| Tag | Content |
|---|
EnhancerAtlas ID | HS044-01085 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr1:204606070-204607810 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr1:204606903-204606914 | CCACACCCTGC | + | 6.62 | | LMX1B | MA0703.2 | chr1:204606996-204607007 | AATTTAATTAA | + | 6.32 | | NFYA | MA0060.3 | chr1:204606426-204606437 | AACCAATCAGA | + | 6.62 | | Nr2f6(var.2) | MA0728.1 | chr1:204607758-204607773 | TGAACTCCTGACCTC | - | 6.22 | | RREB1 | MA0073.1 | chr1:204607225-204607245 | CACCCACCCACCCCCCGCCC | + | 7.01 | | RREB1 | MA0073.1 | chr1:204606808-204606828 | TGTGTGTGTGTGTTTGGGGG | - | 7.55 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 204606879 | 204606993 | | chr1 | 204606530 | 204607469 | | chr1 | 204606613 | 204606768 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I204637 | chr1 | 204606312 | 204608312 |
|
Enhancer Sequence | AAATATTTAG GGAAAAGTGT ACTGATGTCT GCAATTTGCT TTGAAATGCA CCAAAATTAA 60
GATGGATTGA TAGATAGAGG AATGGATAGT TGGAGAGAGA GGTGATAAGG CAAGTCTAAT 120
AATAAGGTTA ATGGTAGAGT CTAGGTGGTG GGTAGATGAT TGCTCACTGT AAAATTCCCT 180
TTACTGTGCG GTATGTTGGA ATTTTTCATA ATAAAGTATT GGGGGGAAAA TCCCCAAATG 240
GTTTGAATGT GAAGCCAGGA CTGAGAACTA TTACTTCTGA AGGAAAAATC CATAAAGCAA 300
ATGAGCTTCT TTCCTCTGCC GTCCACATGT GAAAGAACAT CCCTACTTTC TCATCAAACC 360
AATCAGATCT AGCCCAATGC TTTCTAGCCC AATGCTTCCC AGCCCTTCTC AAGCCAGGGC 420
ACATATAGAT GAGTGTATTT GTACAGTGCA CCAGGGGAGA GGGTGGTGGC TGCTGGCAGC 480
CAGAGGGAGC GGCTCAGGGA GACGCTTGGT TGCCCCAGGC CCCACAGGGC TGCCCTGAGT 540
GCCAAGGGCT GTGCCTGGAG TCCACTGTCC ACAGCCAGAC CAGCTGACCA GCTCTGCTCT 600
GTGCAGATGC CCCTGAGTCT CCCAGTTCTA AACCACAGCT CAGCATTCTT AGCAAGGATT 660
AAATCCTTTC CCAGACCAGA GTCTGCCTAT TGCAGCACGT GACGTGTGTG TGTGTGTGTG 720
TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TTTGGGGGCA GTCGCTGAGA GGGTGGTAGA 780
GAGGACTCCT CTGCGGGAAG GCCCCGACCC CCGGGCCTCA TCTGTATGCT CCTCCACACC 840
CTGCTCACCC TGTGGGGGAG TGCCATGGCA ACACCGTGCT CTTTAAACAC AGGAGTTTGT 900
GCTCCCATCG CAAAGCAGCA TTAGGCAATT TAATTAAGGA GCTGGCAGCA GACAAACTTT 960
GTGAGTTAAA GGCATTTTAT TAAATCCCAT TGTATTATGC AGCTCAATTC CCCCAGGAGC 1020
TGCGGAGCTG GGGGAGGACA GAGGAGAATG TACTAGGGTT TTCTTTTCCT TTCCTTGCTT 1080
TTCTTCTGGT CTCCCTCCCG CCTCGTGAAA GCATTCACTG AGCGTAGGGG GACCCCAACA 1140
GTGATTGCCT GCTCTCACCC ACCCACCCCC CGCCCCGAAC ATCAGGCCTT GGCATGAGGC 1200
CTGCAGGCAG AGGCCTGGGG AATATAATCA CCAGCACTGA TCTCACGCAC TACTGTTCGC 1260
AGAGCCAGAG CGCTGTCATG GTGATCTGGG GCCAGGCCTC CGACCTGCTT TAGTGTTCAC 1320
AACAGGACTC GGCTCTGTGA TTTTGTGCAC CATTTCATTG AATCCCCCCG CACCGTTGGA 1380
GTCAGAACTA CTGGCACCCT TATTTTACAG GCAAGGAAAC TGAGGCTTAC AGATGTGAAG 1440
TAACTTGCCC AAGGTCTTCC TTTTTTTTTT TTTTTTTTTT TTTTTTTGAG ACGGAGTCTC 1500
GCTCTGTCGC CCAGGCTGGA GTGCAGTGGT GCGATCTCGG TTCACTGCAA CCTCCGCCCT 1560
CTAGGTTTAA GCAATTCTCT GCCTCAGCCT CCGGAGTAGC TGAGATTACA GGCATGTGCC 1620
ACCACACCCG GCTAATTTTT TGTATTTTTA GTAGAGATGG GGTTTCACCA TCTTGGCCAG 1680
GCTGGTCTTG AACTCCTGAC CTCGTGATCC ACCCACCTCG GCCTCCCAAA GTGCTGGGAT 1740
|
