| Tag | Content |
|---|
EnhancerAtlas ID | HS133-09557 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr14:90979660-90980760 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxo1 | MA0480.1 | chr14:90980048-90980059 | TCCTGTTTACT | + | 6.32 | | Myog | MA0500.1 | chr14:90979780-90979791 | CCGCAGCTGTC | - | 6.32 |
|
| | Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
| SE_03967 | chr14:90977506-90981551 | Brain_Anterior_Caudate | | SE_05763 | chr14:90977461-90990749 | Brain_Cingulate_Gyrus | | SE_06526 | chr14:90975827-90992794 | Brain_Hippocampus_Middle | | SE_24186 | chr14:90978224-90980896 | Colon_Crypt_2 | | SE_28244 | chr14:90977561-90981612 | Fetal_Intestine | | SE_29280 | chr14:90977514-90981571 | Fetal_Intestine_Large | | SE_31992 | chr14:90977580-90981435 | Gastric | | SE_33611 | chr14:90974537-90981544 | H2171 | | SE_41893 | chr14:90978205-90981022 | LNCaP | | SE_47878 | chr14:90978319-90980144 | Pancreas | | SE_47878 | chr14:90980189-90980919 | Pancreas | | SE_65518 | chr14:90974579-90981557 | Pancreatic_islets | | SE_66921 | chr14:90974537-90981544 | H2171 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I090511 | chr14 | 90977667 | 90981615 |
|
Enhancer Sequence | AGCTGGGCAG CCTCCCTCTA ACCTCCCCGG GGAATGGCCT GGGGACTTAG CCAAACGCTG 60
ACAACCAGTG TGTGAGGGAC AGGTGGACGC TTCCCAAATC AGCTCTGTGC AGAGGACAGA 120
CCGCAGCTGT CAGGCCTATG TTGGCCTGAC CCTCCCCTGT GACCTTGGGC CAGGGACCCC 180
CTCCAGTGTC AGCGTCCCCA TCAGAGCCTC AAGAGCTGAG CCAAGTGACC CTTCTGATGC 240
TCCCTAGCCC TGCCACTCAG CTCCAGCTCA GCCCCAGGGA AGCCCCTCCA CTGTGGGGAC 300
TCACCTGGAG CTACCTGGGG CATGAGCAGC TGAGGAAGGA AAGAAAATGC TCTTTAAGTT 360
GTCATAACAG AGCGGGGCCT CCAGCACCTC CTGTTTACTG AAGGTGAGTA AATACAGCCG 420
GGCCCTTAGC AACAGGCACA AAGGGGCCCT TGTGCCGCCC GCTGCTCGCT GCTCGCTGCT 480
CCCTTGGCTC CCTCCCTGAG CTCAGCCCCA GCTGGGAGCT CTCTGAGAGG CAGGCTGGCC 540
TGGCCCACAG CCCTGGCCTG ACTGGGTGGG GAACGGGGCG GGTGCAAGGA CTGCTGTGTG 600
CCAGTCTCCA GGCGTGTCAG GGAGCCAGGC CTTTAGAGGG CCCTGTCCTC TGCAGGCAGA 660
AAATTCCACC CCATTCTTCT GACCAGCAAA CTGGGGTTCT GAGAGGCCCC TGATTTGAGT 720
TTGTCACTCA GAGATGGAGC GGGTGAGCCT TAGACCAAGA AGCCCTGAGT TGGACGTCAG 780
TCTCGGCCAT GGGCGCTTTG GCGTGTTCTG TGTTACGAGT CCCAGTCTCT TCATTTCTAA 840
CAAGGGGCTC ATGCATCACG CCTGGCTCAC CTGGCTGCGT GCGCATCAAA TCAGATGAGT 900
GTGTGAGGAC GTTCATTCTA AACTTTACAA GCTCTGAGCA AACAGAGGGA GTTATTATTG 960
GGCCAAGCGG GCAGACCAGA CATTAGAGTT GATGATAAAT CGGTCGGGCC CCTGTCAAGC 1020
GCTAGGAGCT TCCAGAGCCC CCTTTTGAAT GATGAGGTGT CACGCCTCCT GGAACCCCAG 1080
GTACTGGCAG CCGACTCCAT 1100
|
