Tag | Content |
---|
EnhancerAtlas ID | HS184-06760 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:120822070-120823560 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SREBF2 | MA0596.1 | chr11:120822510-120822520 | ATCACCCCAT | - | 6.02 | STAT1 | MA0137.3 | chr11:120822157-120822168 | TTTCTGGGAAA | + | 6.02 | STAT3 | MA0144.2 | chr11:120822157-120822168 | TTTCTGGGAAA | + | 6.32 | Spz1 | MA0111.1 | chr11:120822412-120822423 | AGGGTAGCAGC | + | 6.02 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH11I120952 | chr11 | 120823181 | 120824670 |
|
Enhancer Sequence | AGCTTCTTCT AGCTTCCCCT GGATAATGAA AGCTCAGAAG GCTGGTTGAG TTTAGCTCGG 60 TATTGGCAAA GGGAGTTCCC TTTTGTGTTT CTGGGAAACC CAGTGTAAAA ATGACATGCC 120 TTGATAGTGA CAGTAGGTTG CGCCATGACT GATACAATTT TGAGCTTAAA CGCTTACCTG 180 TTCATAGAAC CCTGAGCTTA GTACTGATTT TCAGTCCTAT CCATGGACTT CCTGGATTTC 240 TGGCATCATA GAATCATAGC GTTTTCCATT TACAATAGTC CTTAGGGTGC ATCTAGTCCA 300 GTGGTTTTAT AGTAAATGAA AGAAACCAGC CTGGGACAAG ACAGGGTAGC AGCATGGAGC 360 TGCAGAGAAT ATGCCCTGTC TCCAGTGGGC AGCCCACACT CAGCTTCAGC CAGTTGGGAA 420 GTTGGACTCA GTGGTGTTGG ATCACCCCAT TTTTTAAAAA GCCAGAAATC TAGATTTGTA 480 TGTGAAGTTA CCTAATTATT TAACGCTGGC AACTAATACA AACTAGGTAG ATGCTGCAGG 540 ATAAACAATT CAACTCTGTG GGCCGTATGC ATCCATAAGC CACTGGTGTG TCACCTCGGA 600 TCTATTCCCA CTCCAACTGA GGCCAGAAAG GGGTGGGAAC TTGCCTGAGA CCACACGGCT 660 AAAGACTTGG AGCAGATGAC TTAACTCCAT CCTTCTCATT CCATTTTGTT TTCCCGTGAA 720 GAATGGCGGG GAGCTTGGTG CCCAGGATTC CATTCCTGGC TCCATTGTCT GGCTCACAGG 780 ACTCTGGCCA GACTCATCCC TGGCCTTGCA ACGTGTTTTC CCACGGTGCA GTGGAGTGAG 840 CCCTGGGCTT TGAGTCAGGA AACATGGGCT TTTTTGGGTC CCGGCTCTTC CATTTACGCA 900 CTGTGGAACC TCGGGCACAT CTCTGACTGC CCTCGGCTTT GGCTTCTTCA CTTGTAAAAT 960 GAGAATAATA ATTTGTGCCT CCCAGGACTG TTTTGAGGTT GACGGGGGAA GGTCTCACTG 1020 TGTGAGATCA CCCTGCAAAC AAAACCCAGA GACTCCGGTT GTATTAGCAT CCTGGTGAAA 1080 AAGATGTGAG TGTCTAAGAG GGATGCTGTG GTCGAATTCA GCAATGCAGA CAGCAGCAGC 1140 TCAAAGGTGC TTCCTGAGTC CATCCTCCAC CCCCGATGGA GGACACAGGG TGGTACTTCG 1200 GGGCACTGAG GGTTGTTCCT CTTTGCCAGC ACAAAGCCTG CCTCACCCCA GGGAGTGGCA 1260 TGGCCCCTGC TGCTGTTCTG TGTCACCTGC TGAGGTCAGG GCTGGGTCGT GTCATTTGCG 1320 CAGCCCGGCA ACACCCTCAT TCCCAGTGTC ATTTAAACCA ATCACCCAGA ACCCACAGAA 1380 ATGGGAACTG GGGCCAGACC CACACTCACT ACCTCCTCTA CCCCGCCCTG CCTGCCCCAA 1440 GGTCATGTTG ACTGAATATG TGCGGTGAAT CTTGTTTTTC TCTCCATTTC 1490
|