| Tag | Content |
|---|
EnhancerAtlas ID | HS098-12644 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:26426610-26428330 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata4 | MA0482.1 | chr12:26427483-26427494 | AGGAGATAAGA | - | 6.14 | | HOXA13 | MA0650.2 | chr12:26426734-26426745 | GTTTTATTGGC | - | 6.14 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_36295 | chr12:26423782-26429012 | HMEC | | SE_56564 | chr12:26423624-26427881 | u87 | | SE_56564 | chr12:26427913-26431666 | u87 | | SE_67856 | chr12:26423624-26427881 | u87 | | SE_67856 | chr12:26427913-26431666 | u87 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I026268 | chr12 | 26421461 | 26429582 |
|
Enhancer Sequence | AAGACACAAT TCAGCCCATA CACCATGTCT GTGACTTTCA AGAAGGCTGG GAACCATAGC 60
AACACACCAC ATTTAAATCA TCCAATAATG CCATTCCATT TCCTCTTCTT CCCCAAATGC 120
CCCAGTTTTA TTGGCCTTTC TGAGCTCCTT AGGCCAGTTT TCTCCAGGAT TTCAGTTCTC 180
TGTGGTGCTG AGGACATTCC CTGGAACATT TCCCTTGGGG ACAGCAGCAT TGCCAAGGTG 240
GAGGCCAATG TGCTCCCTCA CCCGCGACTC CTCCCTTGCT GGCCGTTCCC AGCTCAGCCA 300
AAGCAGAAAG TGAGGCCCAG TTAGAGGGTT GTGGTCTTGC CCGAGGAGCC AGGGCTAGCA 360
GACCTCCCAG TCCCCCAGGG GCAACGTTCA AAAAGATAGC CTTCTCCTCA TCAGCTTGTA 420
CGTCCTGTTG TGTTTACAAG CAGGCCTTCT CTGCATGAAA CAGGTTCCAG ATAAGGATGT 480
TCAGAATTTG TTTGGCTTCC CACCACTCCT GAAAAGTAAT TGCCTGGTAG TGCAGGCTGG 540
GAAAGAAGAC AGGATTACTG AGCCCAGAGA TGATCTCTTT TAACCCCTCT GTTTTTTTTT 600
TTCAGATCAA TTTAAAGTTA CTTTTCCTAC CCCTGAACCA GATCAACAAC CATCCCCTTT 660
ACTCTGGGCT TTGCAATTCA ACTCTATTTT CTATGATTGC AGTGCTGAGC TTATTAAACA 720
AAAGCAGCTC TTGTGAATCC TCTCCCTAAG ATGATCGTTC CTGGGTGGTC CTTCTTGGGT 780
GGGTCCCTGG GCACAGAAAC CCCAGGCCAC GTTTCCTCCT CTGCTCAGCA CGCTGGGCAG 840
ATTCTGCCTC CCGCAGCTCA GCTCTGGCTC ATCAGGAGAT AAGATCAGAG ACACTACGGA 900
AGGGCCAGGT TTTAACAAGG CAGAAAATAC AAGCTATTCC AAACATGAGG CCTACTGTGC 960
AAAAAACAAA CCCCCTGGCT TTGGGGGCCC TCTCCTGGAG AGGGTTTCTC TGCTCATAAA 1020
GATTGGTATC AAGGGGTGAG GAGGGAGTCA TGCCATCCCA GCAGGACCTC CAGTTGAGGG 1080
CTTCACTTTC AATTACCCAA GAGCAGCTGT AGACTGCTGC TTATGTAATG GGCTCTGCGC 1140
CTCCTTCTCG GGAGGAGGAT GTGGAACCGT TTTGTGTTTG CTGAATAATG AGTCATGGTC 1200
AGAGTTAGGG AGCAGAAACA GTGACTCTCT CCCCTGCATT GCTTCATCCG GAACTTCTAG 1260
TAAAGAATGA TAAGCCCTGA GTCAGTGCCC AGTGGGGCCT GCCCTGGAAG GGGAAGCACC 1320
ACAGGAGGCT CTGAAATGCA GGCCCCACAG AGCCCACGCA CCAGGCTGAA GGAGACTCTG 1380
GGGGCATTTG AAGCCCAGAT GGGCTGCTTG CAAGAAGATT CACTGTTTAT TTAGGCCTGT 1440
AGCTGAGCTG CCAGGGTTTT CCTATCTCGG GTAATCACAG CTCCTCCAGC CAGGATCCAG 1500
GAGTGTTGGG GTGAAGACTG AGGCTTCAAA ATGAACAGAG CTTTCTCCAA ACCTCATTTT 1560
AGCTCTAAGA AATGAAACAA GTCAGCCGTA CACGGTGGCC CTGCTGTAAT CCCAGCATTT 1620
TGGGAGGCTG AGGCGGGCGG ATCACGAGGT CAGGAGTTTG AGACCAGACT GGCCAACATG 1680
GTGAAACACC ATCTCTACTA AAGATACAAA AAAATTAGCC 1720
|
