| Tag | Content |
|---|
EnhancerAtlas ID | HS184-03214 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr10:5595780-5597080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat6 | MA0520.1 | chr10:5597060-5597075 | CGGTTCCAGAGAAAC | + | 6.01 | | YY1 | MA0095.2 | chr10:5595796-5595808 | CAAGATGGCTGC | + | 6.74 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_01815 | chr10:5586026-5602000 | Aorta | | SE_23255 | chr10:5586122-5596896 | Colon_Crypt_1 | | SE_23903 | chr10:5596019-5596709 | Colon_Crypt_2 | | SE_26546 | chr10:5595302-5597698 | Esophagus | | SE_28423 | chr10:5595944-5597068 | Fetal_Intestine | | SE_29163 | chr10:5595804-5597101 | Fetal_Intestine_Large | | SE_31858 | chr10:5595239-5597663 | Gastric | | SE_33798 | chr10:5595640-5597732 | HCC1954 | | SE_35816 | chr10:5586338-5596910 | HMEC | | SE_43480 | chr10:5585632-5597821 | MCF-7 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I005543 | chr10 | 5585826 | 5597559 |
|
Enhancer Sequence | CAGGGAATCT GCCATTCAAG ATGGCTGCTA GAAAATGGCG ATTCTACCTC CCAGGTGACT 60
CCAAGGGCTC TTACCCAGAG TCCTGAATAG CCACAGCCCA GCCCAGGAGT CCTAAAAGGA 120
ATTCTAGAGT GACCCGGATG GTTGTAAGGG CCTGAGAATG ATCTGTGCCG TTCGGCAGAG 180
ACCCAAGTGC TCTCGGAGTG ACCCAAACCT CAGGGCTGAG AACAGCTCGA GGTTCACCTG 240
GACTTACCCC TGCTCCCCCA CAGATCCTCG GTGCACCCTG GGATTTCCAC AGCCACGTGG 300
ATTTTAAGCC AAATCCAGGA TGATCCCATG ACACACAGGT CTCAGCTCCC CATGGGGCAT 360
TTCTCTCCAA GACCACCTTC CTCCCCAGCT CACCGTCCAC GTCTACAGAG CCATGCACCT 420
CCGTGGCAGA GCTGAGTGCA CGTGGCACAG AGTCAGGGCT GACATTGAGC AGGGCACCCT 480
TGGTCTCCCC CAAGACCCAT CAGAGTGTGC CTGGCACTGC CTTTCAATAA AAAGCCCAGG 540
GTCTGAGCAG GGTGGGGCGT CTCCCCTCCC CCAGCCAGGA TGAAGGTCAG AGCTGAATTT 600
GCTCAGTTCA ACACCAAAAA CAGTCCTGAA GGAAAATGTG TTGAGCTTGG CTGTAAGCCA 660
GGTCGTTAAA CATGGATTCT GATCACAGAT CGTTTCTGCT AATTAAACAA ATATTTTTGC 720
AGAGCTGTCT CGGTTTCCGC TGTTGCCGTT GGCCTAAGTT GCTGGCAAAC CATTGGAGCC 780
ATGCCCCGAA AGTCAGCTCA GATCAGAGGA GAACACACAG AACTTTTGAA GGAACAGCTA 840
AGACAGGTCT TCCAAACAGA GAGCTCTGTT CAGAGAGAAG GAACAGGCAA GAAAACACCG 900
ACACCTCCAG CCCTTACAGT CACCAAGCTG TACTTTCAGA TTCCTGCTGA CATACACACA 960
CACACACACA CACACACACA CACACACACA CTCTCTCTCT CTCTCTCAAT CCCTCCCTCT 1020
CTCAGAATGC ATAGTCCTTC TCCCTGCCTC CATCTCTAAA GCTACACCTG CACACACAAA 1080
TAAGCATTCT AGCAGTGCAA TCACTATTCC AAGTTTGAAG ACTCGTGTGT GTGTGTGTGT 1140
GTGTGTGTGT GTTTTCCTGC TGAAGTGGAG AGAAAAGGGC CAGACAGGAT GGGCCCTGGG 1200
TCCCCATGTG ACGTACCCCA GCAGGGGTCC TTTGCTCCTT CAAAAATGCA ATTATCACAA 1260
ACTTCCCTCG CCCTGGACCG CGGTTCCAGA GAAACGCCCA 1300
|
