| Tag | Content |
|---|
EnhancerAtlas ID | HS182-18289 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr5:178069330-178070280 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GSC | MA0648.1 | chr5:178069575-178069585 | GCTAATCCCC | + | 6.02 | | Stat6 | MA0520.1 | chr5:178069835-178069850 | TTTTTCCTGAGAACT | + | 7.26 | | TFAP2C | MA0524.2 | chr5:178069693-178069705 | TGCCCCAGGGCA | - | 6.44 | | TFAP2C | MA0524.2 | chr5:178069693-178069705 | TGCCCCAGGGCA | + | 7.22 |
|
| | 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 |
| GH05I178641 | chr5 | 178068881 | 178070273 |
|
Enhancer Sequence | GCTCCCGTAT CAATAAACTC GCCCTCCCAG GCTTCTGTTG CACAGCTCTC AATGAGCACC 60
TTTGGGATCC AGCCCATGTT TCCTCTTTCA GCTCCTGCCA GTGCTGTGAA GCAAGTTCAC 120
TGTGCTCTAG TTACCACACT GTCTGAATCT GGTAAGACAG AACACCCACA TATAAATTAC 180
ATGAAGAGGG TTTGTTACTT ACTCATAGGA AGCAAGGGAC AACGGAAGCC CAGGATTCAT 240
TGGAAGCTAA TCCCCAGGGC TCAGGAAAGC CCCCTGAGGT TGGATTGGAG TCTTGCTGTG 300
GTGTGTATGC TCCACTTGGA CTGCAGCCAA AGGGCCATGG AAGAAAGTGC AACCTGGGTT 360
TTATGCCCCA GGGCAACATG ACTCACTGGA ATAAGGCATT GAAGGACATC CTGTTTCTGG 420
GGTAGGGGGG ACTGGAACAG AGCCCAGGCC TTTCCAGCCA GCTTCTCCTT ATCTCACATT 480
GTTGTGTTCC CAGCACATTC TATGGTTTTT CCTGAGAACT GCAAGTAAGA AAGAGGAGAG 540
AACTGGGTTG GTCCAAGGCC ATCTGCAGAA CTGTCCTGCA AGTACTTGTT GGCAAGGTCC 600
TGCAGTTCCT TTGCCTACGG TTCTTTCCTT CCCTTAAGAG GCCCAGCACT TGCCTGGCCA 660
GATTATGTTG TAGCTTGACC CTAGTTACTG GTCTTGGGAC TGGGGAAGAG GGGATTGATC 720
CTGAGAAGGG TGCATGCTTT CCTTTAAAGC AGAAGCCTCC AGATCTTCTT TACATCTTCA 780
AGCATGGAAG CAGCACTGAC CTTTAACAGG GAAGAACGGG CCACTTCTGC AGACCCAGGA 840
GGTTCAGAGC AATCTAATAA TGCAAGATTT TTTAGTGCGT CAACACAGAT ATCCCTATTT 900
CCAGTGTCAG GCTCCTATTC CTTCCCAATT AGGATCCTGA CTTTGGCATA 950
|
