| Tag | Content |
|---|
EnhancerAtlas ID | HS182-04496 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr11:125084070-125085460 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr11:125085431-125085446 | GAGGTCAGGAGTTCA | + | 6.22 | | ZNF263 | MA0528.1 | chr11:125084675-125084696 | CTCTCTTCTCTCTCCTCCCCA | - | 6.38 | | ZNF263 | MA0528.1 | chr11:125084648-125084669 | CTTCCCTCTCCACCCTCCTCT | - | 6.94 | | ZNF263 | MA0528.1 | chr11:125084672-125084693 | TCTCTCTCTTCTCTCTCCTCC | - | 7.21 |
|
| | 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 |
| GH11I125213 | chr11 | 125083390 | 125086768 |
|
Enhancer Sequence | ATGTCAGGAC CCACCTCTTG GAGGGTGGCT TGGAAGAGAG CTAGGCTGTC ATCTGAGTGG 60
GCTCCATGAG CGGCCACCTC CCAGCCCCAC CTACCCTTGA ACCTGAAATT CTACCATTCC 120
CAGTTTGTTC CTCAGAGCTG GCATTTCCTC TTCTGATTCG CTCTTGCTCT CCCTCTTACT 180
CCCTTTCTGT CCCCCTCTTT TGAATGCCCT ACTCGGGAGG GGGTTGCTCT GGAGCATGGA 240
TTTGTGTTGT CAGCCTCTTT TCTTCTGGCT AAGAGTGACA GCCAGAGTAA GAGGTCTAAA 300
TCATGTACCT GGGAGGATAG CTGATCCTGA AAAGGGAAAA AAGGAAAGGC TCCTCCACCT 360
AAGACAAATC TTATACCCTT CTGAGTTTTG CCTGGGCTGG CCCTGCCTGG GTGCAAGTTG 420
AGCCATACCC TGGGCCAGCC TCTGAGGTCT GCGTCCTGCT GTCAGCACCC CCTAGTTAGC 480
ATCTGCACCA TCAATCAGGC AATGCAGCCC CTGCCTGAGG GGTGGAGGGG ATGGGGTGCA 540
GCCTCTCCAA CTCCTTGCCA ACCCTTAGAC ACAGAGCCCT TCCCTCTCCA CCCTCCTCTT 600
TTTCTCTCTC TTCTCTCTCC TCCCCACCTT GATGTGGACA GCTCAGCCCC TCCAAGGCTT 660
CTGTCCACTC CGAGAACCCC TCTCTATCCA TAGTGGCTCA AAGGGCTTTT TGAGTGGGGA 720
AGCAGGCAGC CTGTGGGCCT GGGAGGAGAG ATAAAGGCGT GAGATCCCCC AGGGGCCTGC 780
GGGGTCAGGG GCTGTGTATC TGGTGACTTC TGAATGCAAG CTCCAACAAA GAGAAATCTG 840
TGGTGGGAGA GCGTCCGCGA AGGAAATAAA ATCTCCATGA AAACAAACTT TTGTTGGAAG 900
CTTTCTCCTC TTGTTTTGGC AGCGTTGCTA GGTCCTGGGA GGGGAAGGCC GTGTCTTCCG 960
GAGCAGTTGG GAGGCTCTCG GATTGTCCAA ATATCAGCTT GCTGCAAGAA GGCTGTTCTT 1020
CCCCCACCAG GAAGACGGGG CTTAGGAGTT AGTGCAGTAA TCATTGGTTT TCTAATCAAG 1080
GCTAGAATGG CTGAAAGAAA GGCTGGGGGC CATGGAGAGG GCTCAGGACT GTGAGTTAGG 1140
AGAATCAGCA CTGTGTGTGT CACAGTTCCG TGACTCAGGC CAACCTGAGA TCCCTTCGTG 1200
CCTTACTTTT CTCACCTGTA AAACGAGCAT AACTTGCCCA AGGTCATTCA GCTAGAAAAG 1260
CAGGAGCAGG CCCAGGATAT AAACTGCTAT TTCCATGCTG GGCGCGGTGG CTCATGCCTG 1320
CAATCTCAGC ACTTTGGGAG GCTGAAGCAG GCGGATCACC TGAGGTCAGG AGTTCAAGAC 1380
CAGCCTGACC 1390
|
