| Tag | Content |
|---|
EnhancerAtlas ID | HS182-08041 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr16:11942300-11943350 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr16:11942914-11942925 | GATGAGTCACC | - | 6.32 | | JUND | MA0491.1 | chr16:11942914-11942925 | GATGAGTCACC | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH16I011848 | chr16 | 11942801 | 11942970 | | GH16I011849 | chr16 | 11943061 | 11943210 |
|
Enhancer Sequence | AAACCTAGCT TAATCAGGAC AAGCCTGGTT CAGAATTTTA CCTTCTTTAA AACTCTTAGC 60
TCCATAAACA TAATAACTCT TTCTTCTTTT CCTTTTTTTG AGACAGGGTT TTGCTCAGTA 120
CCCAAGGCTG CAGTGCAGTG GTGTGATCAT AGCTCACGAT AGCCTCCAGC ATAGCTGAGA 180
CTCCAGGCAC GTACCAGTTG GGTGTAGGCC CAGCTAATTT TTGTATTTTT CGTAGAGACA 240
GGGTTTCGCC ACATAGCCTG GGCTGGTCTT GAATTTGTGG GCTCAAGCAA TCCACCTGCC 300
TCAGCCTCCC AAACTGCTGA GATTACAGTG TGAGCCACCA CACTCAGCCA ACATAACTTT 360
TTTTTTTTTT TTTGAGATGG GAGTCTCACT GTCGCCCAGG CTGGAGTCTC TGCAACCTCT 420
GCCTCCTGGG TTCAAATGAT TCTTGCACTT CAGCCTCCCA AACAGCTGGG ATTACAGACG 480
CCCACCATCA TGTCTGGCTA ATTTTTGTAT TTTTAGGAGA CATGGGATTT CGCCATGTTG 540
GGTCAGGATG ATCTCAAACT CCCAGGCCTC AAATGATCCA CCCACCTCAC CTCCCAAAGT 600
GCTGAGATTA CAGGGATGAG TCACCATGCC CAGCATAACA TAACTTTTAA GAATTGAAAC 660
AGCCCAGGCA TGGAGGCTCA TGCCTGTAAT CCCAACACTT TGGGAGACTG AGAGGGAGGA 720
CTGCTTGAGC CTGAGTTCGA GACCAGCCTG GAGAACACAG TGAAACCTCA TCTCCACAAA 780
GATTTCAAAA TTAGCTAGGC ATGGTGGTGT GCACCTGTAG TCCCAGCTAC TTGGAAGGCT 840
GAGGTGGGAG GATCACTTGA GTCAGGTCAG GGAGGTTGAG GTTGCAGTGA ACACAGATCT 900
CACTATTGTA CTCCAGCTGG GCAACAGCGC AAGATCTCGT CTCTTAAAAA AAAAAAAAAA 960
AGGAGAGATA AAAGAATCGA AACCAAAAAC ATGGACTAAA CCAAGAGGGA CCAGCAAACA 1020
CAATTATGCC ACATCTTACA GAAAATAAAA 1050
|
