| Tag | Content |
|---|
EnhancerAtlas ID | HS044-01709 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr10:65332550-65333940 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr10:65332958-65332976 | GCAACCTTCCTTTCTTCC | - | 6.37 | | EWSR1-FLI1 | MA0149.1 | chr10:65332962-65332980 | CCTTCCTTTCTTCCTTTG | - | 6.63 | | FOXC1 | MA0032.2 | chr10:65332626-65332637 | TAAGTAAATAT | + | 6.14 | | STAT1 | MA0137.3 | chr10:65333187-65333198 | TTTCTAGGAAA | + | 6.14 | | Stat4 | MA0518.1 | chr10:65333187-65333201 | TTTCTAGGAAACCA | + | 6.21 |
|
| | 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 |
| GH10I063572 | chr10 | 65332476 | 65334009 |
|
Enhancer Sequence | CTGTACCTAG AACAGTACCT GCTGCATAAT AGGTACTCAA TATTTCTTGA ATAAATAAAT 60
GAGAAAAGTT GACTTTTAAG TAAATATCAA ATATTGTGCT TAATAGCTTG TACATTTCTT 120
AAGTGGATTG ATCTAGTTTA CCAGCTTTGA TTCTGCTGGG TTAGGGAGAA TACAGTCCAG 180
TCTTAACATT TATCCCAAAA CCCAGTTTCT TTGTGGTATT TGGTTATGAC CTAAATTTCA 240
CTGCTATCTA CTTCAAAATT ATTTTCAGAA AGCAAACATT TTCGGTTAAT TTACTTCTTC 300
CCACCCCCAA CTACTACCAT TCCCCTTAAG CCTGCAAATG GTAGATTGCA CCTGATAAAA 360
CAGATGCTGT GCTCAAATCA AAACAAATGG AAAGTACTGT GTATTTTGGC AACCTTCCTT 420
TCTTCCTTTG CCTATTTTTA AAACAGAGCT TTCCTAGGAT ATAATTTCCT GCATAGTGTG 480
GCTGATATGG CCTACTTAAA GACTTTCAGT CTTGCAGTAA TTGAAATGTA AACTTACTGA 540
AGAATTAGTA TGGTTTTGCA AATTTTTTCA GGCTCATTCC ATCTCATGAC TTGAAAATAG 600
AGTGTTTACT TCCAAGTCGT GTGTAATTGC TGTAGCTTTT CTAGGAAACC AGTGTTCTTA 660
TTCTAAGAAT GTTGGAGAAA GCAGCAATGA AAAGATTGGC TAACAGCACT TACAAATCAA 720
AATCAGACAT TTGGTTCTGA GATTTACTGT GAGCAAGAAC AAAGAACAGG AAAAGCTGGG 780
AGATTACTCT CTAAAAGGCC TAGAAATGGC CCTCTAAAAG TCTGCTGACT TGGTTTTTGA 840
AAGTGACCTA ATTTTCGACT GACTATTTAG GTGATATGAA AATGAACAAA TATACCACAT 900
GCCAGTTCTA CAGATCTTAT TGATAATGAA ATCTGAAGTT GTCTGCTAAC TTTAGAGTGG 960
AAATAGAAGG GGAAAAACAT ACTAAAGAAC TTTTCTTTGT TCTCAAGAAG TGTTTCCTAG 1020
GTATCTTTTG ATAATTTTGA TAAAAAGTAT TCATTTCATT TAAAGGTTTT AATAATTTAG 1080
AAAGTTTAAA GATTAGCCTA CTGATTATGA TGGGATTTTT ACTGAAAATT AGTTTTGTCA 1140
GGCTGCTTGC TTGTCTGTGT ATTTTCTATT CTAATTTAGT TTTTATTTTT ATCAAAGCTG 1200
TATTTACTTA TAATGTAAAA AGTCAATTAG TTTTCCAAGG CTTATTATGG AAAACAGTAG 1260
TTCCCCAGGC TCCCATCCCT ATGTCTAACT CTCTAGAGGC AACTAGTTCA AACTCTTTTA 1320
TCTGAATCTT TTAGCATTTA TTGCCATATT CCAAATAACA TACTTATTGT GCTATTTCTT 1380
AATTTTTCAG 1390
|
