Tag | Content |
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EnhancerAtlas ID | HS044-08720 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr3:11407850-11409260 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LMX1B | MA0703.2 | chr3:11408094-11408105 | TTAATTAAATT | - | 6.32 | MEF2A | MA0052.3 | chr3:11408520-11408532 | TTTATTTTTAGC | - | 6.04 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 11408107 | 11409164 | chr3 | 11408320 | 11409243 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I011365 | chr3 | 11407037 | 11409874 |
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Enhancer Sequence | GTCCCCCACA CACAAGGTGG CATTTTTTTT TGACATGCAT GTGTTAATCT TTTCTACAGA 60 GACATTTCAC GTAGGACCCA AAAGACGCGG TAATAACCAT CTATCATAAG GAAGCTGATC 120 TCCAGAGCCT ACCTCTGCTA TTTATGCTGT CGTATCTCAT TTGAATCTTT CCCAAGTCTC 180 CCGCCTTCTT CTGACCTTGA GATGTGCCCT CATCTCCTTT ACAGACTTTA TATTGAGAAG 240 GGCCTTAATT AAATTTTCAG TCATGCCCCT GCACTGGTTT CCTTCTTTAA GTCCTTTATG 300 TTAAATTACT GCAGTTGTAG TTTTCTCAGT GCTGAGGCCA GAGGGCAAAA CAGTCTCTTT 360 ATAGAAGGGG CCCAGTGTCA AAATGCATGT GCCCATGTTT TTAAAGTACT ATGGCAACTA 420 ATCCCTCTCG GTGTTATTTA TCCCCATTGA GCCTCAGAAT TATTTGTCAT TCACCAACTC 480 TTCTAGTTCT TTCTCCTCGT TTTCAAATGT CTGAAGGATT ATTTTGGTTG TTGGCCATCT 540 CTTCATTTGC CCTTTTCAAA GACTGAAGAA TAACGCAGCC ATATATGGGA AAAGCTGTGT 600 GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTTT ACTTGCTTAC ATTGTTTCAA 660 GTTTCAAGCC TTTATTTTTA GCTACTTTCT AAGAAAGAAA GTGGAGAAAG AACTTTAAAA 720 ATTAATCAGG GTTGTGTGGT CCCCATGTAT AGGCTTTAAA CAACTTTTTT CCCCCTAAGT 780 GGAGTGAGTC CATTTATGCA ACCATGTTTT GATTAGGGGA CCATCGTTTC CACGTTTCCA 840 CAAAAACACT GGGCTGTGTT GCAATGCCCT GTTGCAAACT CAGCACTTCC CTCCTCCTCT 900 TCCTGGCTCC TAGAGACAAA TGATTTCCTG TTGGAGAGGA ACTTGGTAAA CTCCTTTGTG 960 TACTTTGTAT GCAAAGAAGA CCAGTGAAGT TTACTGGGCT CATTTTTCTC AGTTCCCAAG 1020 AGGAGAAGTT TTATTAATTG GCCCCTGTGG AAGAGATGTA GTAGAAAAGT GATAGTCCTT 1080 GGACTGAGAA TCACAAGGCC CCCCACCAGC AACTCATTGT GTAATTTGGA GAAAGTTCCT 1140 TAACTTTTCC TGTGCTCTCT GGGTCTCTGC TCTCCTCTGT GTCAGACCTA GGAGGCCTGA 1200 GGATTACTTA GTTGTTCTGT CTCTGGGTCC ACAGGCAGAA TTTGGCCCAT CCAAAGACTG 1260 GCCAAGTGCC AAAAAAAGGC CTGATTAGGC CCTGAAATTC AGTGAAATTC TGCCTGAAGA 1320 AACCTCTTAT TGAATTTGAA AACCATAAAC CATTTCAGGT GAGCTTATGG GTTTGTTTTG 1380 GGTTTTTTTT TTTTTTTTTA AGTCTCTGGC 1410
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