| Tag | Content |
|---|
EnhancerAtlas ID | HS182-12350 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr2:65219170-65220460 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Esrra | MA0592.2 | chr2:65219737-65219748 | CTCAAGGTCAT | + | 6.02 | | Esrrg | MA0643.1 | chr2:65219738-65219748 | TCAAGGTCAT | + | 6.02 | | MAFF | MA0495.3 | chr2:65220324-65220339 | CTGATGAGTCAGCAT | + | 6.38 | | MAFF | MA0495.3 | chr2:65220324-65220339 | CTGATGAGTCAGCAT | - | 6.43 | | MAFK | MA0496.2 | chr2:65220322-65220341 | CTCTGATGAGTCAGCATAG | + | 6.22 | | NFE2L1 | MA0089.2 | chr2:65220325-65220340 | TGATGAGTCAGCATA | + | 6.04 |
|
| | 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 |
| GH02I064991 | chr2 | 65218935 | 65220334 |
|
Enhancer Sequence | TTTAGGTGAG TGCTGAAAAG AAGTCTCCTG AGGTTGAGAG CACCTTTAGC CTATTACCTG 60
TAGGAGGTCG GTCAGCTCTC TCAGGGAGGA AAGGCAATAA TGGGGTTAAA GGATTATTCT 120
TTGCAGGGAT CTGTGGCCCA GGGAGGGAGA ATGGATGTTC AGCTCTGTCC TGCTATGGTC 180
CCGCACCGGG AGCCTCAATA GGATCTTTTA ACTCCAGAAG AGGGGGCAGT GGTGGTAGGG 240
GGTACCTCAT TACCTCCTGA AGGGACTTCT TGTTTCCTGA TCATGGTTTT CTAGTTTTAG 300
ACCCAAGCCC CTTCACCTCC TGCTTCTGAC ATGGATGGTG ACCCAGCGTC ATAGCTTAGT 360
AGTGTGGGTG CAACTTTTCA ATGACTTGGG CTGCACCTGC ATGGAGGGCT AAGAGAGGCT 420
TTGTTGTGGC TTGCTGGGGA TAGGTATTGC TTCATAATTC TTCCAACAGC CAACTTCATC 480
TAATCCAGCA GCTCACGGAT AAAGGTAGGG CAGGTGGTAT ATCCCATTTT ATGACTGACA 540
AAACTGAGAC AGAGATTAAG CGATTTGCTC AAGGTCATGG AGTGGCTTAT AAAGAAGAGA 600
TTAGAAGGAC TGTGGGTCTC CTACCCCACA GTGCAGGGTT CTCTCTCTTT CTCCTAATCC 660
CTCTTCCTCC AAGTCAACAT GCCTTAGTAA TGTCACCTGC CTAGTCTAGT GTGGCTATCT 720
CAGAAATGCT TTCTCTGGGC CCAGAGAGGA ACCAGGTAGG CATATGACTG GGTAAAGACA 780
AATGCTCCTT TCCTCCAGCC AGCGTGGAGG CTGAGCTCCT CAAGTGAAGG AAAGTATGTG 840
TGCACCGCTG AGGTTTGGTC TCAGGCTGAA GCAGCTTGTG AAAGGAAACT AAGTCCCAAG 900
CCACCCGGAA ATGCTTCCTG AGTCTGGAGA GTCTCTGACA TCAAAATTAA AAAATTGCTT 960
CCTTCAAGGA AACTTCACGG ATGTGGATTT CATGTGACTC TGGGCATCTT CTTTGGAAAG 1020
GCAGTGCCCC ATTCCTTTCT TCCTAGGGGC ACGTGAATGA AATGAGACTC TGCCAGTAAA 1080
CGCCTCAGTT ATCCAGCAGG CCCTCTCGAG GTAGCTGCTC AGAACTTAAA CACCTGGAAG 1140
AGTGGGAAAG GCCTCTGATG AGTCAGCATA GCTGCTGCTG AGGCTTTGTG CTAAAGTCCA 1200
TGCCCTTTCC TGATGGTAAA GTGCCCCCAA ATCCCCCAGG GTCTCTCTGT CATGATTTCT 1260
AATTTGGTTT TTAAAGCTGG AACTACAAGT 1290
|
