| Tag | Content |
|---|
EnhancerAtlas ID | HS044-00472 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr1:64648870-64650260 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr1:64649649-64649660 | TCAAGGTCAAT | + | 6.02 | | Nkx2-5(var.2) | MA0503.1 | chr1:64649643-64649654 | AAGCACTCAAG | + | 6.02 |
|
| | 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 |
| GH01I064183 | chr1 | 64648897 | 64650390 |
|
Enhancer Sequence | ATTTGACAAT TAGCTATATT TTTTGAAGTT GTTCCCTTGG ATAGAAAACT GACAACATGT 60
AGTCTTTGTC AAGAAGATAT TCCTCATCCA GTTCACCTGA GACCTAAATT CTTGGATAGT 120
GGCCAAATGC TTTTTCCTTC ATATGGACAA ACTCAAAGAA GTTGGTCTCT TAGTACGCGT 180
TTTTTTGACC CATGAACTGA TGATTGACAA AACAAAACAA AACAAAAATC CCTTCTATGT 240
TGCAACTTAA CAAAGATAAG GTCAAGGATA GGCTGGTCTT TGGGAGGAGG GATAGGCTCA 300
GCCCTAGTAA GCATCAAGCA GGAAGCTGCT GCAGGGGCTC CCCTCCCTCC CTTGCACTTC 360
CTGTGATGCC CTGACCCAGC TGGCTGGATG CAGACACCTG TGGCTTGTTC TGCTGTTTTC 420
CTTGGCCAGC TGGAATCCAT CATCAGTCCC TGGCTGGCCA TGAGTGCTCT TCTGCCCGGA 480
CTTTGCTCTC CTCTGCCTTT AAAGGGCTGA AAGCTCTGAG GAAGGACAGA AAGAGGGATC 540
CAAGGGAGGT TCTGGGGTGC AGTTCATACT CTTCTTAATT TATACGCATT TTTTTCAGCC 600
AATAGCTCTA ATGCTAAAGA GGAAGTGCCA GATTAGCGGA GAAAGAACAA GGGAGCACAC 660
ACAAGAAAGG GTTTTTGCAG CCAAAATATG ACTGCATTGA AGTTTGTTAC CGTAAATGCC 720
AATGGTAATA GGACGCTGTT AGCTCAAGAA AAGGAGAGTC TTACAAACCA TCAAAGCACT 780
CAAGGTCAAT GTAATCCTCT GGGAAATTAG GCTGGGAAGG CTTAAAAATA TAGACATATA 840
GAGGGAGAAG GTCTGCTGAC ATATTTATGA CTAGTTGAAT CTTAAGCACG TATGAATTGC 900
TTACTCACAA ATGAGTACCA TAACATTTGC TGACCGGGAT TGGCAAGATA CCTTACCAAA 960
TGACTATGTT AGTAAATACA GTCATGCATT ACTTAACGAA GGGGATACAT TCTGAGAAAT 1020
GTCCTTAGGT GATTTCGTCA CGGTGCAAAC ATTATGGTGT ACAATTACAC ACACAGTACA 1080
GACTGCTACA AACCTAGGCT ACATAGAGTA TGGCATACTG CTCCCAAGCT ACAAACCTGT 1140
ACAGCATGTT ACAGTACTGA ATACTGTAGG CAACTGTAAT ACAATGGCAA GTATTTGTGA 1200
ATCTAAGCAC TTATCATGAA TGGAGCTTGT AAAACTGGAA GTTGCTCTGG GTGAGTCAGT 1260
GAGTGAGTGG TGGGTATTGT ACACTACTGT AGACTTTATA AACACTGTAC ACTTAAACTA 1320
CACTAAATTT ATTTAAAAAT TCTTCAATCA TAAATTAACC TTTTGATTTA TGAACTTTTT 1380
ATTTTAACTT 1390
|
