| Tag | Content |
|---|
EnhancerAtlas ID | HS182-15277 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr22:44523200-44524610 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr22:44523980-44523993 | GAAGATTCTGGAA | - | 6.16 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTCTTGCCTC ATTTTGTGAA TGTTGTTACA CTGAAATGAC ATAATATACT GTTGATGTGA 60
GATCCTCTTG ATGTGATACT ACTGATGTGA TCACCTGATC CTTGAGCTCC AGGATGCCAG 120
GAATGACACT GATGTAGGCA TTCAGCTCTT TGGCTTTCCA AAGGCAGAAG CCCAAACCAA 180
ATAGGAGATT TTAGCTGAAT ACCAAGGTCA AAGCCAACTT CTGTGCATCC GTAGTAGAGA 240
AGAGGTCTGA GGACTGGGTC TGGGCTGTCA GCCATTAGTG GTCAGGAAGA GGAAGTTCTG 300
GCAAAGGTCA GTCACAAGGG AGGGGGAGCC AGAGGAGTGT TGCATTCAGG AAGGGTAAAG 360
GAGGTGTTTC TAGGAGGTGA GAGGAGGAAA GAGAACAGAC TTCTGGTTTG GCCATGTGGA 420
AATTGCCCAG AGTGAACCAG CAGGACCCCT GAGGAGTCCC TCTTCTTTTT TTTTTTTTCT 480
CTTGAGATAG TGTCTCACTC TGTTGCCCAG GCTGGAGTGC AGTGGCGTGA TCACAGCTCA 540
CTGCAGCCTT GACCCCTAGG CTTGGATGAT CTTCCCACCT CAGCTTCCCC GGGAAGCTGG 600
GATCACAGAT GCATACCACC ATGCCCAGAT AATTTTTGTA TTTTCTGTAG TGCTGAGGTT 660
TTGCCATGTT GCCCAGGCTA GTCTTGAACT GGGCTCAAAC GATCCTCCCA CCTTGGCCTC 720
CCAAAGTGCA GGGATCACAG GGATGAGCCA CTACACCCAG CCGAATCCCT CTTCTTGAGA 780
GAAGATTCTG GAAGCAGCTG CCGGGTTCTC TGCCACATGC CAGGTTTCTG GGGGTGTAGC 840
TCCCCTGTGT TTGCAGTGCA GCCCTCAAGG TAGACTGCAT ATGGCCAGAG TGAGGTGCCC 900
GTGCTGTGGG AGCTCCTGGC TGTCGTCCTG CTGGTCACTC ACGGGCACAC CCTCTCCTTG 960
TGAAGGTGAA GTTCTTCATC ACATGTGTAC TCAACCCCCA TGTGGCCATC ACTCAGGGTC 1020
ACCTGCTACA TGGGAGAATC CTCCCCAGTT TTCTCTCTTT CTGTGCTAGG AAGATAGGGG 1080
TCCTGGCCAC AACAGAGCCC TGAGCTGCTC CTGCGGCCCC CGCCAGTGGG CACAGTGATG 1140
TCTGATGATG CAAGTGATCA TGTGCCGTAT TCTCTGTTGC ACAGGAGTCA CCCAAGACCC 1200
AGCCTAAGGC AGCACACAGG CATGGCCAGT CTCTTTGGTC TCTGTTGCCT GCTGTTTCCA 1260
CCACCAAATT CATATTTTCA AGTCCTACAT GCAGGGCCCA CCCATGTGAC CTCATTTTAC 1320
CTTAACTGCC TCTTTAAATA CAGGCACATT GCAAGGTATG AGAGCCTCGC CCACTAGGAG 1380
AGATGGGTAG CCTGGCAGCC TCCCACTGTC 1410
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