| Tag | Content |
|---|
EnhancerAtlas ID | HS044-00346 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr1:48023990-48025260 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr1:48025232-48025244 | GTTTGTTTGTTT | + | 6.32 | | USF1 | MA0093.2 | chr1:48024732-48024743 | GCCACGTGACC | + | 6.62 | | USF2 | MA0526.2 | chr1:48024730-48024746 | TTGCCACGTGACCAGC | - | 6.52 |
|
| | 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 |
| GH01I047558 | chr1 | 48023941 | 48026628 |
|
Enhancer Sequence | AGGAAGGAGT TGGCCTGAAC TGCATCATAC TGAAGGTGTA GGTGAGATGC TGCATAATGA 60
ACCTGTGTGT GTCTGAATGT GTGGCAGCTG CAAAAGAAGA GGTACTTCAT CCCAGTGGAG 120
ACACAGGTGT AGACAGGTTG GAAGCCTGAA TTTCAGTAAC GCACAATCTC AGCTTACAGT 180
CCACCCTGGT GCTAAGCCCT CTTGCCCAGG AATGCCAAAT GGGCATTACT CATTACCCCA 240
GAGGCCAGTG GGTCCTGGGG TACCCTGGAC CTATAGGCAA CCTTCAGGGC TGGCTTACTG 300
GACAGGGGGC AGGTGACTTC CTGAGATCTG CTCAATCCTT GCCACTGAAA TCCCTCTTGG 360
CACCTGTACC TGGGCAGCAG ATCTGAACCC ATTATTGACC ACAATTGACA CCCTCCCTTC 420
ATTCAAGGGA AGAAAGTCAT GTTGACTCAC CTCCTTACGT TAGGCACAGA CCATTTTATT 480
GAACGTTAAC GCAAATCACA CGGGCAGGAA ATGTCGTAAA GAGAAAAGTA ATCTTCTGAC 540
GGAAAAATAA ATTATCAGCC GTGTTCCGAA GGAAAAGAAA CATTCTTAAA TAATTTCTCT 600
TGCTGTTGGT ATTGGCTGGC AGTGTGGGCC AGCCAAGCAA ATGGTAATTT CCAAATTAGA 660
TTATACATTA TGTCATATTA GTTTTATATT AGAAAAACAA ACGGGATCAG AGGAGAAGTG 720
CCAAGGTTGG CGAGCTGTGC TTGCCACGTG ACCAGCCGTG TTTCCACTGC AGAATGTTTA 780
ATGATTCCGG GAGAGGTGGA AGAGCAAACA TTCAGACCGA CGCGGGGGAG AGTTGAGGTT 840
GGTTGCACAG AGGTAGGCTC TTCCAGGAGG GAAAGGACAG CTCCCAGGCT GGGCCCCTCT 900
GAGTATGGGT ACGCAACCAG GCTGGGGAGG CAGGGAGCAC CCCCACAACA GTCTCGTTTT 960
CTTTTCTCCA GGTATTTGGA CCTTCCCTTG GAAAAGCTGG TCTGGGGCAT GGGCTTTGGA 1020
GTCAGGGCAC CATGGCCAGT CCATGTTCAC AGGAGCAGCA GGTGGAGGTG CCCCATGTCA 1080
GTCCCAGAAG TCTGAGTGGG GCTATGTTGG TGGCCTACTT CCCTAGAGAG CTGCCCTTGG 1140
GCAGTGGGGG CAGATATCTG TCTCCCTAGT GTGCAGGGCC AGGGGAATGA TAAGGAGGAG 1200
ACTTTAAATG AGACTCATAT TGCTAGCTCA TGGTTTTTTT TTGTTTGTTT GTTTTTTGTT 1260
TTTTTTTTTT 1270
|
