| Tag | Content |
|---|
EnhancerAtlas ID | HS044-07127 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr2:62889650-62890980 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP2 | MA0593.1 | chr2:62890410-62890421 | TTTGTTTACAT | - | 6.14 | | Lhx3 | MA0135.1 | chr2:62890876-62890889 | GAATAATTAATTT | - | 7.34 | | Tcf12 | MA0521.1 | chr2:62889867-62889878 | CAGCAGCTGTT | - | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 62889776 | 62889941 | | chr2 | 62890111 | 62890469 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I062659 | chr2 | 62886726 | 62892801 |
|
Enhancer Sequence | ATAGGTTAGA AAAGTTTCCA ATAGCCGAAC ACAAACCCAG GAATCAAAGT CCCCCAAATA 60
TACACAAAGG AAAAAACACA CACACAACCT ACCTAATCTG TAGCTAGAGT GCTTCTGGGC 120
CATGGAACCA CCCCATTGTG CCTTGGCCAC TCCAGCTCAG AAACCAGAGT GTTGCCATGG 180
TGGCAGGGAC CCAACCGTGA GGGCTGGTTT CAATACCCAG CAGCTGTTCA CTTCAGAAAA 240
AGCAGGATGG CAGCCCACTT CTGAATGCGC ATTTTTCTCT AGGCTTTGAC CTGACCTGAA 300
TATTGTTTCT CATTGAATTT CCTTTTATTT ATTTCTTTTT AGATATCAAC TTTCCTTGAA 360
CTTTTCCTGT CATTTGTGTT GCAGTTGGCA GAACTACAGA ACTTCTCCCT TCTGCAAAAA 420
ATGTGTTTTT TTTCTTTAAC CATTTCTAAG TTTTTCCCTG TGTTGTCTTT ATCTCCCCCA 480
CTTCTATATT TTACACACAC ACCTGTGCCT CATTATATGA CGACCCAGGA CAAATTCATC 540
AGGTTTGTTT ATTCCAAGAA GTGTGAAGGC CTCAGGTAGC CCCCTAAAAA ATCCCTCCAT 600
GACTCACCTG ACAGCAGAAA TTTGTCCTAT GAAACTTTGG AGCTGGATTA GAAAATATGA 660
CCCTTTACTC TCTTCATTCT GGCCATGGTC ATAGAATCTG TGTTTAATCC TAAACACATT 720
CTCAATTCAC ACTTGATTCA TAACCTGCTT TTTTCTTCTC TTTGTTTACA TGTTGGCAAA 780
ACATAAGGAA TGTAAAAATA TAAAAACTAT TATGAATTAT GAGCCCTGCT CACAAGGATT 840
GTAGAAAAAC TGTTCTTGAT GCAAAAAGGA GCTGCACTAT ATTTAAGGTG AATTTATCCC 900
TCTCCAGCTC TAAAGGAGTT TGGAATAATT TATAAATGAG GTTGTACTGC TGTTGAATAT 960
TTTTTTTAAC TAGAAACAGT TTGTTTACAA GTTGTTACTA AAGACTGTCA GAAAAAAATG 1020
CTTGTGGACA TGGTATCCAA AAGGCTGACA GAACCCAGAA CTTGCTTGGT ATTCATTTGA 1080
GAGCTCATCC AACATTATCC TGCACAGTGT ATAATTACTT GCATGTTGGG AGCCAAAAAA 1140
GGGAATGTAA CCCTGTGAGT GTGTGTTTAT ACTGAAAAGT TGGAGAAGCA AAACAATTCA 1200
GCAGCATTCT TCATCCCAAC ATCTGGGAAT AATTAATTTG CTAGCTATGA TGTATAACAT 1260
GAAGTTGATA AAGTTGCCTG AAGCTCTGCA TTTAGACCAT TTGCCTTATT TAAAGCTTTC 1320
TGCTTTAGGG 1330
|
