Tag | Content |
---|
EnhancerAtlas ID | HS182-15339 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr22:47249490-47250770 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr22:47250569-47250587 | CCTTGCTTCCCTCTTCCC | - | 6.22 | FOXP1 | MA0481.2 | chr22:47250325-47250337 | TCCTGTTTACAT | - | 6.02 | Foxo1 | MA0480.1 | chr22:47250325-47250336 | TCCTGTTTACA | + | 6.62 | Lhx3 | MA0135.1 | chr22:47249586-47249599 | AATTAATTAATTC | - | 6.29 | Lhx3 | MA0135.1 | chr22:47249585-47249598 | AAATTAATTAATT | + | 6.92 | MYC | MA0147.3 | chr22:47249710-47249722 | GAGCACGTGGCT | - | 6.04 | POU6F1 | MA0628.1 | chr22:47249587-47249597 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr22:47249587-47249597 | ATTAATTAAT | - | 6.02 | ZNF263 | MA0528.1 | chr22:47250276-47250297 | CTTCCCGTTCCCTGCTCCTCC | - | 6.16 |
|
| 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 |
GH22I046853 | chr22 | 47249163 | 47251194 |
|
Enhancer Sequence | TCCCTTAAAA TCTGGTTTTT ACTTACTTCG CTGAAACTGG TCACCAAAGA CACCACATTT 60 GCCTCATTGT ACTTGAGAGC GGAACAGGAA CGGAGAAATT AATTAATTCA GTTTTATAGA 120 TGAAGAAGGG GAGCCTGAAG AGGTTCATTG TTCAACAGAT ACTTACTGAG CACTCACTCG 180 AGGCAGGGCC TCGTCCTCTG GGCCCTGGAG ACTCAGCAGT GAGCACGTGG CTGGTCGGAG 240 TGATGGGCAC AGAGCTGGGC GCAGGCAGTT TTGGAAAGCA CATGAGACTC TTTTCTGCCT 300 CAGGGATCAC TTTCTCAGCC ATGCCGCATG ACCTCAGAGG CATTTTGCAC CAATGGACAC 360 TTCGTGAAAA ATTTTTTCCC AGGGTTCTGT GACATTTTGC CCCGATTTCC CCCGCTGTCT 420 CCGAGTGTCC CCTGTGAGTG GACTCTTTCT CCTTCACACC CATGTGCGTT TCTGGACTTC 480 TTGTTTTAAA CACGCTCTTC CTTGGTTGGG ACTCTGCCTG TCTTTCCGCA CCTCTGAGCC 540 TCATTGCCCA GTGTCCGTGT CTTCCGGAGG TGCCTACTGC ACTGTCTTGG GATTTTGCCC 600 TGTCAGAAAT GTGTCACGTG TGATAGGAAA ATCATGGACG TGGTTGAGAG TCAGGCCCCT 660 GAGTTTCCTT TCCTCATTTG TAAAATGGGG ATGGGAACTG CTCTCCAGGA TGACAAATTG 720 TCACGTGGAA ACCAGTGCAC GGCGCAGACA CTGCTCCACA GTGTCGACAT CCCTTCTCTC 780 CCTCCCCTTC CCGTTCCCTG CTCCTCCTCC ACTGAACAAG CCACCCCTCT CCACTTCCTG 840 TTTACATCAT AGATGGCGCC AATCTCTCCT ACCCAGGGTA ATGTTTGGTC ATTGTCATTT 900 TGGCCTTTCT TTTTCCCCAT ATCTAGTTAT TGCTGAAGCC CACCCCCACC TGTTCTTGTT 960 GTTTCCGGAT GTTCTCGCGC TAATTCCTTC AGCCTTTCCT TTCTGCCTTT GATGGGTCTG 1020 CCCTAGATCA GACCTTTATG ATGTCTGCCC AGGCATTGAA GTAGCTTCCC AGCAAGTCTC 1080 CTTGCTTCCC TCTTCCCCCT GCGATGCATT CCAGGTCCTG GCAGGAGGTG AATCACATTG 1140 AAACGTGGCT TTGACCTCTG CTTTTACAGC TCCCCGTTGC TTGCAGGACA AAGATCACAC 1200 TCCTGATATT TAATGCCTTT CTTAATCGGA CTCCTAATTA CGTGTTCATC CTCTGTTTCA 1260 TCCAGACATA GGAACCTGCT 1280
|