| Tag | Content |
|---|
EnhancerAtlas ID | HS182-02915 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr10:97997710-97999440 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat4 | MA0518.1 | chr10:97998897-97998911 | GTTCCAGGAAAGGG | + | 6.2 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_10441 | chr10:97998637-97999445 | CD19_Primary | | SE_58700 | chr10:97989552-98067150 | Ly1 | | SE_60551 | chr10:97989174-98053492 | DHL6 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I096238 | chr10 | 97998638 | 97999445 |
|
Enhancer Sequence | TTAGCTTAAT GCCCAGAACA GAGTCAATAC TCAACAGATT TTGGATATCT TCCCTTCCCA 60
CAGCAATGCC AGCTGCTTGG GGCAATGCAT TCTGCCCAGT GGGCCAGCAG TTCCTTAGGG 120
GCGATGTTTC CTCCTCAGGG AAAGACTGAA CTGGGATTGC TGGGTCTGAA CTGAAGGCAG 180
CAGGCTCCAC ACTGGCCTGA CCTGCATCCC TGGAGGAGAC CCAGCTCTCC ATTCTTTGTG 240
TAATTCAAGC TTTGTCCTTC TGTACTCTAA CTAGGGAAGA GGGTATGGTG ACTCTTTTAC 300
TGACCTCCTG TGGGGCAGTT GCTGGTCCTT TCTATCCTCT GCTCTCTGAA GGTCAGCATC 360
ACCAAGGTCA ACACACTCTT GGCTTAGAGG GTTTTGGGAA GCCATTTGTT TCCAGAACTG 420
GAAAGAGGAC ATAAATCCAA TGTGTGGGGG GAAAATGGCT GGAGCATTTC AGGAGCCTTT 480
GGTGGATCAA GTGCTCCACA GGGCACGTGA TTGGCCTCCC AGGCTCAGGA GGTCTGGTGG 540
GCTCTGGCCT CCACACACTA CAGTTTCCAA GATCCTAAAG ACTCCCCAGG TTCAGGAGGA 600
GCTCTCAGGG CTGATTTCTG AGGCCCTGGA CGTGCAGCTG TGCAGAAACC TCAAGGCTCA 660
GGGGAAGCAG CTGGAAATGC TCCTGGGATG TGAACTGGGG TGGGGGAGAG AACGGCAAGG 720
GAGGATGCTA ACTGCAGGTG GTGATGGTGG TTTTGGACCA TTTCCGGGGA TTGAGTGTAA 780
GAGCAGGGGA AACTGGGCAA GGCCCCAGTC ATCTGGCAAA GCAATAAGAT GCATTTCCGA 840
GACCCTGGAA CATCAATGGA TTTGCAGGGG TCAGGGATTG AGGGAATAAA ATCTACGTGT 900
CTTTCAGTTC AGGAAAGGCA ATAGGGACAG AGATGGTGGT TTATAGCAGG GTTTCTTAAA 960
TATGATTTAC ATTCAGATCC CCTGGAGATC TTGCTAAAAT GTAAATTCTG ATCCAGTAGT 1020
TCTAGGGTGG GGCCAAGATT CTGCATTTCT AACAAGCTCC AGATGAGGTT GATGCTATCT 1080
TGCTGGGAAT CAAACTTTGT GTTGCAAAGG CTTAGAAGAT CCTGTTGGGC CACACTTCTG 1140
CATTCCAGGA GAGATTAAAT GTTCTGACAT CAAGACTATT TGGAAGGGTT CCAGGAAAGG 1200
GAGCAGGTGT CTGAGGACAA AAAAGAGAAC ACTTCAGAGC ATCAGGGATA TTGGAAGATG 1260
TGAATGCCTA AAGCCAGGGA ATGTTAGGAG AGGCTCACTT TATCACTGGG CCCTGAGCCC 1320
CAGAGATCTG TGTTTCTGCA GGAGTGCAGA ATAATTAGTA TTAGAGGGGA CCTGACAGAT 1380
CTTCTAGTTC AGGCCTGCAT AATATAGATG AGGAAAGGAG CATGAGATGC CCAAGATTAC 1440
ACAGCCAGTT AGTGGCTAAG CTGAAAGACC TTGTATGTGG GCTCAGTGGT TTGCAGTTCC 1500
TCTTGTTAGC AATGTAGAGC CATGAAAAGA TTTAAAGAGA ATTTTATTTC AGAACAATTT 1560
TCTGGTGGAA GTTGAGAGGA CCACATGCAA TCAGGAATTA AGCAGATTAC TTAGAGCCTT 1620
CTACCCTAGG ACAAGCAAGA GATGATGAAG GCCTTAGCTG TAGCAATGGG AATAGAGAGG 1680
GAAAAAATAT TTAAGAGGCA TTTAAGAGCA AATCAATGAG ATTTGGAGAT 1730
|
