| Tag | Content |
|---|
EnhancerAtlas ID | HS183-04031 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr3:196731610-196733410 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr3:196732609-196732626 | TGGGTCACTGTGACCTT | - | 7.26 | | ESR1 | MA0112.3 | chr3:196732609-196732626 | TGGGTCACTGTGACCTT | + | 7.53 | | ESR2 | MA0258.2 | chr3:196732610-196732625 | GGGTCACTGTGACCT | + | 6.66 | | ESR2 | MA0258.2 | chr3:196732610-196732625 | GGGTCACTGTGACCT | - | 7.45 | | PPARG | MA0066.1 | chr3:196732608-196732628 | ATGGGTCACTGTGACCTTGA | + | 6.59 | | PPARG | MA0066.1 | chr3:196732607-196732627 | CATGGGTCACTGTGACCTTG | - | 6.76 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_28391 | chr3:196730035-196732961 | Fetal_Intestine | | SE_29052 | chr3:196730047-196732985 | Fetal_Intestine_Large | | SE_29052 | chr3:196733040-196735809 | Fetal_Intestine_Large |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I197006 | chr3 | 196733041 | 196735809 |
|
Enhancer Sequence | ATGCATGAAT GTCTATGTAA AGTGTTAAGT ACTGATCAAG GAGGAACGAA GGAGTCAGGT 60
GGCTCTCAGT CTTTTTGGAG GGACTCGCAG ATCCTCCTGA AGATCTGATG AAAGCTGTCA 120
GCCTTCTCCC CAGAAAAATG CACATCCACC CAGGATTCTT CTCCCACATT ACTTCAGAGG 180
ACTTAGCAAC CCCCTAGGGA AGCCCAGGGA CCCAGAGTAA AGCACTCCTG GGATAGAGGG 240
GTTCTGTGGG GAAGATGACA GGAAGGAACA TGCGTCAGTT CACAATGTCA AAGTTTAGGA 300
ACAGGCCTGG CGAGCCAGCC AGCTCTGCAG TTCTGTGGTG CTGGTGGGTG TGGAGAAGGC 360
AATTTCAGCA TAAGTCGGGG GAGGGGGAGT GGTTAGAAAC CAGTGGCTCC ATTGTGAGAC 420
AACCTGGGTT TAAATTCTAG GTATATTTTG AAAGCACAAC CAATGGGATC TGCTGATAGA 480
TTGGCTGTAG AGCACGAGAG GAAGACCGGA GTCAAAAATG ACTCCCGAGG AAATGGAAAA 540
GCTAAAGTTG CTCTTAATTG AAGTGGGGAA GACTGAAGGA GGGACGGGGG TCCAACTTTG 600
GACTTGATCC ATTTGAGATG ACTGTTAGAA ACACAAGTCA AAATGTCAAG TATGTAGTTA 660
AATATGCAAG TTTGGGACTG ATGTCTGAAG ATGTAAATTT AGAAGCCATC TGTATATAGA 720
TGGTATTTGA TGACATGGGA TTGGATGAGA TCAAGGGTAA GCTGTAGACA GGGAAGAGGG 780
CTGAGAACTG AATCCTAGGG CTAACAGGTC AGGGAGATGG GGAGGAAATC AGCAGAGAAG 840
ACTGAGGAGT GGCCAGAGAG TGAGAGGACA GCCAGGCAGG GCTGAGGACC TGGGCATCTG 900
CAGGGGAAGG TGTTTCCAGG AGGAGGGAGA GCTGTGGCCA GTGCCACTGA GAGGTCAAGT 960
AAAATGAAGA CTGAGAAATG GCCACTGGGT TTAGCAACAT GGGTCACTGT GACCTTGACA 1020
AGAACAGCTT CAGGGCCCTG GTGGGAGCCT GTCTGGGGTA GTCTCCATCC TTAAGAGGGG 1080
CCAGAGGAGA GGACTTGCTA ACTCAGTCTC CATCCTTAAG AGAGGCCAGA GGAGAGGACT 1140
TGTTAACTCC AGAGCAGACC ACTCTTTGGA GGAGTTTTGC TTCGAAAGGG AGCAGGATTG 1200
GCCGGGCACA GTGGCTCATG CCTGTAATCC CAGCACTTTG GGAGGCCGAG GTGGGCGGAT 1260
CACGAGGTCA GGAGATCGAG ACCATCCTGG CTAACACGGT GAAACCCCTT CTCTACTAAA 1320
AAATAGAAAA AATTAGCCAG GCATGGTGGC GGGTGCCTGT AGTCCCAGCT ACTCAGGAGG 1380
CTGAGGTGGG AGAATGGCGT GAACCCGGGA GGCGGAGCTT GCAGTGAGCC GAGATAGTGC 1440
CACTGCACTC CAGCCTGGGG CGACAGAGTA AGACTCCGTC TCAAAAAAAA AAGAAAAAAA 1500
GGGAGCAGGA TTACAGCTGC AAGAGGATGG ATGTGAGACC AAGAGGTTAG TTTGTTCTTT 1560
AAGGATGGCA GAAGTCACAG CATGTTTCAT GTTGGTGAAA ATGGTCCGAC TGAGAAGGGA 1620
AAATCAACGA TGCAGGAGGC AGAGGGGACA GTTTCTGGAG GGATGTCCTT GCGTAAGTGA 1680
AAATCACAGA ATTTCCCCCG GGCTTCCTCA ATTTCTCTAG AGGTCTGCTC CAGGTAGACT 1740
GAGGCCTCCC AGGGGCTCAG CTTACCTCTG CTGCACACCC CTCAATGAGG TAGCCCCACC 1800
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