| Tag | Content |
|---|
EnhancerAtlas ID | HS182-01172 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:100169820-100170940 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr1:100170163-100170174 | ACCACGCCCCC | + | 6.14 | | KLF4 | MA0039.3 | chr1:100170787-100170798 | CCACACCCTGC | + | 6.62 | | Klf12 | MA0742.1 | chr1:100169986-100170001 | GGGAAGGGCGTGGTC | - | 6.61 | | Klf12 | MA0742.1 | chr1:100170042-100170057 | GAGGAGGGCGTGGTC | - | 6.77 | | MAX | MA0058.3 | chr1:100170637-100170647 | AGCACGTGGT | - | 6.02 | | SP3 | MA0746.2 | chr1:100170162-100170175 | CACCACGCCCCCA | + | 6.16 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_35292 | chr1:100169649-100170656 | HeLa |
|
| | 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 |
| GH01I099704 | chr1 | 100169757 | 100170218 |
|
Enhancer Sequence | CAGGTCTTCT AATTTCCAGT CCTTTTTAAT TTACAGGATC AGCTGCCTCC CATCCCATTT 60
ATAAGGATGG TCAAAACAAA AAGATACCAA TGTTGGACAG CAAGTCAGGG AAGGAGCTAG 120
AACTTGATAA ACTAGCTTTT GTAAGTGATA ACGGGAGGGA AGTGCTGGGA AGGGCGTGGT 180
CCCTTTAAAT AACAGGAAAG GAGGGAAAGG AAGTGCTGGG TAGAGGAGGG CGTGGTCCCT 240
GGCGAGGGCT CCACCCCCAA ACCCGTGCCC ACGGGTCTAA GTGAGGACAG GCACCCCTGC 300
CTTCAGCGCC CAAATGTTGC ATTTCCTAAG ACCACCCTGG CTCACCACGC CCCCATCCTG 360
TGCCTATAAA AACCTCCAAG ATTCTAGCAG GCAGACACAC AAGCAGCTGG ACGTGGAGAG 420
GAACACATCG CAGAAGACAC AAGCAGCTGG ACAGCGAGAG GATGTGGATG GGAGCACGCC 480
AGAGGAAGAG CACACGACAG ATCCCAGCAT GCCGACAGGC CACGACTGGC GGAAGGAGGA 540
ACAGTTGGCG GAGTTTGGCC GGGGCAATCA GAGGAGAGCC CAGGCAGTCT AGCGGCCCAA 600
CTCCAGGGGA AAACCATCTC CCTTCTGGCT CCCCCATCTG CTGAGAGCTA CTTCTACTCA 660
GTAAAACCTT GCACTCGTTC TTCAAGCCCA GGTGTGATCC GATTCTCCTG GTACACCAAG 720
GCAAGAACCC AGGGATACAG AAAGCCCTCT GTCCTTGCAA TAAGGCAGGG GTCTAATTGA 780
GCTAACACAA GCTAACTATG GACAGCTAAA CTAAAAGAGC ACGTGGTAAC ACATGCCCAC 840
TGGGGCTTCA GCTGCAAACA TTCACCCCTA GACATTGCTG TGGGGTCGGA GCCCCACAGC 900
CTGCCCATCT GTATGCTCCC CTAGATTTGA GCAGTGGGGC ACTGAAGAAG CCAGCCACAT 960
CCCCATTCCA CACCCTGCAA GGGGGACAAG GGAACATTTC CCGTTTCACT GAGAAGGGCA 1020
TTCCAGGCTG GTAACCATCT GTGACCTGGG TGCAGAGATG AGCTTGGTAG GGGCTGCACA 1080
AGGAAGAAAG AAGCAGGATG TGGATAGGAA CTGTGAATAT 1120
|
