| Tag | Content |
|---|
EnhancerAtlas ID | HS044-02170 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr11:2751160-2752800 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr11:2751852-2751867 | TGGACTTTGTCCCTA | - | 6.23 | | Hnf4a | MA0114.3 | chr11:2751850-2751866 | GGTGGACTTTGTCCCT | - | 6.62 | | ZNF263 | MA0528.1 | chr11:2752029-2752050 | AGAGGAGGGAAGAATGGAGGG | + | 6.64 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_35355 | chr11:2747987-2755117 | HepG2 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I002724 | chr11 | 2745822 | 2753258 |
|
Enhancer Sequence | GGTGTCAGGG CTAAGAGCAT TGTGGAGAGA GGGTACAGCC ACAGCAAAGG CCCTGAAGTG 60
GGGATGGGCC CACAGGCTGG CAGGACAGCA AGGAGACCCA TGTGCTGGGA CCCCGAGAGC 120
TAGGACACGT GAAGCCCTGG CTGGCCCCGA GTGCGGTGTG GTTGGCGCAG ATGGCAACAG 180
GGTCACTCTG GCTGCAGAGC CAAGAATGGA CCACTGAGGG GCTGGGACAG ACCTGGCAGA 240
CCAGGAGGGA GGCCACTGCA CTAGTCCAGG CGGAGGATGG CAGCTGGACC AGGAGGGCGA 300
GGAGGAAGTA GTAGATTCAG GACTGTTTTG AGAGGGACCA TTTTAGCTTC TTACGGCTGC 360
TGTAATGAAT TCCCACAAAC TTAGTGGCTT TAAGTGACAC GTTTATTATC TAACAGCTCT 420
GGAGGTCAGA TGTCCGACAT GGGCTACATT CAAGGAGCCA GCAGAGCTGG TTCCCACTGG 480
AAGCTCAAAG GGAGGCCCCA CCTCCCTTGG CTTGTGGCCT TTCCCCACGG CCCCCTTGTC 540
TCTGCTTCTG TCCTGCGCTC TTCACAACCT CCCTTCCTCC CTCTTTCTCT TATGGGGAGT 600
GCAGGGGTGA TCTGGAGGAG CCGGTCAATA GCAGCGTGGT GGGGTCTGGC AGAGACAGAC 660
TGCAGGGGGC CTGGGAGGCC CCAGGAGGCA GGTGGACTTT GTCCCTAGGC ATCCAGTGCA 720
GAGGTGAGAC CTGTATGGCC ACAGAGTCTC CCTATCCAGG CCCCATTACC CTGGGGGAGG 780
CGGATTATGG TATGAACTGC TGCAGGTGGT CCAAGAGGGG CTGCCCCTGG GAGACGCAGG 840
GTTCTTCAGT AATGGTGGTT TCGAAGGGCA GAGGAGGGAA GAATGGAGGG ATGGGGGACA 900
GACGCTGGAG CCGTTTTGGT GGCAGGCCTC TGTGGCTGTG GCCAGAAGCA GGGCTGGGCA 960
CCAGGCCAGA TGGACCAGAG GCTGCCCCCA GCTGAACCAA CTACAGAAAT GAGAGCCCCG 1020
GCCCAGCCTC CTCCCAGCCG CCGCTCTCTG GGAGCCCAGC TTTGCTCATA GAAAAGGAAG 1080
GCCCTTGTTG CCCTGCATTG GGAGCAAACA CTTCCTTTGG CCTCACAGCT CAACCTTGGA 1140
CCCAAAGGTC CTCAGGGACC TGGGGGAAAG AGAGGGCAGC CAGGCACCTC TGTTCACGGC 1200
AGGGGCTGCG TTGCCCAGCC TGGCAGAGGG AGGCAGCCCC TAGGTACAGT CCCCTGTGCC 1260
CACTCGAGGG GGTGCTGAAT TCCTCAAGGC CTGAGTCAGA CCTGGTGCAG CTTCATAAAG 1320
CCAAGGGTGG CAGGCGGAAT CCAAGGGGCC TCACCGCCCA TGCACCCCAC TGTTGCATGG 1380
AGAGAACAAT GCCCAAATGC CCTCGTCCCA CAGTCGGCAT GCCAGACCCC TCGGGAATTC 1440
AGGCCTTGGT GAGTCTGGCA CATTCCGGCT GTGTGTCAGC GGGAGAGGCC TGGGAAAGGG 1500
AGCCAGCACT GCAGGCCGCC CACCACACGC CCACTCGGGC ACCGGACACA GGGAAGGCGG 1560
ACACCCAGGG CGGCCATCTC TCGGGACAGG AGGTGCGGCT CCAGGTTCTC ACCCAGGAGA 1620
GGGCTTTCCT CCCATGTCAG 1640
|
