| Tag | Content |
|---|
EnhancerAtlas ID | HS044-09571 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr4:7517530-7519090 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6 | MA0463.2 | chr4:7518397-7518413 | GTGCTTTCCAGGAACA | + | 6.88 | | ZNF263 | MA0528.1 | chr4:7518675-7518696 | CTACCTCCTCCCTCCTCCTCT | - | 6.27 | | ZNF263 | MA0528.1 | chr4:7518672-7518693 | CCTCTACCTCCTCCCTCCTCC | - | 7.01 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGGCTGGAGT AGCCCTGGCA AAGAAACACT GACCTCAGGG CCAGGAGACC TCAGTTAAGA 60
TCACCCACGG GGCTGCTTGG TTGCCGTGTC ACCTCGAGCA AGTGACTCCA CTTCTCTGGG 120
CCTGTGTCCT CACTCATGGG AGGGGTCCAA TGGAGGCCCA GAAGTCTCAA GGGTGCTCTC 180
GGCTCTCGCA GCAGGGTTTA GGGGCTGGGA CCTCAAGTGG GCGTTAGCAG TACCCGTGAT 240
GGTGTCTGGG TGGGCACTGT GGTGCTCATT CATTTATTCA TTCAAGCATT CATTCCACCC 300
GCATTTACCG GTACTCACTC CATGCTGGGC ATTGGGCTGA GAGGTGGCTA GAGAGCTGGT 360
CAGATGCAGT CCTGGTCCTC CTGGAGCTCA CAGGCAGCTC CAAGGAGAGG AAATCCATCA 420
ATGATGAGAC AGGCGTCACA GGTCATTTCA AGCATGCAGA AAGGGAATGA GAAGGCCCAG 480
CTGGGCGTGG GGAGGGACGG CAGGCCTCTT GCTCTTGTTT TCACCTTCCT AAGGCTCTGC 540
CTCTCCTCTC TGAACCTCCC TTCCCTCCCA TCTGGCCTGT TGTTAGGGGC TCTGGCTTCA 600
TCCTGAAGGT GCTGGGACCC TGCAGGTTGT TCAGAGGCTG ATTTGCACCA CGTGGGAGGA 660
GAGGCACCTA GAGTGGGCTG AGGAACAGAG AACGCCGGGT GTTTGGCTGT TGCGTCTGCA 720
GATTTTATCC GCTTGCAAAA CACAGTTCCA TGTGGGCAGG GACCTGGAGG GGTGGGGGCG 780
GTGCTGCTTT TCCTTGGTGG AATGCCCTGG CCTTTTTATG CAGGACAGGC GTCGGGGCTG 840
CACGGAGTCT GGGAGTGTGG GGAGAGGGTG CTTTCCAGGA ACACGGCATG AAGTTCCCAG 900
AAGGAACTGG GCCACACTCA TCCCCTGCCT GCAGCTGAAC CAGGAAGGGA GCCTCCCCTT 960
CTCGGCATGG TCCTAGCTGC CGTTGAATTG TCACTCTCAT CCACGTTTGC AGGTACAGGT 1020
GTGAGAAGTC TCCTCCCTCA TCATCCCCTT CAGGCAGCAG CTACTGCTGA GGAGTTGGGG 1080
CCGCATGTTG TGAGGGCCCC ATTCACAGCT TGGGAGCCAG GCTGCAGTGT TCAAGCTCAG 1140
CCCCTCTACC TCCTCCCTCC TCCTCTGGTT GGTGAGAATG TGCTAGTCCT CCGGCTGGGT 1200
GTTGAAGGGA CTCAACGAGC TAACGCGTCC AGCATACCCA GCGCTTGGAA GTCGACACAG 1260
GCGTGACTGA GGGGATTTGT CATCGCCATG ATTACTACTA CAGCCACCCG ATTTACTGCT 1320
GTCTTTAGGA GTTTTCTGAT CAGACACACT GAGGACACGC ATGGTGATTA TGTCTGTGGG 1380
TCAGTGTTAG TGTTAGCTAG TCAGTGTTGC CGTTGACTTA TCCCTTGTTT TGGATTCCAT 1440
AACATCTTCC CACTCAAAAC TTTCAGCCGG GTTTCCACAA TCGCACGACT CGAAGCATCC 1500
TCTAAGCTTT CCAGAGAGGG GCAGTTGTTT GTGTTAATTG TGTCTTATTT CCTAATGAAT 1560
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