| Tag | Content |
|---|
EnhancerAtlas ID | HS129-16826 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr18:20722860-20724350 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr18:20723113-20723134 | TCCTTGTTTCAGTTTCCACTT | + | 6.14 | | SOX10 | MA0442.2 | chr18:20724334-20724345 | GTCTTTGTTTT | - | 6.14 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_47381 | chr18:20720461-20725099 | Panc1 | | SE_61169 | chr18:20705875-20723336 | HBL1 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH18I023139 | chr18 | 20719530 | 20724890 |
|
Enhancer Sequence | GCAGGCATTA TTCTAAGCAC TTTGATGGGA CTGAGTTCAT ACCTAGAAAC ACCCTGAGAC 60
AGTACTACCT TCACCTCCAT TTGGAAGCAC AGAGAAGTTA AGTAACTTGT CTGGGGTCCT 120
GTGCTCTGAC CCACCTCCCT CTGCTGTGCT ACAATTTACA GGTCAGGCTC ATGCATGCTT 180
GTTAAATAGG CTTCAGCTGA ACTGAGCAGA AGTTGACCTA AATGGCCTCA AGGGTTCCCG 240
ATCACTTGTG ATTTCCTTGT TTCAGTTTCC ACTTTTCTGT CATCTAGGGA AGACCTCTGT 300
GCATTTGGGC CCAGAGGACA GGCCAGGTTT TAAATAGGGA TTCCTGTGAC TCTGGCAATT 360
AACTCCCGCC CTCTGCCTGC CTGTGCTTCC TCTCTTCTTG GCCACAGCTG AATCCCTGAC 420
ACCTTTATTG CCTCTCTGAC TCACCTGGTA CATTACACAT CTTGTGTTAT ATAGAGCATG 480
GTACAATTAG CAACAGGAAC CTGGCCTCCT AAAGTTTAAA GCTCTGCTGG GTCCTCGTCT 540
GTGAAATGGG AATGATACTA CCACCTCCGC CCTGGGCGGG TTTCCCGCTG TATCTTCTCA 600
GCATCACCCT TTCCCCAACT GCCCCTCTGG CTGTTTATAA ATAATACTTT CTTGGAAAAA 660
CCACACCCAC TCGTGCAAGT CTTGCCTTTG GCTGCCTTTG TGCTACAAGG ACAGAATCGA 720
GTAGTTGCGA CAGAGACCAC ATGGCCTATT CCCTGGCTTG TCACAGAGTG GTTGTGCTTC 780
CCCCACCCTA GCCCAGTGCT CTGTGCCCAG GAAGTGTGCA GGTCCCCTTG GCCCCTTCCT 840
GCCTGCCTGC ACCCTCCTTG CCTTGTTTCA CAGCCTGGAT AATGTGGTGG CCCGAGGGGC 900
TCCTGGCTTC TGTTTGGACC CCTGTCAATC CCTCCCCCCC TGGGCTGTCA GAGGGACCCT 960
TCTGAAACCC ACATCTGATC CTGCCAGTCT TAAATTCCTG GTATTTCAGG CGAGGCAGCT 1020
GTTGGCTTGG GTCCTGGTTG CCACTGCAAC CTCCCCCGCT CCCACACACC CTCTGAGGCC 1080
TGTTGCTGCC ATACTGTGTT GTCTTTACAG AGGGCACCCA CGCTGCTCCG TGCCCCAGGC 1140
TCTGGCACTC TCAGGCTTCT CCTGGGGCAA GGCCTCCCAC AAGAGGCCCC TTCCTTCCAG 1200
CTCCGTCAGC CACAGAGCCA GCCGCTGCTC TCCCCATGCT CGTACACGCT CCTGGCTGGG 1260
CCTCTTCCTT CCCTGTGGAT CTGTGCTTCA GCCCTGGTCT GACTGGAGGG CCCCTCCTCC 1320
GTGGTCTGGT CAGAGCTTGA TGGATTGCCC TGGGGCCAGC TTTTGGTGGA ACAGACCACA 1380
TCTCTCCTCC ATAGGGAACA CAAATGAAAC TCCAATTCCC TAACAGTAAG AGGAGGAAAA 1440
TTTGATTCTG TTCCCCCACC CCACAACGTT CTAGGTCTTT GTTTTCATCC 1490
|
