| Tag | Content |
|---|
EnhancerAtlas ID | HS182-07848 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr16:507730-508830 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAX | MA0058.3 | chr16:508259-508269 | ACCACGTGCT | + | 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 |
| GH16I000456 | chr16 | 506628 | 508910 |
| Enhancer Sequence | AAATATTTGG TTAATGTTTC AGAATAAACA ACTTGGTACT TTGTGTTCAA TTAGTAGCTT 60
CAGTGTGGAA ATTCTTAGGA ATCTTCAGGA CAGATTGGCC AGTCTGGACT CCGGATTAGG 120
TAACTCTCAG GTACCCAGCA AGACTCTCAC ATTCTTAGGA ATGAGCTTAG GAATGAGGAC 180
TTTTGTGAGA TAAGTGGGGA GATGTTTTAT AAACTCCAGT TGTCTCCAGG AAGTTGGTTG 240
ATGATGGACT TCCGAGGCTA GAGTCACGCT AGCACACAGA GCCCTAGGAT TGGGGCGATG 300
GCCCCGGCCT CTTCCGTTGT GAAGGGGAAG CGGAAACTCA GTCTCTGGCT CAGGAATTCC 360
ACACTGTGGG GTCCCTTAGC TGGGGCTGGC CCTGTTTGAG CCTGACTTTA TGAGGCATGT 420
TGGCTGACAG TGGCGAGAGG GCCAGCCACG GGGGCCCGGG CCTTGCTCTG GTGCCCTGTG 480
TGCTTCGGGC TCTCTGGATT GCCTCCTGGG CGATGCTATA GCCTTGCTGA CCACGTGCTA 540
CACCCCCCAT CCTTTTCCTG AAACAGAGCA GCTGTGTCCT GGCATCTCCA GCAGGGCTGC 600
CCTTGAGGGT TCTGTGCTTG CTGCTTGGTA GCAGCCCCGG CATCTGGACT TCACCACAGG 660
GCCTAGGGGG CCTTCCTCGG GTTCACCGAT GCCCACAGGG CCTGGGGGGC CTTCCTCGGG 720
TTCACCGATG CCCACAGGGC CTGGGGGGCC TTCCTCGGGT TCACCGATGC CCACAGGGCC 780
TGGGGGGCCT TCCTCGGGTT CACCGATGCC CACAGGGCCT GGGGGGCCTT CCTCGGGTTC 840
ACCGATGCCC ACAGGGCCTG GGGGGCCTTC CTCGGGTTCA CCGATGCTCA TCTGCCGTAA 900
CCTGCCTGAG GCCCTAGGGT TTTGTCAGTT AATGGATGTG GCTACAGCCA GGGCTCCTGC 960
CAGCCTGTTG CCTCTCCCTG TCCCTGAGCA TTTTCACAGT CCAGCCCGCC ACCCAAGAGG 1020
GGCTTTCTTC AGGAGTCTGC CCCCTCTGTG GCTGAATGCT GCCTCCTTTT TCCTTTCTCC 1080
CTGGCCCACA CTTCTTTCTT 1100
|
| |
|
|
|
