| Tag | Content |
|---|
EnhancerAtlas ID | HS182-04863 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr12:26128670-26129920 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYA | MA0060.3 | chr12:26129371-26129382 | TCTGATTGGTT | - | 6.62 | | NFYB | MA0502.1 | chr12:26129372-26129387 | CTGATTGGTTGCTTC | - | 6.31 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_44174 | chr12:26127431-26131321 | NHDF-Ad |
|
| | 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 |
| GH12I025976 | chr12 | 26128952 | 26131009 |
|
Enhancer Sequence | GAAGCTATTT AGAAGGTAGT ACACGCTGAT CAAGGACCAA AGGACCAGAA GAAATAATAC 60
CTGGGGACAG TGGCATAAAG GTGGATGAGA GGTGATGGGG TGCCCTAGGG AGAGGCCACC 120
ACAGCCAGAA AACTGTGGTG GTGGCTGACC CTGGAGCATG GATGTACAGA GTACCTTTGG 180
GAAGCAGCAC AGTGTCTAGA CTCAGTCAGC TTGGGATGAG ACTAGACAGA AATGGGGCCC 240
ATAATGTGAT TGGAACCAGG TGTAGAGGAG CCGCACCCAG AAATTTTGGA CCTTATTCCA 300
AGCCAGTAGG CTTTTATGAA CAGGTCTCCT GGTCTCCTCT CCTCACCCAG GCTGCCAGTG 360
AGGCAGGAGA ATAGGGTCTG GAGGCAGGGA ACCTAAGGCT GTTTCATGCC AACTTCCTAG 420
AACTAAATTG AAAGGAAAAC CCATCAGATC GACTTCCTAG GACTAAATTG AAAGGAAAAC 480
TGTAACCCTC CGCTTAAGGA ACAAGAGGAC CAGAGGCTAC TCCATTTGAC CTTTTCTGTC 540
TGGAGGATGG GAAATTGGCT GTCTGCAACA AATCATACTG AGTGCAGGTG GAGTCTTCAT 600
TTGCAACTTT GTAACTTCAT TCCAGCCTCA GAGTGGTTGC TGTCCACACC AGCGGAGTCT 660
TGGTTTGCAC AGAAGTATAA CTTTGTAACT TCACCTTAGC CTCTGATTGG TTGCTTCTTC 720
TTTTGCATGT GACATTTGTA ACTTCACTTC AGCCTCTGGT TGGCAGCTTT CTGCAACGAA 780
TCAGACTGAT TGTGGGCTAC CACTTCGGTT ACATGAGATG AGCCTGAAGT GGCCAATGGG 840
AAACTTCTAG TGGGTATTTG GACCCAAGAA GATTCAGTAT CTGGGCCATT GAGCTGCTGC 900
TTGGGTCTGC TCCCACACTG TGGAGTGTAC TTTCGTTTTC AGTAAATCCC TGCCTTCGTT 960
CTTTTGTGCT TTATTCTTTC TTTGCTTTGC TGGGCGTTTT GTCCAGTTCT TTTTTCAAAA 1020
TGCCAAGAAC CTGGACAACT TGGAGTCACG ACCCTCTACC GGTGACATGA CTTTCTCCAG 1080
CCTCTCTTCC CCCTGCTGCG TTAAGAACAA GCCCAGTGTG TTACTCCCAA AGCCTAACAC 1140
CACATGCTTG GGACCTCCTG GTTTTGCACG AAAGTTGTGA ATTTAGCCTA TAATTCTAAG 1200
ACGTTTCCCT GGTCCACAGT TTATCCCCTC ATTGTTGGTT CTCCTCACCT 1250
|
