| Tag | Content |
|---|
EnhancerAtlas ID | HS181-15386 |
Organism | Homo sapiens |
Tissue/cell | Sperm |
Coordinate | chr7:150521540-150522530 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX1 | MA0509.2 | chr7:150522077-150522093 | GGTAGCCATGGTAACT | - | 6.71 | | RFX1 | MA0509.2 | chr7:150522077-150522093 | GGTAGCCATGGTAACT | + | 6.72 | | RFX2 | MA0600.2 | chr7:150522077-150522093 | GGTAGCCATGGTAACT | - | 6.7 | | RFX2 | MA0600.2 | chr7:150522077-150522093 | GGTAGCCATGGTAACT | + | 6.86 | | RFX5 | MA0510.2 | chr7:150522077-150522093 | GGTAGCCATGGTAACT | + | 6.17 | | RFX5 | MA0510.2 | chr7:150522077-150522093 | GGTAGCCATGGTAACT | - | 6.26 | | SP2 | MA0516.2 | chr7:150521615-150521632 | GGGGAGGCGGGGCTTAG | - | 6.74 |
|
| | 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 |
| GH07I150825 | chr7 | 150522464 | 150522551 |
|
Enhancer Sequence | AAACCAGGAG TGTTTCCAAA CTCCCCAAAG CTGCGCTACT GGGACACGAG GTGGTGCTGT 60
GCACATTCAT GGGGTGGGGA GGCGGGGCTT AGCACATAGC TCCCTCATCA TTGGCTTTTA 120
GAGAGTGAGC GGCAGGCAGG TTGTCCATTG GATACCAAGA TATGGCGGCC CCCTGACTGG 180
GAAGACATGA CCTTACACAC CTTGGTTCTT TAACTTGACC TTGGGAAGAC AGGGCCAGCC 240
AGCAAGGTGG CTGGGGAGAA GGCCGAGGTC CCCGGGCCGC AGACGGGAAT TGAGGGTCAG 300
GAGCCGAAGT GAAACTGGAG CCGGCGCCAC GAGATGCAGC CCTGAAGGGC ACCTCCACCC 360
AGTGGCCCTC CCCCACCCCA CTCCCGGGGC CCTCCTGGCC CAGCGTCACC CTGCTGCGCT 420
AGGACCTACA AGGGCGGCCT CTGGGAGCCC TCTGCTTTAC CTCCTCTCCT GGGTCAGGCT 480
GCAGAAAGAA CAAGCTCCTC CACCCTGCCT GGTAGGCATG GAAGGAGGGC AAGTGTTGGT 540
AGCCATGGTA ACTCGGGGTA GCCATATTTT CGTGCAGTCA CTCTGACCCC ATCTCGATGG 600
ACAAGGATTG TCCCATCTGT TTCTACAACT GTTTCCCAAA CAGGCAGTGC TGTCCTAAGG 660
AAGCACCCAC CTGGCCCAAA CATGCTGTGC TTTCTTTGTG GCTGCCTTGC CTCCCCAACC 720
AATTGTAACC CCTTGGAATC AGGACTGTCT CCCGTGCGTT TTCTTCTCTC TGCAGCCTCG 780
CCTGCAAAGG CTTCTGTGCC TTCCCTGAGA TGCCCTAGCA AATGGGTCTT TTCGAACATT 840
ACCCACCTCA ACGTAAGTCC TAGGCCAAGC CGGTTCTCTG CTTATTCAGA ACAGAGTGCG 900
TCTTTACTGT CATGCCATTA CCTGGCAAAG GGAATTGCCG GACGGCAGGT GGCACAGAAT 960
TCCTTTGGAA CTCCAAATTC TTTTTTCAGC 990
|
