| Tag | Content |
|---|
EnhancerAtlas ID | HS044-06498 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr19:14528710-14530080 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr19:14529954-14529965 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr19:14529954-14529964 | GCCCCGCCCC | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_09406 | chr19:14526541-14531363 | CD14 | | SE_18377 | chr19:14526473-14531096 | CD4p_CD25-_Il17-_PMAstim_Th |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTGGCTCATG CCTGTAATCC CAGCACTTTG GGAGGCGAAG CGGGCGGATC ACTTGAAGTC 60
GGGAATTAGA GACAAGCCTG GGCAACATGG TGAAACCCCG TCTCTACTAC AAATACAAAA 120
ATTAGCCGGA TGTGCTTGCT TGAACCCGGA AGACGGAGGC TGCAGTGAGC CGAGATAGTG 180
TCACTGCACT CCAGCCTGGG CGACAGAGCA AGGCTCTGTC TCAAAAAAAA AAAAAAAAAA 240
AAAAAAAGAG AGAGAGAGAT AAATAAATTG GGGTGAACCG AATCTGCTAA GATAAAATTT 300
TCGAGAAACC GGGCTGGACA GGATCTAAAG CTCAAAACTG ATTAGATCAG GAAAGGATCC 360
GGCGGGGTTT TCCCCGCCCA AAGTGGGTGG CCATGACCGC TAAGGCGCCA GGAGCGCATG 420
AACTTGAAAG GTGACAGCGG GGAACTCACA ACCCAGACAC GCCACGTGTA CCCAGTTACC 480
CTCAAGTGTC CCCAGGCAGG CTTTCCACCC CGGAGTTTAT TCCCACCTGG GGACTCCTAT 540
TTCCAAAAGA AAATCTTTTT TTCATTCTGT TTTTTTTGAG GCAGAATCTC GCTCTGTCAC 600
CCAGGCTGGA GTGCAGTGTC GCGATCTCGG CTCACTGTAA CCTCCACCTC CCGGGTTCAA 660
GCGATTCTCG TGCCTCAGCC TCCCGAGTAG CTGGGACCAC AGGCGCTCGC CACCACGCTC 720
GGCTGATTTT TTTTTGTATT TTGAGTAGAG ACGAGGTTTC ACCATGTTGG CCAGGCTGGT 780
CTCGAACTCC TGACCTCAAG TGATCCGCCC TCCTTGGTCT CTCCCAAAGT ACTGAGATTA 840
CAAGAGCCAC CGCGCCCGGC CTTCCAAAAT AAAGTCTTAT TTGCTCTAAA TCTCAGAATC 900
CCGAATCCCG TAAAAAGTAG ACCAAGAAGA AGGTAGACTG GGAAAGGGAT CAAGTCCCTC 960
GGACCCAAAG AAACCCCTGA CAACTGAAAG CTCCAACTTC TCCCACCCAG GCCCCAGACC 1020
CCGGCGTCAC CCCCTCGTCC CTCTCCAAAT GGCCCCAGGC CGCCGCGGGG TCTATTCGGA 1080
CGAACTGACA GACTCCAAGT GGGGCTCGGA GCGCCGTAGG CCATGACAGC CCCTCCGAGA 1140
AGCGGGCCCC GAGCCCCGAG CACCGCGCGC CAACGGCTGG CCCACCCCTA GCGCATGCGC 1200
CCCGGTGCCC AACGGCCAAC ACACAGCGCT CTGACACACC AACCGCCCCG CCCCCACCGT 1260
CTCGCGACCC TTTCTCCCCC TCCCCTTAGA TCCCAACGTC TCCCCTCGTC CTCTCGCTCT 1320
CAGTTCAGAC GTCCCCACAC CGCGGCCCCG CGCCCGGGAT CCGCTGCTCA 1370
|
