| Tag | Content |
|---|
EnhancerAtlas ID | HS182-01747 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:203963670-203964980 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr1:203963911-203963926 | ATTGCTGTGTCATTG | - | 6.39 | | REL | MA0101.1 | chr1:203964481-203964491 | GGAAATCCCC | - | 6.02 | | ZNF263 | MA0528.1 | chr1:203964419-203964440 | TTTTTCCCTTCTTGCTCCTCT | - | 6.04 | | ZNF263 | MA0528.1 | chr1:203964416-203964437 | TCCTTTTTCCCTTCTTGCTCC | - | 6.36 |
|
| | 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 |
| GH01I203994 | chr1 | 203963941 | 203964984 |
|
Enhancer Sequence | CAGGCACCAG TTACCTGTGG TGAATACAGG AACAATCAAG ATTGCCCTGT CCTTGAAGAG 60
TTCCATTTTA GTGCCTTACA AGTAACTGAA GGCAGCGGGA AGCCACCAGT GGTTTTACAC 120
AGAGCCAAAA AGTGATCACC TCTATATCTT TGAAAGACAG CTCAGACTAC ATACGGTGAG 180
TGGGAAGAGT ACAGAGGATT GAGGCAGGGG ATTTTGTTCT AGAGGCCAAA TATTGTTCTG 240
CATTGCTGTG TCATTGCTGT CTGTTAATTG CACCCCACGT TCCGCACCAC TTGCCTCATC 300
TATCCCAGAA TCTTATCCCT CACCTTTAGA TTTTTCTCAC CTCAAACCTT CAGTTCCATA 360
CCCACCCTAC CAGAAGTTCA GGGATAGTCA AAGTGGCTTT CTGAGATCAA GAGTCCACAA 420
TGTCTTCATG AATCCATTCT TTGCACATTT ACGAAGCTCT GCATATGCTC TGGGCTCTGC 480
GCTATGGGCT AGAGTTGCAA AGGTGGATCA GACTCAATTC TTGCTTCCAA GGCAGGGACA 540
AAGTTTTTTG CTTCTCTTTC TACTTGAAGA GTATTAAGAA TCTAAACTGA TCTTGGCTAG 600
AGAAGGCAGA TAGAGGAGAC GGGTGGAGCA AGAATCAGAA CAAAAAATGG GTAGCCTGGG 660
ATTGATAGCC ATGAAATCAG GAGGGCAGAT TTGTCCTCAG GGCCCAGTAG TACTTTTCTC 720
TGAAGCCAGA GACGGCCTCC TTCCCTTCCT TTTTCCCTTC TTGCTCCTCT GGTCTCCTCA 780
CAGCCAAGCC TGGCTTCCAT TCAAACTTTC CGGAAATCCC CTACCCAATT TCCAGCTTTT 840
CAAACAATGA CTCTCTGGAG AATATTCCCA TTGTCCTTGG AATTAGAACA ATGAGAGAGT 900
AGAGCCTCCT CTCTGGCTTC AGACTACATC CCTGCTCCCA GCCAGCCTCC CACCAAAGTA 960
AAAGCTTCCT CGACTCTCCA ATCGCTGTTC CCATCTGTAG TGAGGCAGAA AGACAGGGGA 1020
AGTATAAGAA AAAGCATTTT CTACAAGTCA ACCCAGCCCC TTAAGCACTA CCTGGTGCCT 1080
TTCTTCTCCC AGCTAGAACT GAGAAGAATC TCTCTACAGG ACTGGGATTG GACACCTGCC 1140
TATGCTCTGG GTTGGCAAGC AAGCTCCGGG TTTGACTGCT GTGTTTTCTA AATCTCTCTC 1200
TCTCTCTTTC TTTTCTTTTT TTTTCTGAGA CATAGTCTTG CTCTGTCGCC CAGGCTGGAG 1260
TGCAGTGGCG CCATCTCAGC TCACTGCTGC AACCTCCGTC TCCCGGGTTC 1310
|
