| Tag | Content |
|---|
EnhancerAtlas ID | HS182-16235 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr3:124403450-124405450 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr3:124404295-124404306 | TCAAGGTCATA | + | 6.62 | | Esrra | MA0592.2 | chr3:124404294-124404305 | GTCAAGGTCAT | + | 6.32 | | Esrrg | MA0643.1 | chr3:124404295-124404305 | TCAAGGTCAT | + | 6.02 | | Klf1 | MA0493.1 | chr3:124404055-124404066 | AGGGTGTGGCT | - | 6.02 | | Nr5a2 | MA0505.1 | chr3:124404291-124404306 | GAGGTCAAGGTCATA | + | 6.36 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr3 | 124403831 | 124404003 | | chr3 | 124404078 | 124404324 | | chr3 | 124404471 | 124404702 | | chr3 | 124404964 | 124405432 |
|
Enhancer Sequence | GTTTATACAG TGATGTGTAA CCCTTTGAGC ACCATGCACG TCTAAGGTGT GCTAACAAAG 60
GACTTTGCTC TCCAGCACTT CTGACTTTGA AAACATTGAG ATCCCGACCG AAGAGGACGT 120
GGAAGATTCT GTGCTTTGGC CAGCAATTCA CTTTTCAGGG GGTGTGGCGG GAATGGCCTG 180
GGCAGATTTC CTTCTGAGAC TCAACTGGAG TGTCCACTCC TGGCTCTGGG AAGTTTGAGC 240
GGCCAGAGCT GGTACTTTTT TCCTTCCTCA AACCTACAGT TCCCTGGCCC GCCTTTCATG 300
TCCTCAGATC TGAAGAGCCA GCCTACTCCC CGCACCCCAC TCCCCGCCAA CTACCACATC 360
AGCTACTCTG GCCTCCTTAT CCTAGAGCTT CAAAATAACC CGGCCAGACG GATTGAAGGA 420
AACTTTTACA CCCCCAGCCA GGTGACCAAC CTCCTGGCAT CCCCAGTGTG TGTCCACTGA 480
TGCCTGGTTC CGCATTTTAT AAAAAGAATT TTTTCATGAA AAGAACCCTT TGGATGAAAA 540
GAAAGTGAAG CATCACATTC CTGTCGTTTT ATTTTTGCAA AATATTTTCT TTGTAATATA 600
TCTGAAGGGT GTGGCTTGAA GACTTCCTGC CTGGCTTTGT TCTGACTCTC CATGCAGACC 660
GATTTATATT CCGCCACCAA GAGAAGGGAG CTGAGCTTAG TGGCTGCTTC CCTCTCCTGG 720
GAGAATTTTA AGAAGATCGT CCACAGCAGA TTCACATCTA TTATGCTTTT TGTTCCTTGC 780
AATTGCCCTG TGAAGTAAGT AGGGTAGAGT TTCTCACCCT CCTGGGGGAA ACATGTTCAG 840
GGAGGTCAAG GTCATACAGC TAATAAAAAG AGCAAGTCTT GATGGTGGTG CTTTGAGAGA 900
CCAAACTTAG CATGTGCTGT AGAGGAAGTC TACTCGTATG GCTCAAGTAC TTTCTTAACA 960
AGGGTCAGGC TCAGGCCCTC TTTTGCTGCA CATCTGTTTT AGGAGGAGAA TTTCTTCAAC 1020
AACTTTTCAA ATCTCTTGAC TATTGGGATA ATTACTTGGC CTCACCCACG CCCTTTCTCA 1080
ATGACTCAAG AGCCCAGCCA GAGCAACCAA GAAAGGAAGT CCAATTACAT GAGTTGGAAA 1140
TGTCTGAACT GGTTTCTCAG GTCAACATAG TCACTCAGCA CGCCCTGTCA TGCATGTTCC 1200
ATCGCACCCT CACCCTAGAC TGGGGGCCTA ACCCGTTTCG TTTACGTTGT ACACTAATGA 1260
GATTACAAGG TACCATTGAC CCAGAAGTTC CTCTAAGAGC CTGCTATTGA AGAAGCAAAG 1320
ACCATCACCC CCCAACCCCA CCCCCATGCT GTCAAAGTTC ACTCAGCGTG AGTTCCTAGT 1380
CAGTTCAATT TCACACAATT TGATTAACAC AAGGCATTGC AGTGATTATT ATGGAGGACT 1440
AACGAACAAT GTAAGATTGG TTCCCATGCT TAAGGCTTAA GAAGCATAAG AAGGAGGCAG 1500
GTATAAATAA ATGCCCATGT TACACAGCAA ACTTTAAAAC CTGCTCTAAC AGTCATGGTG 1560
AGGGACTGAT TAATCCTGCC TGGAGCCATT TATTCATTCT GTGGATATTT ATGCACCCAC 1620
TCAGGCACTG GGCTCACAAT AATAGTAGCT ACTACTTAGC AGTCTTTCCT GTGTAACTGG 1680
CTCTGTGCTG AGCTCCCAAC AACATCATCA CATAGGTACT ATTCGCGTTA TTCCCACTTT 1740
ATAGATGAGA AAACTGGAGC ACAGTGAGGT TAAGTGACTT TCCCAGGACT GTGTATTCTT 1800
AGGTAGCCTG TCTCCCAGGG AGCCTATGAG TGTGGTCATT GATTCACTGG GCAGCAGTGT 1860
GTGGGTTGGA TGAACTAATA GGATGTGGGC AGTCTTAGAG AAGGCAGAGG GTGAGGAGAG 1920
AGCATGAACA AAAGCCCTGA GGTGGGAGGT GCCTGGCACA TGCTGAGCAG GTATATGGTC 1980
TGAGTACCTG GGGTTAGTTA 2000
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