAGA GAAGGATGAC TGTGATTTTT 1020
ACTTTGGTGA TGGGCATGAA CATAACAAAG AACAGATGGT GGATGCCTTA GTCCCACTGG 1080
TGTTATCAAT TCCGTAGCCC TGAGCCCTGC CCTGCTACAG GCTTATGTAA TTCTCAAGCA 1140
TGTGCTCTCA TGGCCCAAGG GGAGACTATG CAGCACAGAC CCTCCAGCTG CGAGGTTAAC 1200
TCATCAATGC TCCACCCTTG TCATCTTTGG GTTCCAGCAC TCAGGCCCTG GATATGCCTC 1260
TCACCAGAAG TGAACACTTG GTGGGGGCTG CAATAGACCC AATGAACACA TCAGCTGCAG 1320
TTTGCATCTA AAAGAAATGA TTCCAATGTA ACATGACAGG 1360
|
