| Tag | Content |
|---|
EnhancerAtlas ID | HS128-00249 |
Organism | Homo sapiens |
Tissue/cell | MCF-7 |
Coordinate | chr1:19979320-19981500 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:19980354-19980373 | CAGCGCCACCTTTTGGCAG | - | 6.12 | | FOXH1 | MA0479.1 | chr1:19980510-19980521 | TGTGGATTCGA | - | 6.14 | | GFI1 | MA0038.2 | chr1:19980913-19980925 | GAAATCACAGCA | + | 6.22 | | Gfi1b | MA0483.1 | chr1:19980914-19980925 | AAATCACAGCA | + | 6.62 | | TEAD1 | MA0090.2 | chr1:19981247-19981257 | ATGGAATGTG | - | 6.02 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_24802 | chr1:19981234-19982168 | Colon_Crypt_3 | | SE_26994 | chr1:19979780-19980770 | Esophagus | | SE_26994 | chr1:19981202-19982584 | Esophagus | | SE_52799 | chr1:19981212-19982414 | Small_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I019654 | chr1 | 19981203 | 19982711 |
|
Enhancer Sequence | AAATACAAAA ATCAGCCAGG TGTGGTGGCG AATGCCTGTA ATTCCAGCTA TTCTGGAGGC 60
TGAGGCAGGA GAATCACTTG AACCCGGGAG GCGGAGGTTG CAGTGAGCCA AGATCATGCC 120
ATGACACTCC AGCCTGGGCG ACAGAGTGAG ACTCTGTCTC AAAAAAATAG ATAAGTAAGG 180
CCGGGCGCAG TGGCTCACAC CTGTAATCCC AGCACTTTGG GAGGCTGAGG CGGGCGGATC 240
ACGAGGTCAG GAGATCGAGA CCATCCTGGC TAACACGGTG AAACCCCGTC TCTACTGAAA 300
ATACAAAAAA TTAGTGGGGC ATGGTGGTGG GCGCCTGCAG TCCCAGCTAC ACGGGAGGCT 360
GAGGCAGGAG AAGGCGTGAA CCCAGGAGGC GGAGCTTGCA GTGAGCAGAG ATCGTGCCAC 420
TGCACTCCAG CCTGGGCAAC AGAGCGAGAC TCCGTCTCAA AAAAAAAAAA AAAAAAAAAG 480
TACCTGGCTT TGCCATCTCC ATGGCCCATG GTAGGATTGT CCTAAATGGG ATGCCCAGTC 540
CCAAGCCACC TGACTCCTGG TGCTGGGCTT CTGTGGGGCC ACTGGGACCA GGACTTGTCC 600
CCTCTTCCTC CTGATTTAGC CTCATCCAGG CCCCTCTAGG GACTGTCCCA AGGTAAAGAA 660
TCCCTGACTG AGCGCATAGC TGCCTAGGAA GCCTGATCAA AACGCAGACT CCTACCCACC 720
CTAGAACTTT TACTCCACAA GTTCCTAGGG AATTCTGATC AAATTTCAGG TTTGGGAACC 780
ACTGGCCTGG CTCACTGCAC TCATTTTACA GGTGGTGGGG AAACAGGTCT GAGTGTCCCG 840
GTCACCCAGC ACACGTGGAC CCATGCCCTT TCTCGGCTGT GCCGTCCTCC GAGGGTTTGG 900
GGGCCTCCTT GAAGAAGGCA CTGCCCTCAT CTCTGAAGCC TCCCTCTCCC GTGCTTTTTG 960
CACTGGGGGG CATGGGTGAA ACTTACCTGG GGCGAGTCTC CTGAAAGCGG AATCCTTTGA 1020
CACAGACTGC CCTGCAGCGC CACCTTTTGG CAGATCCTGG TATTGTTTTA GTATCTCACT 1080
CCATCCTATA GCAGGGGAAT TTGCAAATGG CCAAGTGCTT AGCTTTGATT GGCTCCCGCT 1140
TGACTCACGT GTTAGAATGG GGCTGGGGAC AGTGATCTGT GTAGAGCCCT TGTGGATTCG 1200
AGTTTCTGGT GAGGCATCTT AGAGAACAAT ACTGTCTGGT TCAGGGTCAG TTTTTTTGCC 1260
TGAGGTCTGG CCAGCCAAGG TGGCCCAGGA ATTCACTGCA GGCCAGGTGC GGTGGCTCAC 1320
GCCTGTAATC CCAGCACTTT GGAATGCTGA AGCAGGAAGA TCGCTTGAGC CCCAGGAGTT 1380
TGAGACCAGC CTGGGCAACA CGGCGAAACC TGGTCTTTAC AGAAATTAGC CAGGTGTGGT 1440
GGCGGACGCC TGTAGTCCCA GCAACTCGGG AGGCTGAGGT GGGAGGATCA CCTGAGCCCA 1500
GGGAAGTCGA GGCTTCAGTG AGCCGTGATC ATGCCACTGC ACTCCAGCGT GGGTGACCGA 1560
GTGAGATCTT TTCTCAAAAA ACAAAACCAA AAAGAAATCA CAGCAACGTG AAGGTTAAGG 1620
CTAACTTTTC AAACATCAGA ATCCTGACAA TGGTTGCAGT AGCTTTCAAG GAGACATGGT 1680
GTGTGGCCAG CCCCTCCAGG GCTGTGTGGA CAGCTTTTTG TGTATTTTCC TGGGTGACTC 1740
ACAGCATCAA AGGGAGAAAG GAGGTAGTAA TTGTTCAGCA CTTGACATGT GCTTGAACAC 1800
TTCGTAATCG CAATCCTGTG CCAGGCAGTG GCACCATCTC CCCTTTTTAG ATGAAGAAAC 1860
CGAGGCACCG AGATAAAAAG TAACTTGCTC AAGGCAATTT AGGAAGTTGT AAAACCAACC 1920
AACACATATG GAATGTGTAT TATCTGCTAG GCTCATTTAA TATCTCATCT GACCTTCCAG 1980
ATACCCATCT GATGTAGGTA CCACTCCCAG CTCCAATTGT GAGATTCAGA GGGGAGAAAT 2040
AACTTGTCCA AAGTTGCACT TGGTTAGTAA GTGGGAGAGC TGGGGTTGCG CCAAGGAGTC 2100
GGATGCCAGA GTCCATGCTG TAACACCACT ACCCGGCCCC CTGCACCTTG CTGTGCCTCA 2160
CCTGGCACCT GTGCTCCGTT 2180
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