| Tag | Content |
|---|
EnhancerAtlas ID | HS182-04442 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr11:120483290-120484640 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crx | MA0467.1 | chr11:120484154-120484165 | CTAATCCCCTT | - | 6.32 | | GSC | MA0648.1 | chr11:120484153-120484163 | GCTAATCCCC | + | 6.02 | | HNF4G | MA0484.1 | chr11:120483867-120483882 | AGAGACCAAAGTTCA | + | 7.09 | | IRF1 | MA0050.2 | chr11:120483929-120483950 | TCACACTTTCTGTTTCTTCTT | + | 6.2 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 120483447 | 120484361 | | chr11 | 120483837 | 120483981 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I120612 | chr11 | 120483220 | 120484689 |
|
Enhancer Sequence | AACGTATAGC ATGTGGGATT CCCCATGACA GGTGGAAATC CAAAGGGTTT TTCTGATCAT 60
TTCCTGAAAG CCACTGATGA CTTCACTGAA GGCAAAAGAT CTCAGTTAAA GGGAATTATT 120
AGACTTGACA CTAGAAGTTG TCAGTGTAGC CCTCATTATC GGGCTACTTT GTGGTGGATG 180
GGAACTGGCT TTGGGGCTTT GTCTGTGACA GGAGAGTGCT CCCTGCTGAC TCTGGGTGGG 240
TCAGACAGAG GCCATACCAG AGCTCTGAGC TTCCACCGTG TGTAGAGCCC TGAGCGGGGC 300
AGGGAACACA GGGACAAAGA GGAGTGAGGT AGGTAGGGGA GGAGGGTCAT GGGCACATGG 360
TGCAAACCCG AGTGTGTGTG TGAGAAAAAA GCATTTCTAA TCAGTGACCC TCGTATTAAG 420
CAGGGTTCTG TGTGTGAGTG GTGGGGTTGC TGGGATAAAG AGCCATTTGA GGCTGGAGGG 480
CTGGTCTCTG CCATTGGGGT CTTGGCTGGT GAGAATGAGG ATGATTACTC ATATCCATGT 540
GTCGTTGTGA CTCAGAGAGC TCGGGTTCTG GAGTTGGAGA GACCAAAGTT CACAGCTGAG 600
CCCAGCTGCT GCTTAGCTGA TTGGCCTTGG GTAAGTTCCT CACACTTTCT GTTTCTTCTT 660
CTCTTGTGTG GGGTATCATA ATAACTGCTT CCTGTTTCTC TGTGTCTTGT ACAAGAAGAC 720
ATGCCCCCAC AGTGGGACTA GCACTCAGGT CTTGTCAATT CTTGTCCTGT GCTTTCTATA 780
CCCTTCAGCC AAGGGAAGGG GGGCTGTCTG CTTAATTAGC TGATGTTGAT AAGAGCTTTG 840
GAGATACAAA GCTCTTGATA AGAGCTAATC CCCTTAATCT GTGTGGGGCT GATGTGTGCA 900
TGTGTTGTAC AAGGCAAATA GCACTGGGGG GATTGACCAG GAATGCAGGG CAGCACACGG 960
AGTGTGCATG TGTTTGCGTG TGTGCATGTG TACACATTGT TCTTGCTCCC TTGAAAGGTG 1020
CTGCAGACAT GATGTGCAGG GATTCATGCC TCAGATGGAG CTTGGAGGAG ATGCCCTCCG 1080
TGTTTTTCCA TCCCCAAAAT GCTGTGATTC TATCCTTGAT TGGAAGGTGG CTCCAGGTCC 1140
TGGGGCAGGG AAGCTCCTGA GCTCTGCAGG AGCGTCTGTG TGGTCCAAGG GAAGGATTTA 1200
AGAGCCCAGA GTCAGGTGTG GGGTGAGCTT TCTGCACACT GCCCTGCTCA CTGTCTCAGG 1260
GTGCTGAGGC ATTTAAAAAT TGTCCTGATA ATCCTTCTGG CAAAGTTGCC AGCCCTACTA 1320
TAGCCTAGAA AAGAGGAATC TGTGAACTCA 1350
|
