| Tag | Content |
|---|
EnhancerAtlas ID | HS182-03904 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr11:64682880-64684430 |
Target genes | | Number: 36 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr11:64683973-64683988 | GGGGTCAAGAGGTCA | + | 8.07 | | Nr2f6 | MA0677.1 | chr11:64683329-64683343 | AAGGTTAGAGGTCA | + | 6.06 | | RARA | MA0729.1 | chr11:64683973-64683991 | GGGGTCAAGAGGTCAGGG | + | 6.56 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGGCCTAGAG ACAGGACTAA TCTAGTCACC CAGTATACAA CAGGGACTGA GACTGGGATG 60
CGGGCCTCTT TCTTTTCATG CCACTTCAGA GGCCCCAGAT ACTCAGTTTC TTTGGGGGCC 120
TTCAAGGCGG GGCCTGCAGG CTGAGCTGGG AGGGAGGAGG GGCTGGTTAT CAAGAAAGCG 180
CCTGCATTCC ACCAGGGCCC TAGAGAAGCC AATTCAATCC CCAACAAGAG GGCAGGGAAC 240
AGGAGTAGGG GCGTTTTCTG GAGCTGAAAG TAAAAAGGGG AAGCCTAGGG CTGGGTATGG 300
TGGTTCATGC CTATAATCTC AGCACTTTGG GAGGCTGAGG TGGGAGGATC CCTTCAGGGG 360
TTCAAGGCTA GCCTGGGCAA CATAGCGAAA TCCTGTCTCT ATAAAAATAA AAAAGGGGCA 420
GCCTAGAGAC GGCCTTAGAG GCTGAGGCTA AGGTTAGAGG TCAGAGAGGG CTTCCTACAC 480
CAGAATTCAC AGACAGCAGG CCACTGGGGG GTGCCCCCAG TTCAGGGCCC ACGATTATCC 540
TACCCCACAT TTGCTCACCA GGGCCTGGCC TACCCCCAAA GCCTAGCTCT TCTGCCCAGA 600
TTAGCAGCCC CCTGAGTCCA GCCACAAAAC TGAGAAGTCC CTGCCTCCAT GCCCACCCCT 660
GCTGCTCTGG ACCTGGTGGA TCGACCAGGA CGCGCCTCTA ATTGGTGGCT CCTTCAAAGC 720
TCCCCAGGTC AGCTGAGCTG TGAGTCAGGG CTCCTCACCG TTCCCAGCCT CAAGCCTCTG 780
ACCTTACACC TCTTGGCCTC CCTAGCATCT CCCTTGGCCT CCTCCCGGCT TGAAGCCAGA 840
TCTCCCCACC TTTCCTCCAG GGCCTCCCTC CAGGCAGGGA CACTGAGCCG GGGGGGTCGG 900
TGGGAGATGT AGGTGGGGGC CATCCAGTCC CTCCCTAGAC ACCCACTTGG CCCATCCCAC 960
TCTCCCAAAA GCAGGAAGTA GGCAGCGACC CAGGCACACG AGGTGTTGAT CAACACTGGT 1020
ACTGACGTAC TGACGCGGTT GTTGACATAC ACATCCGGTG GTTTGTTGAT CCCACCTACG 1080
GGCTCAGGAC CGTGGGGTCA AGAGGTCAGG GCACATGATC CACAGGTGTC CTCGCCAGGG 1140
CTCCGGACCC CTACCAGCTT CCCCCACCAG CTGCGCAGGC CCAAGTCTGT CACTGCCCTG 1200
GCCCAGCTCA GTTCCTACGC TCCCTCCCCA GCCCCTCCTC AGCCCGAGAG CCAACCTCCT 1260
TAACTCAGCC CCCAAACTCG ACGAGTTTGT CTTGCATTCT CCAGACAGGT GATCTTGCCC 1320
TCTCCAGCCT CAGTTTCTCC TCCCGTGGAG ACAGAAACCC CTTCCCGCTC AGTTTCTGGC 1380
TCTGGTAAGG AACTGAAGAG GCCAGCCGGG GTGCCTCTGA CGCCTGGAGA GGGCAAGATT 1440
CCCCTGGCCT CTCTACGCCC GGTGCCTGAT CCCCCAGCCC GATCCTGCCG CAGGGAGCCT 1500
CAGGTCGCTG CGCTCCCACC CTCCGCACCT TCCTGGACTC GGGCCTGGCT 1550
|
