| Tag | Content |
|---|
EnhancerAtlas ID | HS184-04469 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr10:97997770-97999510 |
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 | CAGCAATGCC AGCTGCTTGG GGCAATGCAT TCTGCCCAGT GGGCCAGCAG TTCCTTAGGG 60
GCGATGTTTC CTCCTCAGGG AAAGACTGAA CTGGGATTGC TGGGTCTGAA CTGAAGGCAG 120
CAGGCTCCAC ACTGGCCTGA CCTGCATCCC TGGAGGAGAC CCAGCTCTCC ATTCTTTGTG 180
TAATTCAAGC TTTGTCCTTC TGTACTCTAA CTAGGGAAGA GGGTATGGTG ACTCTTTTAC 240
TGACCTCCTG TGGGGCAGTT GCTGGTCCTT TCTATCCTCT GCTCTCTGAA GGTCAGCATC 300
ACCAAGGTCA ACACACTCTT GGCTTAGAGG GTTTTGGGAA GCCATTTGTT TCCAGAACTG 360
GAAAGAGGAC ATAAATCCAA TGTGTGGGGG GAAAATGGCT GGAGCATTTC AGGAGCCTTT 420
GGTGGATCAA GTGCTCCACA GGGCACGTGA TTGGCCTCCC AGGCTCAGGA GGTCTGGTGG 480
GCTCTGGCCT CCACACACTA CAGTTTCCAA GATCCTAAAG ACTCCCCAGG TTCAGGAGGA 540
GCTCTCAGGG CTGATTTCTG AGGCCCTGGA CGTGCAGCTG TGCAGAAACC TCAAGGCTCA 600
GGGGAAGCAG CTGGAAATGC TCCTGGGATG TGAACTGGGG TGGGGGAGAG AACGGCAAGG 660
GAGGATGCTA ACTGCAGGTG GTGATGGTGG TTTTGGACCA TTTCCGGGGA TTGAGTGTAA 720
GAGCAGGGGA AACTGGGCAA GGCCCCAGTC ATCTGGCAAA GCAATAAGAT GCATTTCCGA 780
GACCCTGGAA CATCAATGGA TTTGCAGGGG TCAGGGATTG AGGGAATAAA ATCTACGTGT 840
CTTTCAGTTC AGGAAAGGCA ATAGGGACAG AGATGGTGGT TTATAGCAGG GTTTCTTAAA 900
TATGATTTAC ATTCAGATCC CCTGGAGATC TTGCTAAAAT GTAAATTCTG ATCCAGTAGT 960
TCTAGGGTGG GGCCAAGATT CTGCATTTCT AACAAGCTCC AGATGAGGTT GATGCTATCT 1020
TGCTGGGAAT CAAACTTTGT GTTGCAAAGG CTTAGAAGAT CCTGTTGGGC CACACTTCTG 1080
CATTCCAGGA GAGATTAAAT GTTCTGACAT CAAGACTATT TGGAAGGGTT CCAGGAAAGG 1140
GAGCAGGTGT CTGAGGACAA AAAAGAGAAC ACTTCAGAGC ATCAGGGATA TTGGAAGATG 1200
TGAATGCCTA AAGCCAGGGA ATGTTAGGAG AGGCTCACTT TATCACTGGG CCCTGAGCCC 1260
CAGAGATCTG TGTTTCTGCA GGAGTGCAGA ATAATTAGTA TTAGAGGGGA CCTGACAGAT 1320
CTTCTAGTTC AGGCCTGCAT AATATAGATG AGGAAAGGAG CATGAGATGC CCAAGATTAC 1380
ACAGCCAGTT AGTGGCTAAG CTGAAAGACC TTGTATGTGG GCTCAGTGGT TTGCAGTTCC 1440
TCTTGTTAGC AATGTAGAGC CATGAAAAGA TTTAAAGAGA ATTTTATTTC AGAACAATTT 1500
TCTGGTGGAA GTTGAGAGGA CCACATGCAA TCAGGAATTA AGCAGATTAC TTAGAGCCTT 1560
CTACCCTAGG ACAAGCAAGA GATGATGAAG GCCTTAGCTG TAGCAATGGG AATAGAGAGG 1620
GAAAAAATAT TTAAGAGGCA TTTAAGAGCA AATCAATGAG ATTTGGAGAT TAATTTTTGT 1680
AGAAGGTGAG GGAAAAGGAG GCATCAAGGT TGATCCCAAG TGTGTGGGTT AGGCAAAAGG 1740
|
