Tag | Content |
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EnhancerAtlas ID | HS044-00983 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr1:181148690-181150300 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr1:181149515-181149527 | GTTTGTTTGTTT | + | 6.32 | REL | MA0101.1 | chr1:181149149-181149159 | GGGGATTTCC | + | 6.02 | RREB1 | MA0073.1 | chr1:181149927-181149947 | TGGTGTGGGGTGGTGTGAGG | - | 6.5 | RREB1 | MA0073.1 | chr1:181149937-181149957 | TGGTGTGAGGTGGTTGGGGG | - | 6.99 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I181179 | chr1 | 181148337 | 181150297 |
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Enhancer Sequence | TCAGTTCCTG CATGAGTTTC CAGCCTGCTA GCCTGCTCCA CAGATCTCAG ACTTGCCAGC 60 CTCCACAACT GTATGAGCCA ATTCCTGAAA TAAATTCCTT TATACATATA TGTAATATGT 120 ACACATACAC ACATCTATGT CATCTAGATT TAGAGCTAAT CTAGCTCCTC CTGGCTCTGT 180 TTGTCTGGAG AACCCCGACT GATACTGATG TGTTTATTTG CTTATCATCC TCCCTACCCC 240 AGACGGAGGC TCTCTAAGGG GAAGATCTTT TGTCTGTTTC CTTCATGCTG TGTCTGAAGT 300 GACCAGGACA GCAGCCGGCA ATAGGACGTG CTCAGTCGAT ATTGTACAAT GGATCTTCAT 360 AATTCTTGCT TATTTGTGTG GTTGTTATCT GTCTGAAATT CAAGAAAGAA GGACATGAGA 420 AAAGAAAAGG ATGAAAGCAC ACTGGTCTTA TCTGAGGCTG GGGATTTCCC CGTTGGGCCC 480 AGTGTTGTGG ATTCTGCAGT TGAGTTGTGT CTGTTTGCAG CTGAAAGAAA GCTGTGGCAG 540 TGAGGAGAGG TTGCAAATTT AGAATCAAGT TCAAGTTCTC CTAGCAACAT GCACACCCCC 600 GCTGCTGGCT GGTGTAATCC AAGCACCAAA CACGTGCAGC TGGGGCAGTG CGTGTTGCTA 660 GGAGAACAAT GACTCTCTTG CTTCCAGAGC TGGTAGGTGA CTGCGGTATT ACCAGGGGCG 720 CACAAAGTGG GTGTTGCCCT TTGTTTCCCA AGTAATTGTT TTAAAGCAAG GTGAGGAGGA 780 GCCTGGGGAA GGGTAGAATG AGAGAAAGCA TGAACCCTGA TTTGTGTTTG TTTGTTTAGG 840 AACTAGAGGT TAGTGAAAAG CCTCTTGTTT CAGAATGTGT CCCAAATGGG TTTACAATTA 900 GTGACAGAGT CTGTAGGAGC TTATGAAACA ACCAATTCCC CACACTGTTT GGCTCTCAGC 960 ATCCACAGAC CATCTGGATC AGCTGAGCAT GAAGTGTGGG GGCGTGCATT GGGGGTGGGG 1020 TCCAGAAACA AAAAAGATCA AGCTGGCATC GGTTGGGGCG GGAGAGGGAT TTGGGTTTTC 1080 AGATTTCCTT TCGCTTAATT ACATTCGCAG GCTGTCCTGA TCCTCATTCC CCTTCCCCAT 1140 TGTTTCTGCC CTGTCAGCGG GGTTGACTGG CTGAAAACAG ACCACCCGGG CAGCCAGAAG 1200 AACTGTGCCT GTCCCGGCAG CCCTGACTCT GGACAGGTGG TGTGGGGTGG TGTGAGGTGG 1260 TTGGGGGACG GGAGAACAGG GAAGCAGGGC CAAGGACAGT AATATCCCTG GCCACTCTTC 1320 ATATATGTAG TCACCAATGC TCAAAGTCCT CCATGCCCCC ACTTCCATCC TGCAAAGGAG 1380 GAAGCTGAGC TGCCAAGGAG TGGCAGAGCT GAGAGCAGCA CCAGCTCCGT CTCTCCCGAA 1440 GACCACCTTC TTTCTCCCAT GTCTGCCTGC AGGATTTGAT GATGAGACAT CGTCTGCTAC 1500 AGGATTTGCA GGGAAACATG GAGTATCACT TTGGGCCTAT TTTCTAAGAG AATGGCCTGA 1560 AGAGAATAGA TTCAAGTTTT CTCCCAGAAA AGCCTCTGCT TCAGGAGCAG 1610
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