| Tag | Content |
|---|
EnhancerAtlas ID | HS182-19668 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr7:29217250-29218330 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TEAD1 | MA0090.2 | chr7:29217669-29217679 | CACATTCCAT | + | 6.02 |
|
| | 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 |
| GH07I029177 | chr7 | 29217470 | 29218610 |
|
Enhancer Sequence | TTTATCTATC TGTCCATCTA TTAATATCTA CCTATTTATC TATCTGTCCA TCCATCCATC 60
TGTGCAGTCA TCCATCCATC CATCCACTTT ACCAGCTATA CCCCAACCCT CTTTACTTCT 120
AAACACCTAC CCATCTCATT ATGCTCCCAC CTATCTATCT GTTCTTTCAT TCATTCACTT 180
TATAACCAAA ATCTTTTTTT CCAACCCAGA CCTCTCTCCA AACCTTGCTA CTTGACATCT 240
CCTTAGACAT TTCATAGGTG CCTCAAACTT CACATGTCCG AAACACAACC CTCGGTTCCA 300
TCCCCACACA AAGTTCCCCC TCCCCAAGCC CTCACCATCA CAGCAAGTGG CACCACCAGC 360
CATTTAACTG CTCAGCTAAA AACCTAGGAG TCACCTTGAT GATTGTTTAT CTCATGCCTC 420
ACATTCCATC ATCAGCAAGT GTTGTCAGAT TCTACCCTAA GTCTGATGGT GTCTTGCCAT 480
CTCCACTGCT ACTATCCTCT GTCCACACCA TCAGCCTTTC TTTGAAACCA CTGGAATAGT 540
CACATAGCCA CCGTGCACCC TGCTCTTCTT ACTATCCTTT TCCATAGCTG CCAAAGTGAT 600
CTTTTCAGTA TGAATCAGAA CATGTTATCC CCTTCCTAAA AGCTTCTGTG GCTTCCCATT 660
GTGTCTAGAA ATAAACAGAA AGTCTCCACT ATGACCCACG TGGCTGCTAG GATCTGACAT 720
CTACTCAGCC TCTGACCTGG TCTTCCTCTG CGTGCGGTTT CATTCCTTTG ACGCCAGCTC 780
CACTGGCCGC CTTTCCTGTT CCTCTAACAT GCCCAGCTCG TGTCTGACTC AGCCCTTTAA 840
ATCTGCTGTT CCCTCCTCCA GACCTGCAAG ATCAAGTCTC TGCTGAAATG TCACATCCTC 900
CGAGAGACGT TGCCTGACAT GCTGTTTTAT GTTCATCTGA ACACATTTTT CAGCATTTGA 960
AGTTATCTTT TTAAAAAAAG CAGTTCATTG TCTGTGCCTC TTAAGGGCAG GGACTTTGTT 1020
TATTGTTATA TTCTCAGGGT CTATACCTAT GCCTGGATCA TAGTAGGGGC TCAGTTATTG 1080
|
