| Tag | Content |
|---|
EnhancerAtlas ID | HS182-04089 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr11:72194320-72195470 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFG | MA0659.1 | chr11:72194637-72194658 | AGCTTGCTGAGTCAGTATTTT | + | 6 | | MAFK | MA0496.2 | chr11:72194638-72194657 | GCTTGCTGAGTCAGTATTT | + | 6.27 | | MAFK | MA0496.2 | chr11:72194638-72194657 | GCTTGCTGAGTCAGTATTT | - | 6 | | Nr2f6(var.2) | MA0728.1 | chr11:72194479-72194494 | CGATCTTTTGACCTC | - | 6.19 |
|
| | 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 |
| GH11I072483 | chr11 | 72194197 | 72195590 |
|
Enhancer Sequence | CGTGGTCTCG GTTCACTGCA ACCTCCGCCT CCCTGGTTCT AGCGATTCTC CTGCCTCAGC 60
CTCCCGAGTA GCTGGGACTA CAGGCGCAGC CACCACGCCC GGCTAATTTT TTGTATTTTT 120
AGTAGAGATG GGGTTTCGCC ATGTGAGCCA GGATGGTCTC GATCTTTTGA CCTCGTGATC 180
CACCTGCCTT AGCCTCCCAA AGTGGTGGGA TTACAGGAGT GAGCCATCAC GCCCGGCCAC 240
GAAGTGATAT TTTTAACCCC ATATTATATG AGAGGAAGTA GATCTCAGAA CATGAGTGTT 300
ATAGTCCAGG TTTGCACAGC TTGCTGAGTC AGTATTTTAA CTCAGGGCTA TGTGTCTGAT 360
TCCAGCACCT CCCTCTGCAC CCGTATTAGA ACACATTGAG AAGGCTCCCC AAGCCATGCC 420
TCCTGTTGGC CTATCTCTCG CTGATCTGCT CCACAGTGGA ACCCTCACAT GCATCTACAT 480
GTTTCAGACA AGGCTCTGGG CACCCAAAGA TTAACAAGAC AGACCCAGAG CTTGCTTTCA 540
TAGAGCCCAC AGTTAGGGGG TGCTCAGGGA AGACAGCTGT TCAAACAACT CATTCCAGAA 600
GTTGTTATGT ACAATTGTGC TGACTGCTAG AAAGGAAAAG CACGGGACAG GAAGTTGTGA 660
AATAGTTTCA GGGAAGCCAT ACTTGTGTAG GAAGTCAGGT CGAACTTCAT GGGAAAGGGG 720
AATTTAGGCT GAGAGTTCAA AATTGAATAG CAGTTGATTG AGCAGTGAGT CATGGAGGAA 780
CTGTCTATAC TAGAAATGAA AAGGCTTTGA GGCTGGGAAA GAACTTGGCC CTAATGGTCA 840
GAAGGGTGAA GGGCAGTGAG CAAGGGATAA ATAATAAAAA TCATAATTCA TAGAGGTAAG 900
TGCAACTAAT GTTTCCACGT GTCTTATTCT AACCAATTCT GGTTAAGAAT ATGGGTTCTG 960
GAGCCAGACA GGCTGGGTTT GAATCCTAGC TCCACCATAT TGGTTGTATG GCACTGGGCA 1020
AGTTCCACCT TCTCTGTGTC TCTATTTCAT CATCTGTAAA ATGGGAGCAA AATTGTCCCT 1080
ATCTTTTCAG GCTGCTGTGA GAATTAAATG AGTTAATATA CGTAAAGCAC TTAGTAAAGC 1140
ACCTGGCACA 1150
|
