| Tag | Content |
|---|
EnhancerAtlas ID | HS044-00113 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr1:16393360-16394300 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX2 | MA0600.2 | chr1:16393731-16393747 | GGTTGCCATGGGGACG | - | 6.02 | | RFX2 | MA0600.2 | chr1:16394034-16394050 | GGCTGCCATGGCAACC | + | 6.14 | | RFX2 | MA0600.2 | chr1:16394034-16394050 | GGCTGCCATGGCAACC | - | 6.18 | | RFX2 | MA0600.2 | chr1:16393731-16393747 | GGTTGCCATGGGGACG | + | 6.29 | | RFX5 | MA0510.2 | chr1:16393731-16393747 | GGTTGCCATGGGGACG | - | 6.07 | | RFX5 | MA0510.2 | chr1:16394034-16394050 | GGCTGCCATGGCAACC | - | 6.68 | | RFX5 | MA0510.2 | chr1:16394034-16394050 | GGCTGCCATGGCAACC | + | 6.76 | | RFX5 | MA0510.2 | chr1:16393731-16393747 | GGTTGCCATGGGGACG | + | 6 | | ZNF263 | MA0528.1 | chr1:16393990-16394011 | GCTCCCTCCCCCACCTCCTCT | - | 6.49 |
|
| | 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 |
| GH01I016066 | chr1 | 16392920 | 16395416 |
|
Enhancer Sequence | AGCCAGGGCC CGCCAAGGTG CAGACAGGTG GCTCTGGCCA TAGGCTGACC CTAGGAACTT 60
GAGAGGTGTT AGGGTATTTC TAGGACCCCT GGCCATCCCC TGAAGCTTTT TTACAACTCT 120
CCAGCCACAG ACCAGGGAGC GAGGTTGATG GGGAGGGGAG CCGGGCACAG AGGAGGCTGG 180
TGGTGATGCC AAAGCCTGGC AGAGGCATGA CTTGAACAAG GTCATTTGTT GAGACGGTGG 240
TGGGCTTGGA GGACTCCTGG CTCCCACCCC CTCCCCAGCC CGCCTGGCTC CCCACCTCAG 300
TTGGGGTTCA GGTGCCTCCA CCAAAGCTGC CTGCTCCCCC TGAGGACTTT GGCCCCATGA 360
TGTCACAGGC TGGTTGCCAT GGGGACGTCA GGTAATGAAC CAGCCCAGGG TGAAATCACA 420
GGCTGTTCTT CGCCCAGCTG GGACTGGTGG TCACGTCACC ACTGGCAACT GGAAAAACAC 480
AGAGTGTCAT GTGGGGTGGG GGCTGGGAGG CAGCCCGAAG GGACCGCTAG CACCTGCTCC 540
TGTGGCTCCC TCTCCCAGAA GGACACCCCC TTTCTTTCAG TCCACACCCT AGTCTCCTGA 600
CCTCAAGGTC AGAATTCCCT TCTCAGACCT GCTCCCTCCC CCACCTCCTC TGTCCACAAG 660
AGTGACAGGC TTCTGGCTGC CATGGCAACC TGGAGAGGGC CATCTTGATT CTTCAAGGAG 720
AGGGTGTCAA CCAGATGTCT CCTCCATCCC TCTGTCTTCA ACCAGAGCTT CTCCTCTGCA 780
TCTTGAGGGT GCTTCCTGCC TTCCTATGCC AGCTCCTCTT CAATCTGCTT TAGAGTCTAA 840
CCTCCCAGAC AGTTCCTCCT GATGTCTAGC CTAAACCCCT CTTGTTGCAG TTCCCATACT 900
GGTTGGTCTT CTCTACTTGA TCCTTGGGTG AGTCTGCAGC 940
|
