| Tag | Content |
|---|
EnhancerAtlas ID | HS133-28158 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:27154600-27155820 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mafb | MA0117.2 | chr7:27155126-27155138 | AAACTGCTGACG | + | 6.02 |
|
| | Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
| SE_00186 | chr7:27153688-27196950 | Adipose_Nuclei | | SE_01778 | chr7:27152517-27156266 | Aorta | | SE_02515 | chr7:27154495-27158695 | Astrocytes | | SE_26049 | chr7:27153676-27170089 | Duodenum_Smooth_Muscle | | SE_27292 | chr7:27152313-27161149 | Esophagus | | SE_27833 | chr7:27135447-27166356 | Fetal_Intestine | | SE_34080 | chr7:27149969-27156855 | HCC1954 | | SE_38361 | chr7:27150046-27165993 | HUVEC | | SE_38872 | chr7:27140071-27158123 | IMR90 | | SE_44881 | chr7:27139764-27158843 | NHLF | | SE_47354 | chr7:27153682-27163924 | Panc1 | | SE_54521 | chr7:27135483-27172379 | Stomach_Smooth_Muscle | | SE_64791 | chr7:27153673-27155561 | NHEK |
|
Enhancer Sequence | TGATTTTCCT CCTAAAGCCT CCTTTGCTCC CAGCTTCAGA AGCAAACTCT GCAAGGGTAC 60
GAGTGTGGCA AAAAGAGAAA TGGAGATTTC TCTCTTTTGC TGCAATCCCA AGGCGTCAAC 120
GGCGGGTCCT TCTCAAAGGA AGGTGTTAAA AATATAAGTA GTATGTTTAA ACTGTCAAGG 180
AGCCAAAGTG TCACCTTAGA GCAAAAACAA AGCCAGGGGA AAAGGGAGAA ATCAAAAAGC 240
ACTCCGGGCC AGGGTGGCCT CATGCATACC AATGGTTTTT GTCATTTATG GCTGGGCAAG 300
ATTTATGACT CGGCGCCCCA AAGCTGTAAA CAGAGCACAA AACAGCAAAC ACTTGCTCCT 360
TATGGCATAT TGCAGAGCAA CTTGAAAGGG GGAGCTGGCC GCGTAGGAGG TGAGAGCCAG 420
CCGCAAAAAT CCGTTCGGCG GCATTTTCTC TTCAAACCCG CCCGGTCGGA TGTGGCATTT 480
GAAGAAAGAA GGCGTGGGTC AATAATCAAC CCGCACTTTC TCCTCCAAAC TGCTGACGCG 540
ACTCTCACCG CCTTCTCAGC TAAGCCAGCT GCCGGGAAGG CCAGCTCTCC GTAAGAACCT 600
GCCAGGGGAA GGGATTCTCT GGGCCAAGGG GACCGAGGGC TCCCGAGCAA GGGCTGGGGC 660
GCCCTGAAAG CATACCTTTC CACTGGCGCC AAGACCCTGC CGGGCAAAAC GCGGGGACCA 720
GACCTGAGGA GCCGTGGGAG CCCAGGGAGA TCTGGGGCGG GAGCTTCGTT CCGGCCAGGG 780
CCTCTATCCG CCCCGATACG TGGCTCCTGG GCCGCGGGCC TCAGCGGGCA GAAGTGGGGC 840
TCCGACCTCA AGATGAAGGT CCAGCGTCCT GGCATGCAGA TGGTCGGTGC CCCAGCCTCA 900
AGCCGCTCTG CTTAAATCCA AAGGACTGGC TTTGGAGCAA GCGTAGGCGA GATTATTTTA 960
AAATAATAAT TTATGCTGGC GGAAGGTTTT TATTTGTTGG TTTGCTATTG GTGTTTTGTT 1020
TTTTAAGCGA AAATGCCGAT TGTTGATTTC CACCTCCAGA AATTACCAGC CGCCGCCGCT 1080
GCGCCCTTTC TAGACAAATC CCACAGCAGT TCACCCGGCT CCCCCAAAAC CGCAGAGCTT 1140
TTCTTTACTG AGAGGACCCC TTGGTTCCAC CAATTCCCCC AAATCCCCGT GGCTCCCGAT 1200
CTCTCATCCA GGGGGACTAG 1220
|
