| Tag | Content |
|---|
EnhancerAtlas ID | HS182-19516 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr7:2322740-2323600 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr7:2322769-2322781 | AAACAAACAAAC | - | 6.32 | | IRF1 | MA0050.2 | chr7:2322757-2322778 | AAAAAAAAAAAGAAACAAACA | - | 6 | | Myod1 | MA0499.1 | chr7:2322929-2322942 | TGCAGCTGTTGCC | + | 6.41 | | Myog | MA0500.1 | chr7:2322928-2322939 | CTGCAGCTGTT | - | 6.02 | | Tcf12 | MA0521.1 | chr7:2322928-2322939 | CTGCAGCTGTT | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 2322849 | 2323284 | | chr7 | 2322934 | 2323003 |
|
Enhancer Sequence | ACCAGACTCC GTCTCAAAAA AAAAAAAAGA AACAAACAAA CAGGATTTAC CGACAAACCC 60
CATGCAAAGA CGCTCCCCCT TCATTGAAGC ACACCTTCGC AAATGCTGAC CTCAGCAGAA 120
GTCACAGGCC CTGCCAGCCT CGGCGCAGGT GGCACGGGAC AGACACTGGA GGGTCCCAAG 180
CAGCACAGCT GCAGCTGTTG CCTGGAGGCC AAGCCCGCCC CGGACTGGCC CGCACACTAC 240
TTCCTGCTGA CCCAGCGTGG GGCTACACTG AGCACTCACA CACACCCCCA GCTCCAGGTC 300
CGCGCCGCCC AGGCACTCCC TGGGGTTCCC CGTGCCGATG GAGAGGCCTT CAGGGCCGGT 360
GCTTTCAGAG CCAGGACAGG GCAGGGGCCT TCCCAAGGAG ACCACGAGTG TGGTTCCTAC 420
TGTCCCGTTT AGTGGCAGGG AGGACCTGAA TGCGCATTCC CATGGACTCC AAGTTCCCTG 480
CTCTTCCACG ACACACGGCT GCTGTCCCCA GCTGCCAGTT CCCTAGAACG GAGGGGAGAT 540
CAGGACCAGC AAGGATGGCA CAGCGTCCCA GGGCTAAATT CCCCAAAGTG GGTGCGTATC 600
AGAATCACCT GGTGGGCTCC TTCAAACACA GAGGGCTGGG CCCACTCCCA GCGTCTCTCC 660
AACAGGAGGG CTGGGGTGGG GACTGGGAAT CTGCTTTTTT TGGAGGGGGT GCCGGAGTCT 720
TACTCTGTCA CCCAAGCTAG AGTGCAGTGG CACAATCTTG GCTCACTGCA ACCTCAGTGT 780
CCAGGGTTCC AGCGATTCTC ATGCCTCAAC CTCCCGAGTA GCTGGGATTA CAGGCATGTG 840
CCACCATACC TGGCTAATTT 860
|
