| Tag | Content |
|---|
EnhancerAtlas ID | HS133-21377 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr22:37821220-37823330 |
Target genes | | Number: 25 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB1 | MA0018.3 | chr22:37821600-37821612 | AGTGACGTCACC | + | 6.22 | | CREB1 | MA0018.3 | chr22:37821600-37821612 | AGTGACGTCACC | - | 6.22 | | Myog | MA0500.1 | chr22:37822626-37822637 | GACAGCTGCTG | + | 6.14 | | SP2 | MA0516.2 | chr22:37823226-37823243 | CCAAGCCCCACCCCCAC | + | 6.3 | | Tcf12 | MA0521.1 | chr22:37822626-37822637 | GACAGCTGCTG | + | 6.02 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_33401 | chr22:37821925-37823844 | H2171 | | SE_34378 | chr22:37821150-37826102 | HCT-116 | | SE_61487 | chr22:37701837-37826067 | Toledo |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH22I037426 | chr22 | 37822081 | 37822370 | | GH22I037427 | chr22 | 37822421 | 37822664 |
|
Enhancer Sequence | GGCCTGGCTG GGATGAAGAG GAAAACAGGG ACTGGGGAGG TCAGATAGGG GGCTGCAGCA 60
CATTGGAGGC CTCCAGGCCC ACCTGGCAAA GGAGTTCAGC AGCCAATGGT GCTGATGTGA 120
GAACCTCCTT CGGGGGTTCC AGTCCTGGAA GGTGCACTCT TCAGGGGGCA GGACTTAAGG 180
AAAGGGGTCC CATGCCCACT CAGGATGCTG GGAAAGGCGG CCTCTTGGGA GGGACCACGC 240
CACGCGTCCT AAGGCTCCAT CCCTCTCCCC TTCCCACCCC TCATATACAA GAGACATAAC 300
CACACTCGGC CACACACACT CCCGTGACAT CACATTTACA CACTCTGGCT GGGGGGAGCA 360
ACCTCCGACA AAACTGTCCC AGTGACGTCA CCTGCGGCCT GGAGCTTATG TCACACCTGA 420
GGTTCTCACT GACCTCACAT ACATACTTTT TCCTGATGTC CCCACAATTA ACACTCTTTC 480
TTCCTGCCTA GGCGTTGATG GCCCAGAGGT ACCCACCTCC CCACCCACAC AGTTGCAGGG 540
CCCCCGGCTC ATCAGGACAG CACCTGCCTG TGCACCCCTC TCAGGGGACA CACATGCCCA 600
CATGCTTTGC TGATGGCCCA GACGTGACAC GTCCCACAGG TGTCCACGGG CCACGAGAAC 660
AGGGGTGTCA GCCATGCACA TACACATACA CACACACACA CACACACACA CACACACACA 720
CACTCCCAGT CCCATCTCAT GATGCAACTT GCATATTAAA ACGCCTCTCG GTAACCGCGC 780
CGGGCAGTCC GCGCCCCACA GCTTCCACCA CATTCCTCCA GGTGCTGCCA GCACCCCCCT 840
CCCTCCAGCT TTCTGACTCC GACAGCCTGG CCTGCTGATA GCGACAGCCG CAGCCCAGAC 900
ACACACACAC ACTCCAGCCC AACACCTGCG TCTCAGCAAG GGACCAAGGC AGTGCCCTCC 960
AGCCGCAGCT GCTGGGTGGG AGGAGTCCAG GGGGAAGGGG CATAGCACAG AGCCCTGAGC 1020
TGCAGAAAGT GCCGAGTACC ACGTTCCTCC CCAGCTGAGT GCACGGTCAG CACCACTGTC 1080
CCCTTCTCGT CTCCCTCCTT GGGCACGCCT GACACACCAT GGCCTGTGGC CTCTGTTTTG 1140
GACACAAGCT CCCCGAGTGT GCATGCACAC GCGCGCGCGC GCACACACAC ACACACATCA 1200
GCTCCCTTCC CTCCAAACAT TCCGAGGAAA TCCTGCCAGG CCACTGACAG TGTGCGTGTG 1260
TGCGCTTGTG TGTGTACAGA CAGAGAGCAG GGTCCACCCC ATGTCCACAC ACACACGCAC 1320
ACACCACACA CACACAGCAC GCACAATCCT CTCCACATGC ACACGGCGCC CCACCAGCCA 1380
ACACACCCAC CCCCTCCCCG TCCCCTGACA GCTGCTGGAG CCCACACACG CACGCACACA 1440
CACACACTGG CACGCGCTCG CACACACACA CAAACACACA CACACACACC CGGCAGTGGC 1500
CCCGGCCCTG CCAGAGCTGC AGTGTCTGCG ATTTATGCCG CCTCCCTGGG CTGCCTCCCT 1560
CCTTGTCCCT GGCCAGCGCC TCTGAAAGGG TCCCCACCCC CCAATTCTGG TCTTACCAAC 1620
CCCACCGCCG TCAAGCCCCA CCCTGGCCCC CCTTCCCCTA GAAGGCATCC ACCCCGTCAA 1680
CCCCTCTTAC CAGCTAGAGG ATGAATGCCT TGACCCGGCA GCACCCCGTG AAAGAGAGGG 1740
GTTAGGGCCC CCGATTCGAA AAGATGAGGG CAGAGAGGTG CAGTGTGGCA CCGGCTGGCA 1800
CACCGTCCAC CATCGAGCCT CTGCACCACC CCCAGAAACG CTCACCTCAC CGACCGTCCT 1860
CGGTGTCCTC CCACCGCCTC CGCCCACCGC CACCACCACC ACCTCCCTCG CGCAGGGTGG 1920
TCCCCCGGGG GTCTCACGGG GATCCCCAGA CCCAGGAGAC ACTGGGGGTG GCTCTCCCCG 1980
TCTCATCCCC CCTTCCGTGT CCCTCTCCAA GCCCCACCCC CACTGACGGA GGGGGTGCCC 2040
TCCGGCTCCA GCCCCGACTC CCACCGTCTC CCCGGTCGGT CGCGGCGCTC GGATCCAGAG 2100
GAATTCACTT 2110
|
