| Tag | Content |
|---|
EnhancerAtlas ID | HS044-06180 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr18:24336630-24338020 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr18:24337538-24337553 | AGTTAATCATTAGCA | - | 6.2 | | HNF1A | MA0046.2 | chr18:24337538-24337553 | AGTTAATCATTAGCA | + | 6.4 | | HNF1B | MA0153.2 | chr18:24337539-24337552 | GTTAATCATTAGC | + | 6.17 | | HNF1B | MA0153.2 | chr18:24337539-24337552 | GTTAATCATTAGC | - | 6.32 | | ZNF263 | MA0528.1 | chr18:24337896-24337917 | TCCCCATTTTCCTTCTCCTTT | - | 6.01 |
|
| | 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 |
| GH18I026757 | chr18 | 24337288 | 24338050 |
|
Enhancer Sequence | TTCCCATGGA CATCTCCCAT TATGGCAAAG GCAGCTGATA GGAAATCAGA GATGAAGCAA 60
TATTAAGTGT TACCCAGGGG ACCTCTCATT TGGAGTTGAG AATGAATCAC CTTTAGCCTC 120
TCTCCTCCAT CTCCGACACC TGCCAAGTAT TGCCTGGGCT GTCAGTAGCT GTGTCTGGCG 180
CCTGTGCAGG GTGGGAGCTT TGTAAGCATT TCTGCTCCTT CTCCTTAGTT CCAAAGCTTG 240
TTTATGTTTC ATTACCTTTT TCTTCCAAGG TGAACATGAG CTGTTAGGCA GTGCTCATGA 300
AGCAATTGTT TGGCTTATAT ACCAAAATTT TCTCACATTC TTGCAGGACT GATTTTCTTC 360
ATGCCAAGCA CAAAAAATGC TGTTCAATAC ACTTTCTCCT TTTCTCCTTG TGTAGTAAAG 420
GAAGGATTCT TGGATATTTA TCCAAAGTTT TGTCACACTG AAAAGAGAAG ACTGCATTGA 480
GGTGATGCTC CAAAAGGAGC AGCTTTGATG CAAAAGAAGC AAAACCCTTT TGTTTCTTGG 540
GCTTATACGA AGGTACTTCC TTTAGATCAG AGTCGGGATG CATACACACT ACAAAAACTG 600
GAATGAAAAA GGCAAACCAT TTTTACTCAA CAGAATTCTC TGTACAGGTC AAGGAAATGC 660
CAAACTTAAC AGATGTCTTA GACTGTGCCC TGCAGGTCAA TAAATTAGAG TTTTGTTGAA 720
CCAGGAAGAG GAAGGAATTC CAGGACTTCA GGTCCCCAAA TGGAAATGCC CCTTAGGACA 780
AGTCTAAACT AGGCAAATAG CACTGGAGCT CCTCCAAGTC AGTTGGCTCA GTCTCGTGTA 840
ACTCATTTCT GGCCCCCCTG AAGCTGTTTG TTCAACTGTG CCTTCTACAA CGCTACAGTG 900
TCAAAGAGAG TTAATCATTA GCAAGTGTGA ATAATGTCAG TGTAACGCAG CATGATTGCA 960
GTTCAGTCTG TTTTGACAAA ATTCTAAGCA TTTGTCAGAG TTTACCAAAA AACAAAAAAC 1020
AACATGACCA CAGAATGTTA AAATAGCATG AAGTTTGGGG AGCAGTTAAT TCACTTTCTA 1080
GCATTTTACA TCACCATTCT CATCGTTTTC CCAGAGGAGA GTGTTGGGTG AGGCCCTCCA 1140
GGTGATGCAG TATTACTGAC TGGCCTGGTA TGGTCTGATT CAGTTCAAGT CAGCTTAATG 1200
CAGCTCACCT CCAGAGATCC AGGCTTTGGA GAATGATCTA AAGGTTTAGG TGTAGGGTCC 1260
TTAACCTCCC CATTTTCCTT CTCCTTTGTC AGAGCCACCT ACTGCCATAG AATTAATATG 1320
GACCCATCTG TGATGCAGAG CCTGTTAGGC CTCCTGCTTG TCCCCTGGGC TGGGGATCAT 1380
AATGAGTCCA 1390
|
