Tag | Content |
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EnhancerAtlas ID | HS044-09790 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr4:77751640-77753870 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Mafb | MA0117.2 | chr4:77752991-77753003 | AAAATGCTGACA | + | 6.62 |
| | 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 |
GH04I076830 | chr4 | 77751420 | 77754491 |
| Enhancer Sequence | CTTAGAGTCA AGAAAATATG AGAATACACC TTCTAGATAG CCATAAAAAT AAATCAAAAT 60 AAAAAATATA TAAGAATAGC GTAATGGGAG TGCGGGGGCT GGGAGAGAGA CTAAGTCAGG 120 TAGGTAGGGA TCTAGAAAGC TTTTTGGAGT GGGCACAGAC ACACAATATG TGCCATACAG 180 ACATAGGAAA GTGGATAGGA AAAGGGGATC TGGCAGAGGT AGCAGCTTAA GCAAAGCCCG 240 GAGGCAAGAG AGCTGGATGA TGTCTAAGCA GAAGCTGAAG GAAAGGAGCT GTGGTGGAAG 300 GGGAGGCTGG AGAGGCAGGC TCGCACACAC CGAGGAGCGC ACCCATGCCA GGCTACAGGC 360 TGCAGCTTTT CAACAGGTCA AGAAAAGCCC TGACATTTCC CCAAGTGCCA GTCTTTAAAA 420 CTTTGGCAAC TCCATATACA AAGGAAATGT ATTATGAAGG CTTCTTCTAG TCACAGGGCA 480 CTGTTACTGA CCCAGCAGGC AGTAAAATCC CCTTTGGAAC TTGAAGCCAG ATGACAAAAA 540 GGTTAGAAAG GCAAAGGGCA TTGTCACCGG AAGCACGGTG TTTAAACAGA CGCTGGGAAA 600 AACTAGGGTT TCTGACAGTG AGCCAAGAAA TTCCAAAGGT CACGTCAGCA GAGCCAGGAA 660 GTGGAAAGAA AGAAGTCATC GCCATGCTAG GAGCCACACA GGAGGAATCA GAGTCACACT 720 TTCTACTCCA AAGGGATTGA AAACTGAGAG TAAAATGAAA TGGGGATGGG GAAGGATGCA 780 GAGTGAGGGA AGGAAAACAA CTGCCACGCC AGCCTGAGGG AGGCCAGCCT CATTCCAGAA 840 GGAGTTCTTG GGCTCAAAAT GCTGTGGTTT GGGAGCTGAA GCCTGAATTT GCCTGCCCTG 900 CACTAAGCAG CATGAGCCTG GTGCCAACGG GAACGGCAAG GTACATAGGA GGTAGGGACG 960 GGGATTGGAA AGGCAGGCTC CCTGGACAAC TCTCCTAAGT CCTTCAGGGA GGGAGTTGAG 1020 CCGGGGACCT TGGGCTCGCC TACTGGGCAG GGGACAAGGG CAGCCCCCTG GGTGCTCTTC 1080 TCCTGTTCTT AGGAAGAGGA TTCCAGGCAG CTCTGCTAAT TCATCCCAGC TCCAAAGCAG 1140 GCAGTGGATG TGTGGAGCAG TGGAAGGGCT GGAGACTGTA TGGCAGCTGA GACCAACCCC 1200 TATAATCAAT AGAAGAAAAT GACCAGGCTC TCATCTGGGT CTCTGTTCTT TACTTATCTC 1260 TTCAGTTTCC AGTAGAGCTT TGGAAGTTTT AAGTGAGACG ATCTCTCAAC TTAAATGATA 1320 TAAACATCGT AGTCCACTGT TATCCTTTCC AAAAATGCTG ACACAGTTCC CAAGATGTAC 1380 AGAGTACTGT GAACTGTGAA AGTTTGCTTC AGAGGACGTG TCCTTTCATG TAGAAGAATA 1440 CTGTGCAGGC TACTCAATAC AGAGCACAGT GGCAGGCCCC AAAATAAATA AAGAAATAAA 1500 GTGAGCTATT GGCGATGTGT GCTAAATTGA ATTGACGTGT TTATTTGCCT GGAGTGTAAG 1560 CCCACCCACT CCCACAAAGG GCTGGAGGCC CCTGAATTGC AGTTTGTGCC TGTTAATACT 1620 CACAGCCTTT GGAGATTCAG TACTGAGGGA CGTCATGCAG TCTGGCTTTT TCCAAACAAA 1680 ACCTGAAACC TTCTCCTCTG GGTCTACCCA TAAAGAGCAG TTACAGGAAG AACTGCTTGG 1740 CCAGTCCTGT GGATCTGATA AGACTCTTGT TTTCTTCCTT AGGGTTGAAG GAGGCCTGTA 1800 CCCTGCCTCT TCCTGGATCC ACGCTCAGCT CTCCTTTTCT CAGCCCAAAG GCTGTGGCAC 1860 CTGGGCACTG GGTCCAGTAG GGCAGGATGG GGCAGAGGAG ACTTAGTCTG GAAGGGCTAT 1920 GGGCTTTTTT TAAAGTAGTG TGACTGAAAG TGGGCATTTC CTGTCAAAAT GGAACGTAGA 1980 GCTGAATGTG GGCTTGGGGA ATGCCTGGGA ATTCATTTGG GCTCAGCCCT AGAAGAAAAG 2040 CATAAGGACT TCCTTGCTCA GAGTTGCTGA TTCTGTAAGG TCTGGGATCA GTGCAGGAAA 2100 CTGCATATTG AAAAGCATCC TGGATCACAC TTCTGATTAA GAATGTTGAA ACAGGGCCAG 2160 GTGTAGTAGC TGACGCCTAT AATCCCAGCA CTTTAGGGGG CCGAGGTAGA CGGATCACTT 2220 GAGGTCAGGA 2230
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