| Tag | Content |
|---|
EnhancerAtlas ID | HS044-04335 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr14:73083770-73085400 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr14:73085346-73085367 | TCTCCCTCCCTCCCCGCCCCC | - | 6.51 |
| | | 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 |
| GH14I072613 | chr14 | 73080021 | 73085927 |
| Enhancer Sequence | CCCTGCCTTG GCCTGGGAGA CCCAGCTGAG GCTCAGCTTG TGTAGGCAGA GCAGACATGG 60
GGCTGAGATC GAACAGGGCT GCCCTATCAC CTGCACTTCT GTGGAAAACA AATTTGCACA 120
TACTCTGAAG AGGACGTGTG AAGTTGTAGA GCCACAGTTT GGGGTTTCGG ACTTGCTTTT 180
TAAACTTTTA AGCTATTGTG GCACTTGGGA ACATTTGGGG AACTTTTTTT TCTAAATTTA 240
AATTAAAATG ACGCTCAAAA CCAATTATTA GCCTTTGGAG ACAGCCTGCT TTGGGTTTTG 300
TGGGAAGAGA GAGAGCTGGA GTAGTCAGGA GAAAAAATGT GCCCCTCTGA TGGAATGTCA 360
CCCTCCCTAT CCCTCCCTGG GCCTTCAGGA TTCAGACAAG CTCACCGACC AGCAGGCGGA 420
AGGAAATTAC TTATGAGGAA GATGAAAATT CCATCCGGTC GGGGGCCCTT TAAATGAGAC 480
CATTATGTAT GTGTGTGATT CCCTCTGAGG CCACAGGCCC CTGCAGGAGA GTGACCCCCA 540
TCGCTTGCCA CAGGTCACTC TGCTGAAGCG TGGGGGAGAC CCACACTGCT TGGTTTCATG 600
CCAGGCTGCC CTGGGTCCAC TGGCCAAGAG CAATTAGCCT AGAGAGGAGC ACTCCTGCCG 660
AGGGACAGCA CAAATACTGC GGCCGGGCAG AGGTGGCCCA ACTAGCCCGA GTCTCCGGGA 720
GCGTCCTCAG GAGCTGAAGA ACTAAAAATA ACCTGGGCCT TTGTTGTGAG CAGCCAGACC 780
ACAGAGATGG AGCTGATTTC AGAGAAGCCA AGCATGCGCG AGGGTTCCGC TCACCGAGAC 840
CTGCCCTTTG GGCAAATGAT TTTTCCAGAA ATATGTCAGT TATTGTGCTG CTGCTGCGAT 900
TCAAAGTCAG CCCAATCCGC TCCAGCCCTC GGGGCTATCT TCCAACACAC AGAGTTCTCG 960
GAAGCTCAGC CTCCCCACCT CTTTCTTCTA GACACATTTT TTTTTGAAAA CAAGAGTCCT 1020
GCATGTTTGG GGAGCTTAGG AGACAAGAGC AGCCCCCGCA CTGAGAGTTC TAAAATGTGG 1080
CCACCCTGGT CGTGAATAAT GACCATGTCA CCCTAATTAT TTGTTTAGAT AACAATCTTC 1140
TCTCCCCCAT CCTAAAATTC CCAGTCAGGT CTCAGTAGAC AATAGCGAAC AAACACTACG 1200
TGGAAGGAAG AAATTACTTG GAAAAAGGAA TTCAGAGCGT CGCATCAATA CTGAAGGTTT 1260
CTCAAAGCTG CAGCCCCCTG TATCCAGCAT TCGGACACAT GATTGGGCAG CCTTCGCTCC 1320
CCTTCCTGGT TCTTCAGTCC CACCAGGAGA AGCTGAACCA GGTCTCCAGA ACCAGGTGGG 1380
CTGAGAGGCA GAGGCTTGAC CGTCTTCCTC TGTCCATAGG CCATGACTGG TCTCACCTAA 1440
AGGATGCCCC AGCTCTGAAG GTCAAGGAAC CAGCCTGGCC TCTTGCAAAG TCTCTCCCGA 1500
TGGATAACAA GTACTGACTG GCTATGGCGG GGCCTTGGCA CCATTTCCAC AATGTTTCCT 1560
CCCATGTCTC TGCGCGTCTC CCTCCCTCCC CGCCCCCATC TAGTAACTTT AAGCAGTGGC 1620
TCAAGACCAG 1630
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