| Tag | Content |
|---|
EnhancerAtlas ID | HS044-07978 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr20:11175490-11177260 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIA | MA0670.1 | chr20:11176535-11176545 | ACTTGGCACC | - | 6.02 | | TBXT | MA0009.2 | chr20:11176485-11176501 | TCACACACATGTGCGA | + | 6.74 | | TBXT | MA0009.2 | chr20:11176485-11176501 | TCACACACATGTGCGA | - | 6.82 | | ZNF263 | MA0528.1 | chr20:11176359-11176380 | TCCTCTCTCTTCCCCTCCTCT | - | 7.42 | | ZNF740 | MA0753.2 | chr20:11176815-11176828 | CCGCCCCCCCCCC | + | 6.64 |
|
| | 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 |
| GH20I011195 | chr20 | 11175658 | 11177760 |
|
Enhancer Sequence | AGCCACAGCA CTCTCATGTT CTTTTTGACC CAAGCCAAAT CACTCAGCCT GCTGAGATCT 60
CAGTTGTTTT TTTTCATCCT GGACAATGGG CATGATGCTG ACTGTCCCTC TGGGTGGTTC 120
TGAGGATCTT GGGAGGATGG ATATAAGTGC AACTTAAACT CTGGAGCCCT TTACAACTGC 180
AAGGCAGCAT TATTCACTCA AACATAAAAA TAGGTCATTA AGCATCATCA AAGGGAAAAG 240
TAAATGTTCA GGGATCATCT CTGCTGCACT GTTGCTGGGG AAAGAGGCTC TTTGTCCCTT 300
TAAGAGCTTT CAGACACATC TCTAGTCACA TCCTAAAAGC CTTCCTAGTT GTGTAGCTTA 360
GGTGCATCCG GTAGCACAGC CGTGTTCTGA TCTTCCTGGC AGATGTCATA ATTTACTGTC 420
ACCCCCATGC AGGAATGCAG GGCGAGGGGC CCCCATGCCG GCTCTGTGAT CCATTGCCTG 480
ACAAGTCCTG AGTGTCAACC TCAGGCAGGC CCAGCGGAGG TGGAACACCA TTTACCTGAT 540
AGTGCCTGTG ATAAAGTGGG CAATTAGACG CACTTGGAAA AGCCTGGCTG GAAACTGGCT 600
GGCATTTACA CAACATTACA GCCAAGTCAG GCTTCATAAA AGTTAATGGA GAAAAATGAA 660
GTCCTTCAAG ATCTACCTTG CTCTCTGAGG AAGTCAGGAA CACAGGACTC TGTAGCTTTA 720
TTTCTTTTTG TGTCTCTCCC ACCTTTTCAC TCTATTTCCC CCAGACAGGG TAATATATTC 780
TCATTGGAGA TGGGAGTAAA GGAAAGCGAA TTGAGAGTTG AGGTCTTAAG TGTTTGATCT 840
CAGAGGCATG TTATTTCTTT AGTCTTCAAT CCTCTCTCTT CCCCTCCTCT CTGTCTCTCT 900
CTCACACACA CACATGCACA CACACACACA CACTCTATAC TTCTATAGAG TATACACACT 960
CTATATTTCT CTGTCTTTCT GTCTCTGTCT CTCTCTCACA CACATGTGCG AGCACACACA 1020
CACACAATCA CAGTGCTAGG ATTTAACTTG GCACCTTGGC TTACAATTTG CCTCTCACTG 1080
GAGTTTCTGG AGTTTGGTGC CAGTTCAAGA GCATGATCTG TTTGACATGA ATTCTACAGC 1140
CCTCTCTTCA TTTCCTCCTA ACTGGATAGC TTCAGTTTGC CGATGATTAA TGAGTCTGGA 1200
AGGTGAGCGA CAGTTATCTT AAGGGCTCTC AAAAGTTTAT TTCAGAGACT AGCCAAACTC 1260
TCCTGCTACA TTAACTGCAG CGAAGTTTCC TGTTTAACAG CCCATGGAAA ATAACTGCCT 1320
GACCCCCGCC CCCCCCCCAA ACCAAGCTGC CATGAGCGCA GCTCTGTTTA TTGGCCAACA 1380
GTGTGCATGT TCTCTCTATC GCTTCCTTTC AGGCAGACGA ACATTTTACC TATGAGAAGT 1440
AGGAAGTCCA TTGTGAGGCT GGTCCAATAC TGGACCTCAT TTGGATGTGG AGGATTTCTG 1500
AAATTGGAAA GTCAGGACTG ATCTGGAAAA TGTGCTTACA GATAGTGGAA CAGGAAAATG 1560
ATTCGCTCCC CAAGGCCAGT TCCTCCTCCT CTGCTGGGTG GAAAAGGTGG GAGGAAGGGA 1620
CAGGGTGTTC TGCCTGTGAT TGGAATTCCC CTGTAGAGTC ATAGAGGATG AGCAAGCCTT 1680
TGGTTTTCCT TTTTCATATT TTATTTTGCA CCTACAATAA TAAGCATGCA GAGAGGAGAC 1740
AGAGAGGCCT AAATGAGTTT TTTTCCTTTC 1770
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