| Tag | Content |
|---|
EnhancerAtlas ID | HS044-02972 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr12:2463250-2464590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr12:2464151-2464171 | GGTCTGGGTGTGGGGTGGGG | - | 6.18 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_01967 | chr12:2462608-2464194 | Aorta | | SE_40585 | chr12:2462206-2464358 | Left_Ventricle |
|
| | 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 |
| GH12I002354 | chr12 | 2463531 | 2463940 |
|
Enhancer Sequence | GCTGGGAGGT TGCTCTGAAA TGCTGATGGG GATGGAGTGG GGGCTGTCGG GAAGGACTGG 60
ATGGAGTCTG TTTTTCCAGA ACCCCTTAAC CCAGTGGAAG CCCCGCCTTT CATGTGGGCC 120
CCGCACAGTT AGGCTGCCCG AGTCCCTCTG TCCTCGCACC CTCACCTGGC TCTCTTGCCT 180
AAGCCTGTCA CAGAAGCCCT GCAGAGCAGG AAACACAGAG CAGAAAGCCA CGCACACAGC 240
TTGTGTTTCC TCTGGCGCCT CTAGGTCGCT CTGCAGCCAC CTGCTTGGAG TGGTGATAAG 300
CCAAATCTTT CTTTAGAGGA GCGAAAACAC AGCTAGCCAG GGCTGCAGCT ATGACTGCAG 360
CCTGTAGGGA AACGCCGGGA GGAACAGGAG ACTGTTGAGA AGGGGACGGA GAACCTCACC 420
AGCAGCTGAA TTGAATTCCA TCTTTGAGAC CCAAGAGAGG GAAAATGCCT TTCCGCATGC 480
ATGCTCTCCT AGCTATGCTT GTAAGAAGTG CGTGCTTCTG GTTGGGAGAG CCCAGGAACG 540
GAGTCCATCC TTTCTCCTGG CCTCCAGGGA GAGCCCAGAC ACTCCTGACC ACAGACTGGC 600
TTGTAATTTG GCTTTTCTGA GCATGGCAAG AGAATCCTGC ATGTCACTTG GGCCTGACAC 660
CTGCTTTTGC CTTCTCCAGA CACGGCAAGA CTGGCCTTGA CTTCTGGTTC CATTCTCGTT 720
TCCCTGGGCT GCTCTCCACC TTCCAGGCTT AGCTGGAGTA ACCATTTCAG AGCTGGTCGT 780
TTCCCCGCAG CTTTAGATTC CATTTTGGTG AGGAAATTTA CATTACCCAG GTGTGCACTT 840
GGGCAGGCTG AGCGACCTGA GTGAAATGAA GCCAAATCCT GGAGGTGCAG GTGTGAGGAT 900
GGGTCTGGGT GTGGGGTGGG GTGGAGGGCT GAAGAAGGAG GCGTAACATT GTGTAAGGTT 960
GGATATTAAA CCTACTGCAG CAAAACCAAC TCTGCCCGCT TCCCCGGGTA TTTATCATGC 1020
TTACCTTCTA CCGCACACAC CGTCAGTGTG AACTATTGCA TAGAAAAGGG TTTTCCAACA 1080
TTGCCAGGTC AGAGCTGATT AAGCTTTCAC TTAAGACCAA GAGTGGATTA AACTTTGGGA 1140
TCTGCCCTCC TCCGGAGGGG GAGAAGCTGG CTGATGTTCA CTGACATGTG GCTGCATGGC 1200
CACATCAGTT GTTAAATATT GAGAAACTTC AGCTGTCCTG TGTCCCTGAG TGCCCATCCC 1260
CCATCCAGGA CCTCCCACCC CCCCACATTT CCTCAGTGGA AGGCTGCTCC CTGGACTCAT 1320
TTCGGTTGGT GGGTGCCACC 1340
|
